U.S. patent application number 12/318829 was filed with the patent office on 2009-08-13 for method of classifying antibody, method of identifying antigen, method of obtaining antibody or antibody set, method of constructing antibody panel and antibody or antibody set and use of the same.
This patent application is currently assigned to Institute for Antibodies Co., Ltd.. Invention is credited to Yasushi Akahori, Masachika Azuma, Nobuhiro Hayashi, Gene Kurosawa, Yoshikazu Kurosawa, Kazuki Matsuda, Miwa Morita, Chiho Muramatsu, Keiko Ogawa, Noriko Satou, Mamoru Shiraishi, Atsushi Sugioka, Mototaka Sugiura, Mariko Sumitomo, Kazuhiro Suzuki, Akihiko Takasaki, Miho Tanaka, Susumu Tsutsumi, Yoshinori Ukai.
Application Number | 20090203538 12/318829 |
Document ID | / |
Family ID | 38923207 |
Filed Date | 2009-08-13 |
United States Patent
Application |
20090203538 |
Kind Code |
A1 |
Sugioka; Atsushi ; et
al. |
August 13, 2009 |
Method of classifying antibody, method of identifying antigen,
method of obtaining antibody or antibody set, method of
constructing antibody panel and antibody or antibody set and use of
the same
Abstract
It is intended to provide a method whereby a plural number of
antibodies against cell surface antigens are quickly classified and
to provide a method whereby antigens of the thus classified
antibodies are quickly identified. Further, it is intended to
provide a method of promoting the utilization of the useful data
obtained by the above methods. Furthermore, it is intended to
provide an antibody which is effective in treating or diagnosing
cancer. Namely, a method of classifying antibodies which comprises:
(1) the step of preparing a plural number of antibodies
respectively recognizing cell surface antigens; (2) the step of
bringing each of these antibodies into contact with a cell of the
same species; (3) the step of analyzing each of the cells having
been treated in the step (2) by flow cytometry and thus obtaining
data indicating the reactivity of each antibody with its cell
surface antigen; and (4) the step of comparing the thus obtained
data and classifying the individual antibodies depending on the
similarity. A method of identifying antigens which further
comprises: (5) the step of selecting one to several antibodies from
each antibody group formed in the step (4) and identifying antigens
thereof; and (6) on the assumption that antigens of the antibodies
belonging to a single antibody group are the same or highly related
to one another, making relations between the antigens having been
identified in the step (5) and the antibody groups to thereby
identify the antigens. An antibody against HER1, an antibody
against HER2, an antibody against CD46, an antibody against ITGA3,
an antibody against ICAM1, an antibody against ALCAM, an antibody
against CD147, an antibody against C1qR, an antibody against CD44,
an antibody against CD73, an antibody against EpCAM and an antibody
against HGFR, each obtained by using the above methods.
Inventors: |
Sugioka; Atsushi;
(Nagoya-shi, JP) ; Sugiura; Mototaka;
(Toyoake-shi, JP) ; Akahori; Yasushi; (Nagoya-shi,
JP) ; Hayashi; Nobuhiro; (Toyoake-shi, JP) ;
Takasaki; Akihiko; (Nagoya-shi, JP) ; Morita;
Miwa; (Toyoake-shi, JP) ; Kurosawa; Gene;
(Nagoya-shi, JP) ; Sumitomo; Mariko; (Nagoya-shi,
JP) ; Tsutsumi; Susumu; (Nagoya-shi, JP) ;
Ogawa; Keiko; (Toyoake-shi, JP) ; Matsuda;
Kazuki; (Nagoya-shi, JP) ; Muramatsu; Chiho;
(Toyoake-shi, JP) ; Satou; Noriko; (Toyoake-shi,
JP) ; Azuma; Masachika; (Nagoya-shi, JP) ;
Ukai; Yoshinori; (Nagoya-shi, JP) ; Suzuki;
Kazuhiro; (Toyota-shi, JP) ; Kurosawa; Yoshikazu;
(Nagoya-shi, JP) ; Tanaka; Miho; (Nagoya-shi,
JP) ; Shiraishi; Mamoru; (Nagoya-shi, JP) |
Correspondence
Address: |
EDWARDS ANGELL PALMER & DODGE LLP
P.O. BOX 55874
BOSTON
MA
02205
US
|
Assignee: |
Institute for Antibodies Co.,
Ltd.
Nagoya-shi
JP
|
Family ID: |
38923207 |
Appl. No.: |
12/318829 |
Filed: |
January 9, 2009 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
PCT/JP2007/063689 |
Jul 9, 2007 |
|
|
|
12318829 |
|
|
|
|
Current U.S.
Class: |
506/9 ; 435/7.2;
435/7.23; 506/18; 506/38; 530/387.7 |
Current CPC
Class: |
A61P 35/02 20180101;
C12N 2310/14 20130101; C07K 2317/565 20130101; C07K 16/303
20130101; C07K 16/32 20130101; C07K 16/28 20130101; C07K 2317/56
20130101; C07K 2317/73 20130101; G01N 33/57492 20130101; C07K
16/005 20130101; C07K 2317/732 20130101; A61P 35/00 20180101; C07K
16/2863 20130101; C07K 16/30 20130101; G01N 33/6854 20130101; C07K
16/2803 20130101; C12N 15/1138 20130101; C07K 16/40 20130101; C07K
16/2896 20130101 |
Class at
Publication: |
506/9 ; 435/7.2;
435/7.23; 530/387.7; 506/18; 506/38 |
International
Class: |
C40B 30/04 20060101
C40B030/04; G01N 33/567 20060101 G01N033/567; G01N 33/574 20060101
G01N033/574; C07K 16/00 20060101 C07K016/00; C40B 40/10 20060101
C40B040/10; C40B 60/10 20060101 C40B060/10 |
Foreign Application Data
Date |
Code |
Application Number |
Jul 10, 2006 |
JP |
2006-189872 |
Mar 8, 2007 |
JP |
2007-058458 |
Claims
1. A method of classifying antibody including the following steps:
(1) preparing a plurality of antibodies recognizing cell surface
antigen; (2) bringing each of the antibodies into contact with
cells of the same kinds; (3) analyzing each cell after step (2) by
flow cytometry so as to obtain data showing reactivity between the
antibody and the cell surface; and (4) comparing the obtained data
and classifying antibodies based on the similarity of the data.
2. The method of classifying antibody according to claim 1, wherein
the cell surface antigen is an intact cell surface antigen.
3. The classifying method according to claim 1, wherein the cell
surface antigen is a cell surface antigen of a cancer cell.
4. The classifying method according to claim 1, wherein the
plurality of antibodies recognize cell surface antigen are composed
of an assembly of antibodies derived from antibody clones selected
as being capable of recognizing a cell surface antigen, from an
antibody library.
5. The classifying method according to claim 4, wherein the
antibody library is a phage antibody library.
6. The classifying method according to claim 1, wherein the
antibody is an antibody to which a label material is bound or
fused.
7. The classifying method according to claim 1, wherein the
antibody does not include a label material and the method includes
a step of labeling the antibody bound to the cell after step
(2).
8. The classifying method according to claim 1, wherein the cell is
an established cell line.
9. The classifying method according to claim 1, wherein the cell is
an established cancer cell line.
10. The classifying method according to claim 1, wherein the data
are shown in a histogram showing a relationship between a binding
amount of antibodies and a number of cells, and the similarity of
the data is determined by comparing the shapes of the
histograms.
11. The classifying method according to claim 1, wherein the data
are shown in a histogram showing a relationship between a binding
amount of antibodies and a number of cells, and the similarity of
the data is determined based on one or more values selected from
the group consisting of a median value, a mode, a maximum value, a
range, a standard deviation, a kurtosis and a skewness of the
histogram.
12. The classifying method according to claim 11, wherein the
similarity of the data is determined based on the values of the
median value, the mode, and the kurtosis and a skewness of the
histogram.
13. The classifying method according to claim 10, wherein the
binding amount of antibody is shown by a fluorescence
intensity.
14. The classifying method according to claim 1, wherein in step
(4), a plurality of antibodies having the identical or high similar
data are classified into one antibody group.
15. The classifying method according to claim 1, wherein two or
more kinds of cells are prepared and each kind of cell is subjected
to steps (2) to (4).
16. The classifying method according to claim 15, wherein a
plurality of antibodies having the identical or high similar data
with respect to two or more kinds of cells in the cells are
classified into one antibody group.
17. The classifying method according to claim 1, wherein an
antibody that has been determined to have a low reactivity with
respect to the cell surface antigen during classification or after
classification is excluded.
18. The classifying method according to claim 1, wherein
classification results of antibodies are displayed as a panel.
19. The classifying method according to claim 1, wherein after step
(4), the following steps are carried out: (i) associating the
classified antibodies to a combination of n pieces of parameters
including a first parameter, a second parameter, . . . , and an
n-th parameter (wherein, n represents an integer of 2 or more, each
parameter has two or more parameter values and the same parameter
value is given to two or more antibodies in each parameter); (ii)
with respect to each parameter, preparing antibody mixtures of the
antibodies having the same parameter value; (iii) examining a
reactivity of each of the antibody mixtures with a target antigen
by an enzyme linked immunosorbent assay (ELISA) so as to specify
the antibody mixture which shows reactivity; (iv) specifying a
combination of a parameter name and a parameter value that are
common to the antibody group contained in the specified antibody
mixture; (v) selecting an antibody corresponding to the combination
specified in the step (iv) in terms of all parameters among the
antibodies subjected to step (i); and (vi) classifying the selected
antibodies into one antibody group.
20. The classifying method according to claim 19, wherein the steps
(i) to (v) are repeated several times under the conditions in which
the combination of parameters is different in each trial; an
antibody in which results of all trials are not contradictory is
selected; and the antibody is subjected to the step (vi).
21. The classifying method according to claim 19, further including
the following steps between the step (v) and the step (vi); (v-1)
newly associating the classified antibodies selected in step (v)
with a combination of n pieces of parameters in a same manner as in
the step (i); (v-2) with respect to each parameter, preparing the
antibody mixture of antibodies having the same parameter value for
each parameter; (v-3) examining a reactivity of each of the
antibody mixtures with a target antigen by an enzyme linked
immunosorbent assay (ELISA) so as to specify the antibody mixture
showing the reactivity; (v-4) determining a combination of a
parameter name and a parameter value that are common to the
antibody group contained in the specified antibody mixture; and
(v-5) selecting an antibody having the combination specified in the
step (v-4) in terms of all parameters among the antibodies
subjected to the step (v-1).
22. The classifying method according to claim 21, wherein the steps
(v-1) to (v-4) are repeated twice or more.
23. The classifying method according to claim 19, wherein n is
3.
24. The classifying method according to claim 19, wherein two or
more kinds of target antigens are prepared and the steps (iii) to
(vi) are carried out by using each target antigen.
25. The classifying method according to claim 19, wherein the
target antigen is an antigen selected from the group consisting of
HER1, HER2, CD46, ITGA3, ICAM1, ALCAM, CD147, IgSF4, BCAM, C1qR,
CD44, CD73, LAR, EpCAM and HGFR.
26. An identifying method of an antigen including the following
steps: (1) preparing a plurality of antibodies recognizing cell
surface antigen; (2) bringing each of the antibodies into contact
with cells of the same kind; (3) analyzing each cell after step (2)
by flow cytometry so as to obtain data showing the reactivity
between the antibody and the cell surface; (4) comparing the
obtained data and classifying antibodies based on the similarity of
the data; (5) selecting one or several antibodies from each
antibody group formed in the step (4) and identifying an antigen
thereof; and (6) associating the antigens identified in the step
(5) with an antibody group, based on the estimation that antigens
to antibodies belonging to the same antibody group are identical or
have high relationship.
27. The identification method according to claim 26, wherein in the
step (5), one antibody is selected from each antibody group.
28. The identification method according to claim 26, wherein in the
step (5), from the results of a flow cytometry analysis, an
antibody that is determined to have a high reactivity with respect
to an antigen is selected.
29. The identification method according to claim 26, wherein in the
step (5), the identification of an antigen is carried out by one or
more methods selected from the group consisting of an
immunoprecipitation test, Western blotting, affinity
chromatography, proteomics techniques (electrophoresis, mass
spectrometry, genome data base retrieve, and analysis by
bioinformatics), and an expression analysis of corresponding
gene.
30. The identification method according to claim 26, further
including a step of examining a reactivity between an antigen
identified in the step (5) and an antibody belonging to an antibody
group with which the antigen is associated in the step (6) so as to
confirm that the estimation is correct.
31. The identification method according to claim 26, wherein an
identification result of antigen is displayed as a panel.
32. The identification method according to claim 31, wherein the
panel is any of the following (a) to (c): (a) a panel displaying a
plurality of antibodies showing identical or high similar data in
the flow cytometry analysis in the step (3) as one antibody group
in which each antibody group is associated with its antigen; (b) a
panel displaying a plurality of antibodies showing identical or
high similar data in the flow cytometry analysis in the step (3) as
one antibody group in which each antibody group is associated with
a cell expressing a cell surface antigen recognized by the each
antibody group; and (c) a panel displaying a plurality of
antibodies showing identical or high similar data in the flow
cytometry analysis in the step (3) as one antibody group in which
each antibody group, its antigen and a cell expressing a cell
surface antigen recognized by the antibody group are associated
with each other.
33. A method of obtaining an antibody having a relationship with
respect to a certain disease, the method comprising the following
steps: (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to claim 1; (2) with respect to one kind or two or more
kinds of diseases, examining a reactivity between an antibody in
each of the selected antibody groups and a certain disease; and (3)
selecting an antibody in the antibody group, to which an antibody
having a specific reactivity to any of diseases belongs, as a
useful antibody.
34. A method of obtaining an antibody having a relationship with
respect to a certain disease, the method comprising the following
steps: (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to claim 19; (2) with respect to one kind or two or more
kinds of diseases, examining a reactivity between an antibody in
each of the selected antibody groups and a certain disease; and (3)
selecting an antibody in the antibody group, to which an antibody
having a specific reactivity to any of diseases belongs, as a
useful antibody.
35. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting one or two or more of antibody
groups from the plurality of antibody groups classified by the
classifying method according to claim 1; (2) with respect to one
kind or two or more kinds of diseases, examining a reactivity
between an antibody in each of the selected antibody groups and a
certain disease; and (3') selecting a disease to which two or more
antibodies show a specific reactivity, then selecting antibodies
from the antibody group, to which the antibody having a specific
reactivity to the disease belongs, and combining the selected
antibodies.
36. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 1;
(2) with respect to two kinds or more diseases, examining a
reactivity between an antibody in each of the selected antibody
groups and a certain disease; and (3) selecting antibodies from the
antibody group, to which the antibody having a specific reactivity
to any of disease belongs, and combining the selected
antibodies.
37. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 1;
(2) with respect to one kind or two or more kinds of diseases,
examining a reactivity between an antibody in each of the selected
antibody groups and a certain disease; and (3) selecting an
antibody from the antibody group to which the antibody having a
specific reactivity to any of diseases belongs, and an antibody
belonging to other antibody group whose antigen is common to that
of the antibody group, and combining the selected antibodies.
38. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing the common antigen from the plurality of antibody
groups classified by the classifying method according to claim 1;
(2) with respect to one kind or two or more kinds of pathologic
conditions, examining a reactivity between an antibody in each of
the selected antibody groups and a pathologic condition; and (3)
connecting information about the reactivity and then combining the
antibodies in the antibody groups.
39. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting one or two or more antibody groups
from the plurality of antibody groups classified by the classifying
method according to claim 19; (2) with respect to one kind or two
or more kinds of diseases, examining a reactivity between an
antibody in each of the selected antibody groups and a certain
disease; and (3') selecting a disease to which two or more
antibodies show a specific reactivity, then selecting antibodies
from an antibody group which the antibodies showing a specific
reactivity to the disease belong to, and combining the selected
antibodies.
40. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 19;
(2) with respect to two or more kinds of diseases, examining a
reactivity between an antibody in each of the selected antibody
groups and a certain disease in two or more kinds of diseases; and
(3) selecting antibodies from the antibody group to which the
antibody having a specific reactivity to any of diseases belong,
and combining the selected antibodies.
41. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 19;
(2) with respect to one kind or two or more kinds of diseases,
examining a reactivity between an antibody in each of the selected
antibody groups and a certain disease; and (3) selecting an
antibody from the antibody group to which the antibody having a
specific reactivity to any of disease belongs, and an antibody
belonging to other antibody group whose antigen is common to that
of the antibody group, and combining the selected antibodies.
42. A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps: (1) selecting two or more antibody groups
recognizing the common antigen from the plurality of antibody
groups classified by the classifying method according to claim 19;
(2) with respect to one kind or two or more kinds of pathologic
conditions, examining a reactivity between an antibody in each of
the selected antibody groups and a pathologic condition; and (3)
associating information about the reactivity and then combining the
antibodies in the antibody groups.
43. The obtaining method according to claim 33, wherein the disease
is selected from the group consisting of: kidney cancer, hepatic
cell carcinoma, gallbladder and liver cancer, alveolar cell
carcinoma, lung squamous cell cancer, pulmonary adenocarcinoma,
pancreas cancer, adenocarcinoma, and ovarian cancer.
44. The obtaining method according to claim 33, wherein in the step
(2), the reactivity is examined by one or more methods selected
from the group consisting of an immunostaining procedure, an
immunoprecipitation method, a flow cytometry analysis, cell ELISA,
an intermolecular interactive analysis between a disease-related
molecule (disease causative gene product and the like) and an
antibody, and application test to a disease model cell (or
animal).
45. An isolated antibody obtained by the method according to claim
33.
46. An antibody set obtained by the method described in claim
35.
47. A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps: (1) selecting one or two or more of antibody
groups from the plurality of antibody groups classified by the
classifying method according to claim 1; (2) with respect to one
kind or two or more kinds of diseases, examining a reactivity
between an antibody in each of the selected antibody groups and a
certain disease; and (3) associating the results of the step (2)
with each antibody and displaying by using a drawing or a tabular
format.
48. A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps: (1) selecting two or more of antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 1;
(2) with respect to one kind or two or more kinds of diseases,
examining a reactivity between an antibody in each of the selected
antibody groups and a certain disease; and (3) associating the
results of the step (2) with each antibody and displaying by using
a drawing or a tabular format.
49. A production method of a panel displaying a relationship
between an antibody and a pathologic condition, the method
comprising the following steps: (1) selecting two or more of
antibody groups recognizing a common antigen from the plurality of
antibody groups classified by the classifying method according to
claim 1; (2) with respect to one kind or two or more kinds of
pathologic condition, examining a reactivity between an antibody in
each of the selected antibody groups and a certain pathologic
condition of disease; and (3) associating the results of the step
(2) with each antibody and displaying by using a drawing or a
tabular format.
50. A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps: (1) selecting one or two or more of antibody
groups from the plurality of antibody groups classified by the
classifying method according to claim 19; (2) with respect to one
kind or two or more kinds of diseases, examining a reactivity
between an antibody in each of the selected antibody groups and a
certain disease; and (3) associating the results of the step (2)
with each antibody and displaying by using a drawing or a tabular
format.
51. A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps: (1) selecting two or more of antibody groups
recognizing different antigens from the plurality of antibody
groups classified by the classifying method according to claim 19;
(2) with respect to one kind or two or more kinds of diseases,
examining a reactivity between an antibody in each of the selected
antibody groups and a certain disease; and (3) associating the
results of the step (2) with each antibody and displaying by using
a drawing or a tabular format.
52. A production method of a panel displaying a relationship
between an antibody and a pathologic condition, the method
comprising the following steps: (1) selecting two or more of
antibody groups recognizing a common antigen from the plurality of
antibody groups classified by the classifying method according to
claim 19; (2) with respect to one kind or two or more kinds of
pathologic condition, examining a reactivity between an antibody in
each of the selected antibody groups and a certain pathologic
condition of disease; and (3) associating the results of the step
(2) with each antibody and displaying by using a drawing or a
tabular format.
53. A panel produced by the method according to claim 47.
54. (canceled)
55. A method of testing a disease in which a cell surface antigen
is an indicator, the method comprising the following steps: (1)
preparing a cell or a tissue separated from a subject; (2)
examining a reactivity between the cell or the tissue and each
antibody displayed on the panel according to claim 53; and (3)
collating the results in the step (2) with the panel.
56. A method of selecting an optimum treatment method for a certain
disease, the method comprising the following steps: (1) preparing a
cell or a tissue separated from a subject; (2) examining a
reactivity between the cell or the tissue and each antibody
displayed on the panel according to claim 53; (3) collating the
results in the step (2) with the panel, and (4) selecting an
effective antibody according to the results of collating.
57. The method according to claim 56, wherein the effective
antibody is an antibody showing a specific reactivity in the step
(2) or an antibody equivalent thereto.
58. The method according to claim 56, wherein the certain disease
is a disease in which a cell surface antigen selected from the
group consisting of HER1, HER2, CD46, ITGA3, ICAM1, ALCAM, CD147,
IgSF4, BCAM, C1qR, CD44, CD73, LAR, EpCAM and HGFR is an
indicator.
59. The method according to claim 56, wherein the panel displays
two or more antibodies selected from the group consisting of
048-006 antibody, 057-091 antibody, 059-152 antibody, 048-040
antibody, 054-101 antibody, 055-147 antibody, 059-173 antibody,
067-149 antibody, 067-176 antibody, 015-126 antibody, 015-044
antibody, 015-102 antibody, 015-136 antibody, 015-143 antibody,
015-209 antibody, 039-016 antibody, 053-216 antibody, 075-024
antibody, 075-110 antibody, 086-032 antibody, 086-035 antibody,
086-036 antibody, 086-061 antibody, 086-138 antibody, 086-182
antibody, 035-224 antibody, 045-011 antibody, 051-144 antibody,
052-053 antibody, 052-073 antibody, 053-049 antibody, 3172-120
antibody, 066-069 antibody, 015-003 antibody, 064-002 antibody,
064-006 antibody, 064-012a antibody, 064-012b antibody, 064-014
antibody, 064-054 antibody, 064-085 antibody, 064-093 antibody,
064-116 antibody, 065-183 antibody, 067-142 antibody, 068-007
antibody, 052-033 antibody, 053-042 antibody, 053-051 antibody,
053-059 antibody, 053-085 antibody, 035-234 antibody, 040-107
antibody, 041-118 antibody, 066-174 antibody, 083-040 antibody,
029-143 antibody, 045-134 antibody, 062-101 antibody, 062-109
antibody, 084-103 antibody, 052-274 antibody, 029-067 antibody,
083-131 antibody, 059-053 antibody, 064-003 antibody, 067-213
antibody, 067-153 antibody, 067-126 antibody, 067-133 antibody,
067-287 antibody, 064-044 antibody, 065-030 antibody, 065-358
antibody, 066-019 antibody, 079-085 antibody, 067-024 antibody and
076-048 antibody.
60. A method of selecting an optimum treatment method of a certain
disease, the method comprising the following steps: (1) preparing a
panel displaying a reactivity between one or more antibodies
selected from the group consisting of 048-006 antibody, 015-126
antibody, 067-133 antibody, 064-044 antibody, 076-048 antibody and
059-053 antibody, and a clinical cancer tissue of one or more
diseases selected from the group consisting of squamous carcinoma,
adenosquamous carcinoma, alveolar adenocarcinoma, adenocarcinoma,
and large cell carcinoma, and a cell or tissue separated from a
subject; (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel; (3) collating the results
in the step (2) with the panel, and (4) selecting an effective
antibody according to the results of collating.
61. The method according to claim 60, wherein the effective
antibody is an antibody showing a specific reactivity in the step
(2) or an antibody equivalent thereto.
62. The method according to claim 60, wherein the certain disease
is a disease selected from the group consisting of squamous
carcinoma, adenosquamous carcinoma, alveolar adenocarcinoma,
adenocarcinoma, and large cell carcinoma.
63-85. (canceled)
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation-in-part of international
application No. PCT/JP2007/063689, filed Jul. 9, 2007, which claims
priority to Japanese applications No. 2006-189872, filed Jul. 10,
2007 and No. 2007-058458, filed Mar. 8, 2008. The contents of these
three applications are hereby incorporated by reference in their
entirety.
FIELD OF THE INVENTION
[0002] The present invention relates to a method of classifying a
plurality of antibodies, a method of identifying antigen, a panel
displaying characteristics of an antibody, and the like, as well as
an antibody related to a disease and a use thereof.
BACKGROUND OF THE INVENTION
[0003] Success of Herceptin to breast cancer (see, non-patent
document 1) and Rituxan (non-patent document 2) to malignant
lymphoma B shows that an antibody is effective as a therapeutic
agent to a cancer. Certain antibodies exhibit an ADCC effect
(non-patent document 3) and/or a CDC effect (non-patent document 4)
by forming a complex with an antigen molecule existing on the cell
membrane and the effects kill a target cell (cell expressing an
antigen). The ADCC effect or the CDC effect may cause apoptosis.
Such an effect of an antibody is specific to an antigen. That is to
say, an antibody acts on cells expressing an antigen which the
antibody recognizes regardless of whether the cells are cancer
cells or normal cells. Therefore, the success in development of
antibody therapeutic agents to cancers is dependent on discovery of
antigens expressing in a cancer-specific manner and recognized by
an antibody so as to cause the ADCC effect or the CDC effect. An
antibody against to such an antigen is a promising candidate of a
therapeutic agent capable of reliably killing target cancer cells
while minimizing the influence (side effect) on normal cells.
[0004] In antibody drug development, it is essential to obtain
antibodies that recognize "intact state" target cancer antigens
existing on the surface of a cell membrane. However, since the
target cancer antigen is membrane protein, it has been difficult to
obtain an antibody against even known cancer antigen. In order to
solve these problems, present inventors have produced a huge human
antibody library including as many as 100 billion independent
clones and established a comprehensive acquisition method for
antibodies to proteins (cell surface antigens) existing on the
surface of the cell membrane of cancer cells and tissues by using
the library (patent documents 1 to 3).
[Patent document 1] WO01/062907 [Patent document 2] WO2001/096401
[Patent document 3] Japanese Patent Unexamined Publication No.
2005-185281 [Non-patent document 1] Mass R, et al.: The Concordance
Between the Clinical Trials Assay (CTA) and Fluorescence in Situ
Hybridization (FISH) in the Herceptin Pivotal Trials.: Proc Am Soci
Clin Oncol 19, 75a, 2000 [Non-patent document 2] Berinstein N L,
Grillo-Lopez A J, White C A, Bence-Bruckler I, Maloney D, Czuczman
M, et al. Association of serum Rituximab (IDEC-C2B8) concentration
and anti-tumor response in the treatment of recurrent low-grade or
follicular non-Hodgkin's lymphoma. Annals of Oncology 1998,
9:995-1001. [Non-patent document 3] Bruggemann M., Williams G. T.,
Bindon C. I., Clark M. R., Walker M. R., Jefferis R., Waldmann H.,
Neuberger M. S. (1987). Comparison of the effector functions of
human immunoglobulins using a matched set of chimeric antibodies.
J. Exp. Med., 166, 1351-1361. [Non-patent document 4] Loos M.
(1982). The classical complement pathway: mechanism of activation
of the first component by antigen-antibody complexes. Prog.
Allergy, 30, 135-192. Mol. Immunol. 1982 May; 19 (5): 651-7.
SUMMARY OF THE INVENTION
[0005] Currently, the present inventors can comprehensively obtain
antibodies to cell surface antigens. As the next step, it is
necessary to identify an antibody to each antibody and to screen
useful antibodies. However, it will take a much labor and time and
considerably high cost to individually identify an antigen for the
comprehensively obtained antibodies.
[0006] Furthermore, the comprehensively obtained antibodies may
include unnecessary antibodies from the viewpoint that they do not
have sufficient affinity and reactivity, or they have substantially
the same as the other antibodies. Therefore, method for efficiently
screening useful antibodies has been demanded.
[0007] On the other hand, the comprehensively obtained antibodies
may include antibodies such as candidates of diagnostic agents and
therapeutic agents, which are extremely important from the medical
viewpoint.
[0008] Under such circumstances, the present invention aims at the
effective use of comprehensively obtained antibodies to cell
surface antigens in medical fields and research fields, and has an
object to provide a useful method therefor. That is to say, the
present invention has an object to provide a method of classifying
a plurality of antibodies to cell surface antigens rapidly. Also,
the present invention has another object to provide a method of
rapidly identifying an antigen for the antibody. Furthermore, the
present invention has a further object to provide a method of
promoting to use useful information obtained by such methods. The
present invention has a yet further object to provide an antibody
effective for treatment and diagnosis of cancers.
[0009] In view of the above-mentioned objects, the present
inventors carry out an analysis of an antibody by the following
approach: preparing cell lines that are expected to express cell
surface antigens for the obtained antibodies; allowing each
antibody to react with the cell lines; and carrying out the flow
cytometry analysis.
[0010] The present inventors focus on the histogram of the results
of the flow cytometry analysis and classify the antibodies based on
the similarity so as to obtain a plurality of antibodies groups.
Then, it is confirmed that antigens to antibodies belonging to the
same antibody group are common. This fact means that it is possible
to determine antigens for all antibodies by selecting the
respective antibody in each antibody group and identifying the
antigen of the representative antibody. Thus, the present inventors
have succeeded in finding a method for identifying antigens
comprehensively and rapidly. On the other hand, the present
inventors carry out classification of antibodies and identification
of an antigen according to the above-mentioned technique and
consider the reactivity between each antibody group and clinical
samples so as to search for clinically applicable antibodies. As a
result, the present inventors have succeeded in finding a novel
antibody specific to certain kinds of cancers. Furthermore, they
have reached the findings that information obtained by using a
clinical sample (relationship between the antibody and disease) is
extremely useful for establishing methods for diagnosis and
treatment.
[0011] The present invention provides, for example, a method of
classifying antibody, and the like, mentioned below based on the
above-mentioned results and findings.
<Method of Classifying Antibody>
[0012] [1] A method of classifying antibody including the following
steps:
[0013] (1) preparing a plurality of antibodies recognizing cell
surface antigen;
[0014] (2) bringing each of the antibodies into contact with cells
of the same kinds;
[0015] (3) analyzing each cell after step (2) by flow cytometry so
as to obtain data showing reactivity between the antibody and the
cell surface; and
[0016] (4) comparing the obtained data and classifying antibodies
based on the similarity of the data.
[2] The method of classifying antibody according to [1], wherein
the cell surface antigen is an intact cell surface antigen. [3] The
classifying method according to [1] or [2], wherein the cell
surface antigen is a cell surface antigen of a cancer cell. [4] The
classifying method according to [1], wherein the plurality of
antibodies recognize cell surface antigen are composed of an
assembly of antibodies derived from antibody clones selected as
being capable of recognizing a cell surface antigen, from an
antibody library. [5] The classifying method according to [4],
wherein the antibody library is a phage antibody library. [6] The
classifying method according to [1], wherein the antibody is an
antibody to which a label material is bound or fused. [7] The
classifying method according to [1], wherein the antibody does not
include a label material and the method includes a step of labeling
the antibody bound to the cell after step (2). [8] The classifying
method according to [1], wherein the cell is an established cell
line. [9] The classifying method according to [1], wherein the cell
is an established cancer cell line. [10] The classifying method
according to [1], wherein the data are shown in a histogram showing
a relationship between a binding amount of antibodies and a number
of cells, and the similarity of the data is determined by comparing
the shapes of the histograms. [11] The classifying method according
to [1], wherein the data are shown in a histogram showing a
relationship between a binding amount of antibodies and a number of
cells, and the similarity of the data is determined based on one or
more values selected from the group consisting of a median value, a
mode, a maximum value, a range, a standard deviation, a kurtosis
and a skewness of the histogram. [12] The classifying method
according to [11], wherein the similarity of the data is determined
based on the values of the median value, the mode, and the kurtosis
and a skewness of the histogram. [13] The classifying method
according to [10] or [11], wherein the binding amount of antibody
is shown by a fluorescence intensity. [14] The classifying method
according to [1], wherein in step (4), a plurality of antibodies
having the identical or high similar data are classified into one
antibody group. [15] The classifying method according to [1],
wherein two or more kinds of cells are prepared and each kind of
cell is subjected to steps (2) to (4). [16] The classifying method
according to [15], wherein a plurality of antibodies having the
identical or high similar data with respect to two or more kinds of
cells in the cells are classified into one antibody group. [17] The
classifying method according to [1], wherein an antibody that has
been determined to have a low reactivity with respect to the cell
surface antigen during classification or after classification is
excluded. [18] The classifying method according to [1], wherein
classification results of antibodies are displayed as a panel. [19]
The classifying method according to any of [.alpha.] to [18],
wherein after step (4), the following steps are carried out:
[0017] (i) associating the classified antibodies to a combination
of n pieces of parameters including a first parameter, a second
parameter, . . . , and an n-th parameter (wherein, n represents an
integer of 2 or more, each parameter has two or more parameter
values and the same parameter value is given to two or more
antibodies in each parameter);
[0018] (ii) with respect to each parameter, preparing antibody
mixtures of the antibodies having the same parameter value;
[0019] (iii) examining a reactivity of each of the antibody
mixtures with a target antigen by an enzyme linked immunosorbent
assay (ELISA) so as to specify the antibody mixture which shows
reactivity;
[0020] (iv) specifying a combination of a parameter name and a
parameter value that are common to the antibody group contained in
the specified antibody mixture;
[0021] (v) selecting an antibody corresponding to the combination
specified in the step (iv) in terms of all parameters among the
antibodies subjected to step (i); and
[0022] (vi) classifying the selected antibodies into one antibody
group.
[20] The classifying method according to [19], wherein the steps
(i) to (v) are repeated several times under the conditions in which
the combination of parameters is different in each trial; an
antibody in which results of all trials are not contradictory is
selected; and the antibody is subjected to the step (vi). [21] The
classifying method according to [19], further including the
following steps between the step (v) and the step (vi);
[0023] (v-1) newly associating the classified antibodies selected
in step (v) with a combination of n pieces of parameters in a same
manner as in the step (i);
[0024] (v-2) with respect to each parameter, preparing the antibody
mixture of antibodies having the same parameter value for each
parameter;
[0025] (v-3) examining a reactivity of each of the antibody
mixtures with a target antigen by an enzyme linked immunosorbent
assay (ELISA) so as to specify the antibody mixture showing the
reactivity;
[0026] (v-4) determining a combination of a parameter name and a
parameter value that are common to the antibody group contained in
the specified antibody mixture; and
[0027] (v-5) selecting an antibody having the combination specified
in the step (v-4) in terms of all parameters among the antibodies
subjected to the step (v-1).
[22] The classifying method according to [21], wherein the steps
(v-1) to (v-4) are repeated twice or more. [23] The classifying
method according to any of [19] to [22], wherein n is 3. [24] The
classifying method according to any of [19] to [23], wherein two or
more kinds of target antigens are prepared and the steps (iii) to
(vi) are carried out by using each target antigen. [25] The
classifying method according to any of [19] to [24], wherein the
target antigen is an antigen selected from the group consisting of
HER1, HER2, CD46, ITGA3, ICAM1, ALCAM, CD147, IgSF4, BCAM, C1qR,
CD44, CD73, LAR, EpCAM and HGFR.
<Identifying Method of Antigen>
[0028] [26] An identifying method of an antigen including the
following steps:
[0029] (1) preparing a plurality of antibodies recognizing cell
surface antigen;
[0030] (2) bringing each of the antibodies into contact with cells
of the same kind;
[0031] (3) analyzing each cell after step (2) by flow cytometry so
as to obtain data showing the reactivity between the antibody and
the cell surface;
[0032] (4) comparing the obtained data and classifying antibodies
based on the similarity of the data;
[0033] (5) selecting one or several antibodies from each antibody
group formed in the step (4) and identifying an antigen thereof;
and
[0034] (6) associating the antigens identified in the step (5) with
an antibody group, based on the estimation that antigens to
antibodies belonging to the same antibody group are identical or
have high relationship, and.
[27] The identification method according to [26], wherein in the
step (5), one antibody is selected from each antibody group. [28]
The identification method according to [26], wherein in the step
(5), from the results of a flow cytometry analysis, an antibody
that is determined to have a high reactivity with respect to an
antigen is selected. [29] The identification method according to
[26], wherein in the step (5), the identification of an antigen is
carried out by one or more methods selected from the group
consisting of an immunoprecipitation test, Western blotting,
affinity chromatography, proteomics techniques (electrophoresis,
mass spectrometry, genome data base retrieve, and analysis by
bioinformatics), and an expression analysis of corresponding gene.
[30] The identification method according to [26], further including
a step of examining a reactivity between an antigen identified in
the step (5) and an antibody belonging to an antibody group with
which the antigen is associated in the step (6) so as to confirm
that the estimation is correct. [31] The identification method
according to [26], wherein an identification result of antigen is
displayed as a panel. [32] The identification method according to
[31], wherein the panel is any of the following (a) to (c):
[0035] (a) a panel displaying a plurality of antibodies showing
identical or high similar data in the flow cytometry analysis in
the step (3) as one antibody group in which each antibody group is
associated with its antigen;
[0036] (b) a panel displaying a plurality of antibodies showing
identical or high similar data in the flow cytometry analysis in
the step (3) as one antibody group in which each antibody group is
associated with a cell expressing a cell surface antigen recognized
by the each antibody group; and
[0037] (c) a panel displaying a plurality of antibodies showing
identical or high similar data in the flow cytometry analysis in
the step (3) as one antibody group in which each antibody group,
its antigen and a cell expressing a cell surface antigen recognized
by the antibody group are associated with each other.
<Method of Obtaining Antibody or Antibody Set, Antibody or
Antibody Set to be Obtained>
[0038] [33] A method of obtaining an antibody having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0039] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to [1];
[0040] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0041] (3) selecting an antibody in the antibody group, to which an
antibody having a specific reactivity to any of diseases belongs,
as a useful antibody.
[34] A method of obtaining an antibody having a relationship with
respect to a certain disease, the method comprising the following
steps:
[0042] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to [19];
[0043] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0044] (3) selecting an antibody in the antibody group, to which an
antibody having a specific reactivity to any of diseases belongs,
as a useful antibody.
[35] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0045] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to [1];
[0046] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0047] (3') selecting a disease to which two or more antibodies
show a specific reactivity, then selecting antibodies from the
antibody group, to which the antibody having a specific reactivity
to the disease belongs, and combining the selected antibodies.
[36] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0048] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [1];
[0049] (2) with respect to two kinds or more diseases, examining a
reactivity between an antibody in each of the selected antibody
groups and a certain disease; and
[0050] (3) selecting antibodies from the antibody group, to which
the antibody having a specific reactivity to any of disease
belongs, and combining the selected antibodies.
[37] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0051] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [1];
[0052] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0053] (3) selecting an antibody from the antibody group to which
the antibody having a specific reactivity to any of diseases
belongs, and an antibody belonging to other antibody group whose
antigen is common to that of the antibody group, and combining the
selected antibodies.
[38] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0054] (1) selecting two or more antibody groups recognizing the
common antigen from the plurality of antibody groups classified by
the classifying method according to [1];
[0055] (2) with respect to one kind or two or more kinds of
pathologic conditions, examining a reactivity between an antibody
in each of the selected antibody groups and a pathologic condition;
and
[0056] (3) connecting information about the reactivity and then
combining the antibodies in the antibody groups.
[39] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0057] (1) selecting one or two or more antibody groups from the
plurality of antibody groups classified by the classifying method
according to [19];
[0058] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0059] (3') selecting a disease to which two or more antibodies
show a specific reactivity, then selecting antibodies from an
antibody group which the antibodies showing a specific reactivity
to the disease belong to, and combining the selected
antibodies.
[40] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0060] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [19];
[0061] (2) with respect to two or more kinds of diseases, examining
a reactivity between an antibody in each of the selected antibody
groups and a certain disease in two or more kinds of diseases;
and
[0062] (3) selecting antibodies from the antibody group to which
the antibody having a specific reactivity to any of diseases
belong, and combining the selected antibodies.
[41] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0063] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [19];
[0064] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0065] (3) selecting an antibody from the antibody group to which
the antibody having a specific reactivity to any of disease
belongs, and an antibody belonging to other antibody group whose
antigen is common to that of the antibody group, and combining the
selected antibodies.
[42] A method of obtaining an antibody set having a relationship
with respect to a certain disease, the method comprising the
following steps:
[0066] (1) selecting two or more antibody groups recognizing the
common antigen from the plurality of antibody groups classified by
the classifying method according to [19];
[0067] (2) with respect to one kind or two or more kinds of
pathologic conditions, examining a reactivity between an antibody
in each of the selected antibody groups and a pathologic condition;
and
[0068] (3) associating information about the reactivity and then
combining the antibodies in the antibody groups.
[43] The obtaining method according any of [33] to [42], wherein
the disease is selected from the group consisting of kidney cancer,
hepatic cell carcinoma, gallbladder and liver cancer, alveolar cell
carcinoma, lung squamous cell cancer, pulmonary adenocarcinoma,
pancreas cancer, adenocarcinoma, and ovarian cancer. [44] The
obtaining method according any of [33] to [42], wherein in the step
(2), the reactivity is examined by one or more methods selected
from the group consisting of an immunostaining procedure, an
immunoprecipitation method, a flow cytometry analysis, cell ELISA,
an intermolecular interactive analysis between a disease-related
molecule (disease causative gene product and the like) and an
antibody, and application test to a disease model cell (or animal).
[45] An isolated antibody obtained by the method according to [33]
or [34]. [46] An antibody set obtained by the method described in
any of [35] to [42].
<Production Method of Panel, Panel, and Combination of Antibody
or Antibody Set and Panel>
[0069] [47] A production method of a panel displaying a
relationship between an antibody and a disease, the method
comprising the following steps:
[0070] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to [1];
[0071] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0072] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[48] A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps:
[0073] (1) selecting two or more of antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [1];
[0074] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0075] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[49] A production method of a panel displaying a relationship
between an antibody and a pathologic condition, the method
comprising the following steps:
[0076] (1) selecting two or more of antibody groups recognizing a
common antigen from the plurality of antibody groups classified by
the classifying method according to [1];
[0077] (2) with respect to one kind or two or more kinds of
pathologic condition, examining a reactivity between an antibody in
each of the selected antibody groups and a certain pathologic
condition of disease; and
[0078] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[50] A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps:
[0079] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to [19];
[0080] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0081] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[51] A production method of a panel displaying a relationship
between an antibody and a disease, the method comprising the
following steps:
[0082] (1) selecting two or more of antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to [19];
[0083] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0084] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[52] A production method of a panel displaying a relationship
between an antibody and a pathologic condition, the method
comprising the following steps:
[0085] (1) selecting two or more of antibody groups recognizing a
common antigen from the plurality of antibody groups classified by
the classifying method according to [19];
[0086] (2) with respect to one kind or two or more kinds of
pathologic condition, examining a reactivity between an antibody in
each of the selected antibody groups and a certain pathologic
condition of disease; and
[0087] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[53] A panel produced by the method according to any of [47] to
[52]. [54] A combination of an antibody or an antibody set and a
panel selected from the group consisting of the following (a) to
(d);
[0088] (a) a combination of the isolated antibody obtained by the
method according to [33] and the panel produced by the method
according to [47];
[0089] (b) a combination of the antibody set obtained by the method
according to [35] and the panel produced by the method according to
[47];
[0090] (c) a combination of the antibody set obtained by the method
according to [36] and the panel produced by the method according to
[48];
[0091] (d) a combination of the antibody set obtained by the method
according to [37] and the panel produced by the method according to
[48];
[0092] (e) a combination of the antibody set obtained by the method
according to [38] and the panel produced by the method according to
[49];
[0093] (f) an isolated antibody obtained by the method according to
[34] and the panel produced by the method according to [50];
[0094] (g) a combination of the antibody set obtained by the method
according to [39] and the panel produced by the method according to
[50];
[0095] (h) a combination of the antibody set obtained by the method
according to [40] and the panel produced by the method according to
[51];
[0096] (i) a combination of the antibody set obtained by the method
according to [41] and the panel produced by the method according to
[51]; and
[0097] (j) a combination of the antibody set obtained by the method
according to [42] and the panel produced by the method according to
[52].
[55] A method of testing a disease in which a cell surface antigen
is an indicator, the method comprising the following steps:
[0098] (1) preparing a cell or a tissue separated from a
subject;
[0099] (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel according to [53]; and
[0100] (3) collating the results in the step (2) with the
panel.
<Method of Selecting Optimum Treatment Method>
[0101] [56] A method of selecting an optimum treatment method for a
certain disease, the method comprising the following steps:
[0102] (1) preparing a cell or a tissue separated from a
subject;
[0103] (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel according to [53];
[0104] (3) collating the results in the step (2) with the panel,
and
[0105] (4) selecting an effective antibody according to the results
of collating.
[57] The method according to [56], wherein the effective antibody
is an antibody showing a specific reactivity in the step (2) or an
antibody equivalent thereto. [58] The method according to [56] or
[57], wherein the certain disease is a disease in which a cell
surface antigen selected from the group consisting of HER1, HER2,
CD46, ITGA3, ICAM1, ALCAM, CD147, IgSF4, BCAM, C1qR, CD44, CD73,
LAR, EpCAM and HGFR is an indicator. [59] The method according to
any of [56] to [58], wherein the panel displays two or more
antibodies selected from the group consisting of 048-006 antibody,
057-091 antibody, 059-152 antibody, 048-040 antibody, 054-101
antibody, 055-147 antibody, 059-173 antibody, 067-149 antibody,
067-176 antibody, 015-126 antibody, 015-044 antibody, 015-102
antibody, 015-136 antibody, 015-143 antibody, 015-209 antibody,
039-016 antibody, 053-216 antibody, 075-024 antibody, 075-110
antibody, 086-032 antibody, 086-035 antibody, 086-036 antibody,
086-061 antibody, 086-138 antibody, 086-182 antibody, 035-224
antibody, 045-011 antibody, 051-144 antibody, 052-053 antibody,
052-073 antibody, 053-049 antibody, 3172-120 antibody, 066-069
antibody, 015-003 antibody, 064-002 antibody, 064-006 antibody,
064-012a antibody, 064-012b antibody, 064-014 antibody, 064-054
antibody, 064-085 antibody, 064-093 antibody, 064-116 antibody,
065-183 antibody, 067-142 antibody, 068-007 antibody, 052-033
antibody, 053-042 antibody, 053-051 antibody, 053-059 antibody,
053-085 antibody, 035-234 antibody, 040-107 antibody, 041-118
antibody, 066-174 antibody, 083-040 antibody, 029-143 antibody,
045-134 antibody, 062-101 antibody, 062-109 antibody, 084-103
antibody, 052-274 antibody, 029-067 antibody, 083-131 antibody,
059-053 antibody, 064-003 antibody, 067-213 antibody, 067-153
antibody, 067-126 antibody, 067-133 antibody, 067-287 antibody,
064-044 antibody, 065-030 antibody, 065-358 antibody, 066-019
antibody, 079-085 antibody, 067-024 antibody and 076-048 antibody.
[60] A method of selecting an optimum treatment method of a certain
disease, the method comprising the following steps:
[0106] (1) preparing a panel displaying a reactivity between one or
more antibodies selected from the group consisting of 048-006
antibody, 015-126 antibody, 067-133 antibody, 064-044 antibody,
076-048 antibody and 059-053 antibody, and a clinical cancer tissue
of one or more diseases selected from the group consisting of
squamous carcinoma, adenosquamous carcinoma, alveolar
adenocarcinoma, adenocarcinoma, and large cell carcinoma, and a
cell or tissue separated from a subject;
[0107] (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel;
[0108] (3) collating the results in the step (2) with the panel,
and
[0109] (4) selecting an effective antibody according to the results
of collating.
[61] The method according to [60], wherein the effective antibody
is an antibody showing a specific reactivity in the step (2) or an
antibody equivalent thereto. [62] The method according to [60] or
[61], wherein the certain disease is a disease selected from the
group consisting of squamous carcinoma, adenosquamous carcinoma,
alveolar adenocarcinoma, adenocarcinoma, and large cell
carcinoma.
<Isolated Antibody>
[0110] [63] An isolated antibody having affinity to HER1,
comprising:
[0111] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) selected from the group consisting of
the following (1) to (3);
[0112] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) selected from the group consisting of the following (4) to
(6);
[0113] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (7) to (9) and (13) to (18); or
[0114] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (10) to (12)
and (19) to (24);
(1) SEQ ID NO: 4 and SEQ ID NO: 8
(2) SEQ ID NO: 12 and SEQ ID NO: 16
(3) SEQ ID NO: 20 and SEQ ID NO: 24
(4) SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 7, and SEQ ID NO: 8
(5) SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 15, and SEQ ID NO:
16
(6) SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 23, and SEQ ID NO:
24
(7) SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID
NO: 7, and SEQ ID NO: 8
(8) SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 14, SEQ
ID NO: 15, and SEQ ID NO: 16
(9) SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 22, SEQ
ID NO: 23, and SEQ ID NO: 24
(10) SEQ ID NO: 1, and SEQ ID NO: 5
(11) SEQ ID NO: 9, and SEQ ID NO: 13
(12) SEQ ID NO: 17, and SEQ ID NO: 21
(13) SEQ ID NO: 484 (VH CDR1), SEQ ID NO: 485 (VH CDR2), SEQ ID NO:
486 (VH CDR3), SEQ ID NO: 488 (VL CDR1), SEQ ID NO: 489 (VL CDR2),
and SEQ ID NO: 490 (VL CDR3)
(14) SEQ ID NO: 492 (VH CDR1), SEQ ID NO: 493 (VH CDR2), SEQ ID NO:
494 (VH CDR3), SEQ ID NO: 496 (VL CDR1), SEQ ID NO: 497 (VL CDR2),
and SEQ ID NO: 498 (VL CDR3)
(15) SEQ ID NO: 500 (VH CDR1), SEQ ID NO: 501 (VH CDR2), SEQ ID NO:
502 (VH CDR3), SEQ ID NO: 504 (VL CDR1), SEQ ID NO: 505 (VL CDR2),
and SEQ ID NO: 506 (VL CDR3)
(16) SEQ ID NO: 508 (VH CDR1), SEQ ID NO: 509 (VH CDR2), SEQ ID NO:
510 (VH CDR3), SEQ ID NO: 512 (VL CDR1), SEQ ID NO: 513 (VL CDR2),
and SEQ ID NO: 514 (VL CDR3)
(17) SEQ ID NO: 516 (VH CDR1), SEQ ID NO: 517 (VH CDR2), SEQ ID NO:
518 (VH CDR3), SEQ ID NO: 520 (VL CDR1), SEQ ID NO: 521 (VL CDR2),
and SEQ ID NO: 522 (VL CDR3)
(18) SEQ ID NO: 524 (VH CDR1), SEQ ID NO: 525 (VH CDR2), SEQ ID NO:
526 (VH CDR3), SEQ ID NO: 528 (VL CDR1), SEQ ID NO: 529 (VL CDR2),
and SEQ ID NO: 530 (VL CDR3)
(19) SEQ ID NO: 483 (VH), and SEQ ID NO: 487 (VL)
(20) SEQ ID NO: 491 (VH), and SEQ ID NO: 495 (VL)
(21) SEQ ID NO: 499 (VH), and SEQ ID NO: 503 (VL)
(22) SEQ ID NO: 507 (VH), and SEQ ID NO: 511 (VL)
(23) SEQ ID NO: 515 (VH), and SEQ ID NO: 519 (VL), and
(24) SEQ ID NO: 523 (VH), and SEQ ID NO: 527 (VL)
[0115] [64] An isolated antibody having affinity to HER2,
comprising:
[0116] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) shown in the following (1);
[0117] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) shown in the following (2);
[0118] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (3) and (5) to (19); or
[0119] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (4) and (20) to
(34);
(1) SEQ ID NO: 28, and SEQ ID NO: 32
(2) SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 31, and SEQ ID NO:
32
(3) SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 30, SEQ
ID NO: 31, and SEQ ID NO:32
(4) SEQ ID NO: 25, and SEQ ID NO: 29
(5) SEQ ID NO: 532 (VH CDR1), SEQ ID NO: 533 (VH CDR2), SEQ ID NO:
534 (VH CDR3), SEQ ID NO: 536 (VL CDR1), SEQ ID NO: 537 (VL CDR2),
and SEQ ID NO: 538 (VL CDR3)
(6) SEQ ID NO: 540 (VH CDR1), SEQ ID NO: 541 (VH CDR2), SEQ ID NO:
542 (VH CDR3), SEQ ID NO: 544 (VL CDR1), SEQ ID NO: 545 (VL CDR2),
and SEQ ID NO: 546 (VL CDR3)
(7) SEQ ID NO: 548 (VH CDR1), SEQ ID NO: 549 (VH CDR2), SEQ ID NO:
550 (VH CDR3), SEQ ID NO: 552 (VL CDR1), SEQ ID NO: 553 (VL CDR2),
and SEQ ID NO: 554 (VL CDR3)
(8) SEQ ID NO: 556 (VH CDR1), SEQ ID NO: 557 (VH CDR2), SEQ ID NO:
558 (VH CDR3), SEQ ID NO: 560 (VL CDR1), SEQ ID NO: 561 (VL CDR2),
and SEQ ID NO: 562 (VL CDR3)
(9) SEQ ID NO: 564 (VH CDR1), SEQ ID NO: 565 (VH CDR2), SEQ ID NO:
566 (VH CDR3), SEQ ID NO: 568 (VL CDR1), SEQ ID NO: 569 (VL CDR2),
and SEQ ID NO: 570 (VL CDR3)
(10) SEQ ID NO: 572 (VH CDR1), SEQ ID NO: 573 (VH CDR2), SEQ ID NO:
574 (VH CDR3), SEQ ID NO: 576 (VL CDR1), SEQ ID NO: 577 (VL CDR2),
and SEQ ID NO: 578 (VL CDR3)
(11) SEQ ID NO: 580 (VH CDR1), SEQ ID NO: 581 (VH CDR2), SEQ ID NO:
582 (VH CDR3), SEQ ID NO: 584 (VL CDR1), SEQ ID NO: 585 (VL CDR2),
and SEQ ID NO: 586 (VL CDR3)
(12) SEQ ID NO: 588 (VH CDR1), SEQ ID NO: 589 (VH CDR2), SEQ ID NO:
590 (VH CDR3), SEQ ID NO: 592 (VL CDR1), SEQ ID NO: 593 (VL CDR2),
and SEQ ID NO: 594 (VL CDR3)
(13) SEQ ID NO: 596 (VH CDR1), SEQ ID NO: 597 (VH CDR2), SEQ ID NO:
598 (VH CDR3), SEQ ID NO: 600 (VL CDR1), SEQ ID NO: 601 (VL CDR2),
and SEQ ID NO: 602 (VL CDR3)
(14) SEQ ID NO: 604 (VH CDR1), SEQ ID NO: 605 (VH CDR2), SEQ ID NO:
606 (VH CDR3), SEQ ID NO:608 (VL CDR1), SEQ ID NO:609 (VL CDR2),
and SEQ ID NO: 610 (VL CDR3)
(15) SEQ ID NO: 612 (VH CDR1), SEQ ID NO: 613 (VH CDR2), SEQ ID NO:
614 (VH CDR3), SEQ ID NO: 616 (VL CDR1), SEQ ID NO: 617 (VL CDR2),
and SEQ ID NO: 618 (VL CDR3)
(16) SEQ ID NO: 620 (VH CDR1), SEQ ID NO: 621 (VH CDR2), SEQ ID NO:
622 (VH CDR3), SEQ ID NO: 624 (VL CDR1), SEQ ID NO: 625 (VL CDR2),
and SEQ ID NO: 626 (VL CDR3)
(17) SEQ ID NO: 628 (VH CDR1), SEQ ID NO: 629 (VH CDR2), SEQ ID NO:
630 (VH CDR3), SEQ ID NO: 632 (VL CDR1), SEQ ID NO: 633 (VL CDR2),
and SEQ ID NO: 634 (VL CDR3)
(18) SEQ ID NO: 636 (VH CDR1), SEQ ID NO: 637 (VH CDR2), SEQ ID NO:
638 (VH CDR3), SEQ ID NO: 640 (VL CDR1), SEQ ID NO: 641 (VL CDR2),
and SEQ ID NO: 642 (VL CDR3)
(19) SEQ ID NO: 644 (VH CDR1), SEQ ID NO: 645 (VH CDR2), SEQ ID NO:
646 (VH CDR3), SEQ ID NO: 648 (VL CDR1), SEQ ID NO: 649 (VL CDR2),
and SEQ ID NO: 650 (VL CDR3)
(20) SEQ ID NO: 531 (VH), and SEQ ID NO: 535 (VL)
(21) SEQ ID NO: 539 (VH), and SEQ ID NO: 543 (VL)
(22) SEQ ID NO: 547 (VH), and SEQ ID NO: 551 (VL)
(23) SEQ ID NO: 555 (VH), and SEQ ID NO: 559 (VL)
(24) SEQ ID NO: 563 (VH), and SEQ ID NO: 567 (VL)
(25) SEQ ID NO: 571 (VH), and SEQ ID NO: 575 (VL)
(26) SEQ ID NO: 579 (VH), and SEQ ID NO: 583 (VL)
(27) SEQ ID NO: 587 (VH), and SEQ ID NO: 591 (VL)
(28) SEQ ID NO: 595 (VH), and SEQ ID NO: 599 (VL)
(29) SEQ ID NO: 603 (VH), and SEQ ID NO: 607 (VL)
(30) SEQ ID NO: 611 (VH), and SEQ ID NO: 615 (VL)
(31) SEQ ID NO: 619 (VH), and SEQ ID NO: 623 (VL)
(32) SEQ ID NO: 627 (VH), and SEQ ID NO: 631 (VL)
(33) SEQ ID NO: 635 (VH), and SEQ ID NO: 639 (VL), and
(34) SEQ ID NO: 643 (VH), and SEQ ID NO: 647 (VL)
[0120] [65] An isolated antibody having affinity to CD46 antigen,
comprising:
[0121] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) selected from the group consisting of
the following (1) to (7);
[0122] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) selected from the group consisting of the following (8) to
(14);
[0123] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (15) to (22); or
[0124] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (23) to
(30);
(1) SEQ ID NO: 36, and SEQ ID NO: 40
(2) SEQ ID NO: 44, and SEQ ID NO: 48
(3) SEQ ID NO: 52, and SEQ ID NO: 56
(4) SEQ ID NO: 60, and SEQ ID NO: 64
(5) SEQ ID NO: 68, and SEQ ID NO: 72
(6) SEQ ID NO: 76, and SEQ ID NO: 80
(7) SEQ ID NO: 84, and SEQ ID NO: 88
(8) SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 39, and SEQ ID NO:
40
(9) SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 47, and SEQ ID NO:
48
(10) SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 55, and SEQ ID NO:
56
(1) SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 63, and SEQ ID NO:
64
(12) SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 71, and SEQ ID NO:
72
(13) SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 79, and SEQ ID NO:
80
(14) SEQ ID NO: 83, SEQ ID NO: 84, SEQ ID NO: 87, and SEQ ID NO:
88
(15) SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 38,
SEQ ID NO: 39, and SEQ ID NO: 40
(16) SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 46,
SEQ ID NO: 47, and SEQ ID NO: 48
(17) SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 54,
SEQ ID NO: 55, and SEQ ID NO: 56
(18) SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 62,
SEQ ID NO: 63, and SEQ ID NO: 64
(19) SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 70,
SEQ ID NO: 71, and SEQ ID NO: 72
(20) SEQ ID NO: 74, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 78,
SEQ ID NO: 79, and SEQ ID NO: 80
(21) SEQ ID NO: 82, SEQ ID NO: 83, SEQ ID NO: 84, SEQ ID NO: 86,
SEQ ID NO: 87, and SEQ ID NO: 88
(22) SEQ ID NO: 756 (VH CDR1), SEQ ID NO: 757 (VH CDR2), SEQ ID NO:
758 (VH CDR3), SEQ ID NO: 760 (VL CDR1), SEQ ID NO: 761 (VL CDR2),
and SEQ ID NO: 762 (VL CDR3)
(23) SEQ ID NO: 33, and SEQ ID NO: 37
(24) SEQ ID NO: 41, and SEQ ID NO: 45
(25) SEQ ID NO: 49, and SEQ ID NO: 53
(26) SEQ ID NO: 57, and SEQ ID NO: 61
(27) SEQ ID NO: 65, and SEQ ID NO: 69
(28) SEQ ID NO: 73, and SEQ ID NO: 77
(29) SEQ ID NO: 81, and SEQ ID NO: 85
(30) SEQ ID NO: 755 (VH), and SEQ ID NO: 759 (VL)
[0125] [66] An isolated antibody having affinity to ITAG3,
comprising:
[0126] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) shown in the following (1);
[0127] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) shown in the following (2);
[0128] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (3) and (5) to (16); or
[0129] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (4) and (17) to
(28);
(1) SEQ ID NO: 92, and SEQ ID NO: 96
(2) SEQ ID NO: 91, SEQ ID NO: 92, SEQ ID NO: 95, and SEQ ID NO:
96
(3) SEQ ID NO: 90, SEQ ID NO: 91, SEQ ID NO: 92, SEQ ID NO: 94, and
SEQ ID NO: 95,
(4) SEQ ID NO: 89, and SEQ ID NO: 93
(5) SEQ ID NO: 676 (VH CDR1), SEQ ID NO: 677 (VH CDR2), SEQ ID NO:
678 (VH CDR3), SEQ ID NO: 680 (VL CDR1), SEQ ID NO: 681 (VL CDR2),
and SEQ ID NO: 682 (VL CDR3)
(6) SEQ ID NO: 684 (VH CDR1), SEQ ID NO: 685 (VH CDR2), SEQ ID NO:
686 (VH CDR3), SEQ ID NO: 688 (VL CDR1), SEQ ID NO: 689 (VL CDR2),
and SEQ ID NO: 690 (VL CDR3)
(7) SEQ ID NO: 692 (VH CDR1), SEQ ID NO: 693 (VH CDR2), SEQ ID NO:
694 (VH CDR3), SEQ ID NO: 696 (VL CDR1), SEQ ID NO: 697 (VL CDR2),
and SEQ ID NO: 698 (VL CDR3)
(8) SEQ ID NO: 700 (VH CDR1), SEQ ID NO: 701 (VH CDR2), SEQ ID NO:
702 (VH CDR3), SEQ ID NO: 704 (VL CDR1), SEQ ID NO: 705 (VL CDR2),
and SEQ ID NO: 706 (VL CDR3)
(9) SEQ ID NO: 708 (VH CDR1), SEQ ID NO: 709 (VH CDR2), SEQ ID NO:
710 (VH CDR3), SEQ ID NO: 712 (VL CDR1), SEQ ID NO: 713 (VL CDR2),
and SEQ ID NO: 714 (VL CDR3)
(10) SEQ ID NO: 716 (VH CDR1), SEQ ID NO: 717 (VH CDR2), SEQ ID NO:
718 (VH CDR3), SEQ ID NO: 720 (VL CDR1), SEQ ID NO: 721 (VL CDR2),
and SEQ ID NO: 722 (VL CDR3)
(11) SEQ ID NO: 724 (VH CDR1), SEQ ID NO: 725 (VH CDR2), SEQ ID NO:
726 (VH CDR3), SEQ ID NO: 728 (VL CDR1), SEQ ID NO: 729 (VL CDR2),
and SEQ ID NO: 730 (VL CDR3)
(12) SEQ ID NO: 732 (VH CDR1), SEQ ID NO: 733 (VH CDR2), SEQ ID NO:
734 (VH CDR3), SEQ ID NO: 736 (VL CDR1), SEQ ID NO: 737 (VL CDR2),
and SEQ ID NO: 738 (VL CDR3)
(13) SEQ ID NO: 740 (VH CDR1), SEQ ID NO: 741 (VH CDR2), SEQ ID NO:
742 (VH CDR3), SEQ ID NO: 744 (VL CDR1), SEQ ID NO: 745 (VL CDR2),
and SEQ ID NO: 746 (VL CDR3)
(14) SEQ ID NO: 748 (VH CDR1), SEQ ID NO: 749 (VH CDR2), SEQ ID NO:
750 (VH CDR3), SEQ ID NO: 752 (VL CDR1), SEQ ID NO: 753 (VL CDR2),
and SEQ ID NO: 754 (VL CDR3)
(15) SEQ ID NO: 764 (VH CDR1), SEQ ID NO: 765 (VH CDR2), SEQ ID NO:
766 (VH CDR3), SEQ ID NO: 768 (VL CDR1), SEQ ID NO: 769 (VL CDR2),
and SEQ ID NO: 770 (VL CDR3)
(16) SEQ ID NO: 772 (VH CDR1), SEQ ID NO: 773 (VH CDR2), SEQ ID NO:
774 (VH CDR3), SEQ ID NO: 776 (VL CDR1), SEQ ID NO: 777 (VL CDR2),
and SEQ ID NO: 778 (VL CDR3)
(17) SEQ ID NO: 675 (VH), and SEQ ID NO: 679 (VL)
(18) SEQ ID NO: 683 (VH), and SEQ ID NO: 687 (VL)
(19) SEQ ID NO: 691 (VH), and SEQ ID NO: 695 (VL)
(20) SEQ ID NO: 699 (VH), and SEQ ID NO: 703 (VL)
(21) SEQ ID NO: 707 (VH), and SEQ ID NO: 711 (VL)
(22) SEQ ID NO: 715 (VH), and SEQ ID NO: 719 (VL)
(23) SEQ ID NO: 723 (VH), and SEQ ID NO: 727 (VL)
(24) SEQ ID NO: 731 (VH), and SEQ ID NO: 735 (VL)
(25) SEQ ID NO: 739 (VH), and SEQ ID NO: 743 (VL)
(26) SEQ ID NO: 747 (VH), and SEQ ID NO: 751 (VL)
(27) SEQ ID NO: 763 (VH), and SEQ ID NO: 767 (VL), and
(28) SEQ ID NO: 771 (VH), and SEQ ID NO: 775 (VL)
[0130] [67] An isolated antibody having affinity to ICAM1,
comprising:
[0131] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) selected from the group consisting of
the following (1) to (5);
[0132] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) selected from the group consisting of the following (6) to
(10);
[0133] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (11) to (15); or
[0134] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (16) to
(20);
(1) SEQ ID NO: 100, and SEQ ID NO: 104
(2) SEQ ID NO: 108, and SEQ ID NO: 112
(3) SEQ ID NO: 116, and SEQ ID NO: 120
(4) SEQ ID NO: 124, and SEQ ID NO: 128
(5) SEQ ID NO: 132, and SEQ ID NO: 136
(6) SEQ ID NO: 99, SEQ ID NO: 100, SEQ ID NO: 103, and SEQ ID NO:
104
(7) SEQ ID NO: 107, SEQ ID NO: 108, SEQ ID NO: 111, and SEQ ID NO:
112
(8) SEQ ID NO: 115, SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO:
120
(9) SEQ ID NO: 123, SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO:
128
(10) SEQ ID NO: 131, SEQ ID NO: 132, SEQ ID NO: 135, SEQ ID NO:
136
(11) SEQ ID NO: 98, SEQ ID NO: 99, SEQ ID NO: 100, SEQ ID NO: 102,
SEQ ID NO: 103, and SEQ ID NO: 104
(12) SEQ ID NO: 106, SEQ ID NO: 107, SEQ ID NO: 108, SEQ ID NO:
110, SEQ ID NO: 111, and SEQ ID NO: 112
(13) SEQ ID NO: 114, SEQ ID NO: 115, SEQ ID NO: 116, SEQ ID NO:
118, SEQ ID NO: 119, and SEQ ID NO: 120
(14) SEQ ID NO: 122, SEQ ID NO: 123, SEQ ID NO: 124, SEQ ID NO:
126, SEQ ID NO: 127, and SEQ ID NO: 128
(15) SEQ ID NO: 130, SEQ ID NO: 131, SEQ ID NO: 132, SEQ ID NO:
134, SEQ ID NO: 135, and SEQ ID NO: 136
(16) SEQ ID NO: 97, and SEQ ID NO: 101
(17) SEQ ID NO: 105, and SEQ ID NO: 109
(18) SEQ ID NO: 113, and SEQ ID NO: 117
(19) SEQ ID NO: 121, and SEQ ID NO: 125
(20) SEQ ID NO: 129, and SEQ ID NO: 133
[0135] [68] An isolated antibody having affinity to ALCAM,
comprising:
[0136] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) selected from the group consisting of
the following (1) to (5);
[0137] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) selected from the group consisting of the following (6) to
(10);
[0138] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (11) to (15) and (21) to (28); or
[0139] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (16) to (20)
and (29) to (36);
(1) SEQ ID NO: 140, and SEQ ID NO: 144
(2) SEQ ID NO: 148, and SEQ ID NO: 152
(3) SEQ ID NO: 156, and SEQ ID NO: 160
(4) SEQ ID NO: 164, and SEQ ID NO: 168
(5) SEQ ID NO: 172, and SEQ ID NO: 176
(6) SEQ ID NO: 139, SEQ ID NO: 140, SEQ ID NO: 143, and SEQ ID NO:
144
(7) SEQ ID NO: 147, SEQ ID NO: 148, SEQ ID NO: 151, and SEQ ID NO:
152
(8) SEQ ID NO: 155, SEQ ID NO: 156, SEQ ID NO: 159, and SEQ ID NO:
160
(9) SEQ ID NO: 163, SEQ ID NO: 164, SEQ ID NO: 167, and SEQ ID NO:
168
(10) SEQ ID NO: 171, SEQ ID NO: 172, SEQ ID NO: 175, and SEQ ID NO:
176
(1) SEQ ID NO: 138, SEQ ID NO: 139, SEQ ID NO: 140, SEQ ID NO: 142,
SEQ ID NO: 143, and SEQ ID NO: 144
(12) SEQ ID NO: 146, SEQ ID NO: 147, SEQ ID NO: 148, SEQ ID NO:
150, SEQ ID NO: 151, and SEQ ID NO: 152
(13) SEQ ID NO: 154, SEQ ID NO: 155, SEQ ID NO: 156, SEQ ID NO:
158, SEQ ID NO: 159, and SEQ ID NO: 160
(14) SEQ ID NO: 162, SEQ ID NO: 163, SEQ ID NO: 164, SEQ ID NO:
166, SEQ ID NO: 167, and SEQ ID NO: 168
(15) SEQ ID NO: 170, SEQ ID NO: 171, SEQ ID NO: 172, SEQ ID NO:
174, SEQ ID NO: 175, and SEQ ID NO: 176
(16) SEQ ID NO: 137, and SEQ ID NO: 141
(17) SEQ ID NO: 145, and SEQ ID NO: 149
(18) SEQ ID NO: 153, and SEQ ID NO: 157
(19) SEQ ID NO: 161, SEQ ID NO: 165
(20) SEQ ID NO: 169, and SEQ ID NO: 173
(21) SEQ ID NO: 780 (VH CDR1), SEQ ID NO: 781 (VH CDR2), SEQ ID NO
782 (VH CDR3), SEQ ID NO: 784 (VL CDR1), SEQ ID NO: 785 (VL CDR2),
and SEQ ID NO: 786 (VL CDR3)
(22) SEQ ID NO: 788 (VH CDR1), SEQ ID NO: 789 (VH CDR2), SEQ ID NO:
790 (VH CDR3), SEQ ID NO: 792 (VL CDR1), SEQ ID NO: 793 (VL CDR2),
and SEQ ID NO: 794 (VL CDR3)
(23) SEQ ID NO: 796 (VH CDR1), SEQ ID NO: 797 (VH CDR2), SEQ ID NO:
798 (VH CDR3), SEQ ID NO: 800 (VL CDR1), SEQ ID NO: 801 (VL CDR2),
and SEQ ID NO: 802 (VL CDR3)
(24) SEQ ID NO: 804 (VH CDR1), SEQ ID NO: 805 (VH CDR2), SEQ ID NO:
806 (VH CDR3), SEQ ID NO: 808 (VL CDR1), SEQ ID NO: 809 (VL CDR2),
and SEQ ID NO: 810 (VL CDR3)
(25) SEQ ID NO: 812 (VH CDR1), SEQ ID NO: 813 (VH CDR2), SEQ ID NO:
814 (VH CDR3), SEQ ID NO: 816 (VL CDR1), SEQ ID NO: 817 (VL CDR2),
and SEQ ID NO: 818 (VL CDR3)
(26) SEQ ID NO: 820 (VH CDR1), SEQ ID NO: 821 (VH CDR2), SEQ ID NO:
822 (VH CDR3), SEQ ID NO: 824 (VL CDR1), SEQ ID NO: 825 (VL CDR2),
and SEQ ID NO: 826 (VL CDR3)
(27) SEQ ID NO: 828 (VH CDR1), SEQ ID NO: 829 (VH CDR2), SEQ ID NO:
830 (VH CDR3), SEQ ID NO: 832 (VL CDR1), SEQ ID NO: 833 (VL CDR2),
and SEQ ID NO: 834 (VL CDR3)
(28) SEQ ID NO: 836 (VH CDR1), SEQ ID NO: 837 (VH CDR2), SEQ ID NO:
838 (VH CDR3), SEQ ID NO: 840 (VL CDR1), SEQ ID NO: 841 (VL CDR2),
and SEQ ID NO: 842 (VL CDR3)
(29) SEQ ID NO: 779 (VH), and SEQ ID NO: 783 (VL)
(30) SEQ ID NO: 787 (VH), and SEQ ID NO: 791 (VL)
(31) SEQ ID NO: 795 (VH), and SEQ ID NO: 799 (VL)
(32) SEQ ID NO: 803 (VH), and SEQ ID NO: 807 (VL)
(33) SEQ ID NO: 811 (VH), and SEQ ID NO: 815 (VL)
(34) SEQ ID NO: 819 (VH), and SEQ ID NO: 823 (VL)
(35) SEQ ID NO: 827 (VH), and SEQ ID NO: 831 (VL), and
(36) SEQ ID NO: 835 (VH), and SEQ ID NO: 839 (VL)
[0140] [69] An isolated antibody having affinity to CD147 antigen,
comprising:
[0141] a heavy chain variable region CDR3 and a light chain
variable region CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR3 and SEQ ID NO showing an amino acid sequence of a light
chain variable region CDR3) shown in the following (1);
[0142] heavy chain variable regions CDR2 and CDR3 and light chain
variable regions CDR2 and CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR2, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR3, SEQ ID NO showing an amino acid
sequence of a light chain variable region CDR2, and SEQ ID NO
showing an amino acid sequence of a light chain variable region
CDR3) shown in the following (2);
[0143] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions
[0144] CDR1 to CDR3 specified by a combination of SEQ ID NOs (SEQ
ID NO showing an amino acid sequence of a heavy chain variable
region CDR1, SEQ ID NO showing an amino acid sequence of a heavy
chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) shown in the following (3);
or
[0145] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the following (4);
(1) SEQ ID NO: 180, and SEQ ID NO: 184
(2) SEQ ID NO: 179, SEQ ID NO: 180, SEQ ID NO: 183, and SEQ ID NO:
184
(3) SEQ ID NO: 178, SEQ ID NO: 179, SEQ ID NO: 180, SEQ ID NO: 182,
SEQ ID NO: 183, and SEQ ID NO: 184, and
(4) SEQ ID NO: 177, and SEQ ID NO: 181
[0146] [70] An isolated antibody having affinity to C1qR,
comprising:
[0147] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) shown in the following (1);
or
[0148] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the following (2);
(1) SEQ ID NO: (VH CDR1) 452, SEQ ID NO: 453 (VH CDR2), SEQ ID NO:
454 (VH CDR3), SEQ ID NO: (VL CDR1) 456, SEQ ID NO: 457 (VL CDR2),
and SEQ ID NO: 458 (VL CDR3), and
(2) SEQ ID NO: 451 (VH), and SEQ ID NO: 455 (VL)
[0149] [71] An isolated antibody having affinity to CD44,
comprising:
[0150] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ. ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) shown in the following (1);
or
[0151] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the following (2);
(1) SEQ ID NO: 460 (VH CDR1), SEQ ID NO: 461 (VH CDR2), SEQ ID NO:
462 (VH CDR3), SEQ ID NO: 464 (VL CDR1), SEQ ID NO: 465 (VL CDR2),
and SEQ ID NO: 466 (VL CDR3), and
(2) SEQ ID NO: 459 (VH), and SEQ ID NO: 463 (VL)
[0152] [72] An isolated antibody having affinity to CD73,
comprising:
[0153] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1; SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) shown in the following (1);
or
[0154] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the following (2);
(1) SEQ ID NO: 468 (VH CDR1), SEQ ID NO: 469 (VH CDR2), SEQ ID NO:
470 (VH CDR3), SEQ ID NO: 472 (VL CDR1), SEQ ID NO: 473 (VL CDR2),
and SEQ ID NO: 474 (VL CDR3), and
(2) SEQ ID NO: 467 (VH), and SEQ ID NO: 471 (VL)
[0155] [73] An isolated antibody having affinity to EpCAM,
comprising:
[0156] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) shown in the following (1);
or
[0157] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the following (2);
(1) SEQ ID NO: 476 (VH CDR1), SEQ ID NO: 477 (VH CDR2), SEQ ID NO:
478 (VH CDR3), SEQ ID NO: 480 (VL CDR1), SEQ ID NO: 481 (VL CDR2),
and SEQ ID NO: 482 (VL CDR3), and
(2) SEQ ID NO: 475 (VH), and SEQ ID NO: 479 (VL)
[0158] [74] An isolated antibody having affinity to HGFR,
comprising:
[0159] heavy chain variable regions CDR1 to CDR3 and light chain
variable regions CDR1 to CDR3 specified by a combination of SEQ ID
NOs (SEQ ID NO showing an amino acid sequence of a heavy chain
variable region CDR1, SEQ ID NO showing an amino acid sequence of a
heavy chain variable region CDR2, SEQ ID NO showing an amino acid
sequence of a heavy chain variable region CDR3, SEQ ID NO showing
an amino acid sequence of a light chain variable region CDR1, SEQ
ID NO showing an amino acid sequence of a light chain variable
region CDR2, and SEQ ID NO showing an amino acid sequence of a
light chain variable region CDR3) selected from the group
consisting of the following (1) to (3); or
[0160] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (4) to (6);
(1) SEQ ID NO: 652 (VH CDR1), SEQ ID NO: 653 (VH CDR2), SEQ ID NO:
654 (VH CDR3), SEQ ID NO: 656 (VL CDR1), SEQ ID NO: 657 (VL CDR2),
and SEQ ID NO: 658 (VL CDR3)
(2) SEQ ID NO: 660 (VH CDR1), SEQ ID NO: 661 (VH CDR2), SEQ ID NO:
662 (VH CDR3), SEQ ID NO: 664 (VL CDR1), SEQ ID NO: 665 (VL CDR2),
and SEQ ID NO: 666 (VL CDR3)
(3) SEQ ID NO: 668 (VH CDR1), SEQ ID NO: 669 (VH CDR2), SEQ ID NO:
670 (VH CDR3), SEQ ID NO: 672 (VL CDR1), SEQ ID NO: 673 (VL CDR2),
and SEQ ID NO: 674 (VL CDR3)
(4) SEQ ID NO: 651 (VH), and SEQ ID NO: 655 (VL)
(5) SEQ ID NO: 659 (VH), and SEQ ID NO: 663 (VL), and
(6) SEQ ID NO: 667 (VH), and SEQ ID NO: 671 (VL)
[0161] [75] An isolated antibody having affinity to LAR,
comprising:
[0162] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
selected from the group consisting of the following (1) to (5);
(1) SEQ ID NO: 944 (VH), and SEQ ID NO: 945 (VL)
(2) SEQ ID NO: 946 (VH), and SEQ ID NO: 947 (VL)
(3) SEQ ID NO: 948 (VH), and SEQ ID NO: 949 (VL)
(4) SEQ ID NO: 950 (VH), and SEQ ID NO: 951 (VL), and
(5) SEQ ID NO: 952 (VH), and SEQ ID NO: 953 (VL)
[0163] [76] An isolated antibody having affinity to BCAM,
comprising:
[0164] a heavy chain variable region and a light chain variable
region specified by a combination of SEQ ID NOs (SEQ ID NO showing
an amino acid sequence of a heavy chain variable region and SEQ ID
NO showing an amino acid sequence of a light chain variable region)
shown in the group consisting of the following (1);
(1) SEQ ID NO: 954 (VH), and SEQ ID NO: 955 (VL)
<Isolated Nucleic Acid Molecule, Vector, and the Like>
[0165] [77] An isolated nucleic acid molecule, which encodes the
heavy chain variable region and/or the light chain variable region
of the antibody according to any of [63] to [76]. [78] A vector
including the nucleic acid molecule according to [77] in a form
capable of being expressed. [79] A transformant into which the
nucleic acid molecule according to [77] is introduced. [80] A
cancer therapeutic agent comprising the antibody according to any
of [63] to [76] as an effective ingredient. [81] A reagent for
examining or studying cancer comprising the antibody according to
any of [63] to [76].
<Examination Method>
[0166] [82] A method for examining gallbladder and liver cancer or
pancreas cancer, the method comprising the following steps:
[0167] (1) preparing subject cells or tissues separated from a
living body; and
[0168] (2) detecting a CD46 antigen in the subject cells or
tissues.
[83] A method for examining gallbladder and liver cancer or
pancreas cancer, the method comprising the following steps:
[0169] (1) preparing subject cells or tissues separated from a
living body; and
[0170] (2) detecting ITGA3 in the subject cells or tissues.
[84] A method for examining kidney cancer, hepatic cell carcinoma
or gallbladder and liver cancer, the method comprising the
following steps:
[0171] (1) preparing subject cells or tissues separated from a
living body; and
[0172] (2) detecting ALCAM in the subject cells or tissues.
[85] A method for examining kidney cancer, the method comprising
the following steps:
[0173] (1) preparing subject cells or tissues separated from a
living body; and
[0174] (2) detecting a CD147 antigen in the subject cells or
tissues.
BRIEF DESCRIPTION OF THE DRAWINGS
[0175] FIG. 1 shows one example of a method of obtaining an
antibody or an antibody set related to a certain disease.
[0176] FIG. 2 shows another example of a method of obtaining an
antibody set related to a certain disease.
[0177] FIG. 3 shows a further example of a method of obtaining an
antibody set related to a certain disease.
[0178] FIG. 4 shows a yet further example of a method of obtaining
an antibody set related to a certain disease.
[0179] FIG. 5 is a schematic view showing a vector used for
producing an scFv antibody gene library.
[0180] FIG. 6 is a schematic view showing a structure of
pscFvCA9-E8VHdVLd.
[0181] FIG. 7-1 shows a base sequence (SEQ ID NO: 401) of an insert
part of pscFvCA9-E8VHdVLd and an amino acid sequence (SEQ ID NO:
402) encoded by the base sequence.
[0182] FIG. 7-2 shows a part continuing to FIG. 7-1.
[0183] FIG. 8-1 shows a base sequence (SEQ ID NO: 405) of an insert
of pscFvCA-E8VHd and a restriction enzyme site and an amino acid
sequence (SEQ ID NO: 406).
[0184] FIG. 8-2 shows a part continuing to FIG. 8-1.
[0185] FIG. 9 shows a process of screening of an antibody clone
specific to liver cancer cell.
[0186] FIG. 10 shows an FCM reactivity (representative example) of
an antibody clone, showing histogram (right) and cell fluorescence
cytology image (left) showing the reactivity between an antibody
clones 035-011 and 041-101 and undifferentiated malignant liver
cancer cell line HLF.
[0187] FIG. 11 shows an FCM reactivity (representative example) of
an antibody clone, showing histogram (right) and cell fluorescence
cytology image (left) showing the reactivity between an antibody
clones 041-129, 045-134 and 052-042 and undifferentiated malignant
liver cancer cell line HLF.
[0188] FIG. 12 shows histograms obtained by FCM of seven kinds of
antibodies, which are overwritten onto each other. This shows that
each histogram has a unique shape.
[0189] FIG. 13 shows histograms obtained by FCM of seven kinds of
antibodies, which are overwritten onto each other. This shows that
all the histograms have high similarity to each other.
[0190] FIG. 14 shows histograms obtained by FCM of four kinds of
antibodies, which are overwritten onto each other. This shows that
all the histograms have high similarity to each other.
[0191] FIG. 15 shows histograms obtained by FCM of two kinds of
antibodies, which are overwritten onto each other. This shows that
two histograms have high similarity to each other.
[0192] FIG. 16 shows histograms obtained by FCM of three kinds of
antibodies in various cells, which are overwritten onto each other.
This shows that even when any cells are used, these antibodies
provide histograms having a high similarity to each other.
[0193] FIG. 17 shows a method for classifying the antibody group
into groups based on the results of the FCM analysis.
[0194] FIG. 18 is a table showing a classification of a plurality
of antibody clones based on the results of the FCM analysis. Each
reference mark in Table is shown by a shift amount from the
histogram (reference histogram) provided by the negative control
antibody. Double circle mark represents that the shift amount is 20
times or more (the peak value of the is 20 times or more of the
reference histogram); "o" (circle mark) represents that the shift
amount is 10 times or more; ".DELTA." (triangle mark) represents
that the shift amount is 3 times or more; and "x" represents that
the shift amount is less than 3, respectively (an oblique line
means no data is obtained).
[0195] FIG. 19 shows the results of RNAi in which CD147 is a
subject antigen. Gray color (a); cells that have not subjected to
RNAi are stained with an anti-influenza antibody YA14 cp3 as a
primary antibody; Green color (b); cells that have not subjected to
RNAi are stained with 059-053 cp3 as a primary antibody; Red color
(c); cells that have subjected to RNAi are stained with 059-053 cp3
as a primary antibody.
[0196] FIG. 20 shows the results of RNAi in which CD166 is a
subject antigen. Gray color (a); cells that have not subjected to
RNAi are stained with an anti-influenza antibody YA14 cp3 as a
primary antibody; Green color (b); cells that have not subjected to
RNAi are stained with 035-234 cp3 as a primary antibody; Red color
(c); cells that have subjected to RNAi are stained with 035-234 cp3
as a primary antibody.
[0197] FIG. 21 shows the results of RNAi in which HER1 is a subject
antigen. Gray color (a); cells that have not subjected to RNAi are
stained with an anti-influenza antibody YA14 cp3 as a primary
antibody; Green color (b); cells that have not subjected to RNAi
are stained with 048-006 cp3 as a primary antibody; Red color (c);
cells that have subjected to RNAi are stained with 048-006 cp3 as a
primary antibody.
[0198] FIG. 22 shows the results of RNAi in which HER2 is a subject
antigen. Gray color (a); cells that have not subjected to RNAi are
stained with an anti-influenza antibody YA14 cp3 as a primary
antibody; Green color (b); cells that have not subjected to RNAi
are stained with 015-126 cp3 as a primary antibody; Red color (c);
cells that have subjected to RNAi are stained with 015-126 cp3 as a
primary antibody.
[0199] FIG. 23 shows the results of RNAi in which IgSF4 is a
subject antigen. Gray color (a); cells that have not subjected to
RNAI are stained with an anti-influenza antibody YA14 cp3 as a
primary antibody; light blue color (b); cells that have not
subjected to RNAi are stained with 035-273 cp3 as a primary
antibody; orange color (c); cells that have subjected to RNAi are
stained with 035-273 cp3 as a primary antibody.
[0200] FIG. 24 shows A: an EGF binding inhibitory activity (using
A431 cells) of 048-006 antibody and 059-152 antibody; B: an EGF
binding inhibitory activity of 048-006 antibody (using low
concentration range, A431 cells), and C: an EGF binding inhibitory
activity of 048-006 antibody (using low concentration range, A431
cells).
[0201] FIG. 25 shows A: HER1 phosphorylation signal inhibitory
activity of 048-006 antibody and 059-152 antibody (results of
Western blotting). Lane 1; antibody is not added, lane 2; HR1-007
added (10 .mu.g/ml), lane 3; 048-006 antibody added (10 .mu.g/ml),
lane 4; 048-006 antibody added (10 .mu.g/ml), lane 5; 059-152
antibody added (10 .mu.g/ml), lane 6; and 059-152 antibody added
(10 .mu.g/ml). Upper part shows the results of Western blotting by
using anti-phosphorylation tyrosine antibody (mouse monoclonal
antibody). Lower part shows the results of Western blotting by
using anti-.beta. actin antibody (rabbit polyclonal antibody). B:
HER1 phosphorylation signal inhibitory activity of a 048-006
antibody (low concentration range). Lane 1; not treated, lane 2;
antibody is not added, lane 3; HR1-007 is added (1 .mu.g/ml), lane
4; 048-006 antibody added (0.5 .mu.g/ml), lane 5; 048-006 antibody
added (0.1 .mu.g/ml), lane 6; and 048-006 antibody added (0.05
.mu.g/ml). After incubation with an antibody for 30 minutes, Her1
was added. Upper part shows the results of Western blotting by
using anti-phosphorylation tyrosine antibody (mouse monoclonal
antibody). Lower part shows the results of Western blotting by
using anti-.beta. actin antibody (rabbit polyclonal antibody). C:
Comparison of HER1 phosphorylation signal inhibition effects of
048-006 antibody, 059-152 antibody and ERBITUX (using A-431 cells.
Lane 1; HR1-007, lane 2; 048-006 antibody, lane 3; 059-152
antibody, lane 4; ERBITUX, lane 5; antibody is not added (EGF (+)),
lane 6; antibody is not added (EGF (-)). D: Comparison of HER1
phosphorylation signal inhibition effects of 048-006 antibody,
059-152 antibody and ERBITUX (using CCF-RC1 cells). Lane 1;
HR1-007, lane 2; 048-006 antibody, lane 3; 059-152 antibody, lane
4; ERBITUX, lane 5; antibody is not added (EGF (+)), lane 6;
antibody is not added (EGF (-)). E: Comparison of HER1
phosphorylation signal inhibition effects of 048-006 antibody and
059-152 antibody clone and ERBITUX (using Caki-1 cells). Lane 1;
HR1-007, lane 2; 048-006 antibody, lane 3; 059-152 antibody, lane
4; ERBITUX, lane 5; antibody is not added (EGF (+)), lane 6;
antibody is not added (EGF (-)).
[0202] FIG. 26 shows a result of BIACORE experiment. Fixation
method: CM5 chip of BIAcore is used and NHS is used so as to fix a
partial sequence of HER1 to sensor. 048-006 antibody is allowed to
flow at the above-mentioned concentration to observe signals.
[0203] FIG. 27 shows a result of an ADCC activity test. An antibody
to be used: anti-ITGA3 antibody, a target culture cell: HLF.
[0204] FIG. 28 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell: A-431.
[0205] FIG. 29 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell: A549.
[0206] FIG. 30 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell: ACHN.
[0207] FIG. 31 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell:
CCF-RC-1.
[0208] FIG. 32 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell:
NCI-H1373.
[0209] FIG. 33 shows a result of an ADCC activity test. An antibody
to be used: anti-HER1 antibody, a target culture cell: SK-OV-3.
[0210] FIG. 34 shows a result of an ADCC activity test. An antibody
to be used: anti-HER2 antibody, a target culture cell: BT-474.
[0211] FIG. 35 shows a result of an ADCC activity test. (a) An
antibody to be used: anti-ALCAM antibody, 066-174 whose, a target
culture cell: NCI-H1373. (b) An antibody to be used: anti-ALCAM
antibody, 066-174, target culture cell: CW2. (c) An antibody to be
used: anti-ALCAM antibody, 066-174, target culture cell:
NCI-H441.
[0212] FIG. 36 shows a result of an ADCC activity test. (a) An
antibody to be used: anti-ALCAM antibody, 035-234, target culture
cell: CW2. (b) An antibody to be used: anti-ALCAM antibody,
035-234, target culture cell: NCI-H441.
[0213] FIG. 37 shows a result of an ADCC activity test. (a) An
antibody to be used: anti-ICAM1 antibody, 053-051, target culture
cell: NCI-H441. (b) An antibody to be used: anti-ICAM1 antibody,
053-051, target culture cell: HepG2.
[0214] FIG. 38 shows a result of an ADCC activity test. (a) An
antibody to be used: anti-ICAM1 antibody, 053-059, target culture
cell: NCI-H441. (b) An antibody to be used: anti-ICAM1 antibody,
053-059, target culture cell: HepG2.
[0215] FIG. 39 shows a result of an ADCC activity test. (a) An
antibody to be used: anti-ICAM1 antibody, 053-085, target culture
cell: NCI-H441. (b) An antibody to be used: anti-ICAM1 antibody,
053-085, target culture cell: HepG2.
[0216] FIG. 40 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 048-006
antibody or 059-152 antibody,
[0217] target culture cell: CCF-RC-1.
[0218] FIG. 41 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 048-006
antibody or 059-152 antibody, target culture cell: NCI-H1373.
[0219] FIG. 42 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 048-006
antibody or 059-152 antibody,
[0220] target culture cell: A-431.
[0221] FIG. 43 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 041-118
antibody, target culture cell: NCI-H1373.
[0222] FIG. 44 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-EpCAM antibody, 067-153
antibody, target culture cell: MKN-45.
[0223] FIG. 45 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-EpCAM antibody, 067-153
antibody, target culture cell: HT-29.
[0224] FIG. 46 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-EpCAM antibody, 067-153
antibody, target culture cell: NCI-H1373.
[0225] FIG. 47 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HGFR antibody, 067-133
antibody, target culture cell: NCI-H1373.
[0226] FIG. 48 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 055-147
antibody or 059-173 antibody, target culture cell: CCF-RC1.
[0227] FIG. 49 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody. 048-006
antibody, 059-152 antibody, 055-147 antibody or 059-173 antibody,
target culture cell: HT-29.
[0228] FIG. 50 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 048-006
antibody, 055-147 antibody or 059-173 antibody, target culture
cell: A431.
[0229] FIG. 51 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HER1 antibody, 048-006
antibody or 059-152 antibody, target culture cell: ACHN.
[0230] FIG. 52 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 035-234
antibody or 066-174 antibody,
[0231] target culture cell: NCI-H1373.
[0232] FIG. 53 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 035-234
antibody or 066-174 antibody, target culture cell: SKOv3.
[0233] FIG. 54 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 035-234
antibody or 066-174 antibody, target culture cell: CW-2.
[0234] FIG. 55 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 041-118
antibody, target culture cell: EBC-1.
[0235] FIG. 56 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ALCAM antibody, 080-040
antibody, target culture cell: NCI-H1373.
[0236] FIG. 57 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ICAM1 antibody, 053-042
antibody, target culture cell: NCI-H1373.
[0237] FIG. 58 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ICAM1 antibody, 053-051
antibody, 053-059 antibody or 053-085 antibody, target culture
cell: NCI-H1373.
[0238] FIG. 59 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-EpCAM antibody, 067-153
antibody, target culture cell: EBC-1.
[0239] FIG. 60 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HGFR antibody 067-133
antibody, target culture cell: MKN-45.
[0240] FIG. 61 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-HGFR antibody 067-133
antibody, target culture cell: EBC-1.
[0241] FIG. 62 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-ITGA3 antibody, 015-003
antibody, target culture cell: ACHN.
[0242] FIG. 63 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-CD147 antibody, 059-053
antibody, target culture cell: CCF-RC1.
[0243] FIG. 64 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-CD147 antibody, 059-053
antibody, target culture cell: ACHN.
[0244] FIG. 65 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-PTP-LAR antibody, 064-044
antibody or 079-085 antibody, target culture cell: PC-14.
[0245] FIG. 66 shows antibody dosage dependence of the ADCC
activity. An antibody to be used: anti-CD44 antibody. 064-003
antibody, target culture cell: PC-14.
[0246] FIG. 67 shows a result of a cell proliferation inhibition
test. An antibody to be used: anti-HER1 antibody (048-006), target
subjected cultured cell: A-431.
[0247] FIG. 68 shows a result of a cell proliferation inhibition
test. An antibody to be used: anti-HER1 antibody (048-006), target
subjected cultured cell: ACHN.
[0248] FIG. 69 shows a result of a cell proliferation inhibition
test. An antibody to be used: anti-HER1 antibody (048-006), target
subjected cultured cell: NCI-H1373.
[0249] FIG. 70 shows a result of a cell proliferation inhibition
test. An antibody to be used: anti-HER1 antibody (048-006), target
subjected cultured cell: SK-OV-3.
[0250] FIG. 71 shows a result of a cell proliferation inhibition
test. An antibody to be used: anti-HER2 antibody (015-126), target
subjected cultured cell: BT-474.
[0251] FIG. 72 shows a result of an antitumor experiment using
mouse. An antibody to be used: anti-HER1 antibody (048-006),
subject transplant cell: human lung cancer cell H1373 cell.
[0252] FIG. 73 shows a result of an antitumor experiment using
mouse. An antibody to be used: anti-HER1 antibody (048-006),
subject transplant cell: epidermoid tumor A-431.
[0253] FIG. 74 shows a result of an antitumor experiment using
mouse. An antibody to be used: anti-HER1 antibody (048-006),
subject transplant cell: epidermoid tumor A-431.
[0254] FIG. 75 shows a result of an antitumor experiment using
mouse. An antibody to be used: anti-HER1 antibody (059-152),
subject transplant cell: epidermoid tumor A-431.
[0255] FIG. 76 is a table showing culture conditions of cell lines
to be used in experiments.
[0256] FIG. 77 is a conceptual diagram of three-dimensional ELISA,
showing how each mixture antibody is prepared.
[0257] FIG. 78 is a conceptual diagram of three-dimensional ELISA,
showing a procedure of specifying an antibody clone.
[0258] FIG. 79 shows a result of ELISA using a plate mixed antibody
(antigen is CD147).
[0259] FIG. 80 shows a result of ELISA using a row mixed antibody
(antigen is CD147).
[0260] FIG. 81 shows a result of ELISA using a column mixed
antibody (antigen is CD147).
[0261] FIG. 82 shows a result of ELISA using a plate mixed antibody
(antigen is HER1).
[0262] FIG. 83 shows a result of ELISA using a row mixed antibody
(antigen is HER1).
[0263] FIG. 84 shows a result of ELISA using a column mixed
antibody (antigen is HER1).
[0264] FIG. 85 shows a result of ELISA using a selected antibody
clone (antigen is HER1).
[0265] FIG. 86 shows a RNAi effect on SKOv-3 cells. A: anit-ITGA3
antibody, B: anit-ITGB1 antibody, C: 015-003 cp3 antibody. Broken
line: no RNAi, solid line: ITGA3 RNAi, light-colored solid line:
ITGB1 RNAi, gray: and no primary antibody.
[0266] FIG. 87 shows a correspondence between a tissue that has
been diagnosed to be specific in immunostaining using a clinical
cancer specimen and each antibody clone.
[0267] FIG. 88 shows a reactivity of a clinical cancer specimen and
each antibody clone. + represents positive to the immunostaining;
.+-. represents weakly positive to the immunostaining; and -
represents negative to the immunostaining.
DETAILED DESCRIPTION OF THE INVENTION
Terms
[0268] For convenience, certain terms employed in the specification
are collected herein.
[0269] In the specification, the terms "comprise/include" and
"comprising/including" are used to include the meaning of
"consisting of:" Therefore, for example, "a product (or method)
comprising/including a plurality of elements (members)" necessarily
includes also the terms "a product (or method) consisting of a
plurality of elements (members)"
[0270] The term "disease" herein is used interchangeably with the
terms meaning that some function failure occurs, for example,
illness and sickness. Furthermore, unless otherwise noted, in this
specification, this term is used to encompass the words meaning the
condition (state) of disease such as condition, pathologic
condition, symptom, and state of health. That is to say, the term
"disease" is used interchangeably with the terms such as condition
and pathologic condition.
[0271] The term "isolated" used herein means a state in which it is
taken out from the original environment (for example, a natural
environment in the case of a natural material), that is to say,
means a state that is a different state from the original existing
state by an artificial manipulation.
[0272] An "isolated antibody" does not include an antibody in a
state in which it is natural state and no external manipulation
(artificial manipulation) is given. It does not include an antibody
produced in the individual body and remaining therein. An isolated
antibody is typically present in a state in which other kinds of
antibodies are not contaminated, that is, present singly (as an
assembly of the same kinds of antibodies). In the case of an
"isolated" state of the CDR region, in addition to the state which
is present singly, a state which is present together with the other
regions of the antibody is included. That is, the term "isolated
CDR" includes not only a CDR that is present singly but also a CDR
that is present as a part of an isolated antibody is included.
[0273] "HER1" is also referred to as erbB1, c-erbB-1, EGFR
(Epidermal Growth Factor Receptor), or v-erbB. Originally, a gene
corresponding to a cancer gene erbB found in the retrovirus that
infects chicken and causes carcinogenesis (erythroleukemia) on the
genome is isolated. And this gene is determined to be a receptor of
EGF. By the way, EGF (Epidermal Growth Factor) as a ligand was
found as a factor for promoting the cleavage of the eyelids of
newly born mouse and development of an incisor in an extracted
solution of the mouse submaxillary gland in 1962, and has been
studied widely as cell proliferation, differentiation and survival
factors. EGF is a peptide composed of 53 amino acids and has a
characteristic structure including three disulfide loops formed of
six cysteine residues. Thereafter, this structure has been found in
a large number of proteins and is referred to as EGF-like domain.
The EGF family has one or more EGF-like domains and directly binds
to a receptor type tyrosine kinase EGF receptor (EGFR) family
(another name: ErbB family) so as to activate this.
[0274] On the other hand, currently, four kinds of receptor ErbB
families has been found and they are called EGFR (ErbB-1), ErbB-2,
ErbB-3, and ErbB-4. ErbB-1 and ErbB-2 overexpress in various human
tumors and are involved in the deterioration of the prognosis or
survival rate. Furthermore, stimuli of these receptors are involved
in cell proliferation and in turn involved in several processes
related to progress, infiltration, and metastasis of tumor. To
date, a phosphorylation inhibiting agent specific to EGFR have been
approved as a therapeutic agent for lung cancer. They are found to
highly express in many cancers. Cetuximab (ERBITUX, which is
mouse/human chimeric antibody) has been developed by ImClone
Systems and already marketed. ERBITUX inhibits the initial process
of activation of the information transmission passage by the
phosphorylation of dimerized-EGFR when it binds to a receptor of
EGF as a ligand. Note here that the amino acid sequence of HER1 is
shown in SEQ ID NO: 369.
[0275] "HER2" is also referred to as erbB-2, c-erbB-2, or neu. HER2
belongs to a receptor type tyrosine kinase family and its
over-expression and gene amplification in the breast cancer,
ovarian cancer, stomach cancer, and the like, have been reported.
HER2 is a molecule that was found in 1985 when DNA containing a
region of gene similar to EGFR was amplified (gene amplification)
in the brain tumor and breast cancer derived from glia cells was
observed. HER2 has low shedding level and is thought to be very
effective as a target molecule in treating cancers. In many
institutions, the monoclonal antibody (MoAb) showing effects of
promoting or suppressing the tumor proliferation has been produced.
MoAb showing a tumor proliferation suppressing effect is used for
clinical test as a simple substance of the antibody or in
combination with anti-cancer drugs such as cisplatin, and its
efficacy has been reported. The EGFR family includes four kinds,
but only EGFR (HER1) and HER4 have both the ligand binding sites
and tyrosine phosphorylation enzymatic activity sites. HER2 does
not have the ligand binding site. Instead using a ligand, HER2 has
a structure that is activated from the first in terms of dimer
formation ability. Incidentally, HER3 lacks the tyrosine
phosphorylation activity. Therefore, HER2-HER3 hetero-dimer is a
functional molecule. Genentech isolated 11 kinds of mouse
monoclonal antibodies to HER2 in 1989. Among them, 4D5 was made
into a humanized antibody and succeeded in developing Trastuzumab
(Herceptin). Note here that the amino acid sequence of HER2 is
shown in SEQ ID NO: 370.
[0276] "CD46 antigen" is an O-type sugar chain bonded non-disulfide
bonded dimer protein having a molecule weight of 56 to 66 kDa,
which is also referred to as MCP (Membrane Co-factor Protein),
gp45-70, HuLY-m5, measles virus receptor, MIC10, TLX-B antigen,
TRA2, trophoblast leucocyte common antigen, and
trophoblast-lymphocyte cross-reactive antigen. This molecule binds
to C3b or C4b and is known as Membrane Co-factor Protein (MCP) that
is a co-factor for promoting the degradation by serine protease or
I factor in plasma. It is also a receptor of the surface protein of
measles virus agglutinin and Streptococcus group A. It has been
reported that it is expressed in the thymus gland cells, T
lymphocyte, B lymphocyte, monocyte, granulocyte, NK cells,
platelet, endothelial cell, epithelium cells and fibroblast but
does not express in the erythrocyte. On the assumption that only
cells inducing the production of antibody to cancer specific
antigen abnormally expressing in carcinogenicity and escaping from
the attack of cancer tissue by complement (complement-dependent
cytotoxicity, CDC) may actually grow into cancer, the expression of
molecule group having an effect of inhibiting the complement has
been analyzed in detail. There have been many reports about the
abnormal expression of CD46 in cancer cells, however, few evidence
showing that the production of antibody against antigen specific to
cancer cells are induced. An amino acid sequence of CD46 antigen is
shown in SEQ ID NO: 371.
[0277] "ITGA3 (integrin alpha 3)" is also referred to as alpha 3
beta 1 Epiligrin Receptor, alpha 3 beta 1 Integrin, Epiligrin
Receptor, CD49c, VLA-3, Gap b3, Galactoprotein b3, or Laminin-5
Receptor in which integrin .alpha.3 chain having a molecular weight
of 150 kDa and integrin .beta.1 chain (CD29 molecule) having a
molecular weight of 130 kDa are bonded to each other non-covalently
to form a VLA-3 complex (.alpha.3.beta.1 or CD49c/CD29). It is
known as a receptor of laminin, collagen, fibronectin, invasion and
epiligrin. Integrin is a hetero dimer molecule composed of .alpha.
chain and .beta. chain. Twenty four types of .alpha. chains and
nine types of .beta. chain form a variety of molecule groups by
various combination and selective splicing. The extracellular
domain binds to the extracellular matrix (for example, collagen,
fibronectin, laminin). The side of cytoplasm is bonded to actin
filament via talin, filanin, and .alpha.-actinin. It functions as
an adhesive molecule and further functions as an important role as
information transmission molecule. Above all, .alpha.3.beta.1
molecule is associated with a tetraspanin molecule C151. Note here
that the amino acid sequence of ITGA3 is shown in SEQ ID NO:
372.
[0278] The "ICAM1 (Intercellular adhesion molecule-1)" is also
referred to Intercellular Adhesion Molecule 1 or CD54 Antigen and
is transmembrane glycoprotein having seven binding sites of the
N-bonding sugar chain. The molecular weight is 90 kDa. ICAM belongs
to Ig-superfamily and is known to be mainly involved with adhesion
of leukocyte. It also mediates T lymphocyte adhesion to an antigen
presenting cell (APC) and is involved with the interaction between
T cell and T cell or between T cell and B cell. It also involved
with the adhesion to endothelial cell in which monocyte,
lymphocyte, and neutrophil are activated. ICAM is bonded to
integrin of LFA-1 (CD11a/CD18) and Mac-1 (CD11b/CD18). Furthermore,
it also is a receptor of rhinovirus. It is expressed on various
kinds of activated cells in addition to the endothelial cells. For
example, it is expressed on the monocyte. On B- and T-lymphocytes,
thymus gland cells, dendritic cells, endothelial cells, fibroblast,
keratinocyte, chondrocyte and epithelium cells, expression is
enhanced. The characteristics required to obtain during the
cancerization process of epithelium cells include capability of
invading into cells, and furthermore migrating and being fixed in
metastasis. Therefore, it is thought that the expression of
adhesion factor contributes to carcinogenesis. The adhesion factor
is roughly classified into five groups, i.e., selectin (E-, P-, and
L-), molecules (Ig-superfamily) having an immunoglobulin-like
domain, integrin, Cadherin, and CD44. In cancerization, it is
recognized that the expression of E Cadherin is suppressed.
Abnormal expression in some cancer cases has been reported. Note
here that the amino acid sequence of ICAM1 is shown in SEQ ID NO:
373.
[0279] "ALCAM (Activaed leukocyte cell adhesion molecule)" is
transmembrane protein that is also referred to as CD166 antigen,
KG-CAM, CD6 Ligand, and Neurolin. ALCAM is an immunoglobulin
superfamily molecule including ten N-bonding type sugar chain added
sites. ALCAM has a molecular weight of 100 to 105 kDa and is
composed of five extracellular Ig-like domains and the
intracellular terminus having 32 amino acid, and short
transmembrane region. ALCAM is one of the adhesive molecules, is
present on the activated leukocyte and is identified as a ligand
molecule to CD6 molecule (which functions as a signal receptor in T
cells). ALCAM also functions as an adhesion factor in homophylic
(ALCAM-ALCAM) or heterophylic (ALCAM-CD6) interaction. It is
suggested that ALCAM can form oligomer at intercellular adhesion
site via three C2-like domains near the membrane. The distribution
of ALCAM is not restricted by cell strains and ALCAM is expressed
in various types of cells such as hematopoietic cells, endothelial
cells, epithelium cells of the thymic cortex and thymic medulla,
mesenchymal cell of the bone marrow, fibroblast, liver cells, and
the like. In the peripheral blood, it is weakly expressed in
activated T- and B-cells, monocyte, circulated dendritic cells, and
granulocyte. Although ALCAM shows wide dispersion of tissues, the
expression of ALCAM is generally limited to cell populations
involved in proliferation or migration. In the thymus gland, since
ALCAM is expressed in CD6+thymus gland cells, and thymus gland
epithelium cells, its interaction with CD6 molecule is thought to
play a role in the differentiation of T cells. In addition, it is
suggested that ALCAM adhesive molecules are involved in the fetal
blood formation, differentiation of angioblastic cells, and
capillary angiogenesis. The roles of ALCAM in cancerization is
variously assumed (e.g., controlling of MMP activation, causing
internalization and recycling, functioning as a substrate of ADM17
and ADAM10 (abbreviation of a disintegrin and metalloprotease),
protecting from apoptosis and autophasy), however, no decisive
roles have not reported. The interaction of ALCAM-CD6 is thought to
be carried out in the both direction. The amino acid sequence of
ALCAM is shown in SEQ ID NO: 374.
[0280] "CD147 antigen" is membrane glycoprotein belonging to an
immunoglobulin superfamily and is also referred to as BSG, TCSF
(Tumor cell-derived collagenase stimulatory factor), 5F7 protein,
OK blood group protein, basigin protein, collagenase stimulatory
factor protein, EMMPRIN (Extracellular matrix metalloproteinase
Inducer), M6 activation antigen, human leukocyte activation antigen
M6, or the like. D147 antigen has two aspects. One is observed when
it functions on the cell surface, it exhibits the activation of
MMP-1, 2, 3 (matrix metalloprotease) and the lectin activity
recognizing oligomannose as membrane glycoprotein having two Ig
domains. The activation of MMP receives much attention in cancers
(which is also known as EMMPRIN in Europe and America). That is to
say, CD147 antigen expressing in cancer cells activates MMP
expressing in the surrounding fibroblast and contributes to the
infiltration of cancers. On the other hand, the activation of
oligomannose lectin is especially important in the interaction of
nerve cells and indicated to have a relationship with respect to
neurite outgrowth. The second aspect is a function in cells. CD147
antigen forms a homo dimer. It is reported that this formation
needs N-terminal Ig domain and does not need addition of sugar
chain. CD147 has the following interesting reports: integrin
.alpha.3.beta.1 and CD147 form a complex, and in this case, TM4SF
(tetraspanin) molecule does not join the complex. In cancerization,
the production of D147 changes anchorage-dependent growth to
independent growth, which is promoted by the production of
hyaluronic acid (hyaluronam). It is interesting that the receptor
of hyaluronic acid includes CD44 and RHAMM. CD147 induces the
production of MMP, and a part of CD147 is solubilized due to the
effect of the MMP. CD147 acts on integrin so as to change the
structure of cells. CD147 affects the angiogenesis. Furthermore,
mass expression-cell proliferation of CD147 and Cyclophin A has
been found.
[0281] The amino acid sequence of the CD147 antigen is shown in SEQ
ID NO: 375.
[0282] "IgSF4" is an abbreviation of immunogloblin superfamily
member 4 and is also referred to as BL2, ST17, NECL2, TSLC1,
IGSF4A, SYNCAM, and sTSLC-1. IgSF4 has homology of NCAM (neural
cell adhesion molecule) and amino acid sequence. IgSF4 is thought
to be expressed from human 11-chromosome, 11q23.2. It has been
reported that IgSF4 expressed as a suppression gene in a lung
cancer specific manner and that IgSF4 is involved in the nerve
adhesion in the brain (Biederer T et al. Science. 2002 Aug. 30; 297
(5586): 1525-31). The sequence information of IgSF4 is recorded in
a NCBI-PUBMED database (Accession No. NM.sub.--01433, Definition:
Homo sapiens immunoglobulin superfamily, member 4 (IGSF4), mRNA).
As to the relationship with respect to the carcinogenesis, as shown
by the name TSLC1 (tumor suppressor in lung cancer 1), it receives
attention as a tumor suppressor gene. However, IgSF4 shows high
expression in 100% adult T cell leukemia (ATL) cells and it is
suggested that IgSF4 may work as oncogene. The amino acid sequence
of IgSF4 is shown in SEQ ID NO: 376.
[0283] "C1qR" is a complement receptor encoding a type I membrane
protein. This protein functions as a receptor for complement
protein C1q, mannose binding lictin, and lung surfactant protein A.
Two or more polypeptides of 70 kDa are bonded by disulfide bonding
so as to form C1qR. Removing an immune complex is an important
function of the complement and the C1q receptor is a functional
receptor that is bonded to a collagen portion of C1q thereby
linking the immune complex to phagocyte. It is suggested that C1qR
forms complex with CD43. The amino acid sequence of C1 qR is shown
in SEQ ID NO: 446.
[0284] "CD44" is a transmembrane protein belonging to a hyaladherin
family, which is cell surface glycoprotein related to cellular
interaction, cell adhesion and cell migration. It is a hyaluronic
acid receptor. It is thought that a wide variety of the structural
and functional isoforms of proteins by the selective splicing or
post-translation modification of this molecule may be involved in
tumor metastasis. The CD44 molecule is expressed in almost all the
cells and tissues. However, in general, it is not expressed in the
platelet, liver cell, cardiac muscle, uridiferous tubule
epithelium, testis, and skin. The amino acid sequence of CD44 is
shown in SEQ ID NO: 447.
[0285] "CD73" is also referred to as 5-prime-ribonucleotide
phosphohydrolase and transforms purine 5-prime mononucleotides into
nucleosides at the neutral pH. The enzyme mediates
glycosylphosphatidyl inositol to the surface of the outside of the
plasma membrane and is bonded to the surface of the outside of the
plasma membrane. CD73 is a homodimer composed of two 70 kDA
subunits. CD73 is used as a marker of the lymphocyte
differentiation. It has been known that the deletion of this gene
is related to various immune defective diseases. The amino acid
sequence of CD73 is shown in SEQ ID NO: 448.
[0286] "EpCAM" has 22 or more names as to only the number of names
used and cited several times in research paper. This antigen exists
on genome 2p21. This antigen is a protein having a full length of
314aa, and 34920 Da. In the documents in which this molecule is
examined at the mRNA level, it is detected in healthy human
individuals, 100% in the peripheral blood (PB) level and 40% in the
bone marrow (BM) level. It has been reported that it can be
detected in large intestine but cannot detected in the liver,
prostate, and lung. In cancer cell line, in the relationship with
respect to p53, the methylation of EpCAM is lost due to the
mutation or deletion of p53 and the amplification is induced. The
amino acid sequence of EpCAM is shown in SEQ ID NO: 449.
[0287] The first Met gene discovered as a search product of
oncogene using NIH3T3 gene is HGFR (Hepatocyte growth factor
receptor). HGF is also referred to as a scatter factor and is
utterly independently isolated as a molecule having an extremely
different apparent function. Similar to HER1 and PDGF, HGFR is a
receptor having a ligand binding domain outside the cells and has a
tyrosine phosphorylation enzymatic activity site at the cytoplasm
side, however, the function is extremely different. In general,
when the cell proliferation factor or a differentiation induction
factor is bonded to a receptor so as to cause the phosphorylation
of protein, it finally activates the transcription factor and
expresses a certain gene set by way of some of the limited
information transmission pathway (Ras/MAP kinase pathway, and the
like). In this case, the type of the cell response is finally
determined by transcription factor. Thus, when the cancerization
may activate some of the proliferation factors-receptor, it is
thought that changes other than cancerization are not likely to
occur in the cells. Currently, as to the cancerization, the
phenomenon called epithelial-mesenchymal transition (EMT) receives
much attention and the factor plays a core role in the phenomenon.
In such examples, since a large number of molecules cooperatively
function, detail analysis is needed. The amino acid sequence of
HGFR is shown in SEQ ID NO: 450.
[0288] LAR (Leukocyte common Antigen-Related) belongs to a PTP
(protein tyrosine phosphatase) family. The PTPs are known to be
molecules to modulate the process in the various aspects of the
cancerization, division cycle, differentiation, cell growth, and
the like. The structure thereof includes an extracellular region,
mono-transmembrane region, and two tandem catalyzing domain in the
cytoplasm (homolog of protein tyrosine phosphatase). The
extracellular region has a structure similar to nerve cell adhesion
factor, which includes three Ig-like domains and nine non-Ig like
domains (homolog of NCAM). The function of this molecule is
involved in the cell adhesion in the formation adherents junctions
in the epithelium. Note here that it is confirmed that this
molecule is highly expressed in insulin sensitive mast cells, and
insulin resistant cells. Therefore, it is suggested that it is
related to insulin. Furthermore, it is reported that anti-LAR
antibody has an insulin receptor inhibitory activity of the insulin
receptor forced expressing body (Knock-down of LAR protein tyrosine
phosphatase induces insulin resistance: Mander A, Hodgkinson C P,
Sale G J.: FEBS Lett. 2005 Jun. 6; 579 (14): 3024-8.).
[0289] Furthermore, LAR is expressed on the membrane of all the
leukocytes and is referred to as protein tyrosine phosphatase
receptor type F (PTPRF) and protein sequence (SEQ ID NO: 941)
thereof is registered as TDHULK in Protein sequence database of the
Protein Information Resource (PIR).
[0290] BCAM (basal cell adhesion molecule) (Lutheran blood group)
is referred to as CD239 antigen and its protein sequence is
registered as Q86VC7 (UniProtKB/Swiss-Prot) and 13800 (PIR) (SEQ ID
NO: 942). It produces a selective splicing product from a single
gene in the chromosome 19q13.2-q13.3. It is a glycoprotein having
an immunoglobulin-like domain. It is a mono-transmembrane type and
expressed widely. Its expression in the pancreas is high and its
expression in the brain is low. The BCAM antigen is modulated
excessively in certain cells, thus inducing the malignant
alteration of cancers. Also, it is shown that it is overexpressed
in the living body with ovarian cancers.
[0291] In the present invention, "liver cancer" is intended to be
widely interpreted and it includes liver carcinoma and liver
sarcoma. Furthermore, the term "cancer" in the present invention is
interchangeably with "tumor." Furthermore, in the stages before the
pathological diagnosis is not established, that is, before whether
the tumor is benign or malignant has not been determined, the term
may include benign tumor, benign-malignant borderline lesion, and
malignant tumor collectively.
[0292] Cancers are called under the name of the organs in which the
cancers are developed or the name of development body tissue. Main
examples include tongue cancer, gingival cancer, pharynx cancer,
maxillary cancer, laryngeal cancer, salivary gland cancer,
esophageal cancer, stomach cancer, small intestinal cancer, large
bowel cancer, rectum cancer, liver cancer, biliary tract cancer,
gallbladder cancer, pancreas cancer, lung cancer, breast cancer,
thyroid gland cancer, adrenal gland cancer, hypophyseal tumor,
pinealoma, uterine cancer, ovarian cancer, vaginal cancer, urinary
bladder cancer, kidney cancer, prostate cancer, urethral cancer,
retinoblastoma, conjunctival cancer, gliocystoma, glioblastoma,
skin cancer, leukemia, malignant lymphoma, testicular tumor,
osteosarcoma, rhabdomyoblastoma, leiomyosarcoma, blood vessel
sarcoma, liposarcoma, chondrosarcoma, Ewing's sarcoma, and the
like. Furthermore, depending upon the characteristics of the sites
of the organs of development, cancers are subclassified into, for
example, upper, middle, and lower pharynx cancers, upper, middle,
and lower esophageal cancers, gastric cardia cancer, gastropyloric
cancer, cervical cancer, cancer of uterine body, and the like.
These cancers are included in the "cancers" of the present
invention but the cancers are not limited to these alone.
[0293] In the specification, if necessary, the following
abbreviations (in parentheses) are used according to the
practice.
[0294] Heavy chain (H chain), light chain (L chain), heavy chain
variable region (VH), light chain variable region (VL),
complementarity determining region (CDR), first complementarity
determining region (CDR1), second complementarity determining
region (CDR2), third complementarity determining region (CDR3),
first complementarity determining region of heavy chain (VH CDR1),
second complementarity determining region of heavy chain (VH CDR2),
third complementarity determining region of heavy chain (VH CDR3),
first complementarity determining region of light chain (VL CDR1),
second complementarity determining region of light chain (VL CDR2),
third complementarity determining region of light chain (VL
CDR3)
[0295] The first aspect of the present invention relates to a
method of classifying antibody. The classifying method of the
present invention includes the following steps.
[0296] (1) preparing a plurality of antibodies recognizing cell
surface antigen;
[0297] (2) bringing each of the antibodies into contact with cells
of the same kinds;
[0298] (3) analyzing each cell after step (2) by flow cytometry so
as to obtain data showing reactivity between the antibody and the
cell surface; and
[0299] (4) comparing the obtained data and classifying antibodies
based on the similarity of the data.
Step (1)
[0300] In the classifying method of the present invention, firstly,
a plurality of antibodies recognizing cell surface antigen are
prepared. For convenience of explanation, the antibody classified
by the classifying method of the present invention is also referred
to as a "sample antibody."
[0301] In the present invention, the "cell surface antigen" is a
molecule in which at least a part thereof exists outside the cell
and which forms an antigenic determinant on the surface of the
cell. For example, protein such as transmembrane type protein
having a cell membrane transmembrane domain and an extracellular
domain and GPI anchor type protein, which are linked to cell
membrane via glycolipid and the like and existing on the surface of
the extracellular surface, can form such an antigenic determinant.
The cell surface antigen can be formed by a simple protein
(basically, constituent includes only amino acids), a conjugated
protein (constituent other than amino acid are contained. For
example, glycoprotein and lipoprotein), or a modified protein (a
protein modified by, for example, phosphorylation, acetylation, and
methylation), and the like. Furthermore, two or more same types or
different types of molecules may cooperatively form an antigen
determinant.
[0302] The "cell surface antigen" of the present invention is not
particularly limited to animal cells and may include cell surface
antigens of plant cells, microorganism cells, and the like.
Preferably, "cell surface antigen" of the present invention is the
cell surface antigen of animal cells. It is known that the animal
cells have various cell surface antigens. The "animal cells" herein
include mammalian cells and non-mammalian cells, but preferably
mammalian cells. Above all, human cells are preferable.
[0303] Preferably, a plurality of antibodies recognizing the intact
cell surface antigen are prepared. The "intact state" means that
the original state is maintained. It has the same meaning that "not
denatured state."
[0304] The "antibody recognizing cell surface antigen" represents
an antibody recognizing and binding the cell surface antigen with
highly specific recognition mechanism between the antigen and the
antibody. The origins, types, classes, forms and the like, of
antibodies are not particularly limited. Therefore, the "antibody"
in the present invention includes an antibody of non-human animals
such as mouse and rat, a chimeric antibody in which a part of the
region is substituted with that of other animal (including human),
a humanized antibody, and human antibody. Preferably, human
antibody or human type antibody (humanized antibody) are used.
Antibody fragments such as Fab, Fab', F(ab')2, scFv, and dsFv
antibody may be used. An antibody for treatment application
includes an antibody in which VH and VL (Fv region) are converted
into IgG type is included.
[0305] An antibody recognizing a cell surface antigen can be
prepared by, for example, bringing an antibody library into contact
with the cell surface antigens and recovering the antibodies bound
to the cell surface antigens. One of such preparation methods is a
method reported by the present inventors before (Japanese Patent
Unexamined Publication No. 2005-185281). This method makes it
possible to select an antibody clone recognizing intact cell
surface antigen from the phage antibody library. The present
invention can preferably use the antibody assembly derived from
each antibody clone. The "assembly derived from each antibody
clone" herein includes the selected antibody clone itself, or the
product prepared by using the gene. The latter example includes an
antibody in which genes of the selected antibody clone is
transformed by an appropriate host (for example, E. coli) and the
host is expressed, or an antibody to which further genetic
engineering modification is added in the host or by the use of the
host and then the modified antibody is expressed.
[0306] The above-mentioned publication discloses as the antibody
having a human Fv region, scFv-CL-cp3 antibody (an antibody in
which a phage protein cpIII is fused to scFV via the light chain
constant region), scFv-CL-pp antibody (an: antibody in which two
proteins A are fused to scFV via the light chain constant region),
scFv-CL-pp-Avi antibody (an antibody in which avidin is fused to
scFv-CL-pp antibody), scFv-CL-Avi antibody (an antibody in which
avidin is fused to scFV via the light chain constant region),
scFv-CL-pp-Avi or antibody obtained by biotining scFv-CL-Avi
antibody (an antibody in which biotin is bonded to an avidin part),
and the like. The present invention can preferably use any of these
types of antibodies. These antibodies having a human Fv region are
very useful in providing an antibody for treatment (production of
an antibody for treatment can be proceeded advantageously).
[0307] Note here that the contents disclosed Japanese Patent
Unexamined Publication No. 2005-185281 are herein incorporated by
reference in its entity.
[0308] A combination of separately prepared antibodies may be used
as the "plurality of antibodies recognizing cell surface antigen"
in the present invention. In this case, the preparation method of
each antibody may be the same as or different from each other.
[0309] An antibody in which a label material has been bound or
fused in advance (which is collectively referred to as "labeled
sample antibody") may be used. The former example can include an
antibody labeled with fluorescence pigment. The latter example can
include an antibody in which fluorescence proteins (fluorescence
protein fused antibody) such as GFP (Green Fluorescent Protein) and
RFP (Red Fluorescent Protein) have been fused. Such fluorescence
protein fused antibody can be prepared easily by using genetic
engineering technique.
Step (2)
[0310] Next, the sample antibodies are brought into contact with
cells of the same kinds, respectively. That is to say, cells to be
used are determined, and then the cells are brought into contact
with the sample antibody for each sample antibody. The sample
antibody recognizing the surface antigen of the cells to be used
binds to the cell surface. The binding amount of the sample
antibody is dependent upon the expression amount of the cell
surface antigen recognized by the antibody.
[0311] Cells that are brought into contact with the sample antibody
are not particularly limited and may be arbitrarily selected from
animal cells, plant cells, microorganism cells, and the like. For
example, in one preferable embodiment, cells derived from a patent
having a certain disease (or having a certain pathologic condition)
are used. The "certain disease" includes various kinds of cancers,
for example. The tissues or organs from which the cells are derived
are not particularly limited. An example of the certain disease
include kidney cancer, hepatic cell carcinoma, gallbladder and
liver cancer, alveolar cell carcinoma, lung squamous cell cancer,
pulmonary adenocarcinoma, pancreas cancer, adenocarcinoma, ovarian
cancer, and the like.
[0312] Cells forming a highly uniform cell population are
preferably used. It is preferable because such cells can provide
easier or simpler data, facilitates the comparison of data and
provides more reliable comparison results in the below-mentioned
flow cytometry analysis. The typical example of such cells is
established cell line (cell line). Preferable examples include
established cancer cell line such as liver cancer cell line HepG2,
undifferentiated liver cancer cell line HLF, liver cancer cell line
OCTH, intrahepatic bile duct cancer cell line RBE, pancreatic
cancer cell line PANC-1, pancreas cancer cell line MIA-Paca2,
kidney cancer cell line CCFRC1, kidney cancer cell line Caki-1,
kidney cancer cell line ACHN, kidney cancer cell line 293T, ovarian
cancer cell line KF28, ovarian cancer cell line SKOv3, ovarian
cancer cell line KF-28, ovarian cancer cell line RMG-1, ovarian
cancer cell line RMG-2, breast cancer cell line BT474, vulvar
mucosa epithelium cell line A431, stomach cancer cell line SNU-5,
stomach cancer cell line MKN45, stomach cancer cell line NCI-N87,
cancer cell line RERF-LC-AI, pulmonary adenocarcinoma cell line
PCI4, lung cancer cell line NCI-H441, lung squamous cell canceEBC1,
pulmonary adenocarcinoma cell line H1373, pulmonary adenocarcinoma
cell line A549, pulmonary adenocarcinoma cell line Calu-3,
pulmonary adenocarcinoma cell line PC14, large bowel cancer cell
line CaCo2, large bowel cancer cell line CW2, hamster ovarian
cancer cell line CHO, and the like. Note here that cells whose
uniformity is improved by culture operation is one of the most
preferable cells.
[0313] Each sample antibody is brought into contact with cells in
an appropriate solution. At this time, it is preferable that the
conditions are set so that the properties of the sample antibody
are not affected and cells are not damaged. For example, cells and
the sample antibodies are co-existed in the culture solution
suitable for the existence and proliferation of the cells, in the
phosphoric acid buffer and citric acid buffer, in physiologic
saline, or in a solution in which BSA for suppressing non-specific
adsorption is added, at room temperature to low temperatures (for
example, 0.degree. C. to 25.degree. C., preferably 4.degree. C. to
15.degree. C.), for 20 minutes to 3 hours. During this time, the
solution may be stirred.
[0314] The conditions under which each sample antibody and cells
are brought into contact with each other are made to be uniform in
order to obtain highly reliable data.
[0315] After contacting operation mentioned above, labeling is
carried out if necessary (other than the case when a labeled sample
antibody is used). The "labeling" herein denotes labeling the
sample antibody bound to the surface of the cells. For example,
labeling can be carried out by reacting (contacting) an antibody
having a specific binding ability to the sample antibody to which a
label material has been bound (antibody to be detected) with cells
after the contacting operation. Instead of directly binding an
antibody to be detected to the sample antibody, other antibodies
and the like may be interposed therebetween. Thus, various labeling
techniques can be employed and a person skilled in the art can
select an appropriate technique. In the flow cytometry analysis, in
general, fluorescent dye is used as a label material. Fluorescent
dye such as Alexa488, AMCA, Cascade Blue (registered trademark),
FITC, PerCPTM, CyTM3, Texas Red (registered trademark), CyTM5, APC,
TRITC, and the like, can be used.
Step (3)
[0316] Subsequently, cells after subjecting to the step (2) are
analyzed by flow cytometry so as to obtain data showing the
reactivity between the antibody and the cell surface. That is to
say, cells after subjecting the contacting operation to the sample
antibody are subjected to the flow cytometry analysis, and the
binding property to the sample antibody is examined. Preferably, as
the data showing the "reactivity" herein, histogram showing the
relationship between the antibody binding amount and the number of
cells is used. That is to say, one-parameter histogram in which the
antibody binding amount is used as a parameter is used. The
one-parameter histogram is one display method in the flow
cytometry. The one-parameter histogram is generally shown in a
graph in which X-axis represents one indicator (parameter) and
Y-axis represents the number of cells. For the device used for the
flow cytometry analysis, for example, devices from BECKMAN COULTER,
Japan Becton, Dickinson and Company, and the like can be used in
the present invention. The operation may be carried out according
to the basic operation and analysis conditions attached to the
device. Furthermore, many research paper and documents about the
flow cytometry analysis are published. See, for example, Cao T M,
et al. Cancer. 2001 Jun. 15; 91 (12): 2205-13., Storek K J, et al.
Blood 97: 3380-3389, WEIR'S HANDBOOK OF EXPERIMENTAL IMMUNOLOGY
Vol. II <Blackwell Science>, Little MT and R. Storb Nature
Reviews Cancer 2002 2: 231-238.
[0317] Typical procedure of the flow cytometry analysis is
described below. The sample antibody and cells are reacted with
each other, then reacted with antibody to be detected labeled with
fluorescent dye, so that cells are labeled with fluorescence. The
amount of sample antibody to be bound varies depending upon the
amount of antigen existing on the surface of the cells. As a
result, the amount of fluorescent label of the cells becomes
different. Therefore, by measuring the fluorescence intensity, the
affinity between the antigen existing on the surface of the cell
and the ample antibody and the amount of antigen can be estimated.
In general, prior to the detection of the fluorescence intensity,
forward scatter light (FSC) and side scatter light (SSC) are
measured and gated, so that the fluorescence intensity of only the
target cell population is measured. Specifically, for example, the
forward scatter light and the side scatter light are shown in
X-axis and Y-axis, respectively. The cell population (when
established cell lines or cultured cells are used, the cell
population becomes extremely uniform) that are assumed to be living
cells from the data obtained by dot plot expansion are gated, and
the fluorescence intensity within the gate is measured. The
measurement result is shown in a form of, for example, histogram.
Note here that the terms related to the histogram obtained in the
flow cytometry analysis are mentioned below.
[0318] The "number of samples" denotes number of data and generally
represented by n. The "total" denotes a total of data and generally
represented by T. "Mean value" denotes an average of data and is
calculated by dividing the total by the number of samples. The mean
value is susceptible to abnormal data. The "median value" is a
value located in the middle when the data are aligned in ascending
numeric order. When the number of data is odd number, the average
of two middle values is defined as a median value. The median value
is less susceptible to abnormal data as compared with the mean
value and shows the characteristics of the population more
accurately. The "mode" denotes a value whose frequency is maximum
in the data. In the case of the flow cytometry analysis, the mode
is the same as a peak value. The mode is less susceptible to
abnormal data as compared with the mean value. The "maximum value"
is a maximum value of data and generally represented by Max.
[0319] The "range value" is difference between the maximum value
and the minimum value and generally called range and referred to as
R. The "dispersion" is a value showing the degree of variation of
data. The larger the dispersion is, the larger the variation is. In
general, it is referred to as V. The dispersion is obtained by
dividing the sum of squares deviation by the number of samples (in
the case of sample survey, divided by (number of samples -1)). The
"standard deviation" denotes square root of the dispersion and is
generally referred to as u. The "coefficient of variation" is a
value obtained by dividing the standard deviation by an average
value and is generally referred to as CV. Since the standard
deviation does not clearly shows the degree of variation of data,
the standard deviation is normalized by dividing it by the average
value. In the flow cytometry analysis, it is frequently used as a
value showing the resolving power of the device. The "kurtosis" is
one of the indicators representing the distribution in the
population and generally is referred to as H. The distribution in
which the kurtosis is 0 is defined as normal distribution. When the
kurtosis is larger than 0, the distribution has sharper apex than
the normal distribution. When the kurtosis is smaller than 0, the
distribution becomes more flatness than the normal distribution.
The "skewness" denotes a value showing the left-right symmetry of
the population and generally is referred to as G. When the skewness
is 0, distribution becomes left-right symmetric. When the skewness
is larger than 0, the distribution distorts in the right direction.
When the skewness is smaller than 0, the distribution distorts in
the left direction.
Step (4)
[0320] Next, the obtained data are compared and sample antibodies
are classified based on the similarity of the obtained data.
Herein, "based on the similarity" means that the similarly of data
are used as a criterion of classification. An example of criterion
(classification criterion) based on the similarity of data is shown
below.
[0321] (a) A plurality of antibodies having the identical or highly
similar data are classified into one antibody group. Specifically,
for example, plurality of antibodies having extremely similar
histogram is defined as one group when the shape of the histogram
showing the distribution of cells is determined by the kurtosis,
skewness and the like.
[0322] (b) An antibody providing specific data forms one antibody
group by itself.
[0323] (c) An antibody having a low reactivity with respect to the
antigen is excluded
[0324] (the antibody does not belong to any groups).
[0325] In the present invention, each antibody is classified by one
or two or more criteria selected from the above-mentioned
classification criteria (a) to (c).
[0326] The similarity of data can be determined based on the
parameter specifying the data. However, the specific determination
method is dependent upon the types of data. In the case where data
are represented by numeric values, it is possible to determine the
similarity based on the degree of similarity of numeric values (for
example, when 1, 2, and 5 are given as data, it is determined that
the similarity between 1 and 2 has high similarity).
[0327] Furthermore, when a histogram is given as data, it is
possible to determine the similarity of data based on the shape of
the histogram. As a result of the investigation by the present
inventors, it is determined that the shape of the histogram in the
flow cytometry analysis is highly dependent upon the kinds of the
antigen. In other words, when the antigens to be recognized are the
same, regardless of the kinds of antibodies, it is determined that
the histogram having an identity or high similarity can be
obtained. Base on this fact, in one embodiment of the present
invention, by comparing the shapes of the histogram showing the
results of the flow cytometry analysis, the similarity of data is
determined. Specifically, the similarity of data can be determined
by comparison by visual observation or by comparison of one or two
or more of parameters specifying the histogram. The parameters
herein can employ one or more values selected from the group
consisting of median value, mode, maximum value, range, standard
deviation, kurtosis, and skewness of the histogram. Preferably,
determination is carried out in terms of two or more values,
furthermore preferably three or more values, and yet furthermore
preferably four or more values. By increasing parameters to be used
in determination, the determination accuracy can be improved. Among
these parameters, it is said to be advantageous that the median
value, mode, or kurtosis that are parameters deeply related to the
shapes of the histogram are employed for carrying out the
determination at high accuracy. Preferably, a combination of two or
more of these parameters is used. Specifically, for example, the
similarity of the histogram may be determined based on the median
value, mode, and kurtosis.
[0328] When two data to be compared have similar values in terms of
employed parameters, the similarity between the two data is
determined to be high. When the difference between two values
(100.times.(A-B)/A (%) when the two values are A, B (A.gtoreq.B))
is within 10%, preferably within 5%, and furthermore preferably
within 3%, the two values are determined to be similar.
[0329] In one embodiment of the present invention, when or after
the sample antibodies are classified, sample antibodies having a
low reactivity to the cell surface antigen are removed. Thereby, an
antibody group including highly useful sample antibodies can be
formed. The degree of the reactivity of the antibody can be
determined by using the results of the flow cytometry analysis.
Specifically, the mode (peak value) of the histogram obtained with
respect to the sample antibody to be determined and the mode (that
is to say, the maximum mode in the group) of the histogram obtained
with respect to the sample antibody having the maximum reactivity
in the antibody group to which the sample antibody belongs. As a
result, when the former is 1/2 or less of the latter, preferably
1/5 or less, furthermore preferably 1/10, it is determined that the
sample antibody to be determined has low reactivity.
[0330] In one embodiment of the present invention, the reactivity
of each sample antibody is examined in two or more kinds of cells
and the sample antibodies are classified by using the results. That
is to say, two or more kinds of cells are prepared and by using the
prepared cells, steps (2) to (4) are carried out.
[0331] The expression amount, distribution, and the like of the
cell surface antigens are dependent upon the kinds of cells.
Therefore, two antibodies having high similarity in data obtained
by using certain cells, that is, two antibodies having the common
antigens should provide data having high similarity when the other
cells are used. Thus, when the two antibodies to be compared
provide data with high similarity with respect to more than two
kinds of cells, the probability that the antibodies have the common
antigens is extremely high. Furthermore, when such results are
obtained, it can be easily determined that the two antibodies have
the common antigens. Thus, the use of two kinds or more cells can
make it accurate and easy to determine the identity of
antigens.
[0332] In one preferable embodiment of the present invention,
sample antibodies having identical or highly similar data with
respect to at least two kinds of cells are classified into one
antibody group.
[0333] Furthermore, by observing the classification results of the
case where two or more kinds of cells are used, kinds or amount of
antigens to be expressed can be compared between the cells.
Therefore, more useful information can be provided in studying the
properties of these cells.
[0334] In one embodiment of the present invention, a classification
result is displayed as a panel. The "panel" in this specification
is a product in which a plurality of elements (for example,
antigen, antibody, antibody group, cell, name of disease, name of
pathologic condition), are displayed in the form of tables or
drawings, in which the elements are associated with each other, on
media such as a display and paper. Each element is represented by
general name, abbreviation, alias, or symbol or code representing
thereof, and the like. The panel of the present invention shows the
relationship with respect to two kinds or more of elements.
[0335] The term "associating to" in the present invention means
that two or more elements are linked. Therefore, in the tabular
format panel showing the association between an antigen and an
antibody group, for example, both elements are displayed in
adjacent to each other, or both elements are displayed in the same
cells, or both elements are linked by a line or something, so that
it can be understood that the both elements form a pair.
[0336] In the panel herein, typically, antibody groups are
displayed in a way in which they are associated with each other for
each antigen (or for each antigen having high association)
expressed by the cells that have been subjected to the flow
cytometry analysis. Therefore, this panel makes it possible to
access antibodies useful for studying surface antigens of the
cells. Thus, the panel itself of the present invention has a great
value. A panel formed by using two kinds or more of cells makes it
possible to understand the presence, expression amount, and the
like, of antigens expressing between cells. Such a panel has
further higher values.
[0337] In the panel of the present invention, antibodies may be
arranged regularly in accordance with the reactivity to antigens.
Thus, the difference in the reactivity between antibodies can be
made obvious.
[0338] According to the classifying method in the present
invention, a plurality of antibodies recognizing the same antigen
(or antigens having high association) are associated with each
other. In other words, for each antigen (or for each antigen having
high association), antibody assembly (antibody group) recognizing
the antigen can be obtained. These antibody groups are useful for
studying cell surface antigen and have high usability. Furthermore,
according to the classifying method of the present invention, a
large number of antibodies can be classified rapidly for each
antigen (or for each antigen having high association). That is to
say, the classifying method of the present invention is useful for
classification of a large number of antibodies and allows
comprehensive classification of antibodies. The term "highly
associated" or "having high association" used for antigen means
that two or more antigens have a close association in a living
body, for example, the antigens are not the same molecules but
exhibit one function cooperatively (for example, two antigens are
bound so as to form one complex functionally).
[0339] According to the classifying method of the present
invention, typically, plurality of antibodies are associated with
each other for each antigen (or for each antigen having high
association). Therefore, in studying certain antigens, a plurality
of antibodies can be used or suitable antibodies can be selectively
used if necessary, which leads to better results or significant
findings and means that studying can be proceeded
advantageously.
[0340] On the other hand, by executing the classifying method of
the present invention, it is possible to understand the expression
amount of distribution of cell surface antigens (antigen are
unknown) in certain cells (that is, cells that are brought into
contact with the sample antibody). Thus, the classifying method of
the present invention provides useful information on the properties
of the certain cells and is useful for studying the cells (in
particular, the surface antigens).
[0341] Note here that when antigens to all the sample antibodies
are unknown, antigens to which each antibody group is associated
are not identified. On the other hand, when some identified
antigens are contained in a part of the sample antibodies, an
antigen to which the antibody group containing the antibody becomes
an identified antigen. Thus, it is also possible to associate an
antibody group with the identified antigen.
[0342] According to the above-mentioned classifying method,
antibodies are classified based on the reactivity between the
antigens and certain cell surfaces and the antibody groups are
formed. Therefore, antibodies belonging to the same antibody group
have the same (or highly similar) reactivity to the surface of
cells used for classification. However, it is not necessarily
ensured that all the antibodies belonging to the same antibody
group can recognize the same antigens. Even if the recognizing
antigen is the same, the reactivity to cells expressing antigens on
the cell surface may be different. Furthermore, the opposite case
may occur (even if the recognizing antigen is different, the
reactivity to cells expressing antigens on the cell surface may be
the same, for example, one of the complex may be recognized).
[0343] Therefore, in order to form an antibody for each recognizing
antigen, one embodiment of the present invention carries out the
following steps (i) to (vi) after the step (4).
[0344] (i) associating the classified antibodies with a combination
of n pieces of parameters including a first parameter, a second
parameter, . . . , and an n-th parameter (wherein, n represents an
integer of 2 or more, each parameter has two or more parameter
values and the same parameter value is given to two or more
antibodies in each parameter);
[0345] (ii) with respect to each parameter, preparing an antibody
mixture of the antibodies having the same parameter value;
[0346] (iii) examining a reactivity of each of the antibody
mixtures with a target antigen by an enzyme linked immunosorbent
assay (ELISA) so as to specify the antibody mixture which shows
reactivity;
[0347] (iv) specifying a combination of a parameter name and a
parameter value that are common to the antibody group contained in
the specified antibody mixture;
[0348] (v) selecting an antibody corresponding to the combination
specified in the step (iv) in terms of all parameters among the
antibodies subjected to step (i); and
[0349] (vi) classifying the selected antibodies into one antibody
group.
[0350] According to the classifying method of this embodiment, an
antibody group can be formed for each antigen to be recognized.
That is to say, antibody groups having various individualities
recognizing the same antigen can be obtained. Furthermore, the
combination of the plurality of parameters is associated with each
antigen and then an antibody mixture is prepared according to a
predetermined regulation. Then, based on the results of ELISA
(Enzyme-Linked immunosorbent assay) using the antibody mixture, an
antibody recognizing a target antigen is determined. By this unique
technique, antibodies can be classified rapidly and efficiently.
Furthermore, at the same time when the antibodies are classified,
as to at least a part of the antibodies, an antigen is identified.
That is to say, the classifying method of this embodiment is a
method of rapidly and efficiently obtaining an antibody whose
antigen has been identified, which dramatically promote the
increase in the number of antibodies whose antigens have been
identified. On the other hand, the classification results show the
presence form or expression from on the cell surface used in flow
cytometry analysis, which provides extremely useful information for
study and development of the application of antibody (for example,
treatment of cancer). Furthermore, when the presence of a certain
antigen is clarified based on the classification results, it is
possible to obtain an unknown antigen (for example, complex
counterpart) that is thought to be possible to exist in a form of a
complex with the antigen. That is to say, the classifying method of
this embodiment efficiently functions as determining a novel
antigen or novel molecule complex. Hereinafter, each step is
described in detail. For convenience of explanation, the
classifying method of this embodiment is also referred to as "n
dimensional ELISA method."
Step (i)
[0351] In this step, a combination of n pieces of parameters
consisting of the first parameter, the second parameter, . . . ,
and the n-th parameter are associated with antibodies classified by
the preceding steps (steps (1) to (4)). Thus, each antibody has
n-dimensional address (a parameter value of the first parameter, a
parameter value of the second parameter, . . . , and a parameter
value of the n-th parameter).
[0352] In general, association is carried out with respect to all
the antibodies that have been classified in the preceding steps,
although the association is not limited to this. That is to say,
the association may be carried out only a part of the antibodies
that has been classified in the preceding steps. In this case, a
part of antibodies are excluded from the antibodies to be
classified.
[0353] Herein, "n" is an integer of two or more. That is to say, to
each antibody, two or more combinations of parameters are
associated. The number of "n" does not have an upper limit. When
the number of "n" is too large, operations in the subsequent steps
(for example, preparation of an antibody mixture, specification of
an antibody mixture showing the reactivity) may be excessively
complicated. Therefore, "n" is preferably three to five.
[0354] On the other hand, each parameter is made to have two or
more parameter values and the same parameter values of each
parameter are made to be provided to two or more kinds of
antibodies. Specifically, parameter values of the first parameter
may be 1, 2, 3 and 4, and each parameter value is provided to five
kinds of antibodies, respectively. The number of the parameter
values is set for each parameter. Furthermore, similar to the
number of parameters, the number of the parameter values does not
have an upper limit. In order to make the analysis in the following
steps (iv) and (v) be efficient and improve the accuracy thereof,
it is preferable that the kinds of antibodies contained in each
antibody mixture are not excessively large number. Therefore, each
parameter value may be set so that the kinds of antibodies
contained in each antibody mixture is preferably 200 or less, and
furthermore preferably, 100 or less. Specifically, for example, the
number of the parameter values can be set to between 2 and 100.
Note here that the kind of antibodies contained in each antibody
mixture is dependent upon the setting of the parameter, and may not
be equal between antibody mixtures.
Step (ii)
[0355] In this step, an antibody mixture, in which antibodies
having the same parameter value are mixed, is prepared. The
antibody mixture is prepared for each parameter. For example, when
the values of the first parameter is 1, 2, 3 and 4, an antibody
mixture mixing antibodies to which 1 is given as the first
parameter, an antibody mixture mixing antibodies to which 2 is
given as the first parameter, an antibody mixture mixing antibodies
to which 3 is given as the first parameter, and an antibody mixture
mixing antibodies to which 4 is given as the first parameter are
prepared. By the same procedure, as to the remaining parameters,
antibody mixtures are prepared. Thus, antibody mixtures in the same
number as the total number of the number of the first parameter,
the number of the second parameter, and the number of the n-th
parameter are prepared.
[0356] In general, an antibody mixture, in which all antibodies
having the same parameter values are mixed, are prepared although
the antibody mixture is not limited to this. An antibody mixture
may be prepared by selecting a part of all antibodies having the
same parameter values and mixing thereof. Thus, the selection of
antibodies may be carried out in this stage.
[0357] It is preferable that an antibody mixture is prepared so
that all antibodies are contained in equal amount and the amount of
each antibody (that is, concentration for each antibody) is equal
between antibody mixtures. Adjusting the amount of antibodies in
this way facilitates the specification of the antibody mixture
based on the reactivity in the following ELISA.
Step (iii)
[0358] In this step, the reactivity between each of the antibody
mixtures and the target antigen is examined by ELISA so as to
specify the antibody mixture showing the reactivity. When at least
one of the antibodies recognizing the target antigen is contained
in the antibody to be used for preparing the antibody mixture, a
plurality of antibody mixtures shows the reactivity. On the other
hand, when the antibody recognizing the target antigen is not
contained, any of the antibody mixtures will not show reactivity.
In this case, the operation is terminated without continuing the
following operations.
[0359] The target antigen herein nay include HER1, HER2, CD46,
ITGA3, ICAM1, ALCAM, CD147, IgSF4, BCAM, CIqR, CD44, CD73, LAR,
EpCAM, HGFR, and the like. The target antigen can be arbitrarily
selected. The antigen determined by the below-mentioned
identification methods (step (5) and (6)) may be used as the target
antigen herein.
Step (iv)
[0360] In this step, a combination of a parameter name and a
parameter value that are common to the antibody group contained in
the specified antibody mixture is specified. In the present
invention, the combination specified herein is referred to as
"positive combination." Specifically, the positive combination is
specified like (first parameter, parameter value a1), (second
parameter, parameter value a2), . . . , (the n-th parameter,
parameter value an). When a plurality of antibody mixtures having
the different degree of reactivity are recognized in the step
(iii), similarly, specification may be carried out for each level
of the reactivity. For example, the middle level of positive
combination may be specified like (first parameter, parameter value
a1), (second parameter, parameter value a2), . . . , (the n-th
parameter, parameter value an); and the high level of positive
combination may be specified like (first parameter, parameter value
b1), (second parameter, parameter value b2), . . . , (the n-th
parameter, parameter value bn).
Step (v)
[0361] In this step, antibodies corresponding to the combination
specified in step (iv) as to all parameters are selected from the
antibody subjected to step (i). That is to say, antibodies in which
all parameters are positive combination are selected. For example,
when (first parameter, parameter value a1), (second parameter,
parameter value a2), . . . , (the n-th parameter, parameter value
an) are specified as the positive combination, antibodies having
(parameter value a1, parameter value a2, . . . , parameter value
an) is selected.
Step (vi)
[0362] In this step, the selected antibodies are classified into
one antibody group. Thus, an antibody group showing the reactivity
to the target antigen can be made into one group. In other words,
an antibody group whose antigen is determined can be obtained. Note
here that when only one antibody is selected in the step (v), this
only one antibody makes one an antibody group.
[0363] When two or more kinds of target antigens are prepared and
the above-mentioned steps (iii) to (vi) are carried out by using
each target antigen, two or more antibody groups recognizing
different antigens can be obtained.
[0364] In one embodiment of the present invention, the steps (i) to
(v) are tried a plurality of times under the conditions in which
the combination of parameters is changed every trial. For example,
in the first trial, analysis is carried out in which four parameter
combinations composed of numeric values (for example, antibody 1
(001, 001, 001, 001), antibody 2 (002, 002, 002, 002), . . . ) are
associated with each antibody. In the second trial, analysis is
carried out in which three parameter combinations composed of
alphabets (for example, antibody 1 (.alpha..alpha..alpha.,
.alpha..alpha..alpha., .alpha..alpha..alpha.), antibody 2
(.beta..beta..beta., .beta..beta..beta., .beta..beta..beta.,
.beta..beta..beta.), . . . ) are associated with each antibody.
Note here that each trial is carried out so that the antibody group
formed in each trial is not completely identical. The "antibody
group is completely identical" means that the numbers of groups are
the same and the kinds of antibodies contained in each group are
the same over the all groups.
[0365] After a plurality of times of trials, antibodies in which
the results in all trials are not contradictory and which show the
binding positive reaction to the target antigen are selected. Then,
the step (vi) is carried out by using the selected antibody (a
plurality of antibodies).
[0366] When trials are carried out at a plurality of times and only
an antibody that provides not-contradictory (that is, consistent)
results are selected, an antibody having a target antigen
reactivity (intended antibody) can be efficiently obtained.
[0367] The number of times of trial in the steps (i) to (v) is not
particularly limited. It may be arbitrarily set by considering the
number of antibodies to be treated, the number of "positive
combinations" that is anticipated at one trial. For example, the
number of times of trial can be twice to five times.
[0368] In a further embodiment of the present invention, the
following steps are carried out between the step (v) and the step
(vi).
[0369] (v-1) newly associating the classified antibodies selected
in step (v) with a combination of n pieces of parameters in a same
manner as in the step (i);
[0370] (v-2) with respect to each parameter, preparing the antibody
mixture of antibodies having the same parameter value;
[0371] (v-3) examining a reactivity of each of the antibody
mixtures with a target antigen by an enzyme linked immunosorbent
assay (ELISA) so as to specify the antibody mixture showing the
reactivity;
[0372] (v-4) determining a combination of a parameter name and a
parameter value that are common to the antibody group contained in
the specified antibody mixture; and
[0373] (v-5) selecting an antibody having the combination specified
in the step (v-4) in terms of all parameters among the antibodies
subjected to the step (v-1).
[0374] Note here that the steps (v-1) to (v-4) are repeated twice
or more, if necessary. In this embodiment, a combination of
parameters is newly associated with antibodies selected in one
trial. Then, the selection of antibody is carried out again. By
repeating trials, the intended antibody is narrowed. Thus,
classification accuracy is improved.
[0375] Herein, with reference to FIGS. 77 and 78, the principle of
the n-dimensional ELISA method is described more particularly.
FIGS. 77 and 78 are conceptual diagrams in a case where n is 3
(three dimensional ELISA method). In this example, a
general-purposed 96-well microwell plate is used. Firstly, plates
in the number necessary to the number of antibody clones are
prepared. In this example, the number of antibody clones is made to
be 4,800 and 50 plates (4,800 well in total) are prepared.
[0376] Next, the antibody clone is placed in the well sequentially
and the antibody clones are arranged in the plate. Thus, each
antibody clone is associated with an address consisting of a plate
number (first parameter), a plate row name (second parameter), and
a plate column number (third parameter). For example, the address
of the antibody clone in the first plate, row A and first column in
a well becomes (1, A, 1).
[0377] Subsequently, a mixture of antibody clones having the same
plate number (referred to as a plate mixed antibody), a mixture of
antibody clones having the same plate row name (referred to as a
row mixed antibody), and a mixture of antibody clones having the
same plate column number (referred to as a column mixed antibody)
are prepared, respectively (FIG. 77). The number of the respective
mixed antibodies are 50 (first plate mixed antibody to fifth plate
mixed antibody), 8 (row A mixed antibody to row H mixed antibody),
and 12 (first column mixed antibody to twelfth column mixed
antibody), sequentially.
[0378] The mixed antibodies prepared as mentioned above are placed
in wells in a newly prepared 96-well microwell plate sequentially,
and the mixed antibodies are aligned in the plate. In this example,
in the plate, the first to seventh columns are assigned to the
plate mixed antibody, the eighth column is assigned to the row
mixed antibody, and the ninth to tenth columns are assigned to the
column mixed antibody (upper part of FIG. 78). The thus obtained
plates are used and ELISA method is carried out. Then, by examining
the well showing the reactivity, the address of the intended
antibody clone (antibody clone showing the reactivity to the target
antigen) is specified. In this example, a well in which the plate
mixed antibody of the third plate is placed, a well in which the
row mixed antibody of the row E is placed, and a well in which the
column mixed antibody of the third column show the reactivity, (3,
E, 3) is specified as an address of the intended antibody (lower
part of FIG. 78). Finally, antibody clone to which the specified
address is associated with is obtained as the intended
antibody.
[0379] The second aspect of the present invention provides an
identifying method of an antigen to each antibody classified in the
classifying method of the present invention. In the identification
method of the present invention, following the above-mentioned
steps (1) to (4) in the classifying method of the present
invention, the below-mentioned steps are carried out.
[0380] (5) selecting one or several antibodies from each antibody
group formed in the step (4) and identifying an antigen thereof,
and
[0381] (6) associating the antigens identified in the step (5) with
an antibody group, on the estimation that antigens to antibodies
belonging to the same antibody group are identical or have high
relationship, and
Step (5)
[0382] In this step, antibodies to be identified are selected. The
criteria of selection are not particularly limited, and antibodies
that are judged to have high reactivity with respect to antigen
from the results of the flow cytometry analysis may be selected.
This is because when such an antibody is used, the identification
operation using the antigen antibody reaction can be carried out
advantageously.
[0383] The number of antibody to be selected is typically one, but
the number is not necessarily limited to one. If necessary, several
antibodies (for example, two or three antibodies) are selected.
When a plurality of antibodies are selected from one antibody
group, the identification results of antibodies can be compared
with each other, and thereby the reliability of the identification
results can be improved. On the other hand, when the identification
operation is carried out by selecting a more than necessary number
of antibodies, excessive workload is applied. As a result, the
effect that is originally intended by the present invention is
decreased. Then, it is preferable that the number of antibodies to
be selected is small. Specifically, the number is preferably five
or less, further preferably three or less, and the most preferably
two or less. In order to maximize the effect of the present
invention, the number of antibody to be selected from each antibody
group is one.
[0384] Identification of an antigen to an selected antibody
(hereinafter, referred to as "selected antibody") can be carried
out by using a method such as mass spectrometry,
immunoprecipitation test, Western blotting, affinity
chromatography, RNAi, proteomics techniques (analysis by
electrophoresis, mass spectrometry, genome data base retrieve, and
bioinformatics), and analysis of expression of corresponding gene.
Among them, a method by the proteomics technique based on the mass
spectrometry is suitable for identification of unknown antigen and
preferable for the identification method employed in the present
invention. Note here that these methods are not exclusive to each
other and two or more of them can be used if necessary.
[0385] The mass spectrometry is a method of determining the mass of
samples by separating ions generated from samples such as protein
and peptide according to mass/electric charge (m/z), and measuring
the intensity thereof. Since soft ionization methods such as an ESI
method (Electro Spray Ionization) and an MALDI method (Matrix
Assisted Laser Deporption Ionization) are developed, the mass
spectrometry is widely used for analyzing living body sample such
as protein and peptide.
[0386] A mass spectrometer is generally composed of ion source,
mass spectrometer, and detector. According to sample types and
analysis purposes, various mass spectrometers are commercially
available. For identification of protein or peptide, MS/MS (Mass
spectrometry/mass spectrometry) by a tandem mass spectrometry such
as ESI Q-TOF MS, MALDI-TOF MS, and the like are used. A measurement
method combining liquid chromatography and mass spectrometer
(LC-MAS (liquid chromatography/Electro Spray Ionization mass
spectrometer), LC-MS/MS, etc.), and the like, can be also used.
[0387] In the tandem mass spectrometer, two mass spectrometers are
linked in series in which ions generated in the ion source are
separated in the first mass spectrometer (MS 1) and allowed to pass
through only a single ion peak. Then, inactive gas particles are
allowed to collide with the ions so as to be degraded into product
ions. This product ion is analyzed by the second mass spectrometer
(MS 2). According to the combination of the first mass spectrometer
(MS 1) and the second mass spectrometer (MS 2), tandem mass
spectrometers such as Q-TOF, TOF-TOF, Q-Q, and Q-IT (Iontrap) are
present. Like Q-TOF (a tandem mass spectrometer in which Quadrupole
mass spectrometer: Q-MS and TOF mass spectrometer (Time-of-flight
mass spectrometer: TOF-MS are linked in series), hybrid type tandem
mass spectrometer composed of two different kinds of mass
spectrometers is excellent in MS/MS measurement ability and
suitable for identifying the amino acid sequence of protein and
peptide.
[0388] In order to identify the amino acid sequence from the
results of the mass spectrometer, a PMF method (peptide mass
fingerprinting method) of carrying out genome data search by using
experiment results, MS/MS ion search method and the like, are used.
Furthermore, de novo sequencing method of determining the amino
acid sequence by mathematical operation from the MS/MS spectrum
without carrying out genome data search may be used.
[0389] On the other hand, an immunoprecipitation test, Western
blotting technique, affinity chromatography, RNAi, and the like,
are effective method when a selected antibody is anticipated to
recognize the known antigen. These methods can examine the
reactivity between the selected antibody and well-known antigen.
That is to say, in the immunoprecipitation test, it is examined
whether or not the selected antibody and certain known antigen form
an immunoprecipitate. When an immunoprecipitate is formed, the
known antigen is determined to be the antigen of the selected
antibody. On the other hand, in the Western blotting technique, it
is examined whether or not the selected antibody can recognize an
antigen protein transferred to a PVDF membrane etc. Furthermore, in
the affinity chromatography, the adsorption property of the
selective antibody to a column supporting a certain known antigen
is examined. The presence or the degree of adsorption property is
determined. Herein, as the known antigen, commercially available
antigens, or antigens expressed from a gene and purified can be
used. Furthermore, operations of the immunoprecipitation test,
Western blotting technique, affinity chromatography, and the like,
can be carried out in the usual manner. In the investigation in
RNAi, RNAi of the known antigen is allowed to act on forcedly
expressed cells or cells to which an antibody is reacted. It is
determined that the subject antibody recognizes the subject antigen
when the staining property FCM or the degree of cell immunostaining
is reduced.
Step (6)
[0390] In the identification method of the present invention,
following the step (5), it is assumed that antigens to each antigen
belonging to the same antibody group are identical or have high
association. According to the assumption, the antigens identified
in the step (5) are associated with an antibody group. Thus, all
antibodies belonging to the same antibody group are associated with
one antigen.
[0391] In one embodiment of the present invention, the above
assumption (estimation as to the association of antigen) is
verified. That is to say, in this embodiment, the reactivity
between the antigen identified in the step (5) and the antibody
belonging to the antibody group with which the antigen is
associated in the step (6) is examined so as to confirm that the
above assumption is correct. Specifically, firstly, antibodies are
selected from the antibody group that needs verification.
Preferably, all the antibodies are selected, and the reactivity
thereof is verified. Next, the reactivity of each antibody to the
identified antigen (hereinafter, referred to as "identified
antigen") is examined by using the immunoprecipitation test or
ELISA (including cell ELISA), and RNAi. For example, in the
immunoprecipitation test, by reacting the antibody to an solution
or an extracted solution of cells that express the identified
antigen, then, proteins recovered as the immunoprecipitates are
detected by, for example, electrophoresis. Thereby, the reactivity
of each antibody to the identified antigen can be confirmed. On the
other hand, in ELISA, for example, by a series of operations
including preparation of well in which an identified antigen is
fixed, addition of antibody, addition of labeled antibody, and
measurement amount of labeled antibodies, the reactivity of each
antibody with respect to the identified antigen can be confirmed.
Furthermore, also by examining the binding property to cells
forcedly expressing the identified antigen, the reactivity of each
antigen to the identified antigen can be confirmed. In the
verification by RNAi, by allowing the known RNAi to act on cells
forcedly expression the identified antigen or subjected cells
showing the antibody reaction. When, the staining property of the
subjected antibody in FCM and cell immunostaining is reduced, it is
recognized that the subjected antigen is recognized.
[0392] Furthermore, when disease-related molecules (disease
causative gene products, etc.) can be obtained in same forms such
as purified protein or recombinant protein, the intermolecular
interaction between such molecules and the antibodies can be
examined in vitro (classical methods using fluorescence
spectroscopy, gel filtration, and ultracentrifugation; a method
using surface plasmon resonance phenomenon; a method using
quartz-crystal resonator microbalance, and the like) or in vivo
(monomolecular tracing method, fluorescence resonance energy
metastasis (fluorescence resonance energy transfer: FRET)
observation method, and the like).
[0393] When specific reactivity is observed between the identified
antigen and each antibody, it is judged that the above assumption
is correct.
[0394] In one embodiment of the present invention, identification
results are displayed on a panel. Specifically, the panel is any of
the following (a) to (c).
[0395] (a) a panel displaying as one antibody group a plurality of
antibodies providing data identical to or similar to each other in
the flow cytometry analysis in the step (3) in which each antibody
group is associated with its antigen;
[0396] (b) a panel displaying as one antibody group a plurality of
antibodies providing data identical to or similar to each other in
the flow cytometry analysis in the step (3) in which each antibody
in the antibody group is associated with a cell expressing a cell
surface antigen recognized by the each antibody group; and
[0397] (c) a panel displaying as one antibody group a plurality of
antibodies providing histogramidentical to or similar to each other
in the flow cytometry analysis in the step (3) in which each
antibody group, its antigen and a cell expressing a cell surface
antigen recognized by the antibody are associated with each
other.
[0398] The above-mentioned panels are useful for studying
identified antigens, and for studying or classifying certain cells
displayed on the panel.
[0399] The panel (a) displays the relationship between each antigen
to the antibody group. Therefore, it is useful in searching an
antibody to a certain antigen. The panel (a) can be formed by
displaying by the use of diagrams or tabular formats the
association between each antibody group and the antigen by using
identification results by steps (5) and (6) of the present
invention in which a plurality of antibodies providing identical or
highly similar data in the flow cytometry analysis in the step (3)
of the present invention are defined as one group.
[0400] The panel (b) shows the association between the antibody
group and cells. Therefore, it is useful in searching an antibody
to a certain cell surface antigen. Furthermore, when the panel
displays the association between the antibody group and a plurality
of cells, useful information on the distribution of cell surface
antigen can be provided. The panel (b) can be formed by displaying
by the use of diagrams or tabular formats the association between
each antibody group and cells expression the cell surface antigen
recognized thereby by using identification results by steps (5) and
(6) of the present invention in which a plurality of antibodies
providing identical or highly similar data in the flow cytometry
analysis in the step (3) of the present invention are defined as
one group.
[0401] The panel (c) combines the panel (a) and the panel (b). This
panel shows that the kinds or distribution state of a cell surface
antigen expressed by certain cells and allows easy and rapid search
of antibodies to the antigens of interest. The panel (c) can be
formed by displaying by the use of diagrams or tabular formats the
association between each antibody group and cells expression the
cell surface antigen recognized by the antigen and each antibody
group by using identification results by steps (5) and (6) of the
present invention in which a plurality of antibodies providing
identical or highly similar histogram in the flow cytometry
analysis in the step (3) of the present invention are defined as
one group.
[0402] In the identification method of the present invention,
identification of antigen with respect to only a part of the
antibodies in the antibody group, and as to the other antibodies,
antigens are determined by estimation. Therefore, as compared with
the case where identification operation is carried out for each
antibody, necessary labor and time can be radically reduced. In
other words, according to the identification method of the present
invention, antigen of each antibody can be determined rapidly and
easily. Note here that as shown in the below-mentioned Examples, as
far as the present inventors have investigated, error in estimation
has not been confirmed. The reliability of this method has been
confirmed.
[0403] On the other hand, according to the identification method of
the present invention, it is possible to understand the kinds of
surface antigens expressed by certain cells. Furthermore,
information on the expression amount can be obtained. When the
classification of antibodies is carried out by using two kinds or
more cells, information on the distribution state of the cell
surface antigens can be obtained. Thus, the identification method
of the present invention brings useful information as to the cell
surface antigen.
[0404] As a result, according to the identification method of the
present invention, it is possible to obtain an assembly of
antibodies capable of recognizing antigens for each identified
antigen (or for each of the plurality of antigens having high
association). These antibody groups are useful for study of the
cell surface antigens, classification and diagnosis of diseases,
and the like. These antibody groups are expected to be applied to
the field of treatment.
[0405] The present invention further provides an application of
information obtained by the classifying method or the
identification method of the present invention. As one of the
applications, the third aspect of the present invention relates to
a method of obtaining an antibody or an antibody set having a
association with respect to a certain disease. The method of
obtaining the antibody of the present invention (the first
embodiment of the third aspect) includes the following steps.
[0406] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to the present invention;
[0407] (2) with respect to one kind or two or more kinds of
diseases examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0408] (3) selecting an antibody in the antibody group, to which an
antibody having a specific reactivity to any of diseases belongs,
as a useful antibody.
[0409] On the other hand, a method of obtaining an antibody set of
the present invention (the second embodiment of the third aspect)
includes the step (3') instead of the step (3):
[0410] (3') selecting diseases to which two or more antibodies show
a specific reactivity, then selecting antibodies from the antibody
group, to which the antibody having a specific reactivity to the
disease belongs, and combining the selected antibodies.
[0411] Hereinafter, the detail of each step is described with
reference to FIG. 1. For convenience of explanation, in FIG. 1, it
is assumed that the antibody groups 1 to 5 are obtained by the
classifying method of the present invention and three antibodies
belong to each antibody group. Furthermore, in this example, it is
assumed that antigens to each antibody group have been already
identified.
[0412] Firstly, in the step (1), focused antibody group (antibody
groups 1, 3, and 5) are selected (FIG. 1, (1)). As in this example,
two or more antibody groups may be selected.
[0413] Next, in the step (2), the reactivity between an antibody to
each of the selected antibody groups and a certain disease is
examined. Specifically, a sample (cells or tissues) derived from a
patient having a certain disease is prepared, and then, the
reactivity of each antibody to the sample is examined (FIG. 1,
(2)). Two or more antibodies from each of the selected antibody
groups are selected, and thereby the reactivity of them may be
examined. The "certain disease" herein is not particularly limited
but it may include various kinds of cancers, for example, kidney
cancer, hepatic cell carcinoma, gallbladder and liver cancer,
alveolar cell carcinoma, lung squamous cell cancer, pulmonary
adenocarcinoma, pancreas cancer, adenocarcinoma, or ovarian cancer.
In the example shown in FIG. 1, the reactivity with respect to two
kinds or more of diseases are examined simultaneously. However, the
examination is not limited to this alone. The reactivity to one
disease may be examined. Furthermore, the reactivity with respect
to a certain pathologic condition in the certain disease may be
examined.
[0414] The reactivity with respect to the samples derived from a
patient can be detected and evaluated by using an
immunohistochemical staining technique, an immunoprecipitation
method, flow cytometry analysis, cell ELISA and the like. These
methods are not exclusive to each other and therefore two or more
of these methods can be used if necessary. Among them, it is
preferable to employ the immunohistochemical staining technique.
The immunohistochemical staining technique permits rapid and
sensitive detection. Furthermore, its operation is relatively
simple.
[0415] In the immunohistochemical staining technique, tissues
collected from a patient and an antibody are brought into contact
with each other, and then, specifically bonded antibodies are
detected. Concretely, the method of the present invention can be
carried out according to the following immunohistochemical staining
technique.
[0416] The immunohistochemical staining of living tissue is
generally carried out by the following procedures (a) to 0). Note
here that the immunohistochemical staining of living tissue can be
referred to as various documents and publications (for example,
"Enzyme-labeled Antibody Method" 3rd revised edition, K. Watanabe
and K. Nakane (ed), Gakusai Kikaku).
(a) Immobilization--Paraffin Embedding Method Tissue surgically
collected from a living body is immobilized in formalin,
paraformaldehyde, absolute ethyl alcohol, and the like, and then
embedded in paraffin. In general, it is dehydrated with alcohol,
treated with xylene and embedded in paraffin. The paraffin embedded
specimen is cut into a desired thickness (for example, 3 to 5 .mu.m
thick) and extended on a slide glass. Instead of the paraffin
embedding specimen, an alcohol immobilized specimen, a dry sealed
specimen, a frozen specimen, and the like may be used.
(b) Deparaffinization
[0417] In general, treatment is carried out with xylene, alcohol,
and purified water sequentially in this order.
(c) Pretreatment (Antigen Activation)
[0418] If necessary, for antigen activation, for example, enzyme
treatment, heat treatment and/or pressurization treatment are
carried out.
(d) Removal of Endogeneous Peroxidase
[0419] When peroxidase is used as a labeling material for staining,
endogeneous peroxidase activation is removed by carrying out with
hydrogen peroxide solution.
(e) Non-Specific Reaction Inhibition
[0420] Non-specific reaction is inhibited by treating a section
with bovine serum albumin solution (for example, 1% solution) for
several minutes to several tens of minutes. Note here that this
process may be omitted when the following primary antibody reaction
is carried out by using an antibody solution impregnated with
bovine serum albumin.
(f) Primary Antibody Reaction
[0421] An antibody diluted to an appropriate concentration is
dropped on the slide glass and allowed to react for ten minutes to
several hours. After reaction, the reacted produce is washed with
an appropriate buffer solution such as phosphate buffer.
(g) Addition of Labeling Reagent
[0422] As the label material, peroxidase is frequently used.
Secondary antibody bonded to peroxidase is dropped on the section
and then allowed to react for ten minutes to several hours. After
reaction, the reacted product is washed with an appropriate buffer
solution such as phosphate buffer.
(h) Color Reaction
[0423] DAB (3,3'-diaminobenzidine) is dissolved in Tris buffer.
Then, hydrogen peroxide solution is added. The thus prepared
coloring solution is impregnated into a section for several minutes
(for example, five minutes) so as to color the section. After
coloring, the section is sufficiently washed with tapped water so
as to remove DAB.
(i) Nuclear Staining
[0424] The section is subjected to nuclear staining by reacting it
with Mayer hematoxylin for several seconds to several tens seconds.
It was washed with flowing water for saddening (in general, for
several minutes).
(j) Dehydration, Clearing, Encapsulation
[0425] The section is dehydrated with alcohol, clearing treated
with xylene, and finally encapsulated with synthesized resin,
glycerine, rubber syrup, and the like.
[0426] An antibody that is recognized to have specific reactivity
to any of diseases can detect a cell surface antigen characterizing
the disease with high sensitivity. Such an antibody is expected to
be used as a diagnosis or treatment antibody of the disease. Then,
in the step (3), an antibody of the antibody group including such
an antibody is selected (FIG. 1 (3)). As a result, in this example,
as to disease A, an antibody (antibody 1-1, 1-2 or 1-3) of the
antibody group 1 and an antibody of the antibody group 3 (antibody
3-1, 3-2 or 3-3) are selected. As to disease B, an antibody
(antibody 5-1, 5-2 or 5-3) of the antibody group 5 is selected. In
this way, a specific antibody for a certain diseases can be
obtained.
[0427] In the step (3'), a disease in which two or more antibodies
show the specific reactivity is selected, and then, each antibody
is selected from the antibody group to which the antibody showing
the specific reactivity to the disease belongs, is selected, and
the selective antibodies are combined (FIG. 1, (3')). That is to
say, in this example, the disease A is selected and the antibodies
of antibody groups 1 and 3, which are antibody groups to which the
antibody showing the specific reactivity to the disease A belongs,
are combined. Thus, the antibody set showing specific to a certain
disease is obtained.
[0428] Herein, by comparing the specificities (cross reactivity) of
the antibodies in the antibody group, an antibody having the most
excellent property may be selected (in this example, antibody 1-2,
antibody 3-3, and antibody 5-3 are selected. See, FIG. 1, (4)). By
adding this step, more useful antibody or antibody set can be
obtained.
[0429] Furthermore, an antibody set may be structured by combining
an arbitrary antibody that does not have reactivity to the diseases
with the antibodies selected as the antibodies showing the
reactivity to a certain disease (in this example, for example, the
antibody 4-1 is combined to an antibody of the antibody group 1 and
antibody of antibody group 3). By using such an antibody set,
detail characterization of the disease can be possible.
[0430] According to the obtaining method of the present invention,
an antibody (or antibody set) to a disease-specific antigen can be
obtained. The antibody (or antibody set), which are as it is or to
which necessary modification is added, is useful for study,
classifying, diagnosing and treating the disease or the pathologic
condition. Thus, this method provides an extremely useful tool in
the field of medicine.
[0431] The third embodiment of this aspect provides the obtaining
method of antibody set including the following steps.
[0432] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to the present invention;
[0433] (2) with respect to two kinds or more of diseases, examining
a reactivity between an antibody in each of the selected antibody
groups and a certain disease; and
[0434] (3) selecting antibodies from the antibody group, to which
the antibody having a specific reactivity to any of disease
belongs, and combining the selected antibodies.
[0435] Hereinafter, the detail of each step is described with
reference to FIG. 2. For convenience of explanation, in FIG. 2, it
is assumed that the antibody groups 1 to 6 are obtained by the
classifying method of the present invention and three antibodies
belong to each antibody group. The antigens (antigen A) in the
antibody groups 1 to 3 are common. Similarly, the antigens (antigen
B) in the antibody groups 4 and 5 are also common.
[0436] In the step (1) of this embodiment, two or more antibody
groups recognizing different antigens (antibody groups 1, 4, and 6)
are selected (see, FIG. 2 (1)). In the following step (2), the
reactivity between the antibodies (antibodies 1-1, 4-1, and 6-1) in
each of the selected antibody groups and certain diseases (diseases
A to D) are examined (FIG. 2, (2)). In the step (3), antibodies in
the antibody groups to which the antibody belong showing specific
reactivity to any of diseases are combined. That is to say, in this
example, an antibody of antibody group 1 to which an antibody 1-1
showing specific reactivity to disease A and an antibody of
antibody group 4 to which an antibody 4-1 showing specific
reactivity to disease B are combined to form an antibody set (FIG.
2, (3)). Thus, an antibody set (the antibody 1-1 and the antibody
4-1) including an antibody specific to disease A and an antibody
specific to disease B is obtained. This antibody set is useful for
detecting, for example, disease A or disease B and this antibody is
a reagent effective to the discrimination of the diseases A and
B.
[0437] Note here that by comparing the specificity (cross
reactivity) and the like between the antibodies in the antibody
group, an antibody having the most excellent property may be
selected (In this example, the antibody 1-2 and the antibody 4-3
are selected. FIG. 2, (4)). By adding this step, it is possible to
obtain a more useful antibody set.
[0438] As a result of carrying out the classifying method and the
identification method of the present invention, assuming that a
plurality of antibodies groups recognizing the same antigen are
obtained, the fourth embodiment of this aspect provides a obtaining
method of an antibody set including the following steps.
[0439] (1) selecting two or more antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to the present invention;
[0440] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0441] (3) selecting an antibody from the antibody group to which
the antibody having a specific reactivity to any of disease
belongs, and an antibody belonging to other antibody group whose
antigen is common to that of the antibody group, and combining the
selected antibodies.
[0442] Hereinafter, the detail of each step is described with
reference to FIG. 3. For convenience of explanation, in FIG. 3, it
is assumed that the antibody groups 1 to 6 are obtained by the
classifying method of the present invention and three antibodies
belong to each antibody group. The antigens (antigen A) in the
antibody groups 1 to 3 are common. Similarly, the antigens (antigen
B) in the antibody groups 4 and 5 are also common.
[0443] In the step (1) of this embodiment, two or more antibody
groups recognizing different antigens (antibody groups 1, 4, and 6)
are selected (see, FIG. 3 (1)). In the following step (2), the
reactivity between the antibodies (antibodies 1-1, 4-1, and 6-1) in
each of the selected antibody groups- and certain diseases
(diseases A to D) are examined (FIG. 3, (2)). In the step (3), an
antibody of the antibody group to which an antibody showing the
specific reactivity to any of diseases and an antibody belonging to
other antibody group whose antigen is common to the group are
selected, respectively. The selected antibodies are combined so as
to form an antibody set (FIG. 3, (3)). That is to say, in this
example, an antibody in antibody group 1 to which antibody 1-1
belongs showing specific reactivity to disease A and an antibody of
the antibody groups 2 and 3 whose antigens are common are combined.
Thus, an antibody set specific to the disease A is obtained.
Similarly, an antibody in antibody group 4 to which antibody 4-1
belongs showing specific reactivity to disease B and an antibody of
the antibody group 5 whose antigen is common to that of antibody
group 4. Thus, an antibody set specific to the disease B is
obtained. As shown in this example, "another antibody group" herein
is not particularly one but a plurality antibody groups may be
present.
[0444] Herein, even in the case of cancers of the same organ,
depending upon patients, the pathologic condition (grade of
malignancy) may be largely different. The difference in such
pathologic conditions is thought to be involved to the expression
forms of the specific antigens. On the other hand, the antibody
sets obtained in this embodiment are not different in the level
recognized by an antigen but include antibodies that are different
in the level of epitope. That is to say, this is an antibody set
including a plurality of antibodies that are different in the
epitope to be recognized. Such an antibody set permits multilateral
detection or evaluation of expression forms of antigen. For
example, such an antibody set is useful for detection of certain
pathologic conditions in, for example, cancers, or a determination
of the grade of malignancy.
[0445] Note here that by comparing the specificity (cross
reactivity) and the like in the antibodies in the antibody group,
an antibody having the most excellent property may be finally
selected (FIG. 3, (4)). By adding this step, it is possible to
obtain a more useful antibody set.
[0446] As a result of carrying out the classifying method and the
identification method of the present invention, assuming that a
plurality of antibodies groups recognizing the same antigen are
obtained, the fifth embodiment of this aspect provides a obtaining
method of an antibody set including the following steps.
[0447] (1) selecting two or more antibody groups recognizing the
same antigen from the plurality of antibody groups classified by
the classifying method according to the present invention;
[0448] (2) with respect to one kind or two or more kinds of
pathologic conditions, examining a reactivity between an antibody
in each of the selected antibody groups and a pathologic condition;
and
[0449] (3) associating information about the reactivity and then
combining the antibodies in the antibody groups.
[0450] Hereinafter, the detail of each step is described with
reference to FIG. 4. For convenience of explanation, in FIG. 4, it
is assumed that the antibody groups 1 to 6 are obtained by the
classifying method of the present invention and three antibodies
belong to each antibody group. The antigens (antigen A) in the
antibody groups 1 to 3 are common. Similarly, the antigens (antigen
B) in the antibody groups 4 and 5 are also common.
[0451] In the step (1) of this embodiment, two or more antibody
groups recognizing common antigen (antibody groups 1 to 3) are
selected (see, FIG. 4 (1)). In the following step (2), the
reactivity between the antibodies (antibodies 1-1, 2-1, and 3-1) in
each of the selected antibody groups and certain various diseases
are examined (FIG. 4, (2)). Specifically, as to various pathologic
conditions of certain disease, samples (cells or tissue) derived
from a patient are prepared, and the reactivity between the samples
and each antibody is examined. In the step (3), the obtained
reactivity is associated with each other (FIG. 4, (2), right
column), and then antibodies of each of the selected antibody
groups (antibody groups 1 to 3) are combined so as to form an
antibody set (FIG. 4, (3)). Thus, antibody sets specific to the
certain pathologic condition of certain disease is obtained (in
this example, an antibody set specific to pathologic condition of
disease A including antibodies of the antibody groups 1 to 3 is
obtained). The antibody set obtained in this embodiment is
typically not different in the level of an antigen but include
antibodies that are different in the level of epitope. Therefore,
similar to the antibody set according to the above-mentioned
embodiment, for example, the antibody set is useful detecting the
certain pathologic condition in, for example, cancer, or a
determination of the grade of malignancy. Note here that it is
preferable that an antibody set is constructed by excluding
antibodies showing no specific reactivity with respect to any
pathologic conditions.
[0452] By comparing the specificity (cross reactivity) and the like
in the antibodies in the antibody group, an antibody having the
most excellent property may be finally selected (in this example,
antibodies 1-2, 2-1 and 3-3 are selected, FIG. 4, (4)). By adding
this step, it is possible to obtain a more useful antibody set.
[0453] A further aspect of the present invention provides a
production method of a panel displaying a association between an
antibody and a disease (or pathologic condition). In the first
embodiment of this aspect, the following steps are carried out.
[0454] (1) selecting one or two or more of antibody groups from the
plurality of antibody groups classified by the classifying method
according to the present invention;
[0455] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0456] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[0457] When one antibody group is selected in the step (1), as to
one antibody or a plurality of antibodies whose antigen is common,
a panel displaying the association with respect to a certain
disease can be obtained. In the latter case, as to a plurality of
antibodies whose antigen is common antigen, from the viewpoint of
the association with respect to the disease, difference or points
of difference (one caused by the cross reactivity and the like) can
be read out. That is to say, the panel gives an important
suggestion as to the property of the antibody. On the other hand,
when two or more antibody groups are selected in the step (1), as
to a plurality of antibodies whose antigen is different (however,
when several antibodies from each antibody group in the step (1),
antibodies whose antigen is common is contaminated), a panel
displaying the association with respect to the certain disease is
obtained. This panel gives information on the antibody group useful
for study, classification and diagnosis. The panel itself has a
great value. Form this panel, the association between a plurality
of antigen and disease can be read out. That is to say, the panel
gives an important suggestion as to the association between each
antigen and disease.
[0458] Herein, in the step (2), it is preferable to examine the
reactivity of the antibody as to two or more diseases. Thus, a
panel displaying the association (linkage) between each antibody
and two or more diseases can be obtained. The panel displays more
pieces of information and further displays the association between
diseases. Suggestion that is useful and important for study,
classification and diagnosis of the diseases can be obtained.
[0459] In the second embodiment of this aspect, the following steps
are carried out.
[0460] (1) selecting two or more of antibody groups recognizing
different antigens from the plurality of antibody groups classified
by the classifying method according to the present invention;
[0461] (2) with respect to one kind or two or more kinds of
diseases, examining a reactivity between an antibody in each of the
selected antibody groups and a certain disease; and
[0462] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[0463] In this embodiment, a panel displaying the association
between a plurality of antibodies whose antigen is different and a
certain disease can be obtained. This panel gives information on an
antibody group useful for study, classification and diagnosis for a
disease and the panel itself has a great value. Form this panel,
the association (linkage) between a plurality of antigens and
disease can be read out. That is to say, the panel gives important
suggestions as to the association between each antigen and disease
as well as the association between antigens.
[0464] Herein, in the step (2), it is preferable to examine the
reactivity of the antibody as to two or more diseases. Thus, a
panel displaying the association between each antibody and two or
more diseases can be obtained. The panel displays more pieces of
information and further displays the association between diseases.
Suggestion that is useful and important for study, classification
and diagnosis of the diseases can be obtained.
[0465] In the third embodiment of this aspect, the following steps
are carried out.
[0466] (1) selecting two or more of antibody groups recognizing a
common antigen from the plurality of antibody groups classified by
the classifying method according to the present invention;
[0467] (2) with respect to one kind or two or more kinds of
pathologic condition, examining a reactivity between an antibody in
each of the selected antibody groups and a certain pathologic
condition of disease; and
[0468] (3) associating the results of the step (2) with each
antibody and displaying by using a drawing or a tabular format.
[0469] In this embodiment, as to a plurality of antibodies whose
antigen is common, a panel displaying the association with respect
to a pathologic condition of a certain disease can be obtained.
This panel gives information on antibody group that is useful for
study of each pathologic condition, study of difference between
pathologic conditions, classification of pathologic conditions, or
diagnosis on the level of the pathologic condition. The panel
itself has a great value.
[0470] Herein, in the step (2), it is preferable to examine the
reactivity of the antibody as to two or more pathologic conditions.
Thus, a panel displaying the association between each antibody and
two or more pathologic conditions can be obtained. This panel
displays not only more pieces of information but also the
association between the pathologic conditions. Suggestion that is
useful and important to study, classification and diagnosis of each
pathologic condition can be obtained.
[0471] Note here that the first embodiment of this aspect
corresponds to the first and second embodiments of the third
aspect. Similarly, the third aspect of the second embodiment
corresponds to the third and fourth embodiments of the third
aspect, respectively. Therefore, as to the matters that are not
specifically noted in this aspect, the explanation of the
corresponding third aspect is employed. In the panel of the present
invention, the term "association between antibody and disease (or
pathologic condition)" is displayed by characters showing subject
diseases (or pathologic conditions) are positive or negative to the
antibody (for example, "to positive," "to negative," "positive,"
and "negative") or marks (for example, "o," "x," "P," and "N") etc.
The display is not limited to two-stage display and, display may be
carried out in four stages, for example, strongly positive,
moderate positive, weak positive, and negative.
[0472] The number of antibodies displayed in one panel is not
particularly limited. For example, the number is 1 to 1000,
preferably 2 to 100, and further preferably 5 to 59.
[0473] Furthermore, in addition to the association between an
antibody and a certain disease (or pathologic condition), an
antigen to each antibody may be shown. The combination of the panel
of this aspect and the antibody (or antibody set) obtained in the
above-mentioned obtaining method of the present invention becomes
an effective tool for study, classification and diagnosis of
diseases, pathologic conditions, or the like. That is to say,
according to the combination, both information, i.e., an antibody
(or an antibody set) specific to a disease or a pathologic
condition and the association between the antibody (or the antibody
set) and the disease or the pathologic condition can be obtained
simultaneously.
[0474] The present invention further relates to a method of testing
a disease in which a cell surface antigen is an indicator, the
method comprising the following steps.
[0475] (1) preparing a cell or a tissue separated from a
subject;
[0476] (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel (panel displaying the
association between an antibody and a disease (or a pathologic
condition)) according to the present invention; and
[0477] (3) collating the results in the step (2) with the
panel.
[0478] According to the testing method of the present invention, as
to a disease or a pathologic condition to be tested (hereinafter,
referred to as "diseased to be tested"), information about the
presence of contraction of a subject, contraction risk, pathologic
conditions, and the like, can be obtained. That is to say, the
testing method of the present invention is effective means for
diagnosing the subjected disease. Furthermore, when the testing
method of the present invention is carried out along with the
treatment, the therapeutic effect can be evaluated based on the
testing results. Thus, the testing method of the present invention
may be used for monitoring the therapeutic effect.
[0479] In the step (1), cells or tissue separated from a subject
(that is, a living body) (hereinafter, referred to as "subject
cell, and the like") are prepared. The term "separated from a
subject" means a state in which a part of cells or tissue of a
subject is extracted and completely isolated form a subject as a
living body. A person who needs information about a disease to be
tested is a subject. A subject may be a patient of a disease to be
tested or may be an apparent healthy person. The "apparent healthy
person" means a person who has not recognized to be a patient of a
disease to be tested prior to the application of the testing method
of the present invention.
[0480] In the step (2), the reactivity between the subject cells
and the like and each antibody displayed on the panel of the
present invention is examined. That is to say, by using an
immunologic procedure (for example, immunohistochemical staining
technique), whether or not the tested cells express an antigen
recognized by each antibody is examined. According to the
immunologic procedure, in general, information on the expression
amount of antigens can be obtained. Therefore, in addition to the
presence of expression antigen, the expression amount may be also
examined. An example of the immunologic procedure includes ELISA
method, radioimmunoassay, flow cytometry analysis,
immunoprecipitation method, immune-blotting, and the like.
[0481] In the step (3), the results of the step (2) (reactivity of
each antibody) is collated with the panel of the present invention.
The panel of the present invention displays the association between
each antibody and a disease or a pathologic condition. Therefore,
this step clarifies the association between the tested cells etc.
and the disease via the reactivity with respect to each
antibody.
[0482] A further application of the above-mentioned panel also
includes the following method of the present invention, that is,
the optimum method of treating certain diseases, which includes the
following steps.
[0483] (1) preparing a cell or a tissue separated from a
subject;
[0484] (2) examining a reactivity between the cell or the tissue
and each antibody displayed on the panel (a panel displaying the
association between the antibody and disease (or pathologic
condition)) according to the present invention;
[0485] (3) collating the results in the step (2) with the panel,
and
[0486] (4) selecting an effective antibody according to the results
of collating.
[0487] In the selection method of the present invention, similar to
the above-mentioned testing method, after the steps (1) to (3) are
carried out, according to the collation results, an effective
antibody is selected (the step (4)). As the effective antibody,
typically, an antibody showing a specific reactivity in the step
(2) is selected. An antibody equivalent to the antibody showing a
specific reactivity in the step (2) may be also selected. The
"equivalent antibody" means an antibody having equivalent
properties (reactivity or activity) to the reference antibody. An
example of the equivalent antibody may be an antibody in which the
sequence of the heavy chain variable region and the sequence of the
light chain variable region are not substantially different from
that of the reference antibody (completely identical, or slightly
different so that the reactivity or activity is not affected).
Another example of the equivalent antibody may be an antibody in
which no difference is observed in all of the sequence of each CDR
constituting heavy chain variable region and the sequence of each
CDR constituting light chain variable region when it is compared
with the reference antibody.
[0488] Diseases to which the selection method of the present
invention is applied is a disease in which cell surface antigen
selected from the group consisting of HER1, HER2, CD46, ITGA3,
ICAM1, ALCAM, CD147, IgSF4, BCAM, C1qR, CD44, CD73, LAR, EpCAM and
HGFR is an indicator. That is to say, for selecting optimum
treatment methods suitable for various diseases characterized by
the expression of the cell surface antigen, the present invention
can be used. According to the present invention, optimum treatment
method suitable for each patient can be selected. Thus, tailor-made
medicine can be realized.
[0489] It is preferable that the panel used in the selection method
of the present invention displays two or more antibodies selected
from the group consisting of 048-006 antibody, 057-091 antibody,
059-152 antibody, 048-040 antibody, 054-101 antibody, 055-147
antibody, 059-173 antibody, 067-149 antibody, 067-176 antibody,
015-126 antibody, 015-044 antibody, 015-102 antibody, 015-136
antibody, 015-143 antibody, 015-209 antibody, 039-016 antibody,
053-216 antibody, 075-024 antibody, 075-110 antibody, 086-032
antibody, 086-035 antibody, 086-036 antibody, 086-061 antibody,
086-138 antibody, 086-182 antibody, 035-224 antibody, 045-011
antibody, 051-144 antibody, 052-053 antibody, 052-073 antibody,
053-049 antibody, 3172-120 antibody, 066-069 antibody, 015-003
antibody, 064-002 antibody, 064-006 antibody, 064-012a antibody,
064-012b antibody, 064-014 antibody, 064-054 antibody, 064-085
antibody, 064-093 antibody, 064-116 antibody, 065-183 antibody,
067-142 antibody, 068-007 antibody, 052-033 antibody, 053-042
antibody, 053-051 antibody, 053-059 antibody, 053-085 antibody,
035-234 antibody, 040-107 antibody, 041-118 antibody, 066-174
antibody, 083-040 antibody, 029-143 antibody, 045-134 antibody,
062-101 antibody, 062-109 antibody, 084-103 antibody, 052-274
antibody, 029-067 antibody, 083-131 antibody, 059-053 antibody,
064-003 antibody, 067-213 antibody, 067-153 antibody, 067-126
antibody, 067-133 antibody, 067-287 antibody, 064-044 antibody,
065-030 antibody, 065-358 antibody, 066-019 antibody, 079-085
antibody, 067-024 antibody, and 076-048 antibody.
[0490] In one embodiment of the selecting method of the present
invention, the following steps are carried out.
[0491] (1) preparing a panel displaying a reactivity between one or
more antibodies selected from the group consisting of 048-006
antibody, 015-126 antibody, 067-133 antibody, 064-044 antibody,
076-048 antibody and 059-053 antibody, and a clinical cancer tissue
of one or more diseases selected from the group consisting of
squamous carcinoma, adenosquamous carcinoma, alveolar
adenocarcinoma, adenocarcinoma, and large cell carcinoma, and a
cell or tissue separated from a subject;
[0492] (2) examining reactivity between the cell or the tissue and
each antibody displayed on the panel;
[0493] (3) collating the results in the step (2) with the panel,
and
[0494] (4) selecting an effective antibody according to the results
of collating. In the step (1) of this embodiment, a panel
displaying the reactivity between an antibody successfully obtained
by the present inventor and clinical cancer tissue of a certain
disease is prepared. In addition, cells or tissue separated from a
subject are prepared. The step (2) or later are carried out similar
to the above-mentioned embodiments. Note here that, a specific
example of the panel to be used in this embodiment is a panel shown
in FIG. 69.
[0495] Also in this embodiment, an antibody showing the specific
reactivity in the step (2) or the equivalent antibody thereto is
selected as an effective antibody. The selection method of this
embodiment is preferred for selecting the suitable treatment method
of squamous carcinoma, adenosquamous carcinoma, alveolar
adenocarcinoma, adenocarcinoma, or large cell carcinoma.
[0496] As a further aspect of the present invention provides an
isolated antibody (or an antibody set) obtained in the
above-mentioned obtaining method of an antibody (or an obtaining
method of an antibody set). As shown in the below-mentioned
Examples, the present inventors have succeeded in actually
obtaining by the method of the present invention, an antibody
relevant to HER1, an antibody relevant to HER2, an antibody
relevant to CD46, an antibody relevant to ITGA3, an antibody
relevant to ICAM1, an antibody relevant to ALCAM, an antibody
relevant to CD147, an antibody relevant to C1qR, an antibody
relevant to CD44, an antibody relevant to CD73, an antibody
relevant to EpCAM, an antibody relevant to HGFR, an antibody
relevant to LAR, and an antibody relevant to BCAM. Furthermore, in
the current testing method, it is possible to obtain an antibody
capable of recognizing two clinical specimen s that are determined
to have the same disease (pathologic condition). With this
antibody, a certain disease can be newly classified based on the
expression state of an antigen and further such a disease can be
examined.
[0497] A further aspect of the present invention provides an
antibody successfully obtained by the present inventors and the
application thereof. As shown in the below-mentioned Examples, the
present inventors succeeded in obtaining nine kinds of antibodies
to HER1 (048-006 antibody, 057-091 antibody, 059-152 antibody,
048-040 antibody, 054-101 antibody, 055-147 antibody, 059-173
antibody, 067-149 antibody, and 067-176 antibody), 16 kinds of
antibodies to HER2 (015-126 antibody, 015-044 antibody, 015-102
antibody, 015-136 antibody, 015-143 antibody, 015-209 antibody,
039-016 antibody, 053-216 antibody, 075-024 antibody, 075-110
antibody, 086-032 antibody, 086-035 antibody, 086-036 antibody,
086-061 antibody, 086-138 antibody, and 086-182 antibody), eight
kinds of antibodies to CD46 (035-224 antibody, 045-011 antibody,
051-144 antibody, 052-053 antibody, 052-073 antibody, 053-049
antibody, 3172-120 antibody, and 066-069 antibody), 13 kinds of
antibodies to ITGA3 (015-003 antibody, 064-002 antibody, 064-006
antibody, 064-012a antibody, 064-012b antibody, 064-014 antibody,
064-054 antibody, 064-085 antibody, 064-093 antibody, 064-116
antibody, 065-183 antibody, 067-142 antibody, and 068-007
antibody), five kinds of antibodies to ICAM1 (052-033 antibody,
053-042 antibody, 053-051 antibody, 053-059 antibody, and 053-085
antibody), 13 kinds of antibodies to ALCAM (035-234 antibody,
040-107 antibody, 041-118 antibody, 066-174 antibody, 083-040
antibody, 029-143 antibody, 045-134 antibody, 062-101 antibody,
062-109 antibody, 084-103 antibody, 052-274 antibody, 029-067
antibody, and 083-131 antibody), one kind of antibody to CD147
antibody (059-053 antibody), one kind of antibody to C1qR (070-016
antibody), one kind of antibody to CD44 (064-003 antibody), one
kind of antibody to CD73 (067-213 antibody), one kind of antibody
to EpCAM (067-153 antibody), three kinds of antibodies to HGFR
(067-126 antibody, 067-133 antibody, and 067-287 antibody), five
kinds of antibodies to LAR (064-044 antibody, 065-030 antibody,
065-358 antibody, 066-019 antibody, and 079-085 antibody), and one
kind of antibody to BCAM (067-024 antibody). Since these antibodies
are recognize an extracellular domain of antigen in a state in
which it is expressed on the surface of the cell membrane, they are
useful for staining cells and tissues, and the like. As a result of
analysis of sequences of each antibody, the following sequence
information is obtained. Note here that, following to the antibody
name, the amino acid sequence of the heavy chain variable region;
the amino acid sequence of the heavy chain CDR1; the amino acid
sequence of the heavy chain CDR2; the amino acid sequence of the
heavy chain CDR3; the amino acid sequence of the light chain
variable region; the amino acid sequence of the light chain CDR1;
the amino acid sequence of the light chain CDR2; and the amino acid
sequence of the light chain CDR3 are described sequentially in this
order.
1. Antibody to HER1
[0498] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned nine kinds of antibody clones, the sequences
are analyzed.
[0499] 048-006 antibody: SEQ ID NO: 1 (VH); SEQ ID NO: 2 (VH CDR1);
SEQ ID NO: 3 (VH CDR2); SEQ ID NO: 4 (VH CDR3); SEQ ID NO: 5 (VL);
SEQ ID NO: 6 (VL CDR1); SEQ ID NO: 7 (VL CDR2); SEQ ID NO: 8 (VL
CDR3)
[0500] 057-091 antibody: SEQ ID NO: 9 (VH); SEQ ID NO: 10 (VH
CDR1); SEQ ID NO: 11 (VH CDR2); SEQ ID NO: 12 (VH CDR3); SEQ ID NO:
13 (VL); SEQ ID NO: 14 (VL CDR1); SEQ ID NO: 15 (VL CDR2); SEQ ID
NO: 16 (VL CDR3)
[0501] 059-152 antibody: SEQ ID NO: 17 (VH); SEQ ID NO: 18 (VH
CDR1); SEQ ID NO: 19 (VH CDR2); SEQ ID NO: 20 (VH CDR3); SEQ ID NO:
21 (VL); SEQ ID NO: 22 (VL CDR1); SEQ ID NO: 23 (VL CDR2); SEQ ID
NO: 24 (VL CDR3)
[0502] 048-040 antibody: SEQ ID NO: 483 (VH); SEQ ID NO: 484 (VH
CDR1); SEQ ID NO: 485 (VH CDR2); SEQ ID NO: 486 (VH CDR3); SEQ ID
NO: 487 (VL); SEQ ID NO: 488 (VL CDR1); SEQ ID NO: 489 (VL CDR2);
SEQ ID NO: 490 (VL CDR3)
[0503] 054-101 antibody: SEQ ID NO: 491 (VH); SEQ ID NO: 492 (VH
CDR1); SEQ ID NO: 493 (VH CDR2); SEQ ID NO: 494 (VH CDR3); SEQ ID
NO: 495 (VL); SEQ ID NO: 496 (VL CDR1); SEQ ID NO: 497 (VL CDR2);
SEQ ID NO: 498 (VL CDR3)
[0504] 055-147 antibody: SEQ ID NO: 499 (VH); SEQ ID NO: 500 (VH
CDR1); SEQ ID NO: 501 (VH CDR2); SEQ ID NO: 502 (VH CDR3); SEQ ID
NO: 503 (VL); SEQ ID NO: 504 (VL CDR1); SEQ ID NO: 505 (VL CDR2);
SEQ ID NO: 506 (VL CDR3)
[0505] 059-173 antibody: SEQ ID NO: 507 (VH); SEQ ID NO: 508 (VH
CDR1); SEQ ID NO: 509 (VH CDR2); SEQ ID NO: 510 (VH CDR3); SEQ ID
NO: 511 (VL); SEQ ID NO: 512 (VL CDR1); SEQ ID NO: 513 (VL CDR2);
SEQ ID NO: 514 (VL CDR3)
[0506] 067-149 antibody: SEQ ID NO: 515 (VH); SEQ ID NO: 516 (VH
CDR1); SEQ ID NO: 517 (VH CDR2); SEQ ID NO: 518 (VH CDR3); SEQ ID
NO: 519 (VL); SEQ ID NO: 520 (VL CDR1); SEQ ID NO: 521 (VL CDR2);
SEQ ID NO: 522 (VL CDR3)
[0507] 067-176 antibody: SEQ ID NO: 523 (VH); SEQ ID NO: 524 (VH
CDR1); SEQ ID NO: 525 (VH CDR2); SEQ ID NO: 526 (VH CDR3); SEQ ID
NO: 527 (VL); SEQ ID NO: 528 (VL CDR1); SEQ ID NO: 529 (VL CDR2);
SEQ ID NO: 530 (VL CDR3)
[0508] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and pancreatic cancer cell
line PANC-1, kidney cancer cell line CCFRC1, kidney cancer cell
line Caki-1, ovarian cancer cell line KF28, stomach cancer cell
line SNU-5, lung squamous cell carcinoma line RERF-LC-AI, ovarian
cancer cell line RMG-1, undifferentiated hepatic cell carcinoma
cancer cell line HLF, ovarian cancer cell line SKOv3, pulmonary
adenocarcinoma cell line PC14, kidney cancer cell line ACHN, lung
squamous cell carcinoma line EBC1, vulva mucosal epithelial cell
line A431, pulmonary adenocarcinoma cell line H1373, hepatic cell
carcinoma cell line HepG2, and kidney cancer clinical specimen
established cell line (as to the above mention, based on the
results of the cell line staining), as well as the relationships
between these antibodies and kidney cancer, hepatic cell carcinoma,
gallbladder and liver cancer, lung squamous cell cancer, pulmonary
adenocarcinoma, and pancreas cancer (as to the above mention, based
on the results of the tissue staining) are experimentally
confirmed.
2. Antibody to HER2
[0509] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned 16 kinds of antibody clones, the sequences are
analyzed.
[0510] 015-126 antibody SEQ ID NO: 25 (VH); SEQ ID NO: 26 (VH
CDR1); SEQ ID NO: 27 (VH CDR2); SEQ ID NO: 28 (VH CDR3); SEQ ID NO:
29 (VL); SEQ ID NO: 30 (VL CDR1); SEQ ID NO: 31 (VL CDR2); SEQ ID
NO: 32 (VL CDR3)
[0511] 015-044 antibody SEQ ID NO: 531 (VH); SEQ ID NO: 532 (VH
CDR1); SEQ ID NO: 533 (VH CDR2); SEQ ID NO: 534 (VH CDR3); SEQ ID
NO: 535 (VL); SEQ ID NO: 536 (VL CDR1); SEQ ID NO: 537 (VL CDR2);
SEQ ID NO: 538 (VL CDR3)
[0512] 015-102 antibody SEQ ID NO: 539 (VH); SEQ ID NO: 540 (VH
CDR1); SEQ ID NO: 541 (VH CDR2); SEQ ID NO: 542 (VH CDR3); SEQ ID
NO: 543 (VL); SEQ ID NO: 544 (VL CDR1); SEQ ID NO: 545 (VL CDR2);
SEQ ID NO: 546 (VL CDR3)
[0513] 015-136 antibody SEQ ID NO: 547 (VH); SEQ ID NO: 548 (VH
CDR1); SEQ ID NO: 549 (VH CDR2); SEQ ID NO: 550 (VH CDR3); SEQ ID
NO: 551 (VL); SEQ ID NO: 552 (VL CDR1); SEQ ID NO: 553 (VL CDR2);
SEQ ID NO: 554 (VL CDR3)
[0514] 015-143 antibody SEQ ID NO: 555 (VH); SEQ ID NO: 556 (VH
CDR1); SEQ ID NO: 557 (VH CDR2); SEQ ID NO: 558 (VH CDR3); SEQ ID
NO: 559 (VL); SEQ ID NO: 560 (VL CDR1); SEQ ID NO: 561 (VL CDR2);
SEQ ID NO: 562 (VL CDR3)
[0515] 015-209 antibody SEQ ID NO: 563 (VH); SEQ ID NO: 564 (VH
CDR1); SEQ ID NO: 565 (VH CDR2); SEQ ID NO: 566 (VH CDR3); SEQ ID
NO: 567 (VL); SEQ ID NO: 568 (VL CDR1); SEQ ID NO: 569 (VL CDR2);
SEQ ID NO: 570 (VL CDR3)
[0516] 039-016 antibody SEQ ID NO: 571 (VH); SEQ ID NO: 572 (VH
CDR1); SEQ ID NO: 573 (VH CDR2); SEQ ID NO: 574 (VH CDR3); SEQ ID
NO: 575 (VL); SEQ ID NO: 576 (VL CDR1); SEQ ID NO: 577 (VL CDR2);
SEQ ID NO: 578 (VL CDR3)
[0517] 053-216 antibody SEQ ID NO: 579 (VH); SEQ ID NO: 580 (VH
CDR1); SEQ ID NO: 581 (VH CDR2); SEQ ID NO: 582 (VH CDR3); SEQ ID
NO: 583 (VL); SEQ ID NO: 584 (VL CDR1); SEQ ID NO: 585 (VL CDR2);
SEQ ID NO: 586 (VL CDR3)
[0518] 075-024 antibody SEQ ID NO: 587 (VH); SEQ ID NO: 588 (VH
CDR1); SEQ ID NO: 589 (VH CDR2); SEQ ID NO: 590 (VH CDR3); SEQ ID
NO: 591 (VL); SEQ ID NO: 592 (VL CDR1); SEQ ID NO: 593 (VL CDR2);
SEQ ID NO: 594 (VL CDR3)
[0519] 075-110 antibody SEQ ID NO: 595 (VH); SEQ ID NO: 596 (VH
CDR1); SEQ ID NO: 597 (VH CDR2); SEQ ID NO: 598 (VH CDR3); SEQ ID
NO: 599 (VL); SEQ ID NO: 600 (VL CDR1); SEQ ID NO: 601 (VL CDR2);
SEQ ID NO: 602 (VL CDR3)
[0520] 086-032 antibody SEQ ID NO: 603 (VH); SEQ ID NO: 604 (VH
CDR1); SEQ ID NO: 605 (VH CDR2); SEQ ID NO: 606 (VH CDR3); SEQ ID
NO: 607 (VL); SEQ ID NO: 608 (VL CDR1); SEQ ID NO: 609 (VL CDR2);
SEQ ID NO: 610 (VL CDR3)
[0521] 086-035 antibody SEQ ID NO: 611 (VH); SEQ ID NO: 612 (VH
CDR1); SEQ ID NO: 613 (VH CDR2); SEQ ID NO: 614 (VH CDR3); SEQ ID
NO: 615 (VL); SEQ ID NO: 616 (VL CDR1); SEQ ID NO: 617 (VL CDR2);
SEQ ID NO: 618 (VL CDR3)
[0522] 086-036 antibody SEQ ID NO: 619 (VH); SEQ ID NO: 620 (VH
CDR1); SEQ ID NO: 621 (VH CDR2); SEQ ID NO: 622 (VH CDR3); SEQ ID
NO: 623 (VL); SEQ ID NO: 624 (VL CDR1); SEQ ID NO: 625 (VL CDR2);
SEQ ID NO: 626 (VL CDR3)
[0523] 086-061 antibody SEQ ID NO: 627 (VH); SEQ ID NO: 628 (VH
CDR1); SEQ ID NO: 629 (VH CDR2); SEQ ID NO: 630 (VH CDR3); SEQ ID
NO: 631 (VL); SEQ ID NO: 632 (VL CDR1); SEQ ID NO: 633 (VL CDR2);
SEQ ID NO: 634 (VL CDR3)
[0524] 086-138 antibody SEQ ID NO: 635 (VH); SEQ ID NO: 636 (VH
CDR1); SEQ ID NO: 637 (VH CDR2); SEQ ID NO: 638 (VH CDR3); SEQ ID
NO: 639 (VL); SEQ ID NO: 640 (VL CDR1); SEQ ID NO: 641 (VL CDR2);
SEQ ID NO: 642 (VL CDR3)
[0525] 086-182 antibody SEQ ID NO: 643 (VH); SEQ ID NO: 644 (VH
CDR1); SEQ ID NO: 645 (VH CDR2); SEQ ID NO: 646 (VH CDR3); SEQ ID
NO: 647 (VL); SEQ ID NO: 648 (VL CDR1); SEQ ID NO: 649 (VL CDR2);
SEQ ID NO: 650 (VL CDR3)
[0526] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and pulmonary adenocarcinoma
cell line Calu-3, ovarian cancer cell line SKOv3, and breast cancer
cell line BT474 (based on the results of the cell line staining)
are experimentally confirmed.
3. Antibody to CD46
[0527] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included.
Finally 87 kinds of antibody clones are identified. As to the
below-mentioned eight kinds of antibody clones, the sequences are
analyzed.
[0528] 035-224 antibody SEQ ID NO: 33 (VH); SEQ ID NO: 34 (VH
CDR1); SEQ ID NO: 35 (VH CDR2); SEQ ID NO: 36 (VH CDR3); SEQ ID NO:
37 (VL); SEQ ID NO: 38 (VL CDR1); SEQ ID NO: 39 (VL CDR2); SEQ ID
NO: 40 (VL CDR3)
[0529] 045-011 antibody SEQ ID NO: 41 (VH); SEQ ID NO: 42 (VH
CDR1); SEQ ID NO: 43 (VH CDR2); SEQ ID NO: 44 (VH CDR3); SEQ ID NO:
45 (VL); SEQ ID NO: 46 (VL CDR1); SEQ ID NO: 47 (VL CDR2); SEQ ID
NO: 48 (VL CDR3)
[0530] 051-144 antibody SEQ ID NO: 49 (VH); SEQ ID NO: 50 (VH
CDR1); SEQ ID NO: 51 (VH CDR2); SEQ ID NO: 52 (VH CDR3); SEQ ID NO:
53 (VL); SEQ ID NO: 54 (VL CDR1); SEQ ID NO: 55 (VL CDR2); SEQ ID
NO: 56 (VL CDR3)
[0531] 052-053 antibody SEQ ID NO: 57 (VH); SEQ ID NO: 58 (VH
CDR1); SEQ ID NO: 59 (VH CDR2); SEQ ID NO: 60 (VH CDR3); SEQ ID NO:
61 (VL); SEQ ID NO: 62 (VL CDR1); SEQ ID NO: 63 (VL CDR2); SEQ ID
NO: 64 (VL CDR3)
[0532] 052-073 antibody SEQ ID NO: 65 (VH); SEQ ID NO: 66 (VH
CDR1); SEQ ID NO: 67 (VH CDR2); SEQ ID NO: 68 (VH CDR3); SEQ ID NO:
69 (VL); SEQ ID NO: 70 (VL CDR1); SEQ ID NO: 71 (VL CDR2); SEQ ID
NO: 72 (VL CDR3)
[0533] 053-049 antibody SEQ ID NO: 73 (VH); SEQ ID NO: 74 (VH
CDR1); SEQ ID NO: 75 (VH CDR2); SEQ ID NO: 76 (VH CDR3); SEQ ID NO:
77 (VL); SEQ ID NO: 78 (VL CDR1); SEQ ID NO: 79 (VL CDR2); SEQ ID
NO: 80 (VL CDR3)
[0534] 3172-120 antibody SEQ ID NO: 81 (VH); SEQ ID NO: 82 (VH
CDR1); SEQ ID NO: 83 (VH CDR2); SEQ ID NO: 84 (VH CDR3); SEQ ID NO:
85 (VL); SEQ ID NO: 86 (VL CDR1); SEQ ID NO: 87 (VL CDR2); SEQ ID
NO: 88 (VL CDR3)
[0535] 066-069 antibody SEQ ID NO: 755 (VH); SEQ ID NO: 756 (VH
CDR1); SEQ ID NO: 757 (VH CDR2); SEQ ID NO: 758 (VH CDR3); SEQ ID
NO: 759 (VL); SEQ ID NO: 760 (VL CDR1); SEQ ID NO: 761 (VL CDR2);
SEQ ID NO: 762 (VL CDR3)
[0536] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and large bowel cancer cell
line CaCo2, stomach cancer cell line MKN45, undifferentiated
hepatic cell carcinoma cell line HLF, liver cancer cell line HepG2,
intrahepatic bile duct cell cancer cell line RBE, pancreas cancer
cell line PANC1, kidney cancer cell line CCFRC1, kidney cancer cell
line Caki-1, lung cancer cell line NCI-H441, lung squamous cell
cancer EBC1, stomach cancer cell line NCI-N87, stomach cancer cell
line SNU-5, lung squamous cell carcinoma line RERF-LC-AI, hepatic
cell carcinoma clinical specimen s, breast cancer cell line BT474,
kidney cancer cell line 293T, pulmonary adenocarcinoma cell line
PC14, kidney cancer cell line ACHN, and pulmonary adenocarcinoma
cell line H1373 (as to the above mention, based on the results of
the cell line staining), as well as the relationships between these
kidney cancer, hepatic cell carcinoma, gallbladder and liver
cancer, pulmonary adenocarcinoma, and pancreas cancer (as to the
above mention, based on the results of the tissue staining) are
experimentally confirmed.
4. Antibody to ITGA3
[0537] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned 13 kinds of antibody clones, the sequences are
analyzed.
[0538] 015-003 antibody SEQ ID NO: 89 (VH); SEQ ID NO: 90 (VH
CDR1); SEQ ID NO: 91 (VH CDR2); SEQ ID NO: 92 (VH CDR3); SEQ ID NO:
93 (VL); SEQ ID NO: 94 (VL CDR1); SEQ ID NO: 95 (VL CDR2); SEQ ID
NO: 96 (VL CDR3)
[0539] 064-002 antibody SEQ ID NO: 675 (VH); SEQ ID NO: 676 (VH
CDR1); SEQ ID NO: 677 (VH CDR2); SEQ ID NO: 678 (VH CDR3); SEQ ID
NO: 679 (VL); SEQ ID NO: 680 (VL CDR1); SEQ ID NO: 681 (VL CDR2);
SEQ ID NO: 682 (VL CDR3)
[0540] 064-006 antibody SEQ ID NO: 683 (VH); SEQ ID NO: 684 (VH
CDR1); SEQ ID NO: 685 (VH CDR2); SEQ ID NO: 686 (VH CDR3); SEQ ID
NO: 687 (VL); SEQ ID NO: 688 (VL CDR1); SEQ ID NO: 689 (VL CDR2);
SEQ ID NO: 690 (VL CDR3)
[0541] 064-012a antibody SEQ ID NO: 691 (VH); SEQ ID NO: 692 (VH
CDR1); SEQ ID NO: 693 (VH CDR2); SEQ ID NO: 694 (VH CDR3); SEQ ID
NO: 695 (VL); SEQ ID NO: 696 (VL CDR1); SEQ ID NO: 697 (VL CDR2);
SEQ ID NO: 698 (VL CDR3)
[0542] 064-012b antibody SEQ ID NO: 699 (VH); SEQ ID NO: 700 (VH
CDR1); SEQ ID NO: 701 (VH CDR2); SEQ ID NO: 702 (VH CDR3); SEQ ID
NO: 703 (VL); SEQ ID NO: 704 (VL CDR1); SEQ ID NO: 705 (VL CDR2);
SEQ ID NO: 706 (VL CDR3)
[0543] 064-014 antibody SEQ ID NO: 707 (VH); SEQ ID NO: 708 (VH
CDR1); SEQ ID NO: 709 (VH CDR2); SEQ ID NO: 710 (VH CDR3); SEQ ID
NO: 711 (VL); SEQ ID NO: 712 (VL CDR1); SEQ ID NO: 713 (VL CDR2);
SEQ ID NO: 714 (VL CDR3)
[0544] 064-054 antibody SEQ ID NO: 715 (VH); SEQ ID NO: 716 (VH
CDR1); SEQ ID NO: 717 (VH CDR2); SEQ ID NO: 718 (VH CDR3); SEQ ID
NO: 719 (VL); SEQ ID NO: 720 (VL CDR1); SEQ ID NO: 721 (VL CDR2);
SEQ ID NO: 722 (VL CDR3)
[0545] 064-085 antibody SEQ ID NO: 723 (VH); SEQ ID NO: 724 (VH
CDR1); SEQ ID NO: 725 (VH CDR2); SEQ ID NO: 726 (VH CDR3); SEQ ID
NO: 727 (VL); SEQ ID NO: 728 (VL CDR1); SEQ ID NO: 729 (VL CDR2);
SEQ ID NO: 730 (VL CDR3)
[0546] 064-093 antibody SEQ ID NO: 731 (VH); SEQ ID NO: 732 (VH
CDR1); SEQ ID NO: 733 (VH CDR2); SEQ ID NO: 734 (VH CDR3); SEQ ID
NO: 735 (VL); SEQ ID NO: 736 (VL CDR1); SEQ ID NO: 737 (VL CDR2);
SEQ ID NO: 738 (VL CDR3)
[0547] 064-116 antibody SEQ ID NO: 739 (VH); SEQ ID NO: 740 (VH
CDR1); SEQ ID NO: 741 (VH CDR2); SEQ ID NO: 742 (VH CDR3); SEQ ID
NO: 743 (VL); SEQ ID NO: 744 (VL CDR1); SEQ ID NO: 745 (VL CDR2);
SEQ ID NO: 746 (VL CDR3)
[0548] 065-183 antibody SEQ ID NO: 747 (VH); SEQ ID NO: 748 (VH
CDR1); SEQ ID NO: 749 (VH CDR2); SEQ ID NO: 750 (VH CDR3); SEQ ID
NO: 751 (VL); SEQ ID NO: 752 (VL CDR1); SEQ ID NO: 753 (VL CDR2);
SEQ ID NO: 754 (VL CDR3)
[0549] 067-142 antibody SEQ ID NO: 763 (VH); SEQ ID NO: 764 (VH
CDR1); SEQ ID NO: 765 (VH CDR2); SEQ ID NO: 766 (VH CDR3); SEQ ID
NO: 767 (VL); SEQ ID NO: 768 (VL CDR1); SEQ ID NO: 769 (VL CDR2);
SEQ ID NO: 770 (VL CDR3)
[0550] 068-007 antibody SEQ ID NO: 771 (VH); SEQ ID NO: 772 (VH
CDR1); SEQ ID NO: 773 (VH CDR2); SEQ ID NO: 774 (VH CDR3); SEQ ID
NO: 775 (VL); SEQ ID NO: 776 (VL CDR1); SEQ ID NO: 777 (VL CDR2);
SEQ ID NO: 778 (VL CDR3)
[0551] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and undifferentiated hepatic
cell carcinoma cell line HLF, ovarian cancer cell line SKOv3,
kidney cancer cell line ACHN, kidney cancer cell line Caki-1,
pulmonary adenocarcinoma cell line H1373, lung squamous cell cancer
EBC1, vulva mucosal epithelial cell line A431, breast cancer cell
line BT474, pulmonary adenocarcinoma cell line PC14, kidney cancer
cell line CCFRC1, hepatic cell carcinoma cell line OCTH,
intrahepatic bile duct cell cancer RBE, pancreas cancer cell line
PANC-1, pancreas cancer cell line MIA-Paca2, pulmonary
adenocarcinoma cell line A549, pulmonary adenocarcinoma cell line
NCI-N441, lung squamous cell carcinoma line Calu-3, lung squamous
cell carcinoma line RERF-LC-AI, stomach cancer cell line SNU5,
stomach cancer cell line MKN45, stomach cancer cell line NCI-N87,
large bowel cancer cell line CW2, ovarian cancer cell line SKOv3,
ovarian cancer cell line KF-28, ovarian cancer cell line RMG-1, and
ovarian cancer cell line RMG-2 (as to the above mention, based on
the results of the cell line staining), as well as the
relationships between these antibodies and gallbladder and liver
cancer and pancreas cancer (as to the above mention, based on the
results of the tissue staining) are experimentally confirmed.
5. Antibody to ICAM1
[0552] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included.
Finally, 22 kinds of antibody clones are identified. As to the
below-mentioned five kinds of antibody clones, the sequences are
analyzed.
[0553] 052-033 antibody SEQ ID NO: 97 (VH); SEQ ID NO: 98 (VH
CDR1); SEQ ID NO: 99 (VH CDR2); SEQ ID NO: 100 (VH CDR3); SEQ ID
NO: 101 (VL); SEQ ID NO: 102 (VL CDR1); SEQ ID NO: 103 (VL CDR2);
SEQ ID NO: 104 (VL CDR3)
[0554] 053-042 antibody SEQ ID NO: 105 (VH); SEQ ID NO: 106 (VH
CDR1); SEQ ID NO: 107 (VH CDR2); SEQ ID NO: 108 (VH CDR3); SEQ ID
NO: 109 (VL); SEQ ID NO: 110 (VL CDR1); SEQ ID NO: 111 (VL CDR2);
SEQ ID NO: 112 (VL CDR3)
[0555] 053-051 antibody SEQ ID NO: 113 (VH); SEQ ID NO: 114 (VH
CDR1); SEQ ID NO: 115 (VH CDR2); SEQ ID NO: 116 (VH CDR3); SEQ ID
NO: 117 (VL); SEQ ID NO: 118 (VL CDR1); SEQ ID NO: 119 (VL CDR2);
SEQ ID NO: 120 (VL CDR3)
[0556] 053-059 antibody SEQ ID NO: 121 (VH); SEQ ID NO: 122 (VH
CDR1); SEQ ID NO: 123 (VH CDR2); SEQ ID NO: 124 (VH CDR3); SEQ ID
NO: 125 (VL); SEQ ID NO: 126 (VL CDR1); SEQ ID NO: 127 (VL CDR2);
SEQ ID NO: 128 (VL CDR3)
[0557] 053-085 antibody SEQ ID NO: 129 (VH); SEQ ID NO: 130 (VH
CDR1); SEQ ID NO: 131 (VH CDR2); SEQ ID NO: 132 (VH CDR3); SEQ ID
NO: 133 (VL); SEQ ID NO: 134 (VL CDR1); SEQ ID NO: 135 (VL CDR2);
SEQ ID NO: 136 (VL CDR3)
[0558] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and liver cancer cell line
HepG2, pulmonary adenocarcinoma cell line PC14, and cell line
established from kidney clinical specimen (as to the above mention,
based on the results of the cell line staining), as well as the
relationships between these antibodies and hepatic cell carcinoma
(as to the above mention, based on the results of the tissue
staining) are experimentally confirmed.
6. Antibody to ALCAM
[0559] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned 13 kinds of antibody clones, the sequences are
analyzed.
[0560] 035-234 antibody SEQ ID NO: 137 (VH); SEQ ID NO: 138 (VH
CDR1); SEQ ID NO: 139 (VH CDR2); SEQ ID NO: 140 (VH CDR3); SEQ ID
NO: 141 (VL); SEQ ID NO: 142 (VL CDR1); SEQ ID NO: 143 (VL CDR2);
SEQ ID NO: 144 (VL CDR3)
[0561] 040-107 antibody SEQ ID NO: 145 (VH); SEQ ID NO: 146 (VH
CDR1); SEQ ID NO: 147 (VH CDR2); SEQ ID NO: 148 (VH CDR3); SEQ ID
NO: 149 (VL); SEQ ID NO: 150 (VL CDR1); SEQ ID NO: 151 (VL CDR2);
SEQ ID NO: 152 (VL CDR3)
[0562] 041-118 antibody SEQ ID NO: 153 (VH); SEQ ID NO: 154 (VH
CDR1); SEQ ID NO: 155 (VH CDR2); SEQ ID NO: 156 (VH CDR3); SEQ ID
NO: 157 (VL); SEQ ID NO: 158 (VL CDR1); SEQ ID NO: 159 (VL CDR2);
SEQ ID NO: 160 (VL CDR3)
[0563] 066-174 antibody SEQ ID NO: 161 (VH); SEQ ID NO: 162 (VH
CDR1); SEQ ID NO: 163 (VH CDR2); SEQ ID NO: 164 (VH CDR3); SEQ ID
NO: 165 (VL); SEQ ID NO: 166 (VL CDR1); SEQ ID NO: 167 (VL CDR2);
SEQ ID NO: 168 (VL CDR3)
[0564] 083-040 antibody SEQ ID NO: 169 (VH); SEQ ID NO: 170 (VH
CDR1); SEQ ID NO: 171 (VH CDR2); SEQ ID NO: 172 (VH CDR3); SEQ ID
NO: 173 (VL); SEQ ID NO: 174 (VL CDR1); SEQ ID NO: 175 (VL CDR2);
SEQ ID NO: 176 (VL CDR3)
[0565] 029-143 antibody SEQ ID NO: 779 (VH); SEQ ID NO: 780 (VH
CDR1); SEQ ID NO: 781 (VH CDR2); SEQ ID NO 782 (VH CDR3); SEQ ID
NO: 783 (VL); SEQ ID NO: 784 (VL CDR1); SEQ ID NO: 785 (VL CDR2);
SEQ ID NO: 786 (VL CDR3)
[0566] 045-134 antibody SEQ ID NO: 787 (VH); SEQ ID NO: 788 (VH
CDR1); SEQ ID NO: 789 (VH CDR2); SEQ ID NO: 790 (VH CDR3); SEQ ID
NO: 791 (VL); SEQ ID NO: 792 (VL CDR1); SEQ ID NO: 793 (VL CDR2);
SEQ ID NO: 794 (VL CDR3)
[0567] 062-101 antibody SEQ ID NO: 795 (VH); SEQ ID NO: 796 (VH
CDR1); SEQ ID NO: 797 (VH CDR2); SEQ ID NO: 798 (VH CDR3); SEQ ID
NO: 799 (VL); SEQ ID NO: 800 (VL CDR1); SEQ ID NO: 801 (VL CDR2);
SEQ ID NO: 802 (VL CDR3)
[0568] 062-109 antibody SEQ ID NO: 803 (VH); SEQ ID NO: 804 (VH
CDR1); SEQ ID NO: 805 (VH CDR2); SEQ ID NO: 806 (VH CDR3); SEQ ID
NO: 807 (VL); SEQ ID NO: 808 (VL CDR1); SEQ ID NO: 809 (VL CDR2);
SEQ ID NO: 810 (VL CDR3)
[0569] 084-103 antibody SEQ ID NO: 811 (VH); SEQ ID NO: 812 (VH
CDR1); SEQ ID NO: 813 (VH CDR2); SEQ ID NO: 814 (VH CDR3); SEQ ID
NO: 815 (VL); SEQ ID NO: 816 (VL CDR1); SEQ ID NO: 817 (VL CDR2);
SEQ ID NO: 818 (VL CDR3)
[0570] 052-274 antibody SEQ ID NO: 819 (VH); SEQ ID NO: 820 (VH
CDR1); SEQ ID NO: 821 (VH CDR2); SEQ ID NO: 822 (VH CDR3); SEQ ID
NO: 823 (VL); SEQ ID NO: 824 (VL CDR1); SEQ ID NO: 825 (VL CDR2);
SEQ ID NO: 826 (VL CDR3)
[0571] 029-067 antibody SEQ ID NO: 827 (VH); SEQ ID NO: 828 (VH
CDR1); SEQ ID NO: 829 (VH CDR2); SEQ ID NO: 830 (VH CDR3); SEQ ID
NO: 831 (VL); SEQ ID NO: 832 (VL CDR1); SEQ ID NO: 833 (VL CDR2);
SEQ ID NO: 834 (VL CDR3)
[0572] 083-131 antibody SEQ ID NO: 835 (VH); SEQ ID NO: 836 (VH
CDR1); SEQ ID NO: 837 (VH CDR2); SEQ ID NO: 838 (VH CDR3); SEQ ID
NO: 839 (VL); SEQ ID NO: 840 (VL CDR1); SEQ ID NO: 841 (VL CDR2);
SEQ ID NO: 842 (VL CDR3)
[0573] As mentioned in the below-mentioned Examples, the
relationships between these antibodies and liver cancer cell line
(HepG2, OCTH, Hep3B, and HLF), kidney cancer cell line (Caki-1,
CCFRC1, ACHN, 293T, and cell line established from the clinical
specimen), lung cancer cell line (PC14, NCI-H441, EB. C-1,
RERF-LC-AI, A549, and H1373), ovarian cancer cell line (SKOv3,
KF-28, RMG1, and RMG2), stomach cancer cell line (NCI-N87), large
bowel cancer cell line (CW2), breast cancer cell line (BT474),
acute myelocytic leukemia AML clinical specimen, and hamster
ovarian cancer cell line CHO (as to the above mention, based on the
results of the cell line staining), as well as the relationships
between these antibodies and kidney cancer, hepatic cell carcinoma,
gallbladder and liver cancer, lung squamous cell cancer, alveolar
cell carcinoma, and adenocarcinoma (as to the above mention, based
on the results of the tissue staining) are experimentally
confirmed.
7. Antibody to CD147
[0574] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed.
[0575] 059-053 antibody SEQ ID NO: 177 (VH); SEQ ID NO: 178 (VH
CDR1); SEQ ID NO: 179 (VH CDR2); SEQ ID NO: 180 (VH CDR3); SEQ ID
NO: 181 (VL); SEQ ID NO: 182 (VL CDR1); SEQ ID NO: 183 (VL CDR2);
SEQ ID NO: 184 (VL CDR3)
[0576] As mentioned in the below-mentioned Examples, the
relationships between this antibody the and liver cancer cell line
HepG2, kidney cancer cell line CCFRC1, kidney cancer cell line
ACHN, kidney cancer cell line Caki-1, pulmonary adenocarcinoma
PC14, and cell line established from kidney cancer clinical
specimen (as to the above mention, based on the results of the cell
line staining), as well as the relationships between these
antibodies and kidney cancer (as to the above mention, based on the
results of the tissue staining) are experimentally confirmed.
8. Antibody to C1qR
[0577] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed.
[0578] 070-016 antibody SEQ ID NO: 451 (VH); SEQ ID NO: (VH CDR1)
452; SEQ ID NO: 453 (VH CDR2); SEQ ID NO: 454 (yH CDR3); SEQ ID NO:
455 (VL); SEQ ID NO: (VL CDR1) 456; SEQ ID NO: 457 (VL CDR2); SEQ
ID NO: 458 (VL CDR3)
[0579] The relationship between this antibody and leukemia is
experimentally confirmed. That is to say, in cell line staining
using this antibody, leukemia AML cell line Nohno 1 and leukemia
AML clinical specimen shows a strong positive property (MFI=20 or
more). Furthermore, in the process of growing the leukemia cell
line, this antibody is added to the growing temperature, rapid
aggregation of cancer cells can be confirmed. Moreover, the
antibody amount necessary to cause these phenomena is relatively
low concentration.
9. Antibody to CD44
[0580] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed.
[0581] 064-003 antibody SEQ ID NO: 459 (VH); SEQ ID NO: 460 (VH
CDR1); SEQ ID NO: 461 (VH CDR2); SEQ ID NO: 462 (VH CDR3); SEQ ID
NO: 463 (VL); SEQ ID NO: 464 (VL CDR1); SEQ ID NO: 465 (VL CDR2);
SEQ ID NO: 466 (VL CDR3)
[0582] The relationships between this antibody and liver cancer,
lung cancer, ovarian cancer, and stomach cancer are experimentally
confirmed. That is to say, in the cell staining using this
antibody, hepatic cell carcinoma HLF, pulmonary adenocarcinoma cell
line PC14, pulmonary adenocarcinoma cell line NCI-H1373, and ovary
adenocarcinoma cell line SKOv3 show the strong positive property
(MFI=20 or more), and epidermoid cancer cell line A431 and lung
squamous cell cancer EBC1 show the weak positive property (MFI=3 or
more). Furthermore, in immunostaining using this antibody, a case
in which a pulmonary adenocarcinoma clinical specimen shows cancer
specific stained image is observed, and cancer portions of alveolar
cell carcinoma and lung squamous cell cancer show the weak positive
property.
10. Antibody to CD73
[0583] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed.
[0584] 067-213 antibody SEQ ID NO: 467 (VH); SEQ ID NO: 468 (VH
CDR1); SEQ ID NO: 469 (VH CDR2); SEQ ID NO: 470 (VH CDR3); SEQ ID
NO: 471 (VL); SEQ ID NO: 472 (VL CDR1); SEQ ID NO: 473 (VL CDR2);
SEQ ID NO: 474 (VL CDR3)
[0585] The relationships between this antibody and liver cancer,
lung cancer, and ovarian cancer are experimentally confirmed. That
is to say, in the cell staining using this antibody, pulmonary
adenocarcinoma cell line NCI-H1373, and lung squamous cell cancer
EBC1 show the strong positive property (MFI=20 or more), and liver
cancer cell line HLF, ovary adenocarcinoma cell line SKOv3, and
pulmonary adenocarcinoma cell line PC14 show the weak positive
property (MFI=3 or more). Furthermore, in immunostaining using this
antibody, a cancer-specific stained image is obtained in a
pulmonary adenocarcinoma clinical specimen and a stained image
showing the weak positive property to a cancer portion is obtained
in lung squamous cell cancer.
11. Antibody to EpCAM
[0586] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed.
[0587] 067-153 antibody SEQ ID NO: 475 (VH); SEQ ID NO: 476 (VH
CDR1); SEQ ID NO: 477 (VH CDR2); SEQ ID NO: 478 (VH CDR3); SEQ ID
NO: 479 (VL); SEQ ID NO: 480 (VL CDR1); SEQ ID NO: 481 (VL CDR2);
SEQ ID NO: 482 (VL CDR3)
[0588] The relationships between this antibody and liver cancer,
lung cancer, ovarian cancer, stomach cancer, and large bowel cancer
are experimentally confirmed. That is to say, in the cell staining
using this antibody, pulmonary adenocarcinoma cell line NCI-H1373
and lung squamous cell carcinoma line LK-2 show the strong positive
property (MFI=20 or more); lung squamous cell cancer EBC1 and
pulmonary adenocarcinoma cell line PCI4 show the positive property
(MFI=10 or more); and ovary adenocarcinoma cell line SKOv3 shows
the weak positive property (MFI=3 or more). Furthermore, in
immunostaining using this antibody, an extremely excellent
cancer-specific stained image is obtained in each clinical specimen
of large bowel cancer, pulmonary adenocarcinoma, lung squamous cell
cancer, stomach cancer. A stained image having a weak cancer
specific positive property is obtained in a part of hepatic cell
carcinoma clinical specimens.
12. Antibody to HGFR
[0589] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included.
Finally 87 kinds of antibody clones are identified. As to the
below-mentioned three kinds of antibody clones, the sequences are
analyzed.
[0590] 067-126 antibody SEQ ID NO: 651 (VH); SEQ ID NO: 652 (VH
CDR1); SEQ ID NO: 653 (VH CDR2); SEQ ID NO: 654 (VH CDR3); SEQ ID
NO: 655 (VL); SEQ ID NO: 656 (VL CDR1); SEQ ID NO: 657 (VL CDR2);
SEQ ID NO: 658 (VL CDR3)
[0591] 067-133 antibody SEQ ID NO: 659 (VH); SEQ ID NO: 660 (VH
CDR1); SEQ ID NO: 661 (VH CDR2); SEQ ID NO: 662 (VH CDR3); SEQ ID
NO: 663 (VL); SEQ ID NO: 664 (VL CDR1); SEQ ID NO: 665 (VL CDR2);
SEQ ID NO: 666 (VL CDR3)
[0592] 067-287 antibody SEQ ID NO: 667 (VH); SEQ ID NO: 668 (VH
CDR1); SEQ ID NO: 669 (VH CDR2); SEQ ID NO: 670 (VH CDR3); SEQ ID
NO: 671 (VL); SEQ ID NO: 672 (VL CDR1); SEQ ID NO: 673 (VL CDR2);
SEQ ID NO: 674 (VL CDR3)
[0593] The relationships between this antibody and lung cancer,
liver cancer, ovarian cancer, large bowel cancer, and stomach
cancer are experimentally confirmed. That is to say, in cell line
staining using this antibody, lung squamous cell cancer EBC1 shows
a strong positive property (MFI=20 or more); alveolar
adenocarcinoma NCI-H1373 shows the positive property (MFI=10 or
more); and epidermoid cancer cell line A431, ovary adenocarcinoma
cell line SKOv3, pulmonary adenocarcinoma cell line PC14, and
hepatic cell carcinoma HLF show the weak positive property (MFI=3
or more). Furthermore, in immunostaining using this antibody, a
weak positive property to cancer portion in a part of lung squamous
cell cancer clinical specimen is obtained.
13. Antibody to LAR
[0594] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned five kinds of antibody clones, the sequence is
analyzed. [0595] 064-044 antibody SEQ ID NO: 944 (VH); and SEQ ID
NO: 945 (VL) 065-030 antibody SEQ ID NO: 946 (VH); and SEQ ID NO:
947 (VL) [0596] 065-358 antibody SEQ ID NO: 948 (VH); and SEQ ID
NO: 949 (VL) [0597] 066-019 antibody SEQ ID NO: 950 (VH); and SEQ
ID NO: 951 (VL) [0598] 079-085 antibody SEQ ID NO: 952 (VH); and
SEQ ID NO: 953 (VL)
[0599] In the immunostaining using these antibodies, a positive
property is observed in a cancer portion in a part of the lung
cancer clinical specimens.
14. Antibody to BCAM
[0600] A plurality of antibodies clones are obtained. Among them,
antibodies having the same amino acid sequence are included. As to
the below-mentioned one kind of antibody clone, the sequence is
analyzed. [0601] 067-024 antibody SEQ ID NO: 954 (VH); and SEQ ID
NO: 955 (VL)
[0602] In the immunostaining using these antibodies, a positive
property is observed in a cancer portion in a part of the clinical
specimens of lung cancer, liver cancer, and kidney cancer.
[0603] The first embodiment of this aspect provides an isolated
antibody having a specific binding property to HER1. The antibody
of this form includes the heavy chain variable region CDR3 and the
light chain variable region CDR3 specified by the combination of
SEQ ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR3, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) selected from the
group consisting of the following (1) to (3). Preferably, it
includes the heavy chain variable regions CDR2 and CDR3 and the
light chain variable regions CDR2 and CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR2, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR3,
SEQ ID NO showing the amino acid sequence of the light chain
variable region CDR2, and SEQ ID NO showing the amino acid sequence
of the light chain variable region CDR3) selected from the group
consisting of the following (4) to (6). Furthermore, preferably, it
includes the heavy chain variable regions CDR1 to CDR3 and the
light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2; and SEQ ID
NO showing the amino acid sequence of the light chain variable
region. CDR3) selected from the group consisting of the following
(7) to (9) and (13) to (18). The most preferably, it includes the
heavy chain variable region and the light chain variable region
specified by the combination of SEQ ID NOs (SEQ ID NO showing the
heavy chain variable region and SEQ ID NO showing the light chain
variable region) selected from the group consisting of the
following (10) to (12) and (19) to (24).
(Combination of CDR3)
(1) SEQ ID NO: 4, SEQ ID NO: 8
(2) SEQ ID NO: 12, SEQ ID NO: 16
(3) SEQ ID NO: 20, SEQ ID NO: 24
(Combination of CDR2 and CDR3)
(4) SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 8
(5) SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 15, SEQ ID NO: 16
(6) SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 23, SEQ ID NO: 24
(Combination of CDR1 to CDR3)
(7) SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 6 SEQ ID
NO: 7, SEQ ID NO: 8
(8) SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 14, SEQ
ID NO: 15, SEQ ID NO: 16
(9) SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 22, SEQ
ID NO: 23, SEQ ID NO: 24
(13) SEQ ID NO: 484 (VH CDR1), SEQ ID NO: 485 (VH CDR2), SEQ ID NO:
486 (VH CDR3), SEQ ID NO: 488 (VL CDR1), SEQ ID NO: 489 (VL CDR2),
SEQ ID NO: 490 (VL CDR3)
(14) SEQ ID NO: 492 (VH CDR1), SEQ ID NO: 493 (VH CDR2), SEQ ID NO:
494 (VH CDR3), SEQ ID NO: 496 (VL CDR1), SEQ ID NO: 497 (VL CDR2),
SEQ ID NO: 498 (VL CDR3)
(15), SEQ ID NO: 500 (VH CDR1), SEQ ID NO: 501 (VH CDR2), SEQ ID
NO: 502 (VH CDR3), SEQ ID NO: 504 (VL CDR1), SEQ ID NO: 505 (VL
CDR2), SEQ ID NO: 506 (VL CDR3)
(16) SEQ ID NO: 508 (VH CDR1), SEQ ID NO: 509 (VH CDR2), SEQ ID NO:
510 (VH CDR3), SEQ ID NO: 512 (VL CDR1), SEQ ID NO: 513 (VL CDR2),
SEQ ID NO: 514 (VL CDR3)
(17) SEQ ID NO: 516 (VH CDR1), SEQ ID NO: 517 (VH CDR2), SEQ ID NO:
518 (VH CDR3), SEQ ID NO: 520 (VL CDR1), SEQ ID NO: 521 (VL CDR2),
SEQ ID NO: 522 (VL CDR3)
(18) SEQ ID NO: 524 (VH CDR1), SEQ ID NO: 525 (VH CDR2), SEQ ID NO:
526 (VH CDR3), SEQ ID NO: 528 (VL CDR1), SEQ ID NO: 529 (VL CDR2),
SEQ ID NO: 530 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(10) SEQ ID NO: 1, SEQ ID NO: 5
(11) SEQ ID NO: 9, SEQ ID NO: 13
(12) SEQ ID NO: 17, SEQ ID NO: 21
(19) SEQ ID NO: 483 (VH), SEQ ID NO: 487 (VL)
(20) SEQ ID NO: 491 (VH), SEQ ID NO: 495 (VL)
(21) SEQ ID NO: 499 (VH), SEQ ID NO: 503 (VL)
(22) SEQ ID NO: 507 (VH), SEQ ID NO: 511 (VL)
(23) SEQ ID NO: 515 (VH), SEQ ID NO: 519 (VL)
(24) SEQ ID NO: 523 (VH), SEQ ID NO: 527 (VL)
[0604] Note here that (1), (4), (7), and (10) correspond to 048-006
antibody; (2), (5), (8), and (11) correspond to 057-091 antibody;
(3), (6), (9), and (12) correspond to 059-152 antibody; (13) and
(19) correspond to 048-040 antibody; (14) and (20) correspond to
054-101 antibody; (15) and (21) correspond to 055-147 antibody;
(16) and (22) correspond to 059-173 antibody; (17) and (23)
correspond to 067-149 antibody; as well as (18) and (24) correspond
to 067-176 antibody. Therefore, the antibody of the present
invention is expected to have high specificity to HER1.
[0605] The second embodiment of this aspect provides an isolated
antibody having a specific binding property to HER2. The antibody
of this form includes the heavy chain variable region CDR3 and the
light chain variable region CDR3 specified by the combination of
SEQ ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR3, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) shown in the
following (1). Preferably, it includes the heavy chain variable
regions CDR2 and CDR3 and the light chain variable regions CDR2 and
CDR3 specified by the combination of SEQ ID NOs (SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR2, and SEQ ID NO showing the
amino acid sequence of the light chain variable region CDR3)
selected from the following (2). Furthermore, preferably, it
includes the heavy chain variable regions CDR1 to CDR3 and the
light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) selected from the group consisting of the following
(3) and (5) to (19). The most preferably, it includes the heavy
chain variable region and the light chain variable region specified
by the combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) selected from the group consisting of the following (4) and
(20) to (34).
(Combination of CDR3)
(1) SEQ ID NO: 28, SEQ ID NO: 32
(Combination of CDR2 and CDR3)
(2) SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 31, SEQ ID NO: 32
(Combination of CDR1 to CDR3)
(3) SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 30, SEQ
ID NO: 31, SEQ ID NO: 32
(5) SEQ ID NO: 532 (VH CDR1), SEQ ID NO: 533 (VH CDR2), SEQ ID NO:
534 (VH CDR3), SEQ ID NO: 536 (VL CDR1), SEQ ID NO: 537 (VL CDR2),
SEQ ID NO: 538 (VL CDR3)
(6) SEQ ID NO: 540 (VH CDR1), SEQ ID NO: 541 (VH CDR2), SEQ ID NO:
542 (VH CDR3), SEQ ID NO: 544 (VL CDR1), SEQ ID NO: 545 (VL CDR2),
SEQ ID NO: 546 (VL CDR3)
(7) SEQ ID NO: 548 (VH CDR1), SEQ ID NO: 549 (VH CDR2), SEQ ID NO:
550 (VH CDR3), SEQ ID NO: 552 (VL CDR1), SEQ ID NO: 553 (VL CDR2),
SEQ ID NO: 554 (VL CDR3)
(8) SEQ ID NO: 556 (VH CDR1), SEQ ID NO: 557 (VH CDR2), SEQ ID NO:
558 (VH CDR3), SEQ ID NO: 560 (VL CDR1), SEQ ID NO: 561 (VL CDR2),
SEQ ID NO: 562 (VL CDR3)
(9) SEQ ID NO: 564 (VH CDR1), SEQ ID NO: 565 (VH CDR2), SEQ ID NO:
566 (VH CDR3), SEQ ID NO: 568 (VL CDR1), SEQ ID NO: 569 (VL CDR2),
SEQ ID NO: 570 (VL CDR3)
(10) SEQ ID NO: 572 (VH CDR1), SEQ ID NO: 573 (VH CDR1), SEQ ID NO:
574 (VH CDR3), SEQ ID NO: 576 (VL CDR1), SEQ ID NO: 577 (VL CDR2),
SEQ ID NO: 578 (VL CDR3)
(11) SEQ ID NO: 580 (VH CDR1), SEQ ID NO: 581 (VH CDR2), SEQ ID NO:
582 (VH CDR3), SEQ ID NO: 584 (VL CDR1), SEQ ID NO: 585 (VL CDR2),
SEQ ID NO: 586 (VL CDR3)
(12) SEQ ID NO: 588 (VH CDR1), SEQ ID NO: 589 (VH CDR2), SEQ ID NO:
590 (VH CDR3), SEQ ID NO: 592 (VL CDR1), SEQ ID NO: 593 (VL CDR2),
SEQ ID NO: 594 (VL CDR3)
(13) SEQ ID NO; 596 (VH CDR1), SEQ ID NO: 597 (VH CDR2), SEQ ID NO:
598 (VH CDR3), SEQ ID NO: 600 (VL CDR1), SEQ ID NO: 601 (VL CDR2),
SEQ ID NO: 602 (VL CDR3)
(14) SEQ ID NO: 604 (VH CDR1), SEQ ID NO: 605 (VH CDR2), SEQ ID NO:
606 (VH CDR3), SEQ ID NO: 608 (VL CDR1), SEQ ID NO: 609 (VL CDR2),
SEQ ID NO: 610 (VL CDR3)
(15) SEQ ID NO: 612 (VH CDR1), SEQ ID NO: 613 (VH CDR2), SEQ ID NO:
614 (VH CDR3), SEQ ID NO: 616 (VL CDR1), SEQ ID NO: 617 (VL CDR2),
SEQ ID NO: 618 (VL CDR3)
(16) SEQ ID NO: 620 (VH CDR1), SEQ ID NO: 621 (VH CDR2), SEQ ID NO:
622 (VH CDR3), SEQ ID NO: 624 (VL CDR1), SEQ ID NO: 625 (VL CDR2),
SEQ ID NO: 626 (VL CDR3)
(17) SEQ ID NO: 628 (VH CDR1), SEQ ID NO: 629 (VH CDR2), SEQ ID NO:
630 (VH CDR3), SEQ ID NO: 632 (VL CDR1), SEQ ID NO: 633 (VL CDR2),
SEQ ID NO: 634 (VL CDR3)
(18) SEQ ID NO: 636 (VH CDR1), SEQ ID NO: 637 (VH CDR2), SEQ ID NO:
638 (VH CDR3), SEQ ID NO: 640 (VL CDR1), SEQ ID NO: 641 (VL CDR2),
SEQ ID NO: 642 (VL CDR3)
(19) SEQ ID NO: 644 (VH CDR1), SEQ ID NO: 645 (VH CDR2), SEQ ID NO:
646 (VH CDR3), SEQ ID NO: 648 (VL CDR1), SEQ ID NO: 649 (VL CDR2),
SEQ ID NO: 650 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(4) SEQ ID NO: 25, SEQ ID NO: 29
(20) SEQ ID NO: 531 (VH), SEQ ID NO: 535 (VL)
(21) SEQ ID NO: 539 (VH), SEQ ID NO: 543 (VL)
(22) SEQ ID NO: 547 (VH), SEQ ID NO: 551 (VL)
(23) SEQ ID NO: 555 (VH), SEQ ID NO: 559 (VL)
(24) SEQ ID NO: 563 (VH), SEQ ID NO: 567 (VL)
(25) SEQ ID NO: 571 (VH), SEQ ID NO: 575 (VL)
(26) SEQ ID NO: 579 (VH), SEQ ID NO: 583 (VL)
(27) SEQ ID NO: 587 (VH), SEQ ID NO: 591 (VL)
(28) SEQ ID NO: 595 (VH), SEQ ID NO: 599 (VL)
(29) SEQ ID NO: 603 (VH), SEQ ID NO: 607 (VL)
(30) SEQ ID NO: 611 (VH), SEQ ID NO: 615 (VL)
(31) SEQ ID NO: 619 (VH), SEQ ID NO: 623 (VL)
(32) SEQ ID NO: 627 (VH), SEQ ID NO: 631 (VL)
(33) SEQ ID NO: 635 (VH), SEQ ID NO: 639 (VL)
(34) SEQ ID NO: 643 (VH), SEQ ID NO: 647 (VL)
[0606] Note here that (1) to (4) correspond to 015-126 antibody;
(5) and (20) correspond to 015-044 antibody; (6) and (21)
correspond to 015-102 antibody; (7) and (22) correspond to 015-136
antibody; (8) and (23) correspond to 015-143 antibody; (9) and (24)
correspond to 015-209 antibody; (10) and (25) correspond to 039-016
antibody; (11) and (26) correspond to 053-216 antibody; (12) and
(27) correspond to 075-024 antibody; (13) and (28) correspond to
075-110 antibody; (14), (29) correspond to 086-032 antibody; (15)
and (30) correspond to 086-035 antibody; (16) and (31) correspond
to 086-036 antibody; (17) and (32) correspond to 086-061 antibody;
(18) and (33) correspond to 086-138 antibody; as well as (19) and
(34) correspond to 086-182 antibody. Therefore, the antibody of the
present invention is expected to have high specificity to HER2.
[0607] The third embodiment of this aspect provides an isolated
antibody having a specific binding property to CD46 antigen. The
antibody of this form includes the heavy chain variable region CDR3
and the light chain variable region CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR3, and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) selected from the following the group consisting of (1) to
(7). Preferably, it includes the heavy chain variable regions CDR2
and CDR3 and the light chain variable regions CDR2 and CDR3
specified by the combination of SEQ ID NOs (SEQ ID NO showing the
amino acid sequence of the heavy chain variable region CDR2, SEQ ID
NO showing the amino acid sequence of the heavy chain variable
region CDR3, SEQ ID NO showing the amino acid sequence of the light
chain variable region CDR2, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) selected from the
following the group consisting of (8) to (14). Furthermore
preferably, it includes the heavy chain variable regions CDR1 to
CDR3 and the light chain variable regions CDR1 to CDR3 specified by
the combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR 1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) selected from the following the group consisting of
(15) to (21). The most preferably, it includes the heavy chain
variable region and the light chain variable region specified by
the combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region and SEQ ID NO showing
the amino acid sequence of the light chain variable region)
selected from the following the group consisting of (22) to
(28).
(Combination of CDR3)
(1) SEQ ID NO: 36, SEQ ID NO: 40
(2) SEQ ID NO: 44, SEQ ID NO: 48
(3) SEQ ID NO: 52, SEQ ID NO: 56
(4) SEQ ID NO: 60, SEQ ID NO: 64
(5) SEQ ID NO: 68, SEQ ID NO: 72
(6) SEQ ID NO: 76, SEQ ID NO: 80
(7) SEQ ID NO: 84, SEQ ID NO: 88
(Combination of CDR2 and CDR3)
(8) SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 39, SEQ ID NO: 40
(9) SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 47, SEQ ID NO: 48
(10) SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 55, SEQ ID NO: 56
(11) SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 63, SEQ ID NO: 64
(12) SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 71, SEQ ID NO: 72
(13) SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 79, SEQ ID NO: 80
(14) SEQ ID NO: 83, SEQ ID NO: 84, SEQ ID NO: 87, SEQ ID NO: 88
(Combination of CDR1 to CDR3)
(15) SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 38,
SEQ ID NO: 39, SEQ ID NO: 40
(16) SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 46,
SEQ ID NO: 47, SEQ ID NO: 48
(17) SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 54,
SEQ ID NO: 55, SEQ ID NO: 56
(18) SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 62,
SEQ ID NO: 63, SEQ ID NO: 64
(19) SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 70,
SEQ ID NO: 71, SEQ ID NO: 72
(20) SEQ ID NO: 74, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 78,
SEQ ID NO: 79, SEQ ID NO: 80
(21) SEQ ID NO: 82, SEQ ID NO: 83, SEQ ID NO: 84, SEQ ID NO: 86,
SEQ ID NO: 87, SEQ ID NO: 88
(22) SEQ ID NO: 756 (VH CDR1), SEQ ID NO: 757 (VH CDR2), SEQ ID NO:
758 (VH CDR3), SEQ ID NO: 760 (VL CDR1), SEQ ID NO: 761 (VL CDR2),
SEQ ID NO: 762 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(23) SEQ ID NO: 33, SEQ ID NO: 37
(24) SEQ ID NO: 41, SEQ ID NO: 45
(25) SEQ ID NO: 49, SEQ ID NO: 53
(26) SEQ ID NO: 57, SEQ ID NO: 61
(27) SEQ ID NO: 65, SEQ ID NO: 69
(28) SEQ ID NO: 73, SEQ ID NO: 77
(29) SEQ ID NO: 81, SEQ ID NO: 85
(30) SEQ ID NO: 755 (VH), SEQ ID NO: 759 (VL)
[0608] Note here that (1), (8), (15) and (23) correspond to 035-224
antibody; (2), (9), (16), and (24) correspond to 045-011 antibody;
(3), (10), (17), and (25) correspond to 051-144 antibody; (4),
(11), (18), and (26) correspond to 052-053 antibody; (5), (12),
(19), and (27) correspond to 052-073 antibody; (6), (13), (20), and
(28) correspond to 053-049 antibody; (7), (14), (21), and (29)
correspond to 3172-120 antibody; as well as (22) and (30)
correspond to 066-069 antibody. Therefore, the antibody of the
present invention is expected to have high specificity to a CD46
antigen.
[0609] The fourth embodiment of this aspect provides an isolated
antibody having a specific binding property to ITGA3. The antibody
of this form includes the heavy chain variable region CDR3 and the
light chain variable region CDR3 specified by the combination of
SEQ ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR3, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) shown in the
following (1). Preferably, it includes the heavy chain variable
regions CDR2 and CDR3 and the light chain variable regions CDR2 and
CDR3 specified by the combination of SEQ ID NOs (SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR2, and SEQ ID NO showing the
amino acid sequence of the light chain variable region CDR3) shown
in the following (2). Furthermore, preferably, it includes the
heavy chain variable regions CDR1 to CDR3 and the light chain
variable regions CDR1 to CDR3 specified by the combination of SEQ
ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR1, SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR2, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR3,
SEQ ID NO showing the amino acid sequence of the light chain
variable region CDR1, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR2, and SEQ ID NO showing the
amino acid sequence of the light chain variable region CDR3)
selected from the group consisting of the following (3) and (5) to
(17). The most preferably, it includes the heavy chain variable
region and the light chain variable region specified by the
combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) selected from the group consisting of the following (4) and
(18) to (30).
(Combination of CDR3)
(1) SEQ ID NO: 92, SEQ ID NO: 96
(Combination of CDR2 and CDR3)
(2) SEQ ID NO: 91, SEQ ID NO: 92, SEQ ID NO: 95, SEQ ID NO: 96
(Combination of CDR 1 to CDR3)
(3) SEQ ID NO: 90, SEQ ID NO: 91, SEQ ID NO: 92, SEQ ID NO: 94, SEQ
ID NO: 95, SEQ ID NO: 96
(5) SEQ ID NO: 676 (VH CDR1), SEQ ID NO: 677 (VH CDR2), SEQ ID NO:
678 (VH CDR3), SEQ ID NO: 680 (VL CDR1), SEQ ID NO: 681 (VL CDR2),
SEQ ID NO: 682 (VL CDR3)
(6) SEQ ID NO: 684 (VH CDR1), SEQ ID NO: 685 (VH CDR2), SEQ ID NO:
686 (VH CDR3), SEQ ID NO: 688 (VL CDR1), SEQ ID NO: 689 (VL CDR2),
SEQ ID NO: 690 (VL CDR3)
(7) SEQ ID NO: 692 (VH CDR1), SEQ ID NO: 693 (VH CDR2), SEQ ID NO:
694 (VH CDR3), SEQ ID NO: 696 (VL CDR1), SEQ ID NO: 697 (VL CDR2),
SEQ ID NO: 698 (VL CDR3)
(8) SEQ ID NO: 700 (VH CDR1), SEQ ID NO: 701 (VH CDR2), SEQ ID NO:
702 (VH CDR3), SEQ ID NO: 704 (VL CDR1), SEQ ID NO: 705 (VL CDR2),
SEQ ID NO: 706 (VL CDR3)
(9) SEQ ID NO: 708 (VH CDR1), SEQ ID NO: 709 (VH CDR2), SEQ ID NO:
710 (VH CDR3), SEQ ID NO: 712 (VL CDR1), SEQ ID NO: 713 (VL CDR2),
SEQ ID NO: 714 (VL CDR3)
(10) SEQ ID NO: 716 (VH CDR1), SEQ ID NO: 717 (VH CDR2), SEQ ID NO:
718 (VH CDR3), SEQ ID NO: 720 (VL CDR1), SEQ ID NO: 721 (VL CDR2),
SEQ ID NO: 722 (VL CDR3)
(11) SEQ ID NO: 724 (VH CDR1), SEQ ID NO: 725 (VH CDR2), SEQ ID NO:
726 (VH CDR3), SEQ ID NO: 728 (VL CDR1), SEQ ID NO: 729 (VL CDR2),
SEQ ID NO: 730 (VL CDR3)
(12) SEQ ID NO: 732 (VH CDR1), SEQ ID NO: 733 (VH CDR2), SEQ ID NO:
734 (VH CDR3), SEQ ID NO: 736 (VL CDR1), SEQ ID NO: 737 (VL CDR2),
SEQ ID NO: 738 (VL CDR3)
(13) SEQ ID NO: 740 (VH CDR1), SEQ ID NO: 741 (VH CDR2), SEQ ID NO:
742 (VH CDR3), SEQ ID NO: 744 (VL CDR1), SEQ ID NO: 745 (VL CDR2),
SEQ ID NO: 746 (VL CDR3)
(14) SEQ ID NO: 748 (VH CDR1), SEQ ID NO: 749 (VH CDR2), SEQ ID NO:
750 (VH CDR3), SEQ ID NO: 752 (VL CDR1), SEQ ID NO: 753 (VL CDR2),
SEQ ID NO: 754 (VL CDR3)
(15) SEQ ID NO: 764 (VH CDR1), SEQ ID NO: 765 (VH CDR2), SEQ ID NO:
766 (VH CDR3), SEQ ID NO: 768 (VL CDR1), SEQ ID NO: 769 (VL CDR2),
SEQ ID NO: 770 (VL CDR3)
(16) SEQ ID NO: 772 (VH CDR1), SEQ ID NO: 773 (VH CDR2), SEQ ID NO:
774 (VH CDR3), SEQ ID NO: 776 (VL CDR1), SEQ ID NO: 777 (VL CDR2),
SEQ ID NO: 778 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(4) SEQ ID NO: 89, SEQ ID NO: 93
(17) SEQ ID NO: 675 (VH), SEQ ID NO: 679 (VL)
(18) SEQ ID NO: 683 (VH), SEQ ID NO: 687 (VL)
(19) SEQ ID NO: 691 (VH), SEQ ID NO: 695 (VL)
(20) SEQ ID NO: 699 (VH), SEQ ID NO: 703 (VL)
(21) SEQ ID NO: 707 (VH), SEQ ID NO: 711 (VL)
(22) SEQ ID NO: 715 (VH), SEQ ID NO: 719 (VL)
(23) SEQ ID NO: 723 (VH), SEQ ID NO: 727 (VL)
(24) SEQ ID NO: 731 (VH), SEQ ID NO: 735 (VL)
(25) SEQ ID NO: 739 (VH), SEQ ID NO: 743 (VL)
(26) SEQ ID NO: 747 (VH), SEQ ID NO: 751 (VL)
(27) SEQ ID NO: 763 (VH), SEQ ID NO: 767 (VL)
(28) SEQ ID NO: 771 (VH), SEQ ID NO. 775 (VL)
[0610] Note here that (1) to (4) correspond to 015-003 antibody;
(5) and (17) correspond to 064-002 antibody; (6) and (18)
correspond to 064-006 antibody; (7) and (19) correspond to 064-012a
antibody; (8) and (20) correspond to 064-012b antibody; (9) and
(21) correspond to 064-014 antibody; (10) and (22) correspond to
064-054 antibody; (11) and (23) correspond to 064-085 antibody;
(12) and (24) correspond to 064-093 antibody; (13) and (25)
correspond to 064-116 antibody; (14) and (26) correspond to 065-183
antibody; (15) and (27) correspond to 067-142 antibody; as well as
(16) and (28) correspond to 068-007 antibody. Therefore, the
antibody of the present invention is expected to have high
specificity to ITGA3.
[0611] The fifth embodiment of this aspect provides an isolated
antibody having a specific binding property to ICAM1. The antibody
of this form includes the heavy chain variable region CDR3 and the
light chain variable region CDR3 specified by the combination of
SEQ ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR3, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) selected from the
following the group consisting of (1) to (5). Preferably, it
includes the heavy chain variable regions CDR2 and CDR3 and the
light chain variable regions CDR2 and CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR2, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR3,
SEQ ID NO showing the amino acid sequence of the light chain
variable region CDR2, and SEQ ID NO showing the amino acid sequence
of the light chain variable region CDR3) selected from the
following the group consisting of (6) to (10). Furthermore
preferably, it includes the heavy chain variable regions CDR1 to
CDR3 and the light chain variable regions CDR1 to CDR3 specified by
the combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) selected from the following the group consisting of
(11) to (15). The most preferably, it includes the heavy chain
variable region and the light chain variable region specified by
the combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region and SEQ ID NO showing
the amino acid sequence of the light chain variable region)
selected from the following the group consisting of (16) to
(20).
(Combination of CDR3)
(1) SEQ ID NO: 100, SEQ ID NO: 104
(2) SEQ ID NO: 108, SEQ ID NO: 112
(3) SEQ ID NO: 116, SEQ ID NO: 120
(4) SEQ ID NO: 124, SEQ ID NO: 128
(5) SEQ ID NO: 132, SEQ ID NO: 136
(Combination of CDR2 and CDR3)
(6) SEQ ID NO: 99, SEQ ID NO: 100, SEQ ID NO: 103, SEQ ID NO:
104
(7) SEQ ID NO: 107, SEQ ID NO: 108, SEQ ID NO: 111, SEQ ID NO:
112
(8) SEQ ID NO: 115, SEQ ID NO: 116, SEQ ID NO: 119, SEQ ID NO:
120
(9) SEQ ID NO: 123, SEQ ID NO: 124, SEQ ID NO: 127, SEQ ID NO:
128
(10) SEQ ID NO: 131, SEQ ID NO: 132, SEQ ID NO: 135, SEQ ID NO:
136
(Combination of CDR1 to CDR3)
(11) SEQ ID NO: 98, SEQ ID NO: 99, SEQ ID NO: 100, SEQ ID NO: 102,
SEQ ID NO: 103, SEQ ID NO: 104
(12) SEQ ID NO: 106, SEQ ID NO: 107, SEQ ID NO: 108, SEQ ID NO:
110, SEQ ID NO: 111, SEQ ID NO: 112
(13) SEQ ID NO: 114, SEQ ID NO: 115, SEQ ID NO: 116, SEQ ID NO:
118, SEQ ID NO: 119, SEQ ID NO: 120
(14) SEQ ID NO: 122, SEQ ID NO: 123, SEQ ID NO: 124, SEQ ID NO:
126, SEQ ID NO: 127, SEQ ID NO: 128
(15) SEQ ID NO: 130, SEQ ID NO: 131, SEQ ID NO: 132, SEQ ID NO:
134, SEQ ID NO: 135, SEQ ID NO: 136
[0612] (Combination of heavy chain variable region and light chain
variable region)
(16) SEQ ID NO: 97, SEQ ID NO: 101
(17) SEQ ID NO: 105, SEQ ID NO: 109
(18) SEQ ID NO: 113, SEQ ID NO: 117
(19) SEQ ID NO: 121, SEQ ID NO: 125
(20) SEQ ID NO: 129, SEQ ID NO: 133
[0613] Note here that (1), (6), (11) and (16) correspond to 052-033
antibody; (2), (7), (12), and (17) correspond to 053-042 antibody;
(3), (8), (13), and (18) correspond to 053-051 antibody; (4), (9),
(14), and (19) correspond to 053-059 antibody; as well as (5),
(10), (15), and (20) correspond to 053-085 antibody. Therefore, the
antibody of the present invention is expected to have high
specificity to ICAM1.
[0614] The sixth embodiment of this aspect provides an isolated
antibody having a specific binding property to ALCAM. The antibody
of this form includes the heavy chain variable region CDR3 and the
light chain variable region CDR3 specified by the combination of
SEQ ID NOs (SEQ ID NO showing the amino acid sequence of the heavy
chain variable region CDR3, and SEQ ID NO showing the amino acid
sequence of the light chain variable region CDR3) selected from the
group consisting of the following (1) to (5). Preferably, it
includes the heavy chain variable regions CDR2 and CDR3 and the
light chain variable regions CDR2 and CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR2, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR3,
SEQ ID NO showing the amino acid sequence of the light chain
variable region CDR2, and SEQ ID NO showing the amino acid sequence
of the light chain variable region CDR3) selected from the group
consisting of the following (6) to (10). Furthermore, preferably,
it includes the heavy chain variable regions CDR1 to CDR3 and the
light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) selected from the group consisting of the following
(11) to (15) and (21) to (28). The most preferably, it includes the
heavy chain variable region and the light chain variable region
specified by the combination of SEQ ID NOs (SEQ ID NO showing the
heavy chain variable region and SEQ ID NO showing the light chain
variable region) selected from the group consisting of the
following (16) to (20) and (29) to (36).
(Combination of CDR3)
(1) SEQ ID NO: 140, SEQ ID NO: 144
(2) SEQ ID NO: 148, SEQ ID NO: 152
(3) SEQ ID NO: 156, SEQ ID NO: 160
(4) SEQ ID NO: 164, SEQ ID NO: 168
(5) SEQ ID NO: 172, SEQ ID NO: 176
(Combination of CDR2 and CDR3)
(6) SEQ ID NO: 139, SEQ ID NO: 140, SEQ ID NO: 143, SEQ ID NO:
144
(7) SEQ ID NO: 147, SEQ ID NO: 148, SEQ ID NO: 151, SEQ ID NO:
152
(8) SEQ ID NO: 155, SEQ ID NO: 156, SEQ ID NO: 159, SEQ ID NO:
160
(9) SEQ ID NO: 163, SEQ ID NO: 164, SEQ ID NO: 167, SEQ ID NO:
168
(10) SEQ ID NO: 171, SEQ ID NO: 172, SEQ ID NO: 175, SEQ ID NO:
176
(Combination of CDR1 to CDR3)
(11) SEQ ID NO: 138, SEQ ID NO: 139, SEQ ID NO: 140, SEQ ID NO:
142, SEQ ID NO: 143, SEQ ID NO: 144
(12) SEQ ID NO: 146, SEQ ID NO: 147, SEQ ID NO: 148, SEQ ID NO:
150, SEQ ID NO: 151, SEQ ID NO: 152
(13) SEQ ID NO: 154, SEQ ID NO: 155, SEQ ID NO: 156, SEQ ID NO:
158, SEQ ID NO: 159, SEQ ID NO: 160
(14) SEQ ID NO: 162, SEQ ID NO: 163, SEQ ID NO: 164, SEQ ID NO:
166, SEQ ID NO: 167, SEQ ID NO: 168
(15) SEQ ID NO: 170, SEQ ID NO: 171, SEQ ID NO: 172, SEQ ID NO:
174, SEQ ID NO: 175, SEQ ID NO: 176
(21) SEQ ID NO: 780 (VH CDR1), SEQ ID NO: 781 (VH CDR2), SEQ ID NO
782 (VH CDR3), SEQ ID NO: 784 (VL CDR1), SEQ ID NO: 785 (VL CDR2),
SEQ ID NO: 786 (VL CDR3)
(22) SEQ ID NO: 788 (VH CDR1), SEQ ID NO: 789 (VH CDR2), SEQ ID NO:
790 (VH CDR3), SEQ ID NO: 792 (VL CDR1), SEQ ID NO: 793 (yL CDR2),
SEQ ID NO: 794 (VL CDR3)
(23) SEQ ID NO: 796 (VH CDR1), SEQ ID NO: 797 (VH CDR2), SEQ ID NO:
798 (VH CDR3), SEQ ID NO: 800 (VL CDR1), SEQ ID NO: 801 (VL CDR2),
SEQ ID NO: 802 (VL CDR3)
(24) SEQ ID NO: 804 (VH CDR1), SEQ ID NO: 805 (VH CDR2), SEQ ID NO:
806 (VH CDR3), SEQ ID NO: 808 (VL CDR1), SEQ ID NO: 809 (VL CDR2),
SEQ ID NO: 810 (VL CDR3)
(25) SEQ ID NO: 812 (VH CDR1), SEQ ID NO: 813 (VH CDR2), SEQ ID NO:
814 (VH CDR3), SEQ ID NO: 816 (VL CDR1), SEQ ID NO: 817 (VL CDR2),
SEQ ID NO: 818 (VL CDR3)
(26) SEQ ID NO: 820 (VH CDR1), SEQ ID NO: 821 (VH CDR2), SEQ ID NO:
822 (VH CDR3), SEQ ID NO: 824 (VL CDR1), SEQ ID NO: 825 (VL CDR2),
SEQ ID NO: 826 (VL CDR3)
(27) SEQ ID NO: 828 (VH CDR1), SEQ ID NO: 829 (VH CDR2), SEQ ID NO:
830 (VH CDR3), SEQ ID NO: 832 (VL CDR1), SEQ ID NO: 833 (VL CDR2),
SEQ ID NO: 834 (VL CDR3)
(28) SEQ ID NO: 836 (VH CDR1), SEQ ID NO: 837 (VH CDR2), SEQ ID NO:
838 (VH CDR3), SEQ ID NO: 840 (VL CDR1), SEQ ID NO: 841 (VL CDR2),
SEQ ID NO: 842 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(16) SEQ ID NO: 137, SEQ ID NO: 141
(17) SEQ ID NO: 145, SEQ ID NO: 149
(18) SEQ ID NO: 153, SEQ ID NO: 157
(19) SEQ ID NO: 161, SEQ ID NO: 165
(20) SEQ ID NO: 169, SEQ ID NO: 173
(29) SEQ ID NO: 779 (VH), SEQ ID NO: 783 (VL)
(30) SEQ ID NO: 787 (VH), SEQ ID NO: 791 (VL)
(31) SEQ ID NO: 795 (VH), SEQ ID NO: 799 (VL)
(32) SEQ ID NO: 803 (VH), SEQ ID NO: 807 (VL)
(33) SEQ ID NO: 811 (VH), SEQ ID NO: 815 (VL)
(34) SEQ ID NO: 819 (VH), SEQ ID NO: 823 (VL)
(35) SEQ ID NO: 827 (VH), SEQ ID NO: 831 (VL)
(36) SEQ ID NO: 835 (VH), SEQ ID NO: 839 (VL)
[0615] Note here that (1), (6), (11), and (16) correspond to
035-234 antibody; (2), (7), (12), and (17) correspond to 040-107
antibody; (3), (8), (13), and (18) correspond to 041-118 antibody;
(4), (9), (14), and (19) correspond to 066-174 antibody; (5), (10),
(15), and (20) correspond to 083-040 antibody; (21) and (29)
correspond to 029-143 antibody; (22) and (30) correspond to 045-134
antibody; (23) and (31) correspond to 062-101 antibody; (24) and
(32) correspond to 062-109 antibody; (25) and (33) correspond to
084-103 antibody; (26) and (34) correspond to 052-274 antibody;
(27) and (35) correspond to 029-067 antibody; as well as (28) and
(36) correspond to 083-131 antibody. Therefore, the antibody of the
present invention is expected to have high specificity to
ALCAM.
[0616] The seventh embodiment of this aspect provides an isolated
antibody having a specific binding property to a CD147 antigen. The
antibody of this form includes the heavy chain variable region CDR3
and the light chain variable region CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR3, and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) shown in the following (1). Preferably, it includes the heavy
chain variable regions CDR2 and CDR3 and the light chain variable
regions CDR2 and CDR3 specified by the combination of SEQ ID NOs
(SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR2, SEQ ID NO showing the amino acid sequence of
the heavy chain variable region CDR3, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) selected from the following (2). Furthermore,
preferably, it includes the heavy chain variable regions CDR1 to
CDR3 and the light chain variable regions CDR1 to CDR3 specified by
the combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2, and SEQ ID
NO showing the amino acid sequence of the light chain variable
region CDR3) shown in the following (3). The most preferably, it
includes the heavy chain variable region and the light chain
variable region specified by the combination of SEQ ID NOs (SEQ ID
NO showing the heavy chain variable region and SEQ ID NO showing
the light chain variable region) shown in the following (4).
(Combination of CDR3)
(1) SEQ ID NO: 180, SEQ ID NO: 184
(Combination of CDR2 and CDR3)
(2) SEQ ID NO: 179, SEQ ID NO: 180, SEQ ID NO: 183, SEQ ID NO:
184
(Combination of CDR1 to CDR3)
(3) SEQ ID NO: 178, SEQ ID NO: 179, SEQ ID NO: 180, SEQ ID NO: 182,
SEQ ID NO: 183, SEQ ID NO: 184
[0617] (Combination of heavy chain variable region and light chain
variable region)
(4) SEQ ID NO: 177, SEQ ID NO: 181
[0618] Note here that (1) to (4) correspond to 059-053 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to a CD147 antigen.
[0619] The eighth embodiment of this aspect provides an isolated
antibody having a specific binding property to C1qR. The antibody
of this form includes the heavy chain variable regions CDR1 to CDR3
and the light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2 and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) shown in the following (1). Preferably, it includes the heavy
chain variable region and the light chain variable region specified
by the combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) shown in the following (2).
(Combination of CDR3)
(1) SEQ ID NO: (VH CDR1) 452, SEQ ID NO: 453 (VH CDR2), SEQ ID NO:
454 (VH CDR3), SEQ ID NO: (VL CDR1) 456, SEQ ID NO: 457 (VL CDR2),
SEQ ID NO: 458 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(2) SEQ ID NO: 451 (VH), SEQ ID NO: 455 (VL)
[0620] Note here that (1) and (2) correspond to 070-016 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to C1qR.
[0621] The ninth embodiment of this aspect provides an isolated
antibody having a specific binding property to CD44. The antibody
of this form includes the heavy chain variable regions CDR1 to CDR3
and the light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2 and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) shown in the following (1). Preferably, it includes the heavy
chain variable region and the light chain variable region specified
by the combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) shown in the following (2).
(Combination of CDR1 to CDR3)
(1) SEQ ID NO: 460 (VH CDR1), SEQ ID NO: 461 (VH CDR2), SEQ ID NO:
462 (VH CDR3), SEQ ID NO: 464 (VL CDR1), SEQ ID NO: 465 (VL CDR2),
SEQ ID NO: 466 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(2) SEQ ID NO: 459 (VH), SEQ ID NO: 463 (VL)
[0622] Note here that (1) and (2) correspond to 064-003 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to CD44.
[0623] The tenth embodiment of this aspect provides an isolated
antibody having a specific binding property to CD73. The antibody
of this form includes the heavy chain variable regions CDR1 to CDR3
and the light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2 and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) shown in the following (1). Preferably, it includes the heavy
chain variable region and the light chain variable region specified
by the combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) shown in the following (2).
(Combination of CDR1 to CDR3)
(1) SEQ ID NO: 468 (VH CDR1), SEQ ID NO: 469 (VH CDR2), SEQ ID NO:
470 (VH CDR3), SEQ ID NO: 472 (VL CDR1), SEQ ID NO: 473 (VL CDR2),
SEQ ID NO: 474 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(2) SEQ ID NO: 467 (VH), SEQ ID NO: 471 (VL)
[0624] Note here that (1) and (2) correspond to 067-213 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to CD73.
[0625] The eleventh embodiment of this aspect provides an isolated
antibody having a specific binding property to EpCAM. The antibody
of this form includes the heavy chain variable regions CDR1 to CDR3
and the light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2 and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) shown in the following (1). Preferably, it includes the heavy
chain variable region and the light chain variable region specified
by the combination of SEQ ID NOs (SEQ ID NO showing the heavy chain
variable region and SEQ ID NO showing the light chain variable
region) shown in the following (2).
(Combination of CDR1 to CDR3)
(1) SEQ ID NO: 476 (VH CDR1), SEQ ID NO: 477 (VH CDR2), SEQ ID NO:
478 (VH CDR3), SEQ ID NO: 480 (VL CDR1), SEQ ID NO: 481 (VL CDR2),
SEQ ID NO: 482 (VL CDR3)
(Combination of Heavy Chain Variable Region and Light Chain
Variable Region)
(2) SEQ ID NO: 475 (VH), SEQ ID NO: 479 (VL)
[0626] Note here that (1) and (2) correspond to 067-153 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to EpCAM.
[0627] The twelfth embodiment of this aspect provides an isolated
antibody having a specific binding property to HGFR. The antibody
of this form includes the heavy chain variable regions CDR1 to CDR3
and the light chain variable regions CDR1 to CDR3 specified by the
combination of SEQ ID NOs (SEQ ID NO showing the amino acid
sequence of the heavy chain variable region CDR1, SEQ ID NO showing
the amino acid sequence of the heavy chain variable region CDR2,
SEQ ID NO showing the amino acid sequence of the heavy chain
variable region CDR3, SEQ ID NO showing the amino acid sequence of
the light chain variable region CDR1, SEQ ID NO showing the amino
acid sequence of the light chain variable region CDR2 and SEQ ID NO
showing the amino acid sequence of the light chain variable region
CDR3) selected from the group consisting of the following (1) to
(3). Preferably, it includes the heavy chain variable region and
the light chain variable region specified by the combination of SEQ
ID NOs (SEQ ID NO showing the heavy chain variable region and SEQ
ID NO showing the light chain variable region) selected from the
group consisting of the following (4) to (6).
(Combination of CDR1 to CDR3)
(1) SEQ ID NO: 652 (VH CDR1), SEQ ID NO: 653 (VH CDR2), SEQ ID NO:
654 (VH CDR3), SEQ ID NO: 656 (VL CDR1), SEQ ID NO: 657 (VL CDR2),
SEQ ID NO: 658 (VL CDR3)
(2) SEQ ID NO: 660 (VH CDR1), SEQ ID NO: 661 (VH CDR2), SEQ ID NO:
662 (VH CDR3), SEQ ID NO: 664 (VL CDR1), SEQ ID NO: 665 (VL CDR2),
SEQ ID NO: 666 (VL CDR3)
(3) SEQ ID NO: 668 (VH CDR1), SEQ ID NO: 669 (VH CDR2), SEQ ID NO:
670 (VH CDR3), SEQ ID NO: 672 (VL CDR1), SEQ ID NO: 673 (VL CDR2),
SEQ ID NO: 674 (VL CDR3)
[0628] (Combination of heavy chain variable region and light chain
variable region)
(4) SEQ ID NO: 651 (VH), SEQ ID NO: 655 (VL)
(5) SEQ ID NO: 659 (VH), SEQ ID NO: 663 (VL)
(6) SEQ ID NO: 667 (VH), SEQ ID NO: 671 (VL)
[0629] Note here that (1) and (4) correspond to 067-126 antibody;
(2) and (5) correspond to 067-133 antibody; and (3) and (6)
correspond to 067-287 antibody. Therefore, the antibody of the
present invention is expected to have high specificity to HGFR.
[0630] The 13rd embodiment of this aspect provides an isolated
antibody having a specific binding property to LAR. The antibody of
this form includes the heavy chain variable region and the light
chain variable region specified by the combination of SEQ ID NOs
(SEQ ID NO showing the heavy chain variable region and SEQ ID NO
showing the light chain variable region) selected from the group
consisting of the following (1) to (5).
(Combination of heavy chain variable region and light chain
variable region)
(1) SEQ ID NO: 944 (VH), SEQ ID NO: 945 (VL)
(2) SEQ ID NO: 946 (VH), SEQ ID NO: 947 (VL)
(3) SEQ ID NO: 948 (VH), SEQ ID NO: 949 (VL)
(4) SEQ ID NO: 950 (VH), SEQ ID NO: 951 (VL)
(5) SEQ ID NO: 952 (VH), SEQ ID NO: 953 (VL)
[0631] Note here that (1) corresponds to 064-044 antibody; (2)
corresponds to 065-030 antibody; (3) corresponds to 065-358
antibody; (4) corresponds to 066-019 antibody; and (5) corresponds
to 079-085 antibody. Therefore, the antibody of the present
invention is expected to have high specificity to LAR.
[0632] The 14th embodiment of this aspect provides an isolated
antibody having a specific binding property to BCAM. The antibody
of this form includes the heavy chain variable region and the light
chain variable region specified by the combination of SEQ ID NOs
(SEQ ID NO showing the heavy chain variable region and SEQ ID NO
showing the light chain variable region) shown in the following
(1).
(Combination of heavy chain variable region and light chain
variable region)
(1) SEQ ID NO: 954 (VH), SEQ ID NO: 955 (VL)
[0633] Note here that (1) corresponds to 067-024 antibody.
Therefore, the antibody of the present invention is expected to
have high specificity to BCAM.
[0634] In the variable region of the antibody of the present
invention, the sequence of the framework region (FR region) is not
particularly limited as long as it does not substantially affect
the specific binding property with respect to corresponding
antigen. For example, when the antibody of the present invention is
constructed as a humanized antibody, the FR region of a known human
antibody can be used. Furthermore, when the antibody of the present
invention is constructed as an antibody used as a reagent for
detection or used for application to non-human animal species, in
some cases, an effect can be expected even if the human antibody FR
region is not used, or the use of the human antibody FR region may
not appropriate. In such cases, the FR region from non-human animal
species (for example, mouse or rat) can be used.
[0635] In one embodiment of the antibody of the present invention,
a constant region (for example, in the case of an IgG type
antibody) is included in addition to the variable region. The
sequence of the constant region in this embodiment is not
particularly limited. For example, as mentioned below, when the
antibody of the present invention is constructed as a humanized
antibody, the constant region of a known human antibody can be
used. Furthermore, similar to the above-mentioned FR region, a
constant region from non-human animal species (for example, mouse
or rat) can be used.
[0636] One embodiment of the antibody of the present invention
relates to a humanized antibody. The "humanized antibody" herein
denotes an antibody that is allowed to resemble the structure of
the human antibody. It includes a humanized chimeric antibody in
which only a constant region is replaced by that of human antibody,
and a humanized CDR-grafted antibody in which a part other than the
CDR (complementarity determining region) existing in the constant
region and the variable region is replaced by that of human
antibody (P. T. Johons et al., Nature 321, 522 (1986)). In order to
improve the antigen binding activity of the humanized CDR-grafted
antibody, improved techniques of a method of selecting a human
antibody FR that is highly homologous to a mouse antibody, a method
of producing a humanized antibody having high homology, and a
method of transplanting a human antibody to a mouse CDR and then
replacing amino acid in the FR region have been already developed
(see, for example, U.S. Pat. Nos. 5,585,089, 5,693,761, 5,693,762,
and 6180370, European Patent Nos. 451216 and 682040, and U.S. Pat.
No. 2,828,340) and such techniques can be used for producing the
humanized antibody of the present invention.
[0637] The humanized chimeric antibody can be produced by, for
example, replacing the constant region of an antibody having the
above-mentioned structure of H chain variable region and/or
structure of L chain variable region by the constant region of a
human antibody. As the constant region of the human antibody, known
region can be employed. Hereinafter, one example of the method of
producing the humanized chimeric antibody is described.
[0638] Firstly, mRNA is extracted from the hybridoma producing a
mouse antibody to certain antigens (for example, antigens
expressing certain cancers, which have been determined this time,
HER1, HER2, CD46, ITGA3, ICAM1, ALCAM, CD147, or the like), and
cDNA is synthesized according to the usual procedure. The
synthesized cDNA is inserted into a vector so as to construct a
cDNA library. From this cDNA library, an H chain gene fragment and
an L chain gene fragment are used as a probe, a vector containing
an H chain gene and an L chain gene is selected. By sequencing the
insertion sequence of the selected vector, the sequences of the
gene in the H chain variable region and the L chain variable region
can be determined. Based on the thus obtained sequence data, DNA
encoding H chain variable region is produced by a chemical
synthesis, biochemical cleavage/recombination and the like. DNA
encoding the obtained H chain variable region is ligated with DNA
encoding a human H chain constant region so as to incorporate it
into an expression vector. Thereby, H chain expression vector is
produced. As the expression vector, for example, an SV40 virus
based vector, an EB virus based vector, and a BPV (papilloma virus)
based vector can be used but not limited to these vectors alone. On
the other hand, by the similar method, an L chain expression vector
is produced. With such H chain expression vector and L chain
expression vector, host cells are co-transformed. As the host cell,
CHO cell (Chinese hamster ovary cell) (A. Wright & S. L.
Morrison, J. Immunol. 160, 3393-3402 (1998)), SP2/0 cell (myeloma)
(K. Motmans et al., Eur. J. Cancer Prev. 5, 512-519 (1996), R. P.
Junghans et al., Cancer Res. 50, 1495-1502 (1990)), and the like
can be suitably used. Furthermore, for transformation, a Lipofectin
method (R. W. Malone et al., Proc. Natl. Acad. Sci. USA 86, 6077
(1989), P. L. Felgner et al., Proc. Natl. Acad. Sci. USA 84, 7413
(1987), an electroporation method, a calcium phosphate method (F.
L. Graham & A. J. van der Eb, Virology 52, 456-467 (1973)), a
DEAE-Dextran method, and the like, are suitably used.
[0639] After the transformant is cultured, a humanized chimeric
antibody is separated from the cells of transformant or the culture
solution. For separation and purification, methods such as
centrifugation, ammonium sulfate fractionation, salting out,
ultrafiltration, affinity chromatography, ion-exchange
chromatography, and gel filtration chromatography can be
appropriately combined and used.
[0640] On the other hand, the humanized CDR-grafted antibody can be
produced by, for example, the following method. Firstly, by the
method described in the production method of chimeric antibody, the
amino acid sequences of the H chain variable region and L chain
variable region of the antibody to the certain antigen and the base
sequences encoding the amino acid sequences are determined. In
addition, the amino acid sequence and the base sequence of each CDR
region are determined.
[0641] As the base sequence of the specific CDRs, any of the
following combinations are used. Note here that they are shown by
SEQ ID NO showing the base sequence of the heavy chain variable
region CDR1, SEQ ID NO showing the base sequence of the heavy chain
variable region CDR2, SEQ ID NO showing the base sequence of the
heavy chain variable region CDR3, SEQ ID NO showing the base
sequence of the light chain variable region CDR1, SEQ ID NO showing
the base sequence of the light chain variable region CDR2, and SEQ
ID NO showing the base sequence of the light chain variable region
CDR3, in this order.
(1) SEQ ID NO 186, SEQ ID NO 187, SEQ ID NO 188, SEQ ID NO 190, SEQ
ID NO 191, SEQ ID NO 192
(2) SEQ ID NO 194, SEQ ID NO 195, SEQ ID NO 196, SEQ ID NO 198, SEQ
ID NO 199, SEQ ID NO 200
(3) SEQ ID NO: 202, SEQ ID NO: 203, SEQ ID NO: 204, SEQ ID NO: 206,
SEQ ID NO: 207, SEQ ID NO: 208
(4) SEQ ID NO: 210, SEQ ID NO: 211, SEQ ID NO: 212, SEQ ID NO: 214,
SEQ ID NO: 215, SEQ ID NO: 126
(5) SEQ ID NO: 218, SEQ ID NO: 219, SEQ ID NO: 220, SEQ ID NO: 222,
SEQ ID NO: 223, SEQ ID NO: 224
(6) SEQ ID NO: 226, SEQ ID NO: 227, SEQ ID NO: 228, SEQ ID NO: 230,
SEQ ID NO: 231, SEQ ID NO: 232
(7) SEQ ID NO: 234, SEQ ID NO: 235, SEQ ID NO: 236, SEQ ID NO: 238,
SEQ ID NO: 239, SEQ ID NO: 240
(8) SEQ ID NO: 242, SEQ ID NO: 243, SEQ ID NO: 244, SEQ ID NO: 246,
SEQ ID NO: 247, SEQ ID NO: 248
(9) SEQ ID NO: 250, SEQ ID NO: 251, SEQ ID NO: 252, SEQ ID NO: 254,
SEQ ID NO: 255, SEQ ID NO: 256
(10) SEQ ID NO: 258, SEQ ID NO: 259, SEQ ID NO: 260, SEQ ID NO:
262, SEQ ID NO: 263, SEQ ID NO: 264
(11) SEQ ID NO: 266, SEQ ID NO: 267, SEQ ID NO: 268, SEQ ID NO:
270, SEQ ID NO: 271, SEQ ID NO: 272
(12) SEQ ID NO: 274, SEQ ID NO: 275, SEQ ID NO: 276, SEQ ID NO:
278, SEQ ID NO: 279, SEQ ID NO: 280
(13) SEQ ID NO: 282, SEQ ID NO: 283, SEQ ID NO: 284, SEQ ID NO:
286, SEQ ID NO: 287, SEQ ID NO: 288
(14) SEQ ID NO: 290, SEQ ID NO: 291, SEQ ID NO: 292, SEQ ID NO:
294, SEQ ID NO: 295, SEQ ID NO: 296
(15) SEQ ID NO: 298, SEQ ID NO: 299, SEQ ID NO: 300, SEQ ID NO:
302, SEQ ID NO: 303, SEQ ID NO: 304
(16) SEQ ID NO: 306, SEQ ID NO: 307, SEQ ID NO: 308, SEQ ID NO:
310, SEQ ID NO: 311, SEQ ID NO: 312
(17) SEQ ID NO: 314, SEQ ID NO: 315, SEQ ID NO: 316, SEQ ID NO:
318, SEQ ID NO: 319, SEQ ID NO: 320
(18) SEQ ID NO: 322, SEQ ID NO: 323, SEQ ID NO: 324, SEQ ID NO:
326, SEQ ID NO: 327, SEQ ID NO: 328
(19) SEQ ID NO: 330, SEQ ID NO: 331, SEQ ID NO: 332, SEQ ID NO:
334, SEQ ID NO: 335, SEQ ID NO: 336
(20) SEQ ID NO: 338, SEQ ID NO: 339, SEQ ID NO: 340, SEQ ID NO:
342, SEQ ID NO: 343, SEQ ID NO: 344
(21) SEQ ID NO: 346, SEQ ID NO: 347, SEQ ID NO: 348, SEQ ID NO:
350, SEQ ID NO: 351, SEQ ID NO: 352
(22) SEQ ID NO: 354, SEQ ID NO: 355, SEQ ID NO: 356, SEQ ID NO:
358, SEQ ID NO: 359, SEQ ID NO: 360
(23) SEQ ID NO: 362, SEQ ID NO: 363, SEQ ID NO: 364, SEQ ID NO:
366, SEQ ID NO: 367, SEQ ID NO: 368
[0642] Note here that these combinations correspond to the
combination in CDR1 to CDR3 in 048-006 antibody, 057-091 antibody,
and 059-152 antibody (which are antibodies to HER1), 015-126
antibody (which is antibody to HER2), 035-224 antibody, 045-011
antibody, 051-144 antibody, 052-053 antibody, 052-073 antibody,
053-049 antibody, and 3172-120 antibody (which are antibodies to
CD46), 015-003 antibody (which is antibody to ITGA3), 052-033
antibody, 053-042 antibody, 053-051 antibody, 053-059 antibody, and
053-085 antibody (which are antibodies to ICAM1), 035-234 antibody,
040-107 antibody, 041-118 antibody, 066-174 antibody, and 083-040
antibody (which are antibodies to ALCAM), 059-053 antibody (which
is antibody to CD147).
[0643] Next, FRs (framework regions) sandwiching the CDR region are
selected. For selecting the FR, approximately three methods can be
employed. The first method is a method using a human antibody frame
whose three dimensional structure has been already identified, for
example, NEWM, REI, and the like (Riechmann L. et al., Nature 332,
323-3Z7 (1988); Tempst, P R. et al., Protein Engineering 7,
1501-1507 (1994); Ellis J H. et al., J. Immunol. 155, 925-937
(1995)). The second method includes selecting a variable region of
a human antibody having the highest homology to a variable region
of the intended mouse antibody from database, and using the FR
thereof (Queen C. et al., Proc Natl Acad Sci USA 86, 10029-10033
(1989); Rozak M J. et al., J Biol Chem 271, 22611-22618 (1996);
Shearman C W. et al., J. Immunol. 147, 4366-4373 (1991)). The third
method is a method of selecting amino acid most commonly used in
the FR of the human antibody (Sato K. et al., Mol Immunol 31,
371-381 (1994); Kobinger F. et al., Protein Engineering 6, 971-980
(1993); Kettleborough C A. et al., Protein Engineering 4, 773-783
(1991)). The present invention can use any of these methods.
[0644] Even if the amino acid sequence is an amino acid sequence
obtained by modifying the amino acid sequence of the selected human
FR, it can be used as an amino acid sequence of the FR as long as a
finally obtained humanized CDR-grafted antibody has a specific
binding property to the corresponding antigens (HER1, HER2, CD46,
ITGA3, ICAM1, ALCAM, CD147, and the like). In particular, a part of
the amino acid of the selected human FR is changed to the amino
acid of the FR of the antibody of the origin of CDR, the property
of the antibody may be maintained. The number of the amino acid to
be modified is preferably 30% or less relative to the entire FR,
further preferably 20% or less relative to the entire FR, and yet
further preferably 10% or less relative to the entire FR.
[0645] Next, by combining the FR selected by any of these methods
and the above-mentioned CDR, DAN encoding the H chain variable
region and L chain variable region is designed. Based on this
design, DNA encoding H chain variable region and DNA encoding L
chain variable region are produced by the chemical synthesis,
biochemical cleavage/recombination, and the like, respectively.
Then, DAN encoding the H chain variable region together with the
DNA encoding H chain constant region of a human immunoglobulin is
incorporated into an expression vector so as to construct an H
chain expression vector. Similarly, DAN encoding the L chain
variable region together with the DNA encoding L chain constant
region of a human immunoglobulin is incorporated into an expression
vector so as to construct an L chain expression vector. As the
expression vector, for example, an SV40 virus based vector, an EB
virus based vector, a BPV (papilloma virus) based vector, and the
like can be used but not necessarily limited to these vectors.
[0646] With the H chain expression vector and L chain expression
vector that are produced by the above-mentioned method, host cells
are co-transformed. As the host cell, CHO cell (Chinese hamster
ovary cell) (A. Wright & S. L. Morrison, J. Immunol. 160,
3393-3402 (1998)), SP2/0 cell (myeloma) (K. Motmans et al., Eur. J.
Cancer Prev. 5, 512-519 (1996), R. P. Junghans et al., Cancer Res.
50, 1495-1502 (1990)), and the like can be suitably used.
Furthermore, for transformation, a Lipofectin method (R. W. Malone
et al., Proc. Natl. Acad. Sci. USA 86, 6077 (1989), P. L. Feigner
et al., Proc. Natl. Acad. Sci. USA 84, 7413 (1987), an
electroporation method, a calcium phosphate method (F. L. Graham
& A. J. van der Eb, Virology 52, 456-467 (1973)), a
DEAE-Dextran method, and the like, are suitably used.
[0647] After the transformant is cultured, a humanized CDR-grafted
antibody is separated from the cells of transformant or the culture
solution. For separation and purification, methods such as
centrifugation, ammonium sulfate fractionation, salting out,
ultrafiltration, affinity chromatography, ion-exchange
chromatography, and gel filtration chromatography can be
appropriately combined and used.
[0648] Based on the antibody of the present invention or based on
the sequence information on the genes encoding the antibody of the
present invention, an antibody fragment can be produced. The
antibody fragment can include Fab, Fab', F(ab').sub.2, scFv, and
dsFv antibodies.
[0649] Fab is a fragment that is obtained by digesting IgG with
papain in the presence of cysteine; includes L chain and H chain
variable regions as well as an H chain fragment consisting of a
C.sub.H1 domain and a part of hinge portion; and has a molecular
weight of about 50000. In the present invention, it can be obtained
by digesting the antibody with papain. Furthermore, DNA encoding a
part of the H chain of the above-mentioned antibody and L chain is
incorporated into an appropriate vector, and the vector is used for
transforming so as to obtain a transformant. From this
transformant, Fab can be prepared.
[0650] Fab' is a fragment having a molecular weight of about 50000,
which can be obtained by cleaving the disulfide bond between H
chains of F(ab').sub.2 mentioned below. In the present invention,
it can be obtained by digesting the above-mentioned antibody with
pepsin and cleaving the disulfide bond by the use of a reducing
agent. Furthermore, similar to Fab, it can also be prepared by gene
engineering with the use of DNA encoding Fab'.
[0651] F(ab').sub.2 is a fragment that is obtained by digesting IgG
with pepsin; a fragment (Fab') is linked by disulfide bond
including L chain and H chain variable regions as well as an H
chain fragment consisting of a C.sub.H1 domain and a part of hinge
portion; and has a molecular weight of about 100000. In the present
invention, it can be obtained by digesting the antibody with
pepsin. Furthermore, similar to Fab, it can also be prepared by
gene engineering with the use of DNA encoding F(ab').sub.2.
[0652] scFv is an antibody fragment obtained by linking Fv
including an H chain variable region and an L chain variable region
to C terminal of one of the chains and N terminal of the other of
the chains by using an appropriate peptide linker so as to produce
a single chain antibody fragment. As the peptide linker, for
example, highly flexible (GGGGS).sub.3 can be used. For example,
DNA encoding an scFv antibody is constructed by using DNA encoding
H chain variable region and L chain variable region of the
above-mentioned antibody and DNA encoding the peptide linker is
constructed. This is incorporated into an appropriate vector and
this vector is used to obtain a transformant. From this
transformant, scFv can be prepared.
[0653] dsFv is an Fv fragment obtained by introducing a Cys residue
into an appropriate positions of the H chain variable region and L
chain variable region and stabilizing the H chain variable region
and chain variable region by disulfide bond. The position in which
the Cys residue is introduced in each chain can be determined based
on the three dimensional structure anticipated by molecule
modeling. In the present invention, for example, the three
dimensional structure is anticipated from the amino acid sequence
of the H chain variable region and the L chain variable region of
the above-mentioned antibody. DNA encoding the H chain variable
region and L chain variable region into which difference based on
such anticipation is constructed and the constructed DNA is
incorporated into the appropriate vector. The vector is used to
obtain a transformant. From this transformant, dsFv can be
prepared.
[0654] Note here that an antibody fragment can be multimerized by
linking an scFv antibody and a dcFv antibody and the like with the
use of an appropriate linker, or by allowing streptavidin to be
fused.
[0655] By fusing or linking a low molecule compound, protein, a
label material, and the like to the antibody of the present
invention (including an antibody fragment), a fused antibody or
labeled antibody can be formed. An example of the label material
may include radioactive material such as .sup.125I, peroxidase,
.beta.-D-galactosidase, micro peroxidase, horseradish peroxidase
(HRP), fluorescein isothiocyanate (FITC), rhodamine isothiocyanate
(RITC), alkaline phosphatase, biotin, and the like.
[0656] The antibody of the present invention (including an antibody
fragment) specifically binds to a cancer cell that specifically
expresses the antigen by the specific binding property to the
corresponding antigen. The use of this property makes it possible
to label and detect a cancer cell (or cancer tissue). By gene
recombination technology, VH and VL having such a specific binding
capacity can be fused to a constant region (Fc region) of IgG so as
to transform into an IgG type antibody. The thus obtained IgG type
antibody is expected to exhibit a cytotoxic effect via Fc receptor
on NK cells. The IgG constant region has subclass. As to the
binding of Fc receptor of each IgG subclass of human, IgG1 and IgG3
have the strongest binding, IgG4 has moderate binding and IgG2 has
weak binding. In transforming into IgG type antibodies, it is
preferable to select a constant region in consideration of this
point. Note here that the present inventors have proposed an assay
of cytotoxic effect via the secondary antibody instead of IgG type
antibody in the previous applications (Japanese Patent Unexamined
Publication No. 2005-185281 and PCT/JP2006/303195).
[0657] Actually, as shown in the below-mentioned Examples, since
015-003 antibody as anti-ITGA3 antibody, 048-006 antibody as
anti-HER1 antibody, and 015-126 antibody as anti-HER2 antibody are
recognized to have an ADCC activity, they themselves can be used
for damaging (killing) cancer cells. Herein, when the antibody of
the present invention that has transformed into human or human IgG
antibody is used, it is less attacked and excluded by the immune
system, thus enabling the expected effect to be well exhibited and
serious side effects to be avoided.
[0658] Furthermore, the antibody of the present invention can be
used as a medium (carrier) for delivering a drug, and the like, to
a specific cancer. That is to say, an anticipated application of
use of the antibody of the present invention includes DDS (Drug
delivery system) targeting a specific cancer cell.
[0659] Note here that each application of the antibody of the
present invention is described in detail below.
(Diagnosis Application)
[0660] Another aspect of the present invention relates to a use as
a diagnosis marker of based on the findings of the expression
(distribution) of CD46 antigen, ITGA3, ALCAM and CD147 antigen.
Specifically, one embodiment of this aspect provides a testing
method of gallbladder and liver cancer or pancreas cancer based on
the findings that a CD46 antigen is expressed in the gallbladder
and liver cancer and the pancreas cancer. The method includes the
following steps.
[0661] Step (1): preparing subject cells or tissues separated from
a living body.
[0662] Step (2): detecting a CD46 antigen in the subject cells or
tissues.
[0663] Information obtained by the testing method of the present
invention is useful for diagnosis of gallbladder and liver cancer
or pancreas cancer. For example, information obtained by subjecting
the above-mentioned method to patients with gallbladder and liver
cancer can be used for evaluating or grasping the pathologic
condition of patients and for evaluating the therapeutic effect.
For example, when the present invention is carried out concurrently
with the treatment of gallbladder and liver cancer, based on the
resultant information, the therapeutic effect can be evaluated.
Specifically, when the method of the present invention is carried
out after administering drugs, the change in the expression amount
of CD46 antigen in the liver cells is examined and the therapeutic
effect can be determined from the increase and decrease of the
expression amount. Thus, the method of the present invention may be
used for monitoring the therapeutic effect.
[0664] On the other hand, information obtained when the subjects
are persons other than the patient, that is, persons that have not
recognized to have gallbladder and liver cancer can be used for
determination of the presence or absence of contraction of
gallbladder and liver cancer, evaluation of contraction risk, and
the like. Since the method of the present invention permits
diagnosis of liver cancer based on the amount of expression amount
of genes, i.e., an objective indicator, its value is extremely
high.
[0665] Hereinafter, the steps constituting the present invention
are respectively described in detail.
1. Step (1)
[0666] In the step (1), cells or tissues separated from a subject
(a subject person, a living body) are prepared. The subjects herein
may include not only patients (gallbladder and liver cancer
patients or pancreas cancer patients) but also healthy persons
(including persons having a risk of contracting gallbladder and
liver cancer or pancreas cancer). For example, a part of tissues
collected from a subject by biopsy can be used as subject cells or
tissues in the method of the present invention.
[0667] The "subject cells or tissues" in the present invention are
cells or tissues that are samples (subjects) in the detection in
the method of the present invention. The subject cells or tissues
are separated from a living body. That is to say, the present
invention is applied to the subject cells or tissues in the state
in which it is separated from the living body. The term "separated
from a living body" means a state in which a part of the living
tissue in which subject cells or tissues exist is extracted,
thereby the subject cells or tissues are completed separated from
the origin living body. In the step (2), when an immunological
detection method is employed, the subject cells are generally
prepared in a state in which they are present in a living body,
that is, in a state in which they are linked to the surrounding
cells (as tissue), and used for the method of the present
invention. Note here that the subject cells may be used for the
method of the present invention after they are separated (isolated)
from the surrounding cells.
2. Step (2)
[0668] In the step (2), a CD46 antigen is detected in the prepared
subject cells or tissues as subjects. The term "CD46 antigen is
detected" means examining whether or not the CD46 antigen is
expressed (presence or absence of expression), or figuring out the
expression amount of the CD46 antigen as an absolute value or a
relative value. The reference of the relative amount herein can be,
for example, an amount of CD46 antigen of the reference samples
prepared according to the grade of malignancy. In general, the
presence of expression of CD46 antigen and the amount if expressed
are examined. In detecting the CD46 antigen, it is not essential to
determine the amount of CD46 antigens strictly.
[0669] In one embodiment of the present invention, a detection
method targeting mRNA that is a transcriptional product of the CD46
antigen is carried out. For the detection (measurement) of mRNA,
routine procedures such as an RT-PCR method and various
hybridization methods using specific probes (for example, northern
hybridization, in situ hybridization) can be employed. In another
embodiment of the present invention, a detection method targeting
the expression product of the CD46 antigen (protein) is carried
out.
[0670] It is preferable that CD46 antigen is detected by
immunologic procedures (for example, immunohistochemical staining
technique). In the immunologic procedure, anti-CD46 antigen
antibody is used, CD46 antigen protein is detected by using the
bonding property (binding amount) of the antibodies as an
indicator. The immunological detection method permits rapid and
sensitive detection. Also, the operation is simple. An example of
the detection methods may include ELISA method, radioimmunoassay,
FCM, an immunoprecipitation method, immunoblotting, and the
like.
[0671] The immunohistochemical staining technique permits rapid and
sensitive detection of CD46 antigens. Also, the operation is
simple. Therefore, burdens to a subject person (patient)
accompanying the detection of CD46 antigen is reduced. In the
immunohistochemical staining technique, in general, firstly, a step
of bringing the subject cells into contact with the anti-CD46
antibody is carried out. Then, the binding amount of the anti-CD46
antibody is examined. Specifically, according to the
above-mentioned immunohistochemical staining technique, the method
of the present invention can be carried out.
[0672] The kind or origin of the anti-CD46 antibody to be used in
immunostaining procedure is not particularly limited as long as it
has a specific binding property to the CD46 antigen. The anti-CD46
antibody may be any of a polyclonal antibody, an oligoclonal
antibody (a mixture of several kinds to several tens of antibodies)
and a monoclonal antibody. As the polyclonal antibody or the
oligoclonal antibody, affinity purification antibody by antigen can
be used besides an IgG fraction derived from anti-serum obtained by
immunizing an animal so as to obtain. The anti-CD46 antibody may be
antibody fragments such as Fab, Fab', F(ab').sub.2, scFv, and dsFv
antibodies.
[0673] The anti-CD46 antibody can be prepared by using an
immunologic procedure, phage display technique, ribosome display
method, and the like.
[0674] The preparation of a polyclonal antibody by the immunologic
procedure can be prepared by the following procedures. An antigen
(CD46 or a part thereof) is prepared. An animal such as a rabbit is
immunized with this antigen. As this antigen, not only human CD46
but also non-human CD46 such as mouse CD46 can be used. Such CD46
can be obtained by purifying a living body sample. Furthermore,
recombinant CD46 may be used. The recombinant human CD46 can be
prepared by, for example, introducing a gene encoding CD46 (which
may include a part of gene) in an appropriate host by using a
vector and expressing the gene within the obtained recombinant
cells.
[0675] In order to strengthen the immunity inducing effect, an
antigen to which a carrier protein is attached may be used. As the
carrier protein, KLH (Keyhole Limpet Hemocyanin), BSA (Bovine Serum
Albumin), OVA (Ovalbumin), and the like are used. For binding of
the carrier protein, a carbodiimide method, a glutaraldehyde
method, a diazo condensation method, an MBS (maleimidobenzoyl oxy
succinimide) method, and the like, can be used. On the other hand,
an antigen expressing CD46 (or a part thereof) as fusion protein
with GST, .beta. galactosidase, maltose bonded protein, or
histidine (His) tag, and the like, can be used. Such a fusion
protein can be purified by a general method in a simple manner.
[0676] If necessary, immunization is repeated. When the antibody
titer is sufficiently increased, blood is collected and subjected
to centrifugation so as to obtain serum. The obtained anti-serum is
subjected to affinity purification. Thus, a polyclonal antibody is
obtained.
[0677] On the other hand, a monoclonal antibody can be prepared by
the following procedures. Firstly, an immunization operation is
carried out by the similar method to the above-mentioned
procedures. If necessary, immunization is repeated. When the
antibody titer is sufficiently increased, antibody-producing cells
are extracted from an immunized animal. Next, the obtained
antibody-producing cells and myeloma cells are fused to each other
so as to obtain a hybridoma. Subsequently, this hybridoma is made
to be monoclonal. Then, a clone producing antibody showing high
specificity to the target protein is selected. A culture solution
of the selected clone is purified, thereby the target antibody can
be obtained. On the other hand, hybridoma is proliferated into a
predetermined number of more, then, transplanted in the abdominal
cavity of an animal (for example, mouse), proliferated in the
abdominal dropsy. By purifying the abdominal dropsy, the target
antibody can be obtained. For purification of the above-mentioned
culture solution or purification of the abdominal dropsy, affinity
chromatography using protein G, protein A, and the like, is
preferably used. Furthermore, affinity chromatography in which an
antigen is made into a solid phase can be used. Furthermore,
methods such as ion-exchange chromatography, gel filtration
chromatography, ammonium sulfate fractionation, and centrifugation
can be used. These methods are used singly or in arbitrary
combination thereof.
[0678] On the conditions that the specific binding property to CD46
antigen is maintained, the obtained antibody may be subjected to
various modifications. In the present invention, such a modified
antibody may be used.
[0679] When a labeled antibody is used as an anti-CD46 antibody,
the amount of bound antibody can be directly detected by using the
labeled amount as an indicator. Therefore, the method is more
simplified. On the contrary, it is necessary to prepare an
anti-CD46 antibody to which a label material is bound and
furthermore, and furthermore, the detection sensitivity is
generally reduced. Therefore, it is preferable that indirect
methods such as a method using a secondary antibody to which a
label material is linked, a method using a polymer to which a
secondary antibody and a label material are linked are used. The
secondary antibody herein is an antibody having a specific binding
property to the anti-CD46 antibody. For example, when an anti-CD46
antibody is prepared as a rabbit antibody, an anti-rabbit IgG
antibody can be used. Label secondary antibodies that can be used
for various species such as rabbit, goat, and mouse are
commercially available (for example, Funakoshi Corporation, COSMO
BIO Co., Ltd., etc.). Proper antibodies can be appropriately
selected depending upon the anti-CD46 antibody used in the present
invention.
[0680] For the label material, the label material arbitrarily
selected from the group consisting of peroxidase,
.beta.-D-galactosidase, micro peroxidase, horseradish peroxidase
(HRP), fluorescein isothiocyanate (FITC), rhodamine isothiocyanate
(RITC), alkaline phosphatase, biotin, and radioactive material is
preferably used. In particular, a method of using biotin as the
label material and reacting avidin peroxidase permits highly
sensitive detection.
[0681] The above-mentioned antibody of the present invention may be
used as the anti-CD46 antibody. Specifically, for example,
antibodies (035-224 antibody, 045-011 antibody, 051-144 antibody,
052-053 antibody, 052-073 antibody, 053-049 antibody, or 3172-120
antibody), which the present inventors have succeeded in obtaining,
can be used.
[0682] Another embodiment of this aspect provides a testing method
of gallbladder and liver cancer or pancreas cancer based on the
findings that ITGA3 is expressed in gallbladder and liver cancer
and pancreas cancer. The method includes the following steps.
[0683] Step (1): preparing subject cells or tissues separated from
a living body
[0684] Step (2): detecting ITGA3 in the subject cells or
tissues
[0685] Information obtained by the testing method of the present
invention is useful for diagnosis of gallbladder and liver cancer
or diagnosis of pancreas cancer. Since the using method and details
of each step are the same as in the case of the CD46 antigen, the
description thereof is not mentioned here.
[0686] A further embodiment of this aspect provides an obtaining
method of information for diagnosis of kidney cancer, hepatic cell
carcinoma or gallbladder and liver cancer based on the findings
that ALCAM is expressed in kidney cancer, hepatic cell carcinoma
and gallbladder and liver cancer. The method includes the following
steps.
[0687] Step (1): preparing subject cells or tissues separated from
a living body
[0688] Step (2): detecting ALCAM in the subject cells or
tissues
[0689] Information obtained by the testing method of the present
invention is useful for diagnosis of kidney cancer, diagnosis of
hepatic cell carcinoma, or diagnosis of gallbladder and liver
cancer. Since the using method and details of each step are the
same as in the case of the CD46 antigen, the description thereof is
not mentioned here.
[0690] A yet further embodiment of this aspect provides a testing
method of kidney cancer based on the findings that CD147 antigen is
expressed in kidney cancer. The method includes the following
steps.
[0691] Step (1): preparing subject cells or tissues separated from
a living body
[0692] Step (2): detecting a CD147 antigen in the subject cells or
tissues
[0693] Information obtained by the testing method of the present
invention is useful for diagnosis of kidney cancer. Since the using
method and details of each step are the same as in the case of the
CD46 antigen, the description thereof is not mentioned here.
(Treatment Application)
[0694] As mentioned in the below-mentioned Examples, the present
inventor have succeeded in obtaining antibodies exhibiting
Antibody-Dependent Cell-mediated Cytotoxicity (hereinafter,
abbreviated as "ADCC") activity to certain antibodies. Furthermore,
the present inventors have transformed these antibodies into IgG
type and investigated the probability of application to an antibody
therapeutic agent. Any antibodies show excellent anti-tumor effect.
Based on these findings, the further aspect of the present
invention relates to an application of the antibodies successfully
obtained by the present inventors in treatment of cancer.
[0695] This aspect firstly provides a drug (cancer therapeutic
agent) capable of affecting and damaging in a cancer cell-specific
manner using by using ITGA3, HER1, HER2, ALCAM, EpCAM or HGFR as a
target, and the treatment method using the same. One embodiment of
the drug of the present invention contains anti-ITGA3 antibody as
an active ingredient. One preferable embodiment of the drug of the
present invention contains an anti-ITGA3 antibody having an ADCC
activity as an active ingredient. The drugs of this embodiment can
obtain the therapeutic effect by the cytotoxicity using the ADCC
activity. As anti-ITGA3 antibody having the ADCC activity, 015-003
antibody (the specific binding property to ITGA3 and it may be
partially modified as long as the ADCC activity is maintained)
shown in the below-mentioned Examples or different types of
antibodies constructed based on the 015-003 antibody (for example,
IgG type antibody) can be used. This antibody has both the specific
binding property to ITGA3 and the ADCC activity. Therefore, it
specifically binds to the cancer cells expressing ITGA3 and then
expresses the ADCC activity. Thus, it can damage a cancer cell. The
target cancer cell of the drug of this embodiment is not
particularly limited, but can target, for example, gallbladder and
liver cancer cells and pancreas cancer cells.
[0696] In another embodiment of the present invention, an anti-HER1
antibody is contained as an active ingredient. In the drug of one
preferable embodiment of the present invention, anti-HER1 antibody
having an ADCC activity is contained as an active ingredient. In
the drug of this embodiment, the therapeutic effect can be obtained
by the cytotoxicity using the ADCC activity. In the drug of the
further preferable embodiment, in addition to the cytotoxicity
using the ADCC activity, since inhibition of binding of EGF as a
ligand to HER1 and/or inhibition of phosphorylation signal by HER1
are provided, higher therapeutic effect can be obtained. As
anti-HER1 antibody having such an ADCC activity, 048-006 antibody,
059-152 antibody, 055-147 antibody or 059-173 antibody shown in the
below-mentioned Example (which may be partially modified as long as
the specific binding property to HER1 and the ADCC activity are
maintained) or different types of antibodies constructed based on
them (for example, IgG type) can be used. These antibodies have the
specific binding property to HER1, inhibition of binding of EGF to
HER1, inhibition of phosphorylation signal of HER1 and ADCC
activity. Therefore, they can specifically bind to a cancer cell
expressing HER1 and inhibit HER1 activity by inhibition of binding
of EGF to HER1 and/or inhibition of phosphorylation signal of HER1,
thereafter, exhibit the ADCC activity so as to damage a cancer
cell. Furthermore, it is confirmed that the antibody exhibits
suppression effect to cancer cells and an anti-tumor effect in
animal model, so that the antibody is greatly expected to be used
in antibody medicine. The target cancer cell by the drug of this
embodiment is not particularly limited, but it can target, for
example, cells of kidney cancer, hepatic cell carcinoma,
gallbladder and liver cancer, lung squamous cell carcinoma,
pulmonary adenocarcinoma, and pancreas cancer.
[0697] In a further embodiment of the present invention, an
anti-HER2 antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-HER2 antibody having an ADCC activity is contained as an
active ingredient. In the drug of this embodiment, the therapeutic
effect can be obtained by the cytotoxicity using the ADCC activity.
As anti-HER2 antibody having such an ADCC activity, 015-126
antibody shown in the below-mentioned Example (which may be
partially modified as long as the specific binding property to HER2
and the ADCC activity are maintained) or different types of
antibodies constructed based on them (for example, IgG type) can be
used. This antibody has the specific binding property to HER2 and
ADCC activity. Therefore, they can specifically bind to a cancer
cell expressing HER2 then exhibits the ADCC activity so as to
damage a cancer cell. Furthermore, it is confirmed that the
antibody exhibits suppression effect to cancer cells, so that the
antibody is greatly expected to be used in antibody medicine. The
target cancer cell by the drug of this embodiment is not
particularly limited, but it can target, for example, cells of
kidney cancer, liver cancer, and pulmonary adenocarcinoma.
[0698] In a further embodiment of the present invention, an
anti-ALCAM antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-ALCAM antibody having an ADCC activity is contained as an
active ingredient. As anti-ALCAM antibody having such an ADCC
activity, 041-118 antibody or 066-174 antibody shown in the
below-mentioned Example (which may be partially modified as long as
the specific binding property to ALCAM and the ADCC activity are
maintained) or different types of antibodies constructed based on
them (for example, IgG type) can be used. This antibody has the
specific binding property to ALCAM and ADCC activity. Therefore,
they can specifically bind to a cancer cell expressing ALCAM then
exhibits the ADCC activity so as to damage a cancer cell. The
target cancer cell by the drug of this embodiment is not
particularly limited, but it can target, for example, cells of
pulmonary adenocarcinoma, ovarian cancer, and large bowel
cancer.
[0699] In a yet further embodiment of the present invention, an
anti-EpCAM antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-EpCAM antibody having an ADCC activity is contained as an
active ingredient. As anti-EpCAM antibody having such an ADCC
activity, 067-153 antibody shown in the below-mentioned Example
(which may be partially modified as long as the specific binding
property to EpCAM and the ADCC activity are maintained) or
different types of antibodies constructed based on them (for
example, IgG type) can be used. This antibody has the specific
binding property to EpCAM and ADCC activity. Therefore, they can
specifically bind to a cancer cell expressing EpCAM then exhibits
the ADCC activity so as to damage a cancer cell. The target cancer
cell by the drug of this embodiment is not particularly limited,
but it can target, for example, cells of gastric solid-type
adenocarcinoma, colon adenocarcinoma, and pulmonary adenocarcinoma
cell.
[0700] In a yet further embodiment of the present invention, an
anti-CD147 antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-CD147 antibody having an ADCC activity is contained as an
active ingredient. As anti-CD147 antibody having such an ADCC
activity, 059-053 antibody shown in the below-mentioned Example
(which may be partially modified as long as the specific binding
property to CD147 and the ADCC activity are maintained) or
different types of antibodies constructed based on them (for
example, IgG type) can be used. This antibody has the specific
binding property to CD147 and ADCC activity. Therefore, they can
specifically bind to a cancer cell expressing CD147 then exhibits
the ADCC activity so as to damage a cancer cell. The target cancer
cell by the drug of this embodiment is not particularly limited,
but it can target, for example, kidney cancer cells.
[0701] In a yet further embodiment of the present invention, an
anti-CD44 antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-CD44 antibody having an ADCC activity is contained as an
active ingredient. As anti-CD44 antibody having such an ADCC
activity, 064-003 antibody shown in the below-mentioned Example
(which may be partially modified as long as the specific binding
property to CD44 and the ADCC activity are maintained) or different
types of antibodies constructed based on them (for example, IgG
type) can be used. This antibody has the specific binding property
to CD44 and ADCC activity. Therefore, they can specifically bind to
a cancer cell expressing CD44 then exhibits the ADCC activity so as
to damage a cancer cell. The target cancer cell by the drug of this
embodiment is not particularly limited, but it can target, for
example, pulmonary adenocarcinoma cells.
[0702] In a yet further embodiment of the present invention, an
anti-HGFR antibody is contained as an active ingredient. In the
drug of one preferable embodiment of the present invention,
anti-HGFR antibody having an ADCC activity is contained as an
active ingredient. As anti-HGFR antibody having such an ADCC
activity, 067-133 antibody shown in the below-mentioned Example
(which may be partially modified as long as the specific binding
property to HGFR and the ADCC activity are maintained) or different
types of antibodies constructed based on them (for example, IgG
type) can be used. This antibody has the specific binding property
to HGFR and ADCC activity. Therefore, they can specifically bind to
a cancer cell expressing HGFR then exhibits the ADCC activity so as
to damage a cancer cell. The target cancer cell by the drug of this
embodiment is not particularly limited, but it can target, for
example, pulmonary adenocarcinoma cells.
[0703] The present invention furthermore provides a method of
reducing the grade of malignancy of a target cell or promoting the
normalization by damaging or suppressing the expression of HER1,
HER2, CD46, ITGA3, ICAM1, ALCAM, or CD147 in the target cell.
[0704] Herein, the present inventors have investigated and
recognized specific expression of CD46 in gallbladder and liver
cancer and pancreas cancer, which had not been particularly
reported about the relationship with respect to CD46 (see the
below-mentioned Example). Similarly, the relationship between
gallbladder and liver cancer and pancreas cancer and the expression
of ITGA3; the relationship between kidney cancer, hepatic cell
carcinoma and gallbladder and liver cancer and ALCAM; as well as
the relationship between kidney cancer and CD147 have been
clarified (see the below-mentioned Example). Based on the findings,
a novel and effective target cell of CD46 is a gallbladder and
liver cancer cell and a pancreas cancer cell; a novel and effective
target cell of ITGA3 is a gallbladder and liver cancer cell and a
pancreas cancer cell; and a novel and effective target cell of
CD147 is a kidney cancer cell.
[0705] Note here that the inhibition or suppression of each antigen
can be carried out by using an antisense method or RNA
interference, or by using ribozyme.
[0706] In the case where expression inhibition by the antisense
method is carried out, for example, when transcription is carried
out in the target cell, an antisense-construct for generating RNA
that is complementary to a portion specific to mRNA encoding this
protein is used. Such an antisense-construct is introduced into the
target cells, for example, in a form of an expression plasmid. On
the other hand, when it is introduced in to the target cells as the
antisense-construct, it is possible to employ an
oligonucleotide-probe that is hybridized with mRNA or genome DNA
sequence encoding this protein and inhibits the expression thereof.
As such an oligonucleotide-probe, one having a low resistance to
endogenous nuclease such as exonuclease and/or endonuclease is
preferably used.
[0707] When DNA molecule is used as an antisense nucleic acid, it
is preferable that oligodeoxyribonucleotide derived from a region
(for example, a region from -10 to +10) including a translation
initiation site of mRNA encoding this protein is used.
[0708] It is preferable that the complementation between the
antisense nucleic acid and the target nucleic acid is strict.
However, some mismatch may be accepted. The hybridization
performance of the antisense nucleic acid with respect to the
target nucleic acid is generally dependent upon both the degree of
complementation of both nucleic acids and the length thereof. In
general, as the antisense nucleic acid to be used is longer, even
if the number of mismatch is increased, stable two heavy chains (or
three heavy chains) can be formed between the antisense nucleic
acid and the target nucleic acid. Persons skilled in the art can
confirm the degree of permissible degree of the mismatch by using a
standard technique.
[0709] The antisense nucleic acid may be DNA, RNA or a chimera
mixture thereof, or derivative or modified type thereof.
Furthermore, it may be single stranded or double stranded. By
modifying a base portion, a sugar portion or a skeleton portion of
phosphoric acid, the stability and hybridization performance and
the like of the antisense nucleic acid can be improved.
Furthermore, to the antisense nucleic acid, materials for urging
the cell membrane transportation (for example, see Letsinger et
al., 1989, Proc. Natl. Acad. Sci. U.S.A. 86:6553-6556; Lemaitre et
al., 1987, Proc. Natl. Acad. Sci. 84:648-652; PCT Publication No.
WO88/09810, published Dec. 15, 1988) or materials capable of
enhancing the affinity with respect to certain cells may be
added.
[0710] The antisense nucleic acid can be synthesized by a
conventional method, for example, by using commercially available
automated DNA synthesizer (for example, Applied Biosystems, and the
like). For producing the modulated product or derivative of nucleic
acid, you can see, for example, Stein et al. (1988), Nucl. Acids
Res. 16:3209, or Sarin et al., (1988), Proc. Natl. Acad. Sci.
U.S.A. 85:7448-7451.
[0711] In order to enhance the effect of antisense nucleic acid in
the target cells, a strong promoter such as pol II and pol III can
be used. That is to say, if a construct including antisense nucleic
acid disposed under control of such promoters is introduced into
the target cells, it is possible to secure the transcription of
sufficient amount of antisense nucleic acid by the effect of the
promoter.
[0712] The antisense nucleic acid can be expressed by using any
promoters (derivative promoters or constitutive promoters) known to
function in the mammalian cells (preferably, human cells). For
example, promoters such as a SV40 initial promoter region (Bernoist
and Chambon, 1981, Nature 290:304-310), a promoter derived from the
3'-terminal region of Rous sarcoma virus (Yamamoto et al., 1980,
Cell 22:787-797), a Herpetic Thymidine Kinase promoter (Wagner et
al., 1981, Proc. Natl. Acad. Sci. U.S.A. 78: 1441-1445), and the
like, can be used.
[0713] In one embodiment of the present invention, the expression
of the protein is inhibited by RNA interference (RNAi). RNAi is a
process of a sequence specific post-transcriptional gene
suppression that can be caused in the eukaryote. In the RNA
interference, double stranded RNA (dsRNA) having a sequence
corresponding to the sequence of the target mRNA is used. It is
known that mammalian cells have two routes (a sequence specific
route and a sequence nonspecific route) affected by dsRNA. In the
sequence specific route, relatively long dsRNA is divided into
short interference RNAs (siRNAs). Each of the siRNAs has sense and
antisense chains of about 21 nucleotides that form siRNA of about
19 nucleotides having protruding portions at the 3' terminal
portion. On the other hand, it is thought that a sequence
nonspecific route can be caused by arbitrary dsRNA regardless of
the sequence as long as it has a predetermined length or longer. In
this route, dsRNA, two enzymes, that is, PKR, which becomes an
active from and stops whole synthesis of proteins by
phosphorylating the translation initiation factor eIF2, and 2', 5'
oligoadenylate synthetase, which is involved in the synthesis of an
RNAase L activated molecule are activated. In the method of the
present invention, in order to minimize the progress of this
nonspecific route, it is preferable to use dsRNA including about 30
base pairs or less (see, for example, Hunter et al. (1975) J Biol
Chem 250: 409-17; Manche et al. (1992) Mol Cell Biol 12: 5239-48;
Minks et al. (1979) J Biol Chem 254: 10180-3; and Elbashir et al.
(2001) Nature 411: 494-8).
[0714] Note here that it is confirmed that RNAi is an effective
means for reducing the gene expression in various cells (for
example, a HeLa cell, a NIH/3T3 cell, a COS cell, a 293 cell, and
the like). Furthermore, in general, it can inhibit expression more
effectively than by the antisense method.
[0715] The dsRNA used in RNAi can be prepared in vitro or in vivo
by chemical synthesis or by using an appropriate expression vector.
In the latter method, it is particularly effective to prepare a
relatively long dsRNA. For designing dsRNA, in general, sequence
peculiar to the target nucleic acid (continuous sequence) is used.
Note here that a program and algorithm for selecting an appropriate
target sequence have been developed.
[0716] In another embodiment of the present invention, the
expression of ITGA3 is carried out by using ribozyme. By using
ribozyme for cleave mRNA at the site specific recognition sequence,
it is possible to destroy mRNA encoding the protein. However,
preferably, a hammerhead ribozyme is used. A method for
constructing the hammerhead ribozyme can be seen in, for example,
Haseloff and Gerlach, 1988, Nature, 334: 585-591.
[0717] Similar to the antisense method, for example, for the
purpose of the stability and target performance, by using a
modified oligonucleotide, ribozyme may be constructed. In order to
produce an effective amount of ribozyme in the target cells, for
example, under the control of a strong promoter (for example, pol
II and pol III), it is preferable that the nucleic acid construct
in which DNA encoding ribozyme is disposed is used.
[0718] Drugs used for the treatment method (including a method of
urging to reducing or normalizing the grade of malignancy of cancer
cells, and the like) of the present invention can be formulated
according to the conventional method. In formulation, other
ingredients acceptable for formulation (for example, carrier,
vehicle, disintegrating agents, buffer agent, emulsifying agent,
suspending agent, soothing agent, stabilizer, preservative,
preservative, physiological saline, and the like) can be contained.
An example of the vehicle may include lactose, starch, sorbitol,
D-mannitol, and sucrose. An example of the disintegrating agents
may include starch, carboxymethyl cellulose, calcium carbonate, and
the like. An example of the buffer agent may include phosphate,
citrate, acetate, and the like. An example of the emulsifying agent
may include gum Arabic, alginate sodium, tragacanth, and the like.
An example of the suspending agent may include glyceryl
monostearate, aluminum monostearate, methylcellulose, carboxymethyl
cellulose, hydroxymethyl cellulose, sodium lauryl sulfate, and the
like. An example of the soothing agent may include benzyl alcohol,
chlorobutanol, sorbitol, and the like. An example of the stabilizer
may include propylene glycol, diethylene sulfite, ascorbic acid,
and the like. An example of the preservative may include phenol,
benzalkonium chloride, benzyl alcohol, chlorobutanol,
methylparaben, and the like. An example of the preservative may
include benzalkonium chloride, parahydroxybenzoate, chlorobutanol,
and the like.
[0719] The dosage form in the formulation is not particularly
limited. An example of the dosage form may include tablet, powdered
drug, fine subtilae, granule, capsules, syrup, injectable drug,
external preparation, and suppository.
[0720] In the treatment using the drug of the present invention,
the drug of the present invention is administered to a subject
(patient) with a cancer cell or adult T cell leukemia. The drug of
the present invention can be administered to a subject (patient) by
oral administration or parenteral administration (intravenous,
intra-arterial, subcutaneous, intramuscular, intraperitoneal
injection, direct introduction to the target cell, and the like)
depending upon the dosage form.
[0721] The dosage amount of the drug of the present invention will
vary depending on the symptoms, age, sex, body weight, and the
like, of the patient, but the person skilled in the art can set an
appropriate dosage amount. For example, the dosage amount can be
set so that the dosage amount of effective ingredient for adult
(body weight: about 60 kg) per day is about 0.001 mg to about 100
mg. The administration schedule can include, for example, once to
several times a day, once per two days, or once per three days. For
setting the administration schedule, conditions of a patient,
efficacy duration time of the drug, and the like, can be
considered.
[0722] In another embodiment, the drug of the present invention
uses anti-HER1 antibody, anti-HER2 antibody, anti-CD46 antibody,
anti-ITGA3 antibody, anti-ICAM1 antibody, anti-ALCAM antibody,
anti-CD147 antibody as a carrier for DDS. That is to say, this
embodiment provides an immunocomplex obtained by combining a drug
(cytotoxin and the like), radioactive isotope, or the like (these
are also referred to as "active ingredient" together) to anti-HER1
antibody, and others. The immunocomplex containing a drug
(cytotoxin) having a cell-killing activity or a cytotoxic activity
is generally referred to as immunotoxin. An example of the
cytotoxin may include Taxol, cytochalasin. B, gramicidin D,
ethidium bromide, emetine, mitomycin, etoposide, tenoposide,
vincristine, vinblastine, colchicines, doxorubicin, daunorubicin,
dihydroxy-anthracene-dione, mitoxantrone, methramycin, actinomycin
D, 1-dehydrotestosterone, glucocorticoid, procaine, tetracaine,
lidocaine, propranolol, and puromycin as well as analogue or
homologue thereof.
[0723] As the active ingredient contained in the immunocomplex of
the present invention, protein or peptide having a desirable
biological activity may be used. An example of the candidate for
protein and the like that can be used for such a purpose may
include abrin, ricin A, Pseudomonas-exotoxin, diphteria toxin,
tumor necrosis factor, interferon-.gamma., interleukin I (IL-1),
interleukin 2 (IL-2), interleukin 6 (IL-6), a granulocyte
macrophage colony stimulating factor (GM-CSF), a granulocyte colony
stimulating factor (G-CSF) lymphokine.
[0724] A technology for combining an active component to an
antibody is well known and you can see in, for example, Monoclonal
Antibodies And Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56
(Alan R. Liss, Inc. 1985), Controlled Drug Delivery (2nd edition.),
Robinson et al. (eds.), pp. 623-53 (Marcel Dekker, Inc. 1987),
Monoclonal Antibodies For Cancer Detection And Therapy, Baldwin et
al. (eds.), pp. 303-16 (Academic Press 1985), Thorpe et al., "The
Preparation And Cytotoxic Properties Of antibody-Toxin Conjugates",
Immunol. Rev., 62:119-58 (1982).
(Kit Used in the Present Invention)
[0725] Each method of the present invention (a method for obtaining
information for diagnosis, and the like) may be carried out by
using a kit of reagent and the like. Another aspect of the present
invention provides a kit used for such a purpose. For example,
nucleic acid (probe and primer), reaction reagent, dilution, a
reactor vessel, and the like, that are used for the method of the
present invention can be contained in the kit. Note here that the
kit of the present invention is generally includes instruction.
[0726] The user of a kit makes it possible to allow the method of
the present invention to be carried out in a simple way and for a
short time.
Example
1. Production of Vector for Producing ScFv Antibody Gene
Library
[0727] 1-1 Production of Vector for Producing scFV Antibody Gene
Library
[0728] As conceptually shown in FIG. 5, pelB (signal sequence) of
M13 phage, His6 tag sequence, cp3 protein of M13 phage (.DELTA.cp3
(198aa-406aa) N-terminal deleted capsid protein 3) sequence,
protein A protein sequence were incorporated in an appropriate
restriction enzyme site of a pTZ19R phagemid vector (Pharmacia) so
as to from a vector pAALFab (see Iba Y. et al., Gene 194: 35-46,
1997.). A vector pFCAH9-E8d for incorporation was produced from
this pAALFab.
[0729] Genes of a heavy chain and a light chain are inserted into
the predetermined position of this vector, thereby completing an
actual antibody protein expression vector. The shape of the
antibody expressed by the completed vector is a scFv and a light
chain constant region CL gene is bonded to the aforementioned cp3
gene. As a result, expression protein has a shape of scFv-CL-cp3.
Specifically, the below-mentioned operation is carried out.
Used primer:
TABLE-US-00001 527 Reverse (SEQ ID NO: 377):
5'-CAGGAAACAGCTATGAC-3' 599 E8VHf-PstR: (SEQ ID NO: 378)
3'-CGGCTCCAAGTCGACGTCGTCA-5' 544 E8VHf-PstF: (SEQ ID NO: 379)
5'-CAGCTGCAGCAGTCTGGGGCAGAGCTTGTGAAGCCAGGGGCCTCAGT
CAAGTTGTCCTGCACAGCTTCTGGCTTCAACATTAA-3' 545 E8VHf-XbaR: (SEQ ID NO:
380) 3'-AGACCGAAGTTGTAATTTCTGTGGATATACGTGACCCACTTCGTCTC
CGGACTTTTCCCAGATCTCACCTAACCTTCCTAA-5' 546 E8VHf-XbaF: (SEQ ID NO:
381) 5'-AAGGGTCTAGAGTGGATTGGAAGGATTGATCCTGCGAGTGGTAATAC
TAAATATGACCCGAAGGACAAGGCCACTATAACAGCA-3' 547 E8VHf-EcoR (SEQ ID NO:
382) 3'-TTCCTGTTCCGGTGATATTGTCGTCTGTGTAGGAGGTTGTGTCGGAT
GGATGTCGACTTAAGGGAC-5' 548 E8VHf-EcoF (SEQ ID NO: 383)
5'-CAGCTGAATTCCCTGACATCTGAGGACACTGCCGTCTATTACTGTGC TGGT-3' 549
E8VHf-BstR (SEQ ID NO: 384):
3'-CAGATAATGACACGACCAATACTAATGCCGTTGAAACTGATGACCCC
GGTTCCGTGGTGCCAGTGGCACAAGG-5' 590 His6-SmaR (SEQ ID NO: 385):
3'-GGTTCTCTAACAGTAGTGGTAGTAGTGGTAATTATTCTCGATAGGGC CCTCGAA-5' 542
E8VLf-SacF (SEQ ID NO: 386):
5'-GACATCGAGCTCACCCAGTCTCCAGCCTCCCTTTCTGCGTCTGTGGG
AGAAACTGTCACCATCACATGT-3' 539 E8VLf-KpnR (SEQ ID NO: 387):
3'-TGACAGTGGTAGTGTACAGCTCGTTCACCCTTATAAGTGTTAATAAA
TCGTACCATGGTCGTC-5' 542 E8VLf-KpnF (SEQ ID NO: 388):
5'-GCATGGTACCAGCAGAAACCAGGGAAATCTCCTCAGCTCCTGGTCTA T-3' 543
E8VLf-BamR (SEQ ID NO: 389):
3'-GGAGTCGAGGACCAGATATTACGTTTTTGGAATCGTCTACCACACGG
TAGTTCCAAGTCACCGTCACCTAGGCCTTGTGTT-5' 562 E8VLf-XhoR (SEQ ID NO:
390): 3'-TCATGAGGCACCTGCAAGCCACCTCCGTGGTTCGAGCTCTAGTT T-5' 563
E8VLf-XhoF (SEQ ID NO: 391):
5'-AGTACTCCGTGGACGTTCGGTGGAGGCACCAAGCTCGAGATCAA A-3' 613 NheR (SEQ
ID NO: 392): 3'-ATCGACAGCT-5' 600 E8VLKpnXhoR (SEQ ID NO: 393):
3'-AAGCCACCTCCATGGTTCGAGCTCTAGTTT-5' LCP3ASC (SEQ ID NO: 394):
3'-TCGAAGTTGTCCTTACTCACAAGCCGCGCGGTCAGCTGAGGTAA-5' hCH1Bst (SEQ ID
NO: 395): 5'-ACCCTGGTCACCGTCTCCTCAGCCTCCACCAAGGGCCCATCGGTCTT
CCCCCTGG-3' hCH1midAS (SEQ ID NO: 396):
3'-GGGAGTCGTCGCAGCACTGGCACGGGAGGTCGTCGAA-5' hCH1midS (SEQ ID NO:
397): 5'-GGACTCTACTCCCTCAGCAGCGTCGTGACCGTGCCC-3' hCH1H6 (SEQ ID NO:
398): 3'-GGGTCGTTGTGGTTCCACCTGTTCTTTCAACTCGGGTTTAGAACAGT
AGTGGTAGTAGTGGTA-5' hCH1H6Sma (SEQ ID NO: 399):
3'-GGGTTTAGAACAGTAGTGGTAGTAGTGGTAATTATTCTCGATAGGGC CCTCGAACG-5' 702
BstXhoF (SEQ ID NO: 400):
5'-GGCACCACGGTCACCGTCTCGAGCGCCTCCACC-3'
<Production of pFCAH3-E8T H Chain Part> 1) By using pAALFab
as a template, PCR using 527-599 and PCR using 547-590 were carried
out so as to produce a DNA fragment. 2) PCR using 544-545, 546-547,
and 548-549 was carried out so as to produce a DNA fragment. 3) 1)
and 2) were mixed and PCR by 527,590 was carried out, which was
cloned to a HindIII-SmaI site of pAALFab. <pFCAH3-E8T L Chain
Part> 4) PCR using 542-562 and 561-613 was carried out so as to
produce a DNA fragment. 5) PCR using 538-539 and 542-543 was
carried out so as to produce a DNA fragment. 6) 4) and 5) were
mixed and PCR by 538, 562 was carried out, which was cloned to a
SacI-NheI site of pAALFab. <pFCAH9-E8d>
7) Production of VH Stuffer Part
[0730] pFCAH3-E8T was digested with XbaI and EcoRI and a klenow
fragment was acted thereon so as to be blunted. Thereafter, the
self ligation was carried out so as to produce a stuffer of the VH
part.
8) Production of VL Stuffer Part
[0731] By using pFCAH3-E8T as a template, PCR with 527-600 was
carried out, which was cloned to the HindIII-XhoI site in 7).
9) This was digested with KpnI and subjected to self ligation so as
to produce a stuffer of a VL part.
10) Introduction of SfiI, NcoI, SpeI Sites
[0732] By using pFCAH3-E8T as a template, PCR with 527-663 was
carried out, which was cloned to the HindIII-SacI site in 1).
11) Introduction of AscI Site
[0733] By using pFCAH3-E8T as a template, PCR with 527-LCP3ASC was
carried out, which was cloned to 2) which was completely digested
with SacI and partially digested with SalI.
12) Transform of GammaCH1 Part into Human Gene
[0734] Since human gamma CH1 part has BstPI site, cloning was
carried out so as to design this site. By using tonsil cDNA as a
template, PCR with hCH1Bst-hCH1midS, hCH1midAS-hCH1H6 was carried
out and then mixed. PCR with hCH1Bst-hCH16Sma was carried out and
the DNA fragment was cloned to the BstPI-Sma site in 3).
13) Introduction of Xho Site
[0735] By using 12) as a template, PCR with 702-663 was carried out
and this was cloned to the BstPI-SacI site in 12).
<Production of pscFvCA9-E8VHdVLd>
[0736] pFCAH9-E8d 3 .mu.g (3 .mu.L) (see FIG. 5D) was mixed with
BstPI (3 U/.mu.L) (3 .mu.L), 10.times.H buffer (5 .mu.L), DW (39
.mu.L) and subjected to restriction enzyme treatment at 37.degree.
C. for two hours. After treatment, precipitates obtained by ethanol
precipitation were dissolved in 10 .mu.L of TE buffer. To this
solution, SacI (10 U/.mu.L) (1 .mu.L), 10.times.L buffer (5 .mu.L)
and DW (34 .mu.L) were mixed. Then, this mixture was subjected to
restriction enzyme treatment at 37.degree. C. for two hours and to
agarose gel electrophoresis. Thus, 4.7 kb fragment was recovered.
The recovered products were subjected to ethanol precipitation to
give 10 .mu.L (pFCAH9-E8d BstPI-SacI fragment).
[0737] On the other hand, a primer linF (100 pmol/.mu.L) (5 .mu.L)
and a primer linR (100 pmol/.mu.L) (5 .mu.L) were mixed and heated
at 94.degree. C. for 5 minutes, and then annealed at 80.degree. C.
for 5 minutes, at 70.degree. C. for 5 minutes, and at room
temperature for 30 minutes. Two .mu.L of which was mixed with the
above-obtained pFCAH9-E8d BstPI-SacI fragment (1 .mu.L), 10.times.
ligation buffer (1.5 .mu.L), DW (9.5 .mu.L), and T4DNA ligase (I
.mu.L) and reacted at 16.degree. C. for 16 hours. After reaction,
the reacted product was subjected to ethanol precipitation to
concentrate to 3 .mu.L. 1.5 .mu.L of them was used to transform E.
coli DH12S competent cells (20 .mu.L) by electroporation. The
obtained plasmid clone was extracted and the base sequence thereof
was confirmed. This was named pscFvCA9-E8VHdVLd. FIG. 6
schematically shows a structure of pscFvCA9-E8VHdVLd. Furthermore,
FIGS. 7-1 to 7-2 show the base sequence (SEQ ID NO: 401) of the
insert part of pscFvCA9-E8VHdVLd and the amino acid sequence (SEQ
ID NO: 402) encoded thereby, respectively.
TABLE-US-00002 primer linF (SEQ ID NO: 403)
GTCACCGTCTCGAGAGGCGGTGGCGGATCAGGTGGCGGTGGAAGTGGCGG
TGGTGGGTCCATGGCCGACATCGAGCT primer linR (SEQ ID NO: 404)
CGATGTCGGCCATGGACCCACCACCGCCACTTCCACCGCCACCTGATCCG
CCACCGCCTCTCGAGACG
1-2 Production of Vector for Temporarily Cloning Heavy Chain
Variable Region (VH)
[0738] According to the well-known technique (see Iba Y. et al.,
Gene 194:35-46, 1997.), firstly, a pAALFab vector (FIG. 5A) was
produced. A portion between XbaI and EcoRI was deleted from the
pAALFab vector, and the restriction enzyme cut sites Kpn I, Sfi I,
Nco I, and Spe I were newly added. Through pFCAH3-E8T (FIG. 5B), a
vector pscFvCA-E8VHd (FIG. 5C) capable of cloning VH (heavy chain
variable region) was produced. Thus, a vector for temporarily
cloning the heavy chain variable region (VH) was obtained. FIGS.
8-1 to 8-2 show the base sequence (SEQ ID NO: 405) of the insert of
pscFvCA-E8VHd, the restriction enzyme site and the amino acid
sequence (SEQ ID NO: 406) encoded by the base sequence.
[0739] Specifically, the primer 610 and the primer 611 were
annealed and annealed produced was cloned to a BstPI-SacI site of
pFCAH3-E8T. Thus, a single chain was produced. Furthermore, PCR
with the primer 527 and the primer 619 was carried out and this was
further cloned to a HindIII-PstI site. Thus, introduction of SfiI,
NcoI site was carried out. Hereinafter, primer sequences used for
producing the vector are shown.
TABLE-US-00003 610 scBstSpeSacF (SEQ ID NO: 407):
5'-CACCACGGTCACCGTCTCCTCAGGCGGTGGCGGATCAGGTGGCGGTG
GAAGTGGCGGTGGTGGGTCTACTAGTGACATCGAGCTCACCCAG-3' 611 scBstSpeSacR
(SEQ ID NO: 408):
3'-GTGGTGCCAGTGGCAGAGGAGTCCGCCACCGCCTAGTCCACCGCCAC
CTTCACCGCCACCACCCAGATGATCACTGTAGCTCGAGTGGGTC-5' 527 Reverse (SEQ ID
NO: 409): 5'-CAGGAAACAGCTATGAC-3' 619 E8VHf-SftNcoPstR (SEQ ID NO:
410): 3'-GACGCCGGGTCGGCCGGTACCGGCTCCAAGTCGACGTCGTCA-5'
2. Production of Immunoglobulin Light Chain Library
2-1 Isolation of Immunoglobulin Light Chain Gene by Using PCR
[0740] From bone marrow cells (sample No. 59) 4.times.10.sup.7
cells, and lymphocytes of cord blood and peripheral blood, by using
a commercially available kit (Pharmacia Biotech, QuickPrep Micro
mRNA Purification Kit), 2.6 .mu.g of mRNA was obtained. From this
mRNA, cDNA was produced. The cDNA was produced by using
SuperScriptPreamplification System (GibcoBRL). As a primer, oligo
dT was used. PCR using the obtained cDNA as a template was carried
out by using 5' primer (.kappa.1-.kappa.6, .lamda.1-.lamda.6) and
3' primer (hCKASC primer or hCLASC primer) for obtaining light
chain genes. The PCR product was treated with phenol, subjected to
ethanol precipitation and suspended in 10 .mu.L of TE buffer. The
base sequence of primer and conditions of PCR are shown below. In
the base sequence of a primer for obtaining light chain genes,
underline part represents NcoI site and AscI site.
TABLE-US-00004 5' primer .kappa.1-.kappa.6 hVK1a (SEQ ID NO: 411):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCCGACATCCAGATGACCCA GTCTCC hVK2a
(SEQ ID NO: 412): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
GATGTTGTGATGACTC AGTCTCC hVK3a (SEQ ID NO: 413):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC GAAATTGTGTTGACGC AGTCTCC hVK4a
(SEQ ID NO: 414): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
GACATCGTGATGACCC AGTCTCC hVK5a (SEQ ID NO: 415):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC GAAACGACACTCACGC AGTCTCC hVK6a
(SEQ ID NO: 416): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
GAAATTGTGCTGACTC AGTCTCC 5' primer .lamda.1-.lamda.6 hVL1 (SEQ ID
NO: 417): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGTCTGTGTTGACGC
AGCCGCC hVL2 (SEQ ID NO: 418): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
CAGTCTGCCCTGACTC AGCCTGC hVK3a (SEQ ID NO: 419):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC TCCTATGTGCTGACTC AGCCACC hVL3b
(SEQ ID NO: 420): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
TCTTCTGAGCTGACTC AGGACCC hVL4 (SEQ ID NO: 421):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CACGTTATACTGACTC AACCGCC hVL5
(SEQ ID NO: 422): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
CAGGCTGTGCTCACTC AGCCGCC hVL6 (SEQ ID NO: 423):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC AATTTTATGCTGACTC AGCCCCA
3'-primer hCKASC (SEQ ID NO: 424):
TCGACTGGCGCGCCGAACACTCTCCCCTGTTGAAGCTCTTTGTG 3'-primer HCLASC (SEQ
ID NO: 425): TCGACTGGCGCGCCGAACATTCTGTAGGGGCCACTGTCTTCTC
Conditions of PCR
TABLE-US-00005 [0741] cDNA 2 .mu.L 10 .times. buffer # 1 (attached
to KOD) 10 .mu.L dNTP mix (2.0 mM) 10 .mu.L 25 mM MgCl2 4 .mu.L 5'
side primer (100 pmol/.mu.L) 1 .mu.L 3' side primer (100
pmol/.mu.L) 1 .mu.L sterilized MilliQ 71 .mu.L
[0742] KOD DNA polymerase (TYOBO CO LTD., 2.5 U/mL) 1 .mu.L
[0743] 35 cycles, each cycle includes 94.degree. C. for one minute,
55.degree. C. for two minutes and 74.degree. C. for one minute
2-2-1 Incorporation of Light Chain Gene into Phagemid
[0744] The PCR product obtained in 1 was treated with a restriction
enzyme in the following conditions.
TABLE-US-00006 PCR product 10 .mu.L 10 .times. NEB4 (attached to
AscI) 5 .mu.L Sterilized MilliQ 33 .mu.L AscI (NEB, 10 U/.mu.L) 1
.mu.L NcoI (TAKARA SHUZO, 10 U/.mu.L) 1 .mu.L
[0745] After the reaction at 37.degree. C. for one hour and at
50.degree. C. for one hour, 10 .mu.L of the reacted product was
subjected to agarose gel electrophoresis and 600 bp band was cut
out to be purified by using geneclean II kit (Funakoshi
Corporation). Similar to the PCR product, restriction
enzyme-treated pscFvCA9-E8VHdVLd was purified by using geneclean II
kit and reacted with the restriction enzyme-treated PCR product at
16.degree. C. for four hours to overnight in the following
conditions, thereby carrying out ligation.
TABLE-US-00007 restriction enzyme-treated pscFvCA9-E8VHdVLd 2 .mu.L
restriction enzyme-treated PCR product 1 .mu.L 10 .times. ligation
buffer 1.5 .mu.L (attached to T4 DNA ligase) 10 mM ATP 1.5 .mu.L
sterilized MilliQ 8 .mu.L T4 DNA Iigase (TAKARA SHUZO 10 U/.mu.L) 1
.mu.L
2-2-2 Introduction of Phagemid into E. coli
[0746] The obtained ligated DNA was used so as to transform E. coli
DH12S as follows. That is to say, ligated DNA was subjected to
ethanol precipitation once, and dissolved in 3 .mu.L of 1/5 TE (TE
that was 5-fold diluted with sterilized MilliQ). 1.5 .mu.L of them
was suspended in 20 .mu.L of competent cell DH12S (GIBCO BRL),
which was subjected to electroporation in the following
conditions.
TABLE-US-00008 Electroporator Cell-Porator (Cat. series 1600),
product of BRL Setting conditions; voltage booster 4 k.OMEGA.
capacitance 330 .mu.F DC volts Low.OMEGA. charge rate Fast
[0747] The above-mentioned transformed E. coli was planted on a
transformation medium (SOB) (2 mL) and shaking cultured at
37.degree. C. for one hour. Then, a part of the cultured product
was planted on agar medium (Amp plate) and a remaining part was
cultured in a 2.times.TY medium containing 0.1% glucose and 100
.mu.g/mL ampicillin to form glycerine stock. The agar medium was
incubated at 30.degree. C. and growing colony was separated by
picking by a picker. A plasmid was prepared, respectively. Then,
the light chain gene and the base sequence were examined.
[0748] SOB medium: to 950 mL of purified water, the following
components were added and shaken so as to be dissolved completely.
Thereafter, 250 mM KCl solution (10 mL) was added so as to adjust
to pH 7.0 with 5N NaOH. Purified water was added to adjust to 1000
mL, then sterilized for 20 minutes in the autoclave. Immediately
before the use, 5 mL of 2M sterilized MgCl.sub.2 was added.
TABLE-US-00009 bacto-tryptone 20 g bacto-yeast extract 5 g NaCl 0.5
g
[0749] 2.times.YT medium: to 900 mL of purified water, the
following components were added and shaken so as to be dissolved
completely. Thereafter, 5 N NaOH was added so as to adjust to pH
7.0 with 5N NaOH. Purified water was added to adjust to 1000 mL,
then sterilized for 20 minutes in the autoclave and used.
TABLE-US-00010 bacto-tryptone 16 g bacto-yeast extract 10 g NaCl 5
g
[0750] The other reagents were purchased form the following
suppliers.
(Manufacture/Product name are described in this order)
SIGMA/ampicillin sodium
Wako Pure Chemical/phenol
SIGMA/BSA
[0751] DIFCO/2.times.YT medium Wako Pure Chemical/kanamycin sulfate
nacalai tesque/polyethylene glycol 6000 nacalai tesque/Tween 20
KATAYAMA CHEMICAL/NaCl
Wako Pure Chemical/IPTG
[0752] Wako Pure Chemical/skim milk Wako Pure Chemical/sodium
azide
Wako Pure Chemical/triethylamine
[0753] Wako Pure Chemical/hydrogen peroxide Wako Pure Chemical/OPD
tablet
Wako Pure Chemical/ethanol
[0754] The above-mentioned operation is carried out with respect to
all of .kappa.1, .kappa.2, .kappa.3, .kappa.4, .kappa.5, and
.kappa.6, as well as .lamda.1, .lamda.2, .lamda.3a, .lamda.3b,
.lamda.4, .lamda.5, .lamda.6, .lamda.7, .lamda.8, .lamda.9, and
.lamda.10 are operated so as to confirm whether or not the intended
clones are obtained. Then, for example, .kappa.1 and .kappa.2,
clones in each group, were mixed so that the ratio becomes near the
frequency of use. The rate of expression of each group of these
light chains in an actual living body is already known. These gene
clones amplified by PCR method and incorporated into a vector are
mixed so that the ratio becomes near the frequency of use. Thus, VL
library was obtained. Constituent ratio in each family in VL
library is shown below.
[Table I]
TABLE-US-00011 [0755] TABLE 1 v.kappa. Usage Constitutive
Constitutive frequency in ratio in VL ratio in family vivo (%)*
library (%) KL200 (%) V.kappa.1 39 37 30.7 V.kappa.2 12 12 19.8
V.kappa.3 36 35 33.7 V.kappa.4 12 12 10.9 V.kappa.5 1 2 5.0
V.kappa.6 --** 2*** 0.0 *Griffith AD et al. EMBO J. (1994) 13,
3245-60. **Published data is not shown ***equal amount of cDNA
produced with primer VK6-2 and cDNA produced with primer VK6-3 were
mixed.
[Table 2]
TABLE-US-00012 [0756] TABLE 2 V.lamda. Usage Constitutive
Constitutive frequency in ratio in VL ratio in family vivo (%)*
library (%) KL200 (%) V.lamda.1 43 41 34.1 V.lamda.2 15 .sup.
15*.sup.3 15.2 V.lamda.3 34 .sup. 32*.sup.4 25.3 V.lamda.4 0 .sup.
1.6*.sup.5 0.0 V.lamda.5 0 .sup. 1.0*.sup.6 11.1 V.lamda.6 0 1.0
14.1 V.lamda.7 6 6 0.0 V.lamda.8 1 1 0.0 V.lamda.9 1 1 0.0
V.lamda.10 --*.sup.2 1 0.0 *Griffith AD et al. EMBO J. (1994) 13,
3245-60. *.sup.2Published data is not shown *.sup.3cDNA produced
with primer VL2 (5%) and cDNA produced with primer VL2-2 (10%) were
mixed. *.sup.4cDNA produced with primer VL3a-2 (17%) and cDNA
produced with primer VL3b (15%) *.sup.5cDNA produced with primer
VL4a (0.5%), cDNA produced with primer VL4b (0.5%) and cDNA
produced with primer VL4c (0.5%) were mixed. *.sup.6cDNA produced
with primer VLSabde (0.5%) and cDNA produced with cDNA (0.5%) were
mixed.
3. Production of Combinatorial Library of Light Chain Gene Library
and Heavy Chain Gene Library (scFv Antibody Gene Library)
3-1-1 Isolation of Immunoglobulin Heavy Chain Gene Using PCR
[0757] By the procedure similar to 2-1, cDNA was prepared by using
cord blood, bone marrow fluid, and lymphocyte of peripheral blood
as well as a human .mu. primer (below-mentioned primer, 634) from
the tonsil or random hexamer. By using this cDNA as a template, a
mixture of equal amount of 5' primer (VH1 to VH7) and 3' primer
(four kinds of human JH primers are mixed in equal amount,
below-mentioned primers 697 to 700) for obtaining a human antibody
heavy chain gene, or human u primer (below-mentioned primer 634)
were subjected to PCR. In Table, underlined parts show the SfiI
site. Since hVH2a did not correspond to a germ line VH2 family,
VH2a-2 was newly designed. Furthermore, since hhVH4a did not
correspond to the entire VH4 family, hVH4a-2 was newly designed.
Also, VH5a did not correspond to a germ line VH5 subfamily, VH5a-2
was newly designed. Furthermore, as a primer corresponding to VH7,
hVH7 was designed. These were also subjected to gene amplification
and incorporated into pscFvCA-E8VHd. Then, as to the obtained
genes, the base sequence was determined. Since the sequence of
hVH5a-2 is extremely similar to that of hVH1a and it is expected
that the gene product similar to that amplified with hVH1a, this
was not used. The PCR products were subjected to phenol treatment
and then ethanol precipitation, and thereafter suspended in 10
.mu.L of TE buffer.
TABLE-US-00013 634 hum .mu. CH1R (SEQ ID NO: 426):
ATGGAGTCGGGAAGGAAGTC Primers used for amplification of each VH
family Human VH primer, SfiI site is underlined. 628 hVH1a (SEQ ID
NO: 427): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTGCAGCTGGTGC
AGTCTGG 629 hVH2a (SEQ ID NO: 428):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTCAACTTAAGGG AGTCTGG 630
hVH3a (SEQ ID NO: 429): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
GAGGTGCAGCTGGTGG AGTCTGG 631 hVH4a (SEQ ID NO: 430):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTGCAGCTGCAGG AGTCGGG 632
hVH5a (SEQ ID NO: 431): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
CAGGTGCAGCTGTTGC AGTCTGC 633 hVH6a (SEQ ID NO: 432):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTACAGCTGCAGC AGTCAGG 629-2
hVH2a-2 (SEQ ID NO: 433): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
CAGRTCACCTTGAAGG AGTCTGGTCC 631-2 hVH4a-2 (SEQ ID NO: 434):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTGCAGCTACAGC AGTGGGG 632-2
hVH5a-2 (SEQ ID NO: 435): GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC
GAGGTGCAGCTGGTGC AGTCTGG 712 hVH7 (SEQ ID NO: 436):
GTCCTCGCAACTGCGGCCCAGCCGGCCATGGCC CAGGTGCAGCTGGTGC AATCTGGGTCTGAGT
Human JH primer, BstPI and XhoI sites underlined. 697 hJH1-2 (SEQ
ID NO: 437): GGTGGAGGCACTCGAGACGGTGACCAGGGTGC 698 hJH3 (SEQ ID NO:
438): GGTGGAGGCACTCGAGACGGTGACCATTGTCC 699 hJH4-5 (SEQ ID NO: 439):
GGTGGAGGCACTCGAGACGGTGACCAGGGTTC 700 hJH6 (SEQ ID NO: 440):
GGTGGAGGCACTCGAGACGGTGACCGTGGTCC
TABLE-US-00014 cDNA 2 .mu.L 10 .times. buffer # 1 (attached to KOD)
10 .mu.L dNTP mix (2.0 mM) 10 .mu.L 25 mM MgCl2 4 .mu.L 5' primer
(100 pmol/(.mu.L) 1 .mu.L 3' primer (100 pmol/.mu.L) 1 .mu.L
sterilized MilliQ 71 .mu.L KOD DNA polymerase (TYOBO CO LTD., 2.5
U/.mu.L) 1 .mu.L
[0758] PCR conditions: 35 cycles, each cycle includes 94.degree. C.
for one minute, 55.degree. C. for two minutes and 74.degree. C. for
one minute
3-1-2 Production of Heavy Chain Gene Library
[0759] The PCR product obtained in 3-1-1 was treated with a
restriction enzyme in the following conditions.
TABLE-US-00015 PCR product 10 .mu.L 10 .times. K buffer NEB4
(TAKARA SHUZO) 5 .mu.L Sterilized MilliQ 33 .mu.L SfiI (NEB, 10
U/.mu.L) 1 .mu.L XhoI (TAKARA SHUZO, 12 U/.mu.L) 1 .mu.L
[0760] After the reaction at 37.degree. C. for two hours, 10 .mu.L
of the reacted product was subjected to agarose electrophoresis and
400 bp band was cut out to be purified by using geneclean II kit
(Funakoshi Corporation). Similar to the PCR product, restriction
enzyme-treated pscFvCA-E8VHd was purified by using geneclean II kit
and reacted with the restriction enzyme-treated PCR product at
16.degree. C. for four hours to overnight in the following
conditions, thereby carrying out ligation.
TABLE-US-00016 restriction enzyme-treated pscFvCA-E8VHd 2 .mu.L
restriction enzyme-treated PCR product 1 .mu.L 10 .times. ligation
buffer 1.5 .mu.L (attached to T4 DNA ligase) 10 mM ATP 1.5 .mu.L
sterilized MilliQ 8 .mu.L T4 DNA ligase (TAKARA SHUZO 10 U/.mu.L) 1
.mu.L
3-1-3 Introduction of Phagemid into E. coli
[0761] The obtained DNA was transformed into E. coli DH12S.
Specifically, DNA was subjected to ethanol precipitation once, and
dissolved in 3 .mu.L of 1/5 TE (TE that was 5-fold diluted with
sterilized MilliQ). 1.5 .mu.L of them was suspended in 20 .mu.L of
competent cell DH12S (GIBCO BRL), which was subjected to
electroporation.
TABLE-US-00017 Electroporator Cell-Porator (Cat. series 1600),
product of BRL Setting conditions; voltage booster 4 k.OMEGA.
capacitance 330 .mu.F DC volts Low.OMEGA. charge rate Fast
[0762] The above-mentioned transformed E. coli was planted on a
transformation medium (SOB) (2 mL) and shaking cultured at
37.degree. C. for one hour. Then, a part of the cultured product
was planted on agar medium (Amp plate) and a remaining part was
cultured in a 2.times.YT medium containing 0.1% glucose and 100
.mu.g/mL ampicillin to form glycerine stock. The agar medium was
incubated at 30.degree. C. and growing colony was separated by
picking by a picker. A plasmid was prepared, respectively. Then,
the heavy chain gene and the base sequence were examined. All of
the VH1 to VH7 were treated in the same way to confirm whether or
not the target clone was obtained. These clones of each group
(family) were mixed so that the ratio was near the use frequency in
vivo. Thus, VH library was produced. The constitution ratio of each
family in the VH library is shown below.
[Table 3]
TABLE-US-00018 [0763] TABLE 3 Usage Constitutive frequency in ratio
in VH family vivo (%)* library (%) VH1 25 29** VH2 6.6 7 VH3 40 40
VH4 19 19*** VH5 5 --** VH6 3.8 4 VH7 1.2 2 *Griffith AD et al.
EMBO J. (1994) 13, 3245-60. **Actually, since VH1 and VH5 are
amplified with the same primer, they cannot be counted separately.
***cDNA produced with VH4 primer and cDNA produced with VH4-2
primer were mixed in this ratio.
3-2 Production of Combinatorial Gene Library
[0764] VH library (200 .mu.g) was digested with HindIII and XhoI
under the following conditions and heavy chain gene is cut out and
purified by using geneclean II kit.
TABLE-US-00019 VH library 200 .mu.g 100 .mu.L 10 .times. K buffer
(TAKARA SHUZO) 40 .mu.L sterilized MilliQ 205 .mu.L HindIII (TAKARA
SHUZO40 U/.mu.L) 30 .mu.L XhoI (TAKARA SHUZO50 U/.mu.L) 25
.mu.L
[0765] A vector pscFvCA9-E8VHdVLd in which a VL library had been
inserted was was digested with HindIII and XhoI under the following
conditions, and a fragment containing a light chain gene was
purified by using geneclean II kit.
TABLE-US-00020 pscFvCA9-E8VHdVLd in which a VL 100 .mu.g, 100 .mu.L
library had been inserted 10 .times. K buffer (TAKARA SHUZO) 40
.mu.L sterilized Milli-Q 230 .mu.L HindIII (TAKARA SHUZO 40
U/.mu.L) 15 .mu.L XhoI (TAKARA SHUZO 50 U/.mu.L) 15 .mu.L
[0766] Next, a VH gene library fragment and a pscFvCA9-E8VHdVLd
vector into which a light chain gene has been inserted were reacted
at 16.degree. C. overnight in the following conditions so as to be
ligated.
TABLE-US-00021 restriction enzyme-treated VH library fragment 10
.mu.g 50 .mu.L pscFvCA9-E8VHdVLd containing restriction 40 .mu.g 50
.mu.L enzyme-treated VL library fragment 10 .times. ligation buffer
(attached to T4 DNA ligase) 100 .mu.L 10 mM ATP 100 .mu.L
Sterilized MilliQ 670 .mu.L T4 DNA ligase (TAKARA SHUZO 10 U/.mu.L)
30 .mu.L
[0767] The DNA in which the reaction had been completed was used to
transform E. coli DH12S. Specifically, DNA was subjected to ethanol
precipitation once, and dissolved in 30 .mu.L of 1/5 TE (TE 5-fold
diluted with sterilized MilliQ). This was suspended in 500 .mu.L of
competent cell DH12S (GIBCO BRL), and electroporation was carried
out.
TABLE-US-00022 Electroporator Cell-Porator (Cat. series 1600),
product of BRL Setting conditions; voltage booster 4 k.OMEGA.
capacitance 330 .mu.F DC volts Low.OMEGA. charge rate Fast
[0768] The above-mentioned transformed E. coli was planted on a
transformation medium (SOB) (12 mL) and shaking cultured at
37.degree. C. for one hour. Then, a part of the cultured product
was planted on agar medium (Amp plate) and a remaining part was
cultured in a 2.times.YT medium (500 mL) containing 0.1% glucose
and 100 .mu.g/mL ampicillin to form glycerine stock. The agar
medium was incubated at 30.degree. C. and the number of clones were
estimated from the number of growing colonies. 8.5.times.10.sup.10
clones were obtained.
4. Production of scFv-CL Antibody Phage Library from scFv-CL
Antibody Gene Library
[0769] To 16 of 5-liter flasks containing 300 mL of 2.times.YT
medium to which 1% glucose and 100 .mu.g/mL ampicillin had been
added, 2.5 mL of AIMS-5 suspension was added and shaking cultured
at 37.degree. C. Every one hour, the absorbance at the wavelength
of 600 nm was measured and the culture solution was proliferated
until the absorbance became 1.0. To the culture solution, 12 mL
each of helper phage solution (M13KO7) was added for each flask so
as to infect the helper phage, culture at 37.degree. C. for two
hours. Thus, phage infected DH12S was obtained.
[0770] To 24 of 5-L flasks, 2.times.YT medium (600 mL), 100
.mu.g/mL ampicillin (0.6 mL), 50 .mu.g/m 38 L kanamycin (0.8 mL),
and helper phage infected DH12S (200 mL) were added and shaking
cultured at 37.degree. C. for 20 hours.
[0771] The bacterial cells were centrifuged at 8000 rpm at
4.degree. C. for 10 minutes, and supernatant was recovered. 4 L of
20% polyethylene glycol/2.5M NaCl was added to the supernatant,
after it was quietly stirred for about 20 minutes, centrifuged at
8000 rpm at 4.degree. C. for 20 minutes. The precipitate was
dissolved in 1 L of PBS, 200 mL of 20% polyethylene glycol/2.5M
NaCl was added thereto, after it was quietly stirred for about 20
minutes, and centrifuged at 8000 rpm at 4.degree. C. for 20
minutes. The supernatant was discarded and further, centrifuged at
8000 rpm at 4.degree. C. for 3 minutes, and the precipitate was
recovered. The precipitate was dissolved in PBS to which 0.05%
NaN.sub.3 was added, after it was centrifuged at 1000 rpm at
4.degree. C. for 15 minutes and the supernatant was recovered,
further, centrifuged at 8000 rpm at 4.degree. C. for 3 minutes and
the supernatant was recovered.
[0772] The titer of the recovered phage solution was checked as
followings: the phage solution was diluted with PBS in 10.sup.6,
10.sup.7 and 10.sup.8-fold, out of these, 10 .mu.L was infected
with 990 .mu.L of DH12S, cultured at 37.degree. C. for one hour.
100 .mu.L of them was plated on LBGA plate and cultured at
30.degree. C. for 18 hours. The titer of the stock solution before
dilution was calculated by counting the number of colonies. The
stock solution of the phage solution was suspended in PBS
containing 0.05% NaN.sub.3 so as to be 2.times.10.sup.14/mL.
5. Obtaining of Antibody Clone Specific to Cancer Cell
5-1 Phage Antibody Screening Using Cancer Cell Line
[0773] Phage antibodies of various cancer cell lines or clinical
specimens were isolated by the following procedure. Kinds of used
cell lines are described below. The culture conditions of the cell
line are show in Table of FIG. 38.
[0774] pancreatic cancer cell lines PANC-1, MIA-Paca2
[0775] kidney cancer cell lines CCFRC1, Caki-1, CCFRC1, Caki-1,
ACHN
[0776] ovarian cancer cell lines KF28, RMG-1, RMG-2, SKOv3
[0777] stomach cancer cell lines SNU-5, MKN45, NCI-N87
[0778] lung squamous cell carcinoma lines RERF-LC-AI, EBC1
[0779] pulmonary adenocarcinoma cell lines Calu-3, NCI-H441, A549,
PC14
[0780] hepatic cell carcinoma cell lines HepG2, OCTH, Hep3B
[0781] hepatic cell carcinoma clinical specimen (HCV positive),
[0782] intrahepatic bile duct cell carcinoma cell line RBE
[0783] stomach cancer cell lines SNU5, MKN45, NCI-N87
[0784] large bowel cancer cell lines CW2, CaCo2
[0785] acute myelocytic leukemia, AML clinical specimen
[0786] An adherent cell line group in 6 well plate (Falcon 3516)
and a suspended cell line such as ATL-derived cell line in
suspended culture flask (70 ml (slant neck)), which had been
cultured in a medium (RPMI-1640: Sigma-Aldrich, 10% fetal calf
serum, 1% penicillin-streptomycin solution) in a CO.sub.2 incubator
at 37.degree. C., were used.
[0787] The adherent cell line was dissociated from culture dish
with 2 mg/ml collagenase I (Gibco BRL)/cell dissociation buffer
(Gibco BRL), and then recovered with 10% FBS/DMEM. On the other
hand, the suspended cells were, as they were, centrifuged
(400.times.g, 4.degree. C., two minutes) to remove the medium
once.
[0788] After such operation, each cell was washed with 1% BSA,
0.05% NaN.sub.3/PBS (BSA solution) and centrifuged (400.times.g,
4.degree. C., two minutes) to remove the supernatant.
[0789] Cells from the clinical specimen derived from clinical
tissue material prepared in 6 well plate (Falcon 3516), which had
been cultured in a medium (RPMI-1640: Sigma-Aldrich, 10% fetal calf
serum, 1% penicillin-streptomycin solution) in a CO.sub.2 incubator
at 37.degree. C., were used.
[0790] Cells were washed with cooled PBS and 4.times.10.sup.7 of
cells were used for screening. This was mixed with
1.times.10.sup.13 cfu of human antibody phage library, so that the
final concentration of the reaction solution was made to be 1%
BSA-0.1% NaN.sub.3/MEM and the volume was made to be 1.6 ml. The
reaction was carried out while rotating slowly at 4.degree. C. for
four hours. After the reaction was completed, the reaction solution
was divided into two parts and each part was stratified on 0.6 ml
of organic solution (dibutyl phtalate cycloheximide 9:1) and
subjected to centrifugation at centrifugal force of 3000 rpm by
using a micro-centrifugal machine for two minutes, so that cells
were allowed to precipitate at the bottom of the tube. From each
tube, the solution was discarded and cells were suspended in 0.7 ml
of 1% BSA/MEM, stratified on 0.7 ml of organic solvent and
subjected to centrifugation. This operation was repeated again.
Then the solution was discarded and cells were suspended in 0.3 ml
PBS, frozen with liquid nitrogen and melted at 37.degree. C.
[0791] This was infected with 20 ml of E. coli DH12S (OD 0.5) for
one hour, the part of it was plated on an Ampicillin plate and the
titer of the collected phage was calculated. Phage infected E. coli
was cultured over night in 600 ml of 2.times.YTGA culture medium
(2.times.YT, 200 .mu.g/ml ampicillin sulfate, 1% glucose) at
30.degree. C. overnight. The cultured product (10 ml) that had been
cultured over night was mixed with 200 ml of 2.times.YTA culture
medium (2.times.YT, 200 .mu.g/ml ampicillin sulfate) and cultured
at 37.degree. C. for 1 hour. Thereafter, helper phage .kappa.07
(1.times.10.sup.11) was placed and cultured at 37.degree. C. for
1.5 hour. Then, 800 ml of 2.times.YTGAK (2.times.YT, 200 .mu.g/ml
ampicillin sulfate, 0.05% glucose, 50 .mu.g/ml kanamycin) was
placed and cultured over night at 30.degree. C. This was
centrifuged at 8000 rpm for ten minutes so as to prepare 1 l of
supernatant. To this, 200 ml of PEG solution (20% polyetyleneglycol
6000, 2.5M NaCl) was mixed and agitated sufficiently. Thereafter,
the mixture was centrifuged at 8000 rpm for 10 minutes so as to
precipitate phage. This was suspended in 10 ml of PBS/0.05%
NaN.sub.3 and the part of it was used so as to examine the number
of infected E. coli. This is the phase of the I st screening.
[0792] For the 2nd screening, 2.times.10.sup.7 of cells and
1.times.10.sup.10 cfu of the 1st screening phages were used, so
that the volume of the reaction solution was made to be 0.8 ml. The
reaction solution was 1% BSA-0.1% NaN.sub.3/MEM and the entire
scale was carried out equal to that of the 1st screening.
[0793] The 3rd screening was carried out in the same conditions as
those of the 2nd screening except that 1.times.10.sup.9 cfu of 2nd
phages were used.
[0794] When the recovering rate of the phages is increased, the
screening round is stopped at the time. When the recovering rate is
not increased, the 4th screening or later are carried out in the
same manner by using the phage recovered immediately before round
and by using 1.times.10.sup.9 cfu of phages.
[0795] The screening of various cell lines was carried out by the
same method as that of the screening mentioned above.
5-2 Selection of Antibody Clone
[0796] In the screening of HepG2 as an example, because the
recovering rate of HepG2 was increased in the 3rd screening (FIG.
9), it was judged that HepG2 cell specific antibody clone was
concentrated in this stage, and several hundreds clones were picked
up. Next, when the base sequence of H-chain portions of these
positive clones was analyzed, antibodies obtained by removing the
overlap from the kinds of base sequences were classified. These
were examined for expression. Furthermore, expression positive
clones were selected by the following procedures.
6. Base Sequence Determination of Antibody Clone
[0797] E. coli, infected with antibody phage, obtained by screening
was diluted and plated on a nutrient agar medium containing 100
Hg/ml of ampicillin. The obtained colonies were picked up and
cultured in 2.times.YTGA culture medium at 30.degree. C. overnight.
DNA was extracted by using KURABO PI-50 and the base sequence was
determined by a dideoxy method. The overlapped clones having the
same base sequence were removed. Furthermore, this culture medium
cultured overnight (0.05 ml) was plated on 1.2 ml of 2.times.YTAI
(2.times.YT, 200 .mu.g/ml ampicillin sulfate, 0.5 mM IPTG) and
cultured overnight at 30.degree. C., centrifuged by using a
micro-centrifugal machine at 15000 rpm for 5 minutes, and
supernatant was obtained.
7. Confirmation of Expression of Antibody Clone
7-1 Selection of Antibody Clone
[0798] Since the antibody was expressed as cp3 fused protein, the
expression using the protein was examined. That is to say, firstly,
the supernatant obtained in the previous paragraph was reacted in
Maxisorp (NUNC) at 37.degree. C. for two hours, liquid was
discarded, and blocking was carried out by reacting 5%
BSA/PBS/0.05% NaN.sub.3 at 37.degree. C. for two hours. The liquid
was discarded and a rabbit anti-cp3 antibody (Medical &
Biological Laboratories Co., Ltd.) that had been diluted 5000-fold
with 0.05% Tween/PBS was reacted at room temperature for one hour,
followed by washing with PBS. Then, a HRP labeled goat anti-rabbit
IgG antibody (Medical & Biological Laboratories Co., Ltd.) that
had been diluted 2000-fold with 0.05% Tween/PBS was reacted at room
temperature for one hour, followed by washing with PBS. Then, 100
.mu.l of OPD solution was reacted at room temperature for 2 to 10
minutes, and the reaction was terminated by using 2N sulfuric acid,
and by using SPECTRAmax 340PC (Molecular Devices), the absorbance
at 492 nm of wavelength was measured.
[0799] In negative well in which the supernatant was not reacted
was made to be a control. It was judged that a control whose
absorbance did not become two times or more did not express. Such a
control was removed from the later analysis.
7-2 Preparation of Antibody Sample
[0800] 7-2-1 Production of cp Type Antibody Expression E. coli
[0801] E. coli (10 ml) infected with phage corresponding to
expressing antibody clones was introduced was plated on YTGA and
shaking cultured at 30.degree. C. one day and one night
(pre-culture solution). This was added to 4 l of YT 0.05GA and
cultured at 30.degree. C. When O.D. of the bacterial cells became
0.5, 4 ml of 1M IPTG was added and shaking cultured at 30.degree.
C. one day and one night. After the culture was terminated, the
bacterial cells were centrifuged by using a cooling centrifugal
machine at 10000 g, 4.degree. C. for 10 minutes. To the obtained
culture supernatant, an equal amount of saturated ammonium sulfate
aqueous solution was added and stirred at room temperature for one
hour. This solution was centrifuged by using a cooling centrifugal
machine at 10000 g, 4.degree. C. for 15 minutes, then supernatant
was discarded, the obtained precipitate was suspended in 20 ml of
PBS-NaN.sub.3 solution, centrifuged by using a cooling centrifugal
machine at 10000 g, 4.degree. C. for 5 minutes, and supernatant was
recovered. This was dialyzed with PBS one day and one night. To
this, a supernatant antibody cp3 mouse monoclonal antibody (Medical
& Biological Laboratories Co., Ltd.) that had been balanced
with 0.05% NaN.sub.3/PBS was chemically immobilized. Antibody
affinity column was produced by using sepharose beads. The
supernatant was naturally dropped, and the components that had not
reacted with beads were allowed to pass through the column. This
column was washed with 100 ml of PBS twice, washed with 0.1% Tween
20/PBS (30 ml) four times, and washed with 100 ml of PBS twice. To
this, 0.2M Glycine-HCl (pH 3, 4 ml) was slowly added three times
and the eluted component was recovered. Then, 3M Tris (80 .mu.l)
was added and neutralize (antibody solution). This was filtrated
through a MILLEX-GP 0.22 .mu.m filter, O.D. was measured, and the
yield of antibodies was calculated.
7-2-2 Production of pp Type Antibody Expressing E. coli
[0802] The obtained antibody clone is originally cp3 type clone.
This DNA was extracted by using KURABO PI-50, digested with a
restriction enzyme SalI, self reconnected, then, introduced into E.
coli DH 12S for transformation. Then, it was plated on a LBGA plate
and cultured at 30.degree. C. overnight at. The obtained E. coli
colonies were cultured in 2.times.YTGA overnight and a pp type
antibody expressing E. coli solution was obtained.
[0803] E. coli (10 ml) into which a plasmid expressing pp type
antibody clones was introduced was plated on YTGA and shaking
cultured at 30.degree. C. one day and one night (pre-culture
solution). This was added to 4 l of YT 0.05GA and cultured at
30.degree. C. When O.D. of the bacterial cells became 0.5, 4 ml of
1 M IPTG was added and shaking cultured at 30.degree. C. one day
and one night. After the culture was terminated, the bacterial
cells were centrifuged by using a cooling centrifugal machine at
10000 g, 4.degree. C. for 10 minutes. To the obtained culture
supernatant, an equal amount of saturated ammonium sulfate aqueous
solution was added and stirred at room temperature for one hour.
This solution was centrifuged by using a cooling centrifugal
machine at 10000 g, 4.degree. C. for 15 minutes, then supernatant
was discarded, the obtained precipitate was suspended in 20 ml of
PBS-NaN.sub.3 solution, centrifuged by using a cooling centrifugal
machine at 10000 g, 4.degree. C. for 5 minutes, and supernatant was
recovered. This was dialyzed with PBS one day and one night. To
this, 2 ml of IgG sepharose 6 Fast Flow (Amersham Biosciences)
balanced with 0.05% NaN.sub.3/PBS was added and reacted while
shaking at 4.degree. C. one day and one night. This mixture
solution was transferred to a column and naturally dropped. The
components that were not reacted with beads were allowed to pass
through the column. This column was washed with 100 ml of PBS
twice, washed with 0.1% Tween 20/PBS (30 ml) four times, and washed
with 100 ml of PBS twice. To this, 0.2M Glycine-HCl (pH 3, 4 ml)
was slowly added three times and the eluted component was
recovered. Then, 3M Tris (80 .mu.l) was added and neutralize
(antibody solution). This was filtrated through a MILLEX-GP 0.22
.mu.m filter, O.D. was measured, and the yield of antibodies was
calculated.
8. Reactivity to Various Cell Lines of Antibody Clone
8-1 FCM (Flow Cytometry) Analysis
[0804] The reactivity of various isolated antibody clones to
various cell lines was confirmed by FCM. Experiment operation was
as follows. Firstly, an adherent cell line in 6 well plate (Falcon
3516) and a suspended cell line such as ATL-derived cell line in
suspended culture flask (70 ml (slant neck)), which had been
cultured in a medium (RPMI-1640: Sigma-Aldrich, 10% fetal calf
serum, 1% penicillin-streptomycin solution) in a CO.sub.2 incubator
at 37.degree. C., were used.
[0805] i) Adherent cell line was dissociated from a culture plate
with 2 mg/ml collagenase I (Gibco BRL)/cell dissociation buffer
(Gibco BRL), and then recovered with 10% FBS/DMEM. On the other
hand, the suspended cells were, as they were, centrifuged
(400.times.g, 4.degree. C., two minutes) to remove the medium once.
After such operation, each cell was washed with 2.5% BSA, 0.05%
NaN.sub.3/PBS (BSA solution), suspended in 100 .mu.l of 2.5% normal
goat serum/BSA solution and stood still on ice for 30 minutes,
dispensed to 10.sup.6 cells/well, and then centrifuged
(400.times.g, 4.degree. C., two minutes) to remove the
supernatant.
[0806] ii-1) In the case of cp3 antibodies, they were added so that
the concentration became 5 .mu.g/ml and left on ice for one hour.
This was washed with a BSA solution once, then suspended in 100
.mu.l of 5 .mu.g/ml BSA solution of anti-cp3 mouse monoclonal
antibody (Medical & Biological Laboratories Co., Ltd.) and left
on ice for one hour. This was washed with a BSA solution once, then
suspended in 100 .mu.l of 5 .mu.g/ml BSA solution of Alexa 488
binding anti-mouse IgG goat antibody (Molecularprobe) and left on
ice for one hour. This was washed with BSA solution twice, and then
suspended in 500 .mu.l of BSA solution. To this solution, 50 .mu.l
of fixation solution (formaldehyde) was added and it was left for
10 minutes. Thereafter, 150 .mu.l of PBS was added, treated by
using Cell Strainer (Becton Dickinson), and then the fluorescence
intensity of the group of cells was analyzed by using FACScaliver
(FCM) (Becton Dickinson) ((1) to (3)).
[0807] ii-2) In the case of the pp type (protein A type)
antibodies, they were added so that the concentration became 5
.mu.g/ml and left on ice for one hour. This was washed with a BSA
solution once, then suspended in 100 .mu.l of 5 .mu.g/ml BSA
solution of Alexa 488 binding anti-mouse IgG goat antibody
(Molecularprobe) and left on ice for one hour. This was washed with
BSA solution twice, and then suspended in 500 .mu.l of BSA
solution. To this solution, 50 .mu.l of fixation solution
(formaldehyde) was added and it was left for 10 minutes.
Thereafter, 150 .mu.l of PBS was added, treated by using Cell
Strainer (Becton Dickinson), and then the fluorescence intensity of
the group of cells was analyzed by using FACScaliver (FCM) (Becton
Dickinson).
[0808] In the analysis, detection antibody was labeled with
fluorescent dye (Alexa 488, etc.) in advance. After sample
antibodies and cells were reacted, they were reacted with detection
antibodies. The difference in the antibody amount occurs depending
upon the amount of antigen existing on the surface of the cell, and
as a result, the fluorescence intensity became different. Thus, the
affinity with respect to the antigen existing on the surface of the
cells and the amount of antigen can be estimated. Furthermore, in
order to remove dead cells and debris, and the like, Forward
Scatter: FSC is expressed in X-axis and Side Scatter: SSC is
expressed in Y-axis, and a group of living cells (substantially the
same group because cultured cells were used) in data obtained by
dot plot expansion were gated, the fluorescence intensity only in
this gate was measured.
8-2 Production of Panel
[0809] From the results of FCM, a histogram showing the
relationship between the antibody binding amount and the number of
cells was formed. One-parameter histogram using the antibody
binding amount a parameter was drawn. The one-parameter histogram
is one of the display methods in the flow cytometry. The
one-parameter histogram is generally shown in a graph in which
X-axis represents one indicator (parameter) and Y-axis represents
the number of cells.
[0810] Typical examples of the results of FCM are shown in FIGS. 10
to 12. As shown in these figures, basically, the behavior of the
FCM becomes unique according to the combination of cells and
antibodies. FIGS. 10 and 11 show histogram (right) and cell
fluorescence cytology image (left), respectively, which show the
reactivity between the scFv antibody and the undifferentiated
malignant liver cancer cell line HLF obtained in the
above-mentioned method. In all the antibodies (five antibodies),
positive patterns are obtained but each has very unique shape of
peak. Such shapes of peaks are thought to reflect the uniqueness of
epitope of antigen. FIG. 12 shows a plurality of histograms
(antibodies to be used was different in each case) which are
overwritten. It is shown that the peak of each histogram has its
own unique shape. However, during the comprehensive FCM analysis,
an antibody group providing histogram having an extremely high
similarity as shown in FIGS. 13 to 15 are observed. Furthermore, as
shown in FIG. 16, an antibody group consistently providing
histogram having a high similarity regardless of cell lines to be
used in the FCM analysis was observed. FIG. 16 show comparison of
histograms obtained in three kinds of antibodies (035-234 antibody,
040-107 antibody, and 041-118 antibody). According to the later
investigation, it is determined that these three kinds of
antibodies recognize ALCAM.
[0811] FIG. 17 shows a method for classifying the antibody group
based on the results of the FCM analysis. That is to say regardless
of kinds of cells to be used, a plurality of antibodies having
similar behavior (shape of histogram) in the FCM analysis are shown
as the same group in a panel. Basically, a plurality of antibodies
having the same shape of histogram (peaks are overlapped when the
shapes are overwritten) are defined as one group. However, a
plurality of antibodies may be classified into groups on the basis
of the factors such as the median value, mode (peak value), and
kurtosis of the histogram.
[0812] A plurality of antibodies are classified based on the
above-mentioned technique. Firstly, the histograms obtained in the
antibody clones are overwritten for each cell line to be used, and
thereby the histograms are compared with each other. Thus,
similarly between the antibody clones and the reactivity between
antibody clones are obtained. Then, based on the similarity and the
reactivity, antibody clones are classified and summarized in table
(FIG. 18). Thus, eight antibody groups (in the description
hereinafter, groups are named 1, 2, 3, 4, 5, 6, 7, and 8
sequentially in this order) are obtained. In FIG. 18, information
on antigen identified later is also displayed. Each mark in Table
shows a shift amount relative from the histogram (reference
histogram) of the negative control antibody. Double circle mark
represents that the shift amount is 20 times or more (the peak
value of the is 20 times or more of the reference histogram); "o"
(circle mark) represents that the shift amount is 10 times or more;
".DELTA." (triangle mark) represents that the shift amount is 3
times or more; and "x" represents that the shift amount is less
than 3, respectively (an oblique line means no data is obtained).
The larger the shift amount is, the higher the reactivity is.
[0813] Next, by the following procedure, it is verified that
antigens of each antibody group in the produced panel are
common.
9. Identification of Protein (Antigen) Recognized by Antibody
Clone
9-1 Preparation of Solid Phase Antibody for Immunoprecipitation
[0814] Firstly, a pp type antibody solution was dialyzed with a
coupling buffer solution (0.1M NaHCO.sub.3--NaOH, pH 9). That is to
say, an antibody solution was enclosed with a dialysis membrane
(Snake Skin Pleated Dialysis Tubing 10,000 MWCO) and this was
allowed to be sunk in 1.5 L of the coupling buffer solution (0.1 M
NaHCO.sub.3--NaOH, pH 9) and stirred by using a stirrer at
4.degree. C. for two to three hours. Then, the buffer solution was
replaced with new one and dialyzed for two to three hours.
Thereafter, the buffer solution was replaced with new one again and
dialyzed one day and one night.
[0815] Next, activated CNBr-activated Sepharose 4B used for making
solid phase was adjusted. That is to say, CNBr-activated Sepharose
4B (Amersham Biosciences) was swollen with 1 mM HCl, then sucked by
using an aspirator. To this, 50 ml of coupling buffer solution was
added, stirred, and then sucked by using an aspirator. In this
sucked state, a coupling buffer solution was added.
[0816] An antibody was made to be solid phased as follows. That is
to say, to 5 mg antibody solution (10 ml), activated gel (1 ml) was
added to cause a reaction at room temperature for two hours. After
the reaction was terminated, the gel was transferred to a column
and washed with a coupling buffer solution (1 ml) ten times. The
presence of non-reacted antibodies was confirmed by measuring the
O.D. The solid phased gel was substituted by 0.2M Glycine-NaOH pH8
solution (5 ml) twice, the same solution (5 ml) was further added
and left at room temperature for two hours, this solution was
naturally dropped, to this, 0.2M Glycine-HCl (pH 3, 5 ml) was added
and substituted, the same solution (5 ml) was further added and
left for 5 minutes, and then naturally dropped. Finally, the column
was substituted by 20 ml of PBS, then naturally dropped, and 1%
NP40, protease inhibitor, and 0.05% NaN.sub.3/PBS were added, and
gel was recovered.
9-2 Biotin Label of Protein on Cell Membrane and Production of Cell
Lysate
[0817] Biotin labeling of the cultured liver cancer cell line was
carried out as follows. That is to say, cultured cells HLF that had
been cultured in five 15 cm-dishes were washed with PBS twice, and
collagenase I (GIBCO) whose concentration had been adjusted to 5
mg/ml by using a cell dissociation buffer (GIBCO) was added and
reacted in a CO.sub.2 incubator at 37.degree. C., so that cells
were liberated. Thereafter, cells were recovered in a culture
medium and washed with PBS(-) twice. Then, the number of cells was
counted by using a hemocytometer. The cells were suspended in
PBS(-) so that the counted number became about 5.times.10.sup.7/ml.
To this, an equal amount of EZ-Link Sulfo-NHS-LC-Biotinylation Kit
(PIERCE) was added so that the concentration had been adjusted to 1
mg/ml with PBS, left at room temperature for 30 minutes and then
washed with PBS twice.
[0818] The cell lysate of biotin labeled cells was adjusted as
follows. That is to say, to the above-mentioned biotin labeled
cells, 4 ml of lysis buffer (1% NP40/detergent base solution, the
composition of the detergent base solution: 20 mM HEPES, pH 8.0,
140 mM NaCl, protease inhibitor) was added and cells were
suspended. This suspension was placed and homogenized in a cooled
Dounce homogenizer. To the solution, 1/2 amount (2 ml) of a
detergent mix solution (1% NP40, tritonX-100, b-D-Maltoside,
n-Octyl b-D-Glucoside, n-Octyl b-D-Maltoside, n-Decyl
b-D-Maltoside, deoxycholic acid, each 0.5%/detergent base solution)
was added and mixed at 4.degree. C. for four hours. This solution
was centrifuged at 100,000 rpm for 30 minutes and filtrated through
MILLEX-GP 0.22 .mu.m filter.
9-3 Immunoprecipitation Reaction
[0819] Firstly, about 60 .mu.l parts (about 150 .mu.l solution
parts) of the solid-phased antibodies (hereinafter, referred to as
"antibody beads") were placed in a 2 ml-tube and 1/10 volume (about
15 .mu.l) of 4 mM biotin was added to the tube. A mixture of 0.5
culture dishs of lysate (600 .mu.l) and 60 .mu.l of biotin solution
was added to the tube and reacted while stirring at 4.degree. C.
for several hours. Then, the tube was centrifuged (5500 g, one
minute, 4.degree. C.) and supernatant was removed. To this, 800
.mu.l of washing biotin/lysis-T buffer (0.5 mM biotin, 0.1% Tween
20/PBS) was added and mixed while falling two or three times, then
the tube was centrifuged (5500 g, one minute, 4.degree. C.), and
supernatant was removed. This washing operation was carried out
again, then 30 .mu.l of citric acid solution (50 mM citric acid, pH
2.5) for elution was added to the antibody beads and stirred. Then,
the tube was centrifuged (5500 g, 1 min, 4.degree. C.) and
supernatant was recovered. To the remaining antibody beads, 30
.mu.l of citric acid solution for elution was added and stirred.
The tube was centrifuged (5500 g, 1 min, 4.degree. C.) and
supernatant was recovered. This elution operation was repeated
further three times, and a sample solution was recovered and 3M
Tris was added to the solution for neutralization. This sample was
migrated by SDS-PAGE so as to confirm the band by silver staining.
At the same time, this sample was subjected to western blotting by
using streptavidin-HRP (Anti-Streptavidin, IgG Fraction, Conjugated
to Peroxidase CORTEX biochem) so as to detect a band of the biotin
membrane protein.
9-4 Mass Spectrometry of Cut-Out Band
9-4-1 Trypsin Digestion in Gel
[0820] A portion corresponding to detected membrane protein was
digested with trypsin in a gel and peptide was recovered. SDS
polyacrylamide gel electrophoresis was carried out in accordance
with a usual method and a band that had been obtained by staining
with Coomassie Brilliant Blue was cut out. This was soaked in 200
mM ammonium bicarbonate 50% acetonitrile solution, shaken at
37.degree. C. for 45 minutes. Then, the solution was discarded and
the operation was repeated twice, thereby removing the Coomassie
Brilliant Blue. This gel was dried under reduced pressure, and 4
.mu.l of trypsin (20 .mu.g/ml) dissolved in 40 mM ammonium
bicarbonate (pH 8.1)-10% acetonitrile was added per unit area
(mm.sup.2) of gel slice, and left at room temperature for one hour
and sufficiently infiltrated. To this, a trypsin solution was added
in an amount that was 25 times as much as the previously added
amount, and left at 37.degree. C. for 18 hours. This was filtrated
by a tube having a filter whose power size was 0.22 .mu.m, and
peptide in which an antigen had been cut with trypsin was
recovered.
9-4-2 Identification of Antigen by Mass Spectrometry
[0821] A specimen obtained by in-gel trypsin digestion was
subjected to HPLC linked with an electrospray ionization type ion
trap quadrupole mass spectrometer. From the reversed phase
chromatography column of HPLC, according to the change of linear
concentration gradient of 0% to 80% acetonitrile containing 0.1%
TFA, each peptide that had been eluted sequentially depending upon
the hydrophobic property was ionized by an electrospray method. The
mass of each peptide was analyzed.
[0822] At the same time, the mass of limited digested product of
each peptide generated by collision with helium atoms placed in the
middle of the fight route of ions was analyzed. When one amino acid
is removed by limited digestion, since ion that is smaller by a
part of the mass of the removed amino acid is observed, the kind of
the removed amino acid can be identified according to the
difference in mass. Furthermore, another amino acid is removed,
since ion that is smaller by a part of the mass of the removed
amino acid is observed, the kind of the removed amino acid can be
identified according to the difference in mass. By proceeding the
same analysis of the experimental data, an inner amino acid
sequence can be determined. The set of the inner sequence of the
obtained amino acid was retrieved by using a published amino acid
sequence database and antigen was identified. As a result, as shown
below, antigen of each antibody clone was identified and it is
confirmed that the antibodies in the same group have the common
antigen. The identification results was confirmed because the total
amount of the identified protein that had been analogized from the
amino acid sequence was not contradictory to the experimental data
of the molecular weight of the SDS polyacrylamide electrophoresis
of antigen before carrying out the trypsin digestion.
[0823] Antigen of antibodies belonging to group 1: HER1 (also known
as: ErbB1, c-erbB-1, EGFR (Epidermal Growth Factor Receptor),
v-erbB)
[0824] Antigen of antibodies belonging to group 2: HER-2 (also
known as: ErbB2, c-erbB-2, neu)
[0825] Antigen of antibodies belonging to group 3: CD46 antigen
(also known as: MCP (membrane cofactor protein), gp45-70, HuLY-m5,
measles virus receptor, MIC10, TLX-B antigen, TRA2, trophoblast
leucocyte common antigen, trophoblast-lymphocyte cross-reactive
antigen)
[0826] Antigen of antibodies belonging to group 4: ITGA3 (integrin
alpha3) (also known as: alpha3beta1 Epiligrin Receptor, alpha3beta1
Integrin, Epiligrin Receptor, CD49c, VLA-3, Gap b3, Galactoprotein
b3, Laminin-5 Receptor)
[0827] Antigen of antibodies belonging to group 5: ICAM1
(Intercellular adhesion molecule-1) (also known as: Intercellular
Adhesion Molecule 1, CD54 Antigen)
[0828] Antigen of antibodies belonging to group 6: ALCAM (Activated
leukocyte cell adhesion molecule) (also known as: KG-CAM, CD166
Antigen, CD6 Ligand,
Activated Leukocyte Cell Adhesion Molecule, Neurolin)
[0829] Antigen of antibodies belonging to group 7: CD147 antigen
(also known as: BSG, TCSF (Tumor cell-derived collagenase
stimulatory factor), 5F7 protein, OK blood group protein, basigin
protein, collagenase stimulatory factor protein, EMMPRIN
(Extracellular matrix metalloproteinase Inducer), M6 activation
antigen, human leukocyte activation antigen M6)
[0830] Antigen of antibodies belonging to group 8: IgSF4 (also
known as: BL2, ST17, NECL2, TSLC1, IGSF4A, SYNCAM, sTSLC-1)
[0831] From the above-mentioned identification results, it has been
clarified that it was possible obtain three antibody clones to HER1
(048-006 antibody, 057-091 antibody, and 059-152 antibody), one
antibody clone to HER-2 (015-126 antibody), seven antibody clones
to CD46 antigen (035-224 antibody, 045-011 antibody, 051-144
antibody, 052-053 antibody, 052-073 antibody, 053-049 antibody, and
3172-120 antibody), one antibody clone to ITGA3 (015-003 antibody),
five antibody clones to ICAM1 (052-033 antibody, 053-042 antibody,
053-051 antibody, 053-059 antibody, and 053-085 antibody), five
antibody clones to ALCAM (035-234 antibody, 040-107 antibody,
041-118 antibody, 066-174 antibody, and 083-040 antibody), one
antibody clone to CD147 antigen (059-053 antibody), and ten
antibody clones to IgSF4. The Note here that the amino acid
sequences of the antibody clones have been identified as mentioned
below (antibody clones to IgSF4 are omitted).
TABLE-US-00023 <Antibodies belonging to group 1> (1) 048-006
antibody SEQ ID NO: 1 (VH), SEQ ID NO: 2 (VH CDR1), SEQ ID NO: 3
(VH CDR2), SEQ ID NO: 4 (VH CDR3), SEQ ID NO: 5 (VL), SEQ ID NO: 6
(VL CDR1), SEQ ID NO: 7 (VL CDR2), SEQ ID NO: 8 (VL CDR3) (2)
057-091 antibody SEQ ID NO: 9 (VH), SEQ ID NO: 10 (VH CDR1), SEQ ID
NO: 11 (VH CDR2), SEQ ID NO: 12 (VH CDR3), SEQ ID NO: 13 (VL), SEQ
ID NO: 14 (VL CDR1), SEQ ID NO: 15 (VL CDR2), SEQ ID NO: 16 (VL
CDR3) (3) 059-152 antibody SEQ ID NO: 17 (VH), SEQ ID NO: 18 (VH
CDR1), SEQ ID NO: 19 (VH CDR2), SEQ ID NO: 20 (VH CDR3), SEQ ID NO:
21 (VL), SEQ ID NO: 22 (VL CDR1), SEQ ID NO: 23 (VL CDR2), SEQ ID
NO: 24 (VL CDR3) <Antibody belonging to group 2> (1) 015-126
antibody SEQ ID NO: 25 (VH), SEQ ID NO: 26 (VH CDR1), SEQ ID NO: 27
(VH CDR2), SEQ ID NO: 28 (VH CDR3), SEQ ID NO: 29 (VL), SEQ ID NO:
30 (VL CDR1), SEQ ID NO: 31 (VL CDR2), SEQ ID NO: 32 (VL CDR3)
<Antibodies belonging to group 3> (1) 035-224 antibody SEQ ID
NO: 33 (VH), SEQ ID NO: 34 (VH CDR1), SEQ ID NO: 35 (VH CDR2), SEQ
ID NO: 36 (VH CDR3), SEQ ID NO: 37 (VL), SEQ ID NO: 38 (VL CDR1),
SEQ ID NO: 39 (VL CDR2), SEQ ID NO: 40 (VL CDR3) (2) 045-011
antibody SEQ ID NO: 41 (VH), SEQ ID NO: 42 (VH CDR1), SEQ ID NO: 43
(VH CDR2), SEQ ID NO: 44 (VH CDR3), SEQ ID NO: 45 (VL), SEQ ID NO:
46 (VL CDR1), SEQ ID NO: 47 (VL CDR2), SEQ ID NO: 48 (VL CDR3) (3)
051-144 antibody SEQ ID NO: 49 (VH), SEQ ID NO: 50 (VH CDR1), SEQ
ID NO: 51 (VH CDR2), SEQ ID NO: 52 (VH CDR3), SEQ ID NO: 53 (VL),
SEQ ID NO: 54 (VL CDR1), SEQ ID NO: 55 (VL CDR2), SEQ ID NO: 56 (VL
CDR3) (4) 052-053 antibody SEQ ID NO: 57 (VH), SEQ ID NO: 58 (VH
CDR1), SEQ ID NO: 59 (VH CDR2), SEQ ID NO: 60 (VH CDR3), SEQ ID NO:
61 (VL), SEQ ID NO: 62 (VL CDR1), SEQ ID NO: 63 (VL CDR2), SEQ ID
NO: 64 (VL CDR3) (5) 052-073 antibody SEQ ID NO: 65 (VH), SEQ ID
NO: 66 (VH CDR1), SEQ ID NO: 67 (VH CDR2), SEQ ID NO: 68 (VH CDR3),
SEQ ID NO: 69 (VL), SEQ ID NO: 70 (VL CDR1), SEQ ID NO: 71 (VL
CDR2), SEQ ID NO: 72 (VL CDR3) (6) 053-049 antibody SEQ ID NO: 73
(VH), SEQ ID NO: 74 (VH CDR1), SEQ ID NO: 75 (VH CDR2), SEQ ID NO:
76 (VH CDR3), SEQ ID NO: 77 (VL), SEQ ID NO: 78 (VL CDR1), SEQ ID
NO: 79 (VL CDR2), SEQ ID NO: 80 (VL CDR3) (7) 3172-120 antibody SEQ
ID NO: 81 (VH), SEQ ID NO: 82 (VH CDR1), SEQ ID NO: 83 (VH CDR2),
SEQ ID NO: 84 (VH CDR3), SEQ ID NO: 85 (VL), SEQ ID NO: 86 (VL
CDR1), SEQ ID NO: 87 (VL CDR2), SEQ ID NO: 88 (VL CDR3)
<Antibody belonging to group 4> (1) 015-003 antibody SEQ ID
NO: 89 (VH), SEQ ID NO: 90 (VH CDR1), SEQ ID NO: 91 (VH CDR2), SEQ
ID NO: 92 (VH CDR3), SEQ ID NO: 93 (VL), SEQ ID NO: 94 (VL CDR1),
SEQ ID NO: 95 (VL CDR2), SEQ ID NO: 96 (VL CDR3) <<Antibodies
belonging to group 5> (1) 052-033 antibody SEQ ID NO: 97 (VH),
SEQ ID NO: 98 (VH CDR1), SEQ ID NO: 99 (VH CDR2), SEQ ID NO: 100
(VH CDR3), SEQ ID NO: 101 (VL), SEQ ID NO: 102 (VL CDR1), SEQ ID
NO: 103 (VL CDR2), SEQ ID NO: 104 (VL CDR3) (2) 053-042 antibody
SEQ ID NO: 105 (VH), SEQ ID NO: 106 (VH CDR1), SEQ ID NO: 107 (VH
CDR2), SEQ ID NO: 108 (VH CDR3), SEQ ID NO: 109 (VL), SEQ ID NO:
110 (VL CDR1), SEQ ID NO: 111 (VL CDR2), SEQ ID NO: 112 (VL CDR3)
(3) 053-051 antibody SEQ ID NO: 113 (VH), SEQ ID NO: 114 (VH CDR1),
SEQ ID NO: 115 (VH CDR2),
SEQ ID NO: 116 (VH CDR3), SEQ ID NO: 117 (VL), SEQ ID NO: 118 (VL
CDR1), SEQ ID NO: 119 (VL CDR2), SEQ ID NO: 120 (VL CDR3) (4)
053-059 antibody SEQ ID NO: 121 (VH), SEQ ID NO: 122 (VH CDR1), SEQ
ID NO: 123 (VH CDR2), SEQ ID NO: 124 (VH CDR3), SEQ ID NO: 125
(VL), SEQ ID NO: 126 (VL CDR1), SEQ ID NO: 127 (VL CDR2), SEQ ID
NO: 128 (VL CDR3) (5) 053-085 antibody SEQ ID NO: 129 (VH), SEQ ID
NO: 130 (VH CDR1), SEQ ID NO: 131 (VH CDR2), SEQ ID NO: 132 (VH
CDR3), SEQ ID NO: 133 (VL), SEQ ID NO: 134 (VL CDR1), SEQ ID NO:
135 (VL CDR2), SEQ ID NO: 136 (VL CDR3) <Antibodies belonging to
group 6> (1) 035-234 antibody SEQ ID NO: 137 (VH), SEQ ID NO:
138 (VH CDR1), SEQ ID NO: 139 (VH CDR2), SEQ ID NO: 140 (VH CDR3),
SEQ ID NO: 141 (VL), SEQ ID NO: 142 (VL CDR1), SEQ ID NO: 143 (VL
CDR2), SEQ ID NO: 144 (VL CDR3) (2) 040-107 antibody SEQ ID NO: 145
(VH), SEQ ID NO: 146 (VH CDR1), SEQ ID NO: 147 (VH CDR2), SEQ ID
NO: 148 (VH CDR3), SEQ ID NO: 149 (VL), SEQ ID NO: 150 (VL CDR1),
SEQ ID NO: 151 (VL CDR2), SEQ ID NO: 152 (VL CDR3) (3) 041-118
antibody SEQ ID NO: 153 (VH), SEQ ID NO: 154 (VH CDR1), SEQ ID NO:
155 (VH CDR2), SEQ ID NO: 156 (VH CDR3), SEQ ID NO: 157 (VL), SEQ
ID NO: 158 (VL CDR1), SEQ ID NO: 159 (VL CDR2), SEQ ID NO: 160
(VLCDR3) (4) 066-174 antibody SEQ ID NO: 161 (VH), SEQ ID NO: 162
(VH CDR1), SEQ ID NO: 163 (VH CDR2), SEQ ID NO: 164 (VH CDR3), SEQ
ID NO: 165 (VL), SEQ ID NO: 166 (VL CDR1), SEQ ID NO: 167 (VL
CDR2), SEQ ID NO: 168 (VLCDR3) (5) 083-040 antibody SEQ ID NO: 169
(VH), SEQ ID NO: 170 (VH CDR1), SEQ ID NO: 171 (VH CDR2), SEQ ID
NO: 172 (VH CDR3), SEQ ID NO: 173 (VL), SEQ ID NO: 174 (VL CDR1),
SEQ ID NO: 175 (VL CDR2), SEQ ID NO: 176 (VL CDR3) <<Antibody
belonging to group 7> (1) 059-053 antibody SEQ ID NO: 177 (VH),
SEQ ID NO: 178 (VH CDR1), SEQ ID NO: 179 (VH CDR2), SEQ ID NO: 180
(VH CDR3), SEQ ID NO: 181 (VL), SEQ ID NO: 182 (VL CDR1), SEQ ID
NO: 183 (VL CDR2), SEQ ID NO: 184 (VL CDR3)
10. Confirmation of Antigen by RNAi and Immunostaining
[0832] In order to reconfirm that the isolated antibodies recognize
the identified antigen, double stranded oligo RNA was allowed to
act on cells so as to carry out antigen gene knockdown. Thus, the
immunostaining property of the antibody identified by the isolated
antigen with respect to the cell was examined.
[0833] Firstly, cells were cultured in a 6-well culture dish to
about 30% confluent. To this, a mixture including Lipofectamin 2000
(5 .mu.l) (Invitrogen) and the following oligo RNA (100 pmol) was
acted. At day 2, cells were peeled off by using collagenase and
recovered. To this, cp3 type purified antibody for verification was
acted at the concentration of 5 .mu.g/ml. After washing, a rabbit
anti-cp3 antibody was acted at the concentration of 2 .mu.g/ml.
After washing, Alexa488 labeled anti-rabbit IgG was acted at 2
.mu.g/ml. This was washed and then immobilized in OptiLyse (NOTECH)
(50 .mu.l) for ten minutes. This was diluted by adding 1 ml of PBS
and this was measured by using FACS Caliver (Beckmann). As the
antibody reaction solution and washing solution, 2.5% BSA/PBS
solution was used.
[0834] Subject antigen: CD147
[0835] Sequence of the used oligo RNA:
TABLE-US-00024 CAGAGCUACACAUUGAGAACCUGAA (SEQ ID NO: 441)
[0836] Subject cell: clear cell renal cell carcinoma CCFRC1
cell
[0837] Verified antibody: 059-053 cp3 antibody
[0838] Subject antigen: CD166
[0839] Sequence of the used oligo RNA:
TABLE-US-00025 UACCUAUGUGCAGAGGAAUUAUGAU (SEQ ID NO: 442)
[0840] Subject cell: clear cell renal cell carcinoma CCFRC1
cell
[0841] Verified antibody: 035-234 cp3 antibody
[0842] Subject antigen: CD166
[0843] Sequence of the used oligo RNA:
TABLE-US-00026 GCAACCAUCUAAACCUGAAAUUGUA (SEQ ID NO: 443)
[0844] Subject cell: hepatic cell carcinoma HLF cell
[0845] Verified antibody: 048-006 cp3 antibody
[0846] Subject antigen: HER2
[0847] Sequence of the used oligo RNA:
TABLE-US-00027 UAAUAGAGGUUGUCGAAGGCUGGGC (SEQ ID NO: 444)
[0848] Subject cell: ovarian cancer SKOv-3 cell
[0849] Verified antibody: 015-126 cp3 antibody
[0850] Subject antigen: IgSF4
[0851] Sequence of the used oligo RNA:
TABLE-US-00028 CCCAACAGGCAGACCAUUUAUUUCA (SEQ ID NO: 445)
[0852] Subject cell: hepatic cell carcinoma HLF cell
[0853] Verified antibody: 035-273 cp3 antibody Results are shown in
FIGS. 19 to 23. FIG. 19 shows the results of RNAi in which CD147 is
a subject antigen. FIG. 20 shows the results of RNAi in which CD166
is a subject antigen. FIG. 21 shows the results of RNAi in which
HER1 is a subject antigen. FIG. 22 shows the results of RNAi in
which HER2 is a subject antigen. FIG. 23 shows the results of RNAi
in which IgSF4 is a subject antigen. As is apparent from these
results, in any of the verified antibodies, in the cell population
that had been subjected to RNAi, as compared with the cell
population that had not been subjected to RNAi, the staining
property by antibodies (i.e., reactivity) was significantly
reduced. In this way, by RNAi experiment using oligo RNA for
knocking down the corresponding antigen it is reconfirmed again
that each of the isolated antibodies recognizes the identified
antigen.
11. Investigation of Reactivity of Each Antibody by Cell Staining
and Tissue Staining
11-1 Experiment Method
(1) Cell Staining
[0854] Cells were dissociated from a culture dish by using 2 mg/ml
collagenase I (Gibco BRL)/cell dissociation buffer (Gibco BRL),
then collected by using 10% FBS/DMEM, and 1.times.10.sup.5 of the
cells were used. These were washed with 2.5% BSA, 0.05%
NaN.sub.3/PBS (BSA solution), then suspended in 100 .mu.l of 2.5%
normal goat serum/BSA solution and left on ice for 30 minutes.
Thereafter, cp3 type antibodies were added so that the
concentration was 5 Hg/ml and left on ice for one hour. This was
washed with a BSA solution once, then suspended in 100 .mu.l of 5
.mu.g/ml BSA solution of anti-cp3 mouse monoclonal antibody
(Medical & Biological Laboratories Co., Ltd.) and left on ice
for one hour. This was washed with a BSA solution once, then
suspended in 1001i of 5 .mu.g/ml BSA solution of ALEXA488 binding
anti-mouse IgG goat antibody (Molecularprobe), and left on ice for
one hour. This was washed with BSA solution twice, and then
supernatant was discarded. To this, 501l of OptiLyse B (BECKMAN
COULTER) was added and left at room temperature for ten minutes so
as to fix the cells. To this, 950 .mu.l of 1 ng DAPI/BSA solution
was added, left at room temperature for 10 minutes, and subjected
to centrifugation for collecting cells. The cells were mounted on
MULTITEST SLIDE (ICN) and observed under microscopy.
(2) Tissue Staining
(2-1) Preparation of Antibody Sample
[0855] E. coli solution cultured overnight (0.5 ml) was planted in
6 ml of 2.times.YTAI (2.times.YT, 200 .mu.g/ml ampicillin sulfate,
0.5 mM IPTG), cultured overnight at 30.degree. C. and centrifuged
at 10000 rpm for 5 minutes by using a micro-centrifugal machine,
and supernatant was recovered. To this, an equal amount of
saturated ammonium sulfate was added and left at room temperature
for 30 minutes. Then, it was centrifuged at room temperature at
10000 rpm for 5 minutes and supernatant was discarded. The obtained
precipitates were suspended in 0.6 ml of PBS-0.05% NaN.sub.3,
complete solution and centrifuged at 4.degree. C. at 15000 rpm for
5 minutes, and supernatant was recovered.
(2) Production of Section
[0856] The extracted tissue was cut into about 5 mm.times.5
mm.times.10 mm, placed in 4% PFA/0.01% glutaraldehyde/0.1
Mcacodylic acid buffer (4.degree. C.) (PFA is a product by Wako
Pure Chemical Institute, glutaraldehyde is a product by KANTO
CHEMICAL CO., INC., sodium cacodylate is a product by SIGMA). By
using a microwave oven (SHARP), it was microwave-fixed. Then, it
was fixed again in this fixation solution at 4.degree. C. for one
hour. Then, it was transferred into 10% sucrose/PBS and immersed
therein at 4.degree. C. for four hours, then substituted by 15%
sucrose/PBS and immersed therein at 4.degree. C. for four hours,
and then substituted by 20% sucrose/PBS and immersed at one night.
It was embedded in an OTC compound and rapidly frozen in dry
ice/hexane. This was thinly cut into 4 .mu.m thickness by using
cryostat (Reichert-Jung 2800 FRIGCUT E), attached to silane coated
slide glass (MATSUNAMI) and dried by using a cold wind drier for 30
minutes.
(2-3) Staining
[0857] The slide glass to which a section was attached was immersed
in PBS three times for five minutes each so as to make hydrophilic.
Next, 50 .mu.l of 0.3% H.sub.2O.sub.2/0.1% NaN.sub.3 was dropped so
as to cause a reaction at room temperature for ten minutes and
blocking of endogenous peroxidase was carried out. Then, it was
washed with PBS three times for five minutes each. Then, it was
reacted in 2% BSA/PBS at room temperature for 10 minutes, and
blocking of a non-specific reaction was carried out. Then, excess
liquid was dropped off and 50 .mu.l of antibody sample was dropped
thereto so as to cause a reaction at room temperature for one hour,
followed by washing with PBS three times for 5 minutes each. Next,
501l of anti-CP3 rabbit antibody (5 .mu.g/ml) was dropped to cause
a secondary antibody reaction at room temperature for 45 minutes,
followed by washing with PBS three times for 5 minutes each. Then,
50 .mu.l of peroxidase labeled dextran binding anti-rabbit
immunoglobulin-goat polyclonal antibody (DAKO) was dropped so as to
cause a tertiary antibody reaction. This was washed with PBS three
times for 5 minutes each, and the 50 .mu.l of DAB-H.sub.2O coloring
solution was dropped. After the color became brown, this was
transferred to a vat filled with distilled water so as to terminate
the reaction. Thereafter, obtained product was washed with water
for 10 minutes, followed by staining nuclear with hematoxylin.
Thereafter, dehydration and penetration were carried out,
encapsulation with marinol and observation under microscopy were
carried out.
11-2 Experiment Results
(1) Anti-HER1 Antibody Group (Group 1)
[0858] Cancers showing positive in the cell line staining
(containing FACS): [0859] pancreatic cancer cell line PANC-1,
kidney cancer cell line CCFRC1, kidney cancer cell line Caki-1,
ovarian cancer cell line KF28, stomach cancer cell line SNU-5, lung
squamous cell carcinoma line RERF-LC-AI, ovarian cancer cell line
RMG-1, undifferentiated hepatic cell carcinoma cell line HLF,
ovarian cancer cell line SKOv3, pulmonary adenocarcinoma cell line
PCI4, kidney cancer cell line ACHN, lung squamous cell carcinoma
line EBC1, vulva mucosal epithelial cell line A431, pulmonary
adenocarcinoma cell line H1373, hepatic cell carcinoma cell line
HepG2, cell line established from kidney clinical specimen
[0860] Cancers showing negative in the cell line staining
(containing FACS): [0861] breast cancer cell line BT474, hamster
ovarian cancer cell line CHO
[0862] Cancers showing positive in the tissue staining: [0863]
kidney cancer, hepatic cell carcinoma, intrahepatic bile duct
cancer, lung squamous cell cancer, pulmonary adenocarcinoma,
pancreas cancer
(2) Anti-HER2 Antibody Group (Group 2)
[0864] Cancers showing positive in the cell line staining
(containing FACS): [0865] pulmonary adenocarcinoma cell line
Calu-3, ovarian cancer cell line SKOv3, breast cancer cell line
BT474
[0866] Cancers showing negative in the cell line staining
(containing FACS): [0867] hepatic cell carcinoma cell line. HLF,
pulmonary adenocarcinoma cell line PC14, kidney cancer cell line
ACHN, kidney cancer cell line 293T, hamster ovarian cancer cell
line CHO, kidney cancer cell line Caki-1, kidney and stomach cancer
cell line CCFRC1, cell line established from kidney clinical
specimen
(3) Anti-CD46 Antibody Group
[0868] Cancers showing positive in the cell line staining
(containing FACS): [0869] large bowel cancer cell line CaCo2,
stomach cancer cell line MKN45, undifferentiated hepatic cell
carcinoma cell line HLF, liver cancer cell line HepG2, intrahepatic
bile duct cell cancer cell line RBE, pancreas cancer cell line
PANC1, kidney cancer cell line CCFRC1, kidney cancer cell line
Caki-1, pulmonary adenocarcinoma cell line NCI-H441, lung squamous
cell cancer EBC1, stomach cancer cell line NCI-N87, stomach cancer
cell line SNU-5, lung squamous cell carcinoma line RERF-LC-AI,
hepatic cell carcinoma clinical specimen, breast cancer cell line
BT474, kidney cancer cell line 293T, pulmonary adenocarcinoma cell
line PC14, kidney cancer cell line ACHN, pulmonary adenocarcinoma
cell line H1373
[0870] Cancers showing negative in the cell line staining
(containing FACS): [0871] hamster ovarian cancer cell line CHO,
vulva mucosal epithelial cell line A431
[0872] Cancers showing positive in the tissue staining: [0873]
kidney cancer, hepatic cell carcinoma, intrahepatic bile duct
cancer, pulmonary adenocarcinoma, pancreas cancer
[0874] Specific expression of CD46 in intrahepatic bile duct cancer
and pancreas cancer, which had not been particularly reported about
the relationship with respect to CD46 was recognized.
(4) Anti-ITGA3 Antibody Group (Group 4)
[0875] Cancers showing positive in the cell line staining
(containing FACS): [0876] undifferentiated hepatic cell carcinoma
cell line HLF, ovarian cancer cell line SKOv3, kidney cancer cell
line ACHN, kidney cancer cell line Caki-1, pulmonary adenocarcinoma
cell line H1373, lung squamous cell cancer EBC1, vulva mucosal
epithelial cell line A431, breast cancer cell line BT474, pulmonary
adenocarcinoma cell line PCI4, kidney cancer cell line CCFRC1,
hepatic cell carcinoma cell line OCTH, intrahepatic bile duct cell
cancer cell line RBE, pancreas cancer cell line PANC-1, pancreas
cancer cell line MIA-Paca2, pulmonary adenocarcinoma cell line
A549, pulmonary adenocarcinoma cell line NCI-N441, pulmonary
adenocarcinoma cell line Calu-3, lung squamous cell carcinoma line
RERF-LC-AI, stomach cancer cell line SNU5, stomach cancer cell line
MKN45, stomach cancer cell line NCI-N87, large bowel cancer cell
line CW2, ovarian cancer cell line SKOv3, ovarian cancer cell line
KF-28, ovarian cancer cell line RMG-1, ovarian cancer cell line
RMG-2
[0877] Cancers showing negative in the cell line staining
(containing FACS): [0878] kidney cancer cell line 293T, hepatic
cell carcinoma cell line HepG2, hamster ovarian cancer cell line
CHO
[0879] Cancers showing positive in the tissue staining: [0880]
intrahepatic bile duct cancer, pancreas cancer
[0881] Specific expression of ITGA3 in gallbladder and liver cancer
and pancreas cancer, which had not been particularly reported about
the relationship with respect to ITGA3 was recognized.
(5) Anti-ICAM I Antibody Group (Group 5)
[0882] Cancers showing positive in the cell line staining
(containing FACS): [0883] Liver cancer cell line HepG2, pulmonary
adenocarcinoma cell line PC14, cell line established from kidney
clinical specimen
[0884] Cancers showing negative in the cell line staining
(containing FACS): [0885] undifferentiated hepatic cell carcinoma
cell line HLF, ovarian cancer cell line SKOv3, breast cancer cell
line BT474, kidney cancer cell line 293T, kidney cancer cell line
ACHN, kidney cancer cell line Caki-1, pulmonary adenocarcinoma cell
line PC 14, kidney cancer cell line CCFRC1, hamster ovarian cancer
cell line CHO
[0886] Cancers showing positive in the tissue staining: [0887]
hepatic cell carcinoma
(6) Anti-ALCAM Antibody Group (Group 6)
[0888] Cancers showing positive in the cell line staining
(containing FACS): [0889] Liver cancer cell line HepG2, OCTH,
Hep3B, and HLF, kidney cancer cell line Caki-1, CCFRC1, ACHN, 293T,
and cell line established from clinical specimen, lung cancer cell
line PC14, NCI-H441, EBC-1, RERF-LC-AI, A549, and H1373, ovarian
cancer cell line SKOv3, KF-28, RMG1, and RMG2, stomach cancer cell
line NCI-N87, large bowel cancer cell line CW2, breast cancer cell
line BT474, acute myelocytic leukemia AMLclinical specimen, hamster
ovarian cancer cell line CHO
[0890] Cancers showing negative in the cell line staining
(containing FACS): [0891] vulva mucosal epithelial cell line
A431
[0892] Cancers showing positive in the tissue staining: [0893]
kidney cancer, hepatic cell carcinoma, intrahepatic bile duct
cancer, lung squamous cell cancer, alveolar cell carcinoma,
adenocarcinoma [0894] Specific expression of ALCAM in kidney
cancer, hepatic cell carcinoma, and gallbladder and liver cancer,
which had not been particularly reported about the relationship
with respect to ALCAM was recognized.
(7) Anti-CD147 Antibody Group (Group 7)
[0895] Cancers showing positive in the cell line staining
(containing FACS): [0896] liver cancer cell line HepG2, kidney
cancer cell line CCFRC1, kidney cancer cell line ACHN, kidney
cancer cell line Caki-1, pulmonary adenocarcinoma PCI4, cell line
established from kidney cancer clinical specimen
[0897] Cancers showing negative in the cell line staining
(containing FACS): [0898] hamster ovarian cancer cell line CHO
[0899] Cancers showing positive in the tissue staining: [0900]
kidney cancer [0901] Specific expression of CD147 in kidney cancer,
which had not been particularly reported about the relationship
with respect to CD147 was recognized.
12. Conversion into IgG Type Antibody
12-1 Construction of IgG Type Antibody Gene
[0902] In order to investigate the efficacy as an antibody
medicine, a part of antibodies is converted into IgG type
[0903] Firstly, by using VH and VL genes of scFVcp3 type antibody,
it is confirmed that there was not a restriction enzyme site
necessary for cloning them to Fc region of IgG1 and the base
sequence of the gene. PCR was carried out by using an antibody gene
as a template and using a primer for amplifying the H chain and L
chain were used. The amplified product was ligated to the
downstream of CMV promoter of the IgG1 construction vector and a
plasmid DNA containing an IgG type antibody gene was obtained.
12-2 Expression of IgG Type Antibody
[0904] For transfection of plasmid DNA into CHO-K1 cell, GenePORTER
Reagent (Gene Therapy Systems: T201007) was used. Firstly, CHO-K1
cells were prepared in a 60 mm-culture dish the day before the
transfection so that they became 2.times.10.sup.4 cells/ml (a
medium, in which .alpha.-MEM (Invitrogen: 12561-056) to which 10%
FCS (Equitech: 268-1) had been added, was used).
[0905] The plasmid DNA (8 .mu.g) was dissolved in 250 .mu.L of
serum free medium (hereinafter, abbreviate as "SFM") (Invtrogen:
12052-098 CHO--S--SFMII)) and subjected to 0.22 .mu.m filter.
GenePORTER Reagent (40 .mu.L) was added to SFM (250
[0906] The plasmid DNA and GenePORTER Reagent dissolved in SFM were
rapidly stirred and stood still at room temperature for 30
minutes.
[0907] The cells were washed with SFM (2 ml) twice, and the plasmid
DNA-GenePORTER mixture (Transfection Medium) was slowly poured in a
plate containing cells and cultured in an incubator at 37.degree.
C. for five hours.
[0908] The medium for transfection was sucked and washed with
.alpha.MEM 10% FCS twice, then 5 ml of .alpha.MEM 10% FCS was
added, which was cultured in an incubator at 37.degree. C. for 48
hours.
[0909] The medium was replaced by a medium (10 mL) of .alpha.MEM
10% FCS+700 .mu.g/ml G418 (Sigma: G7034) and selection was started
(hereinafter, as a medium, .alpha.MEM 110% FCS+700 .mu.g/mL G418
was used). After cultured at 37.degree. C. for 48 hours, cells were
washed with PBS (10 mL), treated with 0.25% Trypsin-EDTA (Sigma
T4049) (750 .mu.L), .alpha.MEM (5 mL) was added. Then, cultured
product was peeled off and recovered from the plate. The number of
cells was measured. Based on the results, limiting dilution was
carried out under the conditions of 10 cells/200 .mu.L/well (two
sheets of 96 well plates). After culturing for 14 days, ELISA was
carried out by using a culture supernatant of each well and the
expression of an IgG type antibody was confirmed.
12-3 Purification of Expression Protein (IgG) from Culture
Supernatant
[0910] Protein G Sepharose 4 Fast Flow (amersham pharmacia biotech:
17-0618-01) (1 mL) was packed in a column and balanced in PBS (5
mL). The culture supernatant was applied, sent at the flow rate of
1 drop/2 seconds, and allowed the expressed protein (IgG) to be
bonded to a column. PBS (10 mL) was sent at the flow rate of 1
drop/2 seconds, non-adsorbed components were washed, then 6 mL of
elute buffer (0.2M glycine-HCl, pH 3) was sent at the flow rate of
1 drop/second, and 1 mL each of eluate was collected in a 1.5 ml
tube. To the collection tube, neutralizing buffer (3M Tris-HCl)
(400 .mu.L) was added in advance. Neutralization was carried out at
the same time of collection. The eluate was collected and
concentrated to 750 .mu.L, and solution substitution (PBS,
complete, 0.01% NaN.sub.3) was carried out. Then, the concentration
of the antibody protein was calculated by SDS-PAGE.
13. Experiment of Inhibition of Binding of EGF by Successfully
Obtained Anti-HER1 Antibody (048-006 Antibody)
13-1 Experimental Procedure
[0911] A431 cells were cultured in 15.phi. culture dish (medium:
DMEM containing 10% FBS and 1% PS), and the cells were peeled off
with the use of cell dissociation buffer (GIBCO: 13151-014) and
recovered at 90% confluence. Two ml of PBS containing 1.0% BSA and
0.05% NaN.sub.3 was added and the recovered cells were suspended.
The suspension was stood still at 4.degree. C. for 30 minutes and
then 100 .mu.l each (about 2.5.times.10.sup.5 cells) was dispensed
into each well of a 96-well V-bottom plate. It was centrifuged (650
G) for 2 minutes, and the cells were precipitated to remove the
supernatant. Each antibody solution (HR1-007 [10 .mu.g/ml], 48-006
[10 .mu.g/ml, 5 .mu.g/ml, 1 .mu.g/ml], and 59-152 [10 .mu.g/ml, 5
.mu.g/ml, 1 .mu.g/ml]) (200 .mu.l), which had been prepared by
using PBS containing 1.0% BSA, was added and the cells were
suspended. The suspension was stood still at 4.degree. C. for one
hour, and then, biotin labeled EGF (biotinated EGF: 50 .mu.g/ml)
was added to each well so that the final concentration became 1
.mu.g/ml, so that the cells were suspended. Note here that the
biotinated EGF was produced by the following method. Firstly, to
EGF (prepared to 1 mg/ml with PBS(-); AUSTRAL Biologicals:
GF-010-5) (50 .mu.l), EZ-Link Sulfo-NHS-LC-Biotin (prepared to 2
mg/ml with PBS(-); PIERCE: 21335) (25 .mu.l) was added. After it
was stood still at room temperature for 30 minutes, 1M glycine
(pH=7.0 to 8.0) (10 .mu.l) was added. After it was stood still at
room temperature for 30 minutes, PBS(-) (15 .mu.l) was added and
stored at 4.degree. C. (final concentration: 500 .mu.g/ml). This
was 10-fold diluted with PBS containing 1.0% BSA and used for
experiment.
[0912] This was stood still at 4.degree. C. for one hour, and
centrifuged (650 G) for 2 minutes so as to remove the supernatant.
PBS containing 1.0% BSA (180 .mu.l) was added and centrifuged (650
G) for 2 minutes so as to remove the supernatant. HRP-labeled
streptavidin (0.2 .mu.g/ml (PBS containing 1.0% BSA); PIERCE:
21126) (100 .mu.l) was added and cells were suspended at 4.degree.
C. for one hour, and centrifuged (650 G) for 2 minutes so as to
remove the supernatant. PBS containing 1.0% BSA (180 .mu.l) was
added and centrifuged (650 G) for 2 minutes so as to remove the
supernatant. This operation was carried out again. OPD (Wako:
154-01673) coloring solution (100 .mu.l) was added and cells were
suspended. After four minutes at room temperature, coloring stop
solution (2NH.sub.2SO.sub.4) (100 .mu.l) was added and centrifuged
(650 G) for 2 minutes. Then, the supernatant was transferred to a
flat-bottom plate. By using a plate reader, the absorbance at 192
nm (A492) was measured and represented by a numeric value.
13-2 Results
[0913] The results are shown in FIG. 24. HR1-007 as a control does
not affect the binding of EGF. 048-006 antibody and 059-152
antibody inhibit the binding of EGF. 048-006 antibody can inhibit
the binding of EGF substantially completely while 059-152 antibody
cannot completely inhibit the binding even if the temperature is
increased. Note here that 048-006 antibody shows an inhibition
effect even at the low level of about 0.02 .mu.g/ml (FIG. 24C).
[0914] The results suggest that the antagonism activity between
each antibody (048-006 antibody and 059-152 antibody) and EGF
provides a part of the pharmacological effect such as anti-tumor
property.
14. Experiment of Phosphorylation Signal Inhibition of HER1 by
Successfully Obtained Anti-HER1 Antibody (048-006 Antibody)
[0915] By using a phosphorylation antibody, it was determined
whether or not the successfully obtained anti-HER1 antibody
(048-006 antibody) inhibited the phosphorylation signal of HER1.
Specifically, by using three kinds of cells (renal cell carcinoma
(CCF-RC1, Caki-1) and epidermoid cancer (A431)), the inhibition
effect of 048-006 antibody and 059-152 antibody and the inhibition
effect of ERBITUX were compared with each other.
14-1 Experimental Procedure
[0916] Each of cells was cultured in 6-well culture dish, and at
60% confluence, a medium (DMEM containing 10% FBS and 1% PS) was
substituted to DMEM. After 16 hours, each antibody (HR1-007,
048-006, 059-152 (prepared to 2 mg/ml with PBS(-))) and ERBITUX
were added to each well so that the final concentration became 10
.mu.g/ml or 1 .mu.g/ml. After 30 minutes, EGF (prepared to 20
.mu.g/ml with PBS(-)) was added to each well so that the final
concentration became 1 .mu.g/ml. After 30 minutes, each well was
washed with PBS(-) and quickly frozen together with the culture
dish by using liquid nitrogen. To each well, lysis buffer (50 mM
Tris (pH 7.4), 150 mM NaCl, 1 mM Na.sub.3VO4, 10 mM NaF, 1%
Triton.times.100, complete (Roche: 11836145001)) were added, and
the cells were suspended and transferred to centrifugation tube.
Centrifugation (10000G) was carried out for 10 minutes so as to
precipitate cell debris. A part of the supernatant was subjected to
SDS-PAGE, which was transferred to a membrane. Western blotting
using an anti-phosphorylation tyrosine antibody (11 g/ml; upstate:
05-321) or an anti-.beta.-actin antibody (1 .mu.g/ml; abcam:
ab25139) as a primary antibody, and a secondary antibody reaction:
HRP labeled anti-mouse IgG as a secondary antibody was carried out.
A431 cells were required to be exposed to light for 1 to 2 seconds;
CCF-RC1 for 10 seconds; and Caki-1 for one minute (there was
originally large difference in cell sensitivity to external
stimulation).
14-2 Results
[0917] The results are shown in FIG. 25 (A and B: the results of
Western blotting using A431 cells; C to E: comparison effect of
inhibiting HER1 phosphorylation signal between the successfully
obtained antibody and ERBITUX). In CCF-RC1 and A-431 cell lines,
HR1-007 as a control does not affect the phosphorylation signal of
HER1. However, 048-006 antibody and 059-152 antibody inhibit signal
in a concentration-dependent manner. 048-006 antibody can inhibits
the binding of EGF substantially completely and also inhibit self
phosphorylation of HER1 substantially completely. 059-152 antibody
inhibits the binding of EGF about 50%. Furthermore, 059-152
antibody inhibits self phosphorylation of HER1 although it is
weaker than 048-006 antibody. 048-006 antibody and 059-152 antibody
have inhibition capabilities superior to that by ERBITUX. In
particular, the inhibition capability of 048-006 antibody is
remarkable.
[0918] The sensitivity to external stimulation by EGF differs
depending upon the kinds of cells. Therefore, when a cell like
Caki-1 that does not show sensitivity to external stimulation by
EGF is used, the difference in signal inhibition effect by the
antibody is not observed.
[0919] The results suggest that each antibody (048-006 antibody and
059-152 antibody) has an activity of suppress the tyrosine kinase
circuit of HER1 with respect to sensitive cells of HER1 by EGF, and
exhibits pharmacological effects such as proliferation suppression
and anti-tumor property.
15. Measurement of Binding Constant by BIAcore
[0920] As to the successfully obtained antibodies 048-006 and
059-152, the dissociation constant with respect to the expression
Her1 was measured.
15-1 Experimental Procedure
(1) Forced Expression of Partial Sequence of Her1
[0921] A sequence from a region after the signal of HER1 to
immediately before the transmembrane region (621 amino acid of the
expression sites from positions 26 to 645 (SEQ ID NO: 943) was
cloned. For cloning and expression, a pSecTagII vector (Invitrogen)
was used. When this vector is inserted, myc and his tags are
added.
(2) Recovering of Expressed Cells
[0922] One 15.phi.-culture dish (80 confluent) in which 293T cells
were cultured was prepared. The medium was replaced with new one so
that cells were not peeled off, and then cultured. Thus, a state in
which cells were aggregated at 90-100% confluence was formed. The
day before recovering cells, final medium replacement was carried
out. DNA (75 .mu.l) was added to D-MEM (serum free) (1.9 ml) and
subjected to tapping adjustment so as to make the solution A.
Furthermore, Lipo (75 .mu.l) was added to D-MEM (serum free) (1.9
ml) and subjected to tapping adjustment (50 ml, Falcon) so as to
make the solution B.
[0923] One minute after the formation of the solution B, the
solution B was added to the solution A by using a 5 ml-pipette,
subjected to pipetting, and incubated at room temperature for 20
minutes. 22.5 ml of D-MEM (serum free) was measured and taken out
into a 50 ml culture container (Falcon) and 2.5 ml of serum was
added thereto, which was incubated at 37.degree. C. for 15 minutes
so as to obtain D-MEM (containing serum).
[0924] The medium was removed from a 15.phi.-culture dish in which
293T cells were aggregated, and D-MEM (serum free) (25 ml) was
added along the wall of the dish carefully so that cells are not
peeled off. The added D-MEM (serum free) was sucked by using an
aspirator and D-MEM (containing serum) (25 ml) was added. Twenty
minutes after D-MEM (containing serum) was formed, the mixture
solution (3.8 ml) of solution A and solution B was added to the
cells by using 25 ml-pipette and the cells were peeled off. The
cells were separated from each other by pipetting, the cells were
stood still in a CO.sub.2 incubator for 2 days. Two days after, the
supernatant was recovered and subjected to protein
purification.
(3) Secretory Protein Purification (Ni-NTA)
[0925] Ni-NTA agarose gel (QIAGEN) (2 ml) (bed volume of 1 ml) was
packed in a column and balanced in PBS. Then, the culture
supernatant recovered in (2) was applied thereto. A flow-through
solution was again applied to a column. The column was washed with
5 ml of PBS, and eluted in stages with 20, 50, 100, 250, and 500 mM
imidazole/PBS (5 ml each) so that the absorbance (280 nm)<0.005
was satisfied. Furthermore, it was eluted with 0.5M EDTA/PBS (10
ml). The solution was replaced by new one by dialysis so as to
obtain BIAcore immobilized sample.
(4) BIAcore Measurement
[0926] The interaction between the antibody clone and the expressed
Her1 was examined so as to determine KD (dissociation constant;
kd/ka). For analysis, BIAcore 1000 biosensor device was used.
[0927] A carboxymethyldextran (Sensor Chip CM5, Research grade,
BIACORE) sensor chip was used. With the electrostatic adsorption to
a CM5 matrix and a covalent linkage between a lysyl group on CM5
and an activated carboxyl group, antigen (Her1) was immobilized on
the chip. By EDC/NHS coupling chemical reaction, a carboxyl group
was activated.
[0928] In the condition of HBS-EP (BIACORE) at a flow rate of 5
.mu.L/minute by using EDC/NHS (amine coupling kit, BIACORE was
mixed with equal amount of EDC and NHS), after the lysyl group on
CM5 was activated (contact time: 2.4 minutes), chip was washed with
HBS-EP (BIACORE). Subsequently, Her1 (20 .mu.g/mL: Sigma, 0.6 mg
protein/ml was diluted with 10 mM acetic acid (pH 4.0)) was added
to the chip. The chip was washed with HBS-EP, then, 1M ethanolamine
(pH 8.5) was added so as to deactivate the remaining activated
carboxyl group. Thereafter, the chip was washed with 50 mM NaOH so
as to remove all Her1 that were not linked covalently. Note here
that all the analysis experiments were carried out under the
conditions of HBS-EP (BIACORE) at a flow rate of 35 .mu.l/minute at
25.degree. C. Reproduction was carried out by using 50 mM NaOH (one
minute).
[0929] 059-152 antibody or 048-006 antibody were reacted at each
concentration shown in the figure and HBS-EP at flow rate of 35
.mu.l/minute, so that the binding constant was analyzed.
15-2 Results
[0930] The results are shown in FIG. 26. 048-006 antibody shows
extremely strong binding force of more than KD=10-11 (M) at every
measurement point. The actual value of Global fitting based on each
detection value was 4.8.times.10.sup.-13 (M). This is beyond the
reliable measurement limit of BIAcore. As to 059-152 antibody, a
bond dissociation curve cannot be detected. This is thought to be
because this antibody cannot recognize the higher-order structure
of artificially produced forced expression product. In other words,
it is suggested that this antibody recognize a higher-order
structure of a complex or a higher-order structure that can be
observed only on an intact membrane.
16. Cytotoxicity test of anti-HER1 antibody, anti-HER2 antibody,
anti-ITGA3 antibody, Anti-ALCAM Antibody, and Anti-ICAM Antibody
(ADCC Activity Measurement)
[0931] Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) is an
immune reaction of killing and attacking cells harmful to a human
body, for example, virus infected cells, in which "effector cells"
mainly consisting of natural-killer cell or monocyte attacks cells
to which antibodies are bonded widely on the membrane surface as a
target. The cytotoxicity by ADCC occurs depending upon the
combination of an antibody specifically bonded to a surface of the
cell membrane antigen and an effector cell.
[0932] Some of antibodies specifically bonded to a tumor surface
antigen have an anti-tumor effect and a therapeutic effect to
cancer and sold as antibody medicine. It has been reported that the
main mechanism of action of these antibodies are ADCC. Then, in
order to evaluate whether or not the cancer antigen specific
antibodies successfully isolated by the present inventor have an
anti-tumor effect, that is, they have promising as a cancer
treatment antibody, the detection of ADCC was carried out. In the
below-mentioned experiments, human IgG type antibody clone
recognizing a subject antigen is reacted to a target cell to
present it to an effector cell. In the detection of ADCC, the
degree of cytotoxicity is calculated by using a cytotoxicity
detection kit which, in principle, detects the enzymatic activity
of lactate dehydrogenase leaking into the medium from the target
cancer cell attached by the effector cell by using the coloring of
the reagent.
16-1 Induction of ADCC I (Case of 015-003 Antibody as Anti-ITGA3
Antibody: scFVcp3 Type Antibody is Used)
[0933] Regarding 015-003 antibody as anti-ITGA3 antibody, a scFVcp3
type antibody was used and the ADCC activity was investigated by an
assay combining an anti-M13 pIII rabbit antibody. Furthermore,
liver cancer HLF cell is used as the target subject cultured cell.
The operation procedure is described below.
[0934] (1) By the following procedures, peripheral blood is
collected from a volunteer and mononucleosis is separated. Firstly,
heparin-added peripheral blood (30 ml) collected from a volunteer
is diluted with PBS to 80 ml and superposed quietly on 10 ml each
of lymphocyte isolation reagent Ficoll Paque Plus (Amersham
Bioscience), which have been dispensed in four centrifugation
tubes, and centrifuged (400.times.g, 20.degree. C. for 40 minutes).
The mononucleosis fractions (including lymphocyte and monocyte) are
recovered, diluted with cooled PBS to 80 ml and centrifuged
(200.times.g, 4.degree. C. for 15 minutes).
[0935] (2) (1) is suspended in a cooled cytotoxicity test medium
(Cytotoxic Medium, hereinafter, abbreviated as "CTM", RPMI-1640
medium, 1% (v/v) fetal calf serum, 1% (v/v) Penicillin-Streptomycin
Solution, 1% (v/v) 1M HEPES buffer (pH 7.0): Invitrogen) so that
the final density becomes 5.0.times.10.sup.6 cells/ml to obtain an
effector cell.
[0936] (3) In a culture dish having a diameter of 150 mm, a target
subject cultured cell is grown in a culture medium I (Minimum
Essential Medium Alpha Medium:Invitrogen, 10% (v/v) fetal calf
serum: Equitic-Bio, 1% (v/v) Penicillin-Streptomycin Solution
Sigma-Aldrich). A liquid medium is removed and cells are washed
with PBS (10 ml) twice so as to remove the solution. Thereafter, 4%
(w/v) collagenase Type IV (Invitrogen) (5 ml) is added and stored
keeping warm at 37.degree. C. for 10 minutes, so that cells are
peeled off from the culture dish. Furthermore, 5 ml of liquid
medium 2 (RPMI-1640, 10% (v/v) fetal calf serum, 1% (v/v)
Penicillin--Streptomycin Solution:Sigma-Aldrich) (RPMI-1640:
Sigma-Aldrich, 10% fetal calf serum, 1% penicillin-streptomycin
solution) is added to stop a collagenase reaction. Then, suspended
cells are recovered to obtain cell suspension.
(4) The cell density of the cell suspension of (3) is measured. The
supernatant is removed by centrifugation and the cells are
suspended in a cooled CTM medium so that the final density becomes
1.5.times.10.sup.5 cells/ml. (5) 100 .mu.l each of target cells is
dispensed in a 96-well V-bottom multi plate on ice. (6) 2 .mu.g/ml
scFv-pIII phage antibody-CTM solution (100 .mu.l each) is dispensed
and reacted on ice for 60 minutes. (7) Centrifugation (Swing rotor:
500.times.g, 4.degree. C. for 10 min) is carried out to remove the
supernatant. (8) Cell pellet is suspended in 5 .mu.g/ml anti-M13
pill rabbit polyclonal antibody-CTM solution (150 .mu.l each), a
part of 100 .mu.l is transferred to a 96-well U-bottom multi plate.
(9) The effector cell of (2) (or 2% Triton X-100-CTM solution) is
added and then centrifuged (Swing rotor: 50.times.g, 4.degree. C.
for 5 min). (10) Reaction is carried out in 5% CO.sub.2 at
37.degree. C. for 4 hours. (11) After the reaction, centrifugation
(Swing rotor: 500.times.g, 4.degree. C. for 10 min) is carried out
and the supernatant (100 .mu.l) is transferred to a flat-bottom 96
well multi plate. (12) LDH activity measurement reagent (Roche)
(100 .mu.l) is added and reaction is carried out at room
temperature for 30 min. (13) OD490 and OD690 are measured by using
a micro plate absorptiometer. 16-2 Induction of ADCC 2 (case of
048-006 antibody as anti-HER1 antibody, 015-126 antibody as
anti-HER2 antibody, 066-174 antibody, 035-234 antibody and 041-118
antibody as anti-ALCAM antibody, 053-051 antibody, 053-059 antibody
and 053-085 antibody as anti-ICAM1 antibody, 067-153 antibody as
anti-EpCAM antibody, 067-133 antibody as anti-HGFR antibody: IgG
type antibody is used)
[0937] Regarding 048-006 antibody as anti-HER1 antibody, an IgG
type antibody was used and the ADCC activity was investigated.
A-431 and A549 (epidermoid tumor), ACHN and CCF-RC-1 (kidney
cancer), NCI-H1373 (lung cancer), as well as SK-OV-3 (ovarian
cancer) were used as the target subject cultured cell.
[0938] Also regarding 015-126 antibody as anti-HER2 antibody, an
IgG type antibody was used, and the ADCC activity was investigated.
Breast cancer BT-474 was used as the target subject cultured
cell.
[0939] Regarding 066-174 antibody and 035-234 antibody as
anti-ALCAM antibody, an IgG type antibody was used, and the ADCC
activity was investigated. NCI-H1373 (pulmonary adenocarcinoma),
CW2 (large bowel cancer), or NCI-H441 (lung cancer) was used as the
target subject cultured cell.
[0940] Regarding 053-051 antibody, 053-059 antibody and 053-085
antibody as anti-ICAM1 antibody, an IgG type antibody was used, and
the ADCC activity was investigated. HepG2 (hepatic cell carcinoma)
and NCI-H441 (lung cancer) were used as the target subject cultured
cell.
[0941] Furthermore, regarding the effect of 048-006 antibody or
059-152 antibody as anti-HER1 antibody on CCF-RC-1 (kidney cancer),
NCI-H1373 (lung cancer) and A-431 (epidermoid cancer), the antibody
dosage dependence of the ADCC activity was investigated so that the
final concentration of the IgG type antibody was in the range from
0.01 to 10 .mu.g/ml.
[0942] Regarding 041-118 antibody as anti-ALCAM antibody, an IgG
type antibody was used and the antibody dosage dependence of the
ADCC activity was investigated. NCI-H1373 (pulmonary
adenocarcinoma) was used as the target subject cultured cell.
[0943] Regarding 067-153 antibody as anti-EpCAM antibody, an IgG
type antibody was used and the antibody dosage dependence of the
ADCC activity was investigated. MKN-45 (solid-type gastric
adenocarcinoma), HT-29 (colon adenocarcinoma) and NCI-H1373 (lung
cancer) were used as the target subject cultured cell.
[0944] Regarding 067-133 antibody as anti-HGFR antibody, an IgG
type antibody was used and the antibody dosage dependence of the
ADCC activity was investigated. NCI-H1373 (lung cancer) was used as
antibody dosage dependence of the ADCC activity.
[0945] The antibody dosage dependence of the ADCC activity was
basically measured at the E/T Ratio (ratio of effector cell:target
cell) of 80:1 at final antibody concentration in the solution of
0.01 .mu.g/ml to 10 .mu.g/ml or 10.sup.-6 .mu.g/ml to 10
.mu.g/ml.
[0946] At each measurement point, the antibody and the effector
cell were added to the target cell, and four hours later, the ADCC
activity was measured. Regarding NCI-H1373, the ADCC activity was
measured at the E/T Ratio of 100:1.
[0947] The operation procedure was carried out in accordance with
the procedures described in 16-1. The detail of the reaction was
made to be as follows. 66 .mu.l/well of the target cells
(2.times.10.sup.4 cells) were placed in 96-well U-bottom plate
(Becton Dickinson) and 66 .mu.l of IgG type antibody (3 .mu.g/ml)
was added and then 66 .mu.l of peripheral blood mononucleosis
suspension (7.5.times.10.sup.5 cells) was added. The E/T
[0948] Ratio (ratio of effector cell:target cell) was made to be
20. In order to promote the association of cells, centrifugation
(60.times.g, 4.degree. C., 5 minutes) so as to allow the cells to
sink, which was stored keeping warm 240 minutes in a culture
container that had been set to the conditions of 37.degree. C. and
5% CO.sub.2. Thus ADCC reaction was induced. Each antibody sample
was prepared as a CTM solution. Furthermore, in each sample, CTM
was used as a negative control and target cell to which 100 .mu.l
of 2% Triton X-100-CTM solution was added was used as a control of
maximum liberation of lactate dehydrogenase (cells had been
destroyed by Triton X-100 in advance). Furthermore, three wells
were used for each experiment groups.
16-3 Measurement of ADCC Activity
[0949] In both the assay using a scFVcp3 type antibody and assay
using an IgG type antibody, the ADCC activity was an indicator of
the damage to the target cell, which is in proportion to the degree
of coloring, that is, the concentration of lactate dehydrogenase
liberating to the culture supernatant. Thirty minutes after the
coloring starts, absorbance (OD490-OD620 (background absorbance))
was measured by using a spectrophotometer. In each experiment
group, absorbance values in the three wells were averaged to
calculate the cytotoxic Index. In advance, the absorbance of only a
medium was subtracted and the calculation was carried out by the
following calculation equation.
Relative LDH activity=OD490-OD690
LDH activity derived from cell=experimental value-(control
containing only solution)
Cytotoxicity (%)=(experimental value-effector cell control-target
cell control)/(cell+Triton X-100 control-target cell
control).times.100 [Equation 1]
[0950] Note here that when the antibody does not have any cytotoxic
activity, the cytotoxicity calculated by this method may be minus
value due to a measurement error because the measurement is carried
in experiments using the living body components.
16-4 Measurement Result
[0951] The measurement results of the ADCC activity are shown in
FIG. 27 (anti-ITGA3 antibody was used; the target culture cell was
HLF), FIG. 28 (anti-HER1 antibody was used; the target culture cell
was A-431), FIG. 29 (anti-HER1 antibody was used; the target
culture cell was A549), FIG. 30 (anti-HER1 antibody was used; the
target culture cell was ACHN), FIG. 31 (anti-HER1 antibody was
used; the target culture cell was CCF-RC-1), FIG. 32 (anti-HER1
antibody was used; the target culture cell was NCI-H1373), FIG. 33
(anti-HER1 antibody was used; the target culture cell was SK-OV-3),
FIG. 34 (anti-HER2 antibody was used; the target culture cell was
BT-474), FIG. 35 (066-174 as anti-ALCAM antibody was used; the
target culture cell was NCI-H1373, CW2, or NCI-H441), FIG. 36
(035-234 as anti-ALCAM antibody was used; the target culture cell
was CW2 or NCI-H441), FIG. 37 (053-051 as anti-ICAM1 antibody was
used; the target culture cell was NCI-H441 and HepG2), FIG. 38
(053-059 as anti-ICAM1 antibody was used; the target culture cell
was NCI-H441 and HepG2), and FIG. 39 (053-085 as anti-ICAM1
antibody was used; the target culture cell was NCI-H441 and HepG2).
I
[0952] The measurement results of the antibody dosage dependence of
the ADCC activity are shown in FIG. 40 (048-006 or 059-152 antibody
as anti-HER I antibody was used; the target culture cell was
CCF-RC-1), FIG. 41 (048-006 or 059-152 antibody as anti-HER1
antibody was used; the target culture cell was NCI-H1373), FIG. 42
(048-006 or 059-152 antibody as anti-HER1 antibody was used; the
target culture cell was A-431), FIG. 43 (041-118 antibody as
anti-ALCAM antibody was used; the target culture cell was
NCI-H1373), FIG. 44 (067-153 antibody as anti-EpCAM antibody was
used; the target culture cell was MKN-45), FIG. 45 (067-153
antibody as anti-EpCAM antibody was used; the target culture cell
was HT-29), FIG. 46 (067-153 antibody as anti-EpCAM antibody was
used; the target culture cell was NCI-H1373), and FIG. 47 (067-133
antibody as anti-HGFR antibody was used; the target culture cell
was NCI-H1373).
[0953] Similarly, the measurement results of the antibody dosage
dependence of the ADCC activity are shown in FIG. 48 (055-147
antibody or 059-173 antibody as anti-HER1 antibody was used; the
target culture cell was CCF-RC1), FIG. 49 (048-006 antibody,
059-152 antibody, 055-147 antibody or 059-173 antibody as anti-HER1
antibody was used; the target culture cell was HT-29), FIG. 50
(048-006 antibody, 055-147 antibody or 059-173 antibody as
anti-HER1 antibody was used; the target culture cell was A431),
FIG. 51 (048-006 antibody or 059-152 antibody as anti-HER1 antibody
was used; the target culture cell was ACHN), FIG. 52 (035-234
antibody or 066-174 antibody as anti-ALCAM antibody was used; the
target culture cell was NCI-H1373), FIG. 53 (035-234 antibody or
066-174 antibody as anti-ALCAM antibody was used; the target
culture cell was target cell SKOv3), FIG. 54 (035-234 antibody or
066-174 antibody as anti-ALCAM antibody was used; the target
culture cell was CW-2), FIG. 55 (041-118 antibody as anti-ALCAM
antibody was used; the target culture cell was EBC-1), FIG. 56
(080-040 antibody as anti-ALCAM antibody was used; the target
culture cell was NCI-H1373), FIG. 57 (053-042 antibody as
anti-ICAM1 antibody was used; the target culture cell was
NCI-H1373), FIG. 58 (053-051 antibody, 053-059 antibody or 053-085
antibody as anti-ICAM I antibody was used; the target culture cell
was NCI-H1373), FIG. 59 (067-153 antibody as anti-EpCAM antibody
was used; the target culture cell was EBC-1), FIG. 60 (067-133
antibody as anti-HGFR antibody was used; the target culture cell
was MKN-45), FIG. 61 (067-133 antibody as anti-HGFR antibody was
used; the target culture cell was EBC-1), FIG. 62 (015-003 antibody
as anti-ITGA3 antibody was used; the target culture cell was ACHN),
FIG. 63 (059-053 antibody as anti-CD147 antibody was used; the
target culture cell was CCF-RC1), FIG. 64 (059-053 antibody as
anti-CD147 antibody was used; the target culture cell was ACHN),
FIG. 65 (064-044 antibody or 079-085 antibody as anti-PTP-LAR
antibody was used; the target culture cell was PC-14), and FIG. 66
(064-003 antibody as anti-CD44 antibody was used; the target
culture cell was PC-14).
[0954] In any of anti-ITGA3 antibody (015-003), anti-HER1 antibody
(048-006) and anti-HER2 antibody (015-126), anti-CD44 antibody
(064-003), the cytotoxicity was increased in the experiment groups
in which the effector cell was added. That is to say, in any of the
antibodies, the cytotoxic activity caused by the effector cell that
recognizes an antibody to which a target cell has been
specifically-bound and attacks the target cell was observed.
[0955] Note here that an anti-habu venom antibody (control
antibody) HR1-007 that is not related to the surface antigen or the
experiment group in which the antibody clone is not added, the
increase in the cytotoxicity is not observed. In any of anti-ALCAM
antibodies (066-174, 035-234, 041-118, and 083-040), anti-ICAM1
antibody (053-051, 053-059, 053-085, and 053-042), and anti-CD147
antibody (059-053), the cytotoxicity is increased more
significantly than in the anti-habu venom antibody (control
antibody) HR1-007 experiment group. As mentioned above, it is
clearly shown that the antibody dependent cytotoxicity is higher
than that of the control antibody (HR1-007) with a significant
difference.
[0956] From the above-mentioned results, it has been confirmed that
an antibody capable of specifically recognizing a cancer cell and
exhibiting a damaging effect by the ADCC activity has been obtained
for each of HER1, HER2, ITGA3, ALCAM, ICAM, CD44, CD147, EPCAM and
HGFR. In other words, an antibody that is a promising as the
antibody medicine targeting each of cancer cells has been
obtained.
[0957] In the results of the antibody dosage dependence test,
anti-HER1 antibody (048-006) shows a significant effect even if the
dosage is 0.01 .mu.g/ml. It is determined that the effect is
expected with low dosage.
[0958] It is observed that the 048-006 antibody and 059-152
antibody tend to have a strong ADCC activity in the cell line in
which HER1 is expressed. However, the activity differs depending
upon the concentration range of the antibody to be used or the
kinds of antibodies. To A431 cell, with 0.001 Hg/ml, the difference
in the activity was observed. Generally, in the low concentration
range, the activity of 059-152 antibody was more significant than
that of 048-006 antibody. Furthermore, 055-147 antibody and 059-173
antibody shows higher ADCC activity than ERBITUX.TM. that is
commercially available drug and is more useful.
[0959] Furthermore, 067-153 antibody as anti-EpCAM antibody shows
an excellent ADCC activity to MKN-45 (solid-type gastric
adenocarcinoma) cell line at the concentration of 0.01 .mu.g/ml or
more, and it shows an excellent ADCC activity to HT-29 (colon
adenocarcinoma) cell line at the concentration of 10 .mu.g/ml or
more with an amazing score of 80% or more in the ADCC activity in
the concentration range of about 1 .mu.g/ml. It shows an amazing
score of 50% or more in the ADCC activity in NCI-H1373 (pulmonary
adenocarcinoma) cell line at the concentration of 0.01 .mu.g/ml or
more.
[0960] Furthermore, 041-118 antibody as anti-ALCAM antibody shows a
remarkable effect to NCI-H1373 (pulmonary adenocarcinoma) cell line
at the concentration of 0.01 .mu.g/ml or more. It is determined
that the effect can be expected with low dosage.
[0961] Furthermore, 066-174 antibody as anti-ALCAM antibody shows
high ADCC activity to various cells such as NCI-H1373 (pulmonary
adenocarcinoma) cell line, SKOv3 (ovarian cancer) cell line, and
CW-2 (large bowel cancer) cell line. Wide application is
expected.
[0962] Furthermore, 067-133 antibody as anti-HGFR antibody shows a
remarkable effect to NCI-H1373 (pulmonary adenocarcinoma) cell line
at the concentration of 0.01 .mu.g/ml or more with strong activity
of 40% or more at the concentration of 10 .mu.g/ml or more.
[0963] Furthermore, 059-053 antibody as anti-CD147 antibody shows
an excellent ADCC effect to CCF-RC1 (kidney cancer) cell line and
ACHN (kidney cancer) cell line, which shows near the upper limit
value at the low concentration. Therefore, it can be expected to
show the maximum activity at a low concentration.
[0964] From the above-mentioned results, it is confirmed that a
promising antibody group showing a sufficient ADCC activity even
with low dosage (at low concentration) can be obtained
successfully. Also in the similar experiments using a plurality of
lymphocyte fractions derived from human, the same results as
mentioned above can be obtained. The high reproducibility is
confirmed.
17. Cancer Cell Proliferation Inhibition Test
[0965] Some antibody medicines exhibit the efficacy by an effect of
inhibiting the proliferation of cancer instead of the ADCC effect
(or in addition to the ADCC effect). Thus, in order to further
investigate the efficacy of antibody medicine, the activity of
inhibiting the proliferation of cancer by antibodies that have been
successfully isolated have been investigated according to the
following procedure.
17-1 Testing Method
[0966] (1) Target culture cells that have grown in a culture dish
are peeled off with 4% Collagenase and suspended in the used
medium. (2) The cell density is measured and then the supernatant
is removed by centrifugation and suspended in a RPMI-1640 (10% FBS,
1% Penicillin--Streptomycin) medium so that the final density is
1.0.times.10.sup.4 cells/ml. (3) 100 .mu.l each of target cells is
dispensed in a flat-bottom 96 well multi plate. (4) 100 .mu.l each
of 20 .mu.g/ml human IgG monoclonal antibody solution is dispensed.
(5) Reaction is carried out in 5% CO.sub.2 at 37.degree. C. for 5
days. (6) Medium is removed, and living cell measurement reagent
(XTT: Roche) is dispensed in each well (150 .mu.l each). (7)
Reaction is carried out in 5% CO.sub.2 at 37.degree. C. for 4
hours. (8) After reaction, OD490 and OD690 are measured by using a
micro plate absorptiometer. Then, the number of living cells is
calculated according to the following equation.
XTT reduction amount (degree of coloring)=OD490-OD690
XTT reducing activity derived from cells=(experimental
value)-(control value using only a solution) [Equation 2]
[0967] Note here that the XTT reducing activity derived from cells
is in proportion to the number of living cells.
17-2 Results
[0968] The results are shown in FIG. 67 (anti-HER1 antibody
(048-006) was used; the target subject cultured cell was A-431),
FIG. 68 (anti-HER1 antibody (048-006) was used; the target subject
cultured cell was ACHN), FIG. 69 (anti-HER1 antibody (048-006) was
used; the target subject cultured cell was NCI-H1373), FIG. 70
(anti-HER1 antibody (048-006) was used; the target subject cultured
cell wasSK-OV-3), and FIG. 71 (anti-HER2 antibody (015-126) was
used; the target subject cultured cell was BT-474).
[0969] As is apparent from these drawings, it is confirmed that the
antibodies inhibiting the proliferation of cancer cell can be
successfully obtained. In other words, it is shown that these
antibodies may be effective as antibody medicine of suppressing the
proliferation of cancer cells.
18. Antitumor Experiment Using Mouse
[0970] Next, whether or not the antibodies that have been
successfully isolated show an anti-tumor activity in vivo is
confirmed by using a cancer cell-transplanted mouse.
18-1 Animals and Cell Line to be Used
[0971] Four-week old female BALB/c nude mouse (Charles River Japan)
was acclimated and bred for one week and then used for experiment.
The animals were bred under the SPF environment and fed with
sterilized water and feed.
[0972] Human lung cancer cell H1373 or epidermoid tumor A-431,
which had been subcultured in a RPMI medium containing 10% FBS at
37.degree. C. in the presence of 5% CO.sub.2, were used.
18-2 Method of Antitumor Experiment
[0973] Human lung cancer cells, H1373 cells (1.times.10.sup.7
cells) were transplanted in the dorsolateral subcutaneous portion
of a nude mouse so as to produce a tumor. At the time the tumor
volume was 1 cm.sup.3, the tumor was cut into a size of 3
mm.times.3 mm, and is was successive-transplanted to the dorsal
subcutaneous portion of the prepared nude mouse. After
transplantation, when a volume of the tumor was estimated to be 200
mm.sup.3, administration of the antibody was started. The diameter
of the tumor and body weight were measure twice a week, estimated
tumor volume was calculated from the equation: W=a.times.b.sup.2/2
(W: estimated tumor volume (mm.sup.3), a: major axis (mm), b: minor
axis (mm)). The experiment group was divided into a control group
(PBS was administered) and 048-006 IgG administered group (0.5
mg/individual). The administration pathway was made to be an
intraperitoneal administration. Administration was carried out
twice a week eight times in total. Then, the anti-tumor effect was
examined.
[0974] Furthermore, ERBITUX (Cetuximab, Bristol-Myers Squibb
Company) was used as a comparative group or an additivity examining
group. When ERBITUX is used singly, the dosage amount was made to
be 0.25 mg/individual. ERBITUX was used together with 048-006 IgG,
the dosage amount of ERBITUX was made to be 0.25 mg/individual and
the dosage amount of 048-006 IgG was made to be 0.25 mg/individual.
After administration, the follow-up was carried out.
[0975] When epidermoid tumor A-431 is used, epidermoid tumors A-431
(5.times.10.sup.6) were similarly transplanted in the dorsolateral
subcutaneous portion of a five-week old female BALB/c nude mouse
nude mouse so as to produce a tumor. At the time the tumor volume
was estimated to be 200 mm.sup.3, administration of the antibody
was started. The administration pathway was made to be an
intraperitoneal administration. 048-006 IgG type antibody was
administered twice a week six times in total. Then, the anti-tumor
effect was examined. 059-152 IgG type antibody administered group
(0.25 mg or 1.00 mg of antibody was diluted in 0.5 ml
PBS/individual) twice a week six times in total. Then, the
anti-tumor effect was examined. And the follow up was also carried
out.
18-3 Results
[0976] In the antibody (048-006 IgG type antibody) administered
group, estimated tumor volume was significantly reduced as compared
with the control group (PBS was administered), showing a clear
anti-tumor effect. It was confirmed that the effect was comparative
to ERBITUX (see FIGS. 72 to 75). On the other hand, in the antibody
(059-152 IgG type antibody) administered group, estimated tumor
volume was significantly reduced as compared with the control group
(PBS was administered), showing a clear anti-tumor effect. The
effect was more excellent than that of ERBITUX (see FIG. 75).
059-152 antibody shows stronger tumor suppression effect than
048-006 antibody and commercially available ERBITUX. Thus, it was
confirmed that the successfully obtained antibodies exhibited the
anti-tumor effect in also in vivo model. In other words, they are
shown to be an extremely promising as the antibody medicine.
[0977] 19. Analysis by Three Dimensional ELISA
(1) Expression of Antibody by Culturing Screened Clone Group and
Preparation of Antibody Mixture
[0978] Clones (about 4000 clones) of phage-infected E. coli, which
were screened by the methods described in 1 to 5, were transferred
to 41 sheets of 96-well plates at 1 clone/well, and they were
shaking cultured in 100 .mu.l/well YTGA medium (YT medium+1%
Glucose+200 .mu.g/ml Ampicillin) at 30.degree. C. overnight. Next,
10 .mu.l each of culture solution was mixed in all wells of the
first to sixth columns for each plate to make one group (however,
as to the 28th plate, the first to seventh columns are made to be
one group). Forty-one plates of the mixed antibodies were obtained
in total. As to 7th to 12th columns were also made into one group
(excluding the 28th plate and 35th plate). Thirty-nine plates of
the mixed antibodies in total were obtained. Furthermore, after the
plates were divided into 7 groups (3, 6 or 7 sheets per group), for
each group, 10 .mu.l each of culture solution was mixed in all
wells in each row and they were made to one group. Thus, 56 rows of
the mixed antibodies in total were obtained. Finally, after the
plates were divided into 5 groups (3, 9 or 10 sheets per group),
for each group, 10 .mu.l each of culture solution was mixed in all
wells in each column and they were made to one group. Thus, 54
columns of the mixed antibodies in total (in a part, two columns
were made to one group) were obtained.
[0979] A YT0.05GA medium (YT medium+0.05% Glucose+200 .mu.g/ml
Ampicillin) (100 ml) was added to each mixed antibody, and shaking
cultured at 30.degree. C. until OD600 nm was about 0.3 to 0.5.
Thereafter, IPTG was added so that the final concentration was 0.5
mM and further shaking cultured at 30.degree. C. The mixture was
centrifuged at 10000 rpm at 4.degree. C. for 15 minutes, and the
culture supernatant was recovered. Then, ammonium sulfate (29.1 g)
was slowly added and mixed, mixture was centrifuged at 10000 rpm at
4.degree. C. for 20 minutes, and sediment was recovered. The
sediment was suspended in 5 ml of PBS/NaN.sub.3/complete. The
suspension was centrifuged at 10000 rpm at 4.degree. C. for 20
minutes, and the culture supernatant was recovered. Thus, 20-fold
concentrated mixed antibodies (190 types) were obtained.
(2) Measurement by Three-Dimensional ELISA
[0980] Three dimensional ELISA was carried out by using the
obtained 20-fold concentrated mixed antibodies (190 types).
Firstly, 50 .mu.l/well of antigen whose concentration was adjusted
to be 20 .mu.g/ml with PBS was added to Maxisorp (Nunc) and reacted
at 37.degree. C. for two hours to be sensitized. After the liquid
in each well was removed, 5% skim milk/PBS (200 .mu.g/well) was
added and reacted at 37.degree. C. for two hours for blocking. The
liquid in each well was removed and washed with PBS, and 20-fold
concentrated mixed antibody (100 .mu.l/well) was added and reacted
at 37.degree. C. for one hour. The reacted product was washed with
PBS, and a rabbit anti-cp3 antibody (MBL) that had been 5000-fold
diluted with 0.05% Tween/PBS was added (100 .mu.l/well) and reacted
at 37.degree. C. for one hour. The mixture was washed with PBS, and
an HRP labeled goat anti-rabbit IgG antibody (MBL) that had been
2000-fold diluted with 0.05% Tween/PBS was added (100 .mu.l/well)
and reacted at 37.degree. C. for one hour. The reacted product was
washed with PBS and a substrate solution (100 .mu.l/well) was
added. The substrate solution was produced as followed. That is to
say, to 12 ml of 0.1 M citric acid-disodium hydrogen-phosphate (pH
5.1), H.sub.2O.sub.2 was added so that the final concentration
became 0.01% and furthermore, OPD tablet (Wako Pure Chemical) was
added.
[0981] 2N sulfuric acid (100 .mu.l/well) was added to stop the
reaction and the absorbance at 492 nm was measured by using a plate
reader (Wako Pure Chemical, SUNRISE Remote).
[0982] The measurement results are shown in FIGS. 79 to 81 (ELISA
using CK147 as an antigen) and FIGS. 82 to 84 (ELISA using HER1 as
an antigen).
[0983] Based on the results of the above-mentioned three
dimensional ELISA, positive clones were selected. That is to say,
from information of plate, row and column providing positive
results, intersection point was searched and antibody clones
existing in the intersection point were selected. The selected
antibody clones were shaking cultured in 75 .mu.l/well YTGA medium
at 30.degree. C. overnight. In 200 .mu.l/well YT0.05GA medium, the
culture solution was plated and standing cultured at 37.degree. C.
for four hours. Thereafter, IPTG was added so that the final
concentration became 1 mM and shaking cultured at 30.degree. C.
overnight. The culture was centrifuged at 3000 rpm at 4.degree. C.
for 10 minutes and the culture supernatant was recovered.
(3) Reactivity of Selected Antibody Clones
[0984] 50 .mu.l/well of antigen (CD147 or HER1) whose concentration
was adjusted to be 10 .mu.g/ml with PBS was added to Maxisorp
(Nunc) and reacted at 37.degree. C. for two hours to be sensitized.
After the liquid in each well was removed, 5% skim milk/PBS (200
.mu.l/well) was added and reacted at 37.degree. C. for two hours
for blocking. The liquid in each well was removed and washed with
PBS. The culture supernatant of the selected clones (100
.mu.l/well) was added and reacted at 37.degree. C. for one hour.
The reacted product was washed with PBS, and a rabbit anti-cp3
antibody (MBL) that had been 5000-fold diluted with 0.05% Tween/PBS
was added (1001l/well) and reacted at 37.degree. C. for one hour.
The mixture was washed with PBS, and an HRP labeled goat
anti-rabbit IgG antibody (MBL) that had been 2000-fold diluted with
0.05% Tween/PBS was added (100 .mu.l/well) and reacted at
37.degree. C. for one hour. The reacted product was washed with PBS
and a substrate solution (100 .mu.l/well) was added. 2N sulfuric
acid (100 .mu.l/well) was added to stop the reaction and the
absorbance at 492 nm was measured by using a plate reader (Wako
Pure Chemical, SUNRISE Remote). The results of ELISA using HER1 as
an antigen is show in FIG. 85. As is apparent from the graph of
FIG. 85, a large number of monoclonal antibodies to HER1 were
obtained.
20. Newly Obtained Antibodies
[0985] By using the classifying method and identification method of
the present invention, it was possible to obtain the following
antibodies successfully.
(1) Antibody to C1qR
[0986] 070-016 antibody
(a) Amino Acid Sequence
[0987] SEQ ID NO: 451 (VH); SEQ ID NO: (VH CDR1) 452; SEQ ID NO:
453 (VH CDR2); SEQ ID NO: 454 (VH CDR3), SEQ ID NO: 455 (VL); SEQ
ID NO: (VL CDR1) 456; SEQ ID NO: 457 (VL CDR2); and SEQ ID NO: 458
(VL CDR3)
(b) Base Sequence
[0988] SEQ ID NO: 843 (VH); and SEQ ID NO: 844 (VL)
(2) Antibody to CD44
[0989] 064-003 antibody
(a) Amino Acid Sequence
[0990] SEQ ID NO: 459 (VH); SEQ ID NO: 460 (VH CDR1); SEQ ID NO:
461 (VH CDR2); SEQ ID NO: 462 (VH CDR3); SEQ ID NO: 463 (VL); SEQ
ID NO: 464 (VL CDR1); SEQ ID NO: 465 (VL CDR2); and SEQ ID NO: 466
(VL CDR3)
(b) Base Sequence
[0991] SEQ ID NO: 845 (VH); and SEQ ID NO: 846 (VL)
(3) Antibody to CD73
[0992] 067-213 antibody
(a) Amino Acid Sequence
[0993] SEQ ID NO: 467 (VH); SEQ ID NO: 468 (VH CDR1); SEQ ID NO:
469 (VH CDR2); SEQ ID NO: 470 (VH CDR3); SEQ ID NO: 471 (VL); SEQ
ID NO: 472 (VL CDR1); SEQ ID NO: 473 (VL CDR2); and SEQ ID NO: 474
(VL CDR3)
(b) Base Sequence
[0994] SEQ ID NO: 847 (VH); and SEQ ID NO: 848 (VL)
(4) Antibody to EpCAM
[0995] 067-153 Antibody
(a) Amino Acid Sequence
[0996] SEQ ID NO: 475 (VH); SEQ ID NO: 476 (VH CDR1); SEQ ID NO:
477 (VH CDR2); SEQ ID NO: 478 (VH CDR3); SEQ ID NO: 479 (VL); SEQ
ID NO: 480 (VL CDR1); SEQ ID NO: 481 (VL CDR2); and SEQ ID NO: 482
(VL CDR3)
(b) Base Sequence
[0997] SEQ ID NO: 849 (VH); and SEQ ID NO: 850 (VL)
(5) Antibody to HER1
[0998] 048-040 antibody
(a) Amino Acid Sequence
[0999] SEQ ID NO: 483 (VH); SEQ ID NO: 484 (VH CDR1); SEQ ID NO:
485 (VH CDR2); SEQ ID NO: 486 (VH CDR3); SEQ ID NO: 487 (VL); SEQ
ID NO: 488 (VL CDR1); SEQ ID NO: 489 (VL CDR2); and SEQ ID NO: 490
(VL CDR3)
(b) Base Sequence
[1000] SEQ ID NO: 851 (VH); and SEQ ID NO: 852 (VL)
[1001] 054-101 antibody
(a) Amino Acid Sequence
[1002] SEQ ID NO: 491 (VH); SEQ ID NO: 492 (VH CDR1); SEQ ID NO:
493 (VH CDR2); SEQ ID NO: 494 (VH CDR3); SEQ ID NO: 495 (VL); SEQ
ID NO: 496 (VL CDR1); SEQ ID NO: 497 (VL CDR2); and SEQ ID NO: 498
(VL CDR3)
(b) Base Sequence
[1003] SEQ ID NO: 853 (VH); and SEQ ID NO: 854 (VL)
[1004] 055-147 antibody
(a) Amino Acid Sequence
[1005] SEQ ID NO: 499 (VH); SEQ ID NO: 500 (VH CDR1); SEQ ID NO:
501 (VH CDR2); SEQ ID NO: 502 (VH CDR3); SEQ ID NO: 503 (VL); SEQ
ID NO: 504 (VL CDR1); SEQ ID NO: 505 (VL CDR2); and SEQ ID NO: 506
(VL CDR3)
(b) Base Sequence
[1006] SEQ ID NO: 855 (VH); and SEQ ID NO: 856 (VL)
[1007] 059-173 antibody
(a) Amino Acid Sequence
[1008] SEQ ID NO: 507 (VH); SEQ ID NO: 508 (VH CDR1); SEQ ID NO:
509 (VH CDR2); SEQ ID NO: 510 (VH CDR3); SEQ ID NO: 511 (VL); SEQ
ID NO: 512 (VL CDR1); SEQ ID NO: 513 (VL CDR2); and SEQ ID NO: 514
(VL CDR3)
(b) Base Sequence
[1009] SEQ ID NO: 857 (VH); and SEQ ID NO: 858 (VL)
[1010] 067-149 antibody
(a) Amino Acid Sequence
[1011] SEQ ID NO: 515 (VH); SEQ ID NO: 516 (VH CDR1); SEQ ID NO:
517 (VH CDR2); SEQ ID NO: 518 (VH CDR3); SEQ ID NO: 519 (VL); SEQ
ID NO: 520 (VL CDR1); SEQ ID NO: 521 (VL CDR2); and SEQ ID NO: 522
(VL CDR3)
(b) Base Sequence
[1012] SEQ ID NO: 859 (VH); and SEQ ID NO: 860 (VL)
[1013] 067-176 antibody
(a) Amino Acid Sequence
[1014] SEQ ID NO: 523 (VH); SEQ ID NO: 524 (VH CDR1); SEQ ID NO:
525 (VH CDR2); SEQ ID NO: 526 (VH CDR3); SEQ ID NO: 527 (VL); SEQ
ID NO: 528 (VL CDR1); SEQ ID NO: 529 (VL CDR2); and SEQ ID NO: 530
(VL CDR3)
(b) Base Sequence
[1015] SEQ ID NO: 861 (VH); and SEQ ID NO: 862 (VL)
(6) Antibody to HER2
[1016] 015-044 antibody
(a) Amino Acid Sequence
[1017] SEQ ID NO: 531 (VH); SEQ ID NO: 532 (VH CDR1); SEQ ID NO:
533 (VH CDR2); SEQ ID NO: 534 (VH CDR3); SEQ ID NO: 535 (VL); SEQ
ID NO: 536 (VL CDR1); SEQ ID NO: 537 (VL CDR2); and SEQ ID NO: 538
(VL CDR3)
(b) Base Sequence
[1018] SEQ ID NO: 863 (VH); and SEQ ID NO: 864 (VL)
[1019] 015-102 antibody
(a) Amino Acid Sequence
[1020] SEQ ID NO: 539 (VH); SEQ ID NO: 540 (VH CDR1); SEQ ID NO:
541 (VH CDR2); SEQ ID NO: 542 (VH CDR3); SEQ ID NO: 543 (VL); SEQ
ID NO: 544 (VL CDR1); SEQ ID NO: 545 (VL CDR2); and SEQ ID NO: 546
(VL CDR3)
(b) Base Sequence
[1021] SEQ ID NO: 865 (VH); and SEQ ID NO: 866 (VL)
[1022] 015-136 antibody
(a) Amino Acid Sequence
[1023] SEQ ID NO: 547 (VH); SEQ ID NO: 548 (VH CDR1); SEQ ID NO:
549 (VH CDR2); SEQ ID NO: 550 (VH CDR3); SEQ ID NO: 551 (VL); SEQ
ID NO: 552 (VL CDR1); SEQ ID NO: 553 (VL CDR2); and SEQ ID NO: 554
(VL CDR3)
(b) Base Sequence
[1024] SEQ ID NO: 867 (VH); SEQ ID NO: 868 (VL)
[1025] 015-143 antibody
(a) Amino Acid Sequence
[1026] SEQ ID NO: 555 (VH); SEQ ID NO: 556 (VH CDR1); SEQ ID NO:
557 (VH CDR2); SEQ ID NO: 558 (VH CDR3); SEQ ID NO: 559 (VL); SEQ
ID NO: 560 (VL CDR1); SEQ ID NO: 561 (VL CDR2); SEQ ID NO: 562 (VL
CDR3)
(b) Base Sequence
[1027] SEQ ID NO: 869 (VH); SEQ ID NO: 870 (VL)
[1028] 015-209 antibody
(a) Amino Acid Sequence
[1029] SEQ ID NO: 563 (VH); SEQ ID NO: 564 (VH CDR1); SEQ ID NO:
565 (VH CDR2); SEQ ID NO: 566 (VH CDR3); SEQ ID NO: 567 (VL); SEQ
ID NO: 568 (VL CDR1); SEQ ID NO: 569 (VL CDR2); SEQ ID NO: 570 (VL
CDR3)
(b) Base Sequence
[1030] SEQ ID NO: 871 (VH); SEQ ID NO: 872 (VL)
[1031] 039-016 antibody
(a) Amino Acid Sequence
[1032] SEQ ID NO: 571 (VH); SEQ ID NO: 572 (VH CDR1); SEQ ID NO:
573 (VH CDR2); SEQ ID NO: 574 (VH CDR3); SEQ ID NO: 575 (VL); SEQ
ID NO: 576 (VL CDR1); SEQ ID NO: 577 (VL CDR2); SEQ ID NO: 578 (VL
CDR3)
(b) Base Sequence
[1033] SEQ ID NO: 873 (VH); SEQ ID NO: 874 (VL)
[1034] 053-216 antibody
(a) Amino Acid Sequence
[1035] SEQ ID NO: 579 (VH); SEQ ID NO: 580 (VH CDR1); SEQ ID NO:
581 (VH CDR2); SEQ ID NO: 582 (VH CDR3); SEQ ID NO: 583 (VL); SEQ
ID NO: 584 (VL CDR1); SEQ ID NO: 585 (VL CDR2); SEQ ID NO: 586 (VL
CDR3)
(b) Base Sequence
[1036] SEQ ID NO: 875 (VH); SEQ ID NO: 876 (VL)
[1037] 075-024 antibody
(a) Amino Acid Sequence
[1038] SEQ ID NO: 587 (VH); SEQ ID NO: 588 (VH CDR1); SEQ ID NO:
589 (VH CDR2); SEQ ID NO: 590 (VH CDR3); SEQ ID NO: 591 (VL); SEQ
ID NO: 592 (VL CDR1); SEQ ID NO: 593 (VL CDR2); SEQ ID NO: 594 (VL
CDR3)
(b) Base Sequence
[1039] SEQ ID NO: 877 (VH); SEQ ID NO: 878 (VL)
[1040] 075-110 antibody
(a) Amino Acid Sequence
[1041] SEQ ID NO: 595 (VH); SEQ ID NO: 596 (VH CDR1); SEQ ID NO:
597 (VH CDR2); SEQ ID NO: 598 (VH CDR3); SEQ ID NO: 599 (VL); SEQ
ID NO: 600 (VL CDR1); SEQ ID NO: 601 (VL CDR2); SEQ ID NO: 602 (VL
CDR3)
(b) Base Sequence
[1042] SEQ ID NO: 879 (VH); SEQ ID NO: 880 (VL)
[1043] 086-032 antibody
(a) Amino Acid Sequence
[1044] SEQ ID NO: 603 (VH); SEQ ID NO: 604 (VH CDR1); SEQ ID NO:
605 (VH CDR2); SEQ ID NO: 606 (VH CDR3); SEQ ID NO: 607 (VL); SEQ
ID NO: 608 (VL CDR1); SEQ ID NO: 609 (VL CDR2); SEQ ID NO: 610 (VL
CDR3)
(b) Base Sequence
[1045] SEQ ID NO: 881 (VH); SEQ ID NO: 882 (VL)
[1046] 086-035 antibody
(a) Amino Acid Sequence
[1047] SEQ ID NO: 611 (VH); SEQ ID NO: 612 (VH CDR1); SEQ ID NO:
613 (VH CDR2); SEQ ID NO: 614 (VH CDR3); SEQ ID NO: 615 (VL); SEQ
ID NO: 616 (VL CDR1); SEQ ID NO: 617 (VL CDR2); SEQ ID NO: 618 (VL
CDR3)
(b) Base Sequence
[1048] SEQ ID NO: 883 (VH); SEQ ID NO: 884 (VL)
[1049] 086-036 antibody
(a) Amino Acid Sequence
[1050] SEQ ID NO: 619 (VH); SEQ ID NO: 620 (VH CDR1); SEQ ID NO:
621 (VH CDR2); SEQ ID NO: 622 (VH CDR3); SEQ ID NO: 623 (VL); SEQ
ID NO: 624 (VL CDR1); SEQ ID NO: 625 (VL CDR2); SEQ ID NO: 626 (VL
CDR3)
(b) Base Sequence
[1051] SEQ ID NO: 885 (VH); SEQ ID NO: 886 (VL)
[1052] 086-061 antibody
(a) Amino Acid Sequence
[1053] SEQ ID NO: 627 (VH); SEQ ID NO: 628 (VH CDR1); SEQ ID NO:
629 (VH CDR2); SEQ ID NO: 630 (VH CDR3); SEQ ID NO: 631 (VL); SEQ
ID NO: 632 (VL CDR1); SEQ ID NO: 633 (VL CDR2); SEQ ID NO: 634 (VL
CDR3)
(b) Base Sequence
[1054] SEQ ID NO: 887 (VH); SEQ ID NO: 888 (VL)
[1055] 086-138 antibody
(a) Amino Acid Sequence
[1056] SEQ ID NO: 635 (VH); SEQ ID NO: 636 (VH CDR1); SEQ ID NO:
637 (VH CDR2); SEQ ID NO: 638 (VH CDR3); SEQ ID NO: 639 (VL); SEQ
ID NO: 640 (VL CDR1); SEQ ID NO: 641 (VL CDR2); SEQ ID NO: 642 (VL
CDR3)
(b) Base Sequence
[1057] SEQ ID NO: 889 (VH); SEQ ID NO: 890 (VL)
[1058] 086-182 antibody
(a) Amino Acid Sequence
[1059] SEQ ID NO: 643 (VH); SEQ ID NO: 644 (VH CDR1); SEQ ID NO:
645 (VH CDR2); SEQ ID NO: 646 (VH CDR3); SEQ ID NO: 647 (VL); SEQ
ID NO: 648 (VL CDR1); SEQ ID NO: 649 (VL CDR2); SEQ ID NO: 650 (VL
CDR3,
(b) Base Sequence
[1060] SEQ ID NO: 891 (VH); SEQ ID NO: 892 (VL)
(7) Antibody to HGFR 067-126 antibody
(a) Amino Acid Sequence
[1061] SEQ ID NO: 651 (VH); SEQ ID NO: 652 (VH CDR1); SEQ ID NO:
653 (VH CDR2); SEQ ID NO: 654 (VH CDR3); SEQ ID NO: 655 (VL); SEQ
ID NO: 656 (VL CDR1); SEQ ID NO: 657 (VL CDR2); SEQ ID NO: 658 (VL
CDR3)
(b) Base Sequence
[1062] SEQ ID NO: 893 (VH); SEQ ID NO: 894 (VL)
[1063] 067-133 antibody
(a) Amino Acid Sequence
[1064] SEQ ID NO: 659 (VH); SEQ ID NO: 660 (VH CDR1); SEQ ID NO:
661 (VH CDR2); SEQ ID NO: 662 (VH CDR3); SEQ ID NO: 663 (VL); SEQ
ID NO: 664 (VL CDR1); SEQ ID NO: 665 (VL CDR2); SEQ ID NO: 666 (VL
CDR3)
(b) Base Sequence
[1065] SEQ ID NO: 895 (VH); SEQ ID NO: 896 (VL)
[1066] 067-287 antibody
(a) Amino Acid Sequence
[1067] SEQ ID NO: 667 (VH); SEQ ID NO: 668 (VH CDR1); SEQ ID NO:
669 (VH CDR2); SEQ ID NO: 670 (VH CDR3); SEQ ID NO: 671 (VL); SEQ
ID NO: 672 (VL CDR1); SEQ ID NO: 673 (VL CDR2); SEQ ID NO: 674 (VL
CDR3)
(b) Base Sequence
[1068] SEQ ID NO: 897 (VH); SEQ ID NO: 898 (VL)
(8) Antibody to ITGA3
[1069] 064-002 antibody
(a) Amino Acid Sequence
[1070] SEQ ID NO: 675 (VH); SEQ ID NO: 676 (VH CDR1); SEQ ID NO:
677 (VH CDR2); SEQ ID NO: 678 (VH CDR3); SEQ ID NO: 679 (VL); SEQ
ID NO: 680 (VL CDR1); SEQ ID NO: 681 (VL CDR2); SEQ ID NO: 682 (VL
CDR3)
(b) Base Sequence
[1071] SEQ ID NO: 899 (VH); SEQ ID NO: 900 (VL)
[1072] 064-006 antibody
(a) Amino Acid Sequence
[1073] SEQ ID NO: 683 (VH); SEQ ID NO: 684 (VH CDR1); SEQ ID NO:
685 (VH CDR2); SEQ ID NO: 686 (VH CDR3); SEQ ID NO: 687 (VL); SEQ
ID NO: 688 (VL CDR1); SEQ ID NO: 689 (VL CDR2); SEQ ID NO: 690 (VL
CDR3)
(b) Base Sequence
[1074] SEQ ID NO: 901 (VH); SEQ ID NO: 902 (VL)
[1075] 064-012a antibody
(a) Amino Acid Sequence
[1076] SEQ ID NO: 691 (VH); SEQ ID NO: 692 (VH CDR1); SEQ ID NO:
693 (VH CDR2); SEQ ID NO: 694 (VH CDR3); SEQ ID NO: 695 (VL); SEQ
ID NO: 696 (VL CDR1); SEQ ID NO: 697 (VL CDR2); SEQ ID NO: 698 (VL
CDR3)
(b) Base Sequence
[1077] SEQ ID NO: 903 (VH); SEQ ID NO: 904 (VL)
[1078] 064-012b antibody
(a) Amino Acid Sequence
[1079] SEQ ID NO: 699 (VH); SEQ ID NO: 700 (VH CDR1); SEQ ID NO:
701 (VH CDR2); SEQ ID NO: 702 (VH CDR3); SEQ ID NO: 703 (VL); SEQ
ID NO: 704 (VL CDR1); SEQ ID NO: 705 (VL CDR2); SEQ ID NO: 706 (VL
CDR3)
(b) Base Sequence
[1080] SEQ ID NO: 905 (VH); SEQ ID NO: 906 (VL)
[1081] 064-014 antibody
(a) Amino Acid Sequence
[1082] SEQ ID NO: 707 (VH); SEQ ID NO: 708 (VH CDR1); SEQ ID NO:
709 (VH CDR2); SEQ ID NO: 710 (VH CDR3); SEQ ID NO: 711 (VL); SEQ
ID NO: 712 (VL CDR1); SEQ ID NO: 713 (VL CDR2); SEQ ID NO: 714 (VL
CDR3)
(b) Base Sequence
[1083] SEQ ID NO: 907 (VH); SEQ ID NO: 908 (VL)
[1084] 064-054 antibody
(a) Amino Acid Sequence
[1085] SEQ ID NO: 715 (VH); SEQ ID NO: 716 (VH CDR1); SEQ ID NO:
717 (VH CDR2); SEQ ID NO: 718 (VH CDR3); SEQ ID NO: 719 (VL); SEQ
ID NO: 720 (VL CDR1); SEQ ID NO: 721 (VL CDR2); SEQ ID NO: 722 (VL
CDR3)
(b) Base Sequence
[1086] SEQ ID NO: 909 (VH); SEQ ID NO: 910 (VL)
[1087] 064-085 antibody
(a) Amino Acid Sequence
[1088] SEQ ID NO: 723 (VH); SEQ ID NO: 724 (VH CDR1); SEQ ID NO:
725 (VH CDR2); SEQ ID NO: 726 (VH CDR3); SEQ ID NO: 727 (VL); SEQ
ID NO: 728 (VL CDR1); SEQ ID NO: 729 (VL CDR2); SEQ ID NO: 730 (VL
CDR3)
(b) Base Sequence
[1089] SEQ ID NO: 911 (VH); SEQ ID NO: 912 (VL)
[1090] 064-093 antibody
(a) Amino Acid Sequence
[1091] SEQ ID NO: 731 (VH); SEQ ID NO: 732 (VH CDR1); SEQ ID NO:
733 (VH CDR2); SEQ ID NO: 734 (VH CDR3); SEQ ID NO: 735 (VL); SEQ
ID NO: 736 (VL CDR1); SEQ ID NO: 737 (VL CDR2); SEQ ID NO: 738 (VL
CDR3)
(b) Base Sequence
[1092] SEQ ID NO: 913 (VH); SEQ ID NO: 914 (VL)
[1093] 064-116 antibody
(a) Amino Acid Sequence
[1094] SEQ ID NO: 739 (VH); SEQ ID NO: 740 (VH CDR1); SEQ ID NO:
741 (VH CDR2); SEQ ID NO: 742 (VH CDR3); SEQ ID NO: 743 (VL); SEQ
ID NO: 744 (VL CDR1); SEQ ID NO: 745 (VL CDR2); SEQ ID NO: 746 (VL
CDR3)
(b) Base Sequence
[1095] SEQ ID NO: 915 (VH); SEQ ID NO: 916 (VL)
[1096] 065-183 antibody
(a) Amino Acid Sequence
[1097] SEQ ID NO: 747 (VH); SEQ ID NO: 748 (VH CDR1); SEQ ID NO:
749 (VH CDR2); SEQ ID NO: 750 (VH CDR3); SEQ ID NO: 751 (VL); SEQ
ID NO: 752 (VL CDR1); SEQ ID NO: 753 (VL CDR2); SEQ ID NO: 754 (VL
CDR3)
(b) Base Sequence
[1098] SEQ ID NO: 917 (VH); SEQ ID NO: 918 (VL)
[1099] 067-142 antibody
(a) Amino Acid Sequence
[1100] SEQ ID NO: 763 (VH); SEQ ID NO: 764 (VH CDR1); SEQ ID NO:
765 (VH CDR2); SEQ ID NO: 766 (VH CDR3); SEQ ID NO: 767 (VL); SEQ
ID NO: 768 (VL CDR1); SEQ ID NO: 769 (VL CDR2); SEQ ID NO: 770 (VL
CDR3)
(b) Base Sequence
[1101] SEQ ID NO: 921 (VH); SEQ ID NO: 922 (VL)
[1102] 068-007 antibody
(a) Amino Acid Sequence
[1103] SEQ ID NO: 771 (VH); SEQ ID NO: 772 (VH CDR1); SEQ ID NO:
773 (VH CDR2); SEQ ID NO: 774 (VH CDR3); SEQ ID NO: 775 (VL); SEQ
ID NO: 776 (VL CDR1); SEQ ID NO: 777 (VL CDR2); SEQ ID NO: 778 (VL
CDR3)
(b) Base Sequence
[1104] SEQ ID NO: 923 (VH); SEQ ID NO: 924 (VL)
(9) Antibody to ALCAM 029-143 antibody
(a) Amino Acid Sequence
[1105] SEQ ID NO: 779 (VH); SEQ ID NO: 780 (VH CDR1); SEQ ID NO:
781 (VH CDR2); SEQ ID NO 782 (VH CDR3); SEQ ID NO: 783 (VL); SEQ ID
NO: 784 (VL CDR1); SEQ ID NO: 785 (VL CDR2); SEQ ID NO: 786 (VL
CDR3)
(b) Base Sequence
[1106] SEQ ID NO: 925 (VH); SEQ ID NO: 926 (VL)
[1107] 045-1.34 antibody
(a) Amino Acid Sequence
[1108] SEQ ID NO: 787 (VH); SEQ ID NO: 788 (VH CDR1); SEQ ID NO:
789 (VH CDR2); SEQ ID NO: 790 (VH CDR3); SEQ ID NO: 791 (VL); SEQ
ID NO: 792 (VL CDR1); SEQ ID NO: 793 (VL CDR2); SEQ ID NO: 794 (VL
CDR3)
(b) Base Sequence
[1109] SEQ ID NO: 927 (VH); SEQ ID NO: 928 (VL)
[1110] 062-101 antibody
(a) Amino Acid Sequence
[1111] SEQ ID NO: 795 (VH); SEQ ID NO: 796 (VH CDR1); SEQ ID NO:
797 (VH CDR2); SEQ ID NO: 798 (VH CDR3); SEQ ID NO: 799 (VL); SEQ
ID NO: 800 (VL CDR1); SEQ ID NO: 801 (VL CDR2); SEQ ID NO: 802 (VL
CDR3)
(b) Base Sequence
[1112] SEQ ID NO: 929 (VH); SEQ ID NO: 930 (VL)
[1113] 062-109 antibody
(a) Amino Acid Sequence
[1114] SEQ ID NO: 803 (VH); SEQ ID NO: 804 (VH CDR1); SEQ ID NO:
805 (VH CDR2); SEQ ID NO: 806 (VH CDR3); SEQ ID NO: 807 (VL); SEQ
ID NO: 808 (VL CDR1); SEQ ID NO: 809 (VL CDR2); SEQ ID NO: 810 (VL
CDR3)
(b) Base Sequence
[1115] SEQ ID NO: 931 (VH); SEQ ID NO: 932 (VL)
[1116] 084-103 antibody
(a) Amino Acid Sequence
[1117] SEQ ID NO: 811 (VH); SEQ ID NO: 812 (VH CDR1); SEQ ID NO:
813 (VH CDR2); SEQ ID NO: 814 (VH CDR3); SEQ ID NO: 815 (VL); SEQ
ID NO: 816 (VL CDR1); SEQ ID NO: 817 (VL CDR2); SEQ ID NO: 818 (VL
CDR3)
(b) Base Sequence
[1118] SEQ ID NO: 933 (VH); SEQ ID NO: 934 (VL)
[1119] 052-274 antibody
(a) Amino Acid Sequence
[1120] SEQ ID NO: 819 (VH); SEQ ID NO: 820 (VH CDR1); SEQ ID NO:
821 (VH CDR2); SEQ ID NO: 822 (VH CDR3); SEQ ID NO: 823 (VL); SEQ
ID NO: 824 (VL CDR1); SEQ ID NO: 825 (VL CDR2); SEQ ID NO: 826 (VL
CDR3)
(b) Base Sequence
[1121] SEQ ID NO: 935 (VH); SEQ ID NO: 936 (VL)
[1122] 029-067 antibody
(a) Amino Acid Sequence
[1123] SEQ ID NO: 827 (VH); SEQ ID NO: 828 (VH CDR1); SEQ ID NO:
829 (VH CDR2); SEQ ID NO: 830 (VH CDR3); SEQ ID NO: 831 (VL); SEQ
ID NO: 832 (VL CDR1); SEQ ID NO: 833 (VL CDR2); SEQ ID NO: 834 (VL
CDR3)
(b) Base Sequence
[1124] SEQ ID NO: 937 (VH); SEQ ID NO: 938 (VL)
[1125] 083-131 antibody
(a) Amino Acid Sequence
[1126] SEQ ID NO: 835 (VH); SEQ ID NO: 836 (VH CDR1); SEQ ID NO:
837 (VH CDR2); SEQ ID NO: 838 (VH CDR3); SEQ ID NO: 839 (VL); SEQ
ID NO: 840 (VL CDR1); SEQ ID NO: 841 (VL CDR2); SEQ ID NO: 842 (VL
CDR3)
(b) Base Sequence
[1127] SEQ ID NO: 939 (VH); SEQ ID NO: 940 (VL)
(10) Antibody to CD46
[1128] 066-069 antibody
(a) Amino Acid Sequence
[1129] SEQ ID NO: 755 (VH); SEQ ID NO: 756 (VH CDR1); SEQ ID NO:
757 (VH CDR2); SEQ ID NO: 758 (VH CDR3); SEQ ID NO: 759 (VL); SEQ
ID NO: 760 (VL CDR1); SEQ ID NO: 761 (VL CDR2); SEQ ID NO: 762 (VL
CDR3)
(b) Base Sequence
[1130] SEQ ID NO: 919 (VH); SEQ ID NO: 920 (VL)
(11) Antibody to LAR 064-044 antibody
(a) Amino Acid Sequence
[1131] SEQ ID NO: 944 (VH); SEQ ID NO: 945 (VL)
(b) Base Sequence
[1132] SEQ ID NO: 956 (VH); SEQ ID NO: 957 (VL)
[1133] 065-030 antibody
(a) Amino Acid Sequence
[1134] SEQ ID NO: 946 (VH); SEQ ID NO: 947 (VL)
(b) Base Sequence
[1135] SEQ ID NO: 958 (VH); SEQ ID NO: 959 (VL)
[1136] 065-358 antibody
(a) Amino Acid Sequence
[1137] SEQ ID NO: 948 (VH); SEQ ID NO: 949 (VL)
(b) Base Sequence
[1138] SEQ ID NO: 960 (VH); SEQ ID NO: 961 (VL)
[1139] 066-019 antibody
(a) Amino Acid Sequence
[1140] SEQ ID NO: 950 (VH); SEQ ID NO: 951 (VL)
(b) Base Sequence
[1141] SEQ ID NO: 962 (VH); SEQ ID NO: 963 (VL)
[1142] 079-085 antibody
(a) Amino Acid Sequence
[1143] SEQ ID NO: 952 (VH); SEQ ID NO: 953 (VL)
(b) Base Sequence
[1144] SEQ ID NO: 964 (VH); SEQ ID NO: 965 (VL)
(12) Antibody to BCAM 067-024 antibody
(a) Amino Acid Sequence
[1145] SEQ ID NO: 954 (VH); SEQ ID NO: 955 (VL)
(b) Base Sequence
[1146] SEQ ID NO: 966 (VH); SEQ ID NO: 967 (VL)
(13) Antibody to IgSF4
[1147] 076-048 antibody
(a) Amino Acid Sequence
[1148] SEQ ID NO: 968 (VH); SEQ ID NO: 969 (VL)
(b) Base Sequence
[1149] SEQ ID NO: 970 (VH); SEQ ID NO: 971 (VL)
21. Experiment to Confirm ITGA3 Antibody
[1150] From the results of the immunoprecipitation-mass
spectrometry, a part of the antibody group, it was shown that the
antibody included therein recognized a VLA complex. However, in a
strict sense, it was not possible to determine what the antibody
was, that is, whether the antigen was ITGA3 or ITGB1 or other
molecules forming a complex such as CD151. Then, the antibody
clones (015-003, 064-002, 064-006, 064-012, 064-014, 064-054,
064-085, 064-091, 064-093, 064-116, 065-183, 067-142, and 068-007)
were subjected to RNAI in order to confirm antigens.
21-1 Experiment Procedure
[1151] ITGA3 stealth oligo RNA (400 pmol) purchased from Invitrogen
and lipofect RNAi MAX (100 .mu.l) (product of Invitrogen) were
mixed with Opti-MEMI (8 ml) (product of GIBCO-BRL) and the mixture
was stood still at a room temperature for 10 minutes. To this
mixture, 4 ml of SKOv-3 cell solution (2.times.10.sup.6 cells) and
28 ml of RPMI1640-10% FBS were added. This mixture was planted on
four 10-cm culture dishes and cultured in a CO.sub.2 incubator for
two days. 1% trypsin solution was allowed to act on the cultured
cells so as to liberate cells. The cells were recovered in 5%
BSA/PBS solution so as to produce 1 ml of cell suspension. The same
experiment was carried out with respect to ITGB1. As to a group
without RNAi (control group), the same experiment was carried out
except that stealth oligo is not allowed to act.
[1152] To the recovered cells (50 .mu.l), 2.5 .mu.l of normal goat
serum was added, and then primary antibody solution was added, so
that the final amount was made to be 100 .mu.l by using 5% BSA/PBS.
The using amount of the primary antibody (anti-ITGA3 antibody or
anti-ITGB1 antibody (mouse monoclonal antibody, product of
CHEMICON)) was made to be 1 .mu.l. As to the subjected sample (for
example, 015-003 cp3 type antibody), 7 .mu.l of 10-fold
concentrated supernatant was used.
[1153] Next, the mixture was stood still at a room temperature for
10 minutes and then subjected to centrifugation. The supernatant
was discarded, followed by washing with 5% BSA/PBS (200 .mu.l).
Next, as to the sample 015-003 cp3 type antibody, 100 .mu.l of
anti-cp3 mouse monoclonal antibody (MBL), which had been diluted
with 5% BSA/PBS so that the concentration became 5 .mu.g/ml, was
added. The mixture was stood still at a room temperature for 10
minutes. After centrifugation, the supernatant was discarded,
followed by washing with 5% BSA/PBS (200 .mu.l). Then, ALEXA488
labeled anti-mouse IgG goat antibody (100 .mu.l), which had been
1000-folded diluted with 5% BSA/PBS, was reacted. The reacted
product was stood still at a room temperature for 10 minutes and
then subjected to centrifugation. The supernatant was discarded,
followed by washing with 5% BSA/PBS (200 .mu.l). The thus obtained
cells were suspended in 50 .mu.l of OptilyseB (BECKMAN COULTER).
This was stood still for 10 minutes, and then 600 .mu.l of PBS was
added to be diluted. Subsequently, the diluted product was treated
with Cell-Strainer (BD Falcon) and subjected to measurement using
FACS Caliber (BECKMAN COULTER).
21-2 Results
[1154] The results of the above-mentioned RNAi experiment are shown
in FIG. 86. It is shown that A (results of FCM using anti-ITGA3
antibody) and B (results of FCM using anti-ITGB1 antibody) have
different peak patterns. The samples (015-003, 064-002, 064-006,
064-012, 064-014, 064-054, 064-085, 064-091, 064-093, 064-116,
065-183, 067-142, and 068-007) show the peak patterns (C) similar
to A. From this result, it is confirmed that antigen recognized by
these antibody clones is ITGA3.
[1155] When the same RNAi experiment is carried out in each
antibody obtained as an anti-HER1 antibody, an anti-HER2 antibody,
an anti-HGFR antibody, an anti-IgSF4 antibody, an anti-EpCAM
antibody, an anti-CD147 antibody, an anti-CD166 antibody, or
anti-MCP antibody, antigen is not wrong, and it is confirmed that
the method (method using a panel, three-dimensional ELISA)) of the
present invention is useful.
22. Cancer Tissue Specificity of Each Antibody Clone
[1156] When the immunostaining property of the obtained antibody
clones with respect to clinical cancer specimens were examined by
the same method as described in the above column 11, results shown
in FIG. 87 were obtained. These antibody clones are useful for
studying and diagnosing the corresponding cancers. Furthermore,
clinical specimens in different stages in some cancers were
prepared and the immunostaining property of the antibody clones
with respect to the specimens was obtained. As a result, some
antibody clones showed the staining property specific to stages in
addition to the staining property specific to cancer (see FIG. 88).
Thus, in the actual clinical tissues, there are differences in the
reactivity to each antibody clone even if the tissue is from the
same cancer or in the same grade of malignancy. This results show
that the use of the antibody set provided by the present invention
enables new tailor-maid diagnosis in cancers to be carried out and
diagnosis that is more detail than conventional criterion to be
carried out. In other words, it is shown that staging of cancer and
re-classification of pathologic conditions can be realized. On the
other hand, the staging of cancer and the re-classification of
pathologic conditions by using the antibody set are useful for
determining a treatment plan. Furthermore, antibodies recognized to
have specific reactivity can be useful as antibodies for treatment
and useful as a tool for drug screening. Thus, the antibody set
provided by the present invention can realize not only tailor-made
diagnosis of cancers but also tailor-made treatment of cancers.
Thus, the antibody set provides extremely great values and
significance.
INDUSTRIAL APPLICABILITY
[1157] The present invention provides a method of classifying a
plurality of antibodies to cell surface antigens rapidly. Also, the
present invention provides a method of rapidly identifying an
antigen to an antibody. The use of these methods makes it possible
to obtain an antibody useful for treatment and diagnosis of
cancers, or study of the onset mechanism of cancers, and the like.
Furthermore, when the classifying method and the identification
method of an antigen of the present invention are used, a panel on
which a useful antibody set and its characteristics are displayed
can be provided, which is expected to greatly contribute to
tailor-made medicine. On the other hand, the present invention
provides antibodies recognizing antigens expressing in a
cancer-specific manner. Such antibodies are expected to be used as
antibody for treatment, antibody for diagnosis, antibody for study,
and the like, which target cancer cells specifically expressing
cancer surface membrane protein recognized by the antibodies.
[1158] The present invention is not limited only to the description
of the above embodiments. A variety of modifications which are
within the scopes of the following claims and which are achieved
easily by a person skilled in the art are included in the present
invention.
[1159] Contents of the theses, Publication of Patent Applications,
Patent Publications, and other published documents referred to in
this specification are herein incorporated by reference in its
entity.
Sequence CWU 1
1
9711120PRTHomo sapiens 1Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu
Val Lys Pro Ser Gln1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser Gly
Gly Ser Ile Ser Ser Gly 20 25 30Gly Tyr Tyr Trp Ser Trp Ile Arg Gln
His Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Tyr Ile Tyr Tyr Ser
Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr Ile
Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu Ser
Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Arg Thr
Pro Trp Glu Leu Leu Ala Phe Asp Ile Trp Gly Gln 100 105 110Gly Thr
Met Val Thr Val Ser Arg 115 12027PRTHomo sapiens 2Ser Gly Gly Tyr
Tyr Trp Ser1 5316PRTHomo sapiens 3Tyr Ile Tyr Tyr Ser Gly Ser Thr
Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 15410PRTHomo sapiens 4Thr Pro
Trp Glu Leu Leu Ala Phe Asp Ile1 5 105109PRTHomo sapiens 5Ser Tyr
Glu Leu Thr Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10 15Thr
Thr Arg Ile Thr Cys Gly Gly Asn Asn Ile Gly Ser Lys Ser Ala 20 25
30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr
35 40 45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly
Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu
Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp Ser
Ser Ser Asp His 85 90 95Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val
Leu Gly 100 105611PRTHomo sapiens 6Gly Gly Asn Asn Ile Gly Ser Lys
Ser Ala His1 5 1077PRTHomo sapiens 7Tyr Asp Ser Asp Arg Pro Ser1
589PRTHomo sapiens 8Gln Val Trp Asp Ser Ser Ser Asp His1
59126PRTHomo sapiens 9Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val
Lys Lys Thr Gly Ser1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly
Gly Ser Phe Ser Ser Ser 20 25 30Ala Ile Ser Trp Val Arg Gln Ala Pro
Gly His Gly Leu Glu Trp Leu 35 40 45Gly Gly Ile Ile Pro Thr Phe Gly
Thr Pro Asn His Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Ile Thr
Ala Asp Glu Ser Thr Gly Thr Ala Tyr65 70 75 80Met Glu Leu Ser Gly
Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Ala His
Cys Gly Gly Gly Arg Cys Tyr Asp Tyr Thr Asp Ala 100 105 110Phe His
Phe Trp Gly Gln Gly Thr Met Val Thr Val Ser Arg 115 120
125105PRTHomo sapiens 10Ser Ser Ala Ile Ser1 51117PRTHomo sapiens
11Gly Ile Ile Pro Thr Phe Gly Thr Pro Asn His Ala Gln Lys Phe Gln1
5 10 15Gly1217PRTHomo sapiens 12Ala His Cys Gly Gly Gly Arg Cys Tyr
Asp Tyr Thr Asp Ala Phe His1 5 10 15Phe13109PRTHomo sapiens 13Ser
Tyr Glu Leu Thr Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10
15Thr Ala Arg Ile Thr Cys Gly Gly Asp Asn Ile Gly Asn Arg Ser Val
20 25 30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Leu Ile
Tyr 35 40 45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Lys Arg Phe Ser
Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val
Glu Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp
Ser Thr Ser Asp His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr
Val Leu Arg 100 1051411PRTHomo sapiens 14Gly Gly Asp Asn Ile Gly
Asn Arg Ser Val His1 5 10157PRTHomo sapiens 15Tyr Asp Ser Asp Arg
Pro Ser1 5169PRTHomo sapiens 16Gln Val Trp Asp Ser Thr Ser Asp His1
517120PRTHomo sapiens 17Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu
Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser Gly
Gly Ser Ile Ser Ser Ser 20 25 30Ser Tyr Tyr Trp Gly Trp Ile Arg Gln
Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Ser Ile Tyr Tyr Ser
Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr Ile
Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu Ser
Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Arg Leu
Pro Met Val Thr Met Ser Phe Asp Tyr Trp Gly Gln 100 105 110Gly Thr
Leu Val Thr Val Ser Arg 115 120187PRTHomo sapiens 18Ser Ser Ser Tyr
Tyr Trp Gly1 51916PRTHomo sapiens 19Ser Ile Tyr Tyr Ser Gly Ser Thr
Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 152010PRTHomo sapiens 20Leu
Pro Met Val Thr Met Ser Phe Asp Tyr1 5 1021109PRTHomo sapiens 21Ser
Tyr Val Leu Thr Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10
15Thr Ala Arg Ile Thr Cys Gly Gly Asn Asn Ile Gly Ser Lys Ser Val
20 25 30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile
Tyr 35 40 45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser
Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val
Glu Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp
Ser Ser Ser Asp His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr
Val Leu Gly 100 1052211PRTHomo sapiens 22Gly Gly Asn Asn Ile Gly
Ser Lys Ser Val His1 5 10237PRTHomo sapiens 23Tyr Asp Ser Asp Arg
Pro Ser1 5249PRTHomo sapiens 24Gln Val Trp Asp Ser Ser Ser Asp His1
525121PRTHomo sapiens 25Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val
Lys Lys Pro Gly Glu1 5 10 15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly
Tyr Ser Phe Thr Ser Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro
Gly Lys Gly Leu Glu Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser
Asp Thr Arg Tyr Ser Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser
Ala Asp Lys Ser Ile Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser
Leu Lys Ala Ser Asp Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg Leu Thr
Leu Ser Tyr Ser Ser Ser Trp Phe Asp Tyr Trp Gly 100 105 110Gln Gly
Thr Leu Val Thr Val Ser Arg 115 120265PRTHomo sapiens 26Ser Tyr Trp
Ile Gly1 52717PRTHomo sapiens 27Ile Ile Tyr Pro Gly Asp Ser Asp Thr
Arg Tyr Ser Pro Ser Phe Gln1 5 10 15Gly2812PRTHomo sapiens 28Leu
Thr Leu Ser Tyr Ser Ser Ser Trp Phe Asp Tyr1 5 1029111PRTHomo
sapiens 29Gln Thr Val Val Thr Gln Glu Pro Ser Phe Ser Val Ser Pro
Gly Gly1 5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val
Ser Thr Ser 20 25 30Tyr Tyr Pro Ser Trp Tyr Gln Gln Thr Pro Gly Gln
Ala Pro Arg Thr 35 40 45Leu Ile Tyr Ser Thr Asn Thr Arg Ser Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Lys Ala Ala
Leu Thr Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr
Tyr Cys Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Ser Val Phe Gly Gly
Gly Thr Lys Leu Thr Val Leu Gly 100 105 1103014PRTHomo sapiens
30Gly Leu Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5
10317PRTHomo sapiens 31Ser Thr Asn Thr Arg Ser Ser1 5328PRTHomo
sapiens 32Val Leu Tyr Met Gly Ser Gly Ile1 533118PRTHomo sapiens
33Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Glu1
5 10 15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe Thr Ser
Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly Leu Glu
Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser
Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys Ser Ile
Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala Ser Asp
Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg Leu Leu Gly Ile Gly Ala Phe
Asp Ile Trp Gly Gln Gly Thr 100 105 110Thr Val Thr Val Ser Arg
115345PRTHomo sapiens 34Ser Tyr Trp Ile Gly1 53517PRTHomo sapiens
35Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser Pro Ser Phe Gln1
5 10 15Gly369PRTHomo sapiens 36Leu Leu Gly Ile Gly Ala Phe Asp Ile1
537110PRTHomo sapiens 37Ser Ser Glu Leu Thr Gln Asp Pro Ala Val Ser
Val Ala Leu Gly Gln1 5 10 15Thr Val Arg Ile Thr Cys Gln Gly Asp Ser
Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp Tyr Gln Gln Lys Pro Gly Gln
Ala Pro Val Leu Val Ile Tyr 35 40 45Gly Lys Asn Asn Arg Pro Ser Gly
Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60Ser Ser Gly Asn Thr Ala Ser
Leu Thr Ile Thr Gly Ala Gln Ala Glu65 70 75 80Asp Glu Ala Asp Tyr
Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn His 85 90 95His Tyr Val Phe
Gly Thr Gly Thr Lys Val Thr Val Leu Gly 100 105 1103811PRTHomo
sapiens 38Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala Ser1 5
10397PRTHomo sapiens 39Gly Lys Asn Asn Arg Pro Ser1 54010PRTHomo
sapiens 40Asn Ser Arg Asp Ser Ser Gly Asn His His1 5 1041116PRTHomo
sapiens 41Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro
Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Thr Phe
Asn Ser Tyr 20 25 30Gly Ile Thr Trp Val Arg Gln Ala Pro Gly Gln Gly
Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Val Tyr Thr Gly Lys Thr Asn
Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Met Thr Thr Asp Thr
Ser Thr Ser Thr Ala Tyr65 70 75 80Leu Asp Leu Arg Ser Leu Thr Ser
Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Gly Gly Asp His His
Glu Tyr Trp Gly Gln Gly Thr Leu Val 100 105 110Thr Val Ser Arg
115425PRTHomo sapiens 42Ser Tyr Gly Ile Thr1 54317PRTHomo sapiens
43Trp Ile Ser Val Tyr Thr Gly Lys Thr Asn Tyr Ala Gln Lys Phe Gln1
5 10 15Gly447PRTHomo sapiens 44Gly Gly Asp His His Glu Tyr1
545107PRTHomo sapiens 45Asn Phe Met Leu Thr Gln Pro Leu Ser Val Ser
Val Ala Leu Gly Gln1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn Asn
Ile Gly Ser Lys Asn Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly Gln
Ala Pro Val Leu Val Ile Tyr 35 40 45Arg Asp Ser Asn Arg Pro Ser Gly
Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr
Leu Thr Ile Ser Arg Ala Gln Ala Gly65 70 75 80Asp Glu Ala Asp Tyr
Tyr Cys Gln Val Trp Asp Ser Ser Thr Val Val 85 90 95Phe Gly Gly Gly
Thr Lys Leu Thr Val Leu Gly 100 1054611PRTHomo sapiens 46Gly Gly
Asn Asn Ile Gly Ser Lys Asn Val His1 5 10477PRTHomo sapiens 47Arg
Asp Ser Asn Arg Pro Ser1 5487PRTHomo sapiens 48Gln Val Trp Asp Ser
Ser Thr1 549128PRTHomo sapiens 49Glu Val Gln Leu Val Glu Ser Gly
Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala
Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25 30Ala Met Ser Trp Val Arg
Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Gly Ile Ser Gly
Ser Gly Gly Arg Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe
Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln
Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala
Lys Asp Pro Leu Ala Leu Arg Asp Phe Asp Trp Leu Ser Pro Gly 100 105
110Arg Asp Phe Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg
115 120 125505PRTHomo sapiens 50Ser Tyr Ala Met Ser1 55117PRTHomo
sapiens 51Gly Ile Ser Gly Ser Gly Gly Arg Thr Tyr Tyr Ala Asp Ser
Val Lys1 5 10 15Gly5219PRTHomo sapiens 52Asp Pro Leu Ala Leu Arg
Asp Phe Asp Trp Leu Ser Pro Gly Arg Asp1 5 10 15Phe Asp
Tyr53111PRTHomo sapiens 53Gln Ser Val Leu Thr Gln Pro Pro Ser Val
Ser Ala Ala Pro Gly Gln1 5 10 15Lys Val Thr Ile Ser Cys Ser Gly Ser
His Ser Asn Ile Gly Asn Asn 20 25 30Tyr Val Ser Trp Ser Gln Gln Leu
Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45Ile Tyr Asp Asn Asn Lys Arg
Pro Ser Gly Ile Pro Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr
Ser Ala Thr Leu Asp Ile Ala Gly Leu Gln65 70 75 80Thr Gly Asp Glu
Ala Asp Tyr Tyr Cys Gly Ala Trp Asp Thr Ser Leu 85 90 95Ser Ser Tyr
Val Phe Gly Ala Gly Thr Lys Val Thr Val Leu Gly 100 105
1105413PRTHomo sapiens 54Ser Gly Ser His Ser Asn Ile Gly Asn Asn
Tyr Val Ser1 5 10557PRTHomo sapiens 55Asp Asn Asn Lys Arg Pro Ser1
5569PRTHomo sapiens 56Gly Ala Trp Asp Thr Ser Leu Ser Ser1
557120PRTHomo sapiens 57Glu Val Gln Leu Val Glu Ser Gly Ala Glu Val
Lys Lys Pro Gly Ser1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly
Gly Thr Phe Ser Ser Tyr 20 25 30Ala Ile Ser Trp Val Arg Gln Ala Pro
Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Gly Ile Ile Pro Ile Phe Gly
Thr Ala Asn Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Ile Thr
Ala Asp Glu Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu Ser Ser
Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Glu Gly
Leu Ser Gly Gly Tyr Gly Met Asp Val Trp Gly Gln 100 105 110Gly Thr
Thr Val Thr Val Ser Ser 115 120585PRTHomo sapiens 58Ser Tyr Ala Ile
Ser1 55917PRTHomo sapiens 59Gly Ile Ile Pro Ile Phe Gly Thr Ala Asn
Tyr Ala Gln Lys Phe Gln1 5 10 15Gly6011PRTHomo sapiens 60Glu Gly
Leu Ser Gly Gly Tyr Gly Met Asp Val1 5 1061112PRTHomo sapiens 61Gln
Ser Val Leu Thr Gln Pro Pro Ser Val Ser Gly Ala Pro Gly Gln1 5 10
15Arg Val Thr Ile Ser Cys Thr Gly Ser Ser Ser Asn Ile Gly Ala Gly
20 25 30Tyr Asp Val His Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys
Leu 35 40 45Leu Ile Tyr Arg Asn Asn Asn Arg Pro Ser Gly Val Pro Asp
Arg Phe 50 55 60Ser Gly Ser Asn Ser Gly Thr Ser Ala Ser Leu Ala Ile
Thr Gly Leu65 70 75 80Arg Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Gln
Ser Tyr Asp Ser Ser 85 90 95Leu Ser Ser Tyr Val Phe Gly Thr Gly Thr
Lys Val Thr Val Leu Gly 100 105 1106214PRTHomo sapiens 62Thr Gly
Ser Ser Ser Asn Ile Gly Ala Gly Tyr Asp
Val His1 5 10637PRTHomo sapiens 63Arg Asn Asn Asn Arg Pro Ser1
5649PRTHomo sapiens 64Gln Ser Tyr Asp Ser Ser Leu Ser Ser1
565125PRTHomo sapiens 65Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu
Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly
Phe Thr Phe Ser Ser Tyr 20 25 30Ala Met Ser Trp Val Arg Gln Ala Pro
Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ala Ile Ser Gly Ser Gly Gly
Ser Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Asn Ser
Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser
Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Lys Ala Tyr
Tyr Asp Ile Leu Thr Gly Tyr Phe Tyr Asn Gly Met 100 105 110Asp Val
Trp Gly Gln Gly Thr Met Val Thr Val Ser Ser 115 120 125665PRTHomo
sapiens 66Ser Tyr Ala Met Ser1 56717PRTHomo sapiens 67Ala Ile Ser
Gly Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Gly6816PRTHomo sapiens 68Ala Tyr Tyr Asp Ile Leu Thr Gly Tyr Phe
Tyr Asn Gly Met Asp Val1 5 10 1569112PRTHomo sapiens 69Gln Ala Val
Leu Thr Gln Pro Ser Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile
Thr Ile Ser Cys Thr Gly Thr Ser Ser Asp Val Gly Gly Tyr 20 25 30Asp
Tyr Val Ser Trp Tyr Gln Gln His Pro Gly Lys Ala Pro Lys Leu 35 40
45Met Ile His Asp Val Arg Asn Arg Pro Ser Gly Val Ser Asn Arg Phe
50 55 60Ser Gly Ser Lys Phe Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly
Leu65 70 75 80Gln Thr Glu Asp Glu Ala Asp Tyr Tyr Cys Ser Ser Tyr
Thr Ser Ser 85 90 95Ser Thr His Val Leu Phe Gly Gly Gly Thr Lys Leu
Thr Val Leu Gly 100 105 1107014PRTHomo sapiens 70Thr Gly Thr Ser
Ser Asp Val Gly Gly Tyr Asp Tyr Val Ser1 5 10717PRTHomo sapiens
71Asp Val Arg Asn Arg Pro Ser1 5729PRTHomo sapiens 72Ser Ser Tyr
Thr Ser Ser Ser Thr His1 573123PRTHomo sapiens 73Gln Val Gln Leu
Val Gln Ser Gly Gly Gly Leu Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg
Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asp Asp Tyr 20 25 30Ala Met
His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser
Gly Ile Ser Trp Asn Ser Gly Ser Ile Gly Tyr Ala Asp Ser Val 50 55
60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Ser Ser Leu Tyr65
70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Leu Tyr Tyr
Cys 85 90 95Ala Lys Gly His Ser Pro Tyr Ser Ser Gly Trp Ser Asp Phe
Asp Tyr 100 105 110Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115
120745PRTHomo sapiens 74Asp Tyr Ala Met His1 57517PRTHomo sapiens
75Gly Ile Ser Trp Asn Ser Gly Ser Ile Gly Tyr Ala Asp Ser Val Lys1
5 10 15Gly7614PRTHomo sapiens 76Gly His Ser Pro Tyr Ser Ser Gly Trp
Ser Asp Phe Asp Tyr1 5 1077112PRTHomo sapiens 77Gln Ser Val Leu Thr
Gln Pro Pro Ser Val Ser Gly Ala Pro Gly Gln1 5 10 15Arg Val Thr Ile
Ser Cys Thr Gly Ser Ser Ser Asn Ile Gly Ala Gly 20 25 30Tyr Asp Val
Gln Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu 35 40 45Leu Ile
His Ala Asn Lys Asn Arg Pro Ser Gly Val Pro Asp Arg Ile 50 55 60Ser
Gly Ser Lys Ser Gly Thr Thr Ala Ser Leu Ala Ile Thr Gly Phe65 70 75
80Gln Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Ser Ser
85 90 95Leu Thr Gly Tyr Val Phe Gly Thr Gly Thr Lys Val Thr Val Leu
Gly 100 105 1107814PRTHomo sapiens 78Thr Gly Ser Ser Ser Asn Ile
Gly Ala Gly Tyr Asp Val Gln1 5 10797PRTHomo sapiens 79Ala Asn Lys
Asn Arg Pro Ser1 5809PRTHomo sapiens 80Gln Ser Tyr Asp Ser Ser Leu
Thr Gly1 581125PRTHomo sapiens 81Glu Val Gln Leu Val Glu Ser Gly
Gly Gly Leu Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg Leu Ser Cys Ala
Ala Ser Gly Phe Thr Phe Ala Asp Tyr 20 25 30Ala Met His Trp Val Arg
Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Trp
Asn Ser Gly Ser Ile Ala Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe
Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln
Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Leu Tyr Tyr Cys 85 90 95Ala
Lys Ala Ser Ala Ala Gly Thr Glu Tyr Tyr His Tyr Tyr Gly Met 100 105
110Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Arg 115 120
125825PRTHomo sapiens 82Asp Tyr Ala Met His1 58317PRTHomo sapiens
83Ser Ile Ser Trp Asn Ser Gly Ser Ile Ala Tyr Ala Asp Ser Val Lys1
5 10 15Gly8416PRTHomo sapiens 84Ala Ser Ala Ala Gly Thr Glu Tyr Tyr
His Tyr Tyr Gly Met Asp Val1 5 10 1585111PRTHomo sapiens 85Ser Tyr
Val Leu Thr Gln Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln1 5 10 15Arg
Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser Asn 20 25
30Thr Ile Asn Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu Leu
35 40 45Ile Tyr Asn Asn His Gln Arg Pro Ser Gly Val Pro Asp Arg Phe
Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile Ser Gly
Leu Gln65 70 75 80Ser Ala Asp Glu Ala Asp Tyr Tyr Cys Gly Ala Trp
Asn Asp Ser Leu 85 90 95Asn Val Tyr Val Phe Gly Thr Gly Thr Lys Val
Thr Val Leu Gly 100 105 1108613PRTHomo sapiens 86Ser Gly Ser Ser
Ser Asn Ile Gly Ser Asn Thr Ile Asn1 5 10877PRTHomo sapiens 87Asn
Asn His Gln Arg Pro Ser1 5889PRTHomo sapiens 88Gly Ala Trp Asn Asp
Ser Leu Asn Val1 589124PRTHomo sapiens 89Gln Val Gln Leu Val Gln
Ser Gly Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser
Cys Lys Ala Ser Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp
Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile
Ser Ala Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly
Arg Val Thr Met Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75
80Met Glu Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys
85 90 95Ala Thr Ala Ala Ser Leu Lys Tyr Tyr Tyr Asp Ser Ser Gly Tyr
Tyr 100 105 110Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115
120905PRTHomo sapiens 90Ser Tyr Gly Ile Ser1 59117PRTHomo sapiens
91Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys Leu Gln1
5 10 15Gly9215PRTHomo sapiens 92Ala Ala Ser Leu Lys Tyr Tyr Tyr Asp
Ser Ser Gly Tyr Tyr Tyr1 5 10 1593110PRTHomo sapiens 93Ser Ser Glu
Leu Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val
Arg Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser
Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Ser 35 40
45Gly Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser
50 55 60Ser Ser Gly Asp Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala
Glu65 70 75 80Asp Glu Ala Asn Tyr Tyr Cys Asn Ser Arg Asp Ser Ser
Gly Tyr Pro 85 90 95Ser Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val
Leu Gly 100 105 1109411PRTHomo sapiens 94Gln Gly Asp Ser Leu Arg
Ser Tyr Tyr Ala Ser1 5 10957PRTHomo sapiens 95Gly Lys Asn Asn Arg
Pro Ser1 59610PRTHomo sapiens 96Asn Ser Arg Asp Ser Ser Gly Tyr Pro
Ser1 5 1097130PRTHomo sapiens 97Gln Val Gln Leu Val Gln Ser Gly Ala
Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Gly
Ser Gly Tyr Val Phe Asn Ser Tyr 20 25 30Gly Ile Thr Trp Val Arg Gln
Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr
Asn Gly Tyr Thr Asp Tyr Ala Gln Lys Val 50 55 60Gln Gly Arg Val Thr
Met Thr Thr Glu Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu
Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg
Asp Tyr Tyr Asp Ser Ser Thr Tyr Tyr Ser Ser Asp Tyr Phe 100 105
110Gln Tyr Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val
115 120 125Ser Ser 130985PRTHomo sapiens 98Ser Tyr Gly Ile Thr1
59917PRTHomo sapiens 99Trp Ile Ser Ala Tyr Asn Gly Tyr Thr Asp Tyr
Ala Gln Lys Val Gln1 5 10 15Gly10021PRTHomo sapiens 100Asp Tyr Tyr
Asp Ser Ser Thr Tyr Tyr Ser Ser Asp Tyr Phe Gln Tyr1 5 10 15Tyr Gly
Met Asp Val 20101111PRTHomo sapiens 101Gln Ala Val Leu Thr Gln Pro
Ala Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile Thr Ile Ser Cys
Thr Gly Thr Ser Ser Asp Val Gly Ala Tyr 20 25 30Asn Tyr Val Ser Trp
Tyr Gln Gln His Pro Gly Lys Ala Pro Lys Leu 35 40 45Met Ile Ser Asp
Val Ser Arg Arg Pro Ser Gly Val Ser Asn Arg Phe 50 55 60Ser Gly Ser
Lys Ser Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75 80Gln
Thr Glu Asp Glu Ala Asp Tyr Tyr Cys Ser Ser Tyr Thr Ser Ser 85 90
95Asn Thr Val Leu Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
105 11010214PRTHomo sapiens 102Thr Gly Thr Ser Ser Asp Val Gly Ala
Tyr Asn Tyr Val Ser1 5 101037PRTHomo sapiens 103Asp Val Ser Arg Arg
Pro Ser1 51048PRTHomo sapiens 104Ser Ser Tyr Thr Ser Ser Asn Thr1
5105122PRTHomo sapiens 105Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Glu1 5 10 15Ser Leu Arg Ile Ser Cys Lys Gly Ser
Gly Tyr Ser Phe Thr Asn Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met
Pro Gly Lys Gly Leu Glu Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp
Ser Asp Thr Arg Tyr Ser Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile
Ala Ala Asp Lys Ser Ile Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser
Ser Leu Met Ala Ser Asp Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg Arg
Gly Ser Arg Ser Ser Gly Glu Asp Ala Phe Glu Val Trp 100 105 110Gly
Gln Gly Thr Thr Val Thr Val Ser Ser 115 1201065PRTHomo sapiens
106Asn Tyr Trp Ile Gly1 510717PRTHomo sapiens 107Ile Ile Tyr Pro
Gly Asp Ser Asp Thr Arg Tyr Ser Pro Ser Phe Gln1 5 10
15Gly10813PRTHomo sapiens 108Arg Gly Ser Arg Ser Ser Gly Glu Asp
Ala Phe Glu Val1 5 10109110PRTHomo sapiens 109Ser Tyr Glu Leu Thr
Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Thr Ile
Thr Cys Gly Gly Asp Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr
Gln Gln Arg Pro Gly Gln Ala Pro Val Leu Val Ile Asn 35 40 45Tyr Asp
Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn
Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu Ala Gly65 70 75
80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Glu Asp Arg Arg Gly Gly Tyr
85 90 95His Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
105 11011011PRTHomo sapiens 110Gly Gly Asp Asn Ile Gly Ser Lys Ser
Val His1 5 101117PRTHomo sapiens 111Tyr Asp Ser Asp Arg Pro Ser1
511210PRTHomo sapiens 112Gln Val Glu Asp Arg Arg Gly Gly Tyr His1 5
10113125PRTHomo sapiens 113Gln Val Gln Leu Val Gln Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Val Ser Ser Asn 20 25 30Tyr Met Ser Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Val Ile Tyr Ser Gly Gly
Ser Thr Tyr Tyr Ala Asp Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser
Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser
Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Glu Gly
Tyr Cys Ser Gly Gly Ser Cys Tyr Ser Tyr Gly Ala Phe 100 105 110Asp
Ile Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser 115 120
1251145PRTHomo sapiens 114Ser Asn Tyr Met Ser1 511516PRTHomo
sapiens 115Val Ile Tyr Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val
Lys Gly1 5 10 1511617PRTHomo sapiens 116Glu Gly Tyr Cys Ser Gly Gly
Ser Cys Tyr Ser Tyr Gly Ala Phe Asp1 5 10 15Ile117108PRTHomo
sapiens 117Asp Ile Val Met Thr Gln Ser Pro Ser Ser Val Ser Ala Ser
Val Gly1 5 10 15Asp Arg Val Thr Ile Ser Cys Arg Ala Ser Gln Asn Ile
Ala Asn Trp 20 25 30Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro
Lys Leu Leu Ile 35 40 45Tyr Ala Ala Ser Asn Leu Gln Ser Gly Val Pro
Ser Arg Phe Ser Gly 50 55 60Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr
Ile Ser Ser Leu Gln Pro65 70 75 80Glu Asp Phe Ala Ser Tyr Tyr Cys
Gln Gln Gly Asn Ser Phe Pro Arg 85 90 95Val Thr Phe Gly Gly Gly Thr
Lys Val Glu Ile Lys 100 10511811PRTHomo sapiens 118Arg Ala Ser Gln
Asn Ile Ala Asn Trp Leu Ala1 5 101197PRTHomo sapiens 119Ala Ala Ser
Asn Leu Gln Ser1 51208PRTHomo sapiens 120Gln Gln Gly Asn Ser Phe
Pro Arg1 5121130PRTHomo sapiens 121Gln Val Gln Leu Val Gln Ser Gly
Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys
Ala Ser Gly Tyr Val Phe Asn Ser Tyr 20 25 30Gly Ile Thr Trp Val Arg
Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala
Tyr Asn Gly Tyr Thr Asp Tyr Ala Gln Lys Val 50 55 60Gln Gly Arg Val
Thr Met Thr Thr Glu Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu
Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala
Arg Asp Tyr Tyr Asp Ser Ser Thr Tyr Tyr Ser Ser Asp Tyr Phe 100 105
110Lys Tyr Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val
115 120 125Ser Ser 1301225PRTHomo sapiens 122Ser Tyr Gly Ile Thr1
512317PRTHomo sapiens 123Trp Ile Ser Ala Tyr Asn Gly Tyr Thr Asp
Tyr Ala Gln Lys Val Gln1 5 10 15Gly12421PRTHomo sapiens 124Asp Tyr
Tyr Asp Ser Ser Thr Tyr Tyr Ser Ser Asp Tyr Phe Lys Tyr1 5 10 15Tyr
Gly Met Asp Val20125111PRTHomo sapiens 125Gln Ala Val Leu Thr
Gln
Pro Ser Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile Thr Ile Ser
Cys Ser Gly Thr Ser Ser Asp Val Gly Ala Tyr 20 25 30Asn Tyr Val Ser
Trp Tyr Gln Gln His Pro Gly Lys Ala Pro Arg Leu 35 40 45Leu Thr Phe
Asp Val Asn Arg Arg Pro Ser Gly Ser Ser Ser Arg Phe 50 55 60Ser Gly
Ser Lys Ser Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75
80Gln Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Ser Ser Tyr Thr Asn Ser
85 90 95Asn Thr Val Val Phe Gly Gly Gly Thr Arg Leu Thr Val Leu Ser
100 105 11012614PRTHomo sapiens 126Ser Gly Thr Ser Ser Asp Val Gly
Ala Tyr Asn Tyr Val Ser1 5 101277PRTHomo sapiens 127Asp Val Asn Arg
Arg Pro Ser1 51288PRTHomo sapiens 128Ser Ser Tyr Thr Asn Ser Asn
Thr1 5129127PRTHomo sapiens 129Gln Val Gln Leu Gln Glu Ser Gly Pro
Gly Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ala Leu Thr Cys Thr Val
Ser Gly Gly Ser Ile Ser Asn Tyr 20 25 30Tyr Trp Ser Trp Ile Arg Gln
Pro Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45Gly Tyr Ile Tyr Asp Ile
Glu Asn Thr Asn Tyr Asn Pro Ser Leu Lys 50 55 60Ser Arg Val Thr Ile
Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu65 70 75 80Lys Leu Ser
Ser Val Thr Ala Asp Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Asp
Ser Arg Val Ile Arg Phe Leu Glu Gly Tyr Ser Tyr Tyr Tyr 100 105
110Gly Val Asp Val Trp Gly Gln Gly Thr Met Val Thr Val Ser Ser 115
120 1251305PRTHomo sapiens 130Asn Tyr Tyr Trp Ser1 513116PRTHomo
sapiens 131Tyr Ile Tyr Asp Ile Glu Asn Thr Asn Tyr Asn Pro Ser Leu
Lys Ser1 5 10 1513219PRTHomo sapiens 132Asp Ser Arg Val Ile Arg Phe
Leu Glu Gly Tyr Ser Tyr Tyr Tyr Gly1 5 10 15Val Asp
Val133111PRTHomo sapiens 133Ser Tyr Glu Leu Thr Gln Pro Pro Ser Ala
Ser Gly Thr Pro Gly Gln1 5 10 15Thr Val Ile Ile Ser Cys Ser Gly Ser
Arg Ser Asn Ile Gly Gly His 20 25 30Gly Val Asn Trp His Gln Gln Val
Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45Ile Tyr Arg Asn Asp Arg Arg
Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr
Ser Ala Ser Leu Val Ile Ser Gly Leu Gln65 70 75 80Phe Glu Asp Glu
Ala Asp Tyr Tyr Cys Val Ala Trp Glu Asp Ser Leu 85 90 95Asp Gly Pro
Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105
11013413PRTHomo sapiens 134Ser Gly Ser Arg Ser Asn Ile Gly Gly His
Gly Val Asn1 5 101357PRTHomo sapiens 135Arg Asn Asp Arg Arg Pro
Ser1 51369PRTHomo sapiens 136Val Ala Trp Glu Asp Ser Leu Asp Gly1
5137115PRTHomo sapiens 137Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Ala Met Ser Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Ser Gly Ser Gly
Gly Ser Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Gly
Ile Val Ala Thr Ser Trp Gly Gln Gly Thr Leu Val Thr 100 105 110Val
Ser Arg 1151385PRTHomo sapiens 138Ser Tyr Ala Met Ser1
513917PRTHomo sapiens 139Thr Ile Ser Gly Ser Gly Gly Ser Thr Tyr
Tyr Ala Asp Ser Val Lys1 5 10 15Gly1406PRTHomo sapiens 140Gly Ile
Val Ala Thr Ser1 5141108PRTHomo sapiens 141Ser Tyr Glu Leu Thr Gln
Pro Pro Ser Val Ser Val Ala Pro Gly Gln1 5 10 15Thr Ala Arg Ile Thr
Cys Gly Gly Asn Lys Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln
Gln Lys Gln Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Leu Asp Arg
Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser
Gly Asn Thr Ala Thr Leu Thr Ile Thr Arg Val Glu Ala Glu65 70 75
80Asp Glu Ala Asp Tyr Tyr Cys His Leu Trp Asp Ser Gly Ser Asp Gln
85 90 95Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
10514211PRTHomo sapiens 142Gly Gly Asn Lys Ile Gly Ser Lys Ser Val
His1 5 101437PRTHomo sapiens 143Leu Asp Arg Asp Arg Pro Ser1
51448PRTHomo sapiens 144His Leu Trp Asp Ser Gly Ser Asp1
5145114PRTHomo sapiens 145Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Val Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Asn Phe Asp Val Tyr 20 25 30Gly Met Asn Trp Val Arg Gln Val
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Leu Ile Asn Gly Asp Gly
Gly Leu Arg Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Val
Ser Arg Asp Asn Ser Arg Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ser Glu Asp Thr Ala Leu Tyr Tyr Cys 85 90 95Val Lys Gly
Asn Phe Gln Gln Trp Gly Gln Gly Thr Leu Val Thr Val 100 105 110Ser
Arg1465PRTHomo sapiens 146Val Tyr Gly Met Asn1 514717PRTHomo
sapiens 147Leu Ile Asn Gly Asp Gly Gly Leu Arg Tyr Tyr Ala Asp Ser
Val Lys1 5 10 15Gly1485PRTHomo sapiens 148Gly Asn Phe Gln Gln1
5149109PRTHomo sapiens 149Ser Tyr Val Leu Thr Gln Pro Pro Ser Val
Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn
Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly
Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Tyr Asp Ser Asp Arg Pro Ser
Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala
Thr Leu Thr Ile Ser Arg Val Glu Ala Gly65 70 75 80Asp Glu Ala Asp
Tyr Tyr Cys Gln Val Trp Asp Ser Ser Ser Asp His 85 90 95Val Val Phe
Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 10515011PRTHomo sapiens
150Gly Gly Asn Asn Ile Gly Ser Lys Ser Val His1 5 101517PRTHomo
sapiens 151Tyr Asp Ser Asp Arg Pro Ser1 51529PRTHomo sapiens 152Gln
Val Trp Asp Ser Ser Ser Asp His1 5153115PRTHomo sapiens 153Glu Val
Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser
Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asp Asp Tyr 20 25
30Ala Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45Ser Leu Ile Ser Gly Asp Gly Gly Ser Thr Tyr Tyr Ala Asp Ser
Val 50 55 60Lys Asp Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Ser
Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala
Val Tyr Tyr Cys 85 90 95Ala Arg Gly Asn Tyr Phe Asp Tyr Trp Gly Gln
Gly Thr Leu Val Thr 100 105 110Val Ser Arg 1151545PRTHomo sapiens
154Asp Tyr Ala Met His1 515517PRTHomo sapiens 155Leu Ile Ser Gly
Asp Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Asp1566PRTHomo sapiens 156Gly Asn Tyr Phe Asp Tyr1 5157106PRTHomo
sapiens 157Ser Tyr Glu Leu Thr Gln Pro Leu Ser Val Ser Val Ala Leu
Gly Gln1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn Asn Ile Gly Ser
Lys Asn Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val
Leu Val Ile Tyr 35 40 45Arg Asp Ser Asn Arg Pro Ser Gly Ile Pro Glu
Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile
Ser Arg Ala Gln Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln
Val Trp Asp Ser Ser Val Val Phe 85 90 95Gly Gly Gly Thr Lys Leu Thr
Val Leu Gly 100 10515811PRTHomo sapiens 158Gly Gly Asn Asn Ile Gly
Ser Lys Asn Val His1 5 101597PRTHomo sapiens 159Arg Asp Ser Asn Arg
Pro Ser1 51606PRTHomo sapiens 160Gln Val Trp Asp Ser Ser1
5161122PRTHomo sapiens 161Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Ser Met Asn Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Tyr Ile Ser Ser Ser Ser
Ser Thr Ile Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Asp Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Val
Met Pro Ser Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val Trp 100 105 110Gly
Gln Gly Thr Thr Val Thr Val Ser Arg 115 1201625PRTHomo sapiens
162Ser Tyr Ser Met Asn1 516317PRTHomo sapiens 163Tyr Ile Ser Ser
Ser Ser Ser Thr Ile Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Gly16413PRTHomo sapiens 164Val Met Pro Ser Tyr Tyr Tyr Tyr Tyr
Gly Met Asp Val1 5 10165111PRTHomo sapiens 165Asn Phe Met Leu Thr
Gln Pro His Ser Val Ser Glu Ser Pro Gly Lys1 5 10 15Thr Val Thr Ile
Ser Cys Thr Gly Ser Ser Gly Ser Ile Ala Ser Asn 20 25 30Tyr Val Gln
Trp Tyr Gln Gln Arg Pro Gly Ser Ala Pro Thr Thr Val 35 40 45Ile Tyr
Glu Asp Ser Glu Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60Gly
Ser Ile Asp Ser Ser Ser Asn Ser Ala Ser Leu Thr Ile Ser Gly65 70 75
80Leu Lys Thr Gln Asp Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Gly
85 90 95Val Asn Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly
100 105 11016613PRTHomo sapiens 166Thr Gly Ser Ser Gly Ser Ile Ala
Ser Asn Tyr Val Gln1 5 101677PRTHomo sapiens 167Glu Asp Ser Glu Arg
Pro Ser1 51687PRTHomo sapiens 168Gln Ser Tyr Asp Gly Val Asn1
5169114PRTHomo sapiens 169Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Val Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Gly Met His Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Val Ile Ser Tyr Asp Gly
Ser Asn Lys Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Asp Tyr
Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val 100 105 110Ser
Arg 1705PRTHomo sapiens 170Ser Tyr Gly Met His1 517117PRTHomo
sapiens 171Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser
Val Lys1 5 10 15Gly1725PRTHomo sapiens 172Tyr Gly Met Asp Val1
5173107PRTHomo sapiens 173Asp Ile Gln Met Thr Gln Ser Pro Ser Ser
Leu Ser Ala Ser Val Gly1 5 10 15Asp Arg Val Thr Ile Thr Cys Arg Ala
Ser Gln Ser Ile Ser Ser Tyr 20 25 30Leu Asn Trp Tyr Gln Gln Lys Pro
Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45Tyr Ala Ala Ser Ser Leu Gln
Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60Ser Gly Ser Gly Thr Asp
Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro65 70 75 80Glu Asp Phe Ala
Thr Tyr Tyr Cys Gln Gln Ser Tyr Ser Thr Pro Val 85 90 95Thr Phe Gly
Gln Gly Thr Lys Val Glu Ile Lys 100 10517411PRTHomo sapiens 174Arg
Ala Ser Gln Ser Ile Ser Ser Tyr Leu Asn1 5 101757PRTHomo sapiens
175Ala Ala Ser Ser Leu Gln Ser1 51767PRTHomo sapiens 176Gln Gln Ser
Tyr Ser Thr Pro1 5177120PRTHomo sapiens 177Gln Val Gln Leu Gln Glu
Ser Gly Pro Gly Leu Val Lys Pro Ser Gln1 5 10 15Thr Leu Ser Leu Thr
Cys Thr Val Ser Gly Gly Ser Ile Ser Ser Gly 20 25 30Gly Tyr Tyr Trp
Ser Trp Ile Arg Gln His Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly
Tyr Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys
Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75
80Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr
85 90 95Cys Ala Arg Asp Arg Gly Thr Gly Asp Ala Phe Asp Ile Trp Gly
Gln 100 105 110Gly Thr Met Val Thr Val Ser Arg 115 1201787PRTHomo
sapiens 178Ser Gly Gly Tyr Tyr Trp Ser1 517916PRTHomo sapiens
179Tyr Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser1
5 10 1518010PRTHomo sapiens 180Asp Arg Gly Thr Gly Asp Ala Phe Asp
Ile1 5 10181111PRTHomo sapiens 181Gln Ser Val Leu Thr Gln Pro Pro
Ser Val Ser Gly Ala Pro Arg Gln1 5 10 15Thr Val Thr Ile Ser Cys Ser
Gly Ser Ser Ser Asn Ile Gly Gln Asn 20 25 30Ser Val Thr Trp Tyr Gln
Arg Leu Pro Gly Glu Ala Pro Lys Leu Leu 35 40 45Ile Tyr Tyr Asp Asp
Leu Leu His Ser Gly Val Ser Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser
Gly Thr Ser Ala Ser Leu Ala Ile Ser Gly Leu Gln65 70 75 80Ser Glu
Asp Glu Ala Glu Tyr Tyr Cys Ala Ser Trp Asp Asp Ser Leu 85 90 95Lys
Gly Pro Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105
11018213PRTHomo sapiens 182Ser Gly Ser Ser Ser Asn Ile Gly Gln Asn
Ser Val Thr1 5 101837PRTHomo sapiens 183Tyr Asp Asp Leu Leu His
Ser1 51849PRTHomo sapiens 184Ala Ser Trp Asp Asp Ser Leu Lys Gly1
5185360DNAHomo sapiens 185caggtgcagc tgcaggagtc gggcccagga
ctggtgaagc cttcacagac cctgtccctc 60acctgcactg tctctggtgg ctccatcagc
agtggtggtt actactggag ctggatccgc 120cagcacccag ggaagggcct
ggagtggatt gggtacatct attacagtgg gagcacctac 180tacaacccgt
ccctcaagag tcgagtcacc atatcagtag acacgtctaa gaaccagttc
240tccctgaagc tgagctctgt gactgccgcg gacacggccg tgtattactg
tgcgaggaca 300ccgtgggagc tactagcttt tgatatctgg ggccaaggga
caatggtcac cgtctcgaga 36018621DNAHomo sapiens 186agtggtggtt
actactggag c 2118748DNAHomo sapiens 187tacatctatt acagtgggag
cacctactac aacccgtccc tcaagagt 4818830DNAHomo sapiens 188acaccgtggg
agctactagc ttttgatatc 30189327DNAHomo sapiens 189tcctatgagc
tgactcagcc accctcagtg tcagtggccc caggaaagac gaccaggatt 60acctgtgggg
gaaacaacat tggaagtaaa agtgcgcact ggtaccagca gaagccaggc
120caggcccctg tgctggtcat ctattatgat agcgaccggc cctcagggat
ccctgagcga 180ttctctggct ccaactctgg gaacacggcc accctgacca
tcagcagggt cgaagccggg 240gatgaggccg actattactg tcaggtgtgg
gatagtagta gtgatcattg ggtgttcggc 300ggagggacca agctgaccgt cctaggt
32719033DNAHomo sapiens 190gggggaaaca acattggaag taaaagtgcg cac
3319121DNAHomo sapiens 191tatgatagcg accggccctc a 2119227DNAHomo
sapiens 192caggtgtggg atagtagtag tgatcat 27193378DNAHomo sapiens
193caggtgcagc tggtgcagtc tggggctgag gtgaagaaga ctgggtcctc
ggtgaaggtc 60tcctgcaagg cctctggagg ctccttcagc agctctgcaa tcagctgggt
gcgacaggcc 120cctggacacg ggcttgaatg gctgggaggg atcatcccta
cctttggtac accaaaccac 180gcacagaagt tccagggcag agtcacaatt
accgcggacg aatcaacggg cacagcctac 240atggagctga gtggcctgag
atctgaggac acggccgtgt attactgtgc gagagcccat 300tgtggtggtg
gtaggtgtta cgactacact gatgcttttc atttctgggg ccaagggaca
360atggtcaccg tctcgaga 37819415DNAHomo sapiens 194agctctgcaa tcagc
1519551DNAHomo sapiens 195gggatcatcc ctacctttgg tacaccaaac
cacgcacaga agttccaggg c 5119651DNAHomo sapiens 196gcccattgtg
gtggtggtag gtgttacgac tacactgatg cttttcattt c 51197327DNAHomo
sapiens 197tcctatgagc tgactcagcc accctcagtg tcagtggccc caggaaagac
ggccaggatt 60acctgtgggg gagacaacat tggaaataga agtgtgcact ggtaccagca
gaagccaggc 120caggcccctg tgctgcttat ctattatgat agcgaccggc
cctcagggat ccctaagcga 180ttctctggct ccaactctgg gaacacggcc
accctgacca tcagcagggt cgaagccggg 240gatgaggccg actattactg
tcaggtgtgg gatagtacta gtgatcatgt ggtattcggc 300ggagggacca
agctgaccgt cctacgt 32719833DNAHomo sapiens 198gggggagaca acattggaaa
tagaagtgtg cac 3319921DNAHomo sapiens 199tatgatagcg accggccctc a
2120027DNAHomo sapiens 200caggtgtggg atagtactag tgatcat
27201360DNAHomo sapiens 201caggtgcagc tgcaggagtc gggcccagga
ctggtgaagc cttcggagac cctgtccctc 60acctgcactg tctctggtgg ctccatcagc
agtagtagtt actactgggg ctggatccgc 120cagcccccag ggaaggggct
ggagtggatt gggagtatct attatagtgg gagcacctac 180tacaacccgt
ccctcaagag tcgagtcacc atatccgtag acacgtccaa gaaccagttc
240tccctgaagc tgagctctgt gaccgccgca gacacggctg tgtattactg
tgcgagactt 300cctatggtta cgatgtcctt tgactactgg ggccagggaa
ccctggtcac cgtctcgaga 36020221DNAHomo sapiens 202agtagtagtt
actactgggg c 2120348DNAHomo sapiens 203agtatctatt atagtgggag
cacctactac aacccgtccc tcaagagt 4820430DNAHomo sapiens 204cttcctatgg
ttacgatgtc ctttgactac 30205327DNAHomo sapiens 205tcctatgtgc
tgactcagcc accctcagtg tcagtggccc caggaaagac ggccaggatt 60acctgtgggg
gaaacaacat tggaagtaaa agtgtgcact ggtaccagca gaagccaggc
120caggcccctg tgctggtcat ctattatgat agcgaccggc cctcagggat
ccctgagcga 180ttctctggct ccaactctgg gaacacggcc accctgacca
tcagcagggt cgaagccggg 240gatgaggccg actattactg tcaggtgtgg
gatagtagta gtgatcatgt ggtattcggc 300ggagggacca agctgaccgt cctaggt
32720633DNAHomo sapiens 206gggggaaaca acattggaag taaaagtgtg cac
3320721DNAHomo sapiens 207tatgatagcg accggccctc a 2120827DNAHomo
sapiens 208caggtgtggg atagtagtag tgatcat 27209363DNAHomo sapiens
209caggtgcagc tggtgcagtc tggagcagag gtgaaaaagc ccggggagtc
tctgaagatc 60tcctgtaagg gttctggata cagctttacc agctactgga tcggctgggt
gcgccagatg 120cccgggaaag gcctggagtg gatggggatc atctatcctg
gtgactctga taccagatac 180agcccgtcct tccaaggcca ggtcaccatc
tcagccgaca agtccatcag caccgcctac 240ctgcagtgga gcagcctgaa
ggcctcggac accgccatgt attactgtgc gagacttact 300ttgtcttata
gcagcagctg gtttgactac tggggccagg gaaccctggt caccgtctcg 360aga
36321015DNAHomo sapiens 210agctactgga tcggc 1521151DNAHomo sapiens
211atcatctatc ctggtgactc tgataccaga tacagcccgt ccttccaagg c
5121236DNAHomo sapiens 212cttactttgt cttatagcag cagctggttt gactac
36213333DNAHomo sapiens 213cagactgtgg tgacccagga gccatcgttc
tcagtgtccc ctggagggac agtcacactc 60acttgtggct tgagctctgg ctcagtctct
actagttact accccagctg gtaccagcag 120accccaggcc aggctccacg
cacgctcatc tacagcacaa acactcgctc ttctggggtc 180cctgatcgct
tctctggctc catccttggg aacaaagctg ccctcaccat cacgggggcc
240caggcagatg atgaatctga ttattactgt gtgctgtata tgggtagtgg
catttcggtg 300ttcggcggag ggaccaagct gaccgtccta ggt 33321442DNAHomo
sapiens 214ggcttgagct ctggctcagt ctctactagt tactacccca gc
4221521DNAHomo sapiens 215agcacaaaca ctcgctcttc t 2121624DNAHomo
sapiens 216gtgctgtata tgggtagtgg catt 24217354DNAHomo sapiens
217caggtgcagc tggtgcagtc tggagcagag gtgaaaaagc ccggggagtc
tctgaagatc 60tcctgtaagg gttctggata cagctttacc agctactgga tcggctgggt
gcgccagatg 120cccgggaaag gcctggagtg gatggggatc atctatcctg
gtgactctga taccagatac 180agcccgtcct tccaaggcca ggtcaccatc
tcagccgaca agtccatcag caccgcctac 240ctgcagtgga gcagcctgaa
ggcctcggac accgccatgt attactgtgc gagacttctg 300gggataggcg
cttttgatat ctggggccaa gggaccacgg tcaccgtctc gaga 35421815DNAHomo
sapiens 218agctactgga tcggc 1521951DNAHomo sapiens 219atcatctatc
ctggtgactc tgataccaga tacagcccgt ccttccaagg c 5122027DNAHomo
sapiens 220cttctgggga taggcgcttt tgatatc 27221330DNAHomo sapiens
221tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gtaaccatca ttatgtcttc 300ggaactggga
ccaaggtcac cgtcctaggt 33022233DNAHomo sapiens 222caaggagaca
gcctcagaag ctattatgca agc 3322321DNAHomo sapiens 223ggtaaaaaca
accggccctc a 2122430DNAHomo sapiens 224aactcccggg acagcagtgg
taaccatcat 30225678DNAHomo sapiens 225caggtgcagc tggtgcagtc
tggagctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgtaagg cttctggtta
cacctttaat agctatggta ttacttgggt gcgacaggcc 120cctggacaag
ggcttgagtg gatgggatgg atcagcgttt acactggtaa gacaaactat
180gcacagaagt tccagggcag agtcaccatg accacagaca catccacgag
tacagcctac 240ctggacctga ggagcctgac atctgacgac acggccgttt
attactgtgc gagaggaggg 300gatcaccatg aatattgggg ccagggaacc
ctggtcaccg tctcgagatc ttctgagctg 360actcaggacc ctgctgtgtc
tgtggccttg ggacagacag tcaggatcac atgccaagga 420gacagcctca
gaagctatta tgcaagctgg taccagcaga agccaggaca ggcccctgta
480cttgtcatct atggtaaaaa caaccggccc tcagggatcc cagaccgatt
ctctggctcc 540agctcaggaa acacagcttc cttgaccatc actggggctc
aggcggaaga tgaggctgac 600tattactgta actcccggga cagcagtggt
aaccatcatt atgtcttcgg aactgggacc 660aaggtcaccg tcctaggt
67822615DNAHomo sapiens 226agctatggta ttact 1522751DNAHomo sapiens
227tggatcagcg tttacactgg taagacaaac tatgcacaga agttccaggg c
5122821DNAHomo sapiens 228ggaggggatc accatgaata t 21229321DNAHomo
sapiens 229aattttatgc tgactcagcc actctcagtg tcagtggccc tgggacagac
ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa aatgtgcact ggtaccagca
gaagccaggc 120caggcccctg tgctggtcat ctatagggat agcaaccggc
cctctgggat ccctgagcga 180ttctctggct ccaactcggg gaacacggcc
accctgacca tcagcagagc ccaagccggg 240gatgaggctg actattactg
tcaggtgtgg gacagcagca ctgtggtatt cggcggaggg 300accaagctga
ccgtcctagg t 32123033DNAHomo sapiens 230gggggaaaca acattggaag
taaaaatgtg cac 3323121DNAHomo sapiens 231agggatagca accggccctc t
2123221DNAHomo sapiens 232caggtgtggg acagcagcac t 21233384DNAHomo
sapiens 233gaggtgcagc tggtggagtc tgggggaggc ttggtacagc cgggggggtc
cctgagactc 60tcctgtgcag cctctggatt cacctttagc agctatgcca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcaggt attagtggta
gtggtggtag aacatactac 180gcagactccg tgaagggccg gttcaccatc
tccagagaca attctaagaa cacgctgtat 240ctgcaaatga acagcctgag
agccgaggac acggccgtat attactgtgc gaaagatccc 300ctcgcattac
gagattttga ctggttatcc cccgggcggg actttgatta ctggggccag
360ggaaccctgg tcaccgtctc gaga 38423415DNAHomo sapiens 234agctatgcca
tgagc 1523551DNAHomo sapiens 235ggtattagtg gtagtggtgg tagaacatac
tacgcagact ccgtgaaggg c 5123657DNAHomo sapiens 236gatcccctcg
cattacgaga ttttgactgg ttatcccccg ggcgggactt tgattac 57237333DNAHomo
sapiens 237cagtctgtgt tgacgcagcc gccctcagtg tctgcggccc cgggacagaa
ggtcaccatc 60tcctgctctg gaagccactc caacattgga aataattatg tatcgtggtc
ccagcaactc 120ccaggaacag cccccaaact cctcatttat gacaataata
agcgaccctc agggattcct 180gaccgattct ctggctccaa gtctggcacg
tcagccaccc tggacatcgc cgggctccag 240actggggacg aggccgatta
ttactgcgga gcatgggata ccagcctgag ttcttatgtc 300ttcggagctg
ggaccaaggt caccgtccta ggt 33323839DNAHomo sapiens 238tctggaagcc
actccaacat tggaaataat tatgtatcg 3923921DNAHomo sapiens
239gacaataata agcgaccctc a 2124027DNAHomo sapiens 240ggagcatggg
ataccagcct gagttct 27241360DNAHomo sapiens 241gaggtgcagc tggtggagtc
tggggctgag gtgaagaagc ctgggtcctc ggtgaaggtc 60tcctgcaagg cttctggagg
caccttcagc agctatgcta tcagctgggt gcgacaggcc 120cctggacaag
ggcttgagtg gatgggaggg atcatcccta tctttggtac agcaaactac
180gcacagaagt tccagggcag agtcacgatt accgcggacg aatccacgag
cacagcctac 240atggagctga gcagcctgag atctgaggac acggccgtgt
attactgtgc gagagaaggt 300ttatcgggtg ggtacggtat ggacgtctgg
ggccaaggga ccacggtcac cgtctcgagc 36024215DNAHomo sapiens
242agctatgcta tcagc 1524351DNAHomo sapiens 243gggatcatcc ctatctttgg
tacagcaaac tacgcacaga agttccaggg c 5124433DNAHomo sapiens
244gaaggtttat cgggtgggta cggtatggac gtc 33245336DNAHomo sapiens
245cagtctgtgt tgacgcagcc gccctcagtg tctggggccc cagggcagag
ggtcaccatc 60tcctgcactg ggagcagctc caacatcggg gcaggttatg atgtacactg
gtaccagcag 120cttccaggaa cagcccccaa actcctcatc tatcgtaaca
acaatcggcc ctcaggggtc 180cctgaccgat tctctggctc caactctggc
acctcagcct ccctggccat cactgggctc 240cgggctgaag atgaggctga
ttattactgc cagtcctatg acagcagcct gagtagttat 300gtcttcggaa
ctgggaccaa ggtcaccgtc ctaggt 33624642DNAHomo sapiens 246actgggagca
gctccaacat cggggcaggt tatgatgtac ac 4224721DNAHomo sapiens
247cgtaacaaca atcggccctc a 2124827DNAHomo sapiens 248cagtcctatg
acagcagcct gagtagt 27249375DNAHomo sapiens 249gaggtgcagc tggtggagtc
tgggggaggc ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt
cacctttagc agctatgcca tgagctgggt ccgccaggct 120ccagggaagg
ggctggagtg ggtctcagct attagtggta gtggtggtag cacatactac
180gcagactccg tgaagggccg gttcaccaac tccagagaca attccaagaa
cacgctgtat 240ctgcaaatga acagcctgag agccgaggac acggccgtat
attactgtgc gaaagcgtat 300tacgatattt tgactggtta tttttacaac
ggtatggacg tctggggcca agggacaatg 360gtcaccgtct cgagc
37525015DNAHomo sapiens 250agctatgcca tgagc 1525151DNAHomo sapiens
251gctattagtg gtagtggtgg tagcacatac tacgcagact ccgtgaaggg c
5125248DNAHomo sapiens 252gcgtattacg atattttgac tggttatttt
tacaacggta tggacgtc 48253336DNAHomo sapiens 253caggctgtgc
tcactcagcc gtcttccgtg tctgggtctc ctggacagtc gatcaccatc 60tcctgcactg
gaaccagcag tgacgttggt ggttatgact atgtctcctg gtaccaacaa
120cacccaggca aagcccccaa actcatgatt catgatgtca ggaatcggcc
ctcaggggtt 180tctaatcgct tctctggctc caagtttggc aacacggcct
ccctgaccat ctctgggctc 240cagactgagg acgaggctga ttattactgc
agttcatata caagcagcag cactcatgtg 300ctattcggcg gagggaccaa
gctgaccgtc ctaggt 33625442DNAHomo sapiens 254actggaacca gcagtgacgt
tggtggttat gactatgtct cc 4225521DNAHomo sapiens 255gatgtcagga
atcggccctc a 2125627DNAHomo sapiens 256agttcatata caagcagcag
cactcat 27257369DNAHomo sapiens 257caggtgcagc tggtgcagtc tgggggaggc
ttggtacagc ctggcaggtc cctgagactc 60tcctgtgcag cctctggatt cacctttgat
gattatgcca tgcactgggt ccggcaagct 120ccagggaagg gcctggagtg
ggtctcaggt attagttgga atagtggtag cataggctat 180gcggactctg
tgaagggccg attcaccatc tccagagaca acgccaagag ctccctgtat
240ctgcaaatga acagtctgag agctgaggac acggccttgt attactgtgc
aaaaggccac 300tctccgtata gcagtggctg gtctgacttt gactactggg
gccagggaac cctggtcacc 360gtctcgagc 36925815DNAHomo sapiens
258gattatgcca tgcac 1525951DNAHomo sapiens 259ggtattagtt ggaatagtgg
tagcataggc tatgcggact ctgtgaaggg c 5126042DNAHomo sapiens
260ggccactctc cgtatagcag tggctggtct gactttgact ac 42261336DNAHomo
sapiens 261cagtctgtgt tgacgcagcc gccctcagtg tctggggccc cagggcagag
ggtcaccatc 60tcctgcaccg ggagcagctc caacatcggg gcaggttatg atgttcagtg
gtaccagcag 120ctcccaggaa cagcccccaa actcctcatc catgctaaca
agaatcggcc ctcaggggtc 180cctgaccgaa tctctggctc caagtctggc
accacagcct ccctggccat cactgggttc 240caggctgagg atgaggctga
ttattactgc cagtcctatg acagcagcct gactggttat 300gtcttcggaa
ctgggaccaa ggtcaccgtc ctaggt 33626242DNAHomo sapiens 262accgggagca
gctccaacat cggggcaggt tatgatgttc ag 4226321DNAHomo sapiens
263gctaacaaga atcggccctc a 2126427DNAHomo sapiens 264cagtcctatg
acagcagcct gactggt 27265375DNAHomo sapiens 265gaggtgcagc tggtggagtc
tgggggaggc ttggtacagc ctggcaggtc cctgagactc 60tcctgtgcag cctctggatt
cacctttgct gattatgcca tgcactgggt ccggcaagct 120ccagggaagg
gcctggagtg ggtctcaagt attagttgga atagtggtag catagcctat
180gcggactctg tgaagggccg attcaccatc tccagagaca acgccaagaa
ctccctgtat 240ctgcaaatga acagtctgag agctgaggac acggccttgt
attactgtgc aaaagcctca 300gcagctggta ctgaatacta ccactactac
ggtatggacg tctggggcca agggaccacg 360gtcaccgtct cgaga
37526615DNAHomo sapiens 266gattatgcca tgcac 1526751DNAHomo sapiens
267agtattagtt ggaatagtgg tagcatagcc tatgcggact ctgtgaaggg c
5126848DNAHomo sapiens 268gcctcagcag ctggtactga atactaccac
tactacggta tggacgtc 48269333DNAHomo sapiens 269tcctatgtgc
tgactcagcc accctcagcg tctgggaccc ccgggcagag ggtcaccatc 60tcttgttctg
gaagcagctc caacatcgga agtaatacta taaactggta ccagcagctc
120ccaggaacgg cccccaaact cctcatctat aataatcatc agcggccctc
aggggtccct 180gaccgattct ctggctcaaa gtctggcacc tcagcctccc
tggccatcag tgggctccag 240tctgcggatg aggctgatta ttactgtgga
gcgtggaatg acagcctgaa tgtctatgtc 300ttcggaactg ggaccaaggt
caccgtccta ggt 33327039DNAHomo sapiens 270tctggaagca gctccaacat
cggaagtaat actataaac 3927121DNAHomo sapiens 271aataatcatc
agcggccctc a 2127227DNAHomo sapiens 272ggagcgtgga atgacagcct
gaatgtc 27273372DNAHomo sapiens 273caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta cacctttacc
agctatggta tcagctgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcagcgctt acaatggtaa cacaaactat 180gcacagaagc
tccagggcag agtcaccatg accacagaca catccacgag cacagcctac
240atggagctga ggagcctgag atctgacgac acggccgtgt attactgtgc
gacagcagca 300agcctaaagt attactatga tagtagtggt tattactact
ggggccaggg aaccctggtc 360accgtctcga ga 37227415DNAHomo sapiens
274agctatggta tcagc 1527551DNAHomo sapiens 275tggatcagcg cttacaatgg
taacacaaac tatgcacaga agctccaggg c 5127645DNAHomo sapiens
276gcagcaagcc taaagtatta ctatgatagt agtggttatt actac
45277330DNAHomo sapiens 277tcttctgagc tgactcagga ccctgctgtg
tctgtggcct tgggacagac agtcaggatc 60acatgccaag gagacagcct cagaagctat
tatgcaagct ggtaccagca gaagccagga 120caggcccctg tacttgtcat
ctctggtaaa aacaaccggc cctcagggat cccagaccga 180ttctctggct
ccagctcagg agacacagct tccttgacca tcactggggc tcaggcggaa
240gatgaggcta actattactg taactctcgg gacagcagtg gttacccctc
ttgggtgttc 300ggcggaggga ccaagctgac cgtcctaggc 33027833DNAHomo
sapiens 278caaggagaca gcctcagaag ctattatgca agc 3327921DNAHomo
sapiens 279ggtaaaaaca accggccctc a 2128030DNAHomo sapiens
280aactctcggg acagcagtgg ttacccctct 30281390DNAHomo sapiens
281caggtgcagc tggtgcagtc tggggctgag gtgaagaagc ctggggcctc
agtgaaggtc 60tcctgcaagg gttctggtta cgtttttaac agttatggta ttacctgggt
gcgacaggcc 120ccaggacaag ggcttgagtg gatgggatgg atcagcgctt
acaatggtta cacagactat 180gcacagaagg tccagggcag agtcaccatg
accacagaga catccacgag cacagcctac 240atggagctga ggagcctgag
atctgacgac acggccgttt attattgtgc gagggattac 300tatgatagta
gtacttatta ctccagtgat tacttccagt actacggtat ggacgtctgg
360ggccaaggga ccacggtcac cgtctcgagc
39028215DNAHomo sapiens 282agttatggta ttacc 1528351DNAHomo sapiens
283tggatcagcg cttacaatgg ttacacagac tatgcacaga aggtccaggg c
5128463DNAHomo sapiens 284gattactatg atagtagtac ttattactcc
agtgattact tccagtacta cggtatggac 60gtc 63285333DNAHomo sapiens
285caggctgtgc tgactcagcc ggcttccgtg tctgggtctc ctggacagtc
gatcaccatc 60tcctgcactg gaaccagcag tgacgttggt gcttataact atgtctcctg
gtaccaacaa 120cacccaggca aagcccccaa actcatgatt tctgatgtca
gtaggcggcc ctcaggggtt 180tctaatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240cagactgagg acgaggctga
ttattactgc agctcatata caagcagcaa cactgtctta 300ttcggcggag
ggaccaagct gaccgtccta ggt 33328642DNAHomo sapiens 286actggaacca
gcagtgacgt tggtgcttat aactatgtct cc 4228721DNAHomo sapiens
287gatgtcagta ggcggccctc a 2128824DNAHomo sapiens 288agctcatata
caagcagcaa cact 24289333DNAHomo sapiens 289caggctgtgc tgactcagcc
ggcttccgtg tctgggtctc ctggacagtc gatcaccatc 60tcctgcactg gaaccagcag
tgacgttggt gcttataact atgtctcctg gtaccaacaa 120cacccaggca
aagcccccaa actcatgatt tctgatgtca gtaggcggcc ctcaggggtt
180tctaatcgct tctctggctc caagtctggc aacacggcct ccctgaccat
ctctgggctc 240cagactgagg acgaggctga ttattactgc agctcatata
caagcagcaa cactgtctta 300ttcggcggag ggaccaagct gaccgtccta ggt
33329015DNAHomo sapiens 290aactactgga tcggc 1529151DNAHomo sapiens
291atcatctatc ctggtgactc tgataccagg tacagtccgt cattccaagg c
5129239DNAHomo sapiens 292cggggctccc gtagtagtgg tgaagatgct
tttgaagtc 39293330DNAHomo sapiens 293tcctatgagc tgactcagcc
accctcagtg tcagtggccc caggaaagac ggccacaatt 60acgtgtgggg gcgacaacat
tggaagtaag agtgtgcact ggtaccagca gaggccaggc 120caggcccctg
tgttggtcat caattatgat agtgaccggc cctcagggat ccctgagcga
180ttctctggct ccaactctgg gaacacggcc accctgacca tcagcagggt
cgaagccggg 240gatgaggccg actattactg tcaggtggaa gatcgccgtg
gtggttatca tgtggtattc 300ggcggaggga ccaagctgac cgtcctaggt
33029433DNAHomo sapiens 294gggggcgaca acattggaag taagagtgtg cac
3329521DNAHomo sapiens 295tatgatagtg accggccctc a 2129630DNAHomo
sapiens 296caggtggaag atcgccgtgg tggttatcat 30297375DNAHomo sapiens
297caggtgcagc tggtgcagtc tgggggaggc ttggtccagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt caccgtcagt agcaactaca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcagtt atttatagcg
gtggtagcac atactacgca 180gactccgtga agggcagatt caccatctcc
agagacaatt ccaagaacac gctgtatctt 240caaatgaaca gcctgagagc
cgaggacacg gctgtgtatt actgtgcgag ggaaggatat 300tgtagtggtg
gtagctgcta ctcctacggc gcttttgata tctggggcca agggaccacg
360gtcaccgtct cgagc 37529815DNAHomo sapiens 298agcaactaca tgagc
1529948DNAHomo sapiens 299gttatttata gcggtggtag cacatactac
gcagactccg tgaagggc 4830051DNAHomo sapiens 300gaaggatatt gtagtggtgg
tagctgctac tcctacggcg cttttgatat c 51301375DNAHomo sapiens
301caggtgcagc tggtgcagtc tgggggaggc ttggtccagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt caccgtcagt agcaactaca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcagtt atttatagcg
gtggtagcac atactacgca 180gactccgtga agggcagatt caccatctcc
agagacaatt ccaagaacac gctgtatctt 240caaatgaaca gcctgagagc
cgaggacacg gctgtgtatt actgtgcgag ggaaggatat 300tgtagtggtg
gtagctgcta ctcctacggc gcttttgata tctggggcca agggaccacg
360gtcaccgtct cgagc 37530233DNAHomo sapiens 302cgggcgagtc
agaatattgc caactggtta gcc 3330321DNAHomo sapiens 303gctgcatcca
atttgcaaag t 2130424DNAHomo sapiens 304caacagggta acagtttccc tcgg
24305390DNAHomo sapiens 305caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta cgtttttaac
agttatggta ttacctgggt gcgacaggcc 120ccaggacaag ggcttgagtg
gatgggatgg atcagcgctt acaatggtta cacagactat 180gcacagaagg
tccagggcag agtcaccatg accacagaga catccacgag cacagcctac
240atggagctga ggagcctgag atctgacgac acggccgttt attattgtgc
gagggactac 300tatgatagta gtacttatta ctccagtgat tacttcaagt
actacggtat ggacgtctgg 360ggccaaggga ccacggtcac cgtctcgagc
39030615DNAHomo sapiens 306agttatggta ttacc 1530751DNAHomo sapiens
307tggatcagcg cttacaatgg ttacacagac tatgcacaga aggtccaggg c
5130863DNAHomo sapiens 308gactactatg atagtagtac ttattactcc
agtgattact tcaagtacta cggtatggac 60gtc 63309333DNAHomo sapiens
309caggctgtgc tcactcagcc gtcttccgtg tctgggtctc ctggacagtc
gatcaccatc 60tcctgctctg gaaccagcag tgacgttggt gcttataact atgtctcctg
gtaccaacaa 120cacccaggca aagcccccag actcctgact tttgatgtca
ataggcgtcc ctcagggtct 180tctagtcgct tctctggctc caagtctggc
aacacggcct ccctgactat ctctgggctc 240caggctgagg acgaggctga
ctattactgc agttcatata caaacagcaa cactgtcgtg 300ttcggcggag
ggaccaggct gaccgtccta agt 33331042DNAHomo sapiens 310tctggaacca
gcagtgacgt tggtgcttat aactatgtct cc 4231121DNAHomo sapiens
311gatgtcaata ggcgtccctc a 2131224DNAHomo sapiens 312agttcatata
caaacagcaa cact 24313381DNAHomo sapiens 313caggtgcagc tgcaggagtc
ggggccagga ctggtgaagc cgtcggagac cctggccctc 60acctgcactg tctctggtgg
ctccatcagt aactactact ggagttggat ccggcagccc 120ccagggaagg
gactggagtg gattgggtat atctatgaca ttgagaatac caactacaac
180ccctccctca agagtcgagt caccatatca gtggacacgt ccaagaacca
gttctccctg 240aagttgagct ctgtgaccgc tgatgacacg gccgtatatt
actgtgcgag agattcaagg 300gtcattcgat ttttggaggg gtactcctac
tactacggtg tggacgtctg gggccaaggg 360acaatggtca ccgtctcgag c
38131415DNAHomo sapiens 314aactactact ggagt 1531548DNAHomo sapiens
315tatatctatg acattgagaa taccaactac aacccctccc tcaagagt
4831657DNAHomo sapiens 316gattcaaggg tcattcgatt tttggagggg
tactcctact actacggtgt ggacgtc 57317333DNAHomo sapiens 317tcctatgagc
tgactcagcc accctcagcg tctgggaccc ccgggcagac ggtcatcatc 60tcttgttctg
gaagcaggtc caacatcgga ggtcatggtg taaattggca ccagcaggtt
120ccaggaacgg cccccaaact cctcatctac cgtaatgatc gccggccctc
aggggtcccg 180gaccgattct ctggctccaa gtctggcact tcagcctccc
tggtcatcag tggactgcag 240tttgaggatg aggctgatta ttactgtgta
gcatgggaag acagcctgga tggtccggtg 300ttcggcggag ggaccaagct
gactgtccta ggt 33331839DNAHomo sapiens 318tctggaagca ggtccaacat
cggaggtcat ggtgtaaat 3931921DNAHomo sapiens 319cgtaatgatc
gccggccctc a 2132027DNAHomo sapiens 320gtagcatggg aagacagcct
ggatggt 27321345DNAHomo sapiens 321gaggtgcagc tggtggagtc tgggggaggc
ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt cacctttagc
agctatgcca tgagctgggt ccgccaggct 120ccagggaagg ggctggagtg
ggtctcaact attagtggta gtggtggtag tacatactac 180gcagactccg
tgaagggccg attcaccatc tccagagaca attccaagaa cacgctatat
240cttcaaatga acagcctgag agccgaggac acggccgtct attattgtgc
gagaggtata 300gtggctacta gctggggcca gggaaccctg gtcaccgtct cgaga
34532215DNAHomo sapiens 322agctatgcca tgagc 1532351DNAHomo sapiens
323actattagtg gtagtggtgg tagtacatac tacgcagact ccgtgaaggg c
5132418DNAHomo sapiens 324ggtatagtgg ctactagc 18325324DNAHomo
sapiens 325tcctatgagc tgactcagcc accctcagtg tcagtggccc caggacagac
ggccagaatt 60acctgtgggg gaaacaagat tggaagcaaa agtgtgcact ggtaccagca
gaagcaaggc 120caggcccctg tattggtcat ctatttggat cgcgaccggc
cctcagggat ccctgaacga 180ttctctggct ccaactctgg gaacacggcc
accctgacca tcaccagggt cgaagccgag 240gatgaggccg actattattg
tcacctgtgg gatagtggta gtgatcaggt gttcggcgga 300gggaccaaac
tgaccgtcct gggt 32432633DNAHomo sapiens 326gggggaaaca agattggaag
caaaagtgtg cac 3332721DNAHomo sapiens 327ttggatcgcg accggccctc a
2132824DNAHomo sapiens 328cacctgtggg atagtggtag tgat
24329342DNAHomo sapiens 329gaggtgcagc tggtggagtc tgggggaggc
gtagtacagc ctggggggtc cctgagactc 60tcctgtgcag cctcaggatt caactttgat
gtttatggca tgaactgggt ccgtcaagtt 120ccagggaagg gtctggagtg
ggtctctctt atcaacgggg atggcggttt aagatattac 180gcagactctg
tgaagggccg attcaccgtc tccagagaca acagcaggaa ttccctatat
240ctgcaaatga acagtctcag aagtgaggac accgccctgt attattgtgt
aaagggaaac 300ttccagcagt ggggccaggg aaccctggtc accgtctcga ga
34233015DNAHomo sapiens 330gtttatggca tgaac 1533151DNAHomo sapiens
331cttatcaacg gggatggcgg tttaagatat tacgcagact ctgtgaaggg c
5133215DNAHomo sapiens 332ggaaacttcc agcag 15333327DNAHomo sapiens
333tcctatgtgc tgactcagcc accctcagtg tcagtggccc caggaaagac
ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa agtgtgcact ggtaccagca
gaagccaggc 120caggcccctg tgctggtcat ctattatgat agcgaccggc
cctcagggat ccctgagcga 180ttctctggct ccaactctgg gaacacggcc
accctgacca tcagcagggt cgaagccggg 240gatgaggccg actattactg
tcaggtgtgg gatagtagta gtgatcatgt ggtattcggc 300ggagggacca
agctgaccgt cctaggt 32733433DNAHomo sapiens 334gggggaaaca acattggaag
taaaagtgtg cac 3333521DNAHomo sapiens 335tatgatagcg accggccctc a
2133627DNAHomo sapiens 336caggtgtggg atagtagtag tgatcat
27337345DNAHomo sapiens 337gaggtgcagc tggtggagtc tgggggaggc
ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt cacctttgat
gattatgcca tgcactgggt ccgtcaagct 120ccagggaagg gtctggagtg
ggtctctctt attagtgggg atggtggtag cacatactat 180gcagactctg
tgaaggaccg attcaccatc tccagagaca acagcaaaaa ctccctgtat
240ctgcaaatga acagcctgag agccgaggac acggccgtgt attactgtgc
gaggggaaac 300tactttgact actggggcca gggaaccctg gtcaccgtct cgaga
34533815DNAHomo sapiens 338gattatgcca tgcac 1533951DNAHomo sapiens
339cttattagtg gggatggtgg tagcacatac tatgcagact ctgtgaagga c
5134018DNAHomo sapiens 340ggaaactact ttgactac 18341318DNAHomo
sapiens 341tcctatgagc tgactcagcc actctcagtg tcagtggccc tgggacagac
ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa aatgtgcact ggtaccagca
gaagccaggc 120caggcccctg tgctggtcat ctatagggat agcaaccggc
cctctgggat ccctgagcga 180ttctctggct ccaactcggg gaacacggcc
accctgacca tcagcagagc ccaagccggg 240gatgaggctg actattactg
tcaggtgtgg gacagcagcg tggtattcgg cggagggacc 300aagctgaccg tcctaggt
31834233DNAHomo sapiens 342gggggaaaca acattggaag taaaaatgtg cac
3334321DNAHomo sapiens 343agggatagca accggccctc t 2134418DNAHomo
sapiens 344caggtgtggg acagcagc 18345366DNAHomo sapiens
345gaggtgcagc tggtggagtc tgggggaggc ttggtacagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt caccttcagt agctatagca tgaactgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtttcatac attagtagta
gtagtagtac catatactac 180gcagactctg tgaagggccg attcaccatc
tccagagaca atgccaagaa ctcactgtat 240ctgcagatga acagcctgag
agacgaggac acggctgtgt attactgtgc gagagtgatg 300ccgagttact
actactacta cggtatggac gtctggggcc aagggaccac ggtcaccgtc 360tcgaga
36634615DNAHomo sapiens 346agctatagca tgaac 1534751DNAHomo sapiens
347tacattagta gtagtagtag taccatatac tacgcagact ctgtgaaggg c
5134839DNAHomo sapiens 348gtgatgccga gttactacta ctactacggt
atggacgtc 39349333DNAHomo sapiens 349aattttatgc tgactcagcc
ccactctgtg tcggagtctc cggggaagac ggtaaccatc 60tcctgcaccg gcagcagtgg
cagcattgcc agcaactatg tgcagtggta ccagcagcgc 120ccgggcagtg
cccccaccac tgtgatctat gaggatagtg aaagaccctc tggggtccct
180gatcggttct ctggctccat cgacagctcc tccaactctg cctccctcac
catctctgga 240ctgaagactc aggacgaggc tgactactac tgtcagtctt
atgatggcgt caattgggtg 300ttcggcggag ggaccaagct gaccgtccta ggt
33335039DNAHomo sapiens 350accggcagca gtggcagcat tgccagcaac
tatgtgcag 3935121DNAHomo sapiens 351gaggatagtg aaagaccctc t
2135221DNAHomo sapiens 352cagtcttatg atggcgtcaa t 21353342DNAHomo
sapiens 353gaggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc
cctgagactc 60tcctgtgcag cctctggatt caccttcagt agctatggca tgcactgggt
ccgccaggct 120ccaggcaagg ggctggagtg ggtggcagtt atatcatatg
atggaagtaa taaatactat 180gcagactccg tgaagggccg attcaccatc
tccagagaca attccaagaa cacgctgtat 240ctgcaaatga acagcctgag
agctgaggac acggctgtgt attactgtgc ggactacggt 300atggacgtct
ggggccaagg gaccacggtc accgtctcga ga 34235415DNAHomo sapiens
354agctatggca tgcac 1535551DNAHomo sapiens 355gttatatcat atgatggaag
taataaatac tatgcagact ccgtgaaggg c 5135615DNAHomo sapiens
356tacggtatgg acgtc 15357321DNAHomo sapiens 357gacatccaga
tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60atcacttgcc
gggcaagtca gagcattagc agctatttaa attggtatca gcagaaacca
120gggaaagccc ctaagctcct gatctatgct gcatccagtt tgcaaagtgg
ggtcccatca 180aggttcagtg gcagtggatc tgggactgat ttcactctca
ccatcagcag tctgcaacct 240gaagattttg caacttacta ctgtcaacag
agttacagta cccccgtgac gttcggccaa 300gggaccaagg tggaaatcaa a
32135833DNAHomo sapiens 358cgggcaagtc agagcattag cagctattta aat
3335921DNAHomo sapiens 359gctgcatcca gtttgcaaag t 2136021DNAHomo
sapiens 360caacagagtt acagtacccc c 21361360DNAHomo sapiens
361caggtgcagc tgcaggagtc gggcccggga ctggtgaagc cttcacagac
cctgtccctc 60acctgcactg tctctggtgg ctccatcagc agtggtggtt actactggag
ctggatccgc 120cagcacccag ggaagggcct ggagtggatt gggtacatct
attacagtgg gagcacctac 180tacaacccgt ccctcaagag tcgagttacc
atatcagtag acacgtctaa gaaccagttc 240tccctgaagc tgagctctgt
gactgccgcg gacacggccg tgtattactg tgcgagagat 300cgggggactg
gggatgcttt tgatatctgg ggccaaggga caatggtcac cgtctcgaga
36036221DNAHomo sapiens 362agtggtggtt actactggag c 2136348DNAHomo
sapiens 363tacatctatt acagtgggag cacctactac aacccgtccc tcaagagt
4836430DNAHomo sapiens 364gatcggggga ctggggatgc ttttgatatc
30365333DNAHomo sapiens 365cagtctgtgt tgacgcagcc gccctcggtg
tctggggccc cccggcagac ggtcaccatc 60tcctgctctg ggagcagctc caacatcgga
caaaattctg ttacctggta ccagcgcctc 120ccgggtgagg ctcccaaact
cctcatctac tatgatgatc tcttgcactc aggagtctct 180gaccgattct
ctggctccaa gtctggcacc tcagcctcac tggccatcag tggactccag
240tctgaggatg aggctgagta ctactgtgcg tcatgggatg acagcctgaa
aggtccggta 300ttcggcggag ggaccaaact gaccgtccta ggt 33336639DNAHomo
sapiens 366tctgggagca gctccaacat cggacaaaat tctgttacc
3936721DNAHomo sapiens 367tatgatgatc tcttgcactc a 2136827DNAHomo
sapiens 368gcgtcatggg atgacagcct gaaaggt 273691200PRTHomo sapiens
369Met Arg Pro Ser Gly Thr Ala Gly Ala Ala Leu Leu Ala Leu Leu Ala1
5 10 15Ala Leu Cys Pro Ala Ser Arg Ala Leu Glu Glu Lys Lys Val Cys
Gln 20 25 30Gly Thr Ser Asn Lys Leu Thr Gln Leu Gly Thr Phe Glu Asp
His Phe 35 40 45Leu Ser Leu Gln Arg Met Phe Asn Asn Cys Glu Val Val
Leu Gly Asn 50 55 60Leu Glu Ile Thr Tyr Val Gln Arg Asn Tyr Asp Leu
Ser Phe Leu Lys65 70 75 80Thr Ile Gln Glu Val Ala Gly Tyr Val Leu
Ile Ala Leu Asn Thr Val 85 90 95Glu Arg Ile Pro Leu Glu Asn Leu Gln
Ile Ile Arg Gly Asn Met Tyr 100 105 110Tyr Glu Asn Ser Tyr Ala Leu
Ala Gly Leu Lys Glu Leu Pro Met Arg 115 120 125Asn Leu Gln Glu Ile
Leu His Gly Ala Val Arg Phe Ser Asn Asn Pro 130 135 140Ala Leu Cys
Asn Val Glu Ser Ile Gln Trp Arg Asp Ile Val Ser Ser145 150 155
160Asp Phe Leu Ser Asn Met Ser Met Asp Phe Gln Asn His Leu Gly Ser
165 170 175Cys Gln Lys Cys Asp Pro Ser Cys Pro Asn Gly Ser Cys Trp
Gly Ala 180 185 190Gly Glu Glu Asn Cys Gln Lys Leu Thr Lys Ile Ile
Cys Ala Gln Gln 195 200 205Cys Ser Gly Arg Cys Arg Gly Lys Ser Pro
Ser Asp Cys Cys His Asn 210
215 220Gln Cys Ala Ala Gly Cys Thr Gly Pro Arg Glu Ser Asp Cys Leu
Val225 230 235 240Cys Arg Lys Phe Arg Asp Glu Ala Thr Cys Lys Asp
Thr Cys Pro Pro 245 250 255Leu Met Leu Tyr Asn Pro Thr Thr Tyr Gln
Met Asp Val Asn Pro Glu 260 265 270Gly Lys Tyr Ser Phe Gly Ala Thr
Cys Val Lys Lys Cys Pro Arg Asn 275 280 285Tyr Val Val Thr Asp His
Gly Ser Cys Val Arg Ala Cys Gly Ala Asp 290 295 300Ser Tyr Glu Met
Glu Glu Asp Gly Val Arg Lys Cys Lys Lys Cys Glu305 310 315 320Gly
Pro Cys Arg Lys Val Cys Asn Gly Ile Gly Ile Gly Glu Phe Lys 325 330
335Asp Ser Leu Ser Ile Asn Ala Thr Asn Ile Lys His Phe Lys Asn Cys
340 345 350Thr Ser Ile Ser Gly Asp Leu His Ile Leu Pro Val Ala Phe
Arg Gly 355 360 365Asp Ser Phe Thr His Thr Pro Pro Leu Asp Pro Gln
Glu Leu Asp Ile 370 375 380Leu Lys Thr Val Lys Glu Ile Thr Gly Phe
Leu Leu Ile Gln Ala Trp385 390 395 400Pro Glu Asn Arg Thr Asp Leu
His Ala Phe Glu Asn Leu Glu Ile Ile 405 410 415Arg Gly Arg Thr Lys
Gln His Gly Gln Phe Ser Leu Ala Val Val Ser 420 425 430Leu Asn Ile
Thr Ser Leu Gly Leu Arg Ser Leu Lys Glu Ile Ser Asp 435 440 445Gly
Asp Val Ile Ile Ser Gly Asn Lys Asn Leu Cys Tyr Ala Asn Thr 450 455
460Ile Asn Trp Lys Lys Leu Phe Gly Thr Ser Gly Gln Lys Thr Lys
Ile465 470 475 480Ile Ser Asn Arg Gly Glu Asn Ser Cys Lys Ala Thr
Gly Gln Val Cys 485 490 495His Ala Leu Cys Ser Pro Glu Gly Cys Trp
Gly Pro Glu Pro Arg Asp 500 505 510Cys Val Ser Cys Arg Asn Val Ser
Arg Gly Arg Glu Cys Val Asp Lys 515 520 525Cys Asn Leu Leu Glu Gly
Glu Pro Arg Glu Phe Val Glu Asn Ser Glu 530 535 540Cys Ile Gln Cys
His Pro Glu Cys Leu Pro Gln Ala Met Asn Ile Thr545 550 555 560Cys
Thr Gly Arg Gly Pro Asp Asn Cys Ile Gln Cys Ala His Tyr Ile 565 570
575Asp Gly Pro His Cys Val Lys Thr Cys Pro Ala Gly Val Met Gly Glu
580 585 590Asn Asn Thr Leu Val Trp Lys Tyr Ala Asp Ala Gly His Val
Cys His 595 600 605Leu Cys His Pro Asn Cys Thr Tyr Gly Cys Thr Gly
Pro Gly Leu Glu 610 615 620Gly Cys Pro Thr Asn Gly Pro Lys Ile Pro
Ser Ile Ala Thr Gly Met625 630 635 640Val Gly Ala Leu Leu Leu Leu
Leu Val Val Ala Leu Gly Ile Gly Leu 645 650 655Phe Met Arg Arg Arg
His Ile Val Arg Lys Arg Thr Leu Arg Arg Leu 660 665 670Leu Gln Glu
Arg Glu Leu Val Glu Pro Leu Thr Pro Ser Gly Glu Ala 675 680 685Pro
Asn Gln Ala Leu Leu Arg Ile Leu Lys Glu Thr Glu Phe Lys Lys 690 695
700Ile Lys Val Leu Gly Ser Gly Ala Phe Gly Thr Val Tyr Lys Gly
Leu705 710 715 720Trp Ile Pro Glu Gly Glu Lys Val Lys Ile Pro Val
Ala Ile Lys Glu 725 730 735Leu Arg Glu Ala Thr Ser Pro Lys Ala Asn
Lys Glu Ile Leu Asp Glu 740 745 750Ala Tyr Val Met Ala Ser Val Asp
Asn Pro His Val Cys Arg Leu Leu 755 760 765Gly Ile Cys Leu Thr Ser
Thr Val Gln Leu Ile Thr Gln Leu Met Pro 770 775 780Phe Gly Cys Leu
Leu Asp Tyr Val Arg Glu His Lys Asp Asn Ile Gly785 790 795 800Ser
Gln Tyr Leu Leu Asn Trp Cys Val Gln Ile Ala Lys Gly Met Asn 805 810
815Tyr Leu Glu Asp Arg Arg Leu Val His Arg Asp Leu Ala Ala Arg Asn
820 825 830Val Leu Val Lys Thr Pro Gln His Val Lys Ile Thr Asp Phe
Gly Leu 835 840 845Ala Lys Leu Leu Gly Ala Glu Glu Lys Glu Tyr His
Ala Glu Gly Gly 850 855 860Lys Val Pro Ile Lys Trp Met Ala Leu Glu
Ser Ile Leu His Arg Ile865 870 875 880Tyr Thr His Gln Ser Asp Val
Trp Ser Tyr Gly Val Thr Val Trp Glu 885 890 895Leu Met Thr Phe Gly
Ser Lys Pro Tyr Asp Gly Ile Pro Ala Ser Glu 900 905 910Ile Ser Ser
Ile Leu Glu Lys Gly Glu Arg Leu Pro Gln Pro Pro Ile 915 920 925Cys
Thr Ile Asp Val Tyr Met Ile Met Val Lys Cys Trp Met Ile Asp 930 935
940Ala Asp Ser Arg Pro Lys Phe Arg Glu Leu Ile Ile Glu Phe Ser
Lys945 950 955 960Met Ala Arg Asp Pro Gln Arg Tyr Leu Val Ile Gln
Gly Asp Glu Arg 965 970 975Met His Leu Pro Ser Pro Thr Asp Ser Asn
Phe Tyr Arg Ala Leu Met 980 985 990Asp Glu Glu Asp Met Asp Asp Val
Val Asp Ala Asp Glu Tyr Leu Ile 995 1000 1005Pro Gln Gln Gly Phe
Phe Ser Ser Pro Ser Thr Ser Arg Thr Pro 1010 1015 1020Leu Leu Ser
Ser Leu Ser Ala Thr Ser Asn Asn Ser Thr Val Ala 1025 1030 1035Cys
Ile Asp Arg Asn Gly Leu Gln Ser Cys Pro Ile Lys Glu Asp 1040 1045
1050Ser Phe Leu Gln Arg Tyr Ser Ser Asp Pro Thr Gly Ala Leu Thr
1055 1060 1065Glu Asp Ser Ile Asp Asp Thr Phe Leu Pro Val Pro Glu
Tyr Ile 1070 1075 1080Asn Gln Ser Val Pro Lys Arg Pro Ala Gly Ser
Val Gln Asn Pro 1085 1090 1095Val Tyr His Asn Gln Pro Leu Asn Pro
Ala Pro Ser Arg Asp Pro 1100 1105 1110His Tyr Gln Asp Pro His Ser
Thr Ala Val Gly Asn Pro Glu Tyr 1115 1120 1125Leu Asn Thr Val Gln
Pro Thr Cys Val Asn Ser Thr Phe Asp Ser 1130 1135 1140Pro Ala His
Trp Ala Gln Lys Gly Ser His Gln Ile Ser Leu Asp 1145 1150 1155Asn
Pro Asp Tyr Gln Gln Asp Phe Phe Pro Lys Glu Ala Lys Pro 1160 1165
1170Asn Gly Ile Phe Lys Gly Ser Thr Ala Glu Asn Ala Glu Tyr Leu
1175 1180 1185Arg Val Ala Pro Gln Ser Ser Glu Phe Ile Gly Ala 1190
1195 12003701255PRTHomo sapiens 370Met Glu Leu Ala Ala Leu Cys Arg
Trp Gly Leu Leu Leu Ala Leu Leu1 5 10 15Pro Pro Gly Ala Ala Ser Thr
Gln Val Cys Thr Gly Thr Asp Met Lys 20 25 30Leu Arg Leu Pro Ala Ser
Pro Glu Thr His Leu Asp Met Leu Arg His 35 40 45Leu Tyr Gln Gly Cys
Gln Val Val Gln Gly Asn Leu Glu Leu Thr Tyr 50 55 60Leu Pro Thr Asn
Ala Ser Leu Ser Phe Leu Gln Asp Ile Gln Glu Val65 70 75 80Gln Gly
Tyr Val Leu Ile Ala His Asn Gln Val Arg Gln Val Pro Leu 85 90 95Gln
Arg Leu Arg Ile Val Arg Gly Thr Gln Leu Phe Glu Asp Asn Tyr 100 105
110Ala Leu Ala Val Leu Asp Asn Gly Asp Pro Leu Asn Asn Thr Thr Pro
115 120 125Val Thr Gly Ala Ser Pro Gly Gly Leu Arg Glu Leu Gln Leu
Arg Ser 130 135 140Leu Thr Glu Ile Leu Lys Gly Gly Val Leu Ile Gln
Arg Asn Pro Gln145 150 155 160Leu Cys Tyr Gln Asp Thr Ile Leu Trp
Lys Asp Ile Phe His Lys Asn 165 170 175Asn Gln Leu Ala Leu Thr Leu
Ile Asp Thr Asn Arg Ser Arg Ala Cys 180 185 190His Pro Cys Ser Pro
Met Cys Lys Gly Ser Arg Cys Trp Gly Glu Ser 195 200 205Ser Glu Asp
Cys Gln Ser Leu Thr Arg Thr Val Cys Ala Gly Gly Cys 210 215 220Ala
Arg Cys Lys Gly Pro Leu Pro Thr Asp Cys Cys His Glu Gln Cys225 230
235 240Ala Ala Gly Cys Thr Gly Pro Lys His Ser Asp Cys Leu Ala Cys
Leu 245 250 255His Phe Asn His Ser Gly Ile Cys Glu Leu His Cys Pro
Ala Leu Val 260 265 270Thr Tyr Asn Thr Asp Thr Phe Glu Ser Met Pro
Asn Pro Glu Gly Arg 275 280 285Tyr Thr Phe Gly Ala Ser Cys Val Thr
Ala Cys Pro Tyr Asn Tyr Leu 290 295 300Ser Thr Asp Val Gly Ser Cys
Thr Leu Val Cys Pro Leu His Asn Gln305 310 315 320Glu Val Thr Ala
Glu Asp Gly Thr Gln Arg Cys Glu Lys Cys Ser Lys 325 330 335Pro Cys
Ala Arg Val Cys Tyr Gly Leu Gly Met Glu His Leu Arg Glu 340 345
350Val Arg Ala Val Thr Ser Ala Asn Ile Gln Glu Phe Ala Gly Cys Lys
355 360 365Lys Ile Phe Gly Ser Leu Ala Phe Leu Pro Glu Ser Phe Asp
Gly Asp 370 375 380Pro Ala Ser Asn Thr Ala Pro Leu Gln Pro Glu Gln
Leu Gln Val Phe385 390 395 400Glu Thr Leu Glu Glu Ile Thr Gly Tyr
Leu Tyr Ile Ser Ala Trp Pro 405 410 415Asp Ser Leu Pro Asp Leu Ser
Val Phe Gln Asn Leu Gln Val Ile Arg 420 425 430Gly Arg Ile Leu His
Asn Gly Ala Tyr Ser Leu Thr Leu Gln Gly Leu 435 440 445Gly Ile Ser
Trp Leu Gly Leu Arg Ser Leu Arg Glu Leu Gly Ser Gly 450 455 460Leu
Ala Leu Ile His His Asn Thr His Leu Cys Phe Val His Thr Val465 470
475 480Pro Trp Asp Gln Leu Phe Arg Asn Pro His Gln Ala Leu Leu His
Thr 485 490 495Ala Asn Arg Pro Glu Asp Glu Cys Val Gly Glu Gly Leu
Ala Cys His 500 505 510Gln Leu Cys Ala Arg Gly His Cys Trp Gly Pro
Gly Pro Thr Gln Cys 515 520 525Val Asn Cys Ser Gln Phe Leu Arg Gly
Gln Glu Cys Val Glu Glu Cys 530 535 540Arg Val Leu Gln Gly Leu Pro
Arg Glu Tyr Val Asn Ala Arg His Cys545 550 555 560Leu Pro Cys His
Pro Glu Cys Gln Pro Gln Asn Gly Ser Val Thr Cys 565 570 575Phe Gly
Pro Glu Ala Asp Gln Cys Val Ala Cys Ala His Tyr Lys Asp 580 585
590Pro Pro Phe Cys Val Ala Arg Cys Pro Ser Gly Val Lys Pro Asp Leu
595 600 605Ser Tyr Met Pro Ile Trp Lys Phe Pro Asp Glu Glu Gly Ala
Cys Gln 610 615 620Pro Cys Pro Ile Asn Cys Thr His Ser Cys Val Asp
Leu Asp Asp Lys625 630 635 640Gly Cys Pro Ala Glu Gln Arg Ala Ser
Pro Leu Thr Ser Ile Ile Ser 645 650 655Ala Val Val Gly Ile Leu Leu
Val Val Val Leu Gly Val Val Phe Gly 660 665 670Ile Leu Ile Lys Arg
Arg Gln Gln Lys Ile Arg Lys Tyr Thr Met Arg 675 680 685Arg Leu Leu
Gln Glu Thr Glu Leu Val Glu Pro Leu Thr Pro Ser Gly 690 695 700Ala
Met Pro Asn Gln Ala Gln Met Arg Ile Leu Lys Glu Thr Glu Leu705 710
715 720Arg Lys Val Lys Val Leu Gly Ser Gly Ala Phe Gly Thr Val Tyr
Lys 725 730 735Gly Ile Trp Ile Pro Asp Gly Glu Asn Val Lys Ile Pro
Val Ala Ile 740 745 750Lys Val Leu Arg Glu Asn Thr Ser Pro Lys Ala
Asn Lys Glu Ile Leu 755 760 765Asp Glu Ala Tyr Val Met Ala Gly Val
Gly Ser Pro Tyr Val Ser Arg 770 775 780Leu Leu Gly Ile Cys Leu Thr
Ser Thr Val Gln Leu Val Thr Gln Leu785 790 795 800Met Pro Tyr Gly
Cys Leu Leu Asp His Val Arg Glu Asn Arg Gly Arg 805 810 815Leu Gly
Ser Gln Asp Leu Leu Asn Trp Cys Met Gln Ile Ala Lys Gly 820 825
830Met Ser Tyr Leu Glu Asp Val Arg Leu Val His Arg Asp Leu Ala Ala
835 840 845Arg Asn Val Leu Val Lys Ser Pro Asn His Val Lys Ile Thr
Asp Phe 850 855 860Gly Leu Ala Arg Leu Leu Asp Ile Asp Glu Thr Glu
Tyr His Ala Asp865 870 875 880Gly Gly Lys Val Pro Ile Lys Trp Met
Ala Leu Glu Ser Ile Leu Arg 885 890 895Arg Arg Phe Thr His Gln Ser
Asp Val Trp Ser Tyr Gly Val Thr Val 900 905 910Trp Glu Leu Met Thr
Phe Gly Ala Lys Pro Tyr Asp Gly Ile Pro Ala 915 920 925Arg Glu Ile
Pro Asp Leu Leu Glu Lys Gly Glu Arg Leu Pro Gln Pro 930 935 940Pro
Ile Cys Thr Ile Asp Val Tyr Met Ile Met Val Lys Cys Trp Met945 950
955 960Ile Asp Ser Glu Cys Arg Pro Arg Phe Arg Glu Leu Val Ser Glu
Phe 965 970 975Ser Arg Met Ala Arg Asp Pro Gln Arg Phe Val Val Ile
Gln Asn Glu 980 985 990Asp Leu Gly Pro Ala Ser Pro Leu Asp Ser Thr
Phe Tyr Arg Ser Leu 995 1000 1005Leu Glu Asp Asp Asp Met Gly Asp
Leu Val Asp Ala Glu Glu Tyr 1010 1015 1020Leu Val Pro Gln Gln Gly
Phe Phe Cys Pro Asp Pro Ala Pro Gly 1025 1030 1035Ala Gly Gly Met
Val His His Arg His Arg Ser Ser Ser Thr Arg 1040 1045 1050Ser Gly
Gly Gly Asp Leu Thr Leu Gly Leu Glu Pro Ser Glu Glu 1055 1060
1065Glu Ala Pro Arg Ser Pro Leu Ala Pro Ser Glu Gly Ala Gly Ser
1070 1075 1080Asp Val Phe Asp Gly Asp Leu Gly Met Gly Ala Ala Lys
Gly Leu 1085 1090 1095Gln Ser Leu Pro Thr His Asp Pro Ser Pro Leu
Gln Arg Tyr Ser 1100 1105 1110Glu Asp Pro Thr Val Pro Leu Pro Ser
Glu Thr Asp Gly Tyr Val 1115 1120 1125Ala Pro Leu Thr Cys Ser Pro
Gln Pro Glu Tyr Val Asn Gln Pro 1130 1135 1140Asp Val Arg Pro Gln
Pro Pro Ser Pro Arg Glu Gly Pro Leu Pro 1145 1150 1155Ala Ala Arg
Pro Ala Gly Ala Thr Leu Glu Arg Pro Lys Thr Leu 1160 1165 1170Ser
Pro Gly Lys Asn Gly Val Val Lys Asp Val Phe Ala Phe Gly 1175 1180
1185Gly Ala Val Glu Asn Pro Glu Tyr Leu Thr Pro Gln Gly Gly Ala
1190 1195 1200Ala Pro Gln Pro His Pro Pro Pro Ala Phe Ser Pro Ala
Phe Asp 1205 1210 1215Asn Leu Tyr Tyr Trp Asp Gln Asp Pro Pro Glu
Arg Gly Ala Pro 1220 1225 1230Pro Ser Thr Phe Lys Gly Thr Pro Thr
Ala Glu Asn Pro Glu Tyr 1235 1240 1245Leu Gly Leu Asp Val Pro Val
1250 1255371392PRTHomo sapiens 371Met Glu Pro Pro Gly Arg Arg Glu
Cys Pro Phe Pro Ser Trp Arg Phe1 5 10 15Pro Gly Leu Leu Leu Ala Ala
Met Val Leu Leu Leu Tyr Ser Phe Ser 20 25 30Asp Ala Cys Glu Glu Pro
Pro Thr Phe Glu Ala Met Glu Leu Ile Gly 35 40 45Lys Pro Lys Pro Tyr
Tyr Glu Ile Gly Glu Arg Val Asp Tyr Lys Cys 50 55 60Lys Lys Gly Tyr
Phe Tyr Ile Pro Pro Leu Ala Thr His Thr Ile Cys65 70 75 80Asp Arg
Asn His Thr Trp Leu Pro Val Ser Asp Asp Ala Cys Tyr Arg 85 90 95Glu
Thr Cys Pro Tyr Ile Arg Asp Pro Leu Asn Gly Gln Ala Val Pro 100 105
110Ala Asn Gly Thr Tyr Glu Phe Gly Tyr Gln Met His Phe Ile Cys Asn
115 120 125Glu Gly Tyr Tyr Leu Ile Gly Glu Glu Ile Leu Tyr Cys Glu
Leu Lys 130 135 140Gly Ser Val Ala Ile Trp Ser Gly Lys Pro Pro Ile
Cys Glu Lys Val145 150 155 160Leu Cys Thr Pro Pro Pro Lys Ile Lys
Asn Gly Lys His Thr Phe Ser 165 170 175Glu Val Glu Val Phe Glu Tyr
Leu Asp Ala Val Thr Tyr Ser Cys Asp 180 185 190Pro Ala Pro Gly Pro
Asp Pro Phe Ser Leu Ile Gly Glu Ser Thr Ile 195 200 205Tyr Cys Gly
Asp Asn Ser Val Trp Ser Arg Ala Ala Pro Glu Cys Lys 210 215
220Val Val Lys Cys Arg Phe Pro Val Val Glu Asn Gly Lys Gln Ile
Ser225 230 235 240Gly Phe Gly Lys Lys Phe Tyr Tyr Lys Ala Thr Val
Met Phe Glu Cys 245 250 255Asp Lys Gly Phe Tyr Leu Asp Gly Ser Asp
Thr Ile Val Cys Asp Ser 260 265 270Asn Ser Thr Trp Asp Pro Pro Val
Pro Lys Cys Leu Lys Val Leu Pro 275 280 285Pro Ser Ser Thr Lys Pro
Pro Ala Leu Ser His Ser Val Ser Thr Ser 290 295 300Ser Thr Thr Lys
Ser Pro Ala Ser Ser Ala Ser Gly Pro Arg Pro Thr305 310 315 320Tyr
Lys Pro Pro Val Ser Asn Tyr Pro Gly Tyr Pro Lys Pro Glu Glu 325 330
335Gly Ile Leu Asp Ser Leu Asp Val Trp Val Ile Ala Val Ile Val Ile
340 345 350Ala Ile Val Val Gly Val Ala Val Ile Cys Val Val Pro Tyr
Arg Tyr 355 360 365Leu Gln Arg Arg Lys Lys Lys Gly Thr Tyr Leu Thr
Asp Glu Thr His 370 375 380Arg Glu Val Lys Phe Thr Ser Leu385
3903721066PRTHomo sapiens 372Met Gly Pro Gly Pro Ser Arg Ala Pro
Arg Ala Pro Arg Leu Met Leu1 5 10 15Cys Ala Leu Ala Leu Met Val Ala
Ala Gly Gly Cys Val Val Ser Ala 20 25 30Phe Asn Leu Asp Thr Arg Phe
Leu Val Val Lys Glu Ala Gly Asn Pro 35 40 45Gly Ser Leu Phe Gly Tyr
Ser Val Ala Leu His Arg Gln Thr Glu Arg 50 55 60Gln Gln Arg Tyr Leu
Leu Leu Ala Gly Ala Pro Arg Glu Leu Ala Val65 70 75 80Pro Asp Gly
Tyr Thr Asn Arg Thr Gly Ala Val Tyr Leu Cys Pro Leu 85 90 95Thr Ala
His Lys Asp Asp Cys Glu Arg Met Asn Ile Thr Val Lys Asn 100 105
110Asp Pro Gly His His Ile Ile Glu Asp Met Trp Leu Gly Val Thr Val
115 120 125Ala Ser Gln Gly Pro Ala Gly Arg Val Leu Val Cys Ala His
Arg Tyr 130 135 140Thr Gln Val Leu Trp Ser Gly Ser Glu Asp Gln Arg
Arg Met Val Gly145 150 155 160Lys Cys Tyr Val Arg Gly Asn Asp Leu
Glu Leu Asp Ser Ser Asp Asp 165 170 175Trp Gln Thr Tyr His Asn Glu
Met Cys Asn Ser Asn Thr Asp Tyr Leu 180 185 190Glu Thr Gly Met Cys
Gln Leu Gly Thr Ser Gly Gly Phe Thr Gln Asn 195 200 205Thr Val Tyr
Phe Gly Ala Pro Gly Ala Tyr Asn Trp Lys Gly Asn Ser 210 215 220Tyr
Met Ile Gln Arg Lys Glu Trp Asp Leu Ser Glu Tyr Ser Tyr Lys225 230
235 240Asp Pro Glu Asp Gln Gly Asn Leu Tyr Ile Gly Tyr Thr Met Gln
Val 245 250 255Gly Ser Phe Ile Leu His Pro Lys Asn Ile Thr Ile Val
Thr Gly Ala 260 265 270Pro Arg His Arg His Met Gly Ala Val Phe Leu
Leu Ser Gln Glu Ala 275 280 285Gly Gly Asp Leu Arg Arg Arg Gln Val
Leu Glu Gly Ser Gln Val Gly 290 295 300Ala Tyr Phe Gly Ser Ala Ile
Ala Leu Ala Asp Leu Asn Asn Asp Gly305 310 315 320Trp Gln Asp Leu
Leu Val Gly Ala Pro Tyr Tyr Phe Glu Arg Lys Glu 325 330 335Glu Val
Gly Gly Ala Ile Tyr Val Phe Met Asn Gln Ala Gly Thr Ser 340 345
350Phe Pro Ala His Pro Ser Leu Leu Leu His Gly Pro Ser Gly Ser Ala
355 360 365Phe Gly Leu Ser Val Ala Ser Ile Gly Asp Ile Asn Gln Asp
Gly Phe 370 375 380Gln Asp Ile Ala Val Gly Ala Pro Phe Glu Gly Leu
Gly Lys Val Tyr385 390 395 400Ile Tyr His Ser Ser Ser Lys Gly Leu
Leu Arg Gln Pro Gln Gln Val 405 410 415Ile His Gly Glu Lys Leu Gly
Leu Pro Gly Leu Ala Thr Phe Gly Tyr 420 425 430Ser Leu Ser Gly Gln
Met Asp Val Asp Glu Asn Phe Tyr Pro Asp Leu 435 440 445Leu Val Gly
Ser Leu Ser Asp His Ile Val Leu Leu Arg Ala Arg Pro 450 455 460Val
Ile Asn Ile Val His Lys Thr Leu Val Pro Arg Pro Ala Val Leu465 470
475 480Asp Pro Ala Leu Cys Thr Ala Thr Ser Cys Val Gln Val Glu Leu
Cys 485 490 495Phe Ala Tyr Asn Gln Ser Ala Gly Asn Pro Asn Tyr Arg
Arg Asn Ile 500 505 510Thr Leu Ala Tyr Thr Leu Glu Ala Asp Arg Asp
Arg Arg Pro Pro Arg 515 520 525Leu Arg Phe Ala Gly Ser Glu Ser Ala
Val Phe His Gly Phe Phe Ser 530 535 540Met Pro Glu Met Arg Cys Gln
Lys Leu Glu Leu Leu Leu Met Asp Asn545 550 555 560Leu Arg Asp Lys
Leu Arg Pro Ile Ile Ile Ser Met Asn Tyr Ser Leu 565 570 575Pro Leu
Arg Met Pro Asp Arg Pro Arg Leu Gly Leu Arg Ser Leu Asp 580 585
590Ala Tyr Pro Ile Leu Asn Gln Ala Gln Ala Leu Glu Asn His Thr Glu
595 600 605Val Gln Phe Gln Lys Glu Cys Gly Pro Asp Asn Lys Cys Glu
Ser Asn 610 615 620Leu Gln Met Arg Ala Ala Phe Val Ser Glu Gln Gln
Gln Lys Leu Ser625 630 635 640Arg Leu Gln Tyr Ser Arg Asp Val Arg
Lys Leu Leu Leu Ser Ile Asn 645 650 655Val Thr Asn Thr Arg Thr Ser
Glu Arg Ser Gly Glu Asp Ala His Glu 660 665 670Ala Leu Leu Thr Leu
Val Val Pro Pro Ala Leu Leu Leu Ser Ser Val 675 680 685Arg Pro Pro
Gly Ala Cys Gln Ala Asn Glu Thr Ile Phe Cys Glu Leu 690 695 700Gly
Asn Pro Phe Lys Arg Asn Gln Arg Met Glu Leu Leu Ile Ala Phe705 710
715 720Glu Val Ile Gly Val Thr Leu His Thr Arg Asp Leu Gln Val Gln
Leu 725 730 735Gln Leu Ser Thr Ser Ser His Gln Asp Asn Leu Trp Pro
Met Ile Leu 740 745 750Thr Leu Leu Val Asp Tyr Thr Leu Gln Thr Ser
Leu Ser Met Val Asn 755 760 765His Arg Leu Gln Ser Phe Phe Gly Gly
Thr Val Met Gly Glu Ser Gly 770 775 780Met Lys Thr Val Glu Asp Val
Gly Ser Pro Leu Lys Tyr Glu Phe Gln785 790 795 800Val Gly Pro Met
Gly Glu Gly Leu Val Gly Leu Gly Thr Leu Val Leu 805 810 815Gly Leu
Glu Trp Pro Tyr Glu Val Ser Asn Gly Lys Trp Leu Leu Tyr 820 825
830Pro Thr Glu Ile Thr Val His Gly Asn Gly Ser Trp Pro Cys Arg Pro
835 840 845Pro Gly Asp Leu Ile Asn Pro Leu Asn Leu Thr Leu Ser Asp
Pro Gly 850 855 860Asp Arg Pro Ser Ser Pro Gln Arg Arg Arg Arg Gln
Leu Asp Pro Gly865 870 875 880Gly Gly Gln Gly Pro Pro Pro Val Thr
Leu Ala Ala Ala Lys Lys Ala 885 890 895Lys Ser Glu Thr Val Leu Thr
Cys Ala Thr Gly Arg Ala His Cys Val 900 905 910Trp Leu Glu Cys Pro
Ile Pro Asp Ala Pro Val Val Thr Asn Val Thr 915 920 925Val Lys Ala
Arg Val Trp Asn Ser Thr Phe Ile Glu Asp Tyr Arg Asp 930 935 940Phe
Asp Arg Val Arg Val Asn Gly Trp Ala Thr Leu Phe Leu Arg Thr945 950
955 960Ser Ile Pro Thr Ile Asn Met Glu Asn Lys Thr Thr Trp Phe Ser
Val 965 970 975Asp Ile Asp Ser Glu Leu Val Glu Glu Leu Pro Ala Glu
Ile Glu Leu 980 985 990Trp Leu Val Leu Val Ala Val Gly Ala Gly Leu
Leu Leu Leu Gly Leu 995 1000 1005Ile Ile Leu Leu Leu Trp Lys Cys
Gly Phe Phe Lys Arg Thr Arg 1010 1015 1020Tyr Tyr Gln Ile Met Pro
Lys Tyr His Ala Val Arg Ile Arg Glu 1025 1030 1035Glu Glu Arg Tyr
Pro Pro Pro Gly Ser Thr Leu Pro Thr Lys Lys 1040 1045 1050His Trp
Val Thr Ser Trp Gln Thr Arg Asp Gln Tyr Tyr 1055 1060
1065373532PRTHomo sapiens 373Met Ala Pro Ser Ser Pro Arg Pro Ala
Leu Pro Ala Leu Leu Val Leu1 5 10 15Leu Gly Ala Leu Phe Pro Gly Pro
Gly Asn Ala Gln Thr Ser Val Ser 20 25 30Pro Ser Lys Val Ile Leu Pro
Arg Gly Gly Ser Val Leu Val Thr Cys 35 40 45Ser Thr Ser Cys Asp Gln
Pro Lys Leu Leu Gly Ile Glu Thr Pro Leu 50 55 60Pro Lys Lys Glu Leu
Leu Leu Pro Gly Asn Asn Arg Lys Val Tyr Glu65 70 75 80Leu Ser Asn
Val Gln Glu Asp Ser Gln Pro Met Cys Tyr Ser Asn Cys 85 90 95Pro Asp
Gly Gln Ser Thr Ala Lys Thr Phe Leu Thr Val Tyr Trp Thr 100 105
110Pro Glu Arg Val Glu Leu Ala Pro Leu Pro Ser Trp Gln Pro Val Gly
115 120 125Lys Asn Leu Thr Leu Arg Cys Gln Val Glu Gly Gly Ala Pro
Arg Ala 130 135 140Asn Leu Thr Val Val Leu Leu Arg Gly Glu Lys Glu
Leu Lys Arg Glu145 150 155 160Pro Ala Val Gly Glu Pro Ala Glu Val
Thr Thr Thr Val Leu Val Arg 165 170 175Arg Asp His His Gly Ala Asn
Phe Ser Cys Arg Thr Glu Leu Asp Leu 180 185 190Arg Pro Gln Gly Leu
Glu Leu Phe Glu Asn Thr Ser Ala Pro Tyr Gln 195 200 205Leu Gln Thr
Phe Val Leu Pro Ala Thr Pro Pro Gln Leu Val Ser Pro 210 215 220Arg
Val Leu Glu Val Asp Thr Gln Gly Thr Val Val Cys Ser Leu Asp225 230
235 240Gly Leu Phe Pro Val Ser Glu Ala Gln Val His Leu Ala Leu Gly
Asp 245 250 255Gln Arg Leu Asn Pro Thr Val Thr Tyr Gly Asn Asp Ser
Phe Ser Ala 260 265 270Lys Ala Ser Val Ser Val Thr Ala Glu Asp Glu
Gly Thr Gln Arg Leu 275 280 285Thr Cys Ala Val Ile Leu Gly Asn Gln
Ser Gln Glu Thr Leu Gln Thr 290 295 300Val Thr Ile Tyr Ser Phe Pro
Ala Pro Asn Val Ile Leu Thr Lys Pro305 310 315 320Glu Val Ser Glu
Gly Thr Glu Val Thr Val Lys Cys Glu Ala His Pro 325 330 335Arg Ala
Lys Val Thr Leu Asn Gly Val Pro Ala Gln Pro Leu Gly Pro 340 345
350Arg Ala Gln Leu Leu Leu Lys Ala Thr Pro Glu Asp Asn Gly Arg Ser
355 360 365Phe Ser Cys Ser Ala Thr Leu Glu Val Ala Gly Gln Leu Ile
His Lys 370 375 380Asn Gln Thr Arg Glu Leu Arg Val Leu Tyr Gly Pro
Arg Leu Asp Glu385 390 395 400Arg Asp Cys Pro Gly Asn Trp Thr Trp
Pro Glu Asn Ser Gln Gln Thr 405 410 415Pro Met Cys Gln Ala Trp Gly
Asn Pro Leu Pro Glu Leu Lys Cys Leu 420 425 430Lys Asp Gly Thr Phe
Pro Leu Pro Ile Gly Glu Ser Val Thr Val Thr 435 440 445Arg Asp Leu
Glu Gly Thr Tyr Leu Cys Arg Ala Arg Ser Thr Gln Gly 450 455 460Glu
Val Thr Arg Lys Val Thr Val Asn Val Leu Ser Pro Arg Tyr Glu465 470
475 480Ile Val Ile Ile Thr Val Val Ala Ala Ala Val Ile Met Gly Thr
Ala 485 490 495Gly Leu Ser Thr Tyr Leu Tyr Asn Arg Gln Arg Lys Ile
Lys Lys Tyr 500 505 510Arg Leu Gln Gln Ala Gln Lys Gly Thr Pro Met
Lys Pro Asn Thr Gln 515 520 525Ala Thr Pro Pro 530374583PRTHomo
sapiens 374Met Glu Ser Lys Gly Ala Ser Ser Cys Arg Leu Leu Phe Cys
Leu Leu1 5 10 15Ile Ser Ala Thr Val Phe Arg Pro Gly Leu Gly Trp Tyr
Thr Val Asn 20 25 30Ser Ala Tyr Gly Asp Thr Ile Ile Ile Pro Cys Arg
Leu Asp Val Pro 35 40 45Gln Asn Leu Met Phe Gly Lys Trp Lys Tyr Glu
Lys Pro Asp Gly Ser 50 55 60Pro Val Phe Ile Ala Phe Arg Ser Ser Thr
Lys Lys Ser Val Gln Tyr65 70 75 80Asp Asp Val Pro Glu Tyr Lys Asp
Arg Leu Asn Leu Ser Glu Asn Tyr 85 90 95Thr Leu Ser Ile Ser Asn Ala
Arg Ile Ser Asp Glu Lys Arg Phe Val 100 105 110Cys Met Leu Val Thr
Glu Asp Asn Val Phe Glu Ala Pro Thr Ile Val 115 120 125Lys Val Phe
Lys Gln Pro Ser Lys Pro Glu Ile Val Ser Lys Ala Leu 130 135 140Phe
Leu Glu Thr Glu Gln Leu Lys Lys Leu Gly Asp Cys Ile Ser Glu145 150
155 160Asp Ser Tyr Pro Asp Gly Asn Ile Thr Trp Tyr Arg Asn Gly Lys
Val 165 170 175Leu His Pro Leu Glu Gly Ala Val Val Ile Ile Phe Lys
Lys Glu Met 180 185 190Asp Pro Val Thr Gln Leu Tyr Thr Met Thr Ser
Thr Leu Glu Tyr Lys 195 200 205Thr Thr Lys Ala Asp Ile Gln Met Pro
Phe Thr Cys Ser Val Thr Tyr 210 215 220Tyr Gly Pro Ser Gly Gln Lys
Thr Ile His Ser Glu Gln Ala Val Phe225 230 235 240Asp Ile Tyr Tyr
Pro Thr Glu Gln Val Thr Ile Gln Val Leu Pro Pro 245 250 255Lys Asn
Ala Ile Lys Glu Gly Asp Asn Ile Thr Leu Lys Cys Leu Gly 260 265
270Asn Gly Asn Pro Pro Pro Glu Glu Phe Leu Phe Tyr Leu Pro Gly Gln
275 280 285Pro Glu Gly Ile Arg Ser Ser Asn Thr Tyr Thr Leu Met Asp
Val Arg 290 295 300Arg Asn Ala Thr Gly Asp Tyr Lys Cys Ser Leu Ile
Asp Lys Lys Ser305 310 315 320Met Ile Ala Ser Thr Ala Ile Thr Val
His Tyr Leu Asp Leu Ser Leu 325 330 335Asn Pro Ser Gly Glu Val Thr
Arg Gln Ile Gly Asp Ala Leu Pro Val 340 345 350Ser Cys Thr Ile Ser
Ala Ser Arg Asn Ala Thr Val Val Trp Met Lys 355 360 365Asp Asn Ile
Arg Leu Arg Ser Ser Pro Ser Phe Ser Ser Leu His Tyr 370 375 380Gln
Asp Ala Gly Asn Tyr Val Cys Glu Thr Ala Leu Gln Glu Val Glu385 390
395 400Gly Leu Lys Lys Arg Glu Ser Leu Thr Leu Ile Val Glu Gly Lys
Pro 405 410 415Gln Ile Lys Met Thr Lys Lys Thr Asp Pro Ser Gly Leu
Ser Lys Thr 420 425 430Ile Ile Cys His Val Glu Gly Phe Pro Lys Pro
Ala Ile Gln Trp Thr 435 440 445Ile Thr Gly Ser Gly Ser Val Ile Asn
Gln Thr Glu Glu Ser Pro Tyr 450 455 460Ile Asn Gly Arg Tyr Tyr Ser
Lys Ile Ile Ile Ser Pro Glu Glu Asn465 470 475 480Val Thr Leu Thr
Cys Thr Ala Glu Asn Gln Leu Glu Arg Thr Val Asn 485 490 495Ser Leu
Asn Val Ser Ala Ile Ser Ile Pro Glu His Asp Glu Ala Asp 500 505
510Glu Ile Ser Asp Glu Asn Arg Glu Lys Val Asn Asp Gln Ala Lys Leu
515 520 525Ile Val Gly Ile Val Val Gly Leu Leu Leu Ala Ala Leu Val
Ala Gly 530 535 540Val Val Tyr Trp Leu Tyr Met Lys Lys Ser Lys Thr
Ala Ser Lys His545 550 555 560Val Asn Lys Asp Leu Gly Asn Met Glu
Glu Asn Lys Lys Leu Glu Glu 565 570 575Asn Asn His Lys Thr Glu Ala
580375385PRTHomo sapiens 375Met Ala Ala Ala Leu Phe Val Leu Leu Gly
Phe Ala Leu Leu Gly Thr1 5 10 15His Gly Ala Ser Gly Ala Ala Gly Phe
Val Gln Ala Pro Leu Ser Gln 20 25 30Gln Arg Trp Val Gly Gly Ser Val
Glu Leu His Cys Glu Ala Val Gly 35 40 45Ser Pro Val Pro Glu Ile Gln
Trp Trp Phe Glu Gly Gln Gly Pro Asn 50 55 60Asp Thr Cys Ser Gln Leu
Trp Asp Gly Ala Arg Leu Asp Arg Val His65 70 75 80Ile His Ala Thr
Tyr His Gln His Ala Ala Ser Thr Ile Ser Ile Asp 85 90 95Thr Leu Val
Glu Glu Asp Thr Gly Thr Tyr Glu Cys Arg Ala Ser Asn 100 105
110Asp Pro Asp Arg Asn His Leu Thr Arg Ala Pro Arg Val Lys Trp Val
115 120 125Arg Ala Gln Ala Val Val Leu Val Leu Glu Pro Gly Thr Val
Phe Thr 130 135 140Thr Val Glu Asp Leu Gly Ser Lys Ile Leu Leu Thr
Cys Ser Leu Asn145 150 155 160Asp Ser Ala Thr Glu Val Thr Gly His
Arg Trp Leu Lys Gly Gly Val 165 170 175Val Leu Lys Glu Asp Ala Leu
Pro Gly Gln Lys Thr Glu Phe Lys Val 180 185 190Asp Ser Asp Asp Gln
Trp Gly Glu Tyr Ser Cys Val Phe Leu Pro Glu 195 200 205Pro Met Gly
Thr Ala Asn Ile Gln Leu His Gly Pro Pro Arg Val Lys 210 215 220Ala
Val Lys Ser Ser Glu His Ile Asn Glu Gly Glu Thr Ala Met Leu225 230
235 240Val Cys Lys Ser Glu Ser Val Pro Pro Val Thr Asp Trp Ala Trp
Tyr 245 250 255Lys Ile Thr Asp Ser Glu Asp Lys Ala Leu Met Asn Gly
Ser Glu Ser 260 265 270Arg Phe Phe Val Ser Ser Ser Gln Gly Arg Ser
Glu Leu His Ile Glu 275 280 285Asn Leu Asn Met Glu Ala Asp Pro Gly
Gln Tyr Arg Cys Asn Gly Thr 290 295 300Ser Ser Lys Gly Ser Asp Gln
Ala Ile Ile Thr Leu Arg Val Arg Ser305 310 315 320His Leu Ala Ala
Leu Trp Pro Phe Leu Gly Ile Val Ala Glu Val Leu 325 330 335Val Leu
Val Thr Ile Ile Phe Ile Tyr Glu Lys Arg Arg Lys Pro Glu 340 345
350Asp Val Leu Asp Asp Asp Asp Ala Gly Ser Ala Pro Leu Lys Ser Ser
355 360 365Gly Gln His Gln Asn Asp Lys Gly Lys Asn Val Arg Gln Arg
Asn Ser 370 375 380Ser385376442PRTHomo sapiens 376Met Ala Ser Val
Val Leu Pro Ser Gly Ser Gln Cys Ala Ala Ala Ala1 5 10 15Ala Ala Ala
Ala Pro Pro Gly Leu Arg Leu Arg Leu Leu Leu Leu Leu 20 25 30Phe Ser
Ala Ala Ala Leu Ile Pro Thr Gly Asp Gly Gln Asn Leu Phe 35 40 45Thr
Lys Asp Val Thr Val Ile Glu Gly Glu Val Ala Thr Ile Ser Cys 50 55
60Gln Val Asn Lys Ser Asp Asp Ser Val Ile Gln Leu Leu Asn Pro Asn65
70 75 80Arg Gln Thr Ile Tyr Phe Arg Asp Phe Arg Pro Leu Lys Asp Ser
Arg 85 90 95Phe Gln Leu Leu Asn Phe Ser Ser Ser Glu Leu Lys Val Ser
Leu Thr 100 105 110Asn Val Ser Ile Ser Asp Glu Gly Arg Tyr Phe Cys
Gln Leu Tyr Thr 115 120 125Asp Pro Pro Gln Glu Ser Tyr Thr Thr Ile
Thr Val Leu Val Pro Pro 130 135 140Arg Asn Leu Met Ile Asp Ile Gln
Arg Asp Thr Ala Val Glu Gly Glu145 150 155 160Glu Ile Glu Val Asn
Cys Thr Ala Met Ala Ser Lys Pro Ala Thr Thr 165 170 175Ile Arg Trp
Phe Lys Gly Asn Thr Glu Leu Lys Gly Lys Ser Glu Val 180 185 190Glu
Glu Trp Ser Asp Met Tyr Thr Val Thr Ser Gln Leu Met Leu Lys 195 200
205Val His Lys Glu Asp Asp Gly Val Pro Val Ile Cys Gln Val Glu His
210 215 220Pro Ala Val Thr Gly Asn Leu Gln Thr Gln Arg Tyr Leu Glu
Val Gln225 230 235 240Tyr Lys Pro Gln Val His Ile Gln Met Thr Tyr
Pro Leu Gln Gly Leu 245 250 255Thr Arg Glu Gly Asp Ala Leu Glu Leu
Thr Cys Glu Ala Ile Gly Lys 260 265 270Pro Gln Pro Val Met Val Thr
Trp Val Arg Val Asp Asp Glu Met Pro 275 280 285Gln His Ala Val Leu
Ser Gly Pro Asn Leu Phe Ile Asn Asn Leu Asn 290 295 300Lys Thr Asp
Asn Gly Thr Tyr Arg Cys Glu Ala Ser Asn Ile Val Gly305 310 315
320Lys Ala His Ser Asp Tyr Met Leu Tyr Val Tyr Asp Pro Pro Thr Thr
325 330 335Ile Pro Pro Pro Thr Thr Thr Thr Thr Thr Thr Thr Thr Thr
Thr Thr 340 345 350Thr Ile Leu Thr Ile Ile Thr Asp Ser Arg Ala Gly
Glu Glu Gly Ser 355 360 365Ile Arg Ala Val Asp His Ala Val Ile Gly
Gly Val Val Ala Val Val 370 375 380Val Phe Ala Met Leu Cys Leu Leu
Ile Ile Leu Gly Arg Tyr Phe Ala385 390 395 400Arg His Lys Gly Thr
Tyr Phe Thr His Glu Ala Lys Gly Ala Asp Asp 405 410 415Ala Ala Asp
Ala Asp Thr Ala Ile Ile Asn Ala Glu Gly Gly Gln Asn 420 425 430Asn
Ser Glu Glu Lys Lys Glu Tyr Phe Ile 435 44037717DNAArtificialAn
artificially synthesized primer sequence 377caggaaacag ctatgac
1737822DNAArtificialAn artificially synthesized primer sequence
378cggctccaag tcgacgtcgt ca 2237983DNAArtificialAn artificially
synthesized primer sequence 379cagctgcagc agtctggggc agagcttgtg
aagccagggg cctcagtcaa gttgtcctgc 60acagcttctg gcttcaacat taa
8338081DNAArtificialAn artificially synthesized primer sequence
380agaccgaagt tgtaatttct gtggatatac gtgacccact tcgtctccgg
acttttccca 60gatctcacct aaccttccta a 8138184DNAArtificialAn
artificially synthesized primer sequence 381aagggtctag agtggattgg
aaggattgat cctgcgagtg gtaatactaa atatgacccg 60aaggacaagg ccactataac
agca 8438266DNAArtificialAn artificially synthesized primer
sequence 382ttcctgttcc ggtgatattg tcgtctgtgt aggaggttgt gtcggatgga
tgtcgactta 60agggac 6638351DNAArtificialAn artificially synthesized
primer sequence 383cagctgaatt ccctgacatc tgaggacact gccgtctatt
actgtgctgg t 5138473DNAArtificialAn artificially synthesized primer
sequence 384cagataatga cacgaccaat actaatgccg ttgaaactga tgaccccggt
tccgtggtgc 60cagtggcaca agg 7338554DNAArtificialAn artificially
synthesized primer sequence 385ggttctctaa cagtagtggt agtagtggta
attattctcg atagggccct cgaa 5438669DNAArtificialAn artificially
synthesized primer sequence 386gacatcgagc tcacccagtc tccagcctcc
ctttctgcgt ctgtgggaga aactgtcacc 60atcacatgt 6938763DNAArtificialAn
artificially synthesized primer sequence 387tgacagtggt agtgtacagc
tcgttcaccc ttataagtgt taataaatcg taccatggtc 60gtc
6338848DNAArtificialAn artificially synthesized primer sequence
388gcatggtacc agcagaaacc agggaaatct cctcagctcc tggtctat
4838981DNAArtificialAn artificially synthesized primer sequence
389ggagtcgagg accagatatt acgtttttgg aatcgtctac cacacggtag
ttccaagtca 60ccgtcaccta ggccttgtgt t 8139045DNAArtificialAn
artificially synthesized primer sequence 390tcatgaggca cctgcaagcc
acctccgtgg ttcgagctct agttt 4539145DNAArtificialAn artificially
synthesized primer sequence 391agtactccgt ggacgttcgg tggaggcacc
aagctcgaga tcaaa 4539210DNAArtificialAn artificially synthesized
primer sequence 392atcgacagct 1039330DNAArtificialAn artificially
synthesized primer sequence 393aagccacctc catggttcga gctctagttt
3039444DNAArtificialAn artificially synthesized primer sequence
394tcgaagttgt ccttactcac aagccgcgcg gtcagctgag gtaa
4439555DNAArtificialAn artificially synthesized primer sequence
395accctggtca ccgtctcctc agcctccacc aagggcccat cggtcttccc cctgg
5539637DNAArtificialAn artificially synthesized primer sequence
396gggagtcgtc gcagcactgg cacgggaggt cgtcgaa 3739736DNAArtificialAn
artificially synthesized primer sequence 397ggactctact ccctcagcag
cgtcgtgacc gtgccc 3639863DNAArtificialAn artificially synthesized
primer sequence 398gggtcgttgt ggttccacct gttctttcaa ctcgggttta
gaacagtagt ggtagtagtg 60gta 6339956DNAArtificialAn artificially
synthesized primer sequence 399gggtttagaa cagtagtggt agtagtggta
attattctcg atagggccct cgaacg 5640033DNAArtificialAn artificially
synthesized primer sequence 400ggcaccacgg tcaccgtctc gagcgcctcc acc
334011916DNAArtificialInsert sequence of pscFvCA9-E8VHdVLd
401aagcttgcat gcaaattcta tttcaaggag acagtcataa tgaaatacct
attgcctacg 60gcagccgctg gattgttatt actcgctgcc caaccagcga tggcccaggt
gcagctgcag 120cagtctgggg cagagcttgt gaagccaggg gcctcagtca
agttgtcctg cacagcttct 180ggcttcaaca ttaaagacac ctatatgcac
tgggtgaagc agaggcctga aaagggtcta 240gaattccctg acatctgagg
acactgccgt ctattactgt gctggttatg attacggcaa 300ctttgactac
tggggccaag gcaccacggt caccgtctcg agaggcggtg gcggatcagg
360tggcggtgga agtggcggtg gtgggtccat ggccgacatc gagctcaccc
agtctccagc 420ctccctttct gcgtctgtgg gagaaactgt caccatcaca
tgtcgagcaa gtgggaatat 480tcacaattat ttagcatggt accaagctcg
agatcaaacg ggctgatgct gcaccaactg 540tatccatctt cccaccatcc
agtgagcagt taacatctgg aggtgcctca gtcgtgtgct 600tcttgaacag
cttctacccc aaagacatca atgtcaagtg gaagattgat ggcagtgaac
660gacaaaatgg cgtcctgaac agttggactg atcaggacag caaagacagc
acctacagca 720tgagcagcac cctcacgttg accaaggacg agtatgaacg
acataacagc tatacctgtg 780aggccactca caagacatca acttcaccca
ttgtcaagag cttcaacagg aatgagtgtt 840cggcgcgcca gtcgactcca
ttcgtttgtg aatatcaagg ccaatcgtct gacctgcctc 900aacctcctgt
caatgctggc ggcggctctg gtggtggttc tggtggcggc tctgagggtg
960gtggctctga gggtggcggt tctgagggtg gcggctctga gggaggcggt
tccggtggtg 1020gctctggttc cggtgatttt gattatgaaa agatggcaaa
cgctaataag ggggctatga 1080ccgaaaatgc cgatgaaaac gcgctacagt
cagacgctaa aggcaaactt gattctgtcg 1140ctactgatta cggtgctgct
atcgatggtt tcattggtga cgtttccggc cttgctaatg 1200gtaatggtgc
tactggtgat tttgctggct ctaattccca aatggctcaa gtcggtgacg
1260gtgataattc acctttaatg aataatttcc gtcaatattt accttccctc
cctcaatcgg 1320ttgaatgtcg cccttttgtc tttggcgctg gtaaaccata
tgaattttct attgattgtg 1380acaaaataaa cttattccgt ggtgtctttg
cgtttctttt atatgttgcc acctttatgt 1440atgtattttc tacgtttgct
aacatactgc gtaataagga gtcttaatca tgccagttct 1500tttgggtgct
agctgtcgac tgcgcaacac gatgaagccg tagacaacaa attcaacaaa
1560gaacaacaaa acgcgttcta tgagatctta catttaccta acttaaacga
agaacaacga 1620aacgccttca tccaaagttt aaaagatgac ccaagccaaa
gcgctaacct tttagcagaa 1680gctaaaaagc taaatgatgc tcaggcgccg
aaagtagaca acaaattcaa caaagaacaa 1740caaaacgcgt tctatgagat
cttacattta cctaacttaa acgaagaaca acgaaacgcc 1800ttcatccaaa
gtttaaaaga tgacccaagc caaagcgcta accttttagc agaagctaaa
1860aagctaaatg atgctcaggc gccgaaagta gacgcgaatt agctgggaat taattc
191640266PRTArtificialAmino acid sequence encoded by insert
sequence of pscFvCA9-E8VHdVLd 402Met Lys Tyr Leu Leu Pro Thr Ala
Ala Ala Gly Leu Leu Leu Leu Ala1 5 10 15Ala Gln Pro Ala Met Ala Gln
Val Gln Leu Gln Gln Ser Gly Ala Glu 20 25 30Leu Val Lys Pro Gly Ala
Ser Val Lys Leu Ser Cys Thr Ala Ser Gly 35 40 45Phe Asn Ile Lys Asp
Thr Tyr Met His Trp Val Lys Gln Arg Pro Glu 50 55 60Lys
Gly6540377DNAArtificialAn artificially synthesized primer sequence
403gtcaccgtct cgagaggcgg tggcggatca ggtggcggtg gaagtggcgg
tggtgggtcc 60atggccgaca tcgagct 7740468DNAArtificialAn artificially
synthesized primer sequence 404cgatgtcggc catggaccca ccaccgccac
ttccaccgcc acctgatccg ccaccgcctc 60tcgagacg
684051774DNAArtificialInsert sequence of pscFvCA-E8VHd
405aagcttgcat gcaaattcta tttcaaggag acagtcataa tgaaatacct
attgcctacg 60gcagccgctg gattgttatt actcgcggcc cagccggcca tggcccaggt
gcagctgcag 120cagtctgggg cagagcttgt gaagccaggg gcctcagtca
agttgtcctg cacagcttct 180ggcttcaaca ttaaagacac ctatatgcac
tgggtgaagc agaggcctga aaagggtcta 240gaattccctg acatctgagg
acactgccgt ctattactgt gctggttatg attacggcaa 300ctttgactac
tggggccaag gcaccacggt caccgtctcc tcaggcggtg gcggatcagg
360tggcggtgga agtggcggtg gtgggtctac tagtgacatc gagctcaccc
agtctccagc 420ctccctttct gcgtctgtgg gagaaactgt caccatcaca
tgtcgagcaa gtgggaatat 480tcacaattat ttagcatggt accagcagaa
accagggaaa tctcctcagc tcctggtcta 540taatgcaaaa accttagcag
atggtgtgcc atcaaggttc agtggcagtg gatccggaac 600acaatattct
ctcaagatca acagcctgca gcctgaagat tttgggagtt attactgtca
660acatttttgg agtactccgt ggacgttcgg tggaggtacc aagctcgagt
cgactccatt 720cgtttgtgaa tatcaaggcc aatcgtctga cctgcctcaa
cctcctgtca atgctggcgg 780cggctctggt ggtggttctg gtggcggctc
tgagggtggt ggctctgagg gtggcggttc 840tgagggtggc ggctctgagg
gaggcggttc cggtggtggc tctggttccg gtgattttga 900ttatgaaaag
atggcaaacg ctaataaggg ggctatgacc gaaaatgccg atgaaaacgc
960gctacagtca gacgctaaag gcaaacttga ttctgtcgct actgattacg
gtgctgctat 1020cgatggtttc attggtgacg tttccggcct tgctaatggt
aatggtgcta ctggtgattt 1080tgctggctct aattcccaaa tggctcaagt
cggtgacggt gataattcac ctttaatgaa 1140taatttccgt caatatttac
cttccctccc tcaatcggtt gaatgtcgcc cttttgtctt 1200tggcgctggt
aaaccatatg aattttctat tgattgtgac aaaataaact tattccgtgg
1260tgtctttgcg tttcttttat atgttgccac ctttatgtat gtattttcta
cgtttgctaa 1320catactgcgt aataaggagt cttaatcatg ccagttcttt
tgggtgctag ctgtcgactg 1380cgcaacacga tgaagccgta gacaacaaat
tcaacaaaga acaacaaaac gcgttctatg 1440agatcttaca tttacctaac
ttaaacgaag aacaacgaaa cgccttcatc caaagtttaa 1500aagatgaccc
aagccaaagc gctaaccttt tagcagaagc taaaaagcta aatgatgctc
1560aggcgccgaa agtagacaac aaattcaaca aagaacaaca aaacgcgttc
tatgagatct 1620tacatttacc taacttaaac gaagaacaac gaaacgcctt
catccaaagt ttaaaagatg 1680acccaagcca aagcgctaac cttttagcag
aagctaaaaa gctaaatgat gctcaggcgc 1740cgaaagtaga cgcgaattag
ctgggaatta attc 177440666PRTArtificialAmino acid sequence encoded
by insert sequence of pscFvCA-E8VHd 406Met Lys Tyr Leu Leu Pro Thr
Ala Ala Ala Gly Leu Leu Leu Leu Ala1 5 10 15Ala Gln Pro Ala Met Ala
Gln Val Gln Leu Gln Gln Ser Gly Ala Glu 20 25 30Leu Val Lys Pro Gly
Ala Ser Val Lys Leu Ser Cys Thr Ala Ser Gly 35 40 45Phe Asn Ile Lys
Asp Thr Tyr Met His Trp Val Lys Gln Arg Pro Glu 50 55 60Lys
Gly6540791DNAArtificialAn artificially synthesized primer sequence
407caccacggtc accgtctcct caggcggtgg cggatcaggt ggcggtggaa
gtggcggtgg 60tgggtctact agtgacatcg agctcaccca g
9140891DNAArtificialAn artificially synthesized primer sequence
408gtggtgccag tggcagagga gtccgccacc gcctagtcca ccgccacctt
caccgccacc 60acccagatga tcactgtagc tcgagtgggt c
9140917DNAArtificialAn artificially synthesized primer sequence
409caggaaacag ctatgac 1741042DNAArtificialAn artificially
synthesized primer sequence 410gacgccgggt cggccggtac cggctccaag
tcgacgtcgt ca 4241156DNAArtificialAn artificially synthesized
primer sequence 411gtcctcgcaa ctgcggccca gccggccatg gccgacatcc
agatgaccca gtctcc 5641256DNAArtificialAn artificially synthesized
primer sequence 412gtcctcgcaa ctgcggccca gccggccatg gccgatgttg
tgatgactca gtctcc 5641356DNAArtificialAn artificially synthesized
primer sequence 413gtcctcgcaa ctgcggccca gccggccatg gccgaaattg
tgttgacgca gtctcc 5641456DNAArtificialAn artificially synthesized
primer sequence 414gtcctcgcaa ctgcggccca gccggccatg gccgacatcg
tgatgaccca gtctcc 5641556DNAArtificialAn artificially synthesized
primer sequence 415gtcctcgcaa ctgcggccca gccggccatg gccgaaacga
cactcacgca gtctcc 5641656DNAArtificialAn artificially synthesized
primer sequence 416gtcctcgcaa ctgcggccca gccggccatg gccgaaattg
tgctgactca gtctcc 5641756DNAArtificialAn artificially synthesized
primer sequence 417gtcctcgcaa ctgcggccca gccggccatg gcccagtctg
tgttgacgca gccgcc 5641856DNAArtificialAn artificially synthesized
primer sequence 418gtcctcgcaa ctgcggccca gccggccatg gcccagtctg
ccctgactca gcctgc 5641956DNAArtificialAn artificially synthesized
primer sequence 419gtcctcgcaa ctgcggccca gccggccatg gcctcctatg
tgctgactca gccacc 5642056DNAArtificialAn artificially synthesized
primer sequence 420gtcctcgcaa ctgcggccca gccggccatg gcctcttctg
agctgactca ggaccc 5642156DNAArtificialAn artificially synthesized
primer sequence 421gtcctcgcaa ctgcggccca gccggccatg gcccacgtta
tactgactca accgcc 5642256DNAArtificialAn artificially synthesized
primer sequence 422gtcctcgcaa ctgcggccca gccggccatg gcccaggctg
tgctcactca gccgcc 5642356DNAArtificialAn artificially synthesized
primer sequence 423gtcctcgcaa ctgcggccca
gccggccatg gccaatttta tgctgactca gcccca 5642444DNAArtificialAn
artificially synthesized primer sequence 424tcgactggcg cgccgaacac
tctcccctgt tgaagctctt tgtg 4442543DNAArtificialAn artificially
synthesized primer sequence 425tcgactggcg cgccgaacat tctgtagggg
ccactgtctt ctc 4342620DNAArtificialAn artificially synthesized
primer sequence 426atggagtcgg gaaggaagtc 2042756DNAArtificialAn
artificially synthesized primer sequence 427gtcctcgcaa ctgcggccca
gccggccatg gcccaggtgc agctggtgca gtctgg 5642856DNAArtificialAn
artificially synthesized primer sequence 428gtcctcgcaa ctgcggccca
gccggccatg gcccaggtca acttaaggga gtctgg 5642956DNAArtificialAn
artificially synthesized primer sequence 429gtcctcgcaa ctgcggccca
gccggccatg gccgaggtgc agctggtgga gtctgg 5643056DNAArtificialAn
artificially synthesized primer sequence 430gtcctcgcaa ctgcggccca
gccggccatg gcccaggtgc agctgcagga gtcggg 5643156DNAArtificialAn
artificially synthesized primer sequence 431gtcctcgcaa ctgcggccca
gccggccatg gcccaggtgc agctgttgca gtctgc 5643256DNAArtificialAn
artificially synthesized primer sequence 432gtcctcgcaa ctgcggccca
gccggccatg gcccaggtac agctgcagca gtcagg 5643359DNAArtificialAn
artificially synthesized primer sequence 433gtcctcgcaa ctgcggccca
gccggccatg gcccagrtca ccttgaagga gtctggtcc 5943456DNAArtificialAn
artificially synthesized primer sequence 434gtcctcgcaa ctgcggccca
gccggccatg gcccaggtgc agctacagca gtgggg 5643556DNAArtificialAn
artificially synthesized primer sequence 435gtcctcgcaa ctgcggccca
gccggccatg gccgaggtgc agctggtgca gtctgg 5643664DNAArtificialAn
artificially synthesized primer sequence 436gtcctcgcaa ctgcggccca
gccggccatg gcccaggtgc agctggtgca atctgggtct 60gagt
6443732DNAArtificialAn artificially synthesized primer sequence
437ggtggaggca ctcgagacgg tgaccagggt gc 3243832DNAArtificialAn
artificially synthesized primer sequence 438ggtggaggca ctcgagacgg
tgaccattgt cc 3243932DNAArtificialAn artificially synthesized
primer sequence 439ggtggaggca ctcgagacgg tgaccagggt tc
3244032DNAArtificialAn artificially synthesized primer sequence
440ggtggaggca ctcgagacgg tgaccgtggt cc 3244125RNAArtificialoligo
RNA 441cagagcuaca cauugagaac cugaa 2544225RNAArtificialoligo RNA
442uaccuaugug cagaggaauu augau 2544325RNAArtificialoligo RNA
443gcaaccaucu aaaccugaaa uugua 2544425RNAArtificialoligo RNA
444uaauagaggu ugucgaaggc ugggc 2544525RNAArtificialoligo RNA
445cccaacaggc agaccauuua uuuca 25446652PRTHomo sapiens 446Met Ala
Thr Ser Met Gly Leu Leu Leu Leu Leu Leu Leu Leu Leu Thr1 5 10 15Gln
Pro Gly Ala Gly Thr Gly Ala Asp Thr Glu Ala Val Val Cys Val 20 25
30Gly Thr Ala Cys Tyr Thr Ala His Ser Gly Lys Leu Ser Ala Ala Glu
35 40 45Ala Gln Asn His Cys Asn Gln Asn Gly Gly Asn Leu Ala Thr Val
Lys 50 55 60Ser Lys Glu Glu Ala Gln His Val Gln Arg Val Leu Ala Gln
Leu Leu65 70 75 80Arg Arg Glu Ala Ala Leu Thr Ala Arg Met Ser Lys
Phe Trp Ile Gly 85 90 95Leu Gln Arg Glu Lys Gly Lys Cys Leu Asp Pro
Ser Leu Pro Leu Lys 100 105 110Gly Phe Ser Trp Val Gly Gly Gly Glu
Asp Thr Pro Tyr Ser Asn Trp 115 120 125His Lys Glu Leu Arg Asn Ser
Cys Ile Ser Lys Arg Cys Val Ser Leu 130 135 140Leu Leu Asp Leu Ser
Gln Pro Leu Leu Pro Ser Arg Leu Pro Lys Trp145 150 155 160Ser Glu
Gly Pro Cys Gly Ser Pro Gly Ser Pro Gly Ser Asn Ile Glu 165 170
175Gly Phe Val Cys Lys Phe Ser Phe Lys Gly Met Cys Arg Pro Leu Ala
180 185 190Leu Gly Gly Pro Gly Gln Val Thr Tyr Thr Thr Pro Phe Gln
Thr Thr 195 200 205Ser Ser Ser Leu Glu Ala Val Pro Phe Ala Ser Ala
Ala Asn Val Ala 210 215 220Cys Gly Glu Gly Asp Lys Asp Glu Thr Gln
Ser His Tyr Phe Leu Cys225 230 235 240Lys Glu Lys Ala Pro Asp Val
Phe Asp Trp Gly Ser Ser Gly Pro Leu 245 250 255Cys Val Ser Pro Lys
Tyr Gly Cys Asn Phe Asn Asn Gly Gly Cys His 260 265 270Gln Asp Cys
Phe Glu Gly Gly Asp Gly Ser Phe Leu Cys Gly Cys Arg 275 280 285Pro
Gly Phe Arg Leu Leu Asp Asp Leu Val Thr Cys Ala Ser Arg Asn 290 295
300Pro Cys Ser Ser Ser Pro Cys Arg Gly Gly Ala Thr Cys Ala Leu
Gly305 310 315 320Pro His Gly Lys Asn Tyr Thr Cys Arg Cys Pro Gln
Gly Tyr Gln Leu 325 330 335Asp Ser Ser Gln Leu Asp Cys Val Asp Val
Asp Glu Cys Gln Asp Ser 340 345 350Pro Cys Ala Gln Glu Cys Val Asn
Thr Pro Gly Gly Phe Arg Cys Glu 355 360 365Cys Trp Val Gly Tyr Glu
Pro Gly Gly Pro Gly Glu Gly Ala Cys Gln 370 375 380Asp Val Asp Glu
Cys Ala Leu Gly Arg Ser Pro Cys Ala Gln Gly Cys385 390 395 400Thr
Asn Thr Asp Gly Ser Phe His Cys Ser Cys Glu Glu Gly Tyr Val 405 410
415Leu Ala Gly Glu Asp Gly Thr Gln Cys Gln Asp Val Asp Glu Cys Val
420 425 430Gly Pro Gly Gly Pro Leu Cys Asp Ser Leu Cys Phe Asn Thr
Gln Gly 435 440 445Ser Phe His Cys Gly Cys Leu Pro Gly Trp Val Leu
Ala Pro Asn Gly 450 455 460Val Ser Cys Thr Met Gly Pro Val Ser Leu
Gly Pro Pro Ser Gly Pro465 470 475 480Pro Asp Glu Glu Asp Lys Gly
Glu Lys Glu Gly Ser Thr Val Pro Arg 485 490 495Ala Ala Thr Ala Ser
Pro Thr Arg Gly Pro Glu Gly Thr Pro Lys Ala 500 505 510Thr Pro Thr
Thr Ser Arg Pro Ser Leu Ser Ser Asp Ala Pro Ile Thr 515 520 525Ser
Ala Pro Leu Lys Met Leu Ala Pro Ser Gly Ser Ser Gly Val Trp 530 535
540Arg Glu Pro Ser Ile His His Ala Thr Ala Ala Ser Gly Pro Gln
Glu545 550 555 560Pro Ala Gly Gly Asp Ser Ser Val Ala Thr Gln Asn
Asn Asp Gly Thr 565 570 575Asp Gly Gln Lys Leu Leu Leu Phe Tyr Ile
Leu Gly Thr Val Val Ala 580 585 590Ile Leu Leu Leu Leu Ala Leu Ala
Leu Gly Leu Leu Val Tyr Arg Lys 595 600 605Arg Arg Ala Lys Arg Glu
Glu Lys Lys Glu Lys Lys Pro Gln Asn Ala 610 615 620Ala Asp Ser Tyr
Ser Trp Val Pro Glu Arg Ala Glu Ser Arg Ala Met625 630 635 640Glu
Asn Gln Tyr Ser Pro Thr Pro Gly Thr Asp Cys 645 650447719PRTHomo
sapiens 447Leu Asn Ile Thr Cys Arg Phe Ala Gly Val Phe His Val Glu
Lys Asn1 5 10 15Gly Arg Tyr Ser Ile Ser Arg Thr Glu Ala Ala Asp Leu
Cys Lys Ala 20 25 30Phe Asn Ser Thr Leu Pro Thr Met Ala Gln Met Glu
Lys Ala Leu Ser 35 40 45Ile Gly Phe Glu Thr Cys Arg Tyr Gly Phe Ile
Glu Gly His Val Val 50 55 60Ile Pro Arg Ile His Pro Asn Ser Ile Cys
Ala Ala Asn Asn Thr Gly65 70 75 80Val Tyr Ile Leu Thr Ser Asn Thr
Ser Gln Tyr Asp Thr Tyr Cys Phe 85 90 95Asn Ala Ser Ala Pro Pro Glu
Glu Asp Cys Thr Ser Val Thr Asp Leu 100 105 110Pro Asn Ala Phe Asp
Gly Pro Ile Thr Ile Thr Ile Val Asn Arg Asp 115 120 125Gly Thr Arg
Tyr Val Gln Lys Gly Glu Tyr Arg Thr Asn Pro Glu Asp 130 135 140Ile
Tyr Pro Ser Asn Pro Thr Asp Asp Asp Val Ser Ser Gly Ser Ser145 150
155 160Ser Glu Arg Ser Ser Thr Ser Gly Gly Tyr Ile Phe Tyr Thr Phe
Ser 165 170 175Thr Val His Pro Ile Pro Asp Glu Asp Ser Pro Trp Ile
Thr Asp Ser 180 185 190Thr Asp Arg Ile Pro Ala Thr Thr Leu Met Ser
Thr Ser Ala Thr Ala 195 200 205Thr Glu Thr Ala Thr Lys Arg Gln Glu
Thr Trp Asp Trp Phe Ser Trp 210 215 220Leu Phe Leu Pro Ser Glu Ser
Lys Asn His Leu His Thr Thr Thr Gln225 230 235 240Met Ala Gly Thr
Ser Ser Asn Thr Ile Ser Ala Gly Trp Glu Pro Asn 245 250 255Glu Glu
Asn Glu Asp Glu Arg Asp Arg His Leu Ser Phe Ser Gly Ser 260 265
270Gly Ile Asp Asp Asp Glu Asp Phe Ile Ser Ser Thr Ile Ser Thr Thr
275 280 285Pro Arg Ala Phe Asp His Thr Lys Gln Asn Gln Asp Trp Thr
Gln Trp 290 295 300Asn Pro Ser His Ser Asn Pro Glu Val Leu Leu Gln
Thr Thr Thr Arg305 310 315 320Met Thr Asp Val Asp Arg Asn Gly Thr
Thr Ala Tyr Glu Gly Asn Trp 325 330 335Asn Pro Glu Ala His Pro Pro
Leu Ile His His Glu His His Glu Glu 340 345 350Glu Glu Thr Pro His
Ser Thr Ser Thr Ile Gln Ala Thr Pro Ser Ser 355 360 365Thr Thr Glu
Glu Thr Ala Thr Gln Lys Glu Gln Trp Phe Gly Asn Arg 370 375 380Trp
His Glu Gly Tyr Arg Gln Thr Pro Lys Glu Asp Ser His Ser Thr385 390
395 400Thr Gly Thr Ala Ala Ala Ser Ala His Thr Ser His Pro Met Gln
Gly 405 410 415Arg Thr Thr Pro Ser Pro Glu Asp Ser Ser Trp Thr Asp
Phe Phe Asn 420 425 430Pro Ile Ser His Pro Met Gly Arg Gly His Gln
Ala Gly Arg Arg Met 435 440 445Asp Met Asp Ser Ser His Ser Ile Thr
Leu Gln Pro Thr Ala Asn Pro 450 455 460Asn Thr Gly Leu Val Glu Asp
Leu Asp Arg Thr Gly Pro Leu Ser Met465 470 475 480Thr Thr Gln Gln
Ser Asn Ser Gln Ser Phe Ser Thr Ser His Glu Gly 485 490 495Leu Glu
Glu Asp Lys Asp His Pro Thr Thr Ser Thr Leu Thr Ser Ser 500 505
510Asn Arg Asn Asp Val Thr Gly Gly Arg Arg Asp Pro Asn His Ser Glu
515 520 525Gly Ser Thr Thr Leu Leu Glu Gly Tyr Thr Ser His Tyr Pro
His Thr 530 535 540Lys Glu Ser Arg Thr Phe Ile Pro Val Thr Ser Ala
Lys Thr Gly Ser545 550 555 560Phe Gly Val Thr Ala Val Thr Val Gly
Asp Ser Asn Ser Asn Val Asn 565 570 575Arg Ser Leu Ser Gly Asp Gln
Asp Thr Phe His Pro Ser Gly Gly Ser 580 585 590His Thr Thr His Gly
Ser Glu Ser Asp Gly His Ser His Gly Ser Gln 595 600 605Glu Gly Gly
Ala Asn Thr Thr Ser Gly Pro Ile Arg Thr Pro Gln Ile 610 615 620Pro
Glu Trp Leu Ile Ile Leu Ala Ser Leu Leu Ala Leu Ala Leu Ile625 630
635 640Leu Ala Val Cys Ile Ala Val Asn Ser Arg Arg Arg Cys Gly Gln
Lys 645 650 655Lys Lys Leu Val Ile Asn Ser Gly Asn Gly Ala Val Glu
Asp Arg Lys 660 665 670Pro Ser Gly Leu Asn Gly Glu Ala Ser Lys Ser
Gln Glu Met Val His 675 680 685Leu Val Asn Lys Glu Ser Ser Glu Thr
Pro Asp Gln Phe Met Thr Ala 690 695 700Asp Glu Thr Arg Asn Leu Gln
Asn Val Asp Met Lys Ile Gly Val705 710 715448574PRTHomo sapiens
448Met Cys Pro Arg Ala Ala Arg Ala Pro Ala Thr Leu Leu Leu Ala Leu1
5 10 15Gly Ala Val Leu Trp Pro Ala Ala Gly Ala Trp Glu Leu Thr Ile
Leu 20 25 30His Thr Asn Asp Val His Ser Arg Leu Glu Gln Thr Ser Glu
Asp Ser 35 40 45Ser Lys Cys Val Asn Ala Ser Arg Cys Met Gly Gly Val
Ala Arg Leu 50 55 60Phe Thr Lys Val Gln Gln Ile Arg Arg Ala Glu Pro
Asn Val Leu Leu65 70 75 80Leu Asp Ala Gly Asp Gln Tyr Gln Gly Thr
Ile Trp Phe Thr Val Tyr 85 90 95Lys Gly Ala Glu Val Ala His Phe Met
Asn Ala Leu Arg Tyr Asp Ala 100 105 110Met Ala Leu Gly Asn His Glu
Phe Asp Asn Gly Val Glu Gly Leu Ile 115 120 125Glu Pro Leu Leu Lys
Glu Ala Lys Phe Pro Ile Leu Ser Ala Asn Ile 130 135 140Lys Ala Lys
Gly Pro Leu Ala Ser Gln Ile Ser Gly Leu Tyr Leu Pro145 150 155
160Tyr Lys Val Leu Pro Val Gly Asp Glu Val Val Gly Ile Val Gly Tyr
165 170 175Thr Ser Lys Glu Thr Pro Phe Leu Ser Asn Pro Gly Thr Asn
Leu Val 180 185 190Phe Glu Asp Glu Ile Thr Ala Leu Gln Pro Glu Val
Asp Lys Leu Lys 195 200 205Thr Leu Asn Val Asn Lys Ile Ile Ala Leu
Gly His Ser Gly Phe Glu 210 215 220Met Asp Lys Leu Ile Ala Gln Lys
Val Arg Gly Val Asp Val Val Val225 230 235 240Gly Gly His Ser Asn
Thr Phe Leu Tyr Thr Gly Asn Pro Pro Ser Lys 245 250 255Glu Val Pro
Ala Gly Lys Tyr Pro Phe Ile Val Thr Ser Asp Asp Gly 260 265 270Arg
Lys Val Pro Val Val Gln Ala Tyr Ala Phe Gly Lys Tyr Leu Gly 275 280
285Tyr Leu Lys Ile Glu Phe Asp Glu Arg Gly Asn Val Ile Ser Ser His
290 295 300Gly Asn Pro Ile Leu Leu Asn Ser Ser Ile Pro Glu Asp Pro
Ser Ile305 310 315 320Lys Ala Asp Ile Asn Lys Trp Arg Ile Lys Leu
Asp Asn Tyr Ser Thr 325 330 335Gln Glu Leu Gly Lys Thr Ile Val Tyr
Leu Asp Gly Ser Ser Gln Ser 340 345 350Cys Arg Phe Arg Glu Cys Asn
Met Gly Asn Leu Ile Cys Asp Ala Met 355 360 365Ile Asn Asn Asn Leu
Arg His Thr Asp Glu Met Phe Trp Asn His Val 370 375 380Ser Met Cys
Ile Leu Asn Gly Gly Gly Ile Arg Ser Pro Ile Asp Glu385 390 395
400Arg Asn Asn Gly Thr Ile Thr Trp Glu Asn Leu Ala Ala Val Leu Pro
405 410 415Phe Gly Gly Thr Phe Asp Leu Val Gln Leu Lys Gly Ser Thr
Leu Lys 420 425 430Lys Ala Phe Glu His Ser Val His Arg Tyr Gly Gln
Ser Thr Gly Glu 435 440 445Phe Leu Gln Val Gly Gly Ile His Val Val
Tyr Asp Leu Ser Arg Lys 450 455 460Pro Gly Asp Arg Val Val Lys Leu
Asp Val Leu Cys Thr Lys Cys Arg465 470 475 480Val Pro Ser Tyr Asp
Pro Leu Lys Met Asp Glu Val Tyr Lys Val Ile 485 490 495Leu Pro Asn
Phe Leu Ala Asn Gly Gly Asp Gly Phe Gln Met Ile Lys 500 505 510Asp
Glu Leu Leu Arg His Asp Ser Gly Asp Gln Asp Ile Asn Val Val 515 520
525Ser Thr Tyr Ile Ser Lys Met Lys Val Ile Tyr Pro Ala Val Glu Gly
530 535 540Arg Ile Lys Phe Ser Thr Gly Ser His Cys His Gly Ser Phe
Ser Leu545 550 555 560Ile Phe Leu Ser Leu Trp Ala Val Ile Phe Val
Leu Tyr Gln 565 570449314PRTHomo sapiens 449Met Ala Pro Pro Gln Val
Leu Ala Phe Gly Leu Leu Leu Ala Ala Ala1 5 10 15Thr Ala Thr Phe Ala
Ala Ala Gln Glu Glu Cys Val Cys Glu Asn Tyr 20 25 30Lys Leu Ala Val
Asn Cys Phe Val Asn Asn Asn Arg Gln Cys Gln Cys 35 40 45Thr Ser Val
Gly Ala Gln Asn Thr Val Ile Cys Ser Lys Leu Ala Ala 50 55 60Lys Cys
Leu Val Met Lys Ala Glu Met Asn Gly Ser Lys Leu Gly Arg65 70 75
80Arg Ala Lys Pro Glu Gly Ala Leu Gln Asn Asn Asp Gly Leu Tyr Asp
85 90 95Pro Asp
Cys Asp Glu Ser Gly Leu Phe Lys Ala Lys Gln Cys Asn Gly 100 105
110Thr Ser Thr Cys Trp Cys Val Asn Thr Ala Gly Val Arg Arg Thr Asp
115 120 125Lys Asp Thr Glu Ile Thr Cys Ser Glu Arg Val Arg Thr Tyr
Trp Ile 130 135 140Ile Ile Glu Leu Lys His Lys Ala Arg Glu Lys Pro
Tyr Asp Ser Lys145 150 155 160Ser Leu Arg Thr Ala Leu Gln Lys Glu
Ile Thr Thr Arg Tyr Gln Leu 165 170 175Asp Pro Lys Phe Ile Thr Ser
Ile Leu Tyr Glu Asn Asn Val Ile Thr 180 185 190Ile Asp Leu Val Gln
Asn Ser Ser Gln Lys Thr Gln Asn Asp Val Asp 195 200 205Ile Ala Asp
Val Ala Tyr Tyr Phe Glu Lys Asp Val Lys Gly Glu Ser 210 215 220Leu
Phe His Ser Lys Lys Met Asp Leu Thr Val Asn Gly Glu Gln Leu225 230
235 240Asp Leu Asp Pro Gly Gln Thr Leu Ile Tyr Tyr Val Asp Glu Lys
Ala 245 250 255Pro Glu Phe Ser Met Gln Gly Leu Lys Ala Gly Val Ile
Ala Val Ile 260 265 270Val Val Val Val Met Ala Val Val Ala Gly Ile
Val Val Leu Val Ile 275 280 285Ser Arg Lys Lys Arg Met Ala Lys Tyr
Glu Lys Ala Glu Ile Lys Glu 290 295 300Met Gly Glu Met His Arg Glu
Leu Asn Ala305 3104501390PRTHomo sapiens 450Met Lys Ala Pro Ala Val
Leu Ala Pro Gly Ile Leu Val Leu Leu Phe1 5 10 15Thr Leu Val Gln Arg
Ser Asn Gly Glu Cys Lys Glu Ala Leu Ala Lys 20 25 30Ser Glu Met Asn
Val Asn Met Lys Tyr Gln Leu Pro Asn Phe Thr Ala 35 40 45Glu Thr Pro
Ile Gln Asn Val Ile Leu His Glu His His Ile Phe Leu 50 55 60Gly Ala
Thr Asn Tyr Ile Tyr Val Leu Asn Glu Glu Asp Leu Gln Lys65 70 75
80Val Ala Glu Tyr Lys Thr Gly Pro Val Leu Glu His Pro Asp Cys Phe
85 90 95Pro Cys Gln Asp Cys Ser Ser Lys Ala Asn Leu Ser Gly Gly Val
Trp 100 105 110Lys Asp Asn Ile Asn Met Ala Leu Val Val Asp Thr Tyr
Tyr Asp Asp 115 120 125Gln Leu Ile Ser Cys Gly Ser Val Asn Arg Gly
Thr Cys Gln Arg His 130 135 140Val Phe Pro His Asn His Thr Ala Asp
Ile Gln Ser Glu Val His Cys145 150 155 160Ile Phe Ser Pro Gln Ile
Glu Glu Pro Ser Gln Cys Pro Asp Cys Val 165 170 175Val Ser Ala Leu
Gly Ala Lys Val Leu Ser Ser Val Lys Asp Arg Phe 180 185 190Ile Asn
Phe Phe Val Gly Asn Thr Ile Asn Ser Ser Tyr Phe Pro Asp 195 200
205His Pro Leu His Ser Ile Ser Val Arg Arg Leu Lys Glu Thr Lys Asp
210 215 220Gly Phe Met Phe Leu Thr Asp Gln Ser Tyr Ile Asp Val Leu
Pro Glu225 230 235 240Phe Arg Asp Ser Tyr Pro Ile Lys Tyr Val His
Ala Phe Glu Ser Asn 245 250 255Asn Phe Ile Tyr Phe Leu Thr Val Gln
Arg Glu Thr Leu Asp Ala Gln 260 265 270Thr Phe His Thr Arg Ile Ile
Arg Phe Cys Ser Ile Asn Ser Gly Leu 275 280 285His Ser Tyr Met Glu
Met Pro Leu Glu Cys Ile Leu Thr Glu Lys Arg 290 295 300Lys Lys Arg
Ser Thr Lys Lys Glu Val Phe Asn Ile Leu Gln Ala Ala305 310 315
320Tyr Val Ser Lys Pro Gly Ala Gln Leu Ala Arg Gln Ile Gly Ala Ser
325 330 335Leu Asn Asp Asp Ile Leu Phe Gly Val Phe Ala Gln Ser Lys
Pro Asp 340 345 350Ser Ala Glu Pro Met Asp Arg Ser Ala Met Cys Ala
Phe Pro Ile Lys 355 360 365Tyr Val Asn Asp Phe Phe Asn Lys Ile Val
Asn Lys Asn Asn Val Arg 370 375 380Cys Leu Gln His Phe Tyr Gly Pro
Asn His Glu His Cys Phe Asn Arg385 390 395 400Thr Leu Leu Arg Asn
Ser Ser Gly Cys Glu Ala Arg Arg Asp Glu Tyr 405 410 415Arg Thr Glu
Phe Thr Thr Ala Leu Gln Arg Val Asp Leu Phe Met Gly 420 425 430Gln
Phe Ser Glu Val Leu Leu Thr Ser Ile Ser Thr Phe Ile Lys Gly 435 440
445Asp Leu Thr Ile Ala Asn Leu Gly Thr Ser Glu Gly Arg Phe Met Gln
450 455 460Val Val Val Ser Arg Ser Gly Pro Ser Thr Pro His Val Asn
Phe Leu465 470 475 480Leu Asp Ser His Pro Val Ser Pro Glu Val Ile
Val Glu His Thr Leu 485 490 495Asn Gln Asn Gly Tyr Thr Leu Val Ile
Thr Gly Lys Lys Ile Thr Lys 500 505 510Ile Pro Leu Asn Gly Leu Gly
Cys Arg His Phe Gln Ser Cys Ser Gln 515 520 525Cys Leu Ser Ala Pro
Pro Phe Val Gln Cys Gly Trp Cys His Asp Lys 530 535 540Cys Val Arg
Ser Glu Glu Cys Leu Ser Gly Thr Trp Thr Gln Gln Ile545 550 555
560Cys Leu Pro Ala Ile Tyr Lys Val Phe Pro Asn Ser Ala Pro Leu Glu
565 570 575Gly Gly Thr Arg Leu Thr Ile Cys Gly Trp Asp Phe Gly Phe
Arg Arg 580 585 590Asn Asn Lys Phe Asp Leu Lys Lys Thr Arg Val Leu
Leu Gly Asn Glu 595 600 605Ser Cys Thr Leu Thr Leu Ser Glu Ser Thr
Met Asn Thr Leu Lys Cys 610 615 620Thr Val Gly Pro Ala Met Asn Lys
His Phe Asn Met Ser Ile Ile Ile625 630 635 640Ser Asn Gly His Gly
Thr Thr Gln Tyr Ser Thr Phe Ser Tyr Val Asp 645 650 655Pro Val Ile
Thr Ser Ile Ser Pro Lys Tyr Gly Pro Met Ala Gly Gly 660 665 670Thr
Leu Leu Thr Leu Thr Gly Asn Tyr Leu Asn Ser Gly Asn Ser Arg 675 680
685His Ile Ser Ile Gly Gly Lys Thr Cys Thr Leu Lys Ser Val Ser Asn
690 695 700Ser Ile Leu Glu Cys Tyr Thr Pro Ala Gln Thr Ile Ser Thr
Glu Phe705 710 715 720Ala Val Lys Leu Lys Ile Asp Leu Ala Asn Arg
Glu Thr Ser Ile Phe 725 730 735Ser Tyr Arg Glu Asp Pro Ile Val Tyr
Glu Ile His Pro Thr Lys Ser 740 745 750Phe Ile Ser Gly Gly Ser Thr
Ile Thr Gly Val Gly Lys Asn Leu Asn 755 760 765Ser Val Ser Val Pro
Arg Met Val Ile Asn Val His Glu Ala Gly Arg 770 775 780Asn Phe Thr
Val Ala Cys Gln His Arg Ser Asn Ser Glu Ile Ile Cys785 790 795
800Cys Thr Thr Pro Ser Leu Gln Gln Leu Asn Leu Gln Leu Pro Leu Lys
805 810 815Thr Lys Ala Phe Phe Met Leu Asp Gly Ile Leu Ser Lys Tyr
Phe Asp 820 825 830Leu Ile Tyr Val His Asn Pro Val Phe Lys Pro Phe
Glu Lys Pro Val 835 840 845Met Ile Ser Met Gly Asn Glu Asn Val Leu
Glu Ile Lys Gly Asn Asp 850 855 860Ile Asp Pro Glu Ala Val Lys Gly
Glu Val Leu Lys Val Gly Asn Lys865 870 875 880Ser Cys Glu Asn Ile
His Leu His Ser Glu Ala Val Leu Cys Thr Val 885 890 895Pro Asn Asp
Leu Leu Lys Leu Asn Ser Glu Leu Asn Ile Glu Trp Lys 900 905 910Gln
Ala Ile Ser Ser Thr Val Leu Gly Lys Val Ile Val Gln Pro Asp 915 920
925Gln Asn Phe Thr Gly Leu Ile Ala Gly Val Val Ser Ile Ser Thr Ala
930 935 940Leu Leu Leu Leu Leu Gly Phe Phe Leu Trp Leu Lys Lys Arg
Lys Gln945 950 955 960Ile Lys Asp Leu Gly Ser Glu Leu Val Arg Tyr
Asp Ala Arg Val His 965 970 975Thr Pro His Leu Asp Arg Leu Val Ser
Ala Arg Ser Val Ser Pro Thr 980 985 990Thr Glu Met Val Ser Asn Glu
Ser Val Asp Tyr Arg Ala Thr Phe Pro 995 1000 1005Glu Asp Gln Phe
Pro Asn Ser Ser Gln Asn Gly Ser Cys Arg Gln 1010 1015 1020Val Gln
Tyr Pro Leu Thr Asp Met Ser Pro Ile Leu Thr Ser Gly 1025 1030
1035Asp Ser Asp Ile Ser Ser Pro Leu Leu Gln Asn Thr Val His Ile
1040 1045 1050Asp Leu Ser Ala Leu Asn Pro Glu Leu Val Gln Ala Val
Gln His 1055 1060 1065Val Val Ile Gly Pro Ser Ser Leu Ile Val His
Phe Asn Glu Val 1070 1075 1080Ile Gly Arg Gly His Phe Gly Cys Val
Tyr His Gly Thr Leu Leu 1085 1090 1095Asp Asn Asp Gly Lys Lys Ile
His Cys Ala Val Lys Ser Leu Asn 1100 1105 1110Arg Ile Thr Asp Ile
Gly Glu Val Ser Gln Phe Leu Thr Glu Gly 1115 1120 1125Ile Ile Met
Lys Asp Phe Ser His Pro Asn Val Leu Ser Leu Leu 1130 1135 1140Gly
Ile Cys Leu Arg Ser Glu Gly Ser Pro Leu Val Val Leu Pro 1145 1150
1155Tyr Met Lys His Gly Asp Leu Arg Asn Phe Ile Arg Asn Glu Thr
1160 1165 1170His Asn Pro Thr Val Lys Asp Leu Ile Gly Phe Gly Leu
Gln Val 1175 1180 1185Ala Lys Gly Met Lys Tyr Leu Ala Ser Lys Lys
Phe Val His Arg 1190 1195 1200Asp Leu Ala Ala Arg Asn Cys Met Leu
Asp Glu Lys Phe Thr Val 1205 1210 1215Lys Val Ala Asp Phe Gly Leu
Ala Arg Asp Met Tyr Asp Lys Glu 1220 1225 1230Tyr Tyr Ser Val His
Asn Lys Thr Gly Ala Lys Leu Pro Val Lys 1235 1240 1245Trp Met Ala
Leu Glu Ser Leu Gln Thr Gln Lys Phe Thr Thr Lys 1250 1255 1260Ser
Asp Val Trp Ser Phe Gly Val Val Leu Trp Glu Leu Met Thr 1265 1270
1275Arg Gly Ala Pro Pro Tyr Pro Asp Val Asn Thr Phe Asp Ile Thr
1280 1285 1290Val Tyr Leu Leu Gln Gly Arg Arg Leu Leu Gln Pro Glu
Tyr Cys 1295 1300 1305Pro Asp Pro Leu Tyr Glu Val Met Leu Lys Cys
Trp His Pro Lys 1310 1315 1320Ala Glu Met Arg Pro Ser Phe Ser Glu
Leu Val Ser Arg Ile Ser 1325 1330 1335Ala Ile Phe Ser Thr Phe Ile
Gly Glu His Tyr Val His Val Asn 1340 1345 1350Ala Thr Tyr Val Asn
Val Lys Cys Val Ala Pro Tyr Pro Ser Leu 1355 1360 1365Leu Ser Ser
Glu Asp Asn Ala Asp Asp Glu Val Asp Thr Arg Pro 1370 1375 1380Ala
Ser Phe Trp Glu Thr Ser 1385 1390451121PRTHomo sapiens 451Gln Val
Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser
Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr Gly Tyr 20 25
30Tyr Met His Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met
35 40 45Gly Trp Ile Asn Pro Asn Ser Gly Gly Thr Asn Tyr Ala Gln Lys
Phe 50 55 60Gln Gly Arg Val Thr Met Thr Arg Asp Thr Ser Ile Ser Thr
Ala Tyr65 70 75 80Met Glu Leu Ser Arg Leu Arg Ser Asp Asp Thr Ala
Val Tyr Tyr Cys 85 90 95Ala Arg Ser Asp Ile Leu Thr Gly Tyr Tyr Ala
Phe Asp Ile Trp Gly 100 105 110Gln Gly Thr Met Val Thr Val Ser Arg
115 1204525PRTHomo sapiens 452Gly Tyr Tyr Met His1 545317PRTHomo
sapiens 453Trp Ile Asn Pro Asn Ser Gly Gly Thr Asn Tyr Ala Gln Lys
Phe Gln1 5 10 15Gly45412PRTHomo sapiens 454Ser Asp Ile Leu Thr Gly
Tyr Tyr Ala Phe Asp Ile1 5 10455107PRTHomo sapiens 455Asp Ile Gln
Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly1 5 10 15Asp Arg
Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Ile Ser Ser Tyr 20 25 30Leu
Asn Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40
45Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly
50 55 60Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln
Pro65 70 75 80Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Ser Tyr Ser
Thr Thr Trp 85 90 95Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys 100
10545611PRTHomo sapiens 456Arg Ala Ser Gln Ser Ile Ser Ser Tyr Leu
Asn1 5 104577PRTHomo sapiens 457Ala Ala Ser Ser Leu Gln Ser1
54587PRTHomo sapiens 458Gln Gln Ser Tyr Ser Thr Thr1 5459129PRTHomo
sapiens 459Glu Val Gln Leu Val Glu Ser Gly Ala Glu Val Lys Lys Pro
Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Thr Phe
Thr Gly Tyr 20 25 30Tyr Met His Trp Val Arg Gln Ala Pro Gly Gln Gly
Leu Glu Trp Met 35 40 45Gly Trp Ile Asn Pro Asn Ser Gly Gly Thr Asn
Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Met Thr Arg Asp Thr
Ser Ile Ser Thr Ala Tyr65 70 75 80Met Glu Leu Ser Arg Leu Arg Ser
Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Asp Leu Trp Tyr Tyr
Tyr Gly Ser Gly Ser Ser Leu Tyr Tyr 100 105 110Tyr Tyr Gly Met Asp
Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser 115 120
125Arg4605PRTHomo sapiens 460Gly Tyr Tyr Met His1 546117PRTHomo
sapiens 461Trp Ile Asn Pro Asn Ser Gly Gly Thr Asn Tyr Ala Gln Lys
Phe Gln1 5 10 15Gly46220PRTHomo sapiens 462Asp Leu Trp Tyr Tyr Tyr
Gly Ser Gly Ser Ser Leu Tyr Tyr Tyr Tyr1 5 10 15Gly Met Asp Val
20463112PRTHomo sapiens 463Gln Ser Val Leu Thr Gln Pro Pro Ser Val
Ser Gly Ala Pro Gly Gln1 5 10 15Arg Val Thr Ile Ser Cys Thr Gly Ser
Ser Ser Asn Ile Gly Ala Gly 20 25 30Tyr Asp Val His Trp Tyr Gln Gln
Leu Pro Gly Thr Ala Pro Lys Leu 35 40 45Leu Ile Tyr Gly Asn Ser Asn
Arg Pro Ser Gly Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly
Thr Ser Ala Ser Leu Ala Ile Thr Gly Leu65 70 75 80Gln Ala Glu Asp
Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Ser Ser 85 90 95Leu Ser Gly
Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105
11046414PRTHomo sapiens 464Thr Gly Ser Ser Ser Asn Ile Gly Ala Gly
Tyr Asp Val His1 5 104657PRTHomo sapiens 465Gly Asn Ser Asn Arg Pro
Ser1 54669PRTHomo sapiens 466Gln Ser Tyr Asp Ser Ser Leu Ser Gly1
5467122PRTHomo sapiens 467Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Asp Asp Tyr 20 25 30Ala Met His Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Gly Ile Ser Trp Asn Ser
Gly Ser Ile Gly Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Leu Tyr Tyr Cys 85 90 95Val Arg Ser
Gly Ser Tyr Asn Tyr Tyr Tyr Tyr Gly Met Asp Val Trp 100 105 110Gly
Gln Gly Thr Thr Val Thr Val Ser Arg 115 1204685PRTHomo sapiens
468Asp Tyr Ala Met His1 546917PRTHomo sapiens 469Gly Ile Ser Trp
Asn Ser Gly Ser Ile Gly Tyr Ala Asp Ser Val Lys1 5 10
15Gly47013PRTHomo sapiens 470Ser Gly Ser Tyr Asn Tyr Tyr Tyr Tyr
Gly Met Asp Val1 5 10471111PRTHomo sapiens 471Gln Ser Val Leu Thr
Gln Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln1 5 10 15Arg Val Thr Ile
Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser Asn 20 25 30Thr Val Asn
Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45Ile Tyr
Ser Asn
Asn Gln Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60Gly Ser Lys
Ser Gly Thr Ser Ala Ser Leu Ala Ile Ser Gly Leu Gln65 70 75 80Ser
Glu Asp Glu Ala Asp Tyr Tyr Cys Ala Ala Trp Asp Asp Ser Leu 85 90
95Asn Gly Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
105 11047213PRTHomo sapiens 472Ser Gly Ser Ser Ser Asn Ile Gly Ser
Asn Thr Val Asn1 5 104737PRTHomo sapiens 473Ser Asn Asn Gln Arg Pro
Ser1 54749PRTHomo sapiens 474Ala Ala Trp Asp Asp Ser Leu Asn Gly1
5475123PRTHomo sapiens 475Gln Val Gln Leu Gln Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Thr Thr Ser
Gly Phe Thr Phe Thr Ser Tyr 20 25 30Ala Met Ser Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly
Gly Ile Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Lys Asp
Arg Val Leu Val Pro Ala Ser Ser Ser Tyr Phe Asp Tyr 100 105 110Trp
Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115 1204765PRTHomo sapiens
476Ser Tyr Ala Met Ser1 547717PRTHomo sapiens 477Ser Ile Ser Gly
Ser Gly Gly Ile Thr Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Gly47814PRTHomo sapiens 478Asp Arg Val Leu Val Pro Ala Ser Ser
Ser Tyr Phe Asp Tyr1 5 10479109PRTHomo sapiens 479Ser Ser Glu Leu
Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg
Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp
Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly
Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55
60Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65
70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn
His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
10548011PRTHomo sapiens 480Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala
Ser1 5 104817PRTHomo sapiens 481Gly Lys Asn Asn Arg Pro Ser1
54829PRTHomo sapiens 482Asn Ser Arg Asp Ser Ser Gly Asn His1
5483120PRTHomo sapiens 483Gln Val Gln Leu Gln Glu Ser Gly Pro Gly
Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser
Gly Gly Ser Ile Ser Ser Ser 20 25 30Ser Tyr Tyr Trp Gly Trp Ile Arg
Gln Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Ser Ile Tyr Tyr
Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr
Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu
Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Arg
Arg Pro Leu Thr Phe Asn Ala Phe Asp Ile Trp Gly Gln 100 105 110Gly
Thr Met Val Thr Val Ser Arg 115 1204847PRTHomo sapiens 484Ser Ser
Ser Tyr Tyr Trp Gly1 548516PRTHomo sapiens 485Ser Ile Tyr Tyr Ser
Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 1548610PRTHomo
sapiens 486Arg Pro Leu Thr Phe Asn Ala Phe Asp Ile1 5
10487109PRTHomo sapiens 487Ser Tyr Val Leu Thr Gln Pro Pro Ser Val
Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn
Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly
Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Tyr Asp Ser Asp Arg Pro Ser
Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala
Thr Leu Thr Ile Ser Arg Val Glu Ala Gly65 70 75 80Asp Glu Ala Asp
Tyr Tyr Cys Gln Val Trp Asp Ser Ser Ser Asp His 85 90 95Val Val Phe
Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 10548811PRTHomo sapiens
488Gly Gly Asn Asn Ile Gly Ser Lys Ser Val His1 5 104897PRTHomo
sapiens 489Tyr Asp Ser Asp Arg Pro Ser1 54909PRTHomo sapiens 490Gln
Val Trp Asp Ser Ser Ser Asp His1 5491120PRTHomo sapiens 491Gln Val
Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu1 5 10 15Thr
Leu Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Ser Ser 20 25
30Ser Tyr Tyr Trp Gly Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu
35 40 45Trp Ile Gly Ser Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro
Ser 50 55 60Leu Lys Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn
Gln Phe65 70 75 80Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr
Ala Val Tyr Tyr 85 90 95Cys Ala Arg Ile Pro Met Tyr Ser Ser Ser Val
Asp Tyr Trp Gly Gln 100 105 110Gly Thr Leu Val Thr Val Ser Arg 115
1204927PRTHomo sapiens 492Ser Ser Ser Tyr Tyr Trp Gly1
549316PRTHomo sapiens 493Ser Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr
Asn Pro Ser Leu Lys Ser1 5 10 1549410PRTHomo sapiens 494Ile Pro Met
Tyr Ser Ser Ser Val Asp Tyr1 5 10495109PRTHomo sapiens 495Ser Tyr
Val Leu Thr Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10 15Thr
Ala Arg Ile Thr Cys Gly Gly Asn Asn Ile Gly Ser Lys Ser Val 20 25
30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr
35 40 45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly
Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu
Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp Ser
Ser Ser Asp His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val
Leu Gly 100 10549611PRTHomo sapiens 496Gly Gly Asn Asn Ile Gly Ser
Lys Ser Val His1 5 104977PRTHomo sapiens 497Tyr Asp Ser Asp Arg Pro
Ser1 54989PRTHomo sapiens 498Gln Val Trp Asp Ser Ser Ser Asp His1
5499120PRTHomo sapiens 499Gln Val Gln Leu Gln Glu Ser Gly Pro Gly
Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser
Gly Gly Ser Ile Ser Ser Ser 20 25 30Ser Tyr Tyr Trp Gly Trp Ile Arg
Gln Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Ser Ile Tyr Tyr
Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr
Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu
Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Arg
Arg Pro Leu Thr Phe Asn Ala Phe Asp Ile Trp Gly Gln 100 105 110Gly
Thr Thr Val Thr Val Ser Arg 115 1205007PRTHomo sapiens 500Ser Ser
Ser Tyr Tyr Trp Gly1 550116PRTHomo sapiens 501Ser Ile Tyr Tyr Ser
Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 1550210PRTHomo
sapiens 502Arg Pro Leu Thr Phe Asn Ala Phe Asp Ile1 5
10503109PRTHomo sapiens 503Ser Tyr Val Leu Thr Gln Pro Pro Ser Val
Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn
Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly
Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Tyr Asp Ser Asp Arg Pro Ser
Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala
Thr Leu Thr Ile Ser Arg Val Glu Ala Gly65 70 75 80Asp Glu Ala Asp
Tyr Tyr Cys Gln Val Trp Asp Ser Ser Ser Asp His 85 90 95Val Val Phe
Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 10550411PRTHomo sapiens
504Gly Gly Asn Asn Ile Gly Ser Lys Ser Val His1 5 105057PRTHomo
sapiens 505Tyr Asp Ser Asp Arg Pro Ser1 55069PRTHomo sapiens 506Gln
Val Trp Asp Ser Ser Ser Asp His1 5507122PRTHomo sapiens 507Glu Val
Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser
Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25
30Ala Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45Ser Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser
Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr
Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala
Val Tyr Tyr Cys 85 90 95Ala Lys Asp Gly Gly Trp Phe Gly Glu Leu Asp
Tyr Phe Gln His Trp 100 105 110Gly Gln Gly Thr Leu Val Thr Val Ser
Arg 115 1205085PRTHomo sapiens 508Ser Tyr Ala Met Ser1
550917PRTHomo sapiens 509Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr
Tyr Ala Asp Ser Val Lys1 5 10 15Gly51013PRTHomo sapiens 510Asp Gly
Gly Trp Phe Gly Glu Leu Asp Tyr Phe Gln His1 5 10511111PRTHomo
sapiens 511Gln Ser Val Leu Thr Gln Pro Pro Ser Val Ser Ala Ala Pro
Gly Gln1 5 10 15Lys Val Thr Val Ser Cys Thr Gly Ser Asn Ser Asn Ile
Glu Lys Asn 20 25 30Asp Val Ser Trp Tyr Gln Gln Gly Pro Gly Ala Ala
Pro Lys Leu Leu 35 40 45Ile Ser Asp Thr Asp Arg Arg Pro Ser Gly Ile
Pro Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Thr Leu
Ala Ile Ala Gly Leu Gln65 70 75 80Ala Glu Asp Glu Ala Asp Tyr Tyr
Cys Gln Ser His Asp Thr Thr Leu 85 90 95Ser Gly Pro Ile Phe Gly Gly
Gly Thr Gln Leu Thr Val Leu Gly 100 105 11051213PRTHomo sapiens
512Thr Gly Ser Asn Ser Asn Ile Glu Lys Asn Asp Val Ser1 5
105137PRTHomo sapiens 513Asp Thr Asp Arg Arg Pro Ser1 55149PRTHomo
sapiens 514Gln Ser His Asp Thr Thr Leu Ser Gly1 5515124PRTHomo
sapiens 515Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Lys Pro
Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Ser Phe
Ser Asp Tyr 20 25 30Tyr Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly
Leu Glu Trp Ile 35 40 45Ser Tyr Ile Thr Ser Ser Ser Ser Asp Thr Asp
Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn
Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala
Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Val Gly Tyr Tyr Tyr
Asp Tyr Tyr Tyr Tyr Tyr Tyr Met Asp 100 105 110Val Trp Gly Lys Gly
Thr Thr Val Thr Val Ser Arg 115 1205165PRTHomo sapiens 516Asp Tyr
Tyr Met Ser1 551717PRTHomo sapiens 517Tyr Ile Thr Ser Ser Ser Ser
Asp Thr Asp Tyr Ala Asp Ser Val Lys1 5 10 15Gly51815PRTHomo sapiens
518Val Gly Tyr Tyr Tyr Asp Tyr Tyr Tyr Tyr Tyr Tyr Met Asp Val1 5
10 15519108PRTHomo sapiens 519Ser Ser Glu Leu Thr Gln Asp Pro Ala
Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg Ile Thr Cys Gln Gly
Asp Ser Leu Arg Gly Tyr Tyr Ala 20 25 30Ser Trp Tyr Gln Gln Lys Pro
Gly Gln Ala Pro Val Leu Val Val Tyr 35 40 45Asp Glu Asn Asn Arg Pro
Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60Ser Ser Gly Asn Thr
Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65 70 75 80Asp Glu Ala
Asp Tyr Tyr Cys Asn Ser Arg Asp Ile Asn Leu Asp Trp 85 90 95Val Phe
Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 10552011PRTHomo sapiens
520Gln Gly Asp Ser Leu Arg Gly Tyr Tyr Ala Ser1 5 105217PRTHomo
sapiens 521Asp Glu Asn Asn Arg Pro Ser1 55228PRTHomo sapiens 522Asn
Ser Arg Asp Ile Asn Leu Asp1 5523120PRTHomo sapiens 523Gln Val Gln
Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu
Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Ser Ser 20 25 30Ser
Tyr Tyr Trp Gly Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu 35 40
45Trp Ile Gly Ser Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser
50 55 60Leu Lys Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln
Phe65 70 75 80Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala
Val Tyr Tyr 85 90 95Cys Ala Arg Arg Val Ile Val Trp Gly Ser Tyr Asp
Tyr Trp Gly Gln 100 105 110Gly Thr Leu Val Thr Val Ser Arg 115
1205247PRTHomo sapiens 524Ser Ser Ser Tyr Tyr Trp Gly1
552516PRTHomo sapiens 525Ser Ile Tyr Tyr Ser Gly Ser Thr Tyr Tyr
Asn Pro Ser Leu Lys Ser1 5 10 1552610PRTHomo sapiens 526Arg Val Ile
Val Trp Gly Ser Tyr Asp Tyr1 5 10527109PRTHomo sapiens 527Ser Tyr
Val Leu Thr Gln Pro Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10 15Thr
Ala Arg Ile Thr Cys Gly Gly Asn Asn Ile Gly Ser Lys Ser Val 20 25
30His Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr
35 40 45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly
Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu
Ala Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp Ser
Ser Ser Asp His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val
Leu Gly 100 10552811PRTHomo sapiens 528Gly Gly Asn Asn Ile Gly Ser
Lys Ser Val His1 5 105297PRTHomo sapiens 529Tyr Asp Ser Asp Arg Pro
Ser1 55309PRTHomo sapiens 530Gln Val Trp Asp Ser Ser Ser Asp His1
5531120PRTHomo sapiens 531Gln Val Gln Leu Gln Glu Ser Gly Pro Gly
Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser
Gly Gly Ser Ile Ser Ser Ser 20 25 30Ser Tyr Tyr Trp Gly Trp Ile Arg
Gln Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Ser Ile Tyr Tyr
Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr
Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu
Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Met
Arg Ala Tyr Gly Ser Gly Ser Tyr Asp Tyr Trp Gly Gln 100 105 110Gly
Thr Leu Val Thr Val Ser Arg 115 1205327PRTHomo sapiens 532Ser Ser
Ser Tyr Tyr Trp Gly1 553316PRTHomo sapiens 533Ser Ile Tyr Tyr Ser
Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 1553410PRTHomo
sapiens 534Arg Ala Tyr Gly Ser Gly Ser Tyr Asp Tyr1 5
10535112PRTHomo sapiens 535Asp Val Val Met Thr Gln Ser Pro Leu Ser
Leu Pro Val Thr Pro Gly1 5
10 15Glu Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Leu Leu His
Ser 20 25 30Asn Gly Tyr Asn Tyr Leu Asp Trp Tyr Leu Gln Lys Pro Gly
Gln Ser 35 40 45Pro Gln Leu Leu Ile Tyr Leu Gly Ser Asn Arg Ala Ser
Gly Val Pro 50 55 60Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe
Thr Leu Lys Ile65 70 75 80Ser Arg Val Glu Ala Glu Asp Val Gly Val
Tyr Tyr Cys Met Gln Ala 85 90 95Leu Gln Thr Pro Phe Thr Phe Gly Pro
Gly Thr Lys Val Asp Ile Lys 100 105 11053616PRTHomo sapiens 536Arg
Ser Ser Gln Ser Leu Leu His Ser Asn Gly Tyr Asn Tyr Leu Asp1 5 10
155377PRTHomo sapiens 537Leu Gly Ser Asn Arg Ala Ser1 55387PRTHomo
sapiens 538Met Gln Ala Leu Gln Thr Pro1 5539121PRTHomo sapiens
539Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1
5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser
Tyr 20 25 30Ala Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu
Trp Val 35 40 45Ser Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr Tyr Ala
Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys
Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp
Thr Ala Ala Tyr Tyr Cys 85 90 95Ala Lys Gly Leu Arg Tyr Ser Ser Ala
Trp Thr Phe Asp Tyr Trp Gly 100 105 110Gln Gly Thr Leu Val Thr Val
Ser Arg 115 1205405PRTHomo sapiens 540Ser Tyr Ala Met Ser1
554117PRTHomo sapiens 541Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr
Tyr Ala Asp Ser Val Lys1 5 10 15Gly54212PRTHomo sapiens 542Gly Leu
Arg Tyr Ser Ser Ala Trp Thr Phe Asp Tyr1 5 10543112PRTHomo sapiens
543Gln Ser Ala Leu Thr Gln Pro Ala Ser Val Ser Gly Ser Pro Gly Gln1
5 10 15Ser Ile Thr Ile Ser Cys Thr Gly Thr Ser Ser Asp Val Gly Gly
Tyr 20 25 30Asn Tyr Val Ser Trp Tyr Gln Gln His Pro Gly Lys Ala Pro
Lys Leu 35 40 45Met Ile Tyr Asp Val Ser Asn Arg Pro Ser Gly Val Ser
Asn Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly Asn Thr Ala Ser Leu Thr
Ile Ser Gly Leu65 70 75 80Gln Ala Glu Asp Glu Ala Asp Tyr Tyr Cys
Ser Ser Tyr Thr Ser Ser 85 90 95Ser Thr Pro Val Val Phe Gly Gly Gly
Thr Lys Leu Thr Val Leu Gly 100 105 11054414PRTHomo sapiens 544Thr
Gly Thr Ser Ser Asp Val Gly Gly Tyr Asn Tyr Val Ser1 5
105457PRTHomo sapiens 545Asp Val Ser Asn Arg Pro Ser1 55469PRTHomo
sapiens 546Ser Ser Tyr Thr Ser Ser Ser Thr Pro1 5547119PRTHomo
sapiens 547Gln Val Gln Leu Val Gln Ser Gly Ser Glu Leu Lys Lys Pro
Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Ile Phe
Thr Arg Tyr 20 25 30Gly Ile Asn Trp Val Arg Gln Ala Pro Gly Gln Gly
Leu Glu Trp Met 35 40 45Gly Trp Ile Asn Thr Asn Thr Gly Asn Pro Thr
Tyr Ala Gln Gly Phe 50 55 60Thr Gly Arg Val Val Phe Ser Leu Asp Thr
Ser Val Ser Thr Ala Tyr65 70 75 80Leu Gln Ile Ser Ser Leu Lys Ala
Glu Asp Thr Ala Met Tyr Tyr Cys 85 90 95Ala Ile Ser Ser Gly Phe Gly
Tyr Tyr Phe Asp Tyr Trp Gly Gln Gly 100 105 110Thr Leu Val Thr Val
Ser Arg 1155485PRTHomo sapiens 548Arg Tyr Gly Ile Asn1
554917PRTHomo sapiens 549Trp Ile Asn Thr Asn Thr Gly Asn Pro Thr
Tyr Ala Gln Gly Phe Thr1 5 10 15Gly55010PRTHomo sapiens 550Ser Ser
Gly Phe Gly Tyr Tyr Phe Asp Tyr1 5 10551107PRTHomo sapiens 551Asp
Ile Gln Met Thr Gln Ser Pro Ser Ser Val Ser Ala Ser Val Gly1 5 10
15Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Ile Ser Arg Trp
20 25 30Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Phe Leu
Ile 35 40 45Tyr Ala Gly Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe
Ser Gly 50 55 60Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser
Leu Gln Pro65 70 75 80Glu Asp Phe Ala Thr Tyr Tyr Cys Gln Gln Thr
Asn Ser Phe Pro Leu 85 90 95Thr Phe Gly Gly Gly Thr Lys Val Glu Ile
Lys 100 10555211PRTHomo sapiens 552Arg Ala Ser Gln Ser Ile Ser Arg
Trp Leu Ala1 5 105537PRTHomo sapiens 553Ala Gly Ser Ser Leu Gln
Ser1 55547PRTHomo sapiens 554Gln Gln Thr Asn Ser Phe Pro1
5555120PRTHomo sapiens 555Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser
Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp Val Arg Gln Ala
Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr Asn
Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly Arg Val Thr Met
Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu Arg
Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Ala
Phe Arg Asp Trp Gly Ser Leu Arg Asp Tyr Trp Gly Gln 100 105 110Gly
Thr Leu Val Thr Val Ser Arg 115 1205565PRTHomo sapiens 556Ser Tyr
Gly Ile Ser1 555717PRTHomo sapiens 557Trp Ile Ser Ala Tyr Asn Gly
Asn Thr Asn Tyr Ala Gln Lys Leu Gln1 5 10 15Gly55811PRTHomo sapiens
558Ala Phe Arg Asp Trp Gly Ser Leu Arg Asp Tyr1 5 10559111PRTHomo
sapiens 559Gln Ser Val Leu Thr Gln Pro Pro Ser Val Ser Ala Ala Pro
Gly Gln1 5 10 15Lys Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile
Gly Asn Asn 20 25 30Tyr Val Ser Trp Tyr Gln Gln Leu Pro Gly Thr Ala
Pro Lys Leu Leu 35 40 45Ile Tyr Asp Asn Asn Lys Arg Pro Ser Gly Ile
Pro Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Thr Leu
Gly Ile Thr Gly Leu Gln65 70 75 80Thr Gly Asp Glu Ala Asp Tyr Tyr
Cys Gly Thr Trp Asp Ser Ser Leu 85 90 95Ser Ala Val Val Phe Gly Gly
Gly Thr Lys Leu Thr Val Leu Gly 100 105 11056013PRTHomo sapiens
560Ser Gly Ser Ser Ser Asn Ile Gly Asn Asn Tyr Val Ser1 5
105617PRTHomo sapiens 561Asp Asn Asn Lys Arg Pro Ser1 55629PRTHomo
sapiens 562Gly Thr Trp Asp Ser Ser Leu Ser Ala1 5563121PRTHomo
sapiens 563Glu Val Gln Leu Val Glu Ser Gly Ala Glu Val Lys Lys Pro
Gly Glu1 5 10 15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe
Thr Ser Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly
Leu Glu Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg
Tyr Ser Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys
Ser Ile Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala
Ser Asp Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg Leu Ala Val Gly Ala
Tyr Gln Tyr Tyr Phe Asp Tyr Trp Gly 100 105 110Gln Gly Thr Leu Val
Thr Val Ser Arg 115 1205645PRTHomo sapiens 564Ser Tyr Trp Ile Gly1
556517PRTHomo sapiens 565Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg
Tyr Ser Pro Ser Phe Gln1 5 10 15Gly56612PRTHomo sapiens 566Leu Ala
Val Gly Ala Tyr Gln Tyr Tyr Phe Asp Tyr1 5 10567111PRTHomo sapiens
567Gln Thr Val Val Thr Gln Glu Pro Ser Phe Ser Val Ser Pro Gly Gly1
5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val Ser Thr
Ser 20 25 30Tyr Tyr Pro Ser Trp Tyr Gln Gln Thr Pro Gly Gln Ala Pro
Arg Thr 35 40 45Leu Ile Tyr Ser Thr Asn Thr Arg Ser Ser Gly Val Pro
Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Lys Ala Ala Leu Thr
Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr Tyr Cys
Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Ser Val Phe Gly Gly Gly Thr
Lys Leu Thr Val Leu Gly 100 105 11056814PRTHomo sapiens 568Gly Leu
Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5 105697PRTHomo
sapiens 569Ser Thr Asn Thr Arg Ser Ser1 55708PRTHomo sapiens 570Val
Leu Tyr Met Gly Ser Gly Ile1 5571119PRTHomo sapiens 571Glu Val Gln
Leu Val Glu Ser Gly Gly Asn Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu
Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Arg Tyr 20 25 30Trp
Met Thr Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile 35 40
45Ser Ser Val Ser Ser Ser Gly Ser Thr Ile Tyr Tyr Ala Asp Ser Val
50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu
Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val
Tyr Tyr Cys 85 90 95Ala Arg Asp Tyr Trp Pro Gly Trp Tyr Phe Asp Leu
Trp Gly Arg Gly 100 105 110Thr Leu Val Thr Val Ser Arg
1155725PRTHomo sapiens 572Arg Tyr Trp Met Thr1 557317PRTHomo
sapiens 573Ser Val Ser Ser Ser Gly Ser Thr Ile Tyr Tyr Ala Asp Ser
Val Lys1 5 10 15Gly57410PRTHomo sapiens 574Asp Tyr Trp Pro Gly Trp
Tyr Phe Asp Leu1 5 10575116PRTHomo sapiens 575Gln Ala Val Leu Thr
Gln Pro Ser Ser Leu Ser Ala Ser Pro Gly Ala1 5 10 15Ser Ala Ser Leu
Thr Cys Thr Phe Arg Ser Asp Ile Ser Val Gly Ser 20 25 30Tyr Arg Ile
Tyr Trp Tyr Gln Gln Lys Pro Gly Ser Pro Pro Gln Phe 35 40 45Leu Leu
Lys Tyr Thr Ser Asp Ser Asp Lys Gln Gln Gly Ser Gly Val 50 55 60Pro
Ser Arg Phe Ser Gly Ser Lys Asp Val Ser Ala Asn Ala Gly Ile65 70 75
80Leu Leu Ile Ser Gly Leu Gln Ser Glu Asp Glu Ala Asp Tyr Tyr Cys
85 90 95Met Thr Trp His Asn Thr Ala Ser Val Phe Gly Gly Gly Thr Lys
Leu 100 105 110Ala Val Leu Gly 11557614PRTHomo sapiens 576Thr Phe
Arg Ser Asp Ile Ser Val Gly Ser Tyr Arg Ile Tyr1 5 1057711PRTHomo
sapiens 577Tyr Thr Ser Asp Ser Asp Lys Gln Gln Gly Ser1 5
105787PRTHomo sapiens 578Met Thr Trp His Asn Thr Ala1
5579119PRTHomo sapiens 579Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Ile Arg Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Thr Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Thr Met Asn Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Leu 35 40 45Ser Tyr Ile Ser Gly Gly Ser
Gly Thr Lys Phe Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Val
Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Glu Met Asn
Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Leu Val
Ser Tyr Ser Ser Pro Gly Phe Asp Tyr Trp Gly Gln Gly 100 105 110Thr
Leu Val Thr Val Ser Ser 1155805PRTHomo sapiens 580Ser Tyr Thr Met
Asn1 558117PRTHomo sapiens 581Tyr Ile Ser Gly Gly Ser Gly Thr Lys
Phe Tyr Ala Asp Ser Val Lys1 5 10 15Gly58210PRTHomo sapiens 582Val
Ser Tyr Ser Ser Pro Gly Phe Asp Tyr1 5 10583107PRTHomo sapiens
583Ser Tyr Glu Leu Thr Gln Pro Pro Ser Val Ser Val Ser Pro Gly Gln1
5 10 15Thr Ala Ser Ile Thr Cys Ser Gly Asp Lys Leu Gly Asp Lys Tyr
Val 20 25 30Tyr Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Ile Leu Leu
Ile Phe 35 40 45Gln Asp Ser Glu Arg Pro Ser Gly Ile Pro Glu Arg Phe
Ser Gly Ser 50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Gly
Thr Gln Ala Met65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Ala Trp
Asp Ser Ser Ala Ala Val 85 90 95Phe Gly Gly Gly Thr Lys Leu Thr Val
Leu Gly 100 10558411PRTHomo sapiens 584Ser Gly Asp Lys Leu Gly Asp
Lys Tyr Val Tyr1 5 105857PRTHomo sapiens 585Gln Asp Ser Glu Arg Pro
Ser1 55867PRTHomo sapiens 586Gln Ala Trp Asp Ser Ser Ala1
5587115PRTHomo sapiens 587Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser
Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp Val Arg Gln Ala
Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr Asn
Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly Arg Val Thr Met
Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu Arg
Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Gly
Gly Ala Phe Asp Ile Trp Gly Gln Gly Thr Thr Val Thr 100 105 110Val
Ser Arg 1155885PRTHomo sapiens 588Ser Tyr Gly Ile Ser1
558917PRTHomo sapiens 589Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn
Tyr Ala Gln Lys Leu Gln1 5 10 15Gly5906PRTHomo sapiens 590Gly Gly
Ala Phe Asp Ile1 5591112PRTHomo sapiens 591Gln Ser Val Leu Thr Gln
Pro Pro Ser Val Ser Gly Ala Pro Gly Gln1 5 10 15Arg Val Thr Ile Ser
Cys Thr Gly Ser Ser Ser Asn Ile Gly Ala Gly 20 25 30Tyr His Val Tyr
Trp Tyr Gln Gln Leu Pro Gly Lys Ala Pro Lys Leu 35 40 45Leu Ile Tyr
Val Asn Ser Asn Arg Pro Ser Gly Val Pro Asp Arg Phe 50 55 60Ser Gly
Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile Thr Gly Leu65 70 75
80Gln Ala Asp Asp Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Ser Ser
85 90 95Leu Ser Gly Arg Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu
Gly 100 105 11059214PRTHomo sapiens 592Thr Gly Ser Ser Ser Asn Ile
Gly Ala Gly Tyr His Val Tyr1 5 105937PRTHomo sapiens 593Val Asn Ser
Asn Arg Pro Ser1 55949PRTHomo sapiens 594Gln Ser Tyr Asp Ser Ser
Leu Ser Gly1 5595119PRTHomo sapiens 595Glu Val Gln Leu Val Glu Ser
Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys
Ser Ala Ser Gly Phe Thr Phe Ser Asn Tyr 20 25 30Trp Met Thr Trp Val
Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45Ser Ser Ile Ser
Ser Ser Gly Ser Thr Ile Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg
Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu
Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys 85 90
95Ala Arg Asp Tyr Trp Pro Gly Trp Tyr Phe Asp Leu Trp Gly Arg Gly
100 105 110Thr Leu Val Thr Val Ser Arg 1155965PRTHomo sapiens
596Asn Tyr Trp Met Thr1 559717PRTHomo sapiens 597Ser Ile Ser Ser
Ser Gly Ser Thr Ile Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Gly59810PRTHomo sapiens 598Asp Tyr Trp Pro Gly Trp Tyr
Phe Asp Leu1 5 10599116PRTHomo sapiens 599Gln Ala Val Leu Thr Gln
Pro Ser Ser Leu Ser Ala Ser Pro Gly Ala1 5 10 15Ser Ala Ser Leu Thr
Cys Thr Phe Arg Ser Asp Ile Ser Val Gly Ser 20 25 30Tyr Arg Ile Tyr
Trp Tyr Gln Gln Lys Pro Gly Ser Pro Pro Gln Phe 35 40 45Leu Leu Lys
Tyr Thr Ser Asp Ser Asp Lys Gln Gln Gly Ser Gly Val 50 55 60Pro Ser
Arg Phe Ser Gly Ser Lys Asp Val Ser Ala Asn Ala Gly Ile65 70 75
80Leu Leu Ile Ser Gly Leu Gln Ser Glu Asp Glu Ala Asp Tyr Tyr Cys
85 90 95Met Thr Trp His Asn Thr Ala Ser Val Phe Gly Gly Gly Thr Lys
Leu 100 105 110Ala Val Leu Gly 11560014PRTHomo sapiens 600Thr Phe
Arg Ser Asp Ile Ser Val Gly Ser Tyr Arg Ile Tyr1 5 1060111PRTHomo
sapiens 601Tyr Thr Ser Asp Ser Asp Lys Gln Gln Gly Ser1 5
106027PRTHomo sapiens 602Met Thr Trp His Asn Thr Ala1
5603127PRTHomo sapiens 603Gln Val Gln Leu Val Gln Ser Gly Ser Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Thr Ser
Gly Tyr Ile Phe Thr Asp Tyr 20 25 30Tyr Met His Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Asn Pro Asn Ser
Gly Gly Thr Tyr Tyr Ala Gln Lys Phe 50 55 60His Gly Arg Val Thr Met
Thr Ser Asp Thr Ser Ile Ser Thr Ala Tyr65 70 75 80Met Glu Leu Ser
Ser Leu Arg Ser Asp Asp Thr Ala Ile Tyr Tyr Cys 85 90 95Ala Arg Glu
Asp Tyr Asp Ile Leu Thr Gly Tyr Tyr Pro Ala Ser Gly 100 105 110His
Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115 120
1256045PRTHomo sapiens 604Asp Tyr Tyr Met His1 560517PRTHomo
sapiens 605Trp Ile Asn Pro Asn Ser Gly Gly Thr Tyr Tyr Ala Gln Lys
Phe His1 5 10 15Gly60618PRTHomo sapiens 606Glu Asp Tyr Asp Ile Leu
Thr Gly Tyr Tyr Pro Ala Ser Gly His Gly1 5 10 15Asp
Tyr607110PRTHomo sapiens 607Gln Ala Val Val Thr Gln Glu Pro Ser Leu
Thr Val Ser Pro Gly Gly1 5 10 15Thr Val Thr Leu Thr Cys Ala Ser Ser
Thr Gly Ala Val Thr Ser Gly 20 25 30Phe Leu Ala Asn Trp Phe Gln Gln
Lys Pro Gly Gln Thr Pro Arg Ser 35 40 45Leu Ile Tyr Lys Thr Ser Asn
Lys His Pro Trp Thr Pro Ala Arg Phe 50 55 60Ser Gly Ser Leu Leu Gly
Gly Lys Ala Ala Leu Thr Leu Ser Gly Val65 70 75 80Gln Pro Glu Asp
Glu Ala Asp Tyr Tyr Cys Leu Leu Leu Ser Gly Gly 85 90 95Ala Trp Val
Phe Gly Gly Gly Thr Lys Leu Ser Val Leu Gly 100 105 11060814PRTHomo
sapiens 608Ala Ser Ser Thr Gly Ala Val Thr Ser Gly Phe Leu Ala Asn1
5 106097PRTHomo sapiens 609Lys Thr Ser Asn Lys His Pro1
56107PRTHomo sapiens 610Leu Leu Leu Ser Gly Gly Ala1 5611122PRTHomo
sapiens 611Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro
Gly Glu1 5 10 15Ser Leu Lys Ile Ser Cys Glu Gly Ser Gly Tyr Thr Phe
Thr Ser Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Asp
Leu Glu Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg
Tyr Ser Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Val Asp Lys
Ser Ile Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala
Ser Asp Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg His Asp Val Val Asp
Gly Tyr Asn Thr Gly Met Asp Val Trp 100 105 110Gly Gln Gly Thr Thr
Val Thr Val Ser Arg 115 1206125PRTHomo sapiens 612Ser Tyr Trp Ile
Gly1 561317PRTHomo sapiens 613Ile Ile Tyr Pro Gly Asp Ser Asp Thr
Arg Tyr Ser Pro Ser Phe Gln1 5 10 15Gly61413PRTHomo sapiens 614His
Asp Val Val Asp Gly Tyr Asn Thr Gly Met Asp Val1 5 10615111PRTHomo
sapiens 615Gln Thr Val Val Thr Gln Glu Pro Ser Phe Thr Val Ser Pro
Gly Gly1 5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val
Ser Thr Ser 20 25 30Tyr Tyr Pro Ser Trp Tyr Gln Gln Thr Pro Gly Gln
Ala Pro Arg Thr 35 40 45Leu Ile Ser Ser Thr Asn Thr Arg Ser Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Arg Ala Ala
Leu Thr Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr
Tyr Cys Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Trp Val Phe Gly Gly
Gly Thr Lys Leu Thr Val Leu Gly 100 105 11061614PRTHomo sapiens
616Gly Leu Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5
106177PRTHomo sapiens 617Ser Thr Asn Thr Arg Ser Ser1 56188PRTHomo
sapiens 618Val Leu Tyr Met Gly Ser Gly Ile1 5619128PRTHomo sapiens
619Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Glu1
5 10 15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe Thr Ser
Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly Leu Glu
Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Ala Arg Tyr Ser
Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys Ser Ile
Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala Ser Asp
Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg Leu Thr Gly Ser Ser Tyr Tyr
Asp Ser Ser Gly Tyr Ser Ser 100 105 110Tyr Gly Met Asp Val Trp Gly
Gln Gly Thr Thr Val Thr Val Ser Arg 115 120 1256205PRTHomo sapiens
620Ser Tyr Trp Ile Gly1 562117PRTHomo sapiens 621Ile Ile Tyr Pro
Gly Asp Ser Asp Ala Arg Tyr Ser Pro Ser Phe Gln1 5 10
15Gly62219PRTHomo sapiens 622Leu Thr Gly Ser Ser Tyr Tyr Asp Ser
Ser Gly Tyr Ser Ser Tyr Gly1 5 10 15Met Asp Val623111PRTHomo
sapiens 623Gln Thr Val Val Thr Gln Glu Pro Ser Phe Ser Val Ser Pro
Gly Gly1 5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val
Ser Thr Ser 20 25 30Tyr Tyr Pro Ser Trp Phe Gln Gln Thr Pro Gly Gln
Ala Pro Arg Thr 35 40 45Leu Ile Tyr Ser Thr Asn Thr Arg Ser Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Lys Ala Ala
Leu Thr Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr
Tyr Cys Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Ser Val Phe Gly Gly
Gly Thr Gln Leu Thr Val Leu Gly 100 105 11062414PRTHomo sapiens
624Gly Leu Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5
106257PRTHomo sapiens 625Ser Thr Asn Thr Arg Ser Ser1 56268PRTHomo
sapiens 626Val Leu Tyr Met Gly Ser Gly Ile1 5627121PRTHomo sapiens
627Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Glu1
5 10 15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe Thr Ser
Tyr 20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly Leu Glu
Trp Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser
Pro Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys Ser Ile
Ser Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala Ser Asp
Thr Ala Met Tyr Tyr Cys 85 90 95Ala Arg His Asn Ser Asn Tyr Tyr Tyr
Tyr Tyr Met Asp Val Trp Gly 100 105 110Lys Gly Thr Leu Val Thr Val
Ser Arg 115 1206285PRTHomo sapiens 628Ser Tyr Trp Ile Gly1
562917PRTHomo sapiens 629Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg
Tyr Ser Pro Ser Phe Gln1 5 10 15Gly63012PRTHomo sapiens 630His Asn
Ser Asn Tyr Tyr Tyr Tyr Tyr Met Asp Val1 5 10631111PRTHomo sapiens
631Gln Thr Val Val Thr Gln Glu Pro Ser Phe Ser Val Ser Pro Gly Gly1
5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val Ser Thr
Ser 20 25 30Tyr Tyr Pro Ser Trp Tyr Gln Gln Thr Pro Gly Gln Ala Pro
Arg Thr 35 40 45Leu Ile Tyr Ser Thr Asn Thr Arg Ser Ser Gly Val Pro
Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Lys Ala Ala Leu Thr
Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr Tyr Cys
Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Ser Val Phe Gly Gly Gly Thr
Lys Leu Thr Val Leu Gly 100 105 11063214PRTHomo sapiens 632Gly Leu
Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5 106337PRTHomo
sapiens 633Ser Thr Asn Thr Arg Ser Ser1 56348PRTHomo sapiens 634Val
Leu Tyr Met Gly Ser Gly Ile1 5635127PRTHomo sapiens 635Gln Val Gln
Leu Val Gln Ser Gly Ser Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val
Lys Val Ser Cys Lys Thr Ser Gly Tyr Ile Phe Thr Asp Tyr 20 25 30Tyr
Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Met 35 40
45Gly Trp Ile Asn Pro Asn Ser Gly Gly Thr Tyr Tyr Ala Gln Lys Phe
50 55 60His Gly Arg Val Thr Met Thr Ser Asp Thr Ser Ile Ser Thr Ala
Tyr65 70 75 80Met Glu Leu Ser Ser Leu Arg Ser Asp Asp Thr Ala Ile
Tyr Tyr Cys 85 90 95Ala Arg Glu Asp Tyr Asp Ile Leu Thr Gly Phe Tyr
Pro Ala Ser Gly 100 105 110His Gly Asp Tyr Trp Gly Gln Gly Thr Leu
Val Thr Val Ser Arg 115 120 1256365PRTHomo sapiens 636Asp Tyr Tyr
Met His1 563717PRTHomo sapiens 637Trp Ile Asn Pro Asn Ser Gly Gly
Thr Tyr Tyr Ala Gln Lys Phe His1 5 10 15Gly63818PRTHomo sapiens
638Glu Asp Tyr Asp Ile Leu Thr Gly Phe Tyr Pro Ala Ser Gly His Gly1
5 10 15Asp Tyr639107PRTHomo sapiens 639Glu Ile Val Leu Thr Gln Ser
Pro Gly Thr Leu Ser Leu Ser Pro Gly1 5 10 15Glu Arg Ala Thr Leu Ser
Cys Arg Ala Ser Gln Ser Val Ser Ser Ser 20 25 30Tyr Leu Ala Trp Tyr
Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu 35 40 45Ile Tyr Gly Ala
Ser Ser Arg Ala Thr Gly Ile Pro Asp Arg Phe Ser 50 55 60Gly Ser Gly
Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg Leu Glu65 70 75 80Pro
Glu Asp Phe Ala Val Tyr Tyr Cys Gln Gln Tyr Gly Ser Ser Leu 85 90
95Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys 100 10564012PRTHomo
sapiens 640Arg Ala Ser Gln Ser Val Ser Ser Ser Tyr Leu Ala1 5
106417PRTHomo sapiens 641Gly Ala Ser Ser Arg Ala Thr1 56426PRTHomo
sapiens 642Gln Gln Tyr Gly Ser Ser1 5643122PRTHomo sapiens 643Gln
Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Glu1 5 10
15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe Thr Ser Tyr
20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly Leu Glu Trp
Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser Pro
Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys Ser Ile Ser
Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala Ser Asp Thr
Ala Met Tyr Tyr Cys 85 90 95Ala Arg His Gly Met Thr Ser Gly Tyr Val
Ala His Asn Asp Tyr Trp 100 105 110Gly Gln Gly Thr Leu Val Thr Val
Ser Arg 115 1206445PRTHomo sapiens 644Ser Tyr Trp Ile Gly1
564517PRTHomo sapiens 645Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg
Tyr Ser Pro Ser Phe Gln1 5 10 15Gly64613PRTHomo sapiens 646His Gly
Met Thr Ser Gly Tyr Val Ala His Asn Asp Tyr1 5 10647111PRTHomo
sapiens 647Gln Thr Val Val Thr Gln Glu Pro Ser Phe Ser Val Ser Pro
Gly Gly1 5 10 15Thr Val Thr Leu Thr Cys Gly Leu Ser Ser Gly Ser Val
Ser Thr Ser 20 25 30Tyr Tyr Pro Ser Trp Tyr Gln Gln Thr Pro Gly Gln
Ala Pro Arg Thr 35 40 45Leu Ile Tyr Ser Thr Asn Thr Arg Ser Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Ile Leu Gly Asn Lys Ala Ala
Leu Thr Ile Thr Gly Ala65 70 75 80Gln Ala Asp Asp Glu Ser Asp Tyr
Tyr Cys Val Leu Tyr Met Gly Ser 85 90 95Gly Ile Trp Val Phe Gly Gly
Gly Thr Lys Leu Thr Val Leu Gly 100 105 11064814PRTHomo sapiens
648Gly Leu Ser Ser Gly Ser Val Ser Thr Ser Tyr Tyr Pro Ser1 5
106497PRTHomo sapiens 649Ser Thr Asn Thr Arg Ser Ser1 56508PRTHomo
sapiens 650Val Leu Tyr Met Gly Ser Gly Ile1 5651117PRTHomo sapiens
651Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Gly1
5 10 15Thr Leu Ser Leu Thr Cys Ala Val Ser Gly Gly Ser Ile Ser Ser
Ser 20 25 30Asn Trp Trp Ser Trp Val Arg Gln Pro Pro Gly Lys Gly Leu
Glu Trp 35 40 45Ile Gly Glu Ile Tyr His Ser Gly Ser Thr Asn Tyr Asn
Pro Ser Leu 50 55 60Lys Ser Arg Val Thr Ile Ser Val Asp Lys Ser Lys
Asn Gln Phe Ser65 70 75 80Leu Lys Leu Ser Ser Val Thr Ala Ala Asp
Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Gly Gly Ser Tyr Tyr Phe Asp
Tyr Trp Gly Gln Gly Thr Leu 100 105 110Val Thr Val Ser Arg
1156526PRTHomo sapiens 652Ser Ser Asn Trp Trp Ser1 565316PRTHomo
sapiens 653Glu Ile Tyr His Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu
Lys Ser1 5 10 156548PRTHomo sapiens 654Gly Gly Ser Tyr Tyr Phe Asp
Tyr1 5655112PRTHomo sapiens 655Gln Ser Ala Leu Thr Gln Pro Ala Ser
Val Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile Thr Ile Ser Cys Thr Gly
Thr Ile Ser Asp Val Gly Gly Tyr 20 25 30Asp Phe Val Ser Trp Tyr Gln
His His Pro Gly Lys Ala Pro Lys Leu 35 40 45Leu Ile Tyr Asp Val Asn
Asn Arg Pro Ser Gly Val Ser His Arg Phe 50 55 60Ser Gly Ser Lys Ser
Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75 80Gln Ala Glu
Asp Glu Ala Thr Tyr Tyr Cys Ser Ser Tyr Ser Asn Arg 85 90 95His Ser
Leu Ile Val Phe Gly Ser Gly Thr Gln Val Val Gly Leu Gly 100 105
11065614PRTHomo sapiens 656Thr Gly Thr Ile Ser Asp Val Gly Gly Tyr
Asp Phe Val Ser1 5 106577PRTHomo sapiens 657Asp Val Asn Asn Arg Pro
Ser1 56589PRTHomo sapiens 658Ser Ser Tyr Ser Asn Arg His Ser Leu1
5659121PRTHomo sapiens 659Gln Val Gln Leu Gln Gln Trp Gly Ala Gly
Leu Leu Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Ala Val Tyr
Gly Gly Ser Phe Ser Gly Tyr 20 25 30Tyr Trp Ser Trp Ile Arg Gln Pro
Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45Gly Glu Ile Asn His Ser Gly
Ser Thr Asn Tyr Asn Pro Ser Leu Lys 50 55 60Ser
Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu65 70 75
80Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala
85 90 95Arg Gly Gly Gly Val Glu Ala Leu Asn Tyr Gly Met Asp Val Trp
Gly 100 105 110Gln Gly Thr Thr Val Thr Val Ser Arg 115
1206605PRTHomo sapiens 660Gly Tyr Tyr Trp Ser1 566116PRTHomo
sapiens 661Glu Ile Asn His Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu
Lys Ser1 5 10 1566213PRTHomo sapiens 662Gly Gly Gly Val Glu Ala Leu
Asn Tyr Gly Met Asp Val1 5 10663112PRTHomo sapiens 663Gln Ser Ala
Leu Thr Gln Pro Ala Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Thr Ile
Thr Ile Ser Cys Thr Gly Thr Ile Ser Asp Val Gly Gly Tyr 20 25 30Asp
Phe Val Ser Trp Tyr Gln His His Pro Gly Lys Ala Pro Lys Leu 35 40
45Leu Ile Tyr Asp Val Asn Asn Arg Pro Ser Gly Val Ser His Arg Phe
50 55 60Ser Gly Ser Lys Ser Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly
Leu65 70 75 80Gln Ala Glu Asp Glu Ala Thr Tyr Tyr Cys Ser Ser Tyr
Ser Asn Arg 85 90 95His Ser Leu Ile Val Phe Gly Ser Gly Thr Gln Val
Val Gly Leu Gly 100 105 11066414PRTHomo sapiens 664Thr Gly Thr Ile
Ser Asp Val Gly Gly Tyr Asp Phe Val Ser1 5 106657PRTHomo sapiens
665Asp Val Asn Asn Arg Pro Ser1 56669PRTHomo sapiens 666Ser Ser Tyr
Ser Asn Arg His Ser Leu1 5667119PRTHomo sapiens 667Gln Val Gln Leu
Gln Gln Trp Gly Ala Gly Leu Leu Lys Pro Ser Glu1 5 10 15Thr Leu Ser
Leu Thr Cys Thr Val His Gly Gly Ser Phe Asp Asp Tyr 20 25 30Tyr Trp
Thr Trp Ile Arg Gln Pro Pro Gly Gly Gly Leu Glu Trp Ile 35 40 45Gly
Glu Met Asn Ser Gly Arg Thr Tyr Asn Tyr Asn Pro Phe Leu Glu 50 55
60Ser Arg Ala Ser Ile Asp Val Asp Thr Phe Lys Lys Gln Phe Ser Leu65
70 75 80Ala Leu Arg Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys
Ala 85 90 95Arg Gly Ala Tyr Val Asn Tyr Tyr Tyr Ile Asp Val Trp Gly
Asp Gly 100 105 110Thr Thr Val Thr Val Ser Arg 1156685PRTHomo
sapiens 668Asp Tyr Tyr Trp Thr1 566916PRTHomo sapiens 669Glu Met
Asn Ser Gly Arg Thr Tyr Asn Tyr Asn Pro Phe Leu Glu Ser1 5 10
1567011PRTHomo sapiens 670Gly Ala Tyr Val Asn Tyr Tyr Tyr Ile Asp
Val1 5 10671112PRTHomo sapiens 671Gln Ser Ala Leu Thr Gln Pro Ala
Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Thr Ile Thr Ile Ser Cys Thr
Gly Thr Ile Ser Asp Val Gly Gly Tyr 20 25 30Asp Phe Val Ser Trp Tyr
Gln His His Pro Gly Lys Ala Pro Lys Leu 35 40 45Leu Ile Tyr Asp Val
Asn Asn Arg Pro Ser Gly Val Ser His Arg Phe 50 55 60Ser Gly Ser Lys
Ser Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75 80Gln Ala
Glu Asp Glu Ala Thr Tyr Tyr Cys Ser Ser Tyr Ser Asn Arg 85 90 95His
Ser Leu Ile Val Phe Gly Ser Gly Thr Gln Val Val Gly Leu Gly 100 105
11067214PRTHomo sapiens 672Thr Gly Thr Ile Ser Asp Val Gly Gly Tyr
Asp Phe Val Ser1 5 106737PRTHomo sapiens 673Asp Val Asn Asn Arg Pro
Ser1 56749PRTHomo sapiens 674Ser Ser Tyr Ser Asn Arg His Ser Leu1
5675125PRTHomo sapiens 675Gln Val Gln Leu Gln Glu Ser Gly Pro Gly
Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser
Gly Gly Ser Ile Ser Ser Tyr 20 25 30Tyr Trp Ser Trp Ile Arg Gln Pro
Ala Gly Lys Gly Leu Glu Trp Ile 35 40 45Gly Arg Ile Tyr Thr Ser Gly
Ser Thr Asn Tyr Asn Pro Ser Leu Lys 50 55 60Ser Arg Val Thr Met Ser
Val Asp Thr Ser Lys Asn Gln Phe Ser Leu65 70 75 80Lys Leu Ser Ser
Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Glu Arg
Ala Tyr Cys Ser Ser Thr Ser Cys Tyr Arg Asn Ala Phe 100 105 110Asp
Ile Trp Gly Gln Gly Thr Thr Val Thr Val Ser Arg 115 120
1256765PRTHomo sapiens 676Ser Tyr Tyr Trp Ser1 567716PRTHomo
sapiens 677Arg Ile Tyr Thr Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu
Lys Ser1 5 10 1567817PRTHomo sapiens 678Glu Arg Ala Tyr Cys Ser Ser
Thr Ser Cys Tyr Arg Asn Ala Phe Asp1 5 10 15Ile679113PRTHomo
sapiens 679Gln Ser Val Leu Thr Gln Pro Pro Ser Val Ser Gly Ala Pro
Gly Gln1 5 10 15Arg Val Asn Ile Ser Cys Ala Gly Ser Ser Ser Asn Ile
Gly Ala Gly 20 25 30Tyr Asp Val His Trp Tyr Gln Gln Ile Pro Gly Thr
Ala Pro Lys Leu 35 40 45Leu Met Tyr Gly Asn Ser Asn Arg Pro Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly Ala Ser Ala Ser
Leu Ala Ile Thr Arg Leu65 70 75 80Gln Ala Glu Asp Glu Ala Asp Tyr
Tyr Cys Gln Ser Tyr Asp Ser Ser 85 90 95Leu Ser Gly Ser Arg Val Phe
Gly Thr Gly Thr Lys Val Thr Val Leu 100 105 110Gly68014PRTHomo
sapiens 680Ala Gly Ser Ser Ser Asn Ile Gly Ala Gly Tyr Asp Val His1
5 106817PRTHomo sapiens 681Gly Asn Ser Asn Arg Pro Ser1
568210PRTHomo sapiens 682Gln Ser Tyr Asp Ser Ser Leu Ser Gly Ser1 5
10683122PRTHomo sapiens 683Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Val Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Gly Met His Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Thr Val Ile Ser Phe Asp Gly
Ser Asn Lys Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Lys Ala
Tyr Thr Asn Thr Trp Trp Pro Asp Ala Phe Asp Ile Trp 100 105 110Gly
Gln Gly Thr Thr Val Thr Val Ser Arg 115 1206845PRTHomo sapiens
684Ser Tyr Gly Met His1 568517PRTHomo sapiens 685Val Ile Ser Phe
Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys1 5 10
15Gly68613PRTHomo sapiens 686Ala Tyr Thr Asn Thr Trp Trp Pro Asp
Ala Phe Asp Ile1 5 10687107PRTHomo sapiens 687Asp Ile Gln Met Thr
Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly1 5 10 15Asp Arg Val Thr
Ile Thr Cys Gln Ala Ser Gln Asp Ile Ser Asn Tyr 20 25 30Leu Asn Trp
Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45Tyr Asp
Ala Ser Asn Leu Glu Thr Gly Val Pro Ser Arg Phe Ser Gly 50 55 60Ser
Gly Ser Gly Thr Asp Phe Thr Phe Thr Ile Ser Ser Leu Gln Pro65 70 75
80Glu Asp Ile Ala Thr Tyr Tyr Cys Gln Gln Tyr Asp Asn Leu Pro Pro
85 90 95Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys 100
10568811PRTHomo sapiens 688Gln Ala Ser Gln Asp Ile Ser Asn Tyr Leu
Asn1 5 106897PRTHomo sapiens 689Asp Ala Ser Asn Leu Glu Thr1
56907PRTHomo sapiens 690Gln Gln Tyr Asp Asn Leu Pro1 5691118PRTHomo
sapiens 691Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro
Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ser Ser Ile
Ser Ser Tyr 20 25 30Tyr Trp Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly
Leu Glu Trp Ile 35 40 45Gly Tyr Ile Tyr Tyr Ser Gly Ser Thr Asn Tyr
Asn Pro Ser Leu Lys 50 55 60Ser Arg Val Thr Ile Ser Val Asp Thr Ser
Lys Asn Gln Phe Ser Leu65 70 75 80Lys Leu Ser Ser Val Thr Ala Ala
Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Asp Leu Tyr Trp Asn Asp
Ala Phe Asp Ile Trp Gly Gln Gly Thr 100 105 110Thr Val Thr Val Ser
Arg 1156925PRTHomo sapiens 692Ser Tyr Tyr Trp Ser1 569316PRTHomo
sapiens 693Tyr Ile Tyr Tyr Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu
Lys Ser1 5 10 1569410PRTHomo sapiens 694Asp Leu Tyr Trp Asn Asp Ala
Phe Asp Ile1 5 10695111PRTHomo sapiens 695Gln Ser Ala Leu Thr Gln
Pro Leu Ser Ala Ser Gly Thr Pro Gly Gln1 5 10 15Arg Val Thr Ile Ser
Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser Asn 20 25 30Thr Val Asn Trp
Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45Ile Tyr Ser
Asn Asn Gln Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60Gly Ser
Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile Ser Gly Leu Gln65 70 75
80Ser Glu Asp Glu Ala Asp Tyr Tyr Cys Ala Ala Trp Asp Asp Ser Leu
85 90 95Asn Gly Pro Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly
100 105 11069613PRTHomo sapiens 696Ser Gly Ser Ser Ser Asn Ile Gly
Ser Asn Thr Val Asn1 5 106977PRTHomo sapiens 697Ser Asn Asn Gln Arg
Pro Ser1 56989PRTHomo sapiens 698Ala Ala Trp Asp Asp Ser Leu Asn
Gly1 5699118PRTHomo sapiens 699Gln Val Gln Leu Gln Glu Ser Gly Pro
Gly Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val
Ser Gly Ser Ser Ile Ser Ser Tyr 20 25 30Tyr Trp Ser Trp Ile Arg Gln
Pro Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45Gly Tyr Ile Tyr Tyr Ser
Gly Ser Thr Asn Tyr Asn Pro Ser Leu Lys 50 55 60Ser Arg Val Thr Ile
Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu65 70 75 80Lys Leu Ser
Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Asp
Leu Tyr Trp Asn Asp Ala Phe Asp Ile Trp Gly Gln Gly Thr 100 105
110Thr Val Thr Val Ser Arg 1157005PRTHomo sapiens 700Ser Tyr Tyr
Trp Ser1 570116PRTHomo sapiens 701Tyr Ile Tyr Tyr Ser Gly Ser Thr
Asn Tyr Asn Pro Ser Leu Lys Ser1 5 10 1570210PRTHomo sapiens 702Asp
Leu Tyr Trp Asn Asp Ala Phe Asp Ile1 5 10703111PRTHomo sapiens
703Gln Ser Val Leu Thr Gln Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln1
5 10 15Ser Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser
Asn 20 25 30Thr Val Asn Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys
Leu Leu 35 40 45Ile Tyr Ser Asn Asn Gln Arg Pro Ser Gly Val Pro Asp
Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile
Ser Gly Leu Gln65 70 75 80Ser Glu Asp Glu Ala Asp Tyr Tyr Cys Ala
Ala Trp Asp Asp Ser Leu 85 90 95Asn Gly Pro Val Phe Gly Gly Gly Thr
Lys Leu Thr Val Leu Gly 100 105 11070413PRTHomo sapiens 704Ser Gly
Ser Ser Ser Asn Ile Gly Ser Asn Thr Val Asn1 5 107057PRTHomo
sapiens 705Ser Asn Asn Gln Arg Pro Ser1 57069PRTHomo sapiens 706Ala
Ala Trp Asp Asp Ser Leu Asn Gly1 5707126PRTHomo sapiens 707Gln Val
Gln Leu Gln Gln Ser Gly Pro Gly Leu Val Lys Pro Ser Gln1 5 10 15Thr
Leu Ser Leu Thr Cys Ala Ile Ser Gly Asp Ser Val Ser Ser Asn 20 25
30Ser Ala Ala Trp Asn Trp Ile Arg Gln Ser Pro Ser Arg Gly Leu Glu
35 40 45Trp Leu Gly Arg Thr Tyr Tyr Arg Ser Lys Trp Tyr Asn Asp Tyr
Ala 50 55 60Val Ser Val Lys Ser Arg Ile Thr Ile Asn Pro Asp Thr Ser
Lys Asn65 70 75 80Gln Phe Ser Leu Gln Leu Asn Ser Val Thr Pro Glu
Asp Thr Ala Val 85 90 95Tyr Tyr Cys Ala Arg Glu Ser Trp Leu Trp Gly
Ile Gly Gly Asp Ala 100 105 110Phe Asp Ile Trp Gly Gln Gly Thr Thr
Val Thr Val Ser Arg 115 120 1257087PRTHomo sapiens 708Ser Asn Ser
Ala Ala Trp Asn1 570918PRTHomo sapiens 709Arg Thr Tyr Tyr Arg Ser
Lys Trp Tyr Asn Asp Tyr Ala Val Ser Val1 5 10 15Lys Ser71014PRTHomo
sapiens 710Glu Ser Trp Leu Trp Gly Ile Gly Gly Asp Ala Phe Asp Ile1
5 10711111PRTHomo sapiens 711Gln Ser Val Leu Thr Gln Pro Pro Ser
Val Ser Gly Ala Pro Arg Gln1 5 10 15Thr Val Thr Ile Ser Cys Ser Gly
Ser Ser Ser Asn Ile Gly Gln Asn 20 25 30Ser Val Thr Trp Tyr Gln Arg
Leu Pro Gly Glu Ala Pro Lys Leu Leu 35 40 45Ile Tyr Tyr Asp Asp Leu
Leu His Ser Gly Val Ser Asp Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly
Thr Ser Ala Ser Leu Ala Ile Ser Gly Leu Gln65 70 75 80Ser Glu Asp
Glu Ala Glu Tyr Tyr Cys Ala Ser Trp Asp Asp Ser Leu 85 90 95Lys Gly
Pro Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105
11071213PRTHomo sapiens 712Ser Gly Ser Ser Ser Asn Ile Gly Gln Asn
Ser Val Thr1 5 107137PRTHomo sapiens 713Tyr Asp Asp Leu Leu His
Ser1 57149PRTHomo sapiens 714Ala Ser Trp Asp Asp Ser Leu Lys Gly1
5715112PRTHomo sapiens 715Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Val Ser Ser Asn 20 25 30Tyr Met Ser Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Val Ile Tyr Ser Gly Gly
Ser Thr Tyr Tyr Ala Asp Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser
Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser
Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg Glu Phe
Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 100 105
1107165PRTHomo sapiens 716Ser Asn Tyr Met Ser1 571716PRTHomo
sapiens 717Val Ile Tyr Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val
Lys Gly1 5 10 157184PRTHomo sapiens 718Glu Phe Asp
Tyr1719105PRTHomo sapiens 719Asp Ile Gln Met Thr Gln Ser Pro Ser
Ser Leu Ser Ala Ser Val Gly1 5 10 15Asp Arg Val Thr Ile Thr Cys Gln
Ala Ser Gln Asp Ile Ser Asn Tyr 20 25 30Leu Asn Trp Tyr Gln Gln Lys
Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45Tyr Asp Ala Ser Asn Leu
Glu Thr Gly Val Pro Ser Arg Phe Ser Gly 50 55 60Ser Gly Ser Gly Thr
Asp Phe Thr Phe Thr Ile Ser Ser Leu Gln Pro65 70 75 80Glu Asp Ile
Ala Thr Tyr Tyr Cys Gln Gln Tyr Asp Asn Pro Ala Phe 85 90 95Gly Gly
Gly Thr Lys Val Glu Ile Lys 100 10572011PRTHomo sapiens 720Gln Ala
Ser Gln Asp Ile Ser Asn Tyr Leu Asn1 5 107217PRTHomo sapiens 721Asp
Ala Ser Asn Leu Glu Thr1 57225PRTHomo sapiens 722Gln Gln Tyr Asp
Asn1 5723121PRTHomo sapiens 723Gln Val Gln Leu Val Gln Ser Gly Ala
Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala
Ser Gly Tyr Thr Phe Thr Ser
Tyr 20 25 30Gly Ile Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu
Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn Tyr Ala
Gln Lys Leu 50 55 60Gln Gly Arg Val Thr Met Thr Thr Asp Thr Ser Thr
Ser Thr Ala Tyr65 70 75 80Met Glu Leu Arg Ser Leu Arg Ser Asp Asp
Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Asp Arg Tyr Tyr Gly Ser Gly
Phe Gly Met Asp Val Trp Gly 100 105 110Gln Gly Thr Met Val Thr Val
Ser Arg 115 1207245PRTHomo sapiens 724Ser Tyr Gly Ile Ser1
572517PRTHomo sapiens 725Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn
Tyr Ala Gln Lys Leu Gln1 5 10 15Gly72612PRTHomo sapiens 726Asp Arg
Tyr Tyr Gly Ser Gly Phe Gly Met Asp Val1 5 10727109PRTHomo sapiens
727Ser Ser Glu Leu Thr Gln Asp Pro Ala Met Ser Val Ala Leu Gly Gln1
5 10 15Thr Val Lys Ile Thr Cys Gln Gly Asp Ser Leu Thr Asn Tyr Tyr
Pro 20 25 30Ser Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val
Met Tyr 35 40 45Gly Lys Asp Ser Arg Pro Ser Gly Ile Ser Asp Arg Phe
Ser Gly Ser 50 55 60Ser Ser Gly Ile Ser Ala Ser Leu Thr Ile Thr Gly
Ala Gln Ala Glu65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg
Asp Gly Ser Ala His Arg 85 90 95Leu Val Phe Gly Gly Gly Thr Lys Leu
Thr Val Leu Gly 100 10572811PRTHomo sapiens 728Gln Gly Asp Ser Leu
Thr Asn Tyr Tyr Pro Ser1 5 107297PRTHomo sapiens 729Gly Lys Asp Ser
Arg Pro Ser1 57309PRTHomo sapiens 730Asn Ser Arg Asp Gly Ser Ala
His Arg1 5731124PRTHomo sapiens 731Gln Val Gln Leu Val Gln Ser Gly
Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys
Ala Ser Gly Tyr Thr Phe Thr Asn Tyr 20 25 30Gly Leu Thr Trp Val Arg
Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Thr
Tyr Asn Ser Asn Thr Asn Tyr Ala Glu Lys Leu 50 55 60Gln Gly Arg Val
Thr Met Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu
Leu Arg Ser Leu Thr Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala
Arg Gly Pro Thr Tyr Ser Phe Asp Ser Ser Gly Tyr Phe Phe Asp 100 105
110Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115
1207325PRTHomo sapiens 732Asn Tyr Gly Leu Thr1 573317PRTHomo
sapiens 733Trp Ile Ser Thr Tyr Asn Ser Asn Thr Asn Tyr Ala Glu Lys
Leu Gln1 5 10 15Gly73415PRTHomo sapiens 734Gly Pro Thr Tyr Ser Phe
Asp Ser Ser Gly Tyr Phe Phe Asp Tyr1 5 10 15735109PRTHomo sapiens
735Ser Ser Glu Leu Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln1
5 10 15Thr Val Arg Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr
Ala 20 25 30Ser Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val
Ile Tyr 35 40 45Gly Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe
Ser Gly Ser 50 55 60Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly
Ala Gln Ala Glu65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg
Asp Ser Ser Gly Asn His 85 90 95Trp Val Phe Gly Gly Gly Thr Lys Leu
Thr Val Leu Gly 100 10573611PRTHomo sapiens 736Gln Gly Asp Ser Leu
Arg Ser Tyr Tyr Ala Ser1 5 107377PRTHomo sapiens 737Gly Lys Asn Asn
Arg Pro Ser1 57389PRTHomo sapiens 738Asn Ser Arg Asp Ser Ser Gly
Asn His1 5739120PRTHomo sapiens 739Gln Val Gln Leu Val Gln Ser Gly
Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys
Ala Ser Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp Val Arg
Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala
Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly Arg Val
Thr Met Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu
Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala
Arg Asp Thr Tyr Ser Ser Gly Trp Tyr Phe Asp Tyr Trp Gly Gln 100 105
110Gly Thr Leu Val Thr Val Ser Arg 115 1207405PRTHomo sapiens
740Ser Tyr Gly Ile Ser1 574117PRTHomo sapiens 741Trp Ile Ser Ala
Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys Leu Gln1 5 10
15Gly74211PRTHomo sapiens 742Asp Thr Tyr Ser Ser Gly Trp Tyr Phe
Asp Tyr1 5 10743110PRTHomo sapiens 743Ser Ser Glu Leu Thr Gln Asp
Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg Ile Thr Cys
Gln Gly Asp Ser Leu Arg Asn Tyr Tyr Ala 20 25 30Ser Trp Tyr Gln Gln
Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly Lys Asn Asn
Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60Ser Ser Gly
Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65 70 75 80Asp
Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn His 85 90
95Leu Tyr Val Phe Gly Thr Gly Thr Lys Val Thr Val Leu Gly 100 105
11074411PRTHomo sapiens 744Gln Gly Asp Ser Leu Arg Asn Tyr Tyr Ala
Ser1 5 107457PRTHomo sapiens 745Gly Lys Asn Asn Arg Pro Ser1
574610PRTHomo sapiens 746Asn Ser Arg Asp Ser Ser Gly Asn His Leu1 5
10747120PRTHomo sapiens 747Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser
Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp Val Arg Gln Ala
Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr Asn
Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly Arg Val Thr Met
Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu Ser
Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Thr Leu
Asn Ile Ser Gly Ser Tyr Tyr Phe Asp Tyr Trp Gly Gln 100 105 110Gly
Thr Leu Val Thr Val Ser Arg 115 1207485PRTHomo sapiens 748Ser Tyr
Gly Ile Ser1 574917PRTHomo sapiens 749Trp Ile Ser Ala Tyr Asn Gly
Asn Thr Asn Tyr Ala Gln Lys Leu Gln1 5 10 15Gly75011PRTHomo sapiens
750Leu Asn Ile Ser Gly Ser Tyr Tyr Phe Asp Tyr1 5 10751110PRTHomo
sapiens 751Ser Ser Glu Leu Thr Gln Asp Pro Ala Val Ser Val Ala Leu
Gly Gln1 5 10 15Thr Val Arg Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser
Tyr Tyr Ala 20 25 30Thr Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val
Leu Val Ile Ser 35 40 45Gly Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp
Arg Phe Ser Gly Ser 50 55 60Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile
Thr Gly Ala Gln Ala Glu65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn
Ser Arg Asp Ser Ser Gly Tyr Pro 85 90 95Ser Trp Val Phe Gly Gly Gly
Thr Lys Leu Thr Val Leu Gly 100 105 11075211PRTHomo sapiens 752Gln
Gly Asp Ser Leu Arg Ser Tyr Tyr Ala Thr1 5 107537PRTHomo sapiens
753Gly Lys Asn Asn Arg Pro Ser1 575410PRTHomo sapiens 754Asn Ser
Arg Asp Ser Ser Gly Tyr Pro Ser1 5 10755118PRTHomo sapiens 755Gln
Val Gln Leu Val Gln Ser Glu Ala Glu Val Lys Lys Pro Gly Glu1 5 10
15Ser Leu Lys Ile Ser Cys Lys Gly Ser Gly Tyr Ser Phe Thr Ser Tyr
20 25 30Trp Ile Gly Trp Val Arg Gln Met Pro Gly Lys Gly Leu Glu Trp
Met 35 40 45Gly Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser Pro
Ser Phe 50 55 60Gln Gly Gln Val Thr Ile Ser Ala Asp Lys Ser Ile Ser
Thr Ala Tyr65 70 75 80Leu Gln Trp Ser Ser Leu Lys Ala Ser Asp Thr
Ala Met Tyr Tyr Cys 85 90 95Ala Arg Thr Ile Gly Leu Gly Ala Phe Asp
Ile Trp Gly Gln Gly Thr 100 105 110Thr Val Thr Val Ser Arg
1157565PRTHomo sapiens 756Ser Tyr Trp Ile Gly1 575717PRTHomo
sapiens 757Ile Ile Tyr Pro Gly Asp Ser Asp Thr Arg Tyr Ser Pro Ser
Phe Gln1 5 10 15Gly7589PRTHomo sapiens 758Thr Ile Gly Leu Gly Ala
Phe Asp Ile1 5759110PRTHomo sapiens 759Ser Ser Glu Leu Thr Gln Asp
Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg Ile Thr Cys
Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp Tyr Gln Gln
Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly Lys Asn Asn
Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60Ser Ser Gly
Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65 70 75 80Asp
Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn His 85 90
95His Tyr Val Phe Gly Thr Gly Thr Lys Val Thr Val Leu Gly 100 105
11076011PRTHomo sapiens 760Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala
Ser1 5 107617PRTHomo sapiens 761Gly Lys Asn Asn Arg Pro Ser1
576210PRTHomo sapiens 762Asn Ser Arg Asp Ser Ser Gly Asn His His1 5
10763119PRTHomo sapiens 763Gln Val Gln Leu Gln Glu Ser Gly Pro Gly
Leu Val Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Thr Val Ser
Gly Gly Ser Ile Ser Ser Ser 20 25 30Ser Tyr Tyr Trp Gly Trp Ile Arg
Gln Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Ser Ile Tyr Tyr
Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg Val Thr
Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu Lys Leu
Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys Ala Arg
His Trp Gly Asn Tyr Ala Phe Asp Ile Trp Gly Gln Gly 100 105 110Thr
Thr Val Thr Val Ser Arg 1157647PRTHomo sapiens 764Ser Ser Ser Tyr
Tyr Trp Gly1 576516PRTHomo sapiens 765Ser Ile Tyr Tyr Ser Gly Ser
Thr Tyr Tyr Asn Pro Ser Leu Lys Ser1 5 10 157669PRTHomo sapiens
766His Trp Gly Asn Tyr Ala Phe Asp Ile1 5767111PRTHomo sapiens
767Gln Ser Val Leu Thr Gln Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln1
5 10 15Arg Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser
Asn 20 25 30Tyr Val Tyr Trp Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys
Leu Leu 35 40 45Ile Tyr Ser Asn Asn Gln Arg Pro Ser Gly Val Pro Asp
Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile
Ser Gly Leu Arg65 70 75 80Ser Glu Asp Glu Ala Asp Tyr Tyr Cys Ala
Ala Trp Asp Asp Ser Leu 85 90 95Ser Gly Gln Val Phe Gly Gly Gly Thr
Gln Leu Thr Val Leu Gly 100 105 11076813PRTHomo sapiens 768Ser Gly
Ser Ser Ser Asn Ile Gly Ser Asn Tyr Val Tyr1 5 107697PRTHomo
sapiens 769Ser Asn Asn Gln Arg Pro Ser1 57709PRTHomo sapiens 770Ala
Ala Trp Asp Asp Ser Leu Ser Gly1 5771120PRTHomo sapiens 771Glu Val
Gln Leu Val Glu Ser Gly Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser
Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr Ser Tyr 20 25
30Gly Ile Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met
35 40 45Gly Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys
Leu 50 55 60Gln Gly Arg Val Thr Met Thr Thr Asp Thr Ser Thr Ser Thr
Ala Tyr65 70 75 80Met Glu Leu Arg Ser Leu Arg Ser Asp Asp Thr Ala
Val Tyr Tyr Cys 85 90 95Ala Arg Glu Lys Tyr Ser Ser Gly Trp Tyr Phe
Asp Tyr Trp Gly Gln 100 105 110Gly Thr Leu Val Thr Val Ser Arg 115
1207725PRTHomo sapiens 772Ser Tyr Gly Ile Ser1 577317PRTHomo
sapiens 773Trp Ile Ser Ala Tyr Asn Gly Asn Thr Asn Tyr Ala Gln Lys
Leu Gln1 5 10 15Gly77411PRTHomo sapiens 774Glu Lys Tyr Ser Ser Gly
Trp Tyr Phe Asp Tyr1 5 10775110PRTHomo sapiens 775Ser Ser Glu Leu
Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg
Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp
Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly
Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55
60Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65
70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn
His 85 90 95His Tyr Val Phe Gly Thr Gly Thr Lys Val Thr Val Leu Gly
100 105 11077611PRTHomo sapiens 776Gln Gly Asp Ser Leu Arg Ser Tyr
Tyr Ala Ser1 5 107777PRTHomo sapiens 777Gly Lys Asn Asn Arg Pro
Ser1 577810PRTHomo sapiens 778Asn Ser Arg Asp Ser Ser Gly Asn His
His1 5 10779115PRTHomo sapiens 779Glu Val Gln Leu Val Glu Ser Gly
Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala
Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25 30Ala Met Ser Trp Val Arg
Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ala Ile Ser Gly
Ser Gly Gly Ser Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe
Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln
Ile Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala
Lys Gly Ser Ile Ala Ala Asp Trp Gly Gln Gly Thr Leu Val Thr 100 105
110Val Ser Arg 1157805PRTHomo sapiens 780Ser Tyr Ala Met Ser1
578117PRTHomo sapiens 781Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr
Tyr Ala Asp Ser Val Lys1 5 10 15Gly7826PRTHomo sapiens 782Gly Ser
Ile Ala Ala Asp1 5783108PRTHomo sapiens 783Ser Ser Glu Leu Thr Gln
Asp Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg Ile Thr
Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp Tyr Gln
Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly Lys Asn
Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55 60Ser Ser
Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65 70 75
80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn Val
85 90 95Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
10578411PRTHomo sapiens 784Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala
Ser1 5 107857PRTHomo sapiens 785Gly Lys Asn Asn Arg Pro Ser1
57868PRTHomo sapiens 786Asn Ser Arg Asp Ser Ser Gly Asn1
5787115PRTHomo sapiens 787Glu Val Gln Leu Val Glu Ser Gly Gly
Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Ser Tyr 20 25 30Ala Met Ser Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ala Ile Ser Gly Ser Gly
Gly Ser Thr Tyr Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Ser Glu
Gln Ala Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr 100 105 110Val
Ser Arg 1157885PRTHomo sapiens 788Ser Tyr Ala Met Ser1
578917PRTHomo sapiens 789Ala Ile Ser Gly Ser Gly Gly Ser Thr Tyr
Tyr Ala Asp Ser Val Lys1 5 10 15Gly7906PRTHomo sapiens 790Glu Gln
Ala Gly Asp Tyr1 5791111PRTHomo sapiens 791Gln Ser Val Leu Thr Gln
Pro Pro Ser Ala Ser Gly Thr Pro Gly Gln1 5 10 15Arg Val Thr Ile Ser
Cys Ser Gly Ser Ser Ser Asn Ile Gly Ser Asn 20 25 30Tyr Val Tyr Trp
Tyr Gln Gln Leu Pro Gly Thr Ala Pro Lys Leu Leu 35 40 45Ile Tyr Arg
Asn Asn Gln Arg Pro Ser Gly Val Pro Asp Arg Phe Ala 50 55 60Gly Ser
Lys Ser Gly Thr Ser Ala Thr Leu Gly Ile Thr Gly Leu Gln65 70 75
80Thr Gly Asp Glu Ala Asp Tyr Tyr Cys Gly Thr Trp Asp Ser Ser Leu
85 90 95Ser Ala Gly Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly
100 105 11079213PRTHomo sapiens 792Ser Gly Ser Ser Ser Asn Ile Gly
Ser Asn Tyr Val Tyr1 5 107937PRTHomo sapiens 793Arg Asn Asn Gln Arg
Pro Ser1 57949PRTHomo sapiens 794Gly Thr Trp Asp Ser Ser Leu Ser
Ala1 5795119PRTHomo sapiens 795Gln Val Gln Leu Val Gln Ser Gly Ala
Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala
Ser Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Tyr Met His Trp Val Arg Gln
Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Ile Ile Asn Pro Ser
Gly Gly Ser Thr Ser Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr
Met Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr65 70 75 80Met Glu Leu
Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg
Glu Leu Ser Ala Ala Thr Ala Phe Asp Ile Trp Gly Gln Gly 100 105
110Thr Met Val Thr Val Ser Arg 1157965PRTHomo sapiens 796Ser Tyr
Tyr Met His1 579717PRTHomo sapiens 797Ile Ile Asn Pro Ser Gly Gly
Ser Thr Ser Tyr Ala Gln Lys Phe Gln1 5 10 15Gly79810PRTHomo sapiens
798Glu Leu Ser Ala Ala Thr Ala Phe Asp Ile1 5 10799107PRTHomo
sapiens 799Glu Thr Thr Leu Thr Gln Ser Pro Phe Ser Val Ser Ala Ser
Val Gly1 5 10 15Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Tyr Ile
Ser Arg Trp 20 25 30Leu Ala Trp Tyr Gln Gln Arg Pro Gly Lys Ala Pro
Lys Leu Leu Ile 35 40 45Tyr Ala Ala Ala Ser Leu Gln Ser Gly Val Pro
Ser Arg Phe Ser Gly 50 55 60Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr
Ile Ser Ser Leu Gln Pro65 70 75 80Glu Asp Phe Ala Thr Tyr Tyr Cys
Gln Gln Ala Asn Ser Phe Pro Val 85 90 95Thr Phe Gly Gln Gly Thr Arg
Leu Glu Ile Lys 100 10580011PRTHomo sapiens 800Arg Ala Ser Gln Tyr
Ile Ser Arg Trp Leu Ala1 5 108017PRTHomo sapiens 801Ala Ala Ala Ser
Leu Gln Ser1 58027PRTHomo sapiens 802Gln Gln Ala Asn Ser Phe Pro1
5803120PRTHomo sapiens 803Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser
Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Gly Ile Ser Trp Val Arg Gln Ala
Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Trp Ile Ser Ala Tyr Asn
Gly Asn Thr Asn Tyr Ala Gln Lys Leu 50 55 60Gln Gly Arg Val Thr Met
Thr Thr Asp Thr Ser Thr Ser Thr Ala Tyr65 70 75 80Met Glu Leu Arg
Ser Leu Arg Ser Asp Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Val
Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val Trp Gly Gln 100 105 110Gly
Thr Thr Val Thr Val Ser Arg 115 1208045PRTHomo sapiens 804Ser Tyr
Gly Ile Ser1 580517PRTHomo sapiens 805Trp Ile Ser Ala Tyr Asn Gly
Asn Thr Asn Tyr Ala Gln Lys Leu Gln1 5 10 15Gly80611PRTHomo sapiens
806Val Gly Tyr Tyr Tyr Tyr Tyr Gly Met Asp Val1 5 10807111PRTHomo
sapiens 807Gln Ser Ala Leu Thr Gln Pro Ala Ser Val Ser Gly Ser Pro
Gly Gln1 5 10 15Ser Ile Thr Ile Ser Cys Thr Gly Thr Ser Ser Asp Val
Gly Ser Tyr 20 25 30Asn Leu Val Ser Trp Tyr Gln Gln His Pro Gly Lys
Ala Pro Lys Leu 35 40 45Met Ile Tyr Glu Gly Ser Lys Arg Pro Ser Gly
Val Ser Asn Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly Asn Thr Ala Ser
Leu Thr Ile Ser Gly Leu65 70 75 80Gln Ala Glu Asp Glu Ala Asp Tyr
Tyr Cys Ser Ser Tyr Thr Ser Ser 85 90 95Ser Thr Trp Val Phe Gly Gly
Gly Thr Lys Leu Thr Val Leu Gly 100 105 11080814PRTHomo sapiens
808Thr Gly Thr Ser Ser Asp Val Gly Ser Tyr Asn Leu Val Ser1 5
108097PRTHomo sapiens 809Glu Gly Ser Lys Arg Pro Ser1 58108PRTHomo
sapiens 810Ser Ser Tyr Thr Ser Ser Ser Thr1 5811118PRTHomo sapiens
811Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ser1
5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser Gly Gly Thr Phe Ser Ser
Tyr 20 25 30Ala Ile Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu
Trp Met 35 40 45Gly Trp Met Asn Pro Asn Ser Gly Asn Thr Gly Tyr Ala
Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Met Thr Arg Asn Thr Ser Ile
Ser Thr Ala Tyr65 70 75 80Met Glu Leu Ser Ser Leu Arg Ser Glu Asp
Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Asp Val Gly Ile Gly Val Phe
Asp Tyr Trp Gly Gln Gly Thr 100 105 110Leu Val Thr Val Ser Arg
1158125PRTHomo sapiens 812Ser Tyr Ala Ile Ser1 581317PRTHomo
sapiens 813Trp Met Asn Pro Asn Ser Gly Asn Thr Gly Tyr Ala Gln Lys
Phe Gln1 5 10 15Gly8149PRTHomo sapiens 814Asp Val Gly Ile Gly Val
Phe Asp Tyr1 5815109PRTHomo sapiens 815Ser Tyr Val Leu Thr Gln Pro
Pro Ser Val Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Arg Ile Thr Cys
Gly Gly Asn Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln Gln
Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Tyr Asp Ser Asp
Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly Ser 50 55 60Asn Ser Gly
Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu Ala Gly65 70 75 80Asp
Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp Ser Ser Ser Asp His 85 90
95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
10581611PRTHomo sapiens 816Gly Gly Asn Asn Ile Gly Ser Lys Ser Val
His1 5 108177PRTHomo sapiens 817Tyr Asp Ser Asp Arg Pro Ser1
58189PRTHomo sapiens 818Gln Val Trp Asp Ser Ser Ser Asp His1
5819121PRTHomo sapiens 819Glu Val Gln Leu Val Glu Ser Gly Gly Gly
Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser
Gly Phe Thr Phe Ser Asp Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala
Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ala Thr Ser Gly Ser Gly
Gly Ser Thr Phe Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile
Ser Arg Asp Asn Ser Lys Ser Thr Leu Tyr65 70 75 80Leu Gln Met Asn
Ser Leu Arg Asp Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Lys Gly
Thr Leu Pro His Tyr Tyr Asp Ser Ser Gly Ile Gly Gly 100 105 110Gln
Gly Thr Leu Val Thr Val Ser Ser 115 1208205PRTHomo sapiens 820Asp
Tyr Ala Met Asn1 582117PRTHomo sapiens 821Ala Thr Ser Gly Ser Gly
Gly Ser Thr Phe Tyr Ala Asp Ser Val Lys1 5 10 15Gly82212PRTHomo
sapiens 822Gly Thr Leu Pro His Tyr Tyr Asp Ser Ser Gly Ile1 5
10823113PRTHomo sapiens 823Gln Ala Val Leu Thr Gln Pro Ser Ser Val
Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile Thr Ile Ser Cys Thr Gly Thr
Ser Ser Asp Val Gly Gly Tyr 20 25 30Asn Tyr Val Ser Trp Tyr Gln Gln
His Pro Gly Lys Ala Pro Lys Leu 35 40 45Met Ile Tyr Asp Val Gly Lys
Arg Pro Ser Gly Val Ser Asn Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly
Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75 80Arg Ala Glu Asp
Glu Ala Asn Tyr Tyr Cys Ser Ser Tyr Thr Ser Ser 85 90 95Ser Thr Trp
Phe Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu 100 105
110Gly82414PRTHomo sapiens 824Thr Gly Thr Ser Ser Asp Val Gly Gly
Tyr Asn Tyr Val Ser1 5 108257PRTHomo sapiens 825Asp Val Gly Lys Arg
Pro Ser1 582610PRTHomo sapiens 826Ser Ser Tyr Thr Ser Ser Ser Thr
Trp Phe1 5 10827121PRTHomo sapiens 827Gln Val Gln Leu Gln Gln Ser
Gly Ala Glu Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys
Lys Ala Ser Gly Tyr Thr Phe Thr Thr Tyr 20 25 30Tyr Met His Trp Val
Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Ile Ile Asn
Pro Ser Gly Glu Asn Thr Asn Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg
Val Thr Met Thr Arg Asp Thr Ser Thr Thr Thr Val Tyr65 70 75 80Met
Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90
95Ala Arg Ser Phe Ile Gly Thr Arg Gly Gly Gly Leu Asp Val Trp Gly
100 105 110Gln Gly Thr Thr Val Thr Val Ser Arg 115 1208285PRTHomo
sapiens 828Thr Tyr Tyr Met His1 582917PRTHomo sapiens 829Ile Ile
Asn Pro Ser Gly Glu Asn Thr Asn Tyr Ala Gln Lys Phe Gln1 5 10
15Gly83012PRTHomo sapiens 830Ser Phe Ile Gly Thr Arg Gly Gly Gly
Leu Asp Val1 5 10831113PRTHomo sapiens 831Gln Ser Val Leu Thr Gln
Pro Pro Ser Val Ser Gly Ala Pro Gly Gln1 5 10 15Arg Val Asn Ile Ser
Cys Ala Gly Ser Ser Ser Asn Ile Gly Ala Gly 20 25 30Tyr Asp Val His
Trp Tyr Gln Gln Ile Pro Gly Thr Ala Pro Lys Leu 35 40 45Leu Met Tyr
Gly Asn Ser Asn Arg Pro Ser Gly Val Pro Asp Arg Phe 50 55 60Ser Gly
Ser Lys Ser Gly Ala Ser Ala Ser Leu Ala Ile Thr Arg Leu65 70 75
80Gln Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Ser Ser
85 90 95Leu Ser Gly Ser Arg Val Phe Gly Thr Gly Thr Lys Val Thr Val
Leu 100 105 110Gly83214PRTHomo sapiens 832Ala Gly Ser Ser Ser Asn
Ile Gly Ala Gly Tyr Asp Val His1 5 108337PRTHomo sapiens 833Gly Asn
Ser Asn Arg Pro Ser1 583410PRTHomo sapiens 834Gln Ser Tyr Asp Ser
Ser Leu Ser Gly Ser1 5 10835117PRTHomo sapiens 835Glu Val Gln Leu
Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg1 5 10 15Ser Leu Arg
Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asp Asp Tyr 20 25 30Ala Met
His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser
Gly Ile Ser Trp Asn Ser Gly Ser Ile Gly Tyr Ala Asp Ser Val 50 55
60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65
70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr
Cys 85 90 95Ala Thr Glu Glu Trp Trp Arg Phe Asp Leu Trp Gly Arg Gly
Thr Leu 100 105 110Val Thr Val Ser Arg 1158365PRTHomo sapiens
836Asp Tyr Ala Met His1 583717PRTHomo sapiens 837Gly Ile Ser Trp
Asn Ser Gly Ser Ile Gly Tyr Ala Asp Ser Val Lys1 5 10
15Gly8388PRTHomo sapiens 838Glu Glu Trp Trp Arg Phe Asp Leu1
5839111PRTHomo sapiens 839Gln Ser Ala Leu Thr Gln Pro Pro Ser Ala
Ser Gly Ser Pro Gly Gln1 5 10 15Ser Val Thr Ile Ser Cys Thr Gly Thr
Ser Ser Asp Val Asp Asp Tyr 20 25 30Asn Tyr Val Ser Trp Tyr Gln Gln
His Pro Gly Lys Ala Pro Lys Leu 35 40 45Met Ile Tyr Glu Val Thr Lys
Arg Pro Ser Gly Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly
Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75 80Gln Ala Glu Asp
Glu Ala Asp Tyr Tyr Cys Ser Ser Tyr Val Gly Ser 85 90 95Asp Asn Arg
Val Phe Gly Thr Gly Thr Lys Val Thr Val Pro Gly 100 105
11084014PRTHomo sapiens 840Thr Gly Thr Ser Ser Asp Val Asp Asp Tyr
Asn Tyr Val Ser1 5 108417PRTHomo sapiens 841Glu Val Thr Lys Arg Pro
Ser1 58428PRTHomo sapiens 842Ser Ser Tyr Val Gly Ser Asp Asn1
5843363DNAHomo sapiens 843caggtgcagc tggtgcagtc tggggctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggata caccttcacc
ggctactata tgcactgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcaacccta acagtggtgg cacaaactat 180gcacagaagt
ttcagggcag ggtcaccatg accagggaca cgtccatcag cacagcctac
240atggagctga gcaggctgag atctgacgac acggccgtgt attactgtgc
gagatccgat 300attttgactg gttattatgc ttttgatatc tggggccaag
ggacaatggt caccgtctcg 360aga 363844321DNAHomo sapiens 844gacatccaga
tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60atcacttgcc
gggcaagtca gagcattagc agctatttaa attggtatca gcagaaacca
120gggaaagccc ctaagctcct gatctatgct gcatccagtt tgcaaagtgg
ggtcccatca 180aggttcagtg gcagtggatc tgggacagat ttcactctca
ccatcagcag tctgcaacct 240gaagattttg caacttacta ctgtcaacag
agttacagta ccacgtggac gttcggccaa 300gggaccaagg tggaaatcaa a
321845387DNAHomo sapiens 845gaggtgcagc tggtggagtc tggggctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggata caccttcacc
ggctactata tgcactgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcaacccta acagtggtgg cacaaactat 180gcacagaagt
ttcagggcag ggtcaccatg accagggaca cgtccatcag cacagcctac
240atggagctga gcaggctgag atctgacgac acggccgtgt attactgtgc
gagagattta 300tggtattact atggttcggg gagttcactg tactactact
acggtatgga cgtctggggc 360caagggacca cggtcaccgt ctcgaga
387846336DNAHomo sapiens 846cagtctgtgt tgacgcagcc gccctcagtg
tctggggccc cagggcagag ggtcaccatc 60tcctgcactg ggagcagctc caacatcggg
gcaggttatg atgtacactg gtaccagcag 120cttccaggaa cagcccccaa
actcctcatc tatggtaaca gcaatcggcc ctcaggggtc 180cctgaccgat
tctctggctc caagtctggc acctcagcct ccttggccat cactgggctc
240caggctgagg atgaggctga ttattactgc cagtcctatg acagcagcct
gagtggtgtg 300gtattcggcg gagggaccaa gctgaccgtc ctaggt
336847366DNAHomo sapiens 847gaggtgcagc tggtggagtc tgggggaggc
ttggtacagc ctggcaggtc cctgagactc 60tcctgtgcag cctctggatt cacctttgat
gattatgcca tgcactgggt ccggcaagct 120ccagggaagg gcctggagtg
ggtctcaggt attagttgga
atagtggtag cataggctat 180gcggactctg tgaagggccg attcaccatc
tccagagaca acgccaagaa ctccctgtat 240ctgcaaatga acagtctgag
agctgaggac acggccttgt attactgtgt acggagtggg 300agctacaact
actactacta cggtatggac gtctggggcc aagggaccac ggtcaccgtc 360tcgaga
366848333DNAHomo sapiens 848cagtctgtgt tgacgcagcc gccctcagcg
tctgggaccc ccgggcagag ggtcaccatc 60tcttgttctg gaagcagctc caacatcgga
agtaatactg taaactggta ccagcagctc 120ccaggaacgg cccccaaact
cctcatctat agtaataatc agcggccctc aggggtccct 180gaccgattct
ctggctccaa gtctggcacc tcagcctccc tggccatcag tgggctccag
240tctgaggatg aggctgatta ttactgtgca gcatgggatg acagcctgaa
tggttgggtg 300ttcggcggag ggaccaagct gaccgtccta ggt 333849369DNAHomo
sapiens 849caggtgcagc tgcaggagtc ggggggaggc ttggtacagc ctggggggtc
cctgagactc 60tcctgtacaa cctctggatt cacctttacc agctatgcca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcatct attagtggta
gtggtggtat cacatactac 180gcagactccg tgaagggccg gttcaccatc
tccagagaca attccaagaa cacactgtat 240ctgcaaatga acagcctaag
agccgaggac acggccgtat attactgtgc gaaagatagg 300gttctagtcc
cagcttcctc ttcgtacttt gactactggg gccagggaac cctggtcacc 360gtctcgaga
369850327DNAHomo sapiens 850tcttctgagc tgactcagga ccctgctgtg
tctgtggcct tgggacagac agtcaggatc 60acatgccaag gagacagcct cagaagctat
tatgcaagct ggtaccagca gaagccagga 120caggcccctg tacttgtcat
ctatggtaaa aacaaccggc cctcagggat cccagaccga 180ttctctggct
ccagctcagg aaacacagct tccttgacca tcactggggc tcaggcggaa
240gatgaggctg actattactg taactcccgg gacagcagtg gtaaccatgt
ggtattcggc 300ggagggacca agctgaccgt cctaggt 327851360DNAHomo
sapiens 851caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac
cctgtccctc 60acctgcactg tctctggtgg ctccatcagc agtagtagtt actactgggg
ctggatccgc 120cagcccccag ggaaggggct ggagtggatt gggagtatct
attatagtgg gagcacctac 180tacaacccgt ccctcaagag tcgagtcacc
atatccgtag acacgtccaa gaaccagttc 240tccctgaagc tgagctctgt
gaccgccgca gacacggctg tgtattactg tgcgagacgt 300cccttaacct
ttaatgcttt tgatatctgg ggccaaggga caatggtcac cgtctcgaga
360852327DNAHomo sapiens 852tcctatgtgc tgactcagcc accctcagtg
tcagtggccc caggaaagac ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa
agtgtgcact ggtaccagca gaagccaggc 120caggcccctg tgctggtcat
ctattatgat agcgaccggc cctcagggat ccctgagcga 180ttctctggct
ccaactctgg gaacacggcc accctgacca tcagcagggt cgaagccggg
240gatgaggccg actattactg tcaggtgtgg gatagtagta gtgatcatgt
ggtattcggc 300ggagggacca agctgaccgt cctaggt 327853360DNAHomo
sapiens 853caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac
cctgtccctc 60acctgcactg tctctggtgg ctccatcagc agtagtagtt actactgggg
ctggatccgc 120cagcccccag ggaaggggct ggagtggatt gggagtatct
attatagtgg gagcacctac 180tacaacccgt ccctcaagag tcgagtcacc
atatccgtag acacgtccaa gaaccagttc 240tccctgaagc tgagctctgt
gaccgccgca gacacggctg tgtattactg tgcgaggatt 300cccatgtata
gcagctcggt tgactactgg ggccagggaa ccctggtcac cgtctcgaga
360854327DNAHomo sapiens 854tcctatgtgc tgactcagcc accctcagtg
tcagtggccc caggaaagac ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa
agtgtgcact ggtaccagca gaagccaggc 120caggcccctg tgctggtcat
ctattatgat agcgaccggc cctcagggat ccctgagcga 180ttctctggct
ccaactctgg gaacacggcc accctgacca tcagcagggt cgaagccggg
240gatgaggccg actattactg tcaggtgtgg gatagtagta gtgatcatgt
ggtattcggc 300ggagggacca agctgaccgt cctaggt 327855360DNAHomo
sapiens 855caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac
cctgtccctc 60acctgcactg tctctggtgg ctccatcagc agtagtagtt actactgggg
ctggatccgc 120cagcccccag ggaaggggct ggagtggatt gggagtatct
attatagtgg gagcacctac 180tacaacccgt ccctcaagag tcgagtcacc
atatccgtag acacgtccaa gaaccagttc 240tccctgaagc tgagctctgt
gaccgccgca gacacggctg tgtattactg tgcgagacgt 300cccttaacct
ttaatgcttt tgatatctgg ggccaaggga ccacggtcac cgtctcgaga
360856327DNAHomo sapiens 856tcctatgtgc tgactcagcc accctcagtg
tcagtggccc caggaaagac ggccaggatt 60acctgtgggg gaaacaacat tggaagtaaa
agtgtgcact ggtaccagca gaagccaggc 120caggcccctg tgctggtcat
ctattatgat agcgaccggc cctcagggat ccctgagcga 180ttctctggct
ccaactctgg gaacacggcc accctgacca tcagcagggt cgaagccggg
240gatgaggccg actattactg tcaggtgtgg gatagtagta gtgatcatgt
ggtattcggc 300ggagggacca agctgaccgt cctaggt 327857366DNAHomo
sapiens 857gaggtgcagc tggtggagtc tgggggaggc ttggtacagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt cacctttagc agctatgcca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcagct attagtggta
gtggtggtag cacatactac 180gcagactccg tgaagggccg gttcaccatc
tccagagaca attccaagaa cacgctgtat 240ctgcaaatga acagcctgag
agccgaggac acggccgtat attactgtgc gaaagatggg 300ggatggttcg
gggagttaga ttacttccag cactggggcc agggcaccct ggtcaccgtc 360tcgaga
366858333DNAHomo sapiens 858cagtctgtgt tgacgcagcc gccctcagtg
tctgcggccc caggacagaa ggtcaccgtc 60tcctgcactg gaagcaactc caacattgag
aagaatgatg tttcctggta ccagcaggga 120ccaggagcag cccccaaact
cctcatttct gacactgata ggcgaccctc agggattcct 180gaccgattct
ctggctccaa gtctggcacg tcagccaccc tggccatcgc tgggctccag
240gctgaggatg aggctgatta ttactgccag tcccatgaca ccactctgag
tggtccgatc 300ttcggcgggg ggacccagct gaccgtccta ggt 333859372DNAHomo
sapiens 859caggtgcagc tgcaggagtc ggggggaggc ttggtcaagc ctggagggtc
cctgagactc 60tcctgtgcag cctctggatt cagtttcagt gactactaca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg gatttcatat attactagta
gtagtagtga cacagactac 180gcagactctg tgaagggccg attcaccatc
tccagagaca acgccaagaa ctcactatat 240ctgcaaatga acagcctgag
agccgacgac acggccgtgt attactgtgc gagagtgggc 300tattattatg
attactacta ctactactac atggacgtct ggggcaaagg gaccacggtc
360accgtctcga ga 372860324DNAHomo sapiens 860tcttctgagc tgactcagga
ccctgctgtg tctgtggcct tgggacagac agtcaggatc 60acatgccaag gagacagcct
cagaggctat tatgcaagct ggtaccagca gaagccagga 120caggcccctg
tccttgtcgt ctatgatgaa aacaaccggc cctcagggat cccagaccga
180ttctctggct ccagctcagg aaacacagct tccttgacca tcactggggc
tcaggcggaa 240gatgaggctg actattactg taactcccgg gacattaacc
ttgattgggt gttcggcgga 300gggaccaagt tgaccgtcct aggt
324861360DNAHomo sapiens 861caggtgcagc tgcaggattc gggcccagga
ctggtgaagc cttcggatac cctgtccctc 60acctgcactg tctctggtgg ctccatcagc
agtattagtt actactgggg ctggatccgc 120cagcccccag ggaaggggct
ggagtgtatt gggagtatct attatagtgg gagcacctac 180tacaacccgt
ccctcaagag tcgagtcacc atatccgtag acacgtccaa gaaccagttc
240tccctgaagc tgagctctgt gaccgccgca gacacggctg tgtattactg
tgcgagacgg 300gtcatagtgt gggggagtga tgactactgg ggccagggaa
ccctggtcac cgtctcgaga 360862327DNAHomo sapiens 862tcctatgtgc
tgactcagcc accctcagtg tcagtggccc caggaaagac ggccaggatt 60acctgtgggg
gaaacaacat tggaagtaaa agtgtgcact ggtaccagca gaagccaggc
120caggcccctg tgctggtcat ctattatgat agcgaccggc cctcagggat
ccctgagcga 180ttctctggct ccaactctgg gaacacggcc accctgacca
tcagcagggt cgaagccggg 240gatgaggccg actattactg tcaggtgtgg
gatagtagta gtgatcatgt ggtattcggc 300ggagggacca agctgaccgt cctaggt
327863360DNAHomo sapiens 863caggtgcagc tgcaggagtc gggcccagga
ctggtgaagc cttcggagac cctgtccctc 60acctgcactg tctctggtgg ctccatcagc
agtagtagtt actactgggg ctggatccgc 120cagcccccag ggaaggggct
ggagtggatt gggagtatct attatagtgg gagcacctac 180tacaacccgt
ccctcaagag tcgagtcacc atatccgtag acacgtccaa gaaccagttc
240tccctgaagc tgagctctgt gaccgccgca gacacggctg tgtattactg
tgcgatgcgg 300gcctatggtt cagggagtta tgactactgg ggccagggaa
ccctggtcac cgtctcgaga 360864336DNAHomo sapiens 864gatgttgtga
tgactcagtc tccactctcc ctgcccgtca cccctggaga gccggcctcc 60atctcctgca
ggtctagtca gagcctcctc catagtaatg gatacaacta tttggattgg
120tacctgcaga agccagggca gtctccgcag ctcctgatct atttgggttc
taatcgggcc 180tccggggtcc ctgacaggtt cagtggcagt ggatcaggca
cagattttac actgaaaatc 240agcagagtgg aggctgagga tgttggggtt
tattactgca tgcaagctct acaaacccca 300ttcactttcg gccctgggac
caaagtggat atcaaa 336865363DNAHomo sapiens 865gaggtgcagc tggtggagtc
tgggggaggc ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt
cacctttagc agctatgcca tgagctgggt ccgccaggct 120ccagggaagg
ggctggagtg ggtctcagct attagtggta gtggtggtag cacatattac
180gcagactccg tgaagggccg gttcaccatc tccagagaca attccaagaa
cacgctgtat 240ctgcaaatga acagcctgag agccgaggac acggccgcat
attactgtgc gaaaggtctt 300aggtatagca gtgcctggac gtttgactac
tggggccagg gaaccctggt caccgtctcg 360aga 363866336DNAHomo sapiens
866cagtctgccc tgactcagcc tgcctccgtg tctgggtctc ctggacagtc
gatcaccatc 60tcctgcactg gaaccagcag tgacgttggt ggttataact atgtctcctg
gtaccaacaa 120cacccaggca aagcccccaa actcatgatt tatgatgtca
gtaatcggcc ctcaggggtt 180tctaatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctggactc 240caggctgagg acgaggctga
ttattactgc agctcatata caagcagtag cactcctgtg 300gtattcggcg
gagggaccaa gctgaccgtc ctaggt 336867357DNAHomo sapiens 867caggtgcagc
tggtgcaatc tgggtctgag ttgaagaagc ctggggcctc agtgaaggtt 60tcctgcaagg
cttctggata catcttcact agatatggca taaattgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggatgg atcaacacca acactgggaa
cccaacgtat 180gcccagggct tcacaggccg ggttgtcttc tccttggaca
cctctgtcag cacggcatat 240ctgcagatca gcagcctaaa ggctgaggac
actgccatgt attactgtgc gatcagcagt 300ggctttgggt actactttga
ctactggggc cagggaaccc tggtcaccgt ctcgaga 357868321DNAHomo sapiens
868gacatccaga tgacccagtc tccatcgtcc gtgtctgcat ctgtgggaga
cagagtcacc 60atcacttgtc gggcgagtca aagtattagt aggtggttag cctggtatca
gcagaaacca 120gggaaagccc ctaagttcct gatctatgct ggatccagtt
tgcaaagtgg ggtcccatcg 180aggttcagcg gcagtgggtc tgggacagat
ttcactctca ccatcagcag cctgcagcct 240gaagactttg caacttatta
ttgtcaacag actaacagtt tccctctcac cttcggcgga 300gggaccaagg
tggagatcaa a 321869360DNAHomo sapiens 869caggtgcagc tggtgcagtc
tggggctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta
cacctttacc agctacggta tcagctgggt gcgacaggcc 120cctggacaag
ggcttgagtg gatgggatgg atcagcgctt acaatggtaa cacaaactat
180gcacagaagc tccagggcag agtcaccatg accacagaca catccacgag
cacagcctac 240atggagctga ggagcctgag atctgacgac acggccgtgt
attactgtgc gagagctttt 300agggactggg gatctcttag ggactactgg
ggccagggca ccctggtcac cgtctcgaga 360870333DNAHomo sapiens
870cagtctgtgt tgacgcagcc gccctcagtg tctgcggccc caggacagaa
ggtcaccatc 60tcctgctctg gaagcagctc caacattggg aataattatg tatcctggta
ccagcagctc 120ccaggaacag cccccaaact cctcatttat gacaataata
agcgaccctc agggattcct 180gaccgattct ctggctccaa gtctggcacg
tcagccaccc tgggcatcac cggactccag 240actggggacg aggccgatta
ttactgcgga acatgggata gcagcctgag tgccgtggta 300ttcggcggag
ggaccaagct gaccgtccta ggt 333871363DNAHomo sapiens 871gaggtgcagc
tggtggagtc tggagcagag gtgaaaaagc ccggggagtc tctgaagatc 60tcctgtaagg
gttctggata cagctttacc agctactgga tcggctgggt gcgccagatg
120cccgggaaag gcctggagtg gatggggatc atctatcctg gtgactctga
taccagatac 180agcccgtcct tccaaggcca ggtcaccatc tcagccgaca
agtccatcag caccgcctac 240ctgcagtgga gcagcctgaa ggcctcggac
accgccatgt attactgtgc gagactggca 300gtgggagcct accagtacta
ctttgactac tggggccagg gaaccctggt caccgtctcg 360aga 363872333DNAHomo
sapiens 872cagactgtgg tgacccagga gccatcgttc tcagtgtccc ctggagggac
agtcacactc 60acttgtggct tgagctctgg ctcagtctct actagttact accccagctg
gtaccagcag 120accccaggcc aggctccacg cacgctcatc tacagcacaa
acactcgctc ttctggggtc 180cctgatcgct tctctggctc catccttggg
aacaaagctg ccctcaccat cacgggggcc 240caggcagatg atgaatctga
ttattactgt gtgctgtata tgggtagtgg catttcggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333873357DNAHomo sapiens 873gaggtgcagc
tggtggagtc tgggggaaac ttggtccagc cgggggggtc cctgagactc 60tcctgtgcag
cctctggatt caccttcagt aggtattgga tgacctgggt ccgccaggct
120ccagggaagg ggctggagtg gatttcatcc gttagtagta gcggcagtac
catatactac 180gcagactctg tgaagggccg attcaccatc tccagagaca
acgccaagaa ctcactgtat 240ctgcaaatga acagcctgag agtcgaggac
acggctgttt attactgtgc gcgagactat 300tggcctggct ggtacttcga
tctctggggc cgtggaaccc tggtcaccgt ctcgaga 357874348DNAHomo sapiens
874caggctgtgc tcactcagcc gtcttccctc tctgcatctc ctggagcatc
agccagtctc 60acctgcacct tccgcagtga catcagtgtt ggttcctata ggatatactg
gtaccagcag 120aagccaggga gtcctcccca gtttctcctg aaatatacgt
cagactcaga taagcagcag 180ggctctggag tccccagccg cttctctgga
tccaaagatg tttcggccaa tgctggcatt 240ttactcatct ctgggctcca
gtctgaggat gaggctgact attactgtat gacttggcac 300aacaccgctt
cggtattcgg cggagggacc aagctggccg tcctaggt 348875357DNAHomo sapiens
875gaggtacagc tggtggagtc tgggggaggt ttgataaggc cgggggggtc
cctgagactc 60tcctgtacag cctctggatt caccttcagt agttatacta tgaattgggt
ccgccaggct 120ccagggaagg ggctggagtg gctttcatat ataagtggtg
gcagtggtac caaattctac 180gcagactctg tgaagggccg gttcaccgtc
tccagagaca atgccaagaa ttcattgtat 240ctggaaatga acagcctgag
acccgaggac acggctgtct attactgtgc gctagtgtca 300tatagttcgc
cgggctttga ctactggggc cagggcaccc tggtcaccgt ctcgagc
357876321DNAHomo sapiens 876tcctatgagc tgactcagcc accctcagtg
tccgtgtccc caggacagac agccagcatc 60acctgctctg gagataaatt gggcgataaa
tatgtttact ggtatcaaca gaagccaggc 120cagtccccta tattgctcat
ctttcaagat agcgagcggc cctcagggat ccctgagcga 180ttctctggct
ccaactctgg gaacacagcc actctgacca tcagcgggac ccaggctatg
240gatgaggctg actattactg tcaggcgtgg gacagcagcg ctgcggtgtt
cggcggaggg 300accaagctga ccgtcctagg t 321877345DNAHomo sapiens
877caggtgcagc tggtgcagtc tggagcagag gtgaaaaagc ctggggcctc
agtgaaggtc 60tcctgcaagg cttctggtta cacctttacc agctatggta tcagctgggt
gcgacaggcc 120cctggacaag ggcttgagtg gatgggatgg atcagcgctt
acaatggtaa cacaaactat 180gcacagaagc tccagggcag agtcaccatg
accacagaca catccacgag cacagcctac 240atggagctga ggagcctgag
atctgacgac acggccgtgt attactgtgc gagagggggt 300gcttttgata
tctggggcca agggaccacg gtcaccgtct cgaga 345878336DNAHomo sapiens
878cagtctgtgt tgacgcagcc gccctcagtg tctggggccc cagggcagag
ggtcaccatc 60tcctgcactg ggagcagctc caacatcggg gcaggttatc atgtatactg
gtaccagcag 120cttccaggaa aagcccccaa actcctcatc tacgttaaca
gcaatcggcc ctcaggggtc 180cctgaccgat tctctggctc caagtctggc
acctcagcct ccctggccat cactgggctc 240caggctgacg atgaggctga
ttactactgc cagtcctatg acagcagcct gagtggtagg 300gttttcggcg
gagggaccaa gctgaccgtc ttaggt 336879357DNAHomo sapiens 879gaggtgcagc
tggtggagtc tgggggcggc ttggtccagc cgggggggtc cctgagactc 60tcctgttcag
cctctggatt cacctttagt aactattgga tgacctgggt ccgtcaggct
120ccagggaagg ggctggagtg gatttcatcc attagtagta gcggcagtac
catatactac 180gcagactctg tgaagggccg attcaccatc tccagagaca
acgccaagaa ctcactgtat 240ctgcaaatga acagcctgag agtcgaggac
acggctgttt attactgtgc gcgagactat 300tggcctggct ggtacttcga
tctctggggc cgtggcaccc tggtcaccgt ctcgaga 357880348DNAHomo sapiens
880caggctgtgc tcactcagcc gtcttccctc tctgcatctc ctggagcatc
agccagtctc 60acctgcacct tccgcagtga catcagtgtt ggttcctata ggatatactg
gtaccagcag 120aagccaggga gtcctcccca gtttctcctg aaatatacgt
cagactcaga taagcagcag 180ggctctggag tccccagccg cttctctgga
tccaaagatg tttcggccaa tgctggcatt 240ttactcatct ctgggctcca
gtctgaggat gaggctgact attactgtat gacttggcac 300aacaccgctt
cggtattcgg cggagggacc aagctggccg tcctaggt 348881381DNAHomo sapiens
881caggtgcagc tggtgcagtc tgggtctgag gtgaagaagc ctggggcctc
agtgaaggtc 60tcctgcaaga cttctggata catcttcacc gactactata tgcactgggt
gcgacaggcc 120cctggaaaag ggcttgagtg gatgggatgg attaacccta
acagtggtgg cacatactat 180gcacagaagt ttcacggcag ggtcaccatg
accagtgaca cgtccatcag cacagcctac 240atggagctga gcagtctgag
atctgacgac acggccatat attactgtgc gagagaggat 300tacgatattt
tgactggtta ttatcccgcg tccggccacg gggactactg gggccaggga
360accctggtca ccgtctcgag a 381882330DNAHomo sapiens 882caggctgtgg
tgactcagga gccctcactg actgtgtccc caggagggac agtcactctc 60acctgtgcat
ccagcactgg agcagtcacc agtggtttcc ttgcaaactg gttccagcag
120aaacctggac aaacacccag gtcactgatt tataaaacaa gcaacaaaca
tccctggacc 180cctgcccggt tctcaggctc cctccttggg ggcaaagctg
ccctgacact gtcaggtgtg 240cagcctgagg acgaggctga ctattactgc
ctgctcttat ctggtggtgc atgggtgttt 300ggcggaggga ccaagctgag
tgtcctaggt 330883366DNAHomo sapiens 883caggtgcagc tggtgcagtc
tggagcagag gtgaaaaagc ccggagagtc tctgaagatc 60tcgtgtgagg gttctggata
cacctttacc agctactgga tcggctgggt gcgccagatg 120cccgggaaag
acctggagtg gatggggatc atctatcctg gtgactctga taccagatac
180agcccgtcct tccaaggcca ggtcaccatc tcagtcgaca agtctatcag
caccgcctac 240ctgcagtgga gcagcctgaa ggcctcggac accgccatgt
attactgtgc gagacacgac 300gtagttgatg gctacaatac cggtatggac
gtctggggcc aagggaccac ggtcaccgtc 360tcgaga 366884333DNAHomo sapiens
884cagactgtgg tgacccagga gccatcgttc acagtgtccc ctggagggac
agtcacactc 60acttgtggct tgagctctgg ctcagtctct actagttact accccagctg
gtaccagcag 120accccaggcc aggctccacg cacgctcatc tccagcacaa
acactcgctc ttctggggtc 180cctgatcgct tctctggctc catccttggg
aacagagctg ccctcaccat cacgggggcc 240caggcagatg atgagtctga
ttattactgt gtgctgtata tgggtagtgg catttgggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333885384DNAHomo sapiens 885caggtgcagc
tggtgcagtc tggagcagag gtgaaaaagc ccggggagtc tctgaagatc 60tcctgtaagg
gttctggata cagctttacc agctactgga tcggctgggt gcgccagatg
120cccgggaaag gcctggagtg gatggggatc atctatcctg gtgactctga
tgccagatac 180agcccgtcct tccaaggcca
ggtcaccatc tcagccgaca agtccatcag caccgcctac 240ctgcagtgga
gcagcctgaa ggcctcggac accgccatgt attactgtgc gagactcacg
300ggcagttctt actatgatag tagtggttat tcctcctacg gtatggacgt
ctggggccaa 360gggaccacgg tcaccgtctc gaga 384886333DNAHomo sapiens
886cagactgtgg tgacccagga gccatcgttc tcagtgtccc ctggagggac
agtcacactc 60acttgtggct tgagctctgg ctcagtctct actagttact accccagctg
gttccagcag 120accccaggcc aggctccacg cacgctcatc tacagcacaa
acactcgctc ttctggggtc 180cctgatcgct tctctggctc catccttggg
aacaaagctg ccctcaccat cacgggggcc 240caggcagatg atgaatctga
ttattactgt gtgctgtata tgggtagtgg catttctgtg 300ttcggaggag
gcacccagct gaccgtcctc ggt 333887363DNAHomo sapiens 887caggtgcagc
tggtgcagtc tggagcagag gtgaaaaagc ccggggagtc tctgaagatc 60tcctgtaagg
gttctggata cagctttacc agctactgga tcggctgggt gcgccagatg
120cccgggaaag gcctggagtg gatggggatc atctatcctg gtgactctga
taccagatac 180agcccgtcct tccaaggcca ggtcaccatc tcagccgaca
agtccatcag caccgcctac 240ctgcagtgga gcagcctgaa ggcctcggac
accgccatgt attactgtgc gagacataac 300agtaactact actactacta
catggacgtc tggggcaaag gaaccctggt caccgtctcg 360aga 363888333DNAHomo
sapiens 888cagactgtgg tgacccagga gccatcgttc tcagtgtccc ctggagggac
agtcacactc 60acttgtggct tgagctctgg ctcagtctct actagttact accccagctg
gtaccagcag 120accccaggcc aggctccacg cacgctcatc tacagcacaa
acactcgctc ttctggggtc 180cctgatcgct tctctggctc catccttggg
aacaaagctg ccctcaccat cacgggggcc 240caggcagatg atgaatctga
ttattactgt gtgctgtata tgggtagtgg catttcggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333889381DNAHomo sapiens 889caggtgcagc
tggtgcagtc tgggtctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaaga
cttctggata catcttcacc gactactata tgcactgggt gcgacaggcc
120cctggaaaag ggcttgagtg gatgggatgg attaacccta acagtggtgg
cacatactat 180gcacagaagt ttcacggcag ggtcaccatg accagtgaca
cgtccatcag cacagcctac 240atggagctga gcagtctgag atctgacgac
acggccatat attactgtgc gagagaggat 300tacgatattt tgactggttt
ttatcccgcg tccggccacg gggactactg gggccaggga 360accctggtca
ccgtctcgag a 381890321DNAHomo sapiens 890gaaattgtgt tgacgcagtc
tccaggcacc ctgtctttgt ctccagggga aagagccacc 60ctctcctgca gggccagtca
gagtgttagc agcagctact tagcctggta ccagcagaaa 120cctggccagg
ctcccaggct cctcatctat ggtgcatcca gcagggccac tggcatccca
180gacaggttca gtggcagtgg gtctgggaca gacttcactc tcaccatcag
cagactggag 240cctgaagatt ttgcagtgta ttactgtcag cagtatggta
gctcactcac tttcggcgga 300gggaccaagg tggagatcaa a 321891366DNAHomo
sapiens 891caggtgcagc tggtgcagtc tggagcagag gtgaaaaagc ccggggagtc
tctgaagatc 60tcctgtaagg gttctggata cagctttacc agctactgga tcggctgggt
gcgccagatg 120cccgggaaag gcctggagtg gatggggatc atctatcctg
gtgactctga taccagatac 180agcccgtcct tccaaggcca ggtcaccatc
tcagccgaca agtccatcag caccgcctac 240ctgcagtgga gcaccctgaa
ggcctcggac accgccatgt attactgtgc gagacatggg 300atgactagtg
gctacgtcgc gcacaatgac tactggggcc agggaaccct ggtcaccgtc 360tcgaga
366892333DNAHomo sapiens 892cagactgtgg tgacccagga gccatcgttc
tcagtgtccc ctggagggac agtcacactc 60acttgtggct tgagctctgg ctcagtctct
actagttact accccagctg gtaccagcag 120accccaggcc aggctccacg
cacgctcatc tacagcacaa acactcgctc ttctggggtc 180cctgatcgct
tctctggctc catccttggg aacaaagctg ccctcaccat cacgggggcc
240caggcagatg atgaatctga ttattactgt gtgctgtata tgggtagtgg
catttgggtg 300ttcggcggag ggaccaagct gaccgtccta ggt 333893351DNAHomo
sapiens 893caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggggac
cctgtccctc 60acctgcgctg tctctggtgg ctccatcagc agtagtaact ggtggagttg
ggtccgccag 120cccccaggga aggggctgga gtggattggg gaaatctatc
atagtgggag caccaactac 180aacccgtccc tcaagagtcg agtcaccata
tcagtagaca agtccaagaa ccagttctcc 240ctgaagctga gctctgtgac
cgccgcggac acggccgtgt attactgtgc gagaggtggg 300agctactact
ttgactactg gggccaggga accctggtca ccgtctcgag a 351894336DNAHomo
sapiens 894cagtctgccc tgactcagcc tgcctccgtg tctgggtctc ctggacagtc
gatcaccatc 60tcctgcactg gaaccatcag tgacgttggt ggttatgact ttgtctcctg
gtaccaacac 120caccccggca aagcccccaa actcctgatt tatgatgtca
ataatcggcc ctctggggtt 180tctcatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240caggctgagg acgaggctac
ttattactgc agttcatatt caaacagaca ttctctcatc 300gtcttcggat
ctgggaccca ggtcgtcggc ctaggt 336895363DNAHomo sapiens 895caggtgcagc
tacagcagtg gggcgcagga ctgttgaagc cttcggagac cctgtccctc 60acctgcgctg
tctatggtgg gtccttcagt ggttactact ggagctggat ccgccagccc
120ccagggaagg ggctggagtg gattggggaa atcaatcata gtggaagcac
caactacaac 180ccgtccctca agagtcgagt caccatatca gtagacacgt
ccaagaacca gttctccctg 240aagctgagct ctgtgaccgc cgcggacacg
gctgtgtatt actgtgcgag aggcgggggg 300gttgaggcgt tgaactacgg
tatggacgtc tggggccaag ggaccacggt caccgtctcg 360aga 363896336DNAHomo
sapiens 896cagtctgccc tgactcagcc tgcctccgtg tctgggtctc ctggacagac
gatcaccatc 60tcctgcactg gaaccatcag tgacgttggt ggttatgact ttgtctcctg
gtaccaacac 120caccccggca aagcccccaa actcctgatt tatgatgtca
ataatcggcc ctctggggtt 180tctcatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240caggctgagg acgaggctac
ttattactgc agttcatatt caaacagaca ttctctcatc 300gtcttcggat
ctgggaccca ggtcgtcggc ctaggt 336897357DNAHomo sapiens 897caggtgcagc
tacagcagtg gggcgcaggg ctgttgaagc cttcggaaac cctgtccctc 60acctgcactg
tccatggtgg gtccttcgat gattactact ggacctggat ccgccagccc
120ccaggggggg ggctggaatg gattggggaa atgaattccg gtagaactta
caactacaac 180ccgttcctgg agagtcgagc ctccatagat gttgacacgt
tcaagaagca gttctccctg 240gcattgcgtt ctgtgaccgc cgcggacaca
gctgtctatt actgtgcgcg gggcgcctat 300gtcaactact actacataga
cgtctggggc gacgggacca cggtcaccgt ctcgaga 357898336DNAHomo sapiens
898cagtctgccc tgactcagcc tgcctccgtg tctgggtctc ctggacagac
gatcaccatc 60tcctgcactg gaaccatcag tgacgttggt ggttatgact ttgtctcctg
gtaccaacac 120caccccggca aagcccccaa actcctgatt tatgatgtca
ataatcggcc ctctggggtt 180tctcatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240caggctgagg acgaggctac
ttattactgc agttcatatt caaacagaca ttctctcatc 300gtcttcggat
ctgggaccca ggtcgtcggc ctaggt 336899375DNAHomo sapiens 899caggtgcagc
tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60acctgcactg
tctctggtgg ctccatcagt agttactact ggagctggat ccggcagccc
120gccgggaagg gactggagtg gattgggcgt atctatacca gtgggagcac
caactacaac 180ccctccctca agagtcgagt caccatgtca gtagacacgt
ccaagaacca gttctccctg 240aagctgagct ctgtgaccgc cgcggacacg
gccgtgtatt actgtgcgag agagagggca 300tattgtagta gtaccagctg
ctatcgaaat gcttttgata tctggggcca agggaccacg 360gtcaccgtct cgaga
375900357DNAHomo sapiens 900cagtctgtgt tgacgcagcc gccctcagtg
tctggggccc cagggcagag ggtcaacatc 60tcctgcgctg ggagcagctc caacatcggg
gcgggttatg atgttcactg gtaccagcag 120attccaggaa cagcccccaa
actcctcatg tatggtaata gtaatcggcc ctcaggggtc 180cctgaccgat
tctctggctc caagtctggc gcctcagcct ccctggccat cactaggctc
240caggctgagg atgaggctga ttattactgc cagtcctatg acagcagcct
gagtggttcg 300agggtcttcg gaactgggac caaggtcacc gtcctaggtc
agtccaacgt cctaggt 357901366DNAHomo sapiens 901gaggtgcagc
tggtggagtc tgggggaggc gtggtccagc ctgggaggtc cctgagactc 60tcctgtgcag
cctctggatt caccttcagt agctatggca tgcactgggt ccgccaggct
120ccaggcaagg ggctggagtg ggtgacagtt atatcatttg atggaagtaa
taaatactat 180gcagactccg tgaagggccg attcaccatc tccagagaca
attccaagaa cacgctgtat 240ctgcaaatga acagcctgag agctgaggac
acggctgtgt attactgtgc gaaagcgtat 300accaacacct ggtggcctga
tgcttttgat atctggggcc aagggaccac ggtcaccgtc 360tcgaga
366902321DNAHomo sapiens 902gacatccaga tgacccagtc tccatcctcc
ctgtctgcat ctgtaggaga cagagtcacc 60atcacttgcc aggcgagtca ggacattagc
aactatttaa attggtatca gcagaaacca 120gggaaagccc ctaagctcct
gatctacgat gcatccaatt tggaaacagg ggtcccatca 180aggttcagtg
gaagtggatc tgggacagat tttactttca ccatcagcag cctgcagcct
240gaagatattg caacatatta ctgtcaacag tatgataatc tccctcccac
tttcggccct 300gggaccaaag tggatatcaa a 321903354DNAHomo sapiens
903caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac
cctgtccctc 60acctgcactg tctctggtag ctccatcagt agttactact ggagctggat
ccggcagccc 120ccagggaagg gactggagtg gattgggtat atctattaca
gtgggagcac caactacaac 180ccctccctca agagtcgagt caccatatca
gtagacacgt ccaagaacca gttctccctg 240aagctgagct ctgtgaccgc
tgcggacacg gccgtgtatt actgtgcgag agatctgtac 300tggaacgacg
cttttgatat ctggggccaa gggaccacgg tcaccgtctc gaga 354904333DNAHomo
sapiens 904cagtctgccc tgactcagcc tctctcagcg tctgggaccc ccgggcagag
ggtcaccatc 60tcttgttctg gaagcagctc caacatcgga agtaatactg taaactggta
ccagcagctc 120ccaggaacgg cccccaaact cctcatctat agtaataatc
agcggccctc aggggtccct 180gaccgattct ctggctccaa gtctggcacc
tcagcctccc tggccatcag tgggctccag 240tctgaggatg aggctgatta
ttactgcgca gcatgggatg acagcctgaa tggtccggta 300ttcggcggag
ggaccaagct gaccgtccta ggt 333905354DNAHomo sapiens 905caggtgcagc
tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60acctgcactg
tctctggtag ctccatcagt agttactact ggagctggat ccggcagccc
120ccagggaagg gactggagtg gattgggtat atctattaca gtgggagcac
caactacaac 180ccctccctca agagtcgagt caccatatca gtagacacgt
ccaagaacca gttctccctg 240aagctgagct ctgtgaccgc tgcggacacg
gccgtgtatt actgtgcgag agatctgtac 300tggaacgacg cttttgatat
ctggggccaa gggaccacgg tcaccgtctc gaga 354906333DNAHomo sapiens
906cagtctgtgt tgacgcagcc gccctcagcg tctgggaccc ccgggcagag
tgtcaccatc 60tcttgttctg gaagcagctc caacatcgga agtaatactg taaactggta
ccagcagctc 120ccaggaacgg cccccaaact cctcatctat agtaataatc
agcggccctc aggggtccct 180gaccgattct ctggctccaa gtctggcacc
tcagcctccc tggccatcag tgggctccag 240tctgaggatg aggctgatta
ttactgtgca gcatgggatg acagcctgaa tggtccggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333907378DNAHomo sapiens 907caggtacagc
tgcagcagtc aggtccagga ctggtgaagc cctcgcagac cctctcactc 60acctgtgcca
tctccgggga cagtgtctct agcaacagtg ctgcttggaa ctggatcagg
120cagtccccat cgagaggcct tgagtggctg ggaaggacat actacaggtc
caagtggtat 180aatgattatg cagtatctgt gaaaagtcga ataaccatca
acccagacac atccaagaac 240cagttctccc tgcagctgaa ctctgtgact
cccgaggaca cggctgtgta ttactgtgca 300agagaatcat ggctttgggg
gattgggggg gatgcttttg atatctgggg ccaagggacc 360acggtcaccg tctcgaga
378908333DNAHomo sapiens 908cagtctgtgt tgacgcagcc gccctcggtg
tctggggccc cccggcagac ggtcaccatc 60tcctgctctg ggagcagctc caacatcgga
caaaattctg ttacctggta ccagcgcctc 120ccgggtgagg ctcccaaact
cctcatctac tatgatgatc tcttgcactc aggagtctct 180gaccgattct
ctggctccaa gtctggcacc tcagcctcac tggccatcag tggactccag
240tctgaggatg aggctgagta ctactgtgcg tcatgggatg acagcctgaa
aggtccggta 300ttcggcggag ggaccaaact gaccgtccta ggt 333909336DNAHomo
sapiens 909gaggtgcagc tggtggagtc tgggggaggc ttggtccagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt caccgtcagt agcaactaca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcagtt atttatagcg
gtggtagcac atactacgca 180gactccgtga agggcagatt caccatctcc
agagacaatt ccaagaacac gctgtatctt 240caaatgaaca gcctgagagc
cgaggacacg gctgtgtatt actgtgcgag ggagtttgac 300tactggggcc
agggaaccct ggtcaccgtc tcgaga 336910315DNAHomo sapiens 910gacatccaga
tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60atcacttgcc
aggcgagtca ggacattagc aactatttaa attggtatca gcagaaacca
120gggaaagccc ctaagctcct gatctacgat gcatccaatt tggaaacagg
ggtcccatca 180aggttcagtg gaagtggatc tgggacagat tttactttca
ccatcagcag cctgcagcct 240gaagatatcg caacatatta ctgtcaacag
tatgataatc ccgctttcgg cggagggacc 300aaggtggaga tcaaa
315911363DNAHomo sapiens 911caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta cacctttacc
agctatggta tcagctgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcagcgctt acaatggtaa cacaaactat 180gcacagaagc
tccagggcag agtcaccatg accacagaca catccacgag cacagcctac
240atggagctga ggagcctgag atctgacgac acggccgtgt attactgtgc
gagagatcgt 300tactatggtt cggggttcgg tatggacgtc tggggccaag
ggacaatggt caccgtctcg 360aga 363912327DNAHomo sapiens 912tcttctgagc
tgactcagga ccctgctatg tctgtggcct tgggacagac agtcaaaatc 60acttgccaag
gagacagcct cacaaactat tatccaagtt ggtatcagca gaagccagga
120caggcccctg tccttgtcat gtatggaaaa gacagccggc cctcagggat
ctcagaccga 180ttctctggct ccagctcagg aatctcagct tccttgacca
tcactggggc tcaggcggaa 240gatgaggctg actactactg taactcccga
gacggcagtg ctcaccgtct ggttttcggc 300ggagggacca agttgaccgt cctgggt
327913372DNAHomo sapiens 913caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta cacctttacc
aactatggtc tcacctgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcagcactt acaatagtaa cacaaactat 180gcagagaagc
tccagggcag agtcaccatg accacagaca catccacgag cacagcctac
240atggagttga ggagcctgac atctgacgac acggccgtgt attactgtgc
gagaggcccc 300acatattcct ttgatagtag tggttatttt tttgactact
ggggccaggg aaccctggtc 360accgtctcga ga 372914327DNAHomo sapiens
914tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gtaaccattg ggtgttcggc 300ggagggacca
agctgaccgt cctaggt 327915360DNAHomo sapiens 915caggtgcagc
tggtgcagtc tggagctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg
cttctggtta cacctttacc agctatggta tcagctgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggatgg atcagcgctt acaatggtaa
cacaaactat 180gcacagaagc tccagggcag agtcaccatg accacagaca
catccacgag cacagcctac 240atggagctga ggagcctgag atctgacgac
acggccgtgt attactgtgc gagagatacg 300tatagcagtg gctggtactt
tgactactgg ggccagggca ccctggtcac cgtctcgaga 360916330DNAHomo
sapiens 916tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaaactat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccga gacagcagtg gtaaccatct ttatgtcttc 300ggaactggga
ccaaggtcac cgtcctaggt 330917360DNAHomo sapiens 917caggtgcagc
tggtgcagtc tggagctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg
cttctggtta cacctttacc agctatggta tcagctgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggatgg atcagcgctt acaatggtaa
cacaaactat 180gcacagaagc tccagggcag agtcaccatg accacagaca
catccacgag cacagcctac 240atggagctga gcagcctgag atctgaggac
acggccgtgt attactgtgc aacccttaac 300attagtggga gctactactt
tgactactgg ggccagggaa ccctggtcac cgtctcgaga 360918344DNAHomo
sapiens 918tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaacct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctctggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gttacccctc ttgggtgttc 300ggcggaggga
ccaagctgac cggaccaagc tgaccgtcct aggt 344919354DNAHomo sapiens
919caggtgcagc tggtgcagtc tgaagcagag gtgaaaaagc ccggggagtc
tctgaagatc 60tcctgtaagg gttctggata cagctttacc agctactgga tcggctgggt
gcgccagatg 120cccgggaaag gcctggagtg gatggggatc atctatcctg
gtgactctga taccagatac 180agcccgtcct tccaaggcca ggtcaccatc
tcagccgaca agtccatcag caccgcctac 240ctgcagtgga gcagcctgaa
ggcctcggac accgccatgt attactgtgc gagaacgatc 300gggcttggtg
cttttgatat ctggggccaa gggaccacgg tcaccgtctc gaga 354920330DNAHomo
sapiens 920tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gtaaccatca ttatgtcttc 300ggaactggga
ccaaggtcac cgtcctaggt 330921357DNAHomo sapiens 921caggtgcagc
tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60acctgcactg
tctctggtgg ctccatcagc agtagtagtt actactgggg ctggatccgc
120cagcccccag ggaaggggct ggagtggatt gggagtatct attatagtgg
gagcacctac 180tacaacccgt ccctcaagag tcgagtcacc atatccgtag
acacgtccaa gaaccagttc 240tccctgaagc tgagctctgt gaccgccgca
gacacggctg tgtattactg tgcgagacac 300tggggaaact atgcttttga
tatctggggc caagggacca cggtcaccgt ctcgaga 357922333DNAHomo sapiens
922cagtctgtgt tgacgcagcc gccctcagcg tctgggaccc ccgggcagag
ggtcaccatc 60tcttgttctg gaagcagctc caacatcgga agtaattatg tatactggta
ccaacagctc 120ccaggaacgg cccccaaact cctcatctat agtaataatc
agcggccctc aggggtccct 180gaccgattct ctggctccaa gtctggcacc
tcagcctccc tggccatcag tgggctccgg 240tccgaggatg aggctgatta
ttactgtgca gcatgggatg acagcctgag tggtcaagtg 300ttcggaggag
gcacccagct gaccgtcctc ggt 333923360DNAHomo sapiens 923gaggtgcagc
tggtggagtc tggagctgag gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg
cttctggtta cacctttacc agctatggta tcagctgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggatgg atcagcgctt
acaatggtaa cacaaactat 180gcacagaagc tccagggcag agtcaccatg
accacagaca catccacgag cacagcctac 240atggagctga ggagcctgag
atctgacgac acggccgtgt attactgtgc gagagagaag 300tatagcagtg
gctggtactt tgactactgg ggccagggca ccctggtcac cgtctcgaga
360924330DNAHomo sapiens 924tcttctgagc tgactcagga ccctgctgtg
tctgtggcct tgggacagac agtcaggatc 60acatgccaag gagacagcct cagaagctat
tatgcaagct ggtaccagca gaagccagga 120caggcccctg tacttgtcat
ctatggtaaa aacaaccggc cctcagggat cccagaccga 180ttctctggct
ccagctcagg aaacacagct tccttgacca tcactggggc tcaggcggaa
240gatgaggctg actattactg taactcccgg gacagcagtg gtaaccatca
ttatgtcttc 300ggaactggga ccaaggtcac cgtcctaggt 330925345DNAHomo
sapiens 925gaggtgcagc tggtggagtc tgggggaggc ttggtacagc ctggggggtc
cctgagactc 60tcctgtgcag cctctggatt cacctttagc agctatgcca tgagctgggt
ccgccaggct 120ccagggaagg ggctggagtg ggtctcagct attagtggta
gtggtggtag cacatactac 180gcagactccg tgaagggccg gttcaccatc
tccagagaca attccaagaa cacgctgtat 240ctgcaaataa acagcctgag
agccgaggac acggccgtat attactgtgc gaaaggttct 300atagcagcgg
actggggcca gggaaccctg gtcaccgtct cgaga 345926324DNAHomo sapiens
926tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gtaacgtggt attcggcgga 300gggaccaagc
tgaccgtcct aggt 324927345DNAHomo sapiens 927gaggtgcagc tggtggagtc
tgggggaggc ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt
cacctttagc agctatgcca tgagctgggt ccgccaggct 120ccagggaagg
ggctggagtg ggtctcagct attagtggta gtggtggtag cacatactac
180gcagactccg tgaagggccg gttcaccatc tccagagaca attccaagaa
ctcactgtat 240ctgcaaatga acagcctgag agccgaggac acggctgtgt
attactgtgc gagtgagcag 300gctggggact actggggcca gggaaccctg
gtcaccgtct cgaga 345928333DNAHomo sapiens 928cagtctgtgt tgacgcagcc
gccctcagcg tctgggaccc ccgggcagag ggtcaccatc 60tcttgttctg gaagcagctc
caacatcgga agtaattatg tatactggta ccagcagctc 120ccaggaacgg
cccccaaact cctcatctat aggaataatc agcggccctc aggggtccct
180gaccgattcg ctggctccaa gtctggcacg tcagccaccc tgggcatcac
cggactccag 240actggggacg aggccgatta ttactgcgga acatgggata
gcagcctgag tgctggggta 300ttcggcggag ggaccaagct gaccgtccta ggt
333929357DNAHomo sapiens 929caggtgcagc tggtgcagtc tggggctgag
gtgaagaagc ctggggcctc agtgaaggtt 60tcctgcaagg catctggata caccttcacc
agctactata tgcactgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggaata atcaacccta gtggtggtag cacaagctac 180gcacagaagt
tccagggcag agtcaccatg accagggaca cgtccacgag cacagtctac
240atggagctga gcagcctgag atctgaggac acggccgtgt attactgtgc
gagagaattg 300tcggctgcta ctgcttttga tatctggggc caagggacaa
tggtcaccgt ctcgaga 357930321DNAHomo sapiens 930gaaacgacac
tcacgcagtc tccattttct gtgtctgcat ctgtaggaga cagagtcacc 60atcacttgtc
gggcgagtca gtatattagc agatggctag cctggtatca gcagagacca
120gggaaagccc ctaagctcct gatctatgct gcagccagtt tgcaaagtgg
ggtcccatca 180aggttcagcg gcagtggatc tgggacagat ttcactctca
ctatcagcag cctgcaacct 240gaagattttg caacttacta ttgccaacag
gctaacagtt tccccgtcac cttcggccaa 300gggacacgac tggagattaa a
321931360DNAHomo sapiens 931caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg cttctggtta cacctttacc
agctatggta tcagctgggt gcgacaggcc 120cctggacaag ggcttgagtg
gatgggatgg atcagcgctt acaatggtaa cacaaactat 180gcacagaagc
tccagggcag agtcaccatg accacagaca catccacgag cacagcctac
240atggagctga ggagcctgag atctgacgac acggccgtgt attactgtgc
gagagtaggt 300tattactact actacggtat ggacgtctgg ggccaaggga
ccacggtcac cgtctcgaga 360932333DNAHomo sapiens 932cagtctgccc
tgactcagcc tgcctccgtg tctgggtctc ctggacagtc gatcaccatc 60tcctgcactg
gaaccagcag tgatgttggg agttataacc ttgtctcctg gtaccaacag
120cacccaggca aagcccccaa actcatgatt tatgagggca gtaagcggcc
ctcaggggtt 180tctaatcgct tctctggctc caagtctggc aacacggcct
ccctgaccat ctctgggctc 240caggctgagg acgaggctga ttattactgc
agctcatata caagcagcag cacttgggtg 300ttcggcggag ggaccaagct
gaccgtccta ggt 333933354DNAHomo sapiens 933caggtgcagc tggtgcagtc
tggggctgag gtgaagaagc ctgggtcctc ggtgaaggtc 60tcctgcaagg cttctggagg
caccttcagc agctatgcta tcagctgggt gcgacaggcc 120cctggacaag
ggcttgagtg gatgggatgg atgaacccta acagtggtaa cacaggctat
180gcacagaagt tccagggcag agtcaccatg accaggaaca cctccataag
cacagcctac 240atggagctga gcagcctgag atctgaggac acggccgtgt
attactgtgc gagagacgtt 300gggattgggg tctttgacta ctggggccag
ggaaccctgg tcaccgtctc gaga 354934327DNAHomo sapiens 934tcctatgtgc
tgactcagcc accctcagtg tcagtggccc caggaaagac ggccaggatt 60acctgtgggg
gaaacaacat tggaagtaaa agtgtgcact ggtaccagca gaagccaggc
120caggcccctg tgctggtcat ctattatgat agcgaccggc cctcagggat
ccctgagcga 180ttctctggct ccaactctgg gaacacggcc accctgacca
tcagcagggt cgaagccggg 240gatgaggccg actattactg tcaggtgtgg
gatagtagta gtgatcatgt ggtattcggc 300ggagggacca agctgaccgt cctaggt
327935363DNAHomo sapiens 935gaggtgcagc tggtggagtc tgggggaggc
ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt cacctttagc
gactatgcca tgaactgggt ccgccaggct 120ccagggaagg ggctggagtg
ggtctcagct actagtggta gtggaggcag cacattctac 180gcagactccg
tgaagggccg gttcaccatc tccagagaca attccaagag tacgttgtat
240ctgcaaatga acagcctgag agacgaggac acggccgtgt attactgtgc
gaaagggacc 300ttaccgcatt actatgatag tagtggtata gggggccagg
gcaccctggt caccgtctcg 360agc 363936339DNAHomo sapiens 936caggctgtgc
tcactcagcc gtcttccgtg tctgggtctc ctggacagtc gatcaccatc 60tcctgcactg
gaaccagcag tgacgttggt ggttataact atgtctcctg gtaccaacag
120cacccaggca aagcccccaa actcatgatt tatgatgtcg gtaagcggcc
ctcaggggtt 180tctaatcgct tctctggctc caagtctggc aacacggcct
ccctgaccat ctctgggctc 240cgggctgagg acgaggctaa ttattactgc
agctcatata caagcagcag cacttggttt 300gtggtattcg gcggagggac
caagctgacc gtcctaggt 339937363DNAHomo sapiens 937caggtacagc
tgcagcagtc aggggctgag gtgaagaagc ctggggcctc agtgaaggtt 60tcctgcaagg
catctggata caccttcacc acctactata tgcactgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggaata atcaatccta gtggtgaaaa
tacaaactac 180gcacagaagt tccagggcag agtcaccatg accagggaca
catccacgac cacagtctac 240atggagctga gcagcctgag atctgaggac
acggccgtgt attactgtgc gagatctttc 300ataggaactc gtgggggcgg
tttggacgtc tggggccaag ggaccacggt caccgtctcg 360aga 363938339DNAHomo
sapiens 938cagtctgtgt tgacgcagcc gccctcagtg tctggggccc cagggcagag
ggtcaacatc 60tcctgcgctg ggagcagctc caacatcggg gcgggttatg atgttcactg
gtaccagcag 120attccaggaa cagcccccaa actcctcatg tatggtaata
gtaatcggcc ctcaggggtc 180cctgaccgat tctctggctc caagtctggc
gcctcagcct ccctggccat cactaggctc 240caggctgagg atgaggctga
ttattactgc cagtcctatg acagcagcct gagtggttcg 300agggtcttcg
gaactgggac caaggtcacc gtcctaggt 339939351DNAHomo sapiens
939gaggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc
cctgagactc 60tcctgtgcag cctctggatt cacctttgat gattatgcca tgcactgggt
ccggcaagct 120ccggggaagg gcctggagtg ggtctcaggt attagttgga
atagtggtag cataggctat 180gcggactctg tgaagggccg attcaccatc
tccagagaca acgccaagaa ctccctgtat 240ctgcaaatga acagtctgag
agctgaggac acggctgtgt attactgtgc gacggaagaa 300tggtggcgct
tcgatctctg gggccgtggc accctggtca ccgtctcgag a 351940333DNAHomo
sapiens 940cagtctgccc tgactcagcc tccctccgcg tccgggtctc ctggacagtc
agtcaccatc 60tcctgcactg gaaccagcag tgacgttgat gattacaact atgtctcctg
gtaccaacag 120cacccaggca aagcccccaa actcatgatt tatgaggtca
ctaagcggcc ctcaggggtc 180cctgatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240caggctgagg atgaggctga
ttattactgc agctcatatg tgggcagcga caatagagtc 300ttcggaactg
ggaccaaggt caccgtccca ggt 3339411897PRTHomo sapiens 941Met Val Pro
Leu Val Pro Ala Leu Val Met Leu Gly Leu Val Ala Gly1 5 10 15Ala His
Gly Asp Ser Lys Pro Val Phe Ile Lys Val Pro Glu Asp Gln 20 25 30Thr
Gly Leu Ser Gly Gly Val Ala Ser Phe Val Cys Gln Ala Thr Gly 35 40
45Glu Pro Lys Pro Arg Ile Thr Trp Met Lys Lys Gly Lys Lys Val Ser
50 55 60Ser Gln Arg Phe Glu Val Ile Glu Phe Asp Asp Gly Ala Gly Ser
Val65 70 75 80Leu Arg Ile Gln Pro Leu Arg Val Gln Arg Asp Glu Ala
Ile Tyr Glu 85 90 95Cys Thr Ala Thr Asn Ser Leu Gly Glu Ile Asn Thr
Ser Ala Lys Leu 100 105 110Ser Val Leu Glu Glu Glu Gln Leu Pro Pro
Gly Phe Pro Ser Ile Asp 115 120 125Met Gly Pro Gln Leu Lys Val Val
Glu Lys Ala Arg Thr Ala Thr Met 130 135 140Leu Cys Ala Ala Gly Gly
Asn Pro Asp Pro Glu Ile Ser Trp Phe Lys145 150 155 160Asp Phe Leu
Pro Val Asp Pro Ala Thr Ser Asn Gly Arg Ile Lys Gln 165 170 175Leu
Arg Ser Gly Ala Leu Gln Ile Glu Ser Ser Glu Glu Ser Asp Gln 180 185
190Gly Lys Tyr Glu Cys Val Ala Thr Asn Ser Ala Gly Thr Arg Tyr Ser
195 200 205Ala Pro Ala Asn Leu Tyr Val Arg Val Arg Arg Val Ala Pro
Arg Phe 210 215 220Ser Ile Pro Pro Ser Ser Gln Glu Val Met Pro Gly
Gly Ser Val Asn225 230 235 240Leu Thr Cys Val Ala Val Gly Ala Pro
Met Pro Tyr Val Lys Trp Met 245 250 255Met Gly Ala Glu Glu Leu Thr
Lys Glu Asp Glu Met Pro Val Gly Arg 260 265 270Asn Val Leu Glu Leu
Ser Asn Val Val Arg Ser Ala Asn Tyr Thr Cys 275 280 285Val Ala Ile
Ser Ser Leu Gly Met Ile Glu Ala Thr Ala Gln Val Thr 290 295 300Val
Lys Ala Leu Pro Lys Pro Pro Ile Asp Leu Val Val Thr Glu Thr305 310
315 320Thr Ala Thr Ser Val Thr Leu Thr Trp Asp Ser Gly Asn Ser Glu
Pro 325 330 335Val Thr Tyr Tyr Gly Ile Gln Tyr Arg Ala Ala Gly Thr
Glu Gly Pro 340 345 350Phe Gln Glu Val Asp Gly Val Ala Thr Thr Arg
Tyr Ser Ile Gly Gly 355 360 365Leu Ser Pro Phe Ser Glu Tyr Ala Phe
Arg Val Leu Ala Val Asn Ser 370 375 380Ile Gly Arg Gly Pro Pro Ser
Glu Ala Val Arg Ala Arg Thr Gly Glu385 390 395 400Gln Ala Pro Ser
Ser Pro Pro Arg Arg Val Gln Ala Arg Met Leu Ser 405 410 415Ala Ser
Thr Met Leu Val Gln Trp Glu Pro Pro Glu Glu Pro Asn Gly 420 425
430Leu Val Arg Gly Tyr Arg Val Tyr Tyr Thr Pro Asp Ser Arg Arg Pro
435 440 445Pro Asn Ala Trp His Lys His Asn Thr Asp Ala Gly Leu Leu
Thr Thr 450 455 460Val Gly Ser Leu Leu Pro Gly Ile Thr Tyr Ser Leu
Arg Val Leu Ala465 470 475 480Phe Thr Ala Val Gly Asp Gly Pro Pro
Ser Pro Thr Ile Gln Val Lys 485 490 495Thr Gln Gln Gly Val Pro Ala
Gln Pro Ala Asp Phe Gln Ala Glu Val 500 505 510Glu Ser Asp Thr Arg
Ile Gln Leu Ser Trp Leu Leu Pro Pro Gln Glu 515 520 525Arg Ile Ile
Met Tyr Glu Leu Val Tyr Trp Ala Ala Glu Asp Glu Asp 530 535 540Gln
Gln His Lys Val Thr Phe Asp Pro Thr Ser Ser Tyr Thr Leu Glu545 550
555 560Asp Leu Lys Pro Asp Thr Leu Tyr Arg Phe Gln Leu Ala Ala Arg
Ser 565 570 575Asp Met Gly Val Gly Val Phe Thr Pro Thr Ile Glu Ala
Arg Thr Ala 580 585 590Gln Ser Thr Pro Ser Ala Pro Pro Gln Lys Val
Met Cys Val Ser Met 595 600 605Gly Ser Thr Thr Val Arg Val Ser Trp
Val Pro Pro Pro Ala Asp Ser 610 615 620Arg Asn Gly Val Ile Thr Gln
Tyr Ser Val Ala His Glu Ala Val Asp625 630 635 640Gly Glu Asp Arg
Gly Arg His Val Val Asp Gly Ile Ser Arg Glu His 645 650 655Ser Ser
Trp Asp Leu Val Gly Leu Glu Lys Trp Thr Glu Tyr Arg Val 660 665
670Trp Val Arg Ala His Thr Asp Val Gly Pro Gly Pro Glu Ser Ser Pro
675 680 685Val Leu Val Arg Thr Asp Glu Asp Val Pro Ser Gly Pro Pro
Arg Lys 690 695 700Val Glu Val Glu Pro Leu Asn Ser Thr Ala Val His
Val Tyr Trp Lys705 710 715 720Leu Pro Val Pro Ser Lys Gln His Gly
Gln Ile Arg Gly Tyr Gln Val 725 730 735Thr Tyr Val Arg Leu Glu Asn
Gly Glu Pro Arg Gly Leu Pro Ile Ile 740 745 750Gln Asp Val Met Leu
Ala Glu Ala Gln Trp Arg Pro Glu Glu Ser Glu 755 760 765Asp Tyr Glu
Thr Thr Ile Ser Gly Leu Thr Pro Glu Thr Thr Tyr Ser 770 775 780Val
Thr Val Ala Ala Tyr Thr Thr Lys Gly Asp Gly Ala Arg Ser Lys785 790
795 800Pro Lys Ile Val Thr Thr Thr Gly Ala Val Pro Gly Arg Pro Thr
Met 805 810 815Met Ile Ser Thr Thr Ala Met Asn Thr Ala Leu Leu Gln
Trp His Pro 820 825 830Pro Lys Glu Leu Pro Gly Glu Leu Leu Gly Tyr
Arg Leu Gln Tyr Cys 835 840 845Arg Ala Asp Glu Ala Arg Pro Asn Thr
Ile Asp Phe Gly Lys Asp Asp 850 855 860Gln His Phe Thr Val Thr Gly
Leu His Lys Gly Thr Thr Tyr Ile Phe865 870 875 880Arg Leu Ala Ala
Lys Asn Arg Ala Gly Leu Gly Glu Glu Phe Glu Lys 885 890 895Glu Ile
Arg Thr Pro Glu Asp Leu Pro Ser Gly Phe Pro Gln Asn Leu 900 905
910His Val Thr Gly Leu Thr Thr Ser Thr Thr Glu Leu Ala Trp Asp Pro
915 920 925Pro Val Leu Ala Glu Arg Asn Gly Arg Ile Ile Ser Tyr Thr
Val Val 930 935 940Phe Arg Asp Ile Asn Ser Gln Gln Glu Leu Gln Asn
Ile Thr Thr Asp945 950 955 960Thr Arg Phe Thr Leu Thr Gly Leu Lys
Pro Asp Thr Thr Tyr Asp Ile 965 970 975Lys Val Arg Ala Trp Thr Ser
Lys Gly Ser Gly Pro Leu Ser Pro Ser 980 985 990Ile Gln Ser Arg Thr
Met Pro Val Glu Gln Val Phe Ala Lys Asn Phe 995 1000 1005Arg Val
Ala Ala Ala Met Lys Thr Ser Val Leu Leu Ser Trp Glu 1010 1015
1020Val Pro Asp Ser Tyr Lys Ser Ala Val Pro Phe Lys Ile Leu Tyr
1025 1030 1035Asn Gly Gln Ser Val Glu Val Asp Gly His Ser Met Arg
Lys Leu 1040 1045 1050Ile Ala Asp Leu Gln Pro Asn Thr Glu Tyr Ser
Phe Val Leu Met 1055 1060 1065Asn Arg Gly Ser Ser Ala Gly Gly Leu
Gln His Leu Val Ser Ile 1070 1075 1080Arg Thr Ala Pro Asp Leu Leu
Pro His Lys Pro Leu Pro Ala Ser 1085 1090 1095Ala Tyr Ile Glu Asp
Gly Arg Phe Asp Leu Ser Met Pro His Val 1100 1105 1110Gln Asp Pro
Ser Leu Val Arg Trp Phe Tyr Ile Val Val Val Pro 1115 1120 1125Ile
Asp Arg Val Gly Gly Ser Met Leu Thr Pro Arg Trp Ser Thr 1130 1135
1140Pro Glu Glu Leu Glu Leu Asp Glu Leu Leu Glu Ala Ile Glu Gln
1145 1150 1155Gly Gly Glu Glu Gln Arg Arg Arg Arg Arg Gln Ala Glu
Arg Leu 1160 1165 1170Lys Pro Tyr Val Ala Ala Gln Leu Asp Val Leu
Pro Glu Thr Phe 1175 1180 1185Thr Leu Gly Asp Lys Lys Asn Tyr Arg
Gly Phe Tyr Asn Arg Pro 1190 1195 1200Leu Ser Pro Asp Leu Ser Tyr
Gln Cys Phe Val Leu Ala Ser Leu 1205 1210 1215Lys Glu Pro Met Asp
Gln Lys Arg Tyr Ala Ser Ser Pro Tyr Ser 1220 1225 1230Asp Glu Ile
Val Val Gln Val Thr Pro Ala Gln Gln Gln Glu Glu 1235 1240 1245Pro
Glu Met Leu Trp Val Thr Gly Pro Val Leu Ala Val Ile Leu 1250 1255
1260Ile Ile Leu Ile Val Ile Ala Ile Leu Leu Phe Lys Arg Lys Arg
1265 1270 1275Thr His Ser Pro Ser Ser Lys Asp Glu Gln Ser Ile Gly
Leu Lys 1280 1285 1290Asp Ser Leu Leu Ala His Ser Ser Asp Pro Val
Glu Met Arg Arg 1295 1300 1305Leu Asn Tyr Gln Thr Pro Gly Met Arg
Asp His Pro Pro Ile Pro 1310 1315 1320Ile Thr Asp Leu Ala Asp Asn
Ile Glu Arg Leu Lys Ala Asn Asp
1325 1330 1335Gly Leu Lys Phe Ser Gln Glu Tyr Glu Ser Ile Asp Pro
Gly Gln 1340 1345 1350Gln Phe Thr Trp Glu Asn Ser Asn Leu Glu Val
Asn Lys Pro Lys 1355 1360 1365Asn Arg Tyr Ala Asn Val Ile Ala Tyr
Asp His Ser Arg Val Ile 1370 1375 1380Leu Thr Ser Ile Asp Gly Val
Pro Gly Ser Asp Tyr Ile Asn Ala 1385 1390 1395Asn Tyr Ile Asp Gly
Tyr Arg Lys Gln Asn Ala Tyr Ile Ala Thr 1400 1405 1410Gln Gly Pro
Leu Pro Glu Thr Met Gly Asp Phe Trp Arg Met Val 1415 1420 1425Trp
Glu Gln Arg Thr Ala Thr Val Val Met Met Thr Arg Leu Glu 1430 1435
1440Glu Lys Ser Arg Val Lys Cys Asp Gln Tyr Trp Pro Ala Arg Gly
1445 1450 1455Thr Glu Thr Cys Gly Leu Ile Gln Val Thr Leu Leu Asp
Thr Val 1460 1465 1470Glu Leu Ala Thr Tyr Thr Val Arg Thr Phe Ala
Leu His Lys Ser 1475 1480 1485Gly Ser Ser Glu Lys Arg Glu Leu Arg
Gln Phe Gln Phe Met Ala 1490 1495 1500Trp Pro Asp His Gly Val Pro
Glu Tyr Pro Thr Pro Ile Leu Ala 1505 1510 1515Phe Leu Arg Arg Val
Lys Ala Cys Asn Pro Leu Asp Ala Gly Pro 1520 1525 1530Met Val Val
His Cys Ser Ala Gly Val Gly Arg Thr Gly Cys Phe 1535 1540 1545Ile
Val Ile Asp Ala Met Leu Glu Arg Met Lys His Glu Lys Thr 1550 1555
1560Val Asp Ile Tyr Gly His Val Thr Cys Met Arg Ser Gln Arg Asn
1565 1570 1575Tyr Met Val Gln Thr Glu Asp Gln Tyr Val Phe Ile His
Glu Ala 1580 1585 1590Leu Leu Glu Ala Ala Thr Cys Gly His Thr Glu
Val Pro Ala Arg 1595 1600 1605Asn Leu Tyr Ala His Ile Gln Lys Leu
Gly Gln Val Pro Pro Gly 1610 1615 1620Glu Ser Val Thr Ala Met Glu
Leu Glu Phe Lys Leu Leu Ala Ser 1625 1630 1635Ser Lys Ala His Thr
Ser Arg Phe Ile Ser Ala Asn Leu Pro Cys 1640 1645 1650Asn Lys Phe
Lys Asn Arg Leu Val Asn Ile Met Pro Tyr Glu Leu 1655 1660 1665Thr
Arg Val Cys Leu Gln Pro Ile Arg Gly Val Glu Gly Ser Asp 1670 1675
1680Tyr Ile Asn Ala Ser Phe Leu Asp Gly Tyr Arg Gln Gln Lys Ala
1685 1690 1695Tyr Ile Ala Thr Gln Gly Pro Leu Ala Glu Ser Thr Glu
Asp Phe 1700 1705 1710Trp Arg Met Leu Trp Glu His Asn Ser Thr Ile
Ile Val Met Leu 1715 1720 1725Thr Lys Leu Arg Glu Met Gly Arg Glu
Lys Cys His Gln Tyr Trp 1730 1735 1740Pro Ala Glu Arg Ser Ala Arg
Tyr Gln Tyr Phe Val Val Asp Pro 1745 1750 1755Met Ala Glu Tyr Asn
Met Pro Gln Tyr Ile Leu Arg Glu Phe Lys 1760 1765 1770Val Thr Asp
Ala Arg Asp Gly Gln Ser Arg Thr Ile Arg Gln Phe 1775 1780 1785Gln
Phe Thr Asp Trp Pro Glu Gln Gly Val Pro Lys Thr Gly Glu 1790 1795
1800Gly Phe Ile Asp Phe Ile Gly Gln Val His Lys Thr Lys Glu Gln
1805 1810 1815Phe Gly Gln Asp Gly Pro Ile Thr Val His Cys Ser Ala
Gly Val 1820 1825 1830Gly Arg Thr Gly Val Phe Ile Thr Leu Ser Ile
Val Leu Glu Arg 1835 1840 1845Met Arg Tyr Glu Gly Val Val Asp Met
Phe Gln Thr Val Lys Thr 1850 1855 1860Leu Arg Thr Gln Arg Pro Ala
Met Val Gln Thr Glu Asp Gln Tyr 1865 1870 1875Gln Leu Cys Tyr Arg
Ala Ala Leu Glu Tyr Leu Gly Ser Phe Asp 1880 1885 1890His Tyr Ala
Thr 1895942628PRTHomo sapiens 942Met Glu Pro Pro Asp Ala Pro Ala
Gln Ala Arg Gly Ala Pro Arg Leu1 5 10 15Leu Leu Leu Ala Val Leu Leu
Ala Ala His Pro Asp Ala Gln Ala Glu 20 25 30Val Arg Leu Ser Val Pro
Pro Leu Val Glu Val Met Arg Gly Lys Ser 35 40 45Val Ile Leu Asp Cys
Thr Pro Thr Gly Thr His Asp His Tyr Met Leu 50 55 60Glu Trp Phe Leu
Thr Asp Arg Ser Gly Ala Arg Pro Arg Leu Ala Ser65 70 75 80Ala Glu
Met Gln Gly Ser Glu Leu Gln Val Thr Met His Asp Thr Arg 85 90 95Gly
Arg Ser Pro Pro Tyr Gln Leu Asp Ser Gln Gly Arg Leu Val Leu 100 105
110Ala Glu Ala Gln Val Gly Asp Glu Arg Asp Tyr Val Cys Val Val Arg
115 120 125Ala Gly Ala Ala Gly Thr Ala Glu Ala Thr Ala Arg Leu Asn
Val Phe 130 135 140Ala Lys Pro Glu Ala Thr Glu Val Ser Pro Asn Lys
Gly Thr Leu Ser145 150 155 160Val Met Glu Asp Ser Ala Gln Glu Ile
Ala Thr Cys Asn Ser Arg Asn 165 170 175Gly Asn Pro Ala Pro Lys Ile
Thr Trp Tyr Arg Asn Gly Gln Arg Leu 180 185 190Glu Val Pro Val Glu
Met Asn Pro Glu Gly Tyr Met Thr Ser Arg Thr 195 200 205Val Arg Glu
Ala Ser Gly Leu Leu Ser Leu Thr Ser Thr Leu Tyr Leu 210 215 220Arg
Leu Arg Lys Asp Asp Arg Asp Ala Ser Phe His Cys Ala Ala His225 230
235 240Tyr Ser Leu Pro Glu Gly Arg His Gly Arg Leu Asp Ser Pro Thr
Phe 245 250 255His Leu Thr Leu His Tyr Pro Thr Glu His Val Gln Phe
Trp Val Gly 260 265 270Ser Pro Ser Thr Pro Ala Gly Trp Val Arg Glu
Gly Asp Thr Val Gln 275 280 285Leu Leu Cys Arg Gly Asp Gly Ser Pro
Ser Pro Glu Tyr Thr Leu Phe 290 295 300Arg Leu Gln Asp Glu Gln Glu
Glu Val Leu Asn Val Asn Leu Glu Gly305 310 315 320Asn Leu Thr Leu
Glu Gly Val Thr Arg Gly Gln Ser Gly Thr Tyr Gly 325 330 335Cys Arg
Val Glu Asp Tyr Asp Ala Ala Asp Asp Val Gln Leu Ser Lys 340 345
350Thr Leu Glu Leu Arg Val Ala Tyr Leu Asp Pro Leu Glu Leu Ser Glu
355 360 365Gly Lys Val Leu Ser Leu Pro Leu Asn Ser Ser Ala Val Val
Asn Cys 370 375 380Ser Val His Gly Leu Pro Thr Pro Ala Leu Arg Trp
Thr Lys Asp Ser385 390 395 400Thr Pro Leu Gly Asp Gly Pro Met Leu
Ser Leu Ser Ser Ile Thr Phe 405 410 415Asp Ser Asn Gly Thr Tyr Val
Cys Glu Ala Ser Leu Pro Thr Val Pro 420 425 430Val Leu Ser Arg Thr
Gln Asn Phe Thr Leu Leu Val Gln Gly Ser Pro 435 440 445Glu Leu Lys
Thr Ala Glu Ile Glu Pro Lys Ala Asp Gly Ser Trp Arg 450 455 460Glu
Gly Asp Glu Val Thr Leu Ile Cys Ser Ala Arg Gly His Pro Asp465 470
475 480Pro Lys Leu Ser Trp Ser Gln Leu Gly Gly Ser Pro Ala Glu Pro
Ile 485 490 495Pro Gly Arg Gln Gly Trp Val Ser Ser Ser Leu Thr Leu
Lys Val Thr 500 505 510Ser Ala Leu Ser Arg Asp Gly Ile Ser Cys Glu
Ala Ser Asn Pro His 515 520 525Gly Asn Lys Arg His Val Phe His Phe
Gly Thr Val Ser Pro Gln Thr 530 535 540Ser Gln Ala Gly Val Ala Val
Met Ala Val Ala Val Ser Val Gly Leu545 550 555 560Leu Leu Leu Val
Val Ala Val Phe Tyr Cys Val Arg Arg Lys Gly Gly 565 570 575Pro Cys
Cys Arg Gln Arg Arg Glu Lys Gly Ala Pro Pro Pro Gly Glu 580 585
590Pro Gly Leu Ser His Ser Gly Ser Glu Gln Pro Glu Gln Thr Gly Leu
595 600 605Leu Met Gly Gly Ala Ser Gly Gly Ala Arg Gly Gly Ser Gly
Gly Phe 610 615 620Gly Asp Glu Cys625943621PRTHomo sapiens 943Leu
Glu Glu Lys Lys Val Cys Gln Gly Thr Ser Asn Lys Leu Thr Gln1 5 10
15Leu Gly Thr Phe Glu Asp His Phe Leu Ser Leu Gln Arg Met Phe Asn
20 25 30Asn Cys Glu Val Val Leu Gly Asn Leu Glu Ile Thr Tyr Val Gln
Arg 35 40 45Asn Tyr Asp Leu Ser Phe Leu Lys Thr Ile Gln Glu Val Ala
Gly Tyr 50 55 60Val Leu Ile Ala Leu Asn Thr Val Glu Arg Ile Pro Leu
Glu Asn Leu65 70 75 80Gln Ile Ile Arg Gly Asn Met Tyr Tyr Glu Asn
Ser Tyr Ala Leu Ala 85 90 95Val Leu Ser Asn Tyr Asp Ala Asn Lys Thr
Gly Leu Lys Glu Leu Pro 100 105 110Met Arg Asn Leu Gln Glu Ile Leu
His Gly Ala Val Arg Phe Ser Asn 115 120 125Asn Pro Ala Leu Cys Asn
Val Glu Ser Ile Gln Trp Arg Asp Ile Val 130 135 140Ser Ser Asp Phe
Leu Ser Asn Met Ser Met Asp Phe Gln Asn His Leu145 150 155 160Gly
Ser Cys Gln Lys Cys Asp Pro Ser Cys Pro Asn Gly Ser Cys Trp 165 170
175Gly Ala Gly Glu Glu Asn Cys Gln Lys Leu Thr Lys Ile Ile Cys Ala
180 185 190Gln Gln Cys Ser Gly Arg Cys Arg Gly Lys Ser Pro Ser Asp
Cys Cys 195 200 205His Asn Gln Cys Ala Ala Gly Cys Thr Gly Pro Arg
Glu Ser Asp Cys 210 215 220Leu Val Cys Arg Lys Phe Arg Asp Glu Ala
Thr Cys Lys Asp Thr Cys225 230 235 240Pro Pro Leu Met Leu Tyr Asn
Pro Thr Thr Tyr Gln Met Asp Val Asn 245 250 255Pro Glu Gly Lys Tyr
Ser Phe Gly Ala Thr Cys Val Lys Lys Cys Pro 260 265 270Arg Asn Tyr
Val Val Thr Asp His Gly Ser Cys Val Arg Ala Cys Gly 275 280 285Ala
Asp Ser Tyr Glu Met Glu Glu Asp Gly Val Arg Lys Cys Lys Lys 290 295
300Cys Glu Gly Pro Cys Arg Lys Val Cys Asn Gly Ile Gly Ile Gly
Glu305 310 315 320Phe Lys Asp Ser Leu Ser Ile Asn Ala Thr Asn Ile
Lys His Phe Lys 325 330 335Asn Cys Thr Ser Ile Ser Gly Asp Leu His
Ile Leu Pro Val Ala Phe 340 345 350Arg Gly Asp Ser Phe Thr His Thr
Pro Pro Leu Asp Pro Gln Glu Leu 355 360 365Asp Ile Leu Lys Thr Val
Lys Glu Ile Thr Gly Phe Leu Leu Ile Gln 370 375 380Ala Trp Pro Glu
Asn Arg Thr Asp Leu His Ala Phe Glu Asn Leu Glu385 390 395 400Ile
Ile Arg Gly Arg Thr Lys Gln His Gly Gln Phe Ser Leu Ala Val 405 410
415Val Ser Leu Asn Ile Thr Ser Leu Gly Leu Arg Ser Leu Lys Glu Ile
420 425 430Ser Asp Gly Asp Val Ile Ile Ser Gly Asn Lys Asn Leu Cys
Tyr Ala 435 440 445Asn Thr Ile Asn Trp Lys Lys Leu Phe Gly Thr Ser
Gly Gln Lys Thr 450 455 460Lys Ile Ile Ser Asn Arg Gly Glu Asn Ser
Cys Lys Ala Thr Gly Gln465 470 475 480Val Cys His Ala Leu Cys Ser
Pro Glu Gly Cys Trp Gly Pro Glu Pro 485 490 495Arg Asp Cys Val Ser
Cys Arg Asn Val Ser Arg Gly Arg Glu Cys Val 500 505 510Asp Lys Cys
Asn Leu Leu Glu Gly Glu Pro Arg Glu Phe Val Glu Asn 515 520 525Ser
Glu Cys Ile Gln Cys His Pro Glu Cys Leu Pro Gln Ala Met Asn 530 535
540Ile Thr Cys Thr Gly Arg Gly Pro Asp Asn Cys Ile Gln Cys Ala
His545 550 555 560Tyr Ile Asp Gly Pro His Cys Val Lys Thr Cys Pro
Ala Gly Val Met 565 570 575Gly Glu Asn Asn Thr Leu Val Trp Lys Tyr
Ala Asp Ala Gly His Val 580 585 590Cys His Leu Cys His Pro Asn Cys
Thr Tyr Gly Cys Thr Gly Pro Gly 595 600 605Leu Glu Gly Cys Pro Thr
Asn Gly Pro Lys Ile Pro Ser 610 615 620944123PRTHomo sapiens 944Gln
Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala1 5 10
15Ser Val Lys Val Ser Cys Lys Val Ser Gly Tyr Thr Leu Thr Glu Leu
20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp
Met 35 40 45Gly Gly Phe Asp Pro Glu Asp Gly Glu Thr Ile Tyr Ala Gln
Lys Phe 50 55 60Gln Gly Arg Val Thr Met Thr Glu Asp Thr Ser Thr Asp
Thr Ala Tyr65 70 75 80Met Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr
Ala Val Tyr Tyr Cys 85 90 95Ala Thr Asp Leu Asp Tyr Tyr Gly Ser Gly
Ser Tyr Ala Phe Asp Ile 100 105 110Trp Gly Gln Gly Thr Thr Val Thr
Val Ser Arg 115 120945111PRTHomo sapiens 945Gln Ser Ala Leu Thr Gln
Pro Ala Ser Val Ser Gly Ser Pro Gly Gln1 5 10 15Ser Ile Thr Ile Ser
Cys Thr Gly Thr Ser Ser Asp Val Gly Ser Tyr20 25 30Asn Leu Val Ser
Trp Tyr Gln Gln His Pro Gly Lys Ala Pro Lys Leu35 40 45Met Ile Tyr
Glu Gly Ser Lys Arg Pro Ser Gly Val Ser Asn Arg Phe50 55 60Ser Gly
Ser Lys Ser Gly Asn Thr Ala Ser Leu Thr Ile Ser Gly Leu65 70 75
80Gln Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Ser Ser Tyr Thr Ser Ser
85 90 95Ser Thr Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly
100 105 110946123PRTHomo sapiens 946Gln Val Gln Leu Gln Gln Trp Gly
Ala Gly Leu Leu Lys Pro Ser Glu1 5 10 15Thr Leu Ser Leu Thr Cys Ala
Ala Tyr Gly Gly Ser Phe Ser Gly Tyr 20 25 30Tyr Trp Ser Trp Ile Arg
Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile 35 40 45Gly Glu Ile Asn His
Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu Lys 50 55 60Ser Arg Val Thr
Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu65 70 75 80Lys Leu
Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95Arg
Thr Tyr Tyr Gly Ser Gly Ser Tyr Gln Tyr Asn Trp Phe Asp Pro 100 105
110Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115 120947112PRTHomo
sapiens 947Gln Ser Val Leu Thr Gln Pro Pro Ser Val Ser Gly Ala Pro
Gly Gln1 5 10 15Arg Val Thr Ile Ser Cys Thr Gly Ser Ser Ser Asn Ile
Gly Ala Gly 20 25 30Tyr Asp Val His Trp Tyr Gln Gln Leu Pro Gly Thr
Ala Pro Lys Leu 35 40 45Leu Ile Tyr Gly Asn Ser Asn Arg Pro Ser Gly
Val Pro Asp Arg Phe 50 55 60Ser Gly Ser Lys Ser Gly Thr Ser Ala Ser
Leu Ala Ile Thr Gly Leu65 70 75 80Gln Ala Glu Asp Glu Ala Asp Tyr
Tyr Cys Gln Ser Tyr Asp Ser Ser 85 90 95Leu Ser Gly Val Val Phe Gly
Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105 110948117PRTHomo
sapiens 948Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro
Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe
Ser Ser Tyr 20 25 30Ser Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly
Leu Glu Trp Val 35 40 45Ser Tyr Ile Ser Ser Ser Ser Ser Thr Ile Tyr
Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn
Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Asp
Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Asp Asn Leu Glu Gly
Leu Asp Tyr Trp Gly Gln Gly Thr Leu 100 105 110Val Thr Val Ser Arg
115949109PRTHomo sapiens 949Ser Tyr Val Leu Thr Gln Pro Pro Ser Val
Ser Val Ala Pro Gly Lys1 5 10 15Thr Ala Arg Ile Thr Cys Gly Gly Asn
Asn Ile Gly Ser Lys Ser Val 20 25 30His Trp Tyr Gln Gln Lys Pro Gly
Gln Ala Pro Val Leu Val Ile Tyr 35 40
45Tyr Asp Ser Asp Arg Pro Ser Gly Ile Pro Glu Arg Phe Ser Gly Ser
50 55 60Asn Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Arg Val Glu Ala
Gly65 70 75 80Asp Glu Ala Asp Tyr Tyr Cys Gln Val Trp Asp Ser Ser
Ser Asp His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu
Gly 100 105950120PRTHomo sapiens 950Gln Val Gln Leu Gln Glu Ser Gly
Pro Gly Leu Val Lys Pro Ser Gln1 5 10 15Thr Leu Ser Leu Thr Cys Thr
Val Ser Gly Gly Ser Ile Ser Ser Gly 20 25 30Asp Tyr Tyr Trp Ser Trp
Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu 35 40 45Trp Ile Gly Tyr Ile
Tyr Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser 50 55 60Leu Lys Ser Arg
Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe65 70 75 80Ser Leu
Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr 85 90 95Cys
Ala Arg Gly Thr Gly Asp Leu Glu Trp Phe Asp Pro Trp Gly Gln 100 105
110Gly Thr Leu Val Thr Val Ser Arg 115 120951111PRTHomo sapiens
951Gln Ser Val Leu Thr Gln Pro Pro Ser Val Ser Gly Ala Pro Arg Gln1
5 10 15Thr Val Thr Ile Ser Cys Ser Gly Ser Ser Ser Asn Ile Gly Gln
Asn 20 25 30Ser Val Thr Trp Tyr Gln Arg Leu Pro Gly Glu Ala Pro Lys
Leu Leu 35 40 45Ile Tyr Tyr Asp Asp Leu Leu His Ser Gly Val Ser Asp
Arg Phe Ser 50 55 60Gly Ser Lys Ser Gly Thr Ser Ala Ser Leu Ala Ile
Ser Gly Leu Gln65 70 75 80Ser Glu Asp Glu Ala Glu Tyr Tyr Cys Ala
Ser Trp Asp Asp Ser Leu 85 90 95Lys Gly Pro Val Phe Gly Gly Gly Thr
Lys Leu Thr Val Leu Gly 100 105 110952121PRTHomo sapiens 952Glu Val
Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser
Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25
30Ser Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45Ser Tyr Ile Ser Ser Ser Ser Ser Thr Ile Tyr Tyr Ala Asp Ser
Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser
Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Asp Glu Asp Thr Ala
Val Tyr Tyr Cys 85 90 95Ala Arg Glu Gly Pro Arg Gly Ser Tyr Tyr Tyr
Phe Asp Tyr Trp Gly 100 105 110Gln Gly Thr Leu Val Thr Val Ser Arg
115 120953111PRTHomo sapiens 953Asn Phe Met Leu Thr Gln Pro His Ser
Val Ser Glu Ser Pro Gly Lys1 5 10 15Thr Val Thr Ile Ser Cys Thr Arg
Ser Ser Gly Ser Ile Ala Ser Asn 20 25 30Tyr Val Gln Trp Tyr Gln Gln
Arg Pro Gly Ser Ala Pro Thr Thr Val 35 40 45Ile Tyr Glu Asp Asn Gln
Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60Gly Ser Ile Asp Ser
Ser Ser Asn Ser Ala Ser Leu Thr Ile Ser Gly65 70 75 80Leu Lys Thr
Glu Asp Glu Ala Asp Tyr Tyr Cys Gln Ser Tyr Asp Ser 85 90 95Ser Asn
Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100 105
110954119PRTHomo sapiens 954Gln Val Gln Leu Val Gln Ser Gly Ala Glu
Val Lys Lys Pro Gly Ala1 5 10 15Ser Val Lys Val Ser Cys Lys Ala Ser
Gly Tyr Thr Phe Thr Ser Tyr 20 25 30Tyr Met His Trp Val Arg Gln Ala
Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Ile Ile Asn Pro Ser Gly
Gly Ser Thr Ser Tyr Ala Gln Lys Phe 50 55 60Gln Gly Arg Val Thr Met
Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr65 70 75 80Met Glu Leu Ser
Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Ala
Lys Arg Arg Gly Ser Ala Phe Asp Ile Trp Gly Gln Gly 100 105 110Thr
Thr Val Thr Val Ser Arg 115955109PRTHomo sapiens 955Ser Ser Glu Leu
Thr Gln Asp Pro Ala Val Ser Val Ala Leu Gly Gln1 5 10 15Thr Val Arg
Ile Thr Cys Gln Gly Asp Ser Leu Arg Ser Tyr Tyr Ala 20 25 30Ser Trp
Tyr Gln Gln Lys Pro Gly Gln Ala Pro Val Leu Val Ile Tyr 35 40 45Gly
Lys Asn Asn Arg Pro Ser Gly Ile Pro Asp Arg Phe Ser Gly Ser 50 55
60Ser Ser Gly Asn Thr Ala Ser Leu Thr Ile Thr Gly Ala Gln Ala Glu65
70 75 80Asp Glu Ala Asp Tyr Tyr Cys Asn Ser Arg Asp Ser Ser Gly Asn
His 85 90 95Val Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu Gly 100
105956369DNAHomo sapiens 956caggtgcagc tggtgcagtc tggagctgag
gtgaagaagc ctggggcctc agtgaaggtc 60tcctgcaagg tttccggata caccctcact
gaattatcca tgcactgggt gcgacaggct 120cctggaaaag ggcttgagtg
gatgggaggt tttgatcctg aagatggtga aacaatctac 180gcacagaagt
tccagggcag agtcaccatg accgaggaca catctacaga cacagcctac
240atggagctga gcagcctgag atctgaggac acggccgtgt attactgtgc
aacagatctc 300gattactatg gttcggggag ttatgctttt gatatctggg
gccaagggac cacggtcacc 360gtctcgaga 369957333DNAHomo sapiens
957cagtctgccc tgactcagcc tgcctccgtg tctgggtctc ctggacagtc
gatcaccatc 60tcctgcactg gaaccagcag tgatgttggg agttataacc ttgtctcctg
gtaccaacag 120cacccaggca aagcccccaa actcatgatt tatgagggca
gtaagcggcc ctcaggggtt 180tctaatcgct tctctggctc caagtctggc
aacacggcct ccctgaccat ctctgggctc 240caggctgagg acgaggctga
ttattactgc agctcatata caagcagcag cacttgggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333958369DNAHomo sapiens 958caggtgcagc
tacagcagtg gggcgcagga ctgttgaagc cttcggagac cctgtccctc 60acctgcgctg
cctatggtgg gtccttcagt ggttactact ggagctggat ccgccagccc
120ccagggaagg ggctggagtg gattggggaa atcaatcata gtggaagcac
caactacaac 180ccgtccctca agagtcgagt caccatatca gtagacacgt
ccaagaacca gttctccctg 240aagctgagct ctgtgaccgc cgcggacacg
gctgtgtatt actgtgcgag gacttactat 300ggttcgggga gttatcagta
caactggttc gacccctggg gccagggaac cctggtcacc 360gtctcgaga
369959336DNAHomo sapiens 959cagtctgtgt tgacgcagcc gccctcagtg
tctggggccc cagggcagag ggtcaccatc 60tcctgcactg ggagcagctc caacatcggg
gcaggttatg atgtacactg gtaccagcag 120cttccaggaa cagcccccaa
actcctcatc tatggtaaca gcaatcggcc ctcaggggtc 180cctgaccgat
tctctggctc caagtctggc acctcagcct ccttggccat cactgggctc
240caggctgagg atgaggctga ttattactgc cagtcctatg acagcagcct
gagtggtgtg 300gtattcggcg gagggaccaa gctgaccgtc ctaggt
336960351DNAHomo sapiens 960gaggtgcagc tggtggagtc tgggggaggc
ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt caccttcagt
agctatagca tgaactgggt ccgccaggct 120ccagggaagg ggctggagtg
ggtttcatat attagtagta gtagtagtac catatactac 180gcagactctg
tgaagggccg attcaccatc tccagagaca atgccaagaa ctcactgtat
240ctgcaaatga acagcctgag agacgaggac acggctgtgt attactgtgc
gagagataat 300cttgaaggcc tggactactg gggccaggga accctggtca
ccgtctcgag a 351961327DNAHomo sapiens 961tcctatgtgc tgactcagcc
accctcagtg tcagtggccc caggaaagac ggccaggatt 60acctgtgggg gaaacaacat
tggaagtaaa agtgtgcact ggtaccagca gaagccaggc 120caggcccctg
tgctggtcat ctattatgat agcgaccggc cctcagggat ccctgagcga
180ttctctggct ccaactctgg gaacacggcc accctgacca tcagcagggt
cgaagccggg 240gatgaggccg actattactg tcaggtgtgg gatagtagta
gtgatcatgt ggtattcggc 300ggagggacca agctgaccgt cctaggt
327962360DNAHomo sapiens 962caggtgcagc tgcaggagtc gggcccagga
ctggtgaagc cttcacagac cctgtccctc 60acctgcactg tctctggtgg ctccatcagc
agtggtgatt actactggag ttggatccgc 120cagcccccag ggaagggcct
ggagtggatt gggtacatct attacagtgg gagcacctac 180tacaacccgt
ccctcaagag tcgagttacc atatcagtag acacgtccaa gaaccagttc
240tccctgaagc tgagctctgt gactgccgca gacacggccg tgtattactg
tgccagaggg 300actggggatc ttgagtggtt cgacccctgg ggccagggca
ccctggtcac cgtctcgaga 360963333DNAHomo sapiens 963cagtctgtgt
tgacgcagcc gccctcggtg tctggggccc cccggcagac ggtcaccatc 60tcctgctctg
ggagcagctc caacatcgga caaaattctg ttacctggta ccagcgcctc
120ccgggtgagg ctcccaaact cctcatctac tatgatgatc tcttgcactc
aggagtctct 180gaccgattct ctggctccaa gtctggcacc tcagcctcac
tggccatcag tggactccag 240tctgaggatg aggctgagta ctactgtgcg
tcatgggatg acagcctgaa aggtccggta 300ttcggcggag ggaccaaact
gaccgtccta ggt 333964363DNAHomo sapiens 964gaggtgcagc tggtggagtc
tgggggaggc ttggtacagc ctggggggtc cctgagactc 60tcctgtgcag cctctggatt
caccttcagt agctatagca tgaactgggt ccgccaggct 120ccagggaagg
ggctggagtg ggtttcatac attagtagta gtagtagtac catatactac
180gcagactctg tgaagggccg attcaccatc tccagagaca atgccaagaa
ctcactgtat 240ctgcaaatga acagcctgag agacgaggac acggctgtgt
attactgtgc gagagagggc 300ccaaggggga gctactacta ctttgactac
tggggccagg gaaccctggt caccgtctcg 360aga 363965333DNAHomo sapiens
965aattttatgc tgactcagcc gcactctgtg tcggagtctc cggggaagac
ggtaaccatc 60tcctgcaccc gcagcagtgg cagcattgcc agcaactatg tgcagtggta
ccagcagcgc 120ccgggcagtg cccccaccac tgtgatctat gaggataacc
aaagaccctc tggggtccct 180gatcggttct ctggctccat cgacagctcc
tccaactctg cctccctcac catctctgga 240ctgaagactg aggacgaggc
tgactactac tgtcagtctt atgatagcag caattgggtg 300ttcggcggag
ggaccaagct gaccgtccta ggt 333966357DNAHomo sapiens 966caggtgcagc
tggtgcagtc tggggctgag gtgaagaagc ctggggcctc agtgaaggtt 60tcctgcaagg
catctggata caccttcacc agctactata tgcactgggt gcgacaggcc
120cctggacaag ggcttgagtg gatgggaata atcaacccta gtggtggtag
cacaagctac 180gcacagaagt tccagggcag agtcaccatg accagggaca
cgtccacgag cacagtctac 240atggagctga gcagcctgag atctgaggac
acggccgtgt attactgtgc gagagcgaag 300agaaggggat ctgcttttga
tatctggggc caagggacca cggtcaccgt ctcgaga 357967327DNAHomo sapiens
967tcttctgagc tgactcagga ccctgctgtg tctgtggcct tgggacagac
agtcaggatc 60acatgccaag gagacagcct cagaagctat tatgcaagct ggtaccagca
gaagccagga 120caggcccctg tacttgtcat ctatggtaaa aacaaccggc
cctcagggat cccagaccga 180ttctctggct ccagctcagg aaacacagct
tccttgacca tcactggggc tcaggcggaa 240gatgaggctg actattactg
taactcccgg gacagcagtg gtaaccatgt ggtattcggc 300ggagggacca
agctgaccgt cctaggt 327968124PRTHomo sapiens 968Gln Val Gln Leu Val
Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ser1 5 10 15Ser Val Lys Val
Ser Cys Arg Ala Ser Gly Gly Thr Phe Ser Ser Tyr 20 25 30Ala Ile Ser
Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45Gly Gly
Ile Ile Pro Ile Phe Gly Thr Ala Asn Tyr Ala Gln Lys Phe 50 55 60Gln
Gly Arg Val Thr Ile Thr Ala Asp Lys Ser Thr Ser Thr Ala Tyr65 70 75
80Met Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95Ala Gly Asp Ile Ser Arg Gly Ser Ser Trp Tyr Gly Tyr Tyr Phe
Asp 100 105 110Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Arg 115
120969106PRTHomo sapiens 969Asp Ile Gln Met Thr Gln Ser Pro Ser Thr
Leu Ala Ala Ser Val Gly1 5 10 15Asp Arg Val Thr Ile Thr Cys Arg Ala
Ser Gln Ser Ile Ser Ser Trp 20 25 30Leu Ala Trp Tyr Gln Gln Lys Pro
Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45Tyr Lys Ala Ser Ser Leu Glu
Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60Ser Gly Ser Gly Thr Glu
Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro65 70 75 80Asp Asp Phe Ala
Thr Tyr Tyr Cys Gln Gln Tyr Asn Ser Tyr Ser Thr 85 90 95Phe Gly Gln
Gly Thr Lys Leu Glu Ile Lys 100 105970372DNAHomo sapiens
970caggtgcagc tggtgcagtc tggggctgag gtgaagaagc ctgggtcctc
ggtgaaggtc 60tcctgcaggg cttctggagg caccttcagc agctatgcta tcagctgggt
gcgacaggcc 120cctggacaag ggcttgagtg gatgggaggg atcatcccta
tctttggtac agcaaactac 180gcacagaagt tccagggcag agtcacgatt
accgcggaca aatccacgag cacagcctac 240atggagctga gcagcctgag
atctgaggac acggccgtgt attactgtgc gggagatatc 300agccgaggca
gcagctggta cgggtactac tttgactact ggggccaggg aaccctggtc
360accgtctcga ga 372971318DNAHomo sapiens 971gacatccaga tgacccagtc
tccttccacc ctggctgcat ctgtaggaga cagagtcacc 60atcacttgcc gggccagtca
gagtattagt agctggttgg cctggtatca gcagaaacca 120gggaaagccc
ctaagctcct gatctataag gcgtctagtt tagaaagtgg ggtcccatca
180aggttcagcg gcagtggatc tgggacagaa ttcactctca ccatcagcag
cctgcagcct 240gatgattttg caacttatta ctgccaacag tataatagtt
attccacttt tggccagggg 300accaagctgg agatcaaa 318
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