U.S. patent application number 14/606568 was filed with the patent office on 2015-12-10 for modified factor viii.
This patent application is currently assigned to Emory University. The applicant listed for this patent is Emory University. Invention is credited to John S. Lollar.
Application Number | 20150352190 14/606568 |
Document ID | / |
Family ID | 46326333 |
Filed Date | 2015-12-10 |
United States Patent
Application |
20150352190 |
Kind Code |
A1 |
Lollar; John S. |
December 10, 2015 |
Modified Factor VIII
Abstract
Methods of treating patients with Factor VIII deficiency by
administration of modified porcine factor VIII are disclosed. The
particular modified porcine factor VIII is one in which most of the
B domain has been removed through genetic engineering. This
modified factor VIII is particularly useful for treatment of
hemophiliacs, especially those undergoing bleeding episodes.
Inventors: |
Lollar; John S.; (Decatur,
GA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Emory University |
Atlanta |
GA |
US |
|
|
Assignee: |
Emory University
Atlanta
GA
|
Family ID: |
46326333 |
Appl. No.: |
14/606568 |
Filed: |
January 27, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13431085 |
Mar 27, 2012 |
8951515 |
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14606568 |
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12491734 |
Jun 25, 2009 |
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13431085 |
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11550366 |
Oct 17, 2006 |
7560107 |
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12491734 |
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10938414 |
Sep 10, 2004 |
7122634 |
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11550366 |
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10187319 |
Jun 28, 2002 |
7012132 |
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10938414 |
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09523656 |
Mar 10, 2000 |
6458563 |
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10187319 |
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09037601 |
Mar 10, 1998 |
6180371 |
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09523656 |
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08670707 |
Jun 26, 1996 |
5859204 |
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09037601 |
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PCT/US97/11155 |
Jun 26, 1997 |
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08670707 |
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Current U.S.
Class: |
424/93.2 ;
514/14.1 |
Current CPC
Class: |
A61P 7/04 20180101; C07K
2319/00 20130101; A61K 9/0019 20130101; A61K 48/00 20130101; A61K
38/37 20130101; C07K 14/755 20130101 |
International
Class: |
A61K 38/37 20060101
A61K038/37; A61K 9/00 20060101 A61K009/00 |
Goverment Interests
ACKNOWLEDGMENT OF FEDERAL RESEARCH SUPPORT
[0002] The government has rights in this invention arising from
National Institutes of Health Grant Nos. HL40921, HL46215, and
HL36094 that partially funded the research leading to this
invention.
Claims
1. A method for treating a patient having factor VIII deficiency
comprising administering a composition comprising a therapeutically
effective amount of a modified porcine factor Vlll protein that
comprises the sequence of amino acids from position 1 through
position 1448 of SEQ ID NO:49.
2. The method according to claim 1, wherein the patient having
factor VIII deficiency has inhibitory antibodies to human factor
VIII.
3. The method according to claim 1, wherein the patient having
factor VIII deficiency suffers from uncontrolled bleeding.
4. The method according to claim 3, wherein the uncontrolled
bleeding is selected from intra-articular, intracranial, and
gastrointestinal hemorrhage.
5. A method for treating a patient having factor VIII deficiency
comprising administering a therapeutically effective amount of a
modified porcine factor Vlll protein, wherein the modified porcine
factor VIII protein is an expression product of the DNA sequence
set forth in SEQ ID NO:48, expressed in a mammalian host cell.
6. The method according to claim 5, wherein the modified porcine
factor Vlll is prepared from the supernatant of cultured mammalian
host cells containing and expressing the DNA sequence set forth in
SEQ ID NO:48.
7. The method according to claim 1, wherein the modified porcine
factor VIII protein consists of the sequence of amino acids 1 to
1448 of SEQ ID NO:49.
8. The method according to claim 1, wherein the composition further
comprises a physiologically acceptable carrier.
9. The method according to claim 8, wherein the composition further
comprises a stabilizer and a delivery vehicle.
10. The method according to claim 1, wherein the composition is
infused intravenously.
11. The method according to claim 1, wherein the patient is an
acquired hemophilia patient or a congenital hemophilia patient.
12. A method of treating a patient having factor VIII deficiency
comprising the step of administering a composition comprising an
effective amount of a modified porcine factor VIII protein, a
human-animal hybrid factor VIII protein or a hybrid equivalent
factor VIII protein.
13. The method according to claim 12, wherein the hybrid equivalent
factor VIII protein is the expression product of SEQ ID NO:38.
14. The method according to claim 12, wherein the hybrid
human-animal factor VIII protein is a human-porcine hybrid factor
VIII protein.
15. A method of treating a patient having factor VIII deficiency
comprising the step of administering a retrovirus modified to
contain and express a hybrid factor VIII protein or a hybrid
equivalent factor VIII protein, wherein said retrovirus does not
produce virus in said patient.
16. The method according to claim 15, wherein the patient is an
acquired hemophilia patient or a congenital hemophilia patient.
17. The method according to claim 13, wherein said hybrid factor
VIII protein or a hybrid equivalent factor VIII protein is the
expression product of SEQ ID NO:37 or SEQ ID NO:48.
18. The method according to claim 13, wherein the patient having
factor VIII deficiency has inhibitory antibodies to human factor
VIII.
19. The method according to claim 12, wherein the patient having
factor VIII deficiency suffers from uncontrolled bleeding.
20. The method according to claim 12, wherein the uncontrolled
bleeding is selected from intra-articular, intracranial, and
gastrointestinal hemorrhage.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 13/431,085, filed Mar. 27, 2012, which is a
continuation of U.S. patent application Ser. No. 12/491,734, filed
Jun. 25, 2009, now abandoned, which is a continuation of U.S.
patent application Ser. No. 11/550,366, filed Oct. 17, 2006, now
U.S. Pat. No. 7,560,107, which is a continuation-in-part of U.S.
patent application Ser. No. 10/938,414, filed Sep. 10, 2004, now
U.S. Pat. No. 7,122,634; which is divisional application of U.S.
patent application Ser. No. 10/187,319 filed Jun. 28, 2002, now
U.S. Pat. No. 7,012,132, which is a continuation-in-part of U.S.
patent application Ser. No. 09/523,656 filed Mar. 10, 2000, now
U.S. Pat. No. 6,458,563; which is a continuation-in-part of U.S.
patent application Ser. No. 09/037,601 filed Mar. 10, 1998, which
issued as U.S. Pat. No. 6,180,371; which is a continuation-in-part
of U.S. patent application Ser. No. 08/670,707 filed Jun. 26, 1996,
which issued as U.S. Pat. No. 5,859,204; and of International
Patent Application No. PCT/US97/11155 filed Jun. 26, 1997. All of
the foregoing priority applications are incorporated herein by
reference to the extent there is no inconsistency with the present
disclosure.
SEQUENCE LISTING
[0003] The Sequence Listing is incorporated by reference
herein.
BACKGROUND OF THE INVENTION
[0004] This invention relates generally to a hybrid factor VIII
having human and animal factor VIII amino acid sequence or having
human factor VIII and non-factor VIII amino acid sequence and
methods of preparation and use thereof.
[0005] Blood clotting begins when platelets adhere to the cut wall
of an injured blood vessel at a lesion site. Subsequently, in a
cascade of enzymatically regulated reactions, soluble fibrinogen
molecules are converted by the enzyme thrombin to insoluble strands
of fibrin that hold the platelets together in a thrombus. At each
step in the cascade, a protein precursor is converted to a protease
that cleaves the next protein precursor in the series. Cofactors
are required at most of the steps.
[0006] Factor VIII circulates as an inactive precursor in blood,
bound tightly and non-covalently to von Willebrand factor. Factor
VIII is proteolytically activated by thrombin or factor Xa, which
dissociates it from von Willebrand factor and activates its
procoagulant function in the cascade. In its active form, the
protein factor VIIIa is a cofactor that increases the catalytic
efficiency of factor IXa toward factor X activation by several
orders of magnitude.
[0007] People with deficiencies in factor VIII or antibodies
against factor VIII who are not treated with factor VIII suffer
uncontrolled internal bleeding that may cause a range of serious
symptoms, from inflammatory reactions in joints to early death.
Severe hemophiliacs, who number about 10,000 in the United States,
can be treated with infusion of human factor VIII, which will
restore the blood's normal clotting ability if administered with
sufficient frequency and concentration. The classic definition of
factor VIII, in fact, is that substance present in normal blood
plasma that corrects the clotting defect in plasma derived from
individuals with hemophilia A.
[0008] The development of antibodies ("inhibitors" or "inhibitory
antibodies") that inhibit the activity of factor VIII is a serious
complication in the management of patients with hemophilia.
Autoantibodies develop in approximately 20% of patients with
hemophilia A in response to therapeutic infusions of factor VIII.
In previously untreated patients with hemophilia A who develop
inhibitors, the inhibitor usually develops within one year of
treatment. Additionally, autoantibodies that inactivate factor VIII
occasionally develop in individuals with previously normal factor
VIII levels. If the inhibitor titer is low enough, patients can be
managed by increasing the dose of factor VIII. However, often the
inhibitor titer is so high that it cannot be overwhelmed by factor
VIII. An alternative strategy is to bypass the need for factor VIII
during normal hemo stasis using factor IX complex preparations (for
example, KONYNE.TM., Proplex.TM.) or recombinant human factor
VIIIa. Additionally, since porcine factor VIII usually has
substantially less reactivity with inhibitors than human factor
VIII, a partially purified porcine factor VIII preparation
(HYATE:C.sup.7) is used. Many patients who have developed
inhibitory antibodies to human factor VIII have been successfully
treated with porcine factor VIII and have tolerated such treatment
for long periods of time. However, administration of porcine factor
VIII is not a complete solution because inhibitors may develop to
porcine factor VIII after one or more infusions.
[0009] Several preparations of human plasma-derived factor VIII of
varying degrees of purity are available commercially for the
treatment of hemophilia A. These include a partially-purified
factor VIII derived from the pooled blood of many donors that is
heat- and detergent-treated for viruses but contain a significant
level of antigenic proteins; a monoclonal antibody-purified factor
VIII that has lower levels of antigenic impurities and viral
contamination; and recombinant human factor VIII, clinical trials
for which are underway. Unfortunately, human factor VIII is
unstable at physiologic concentrations and pH, is present in blood
at an extremely low concentration (0.2 .mu.g/ml plasma), and has
low specific clotting activity.
[0010] Hemophiliacs require daily replacement of factor VIII to
prevent bleeding and the resulting deforming hemophilic
arthropathy. However, supplies have been inadequate and problems in
therapeutic use occur due to difficulty in isolation and
purification, immunogenicity, and the necessity of removing the
AIDS and hepatitis infectivity risk. The use of recombinant human
factor VIII or partially-purified porcine factor VIII will not
resolve all the problems.
[0011] The problems associated with the commonly used, commercially
available, plasma-derived factor VIII have stimulated significant
interest in the development of a better factor VIII product. There
is a need for a more potent factor VIII molecule so that more units
of clotting activity can be delivered per molecule; a factor VIII
molecule that is stable at a selected pH and physiologic
concentration; a factor VIII molecule that is less apt to cause
production of inhibitory antibodies; and a factor VIII molecule
that evades immune detection in patients who have already acquired
antibodies to human factor VIII.
[0012] It is therefore an object of the present invention to
provide a factor VIII that corrects hemophilia in a patient
deficient in factor VIII or having inhibitors to factor VIII.
[0013] It is a further object of the present invention to provide
methods for treatment of hemophiliacs.
[0014] It is still another object of the present invention to
provide a factor VIII that is stable at a selected pH and
physiologic concentration.
[0015] It is yet another object of the present invention to provide
a factor VIII that has greater coagulant activity than human factor
VIII.
[0016] It is an additional object of the present invention to
provide a factor VIII against which less antibody is produced.
SUMMARY OF THE INVENTION
[0017] The present invention provides isolated, purified, hybrid
factor VIII molecules and fragments thereof with coagulant activity
including hybrid factor VIII having factor VIII amino acid sequence
derived from human and pig or other non-human mammal (together
referred to herein as "animal"); or in a second embodiment
including a hybrid equivalent factor VIII having factor VIII amino
acid sequence derived from human or animal or both and amino acid
sequence having no known sequence identity to factor VIII
("non-factor VIII amino acid sequence"), preferably substituted in
an antigenic and/or immunogenic region of the factor VIII, is
described. One skilled in the art will realize that numerous hybrid
factor VIII constructs can be prepared including, but not limited
to, human/animal factor VIII having greater coagulant activity than
human factor VIII ("superior coagulant activity"); non-immunogenic
human/equivalent factor VIII; non-antigenic human/equivalent or
human/animal factor VIII; non-immunogenic human/animal or
human/equivalent factor VIII having superior coagulant activity;
non-antigenic human/animal or human/animal/equivalent factor VIII
having superior coagulant activity; non-immunogenic, non-antigenic
human/equivalent or human/equivalent/animal factor VIII; and
non-immunogenic, non-antigenic human/animal/equivalent factor VIII
having superior coagulant activity.
[0018] The hybrid factor VIII molecule is produced by isolation and
recombination of human and animal factor VIII subunits or domains;
or by genetic engineering of the human and animal factor VIII
genes.
[0019] In a preferred embodiment, recombinant DNA methods are used
to substitute elements of animal factor VIII for the corresponding
elements of human factor VIII, resulting in hybrid human/animal
factor VIII molecules. In a second preferred embodiment,
recombinant DNA methods are used to replace one or more amino acids
in the human or animal factor VIII or in a hybrid human/animal
factor VIII with amino acids that have no known sequence identity
to factor VIII, preferably a sequence of amino acids that has less
immunoreactivity with naturally occurring inhibitory antibodies to
factor VIII ("nonantigenic amino acid sequence") and/or is less apt
to elicit the production of antibodies to factor VIII
("non-immunogenic amino acid sequence") than human factor VIII. An
example of an amino acid sequence that can be used to replace
immunogenic or antigenic sequence is a sequence of alanine
residues.
[0020] In another embodiment, subunits of factor VIII are isolated
and purified from human or animal plasma, and hybrid human/animal
factor VIII is produced either by mixture of animal heavy chain
subunits with human light chain subunits or by mixture of human
heavy chain subunits with animal light chain subunits, thereby
producing human light chain/animal heavy chain and human heavy
chain/animal light chain hybrid molecules. These hybrid molecules
are isolated by ion exchange chromatography.
[0021] Alternatively, one or more domains or partial domains of
factor VIII are isolated and purified from human or animal plasma,
and hybrid human/animal factor VIII is produced by mixture of
domains or partial domains from one species with domains or partial
domains of the second species. Hybrid molecules can be isolated by
ion exchange chromatography.
[0022] Methods for preparing highly purified hybrid factor VIII are
described having the steps of: (a) isolation of subunits of
plasma-derived human factor VIII and subunits of plasma-derived
animal factor VIII, followed by reconstitution of coagulant
activity by mixture of human and animal subunits, followed by
isolation of hybrid human/animal factor VIII by ion exchange
chromatography; (b) isolation of domains or partial domains of
plasma-derived human factor VIII and domains or partial domains of
plasma-derived animal factor VIII, followed by reconstitution of
coagulant activity by mixture of human and animal domains, followed
by isolation of hybrid human/animal factor VIII by ion exchange
chromatography; (c) construction of domains or partial domains of
animal factor VIII by recombinant DNA technology, and recombinant
exchange of domains of animal and human factor VIII to produce
hybrid human/animal factor VIII with coagulant activity; (d)
creation of hybrid human/animal factor VIII by replacement of
specific amino acid residues of the factor VIII of one species with
the corresponding unique amino acid residues of the factor VIII of
the other species; or (e) creation of a hybrid equivalent factor
VIII molecule having human or animal amino acid sequence or both,
in which specific amino acid residues of the factor VIII are
replaced with amino acid residues having no known sequence identity
to factor VIII by site-directed mutagenesis. A preferred factor
VIII is POL1212, which is derived from porcine factor VIII and
lacks most of the B-domain.
[0023] The determination of the entire DNA sequence encoding
porcine factor VIII has enabled the synthesis of full-length
porcine factor VIII by expressing the DNA encoding porcine factor
VIII in a suitable host cell. Purified recombinant porcine factor
VIII is therefore an aspect of the present invention. The DNA
encoding each domain of porcine factor VIII as well as any
specified fragment thereof, can be similarly expressed, either by
itself or in combination with DNA encoding human factor VIII to
make the hybrid human/porcine factor VIII described herein.
Furthermore, porcine fVIII having all or part of the B domain
deleted (B-domainless or substantially B-domainless porcine fVIII)
is made available as part of the present invention, by expression
DNA encoding porcine fVIII having a deletion of one or more codons
of the B-domain.
[0024] Some embodiments of hybrid or hybrid equivalent factor VIII
have specific activity greater than that of human factor VIII and
equal to or greater than that of porcine factor VIII. Some
embodiments of hybrid or hybrid equivalent factor VIII have equal
or less immunoreactivity with inhibitory antibodies to factor VIII
and/or less immunogenicity in humans or animals, compared to human
or porcine factor VIII.
[0025] Also provided are pharmaceutical compositions and methods
for treating patients having factor VIII deficiency comprising
administering the hybrid or hybrid equivalent factor VIII,
especially the POL1212 protein, the amino acid sequence of the
protein after the removal of the signal peptide is provided herein
as SEQ ID NO:49.
[0026] A specific, preferred embodiment of the present invention is
a substantially B-domainless porcine factor VIII protein, called
POL1212 or OBI-1. See SEQ ID NOs:48 and 49. Also within the scope
of the present invention are pharmaceutical compositions comprising
the OBI-1 protein, and optionally a lyoprotectant and/or a
pharmaceutically acceptable carrier or excipient.
BRIEF DESCRIPTION OF THE DRAWINGS
[0027] FIGS. 1A-1H taken together provide an aligned sequence
comparison of the human, pig and mouse factor VIII amino acid
sequences. FIG. 1A compares signal peptide regions (human, SEQ ID
NO:40; porcine, SEQ ID NO:37, amino acids 1-19; murine, SEQ ID
NO:6, amino acids 1-19). Note that the amino acids in FIGS. 1A-1H
are numbered at the first Alanine of the mature protein as number
1, with amino acids of the signal peptide assigned negative
numbers. The Human fVIII sequence in SEQ ID NO:2 also begins with
the first Alanine of the mature protein as amino acid number 1. In
the amino acid sequences of mouse fVIII (SEQ ID NO:6) and porcine
fVIII (SEQ ID No:37), the first amino acid (alanine) of the mature
sequence is amino acid number 20. FIGS. 1A-1H show an alignment of
the corresponding sequences of human, mouse and pig fVIII, such
that the regions of greatest amino acid identity are juxtaposed.
The amino acid numbers in FIGS. 1A-1H apply to human fVIII only.
FIG. 1B gives the amino acid sequences for the A1 domain of human
(SEQ ID NO:2, amino acids 1-372), porcine (SEQ ID NO:37, amino
acids 20-391), and murine (SEQ ID NO:6, amino acids 20-391). FIG.
1C provides amino acid sequences for the factor VIII A2 domains
from human (SEQ ID NO:2, amino acids 373-740), pig (SEQ ID NO:37,
amino acids 392-759) and mouse (SEQ ID NO:6, amino acids 392-759).
FIGS. 1D and 1D-1 provide the amino acid sequences of B domains of
human factor VIII (SEQ ID NO:2, amino acids 741-1648), pig (SEQ ID
NO:37, amino acids 760-1449) and mouse (SEQ ID NO:6, amino acids
760-1640). FIG. 1E compares the amino acid sequences of factor VIII
light chain activation peptides of human, pig and mouse (SEQ ID
NO:2, amino acids 1649-1689; SEQ ID NO:37, amino acids 1450-1490;
and SEQ ID NO:6, amino acids 1641-1678, respectively). FIG. 1F
provides the sequence comparison for human, pig and mouse factor
VIII A3 domains (SEQ ID NO:2, amino acids 1690-2019; SEQ ID NO:37,
amino acids 1491-1820; and SEQ ID NO:6, amino acids 1679-2006,
respectively. FIG. 1G provides the amino acid sequences of the
factor VIII C1 domains of human, pig and mouse (SEQ ID NO:2, amino
acids 2020-2172; SEQ ID NO:37, amino acids 1821-1973; and SEQ ID
NO:6, amino acids 2007-2159, respectively). FIG. 1H provides
sequence data for the C2 domains of the factor VIII C2 domains of
human, pig and mouse (SEQ ID NO:2, amino acids 2173-2332; SEQ ID
NO:37, amino acids 1974-2133; and SEQ ID NO:6, amino acids
2160-2319, respectively).
DETAILED DESCRIPTION OF THE INVENTION
[0028] Unless otherwise specified or indicated, as used herein,
"factor VIII" denotes any functional factor VIII protein molecule
from any animal, any hybrid factor VIII or modified factor VIII,
"hybrid factor VIII" or "hybrid protein" denotes any functional
factor VIII protein molecule or fragment thereof comprising factor
VIII amino acid sequence from human, porcine, and/or non-human,
non-porcine mammalian species. Such combinations include, but are
not limited to, any or all of the following hybrid factor VIII
molecules or fragments thereof: (1) human/porcine; (2)
human/non-human, non-porcine mammalian, such as human/mouse; (3)
porcine/non-human, non-porcine mammalian, such as mouse/dog. Such
combinations also include hybrid factor VIII equivalent molecules
or fragments thereof, as further defined below, comprising factor
VIII amino acid sequence of hybrid, human, porcine, or non-human,
non-porcine mammalian origin in which amino acid sequence having no
known sequence identity to factor VIII is substituted. Such hybrid
combinations also include hybrid factor VIII amino sequence derived
from more than two species, such as human/pig/mouse, or from two or
more species in which amino acid sequence having no known sequence
identity to factor VIII is substituted. Unless otherwise indicated,
"hybrid factor VIII" includes fragments of the hybrid factor VIII,
which can be used, as described below in one exemplary embodiment,
as probes for research purposes or as diagnostic reagents.
[0029] As used herein, "mammalian factor VIII" includes factor VIII
with amino acid sequence derived from any non-human mammal, unless
otherwise specified. "Animal", as used herein, refers to pig and
other non-human mammals.
[0030] A "fusion protein" or "fusion factor VIII or fragment
thereof", as used herein, is the product of a hybrid gene in which
the coding sequence for one protein is extensively altered, for
example, by fusing part of it to the coding sequence for a second
protein from a different gene to produce a hybrid gene that encodes
the fusion protein. As used herein, a fusion protein is a subset of
the hybrid factor VIII protein described in this application.
[0031] A "corresponding" nucleic acid or amino acid or sequence of
either, as used herein, is one present at a site in a factor VIII
or hybrid factor VIII molecule or fragment thereof that has the
same structure and/or function as a site in the factor VIII
molecule of another species, although the nucleic acid or amino
acid number may not be identical. A sequence "corresponding to"
another factor VIII sequence substantially corresponds to such
sequence, and hybridizes to the sequence of the designated SEQ ID
NO. under stringent conditions. A sequence "corresponding to"
another factor VIII sequence also includes a sequence that results
in the expression of a factor VIII or claimed procoagulant hybrid
factor VIII or fragment thereof and would hybridize to a nucleic
molecule of the designated SEQ ID NO. but for the redundancy of the
genetic code.
[0032] A "unique" amino acid residue or sequence, as used herein,
refers to an amino acid sequence or residue in the factor VIII
molecule of one species that is different from the homologous
residue or sequence in the factor VIII molecule of another
species.
[0033] "Specific activity," as used herein, refers to the activity
that will correct the coagulation defect of human factor
VIII-deficient plasma. Specific activity is measured in units of
clotting activity per milligram total factor VIII protein in a
standard assay in which the clotting time of human factor VIII
deficient plasma is compared to that of normal human plasma. One
unit of factor VIII activity is the activity present in one
milliliter of normal human plasma. In the assay, the shorter the
time for clot formation, the greater the activity of the factor
VIII being assayed. Hybrid human/porcine factor VIII has
coagulation activity in a human factor VIII assay. This activity,
as well as that of other hybrid or hybrid equivalent factor VIII
molecules or fragments thereof, may be less than, equal to, or
greater than that of either plasma-derived or recombinant human
factor VIII.
[0034] The human factor VIII cDNA nucleotide and predicted amino
acid sequences are shown in SEQ ID NOs:1 and 2, respectively.
Factor VIII is synthesized as an approximately 300 kDa single chain
protein with internal sequence homology that defines the "domain"
sequence NH.sub.2-A1-A2-B-A3-C1-C2-COOH. In a factor VIII molecule,
a "domain", as used herein, is a continuous sequence of amino acids
that is defined by internal amino acid sequence identity and sites
of proteolytic cleavage by thrombin. Unless otherwise specified,
factor VIII domains include the following amino acid residues, when
the sequences are aligned with the human amino acid sequence (SEQ
ID NO:2): A1, residues Alal-Arg372; A2, residues Ser373-Arg740; B,
residues Ser741-Arg1648; A3, residues Ser1690-Ile2032; C1, residues
Arg2033-Asn2172; C2, residues Ser2173-Tyr2332. The A3-C1-C2
sequence includes residues Ser1690-Tyr2332. The remaining sequence,
residues Glu1649-Arg1689, is usually referred to as the factor VIII
light chain activation peptide. Factor VIII is proteolytically
activated by thrombin or factor Xa, which dissociates it from von
Willebrand factor, forming factor VIIIa, which has procoagulant
function. The biological function of factor VIIIa is to increase
the catalytic efficiency of factor IXa toward factor X activation
by several orders of magnitude. Thrombin-activated factor VIIIa is
a 160 kDa A1/A2/A3-C1-C2 heterotrimer that forms a complex with
factor IXa and factor X on the surface of platelets or monocytes. A
"partial domain" as used herein is a continuous sequence of amino
acids forming part of a domain.
[0035] "Subunits" of human or animal factor VIII, as used herein,
are the heavy and light chains of the protein. The heavy chain of
factor VIII contains three domains, A1, A2, and B. The light chain
of factor VIII also contains three domains, A3, C1, and C2.
[0036] The hybrid factor VIII or fragment thereof can be made (1)
by substitution of isolated, plasma-derived animal subunits or
human subunits (heavy or light chains) for corresponding human
subunits or animal subunits; (2) by substitution of human domains
or animal domains (A1, A2, A3, B, C1, and C2) for corresponding
animal domains or human domains; (3) by substitution of parts of
human domains or animal domains for parts of animal domains or
human domains; (4) by substitution of at least one specific
sequence including one or more unique human or animal amino acid(s)
for the corresponding animal or human amino acid(s); or (5) by
substitution of amino acid sequence that has no known sequence
identity to factor VIII for at least one sequence including one or
more specific amino acid residue(s) in human, animal, or hybrid
factor VIII or fragments thereof. A "B-domainless" hybrid factor
VIII, hybrid equivalent factor VIII, or fragment of either, as used
herein, refers to any one of the hybrid factor VIII constructs
described herein that lacks the B domain.
[0037] The terms "epitope", "antigenic site", and "antigenic
determinant", as used herein, are used synonymously and are defined
as a portion of the human, animal, hybrid, or hybrid equivalent
factor VIII or fragment thereof that is specifically recognized by
an antibody. It can consist of any number of amino acid residues,
and it can be dependent upon the primary, secondary, or tertiary
structure of the protein. In accordance with this disclosure, a
hybrid factor VIII, hybrid factor VIII equivalent, or fragment of
either that includes at least one epitope may be used as a reagent
in the diagnostic assays described below. In some embodiments, the
hybrid or hybrid equivalent factor VIII or fragment thereof is not
cross-reactive or is less cross-reactive with all naturally
occurring inhibitory factor VIII antibodies than human or porcine
factor VIII.
[0038] The term "immunogenic site", as used herein, is defined as a
region of the human or animal factor VIII, hybrid or hybrid
equivalent factor VIII, or fragment thereof that specifically
elicits the production of antibody to the factor VIII, hybrid,
hybrid equivalent, or fragment in a human or animal, as measured by
routine protocols, such as immunoassay, e.g. ELISA, or the Bethesda
assay, described herein. It can consist of any number of amino acid
residues, and it can be dependent upon the primary, secondary, or
tertiary structure of the protein. In some embodiments, the hybrid
or hybrid equivalent factor VIII or fragment thereof is
nonimmunogenic or less immunogenic in an animal or human than human
or porcine factor VIII.
[0039] As used herein, a "hybrid factor VIII equivalent molecule or
fragment thereof" or "hybrid equivalent factor VIII or fragment
thereof" is an active factor VIII or hybrid factor VIII molecule or
fragment thereof comprising at least one sequence including one or
more amino acid residues that have no known identity to human or
animal factor VIII sequence substituted for at least one sequence
including one or more specific amino acid residues in the human,
animal, or hybrid factor VIII or fragment thereof. The sequence of
one or more amino acid residues that have no known identity to
human or animal factor VIII sequence is also referred to herein as
"non-factor VIII amino acid sequence". In a preferred embodiment,
the amino acid(s) having no known sequence identity to factor VIII
sequence are alanine residues. In another preferred embodiment, the
specific factor VIII sequence for which the amino acid(s) having no
known sequence identity to factor VIII sequence are substituted
includes an antigenic site that is immunoreactive with naturally
occurring factor VIII inhibitory antibodies, such that the
resulting hybrid factor VIII equivalent molecule or fragment
thereof is less immunoreactive or not immunoreactive with factor
VIII inhibitory antibodies. In yet another preferred embodiment,
the specific hybrid factor VIII sequence for which the amino
acid(s) having no known sequence identity to factor VIII sequence
are substituted includes an immunogenic site that elicits the
formation of factor VIII inhibitory antibodies in an animal or
human, such that the resulting hybrid factor VIII equivalent
molecule or fragment thereof is less immunogenic.
[0040] "Factor VIII deficiency," as used herein, includes
deficiency in clotting activity caused by production of defective
factor VIII, by inadequate or no production of factor VIII, or by
partial or total inhibition of factor VIII by inhibitors.
Hemophilia A is a type of factor VIII deficiency resulting from a
defect in an X-linked gene and the absence or deficiency of the
factor VIII protein it encodes.
[0041] As used herein, "diagnostic assays" include assays that in
some manner utilize the antigen-antibody interaction to detect
and/or quantify the amount of a particular antibody that is present
in a test sample to assist in the selection of medical therapies.
There are many such assays known to those of skill in the art. As
used herein, however, the hybrid or hybrid equivalent factor VIII
DNA or fragment thereof and protein expressed therefrom, in whole
or in part, can be substituted for the corresponding reagents in
the otherwise known assays, whereby the modified assays may be used
to detect and/or quantify antibodies to factor VIII. It is the use
of these reagents, the hybrid or hybrid equivalent factor VIII DNA
or fragment thereof or protein expressed therefrom, that permits
modification of known assays for detection of antibodies to human
or animal factor VIII or to hybrid human/animal factor VIII. Such
assays include, but are not limited to ELISAs, immunodiffusion
assays, and immunoblots. Suitable methods for practicing any of
these assays are known to those of skill in the art. As used
herein, the hybrid or hybrid equivalent factor VIII or fragment
thereof that includes at least one epitope of the protein can be
used as the diagnostic reagent. Examples of other assays in which
the hybrid or hybrid equivalent factor VIII or fragment thereof can
be used include the Bethesda assay and anticoagulation assays.
General Description of Methods
[0042] U.S. Pat. No. 5,364,771 described the discovery of hybrid
human/porcine factor VIII molecules having coagulant activity, in
which elements of the factor VIII molecule of human or pig are
substituted for corresponding elements of the factor VIII molecule
of the other species. U.S. Pat. No. 5,663,060 and PCT/US94/13200
describe procoagulant hybrid human/animal and hybrid equivalent
factor VIII molecules, in which elements of the factor VIII
molecule of one species are substituted for corresponding elements
of the factor VIII molecule of the other species.
[0043] The present invention provides hybrid human/animal,
animal/animal, and equivalent factor VIII molecules and fragments
thereof, and the nucleic acid sequences encoding such hybrids, some
of which have greater coagulant activity in a standard clotting
assay when compared to highly-purified human factor VIII; and/or
are less immunoreactive to inhibitory antibodies to human or
porcine factor VIII than human or porcine factor VIII; and/or are
less immunogenic in a human or animal than human or porcine factor
VIII. These hybrid factor VIII molecules can be constructed as
follows.
[0044] At least five types of active hybrid human/porcine or hybrid
equivalent factor VIII molecules or fragments thereof, the nucleic
acid sequences encoding these hybrid factor VIII molecules, and the
methods for preparing them are disclosed herein: those obtained (1)
by substituting a human or porcine subunit (i.e., heavy chain or
light chain) for the corresponding porcine or human subunit; (2) by
substituting one or more human or porcine domain(s) (i.e., A1, A2,
A3, B, C1, and C2) for the corresponding porcine or human
domain(s); (3) by substituting a continuous part of one or more
human or porcine domain(s) for the corresponding part of one or
more porcine or human domain(s); (4) by substituting at least one
specific sequence including one or more unique amino acid
residue(s) in human or porcine factor VIII for the corresponding
porcine or human sequence; and (5) by substituting at least one
sequence including one or more amino acid residue(s) having no
known sequence identity to factor VIII ("non-factor VIII amino acid
sequence") for at least one specific sequence of one or more amino
acids in human, porcine, or hybrid human/porcine factor VIII.
[0045] At least five types of active hybrid human/non-human,
non-porcine mammalian or hybrid equivalent factor VIII molecules or
fragments thereof, and the nucleic acid sequences encoding them,
can also be prepared by the same methods: those obtained (1) by
substituting a human or non-human, non-porcine mammalian subunit
(i.e., heavy chain or light chain) for the corresponding non-human,
non-porcine mammalian or human subunit; (2) by substituting one or
more human or non-human, non-porcine mammalian domain(s) (i.e., A1,
A2, A3, B, C1 and C2) for the corresponding non-human, non-porcine
mammalian or human domain(s); (3) by substituting a continuous part
of one or more human or non-human, non-porcine mammalian domain(s)
for the corresponding part of one or more non-human, non-porcine
mammalian or human domain(s); (4) by substituting at least one
specific sequence including one or more unique amino acid
residue(s) in human or non-human, non-porcine mammalian factor VIII
for the corresponding non-human, non-porcine mammalian or human
sequence; and (5) by substituting at least one sequence including
one or more amino acid residue(s) having no known sequence identity
to factor VIII ("non-factor VIII amino acid sequence") for at least
one specific sequence of one or more amino acids in human,
non-human, non-porcine mammalian, or hybrid human/non-human,
non-porcine mammalian factor VIII.
[0046] Further, one skilled in the art will readily recognize that
the same methods can be used to prepare at least five types of
active hybrid factor VIII molecules or fragments thereof,
corresponding to types (1)-(5) in the previous two paragraphs,
comprising factor VIII amino acid sequence from two or more
non-human mammals, such as porcine/mouse, and further comprising
non-factor VIII amino acid sequence.
[0047] Hybrid human/animal, animal/animal, and equivalent factor
VIII proteins or fragments thereof listed above under groups
(1)-(3) are made by isolation of subunits, domains, or continuous
parts of domains of plasma-derived factor VIII, followed by
reconstitution and purification. Hybrid human/animal,
animal/animal, and equivalent factor VIII proteins or fragments
thereof described under groups (3)-(5) above are made by
recombinant DNA methods. The hybrid molecule may contain a greater
or lesser percentage of human than animal sequence, depending on
the origin of the various regions, as described in more detail
below.
[0048] Since current information indicates that the B domain has no
inhibitory epitope and has no known effect on factor VIII function,
in some embodiments the B domain is deleted in the active hybrid or
hybrid equivalent factor VIII molecules or fragments thereof ("B(-)
factor VIII") prepared by any of the methods described herein.
[0049] It is shown in Example 4 that hybrid human/porcine factor
VIII comprising porcine heavy chain and human light chain and
corresponding to the first type of hybrid listed above has greater
specific coagulant activity in a standard clotting assay compared
to human factor VIII. The hybrid human/animal or equivalent factor
VIII with coagulant activity, whether the activity is higher, equal
to, or lower than that of human factor VIII, can be useful in
treating patients with inhibitors, since these inhibitors can react
less with hybrid human/animal or equivalent factor VIII than with
either human or porcine factor VIII.
Preparation of Hybrid Factor VIII Molecules from Isolated Human and
Animal Factor VIII Subunits by Reconstitution
[0050] The present invention provides hybrid human/animal factor
VIII molecules or fragments thereof, with subunit substitutions,
the nucleic acid sequences encoding these hybrids, methods for
preparing and isolating them, and methods for characterizing their
procoagulant activity. One method, modified from procedures
reported by Fay, P. J. et al. (1990) J. Biol. Chem. 265:6197; and
Lollar, J. S. et al. (1988) J. Biol. Chem. 263:10451, involves the
isolation of subunits (heavy and light chains) of human and animal
factor VIII, followed by recombination of human heavy chain and
animal light chain or by recombination of human light chain and
animal heavy chain.
[0051] Isolation of both human and animal individual subunits
involves dissociation of the light chain/heavy chain dimer. This is
accomplished, for example, by chelation of calcium with
ethylenediaminetetraacetic acid (EDTA), followed by MonoS.TM. HPLC
(Pharmacia-LKB, Piscataway, N.J.). Hybrid human/animal factor VIII
molecules are reconstituted from isolated subunits in the presence
of calcium. Hybrid human light chain/animal heavy chain or animal
light chain/human heavy chain factor VIII is isolated from
unreacted heavy chains by MonoS.TM. HPLC by procedures for the
isolation of porcine factor VIII, such as described by Lollar, J.
S. et al. (1988) Blood 71:137-143.
[0052] These methods, used in one embodiment to prepare active
hybrid human/porcine factor VIII, described in detail in the
examples below, result in hybrid human light chain/porcine heavy
chain molecules with greater than six times the procoagulant
activity of human factor VIII.
[0053] Other hybrid human/non-human, non-porcine mammalian factor
VIII molecules can be prepared, isolated, and characterized for
activity by the same methods. One skilled in the art will readily
recognize that these methods can also be used to prepare, isolate,
and characterize for activity hybrid animal/animal factor VIII,
such as porcine/mouse, comprising the light or heavy chain or one
species is combined with the heavy or light chain of the other
species.
Preparation of Hybrid Factor VIII Molecules from Isolated Human and
Animal Factor VIII Domains by Reconstitution
[0054] The present invention provides hybrid human/animal factor
VIII molecules or fragments thereof with domain substitutions, the
nucleic acid sequences encoding them, methods for preparing and
isolating them, and methods for characterizing their procoagulant
activity. One method involves the isolation of one or more domains
of human and one or more domains of animal factor VIII, followed by
recombination of human and animal domains to form hybrid
human/animal factor VIII with coagulant activity, as described by
Lollar, P. et al. (1992) J. Biol. Chem. 267(33):23652-23657, for
hybrid human/porcine factor VIII.
[0055] Specifically provided is a hybrid human/porcine factor VIII
with substitution of the porcine A2 domain for the human A2 domain,
which embodiment illustrates a method by which domain-substituted
hybrid human/non-human, non-porcine mammalian factor VIII can be
constructed. Plasma-derived non-human, non-porcine mammalian and
human A1/A3-C1-C2 dimers are isolated by dissociation of the A2
domain from factor VIIIa. This is accomplished, for example, in the
presence of NaOH, after which the mixture is diluted and the dimer
is eluted using MonoS.TM. HPLC (Pharmacia-LKB, Piscataway, N.J.).
The A2 domain is isolated from factor VIIIa as a minor component in
the MonoS.TM. HPLC. Hybrid human/animal factor VIII molecules are
reconstituted by mixing equal volumes of the A2 domain of one
species and the A1/A3-C1-C2 dimer of the other species.
[0056] Hybrid human/animal factor VIII or fragments thereof with
one or more domain substitutions is isolated from the mixture of
unreacted dimers and A2 by MonoS.TM. HPLC by procedures for the
isolation of porcine factor VIII, as described by Lollar, J. S. et
al. (1988) Blood 71:137-143. Routine methods can also be used to
prepare and isolate the A1, A3, C1, C2, and B domains of the factor
VIII of one species, any one or more of which can be substituted
for the corresponding domain in the factor VIII of the other
species. One skilled in the art will readily recognize that these
methods can also be used to prepare, isolate, and characterize for
activity domain-substituted hybrid animal/animal factor VIII, such
as porcine/mouse.
[0057] These methods, described in detail in the examples below,
result in hybrid factor VIII molecules with procoagulant
activity.
Preparation of Hybrid Factor VIII Molecules by Recombinant
Engineering of the Sequences Encoding Human, Animal, and Hybrid
Factor VIII Subunits, Domains, or Parts of Domains:
Substitution of Subunits, Domains, Continuous Parts of Domains
[0058] The present invention provides active, recombinant hybrid
human/animal and hybrid equivalent factor VIII molecules and
fragments thereof with subunit, domain, and amino acid sequence
substitutions, the nucleic acid sequences encoding these hybrids,
methods for preparing and isolating them, and methods for
characterizing their coagulant, immunoreactive, and immunogenic
properties.
[0059] The human factor VIII gene was isolated and expressed in
mammalian cells, as reported by Toole, J. J. et al. (1984) Nature
312:342-347 (Genetics Institute); Gitschier, J. et al. (1984)
Nature 312:326-330 (Genentech); Wood, W. I. et al. (1984) Nature
312:330-337 (Genentech); Vehar, G. A. et al. (1984) Nature
312:337-342 (Genentech); WO 87/04187; WO 88/08035; WO 88/03558;
U.S. Pat. No. 4,757,006, and the amino acid sequence was deduced
from cDNA. U.S. Pat. No. 4,965,199 to Capon et al. discloses a
recombinant DNA method for producing factor VIII in mammalian host
cells and purification of human factor VIII. Human factor VIII
expression in CHO (Chinese hamster ovary) cells and BHKC (baby
hamster kidney cells) has been reported. Human factor VIII has been
modified to delete part or all of the B domain (U.S. Pat. No.
4,868,112), and replacement of the human factor VIII B domain with
the human factor V B domain has been attempted (U.S. Pat. No.
5,004,803). The cDNA sequence encoding human factor VIII and
predicted amino acid sequence are shown in SEQ ID NOs:1 and 2,
respectively.
[0060] Porcine factor VIII has been isolated and purified from
plasma (Fass, D. N. et al. (1982) Blood 59:594). Partial amino acid
sequence of porcine factor VIII corresponding to portions of the
N-terminal light chain sequence having homology to ceruloplasmin
and coagulation factor V and largely incorrectly located were
described by Church et al. (1984) Proc. Natl. Acad. Sci. USA
81:6934. Toole, J. J. et al. (1984) Nature 312:342-347 described
the partial sequencing of the N-terminal end of four amino acid
fragments of porcine factor VIII but did not characterize the
fragments as to their positions in the factor VIII molecule. The
amino acid sequence of the B and part of the A2 domains of porcine
factor VIII were reported by Toole, J. J. et al. (1986) Proc. Natl.
Acad. Sci. USA 83:5939-5942. The cDNA sequence encoding the
complete A2 domain of porcine factor VIII and predicted amino acid
sequence and hybrid human/porcine factor VIII having substitutions
of all domains, all subunits, and specific amino acid sequences
were disclosed in U.S. Pat. No. 5,364,771 and in WO 93/20093. The
cDNA sequence encoding the A2 domain of porcine factor VIII having
sequence identity to residues 373-740 in mature human factor VIII,
as shown in SEQ ID NO:1, and the predicted amino acid sequence are
shown in SEQ ID NOs:3 and 4, respectively. More recently, the
nucleotide and corresponding amino acid sequences of the A1 and A2
domains of porcine factor VIII and a chimeric factor VIII with
porcine A1 and/or A2 domains substituted for the corresponding
human domains were reported in WO 94/11503.
[0061] Both porcine and human factor VIII are isolated from plasma
as a two subunit protein. The subunits, known as the heavy chain
and light chain, are held together by a non-covalent bond that
requires calcium or other divalent metal ions. The heavy chain of
factor VIII contains three domains, A1, A2, and B, which are linked
covalently. The light chain of factor VIII also contains three
domains, designated A3, C1, and C2. The B domain has no known
biological function and can be removed from the molecule
proteolytically or by recombinant DNA technology methods without
significant alteration in any measurable parameter of factor VIII.
Human recombinant factor VIII has a similar structure and function
to plasma-derived factor VIII, though it is not glycosylated unless
expressed in mammalian cells.
[0062] Both human and porcine activated factor VIII ("factor
VIIIa") have three subunits due to cleavage of the heavy chain
between the A1 and A2 domains. This structure is designated
A1/A2/A3-C1-C2. Human factor VIIIa is not stable under the
conditions that stabilize porcine factor VIIIa, presumably because
of the weaker association of the A2 subunit of human factor VIIIa.
Dissociation of the A2 subunit of human and porcine factor VIIIa is
associated with loss of activity in the factor VIIIa molecule.
[0063] Using as probes the known sequence of parts of the porcine
factor VIII molecule, the domains of the porcine factor VIII
molecule that have not been sequenced to date can be sequenced by
standard, established cloning techniques, such as those described
in Weis, J. H., "Construction of recombinant DNA libraries," in
Current Protocols in Molecular Biology, F. M. Ausubel et al., eds.
(1991); and Sambrook, J. (1989), et al., Molecular Cloning, A
Laboratory Manual, so that full length hybrids can be
constructed.
[0064] Specifically provided as an exemplary and a preferred
embodiment is active recombinant hybrid human/porcine factor VIII
having substituted A2 domain, the nucleic acid sequence encoding
it, and the methods for preparing, isolating, and characterizing
its activity. The methods by which this hybrid construct is
prepared can also be used to prepare active recombinant hybrid
human/porcine factor VIII or fragments thereof having substitution
of subunits, continuous parts of domains, or domains other than A2.
One skilled in the art will recognize that these methods also
demonstrate how other recombinant hybrid human/non-human,
non-porcine mammalian or animal/animal hybrid factor VIII molecules
or fragments thereof can be prepared in which subunits, domains, or
continuous parts of domains are substituted.
[0065] Recombinant hybrid human/porcine factor VIII is prepared
starting with human cDNA (Biogen, Inc.) or porcine cDNA (described
herein) encoding the relevant factor VIII sequence. In a preferred
embodiment, the factor VIII encoded by the cDNA includes domains
A1-A2-A3-C1-C2, lacking the entire B domain, and corresponds to
amino acid residues 1-740 and 1649-2332 of single chain human
factor VIII (see SEQ ID NO:2), according to the numbering system of
Wood et al. (1984) Nature 312:330-337.
[0066] Individual subunits, domains, or continuous parts of domains
of porcine or human factor VIII cDNA can be and have been cloned
and substituted for the corresponding human or porcine subunits,
domains, or parts of domains by established mutagenesis techniques.
For example, Lubin, I. M. et al. (1994) J. Biol. Chem.
269(12):8639-8641 describes techniques for substituting the porcine
A2 domain for the human domain using convenient restriction sites.
Other methods for substituting any arbitrary region of the factor
VIII cDNA of one species for the factor VIII cDNA of another
species include splicing by overlap extension ("SOE"), as described
by Horton, R. M. et al. (1993) Meth. Enzymol 217:270-279.
[0067] The hybrid factor VIII cDNA encoding subunits, domains, or
parts of domains or the entire hybrid cDNA molecules are cloned
into expression vectors for ultimate expression of active hybrid
human/porcine factor VIII protein molecules in cultured cells by
established techniques, as described by Selden, R. F.,
"Introduction of DNA into mammalian cells," in Current Protocols in
Molecular Biology, F. M. Ausubel et al., eds (1991).
[0068] In an embodiment, a hybrid human/porcine cDNA encoding
factor VIII, in which the porcine sequence encodes a domain or part
domain, such as the A2 domain or part domain, is inserted in a
mammalian expression vector, such as ReNeo, to form a hybrid factor
VIII construct. Preliminary characterization of the hybrid factor
VIII is accomplished by insertion of the hybrid cDNA into the ReNeo
mammalian expression vector and transient expression of the hybrid
protein in COS-7 cells. A determination of whether active hybrid
protein is expressed can then be made. The expression vector
construct is used further to stably transfect cells in culture,
such as baby hamster kidney cells, using methods that are routine
in the art, such as liposome-mediated transfection (LipofectinJ,
Life Technologies, Inc.). Expression of recombinant hybrid factor
VIII protein can be confirmed, for example, by sequencing, Northern
and Western blotting, or polymerase chain reaction (PCR). Hybrid
factor VIII protein in the culture media in which the transfected
cells stably expressing the protein are maintained can be
precipitated, pelleted, washed, and resuspended in an appropriate
buffer, and the recombinant hybrid factor VIII protein purified by
standard techniques, including immunoaffinity chromatography using,
for example, monoclonal anti-A2-Sepharose.TM..
[0069] In a further embodiment, the hybrid factor VIII comprising
subunit, domain, or amino acid sequence substitutions is expressed
as a fusion protein from a recombinant molecule in which sequence
encoding a protein or peptide that enhances, for example,
stability, secretion, detection, isolation, or the like is inserted
in place adjacent to the factor VIII encoding sequence. Established
protocols for use of homologous or heterologous species expression
control sequences including, for example, promoters, operators, and
regulators, in the preparation of fusion proteins are known and
routinely used in the art. See Current Protocols in Molecular
Biology (Ausubel, F. M., et al., eds), Wiley Interscience, N.Y.
[0070] The purified hybrid factor VIII or fragment thereof can be
assayed for immunoreactivity and coagulation activity by standard
assays including, for example, the plasma-free factor VIII assay,
the one-stage clotting assay, and the enzyme-linked immunosorbent
assay using purified recombinant human factor VIII as a
standard.
[0071] Other vectors, including both plasmid and eukaryotic viral
vectors, may be used to express a recombinant gene construct in
eukaryotic cells depending on the preference and judgment of the
skilled practitioner (see, for example, Sambrook et al., Chapter
16). Other vectors and expression systems, including bacterial,
yeast, and insect cell systems, can be used but are not preferred
due to differences in, or lack of, glycosylation.
[0072] Recombinant hybrid or other modified factor VIII protein can
be expressed in a variety of cells commonly used for culture and
recombinant mammalian protein expression. In particular, a number
of rodent cell lines have been found to be especially useful hosts
for expression of large proteins. Preferred cell lines, available
from the American Type Culture Collection, Manassas, Va., include
baby hamster kidney cells, and Chinese hamster ovary (CHO) cells
which are cultured using routine procedures and media.
[0073] The same methods employed for preparing hybrid human/porcine
factor VIII having subunit, domain, or amino acid sequence
substitution can be used to prepare other recombinant hybrid factor
VIII protein and fragments thereof and the nucleic acid sequences
encoding these hybrids, such as human/non-human, non-porcine
mammalian or animal/animal. Starting with primers from the known
human DNA sequence, the murine and part of the porcine factor VIII
cDNA have been cloned. Factor VIII sequences of other species for
use in preparing a hybrid human/animal or animal/animal factor VIII
molecule can be obtained using the known human and porcine DNA
sequences as a starting point. Other techniques that can be
employed include PCR amplification methods with animal tissue DNA,
and use of a cDNA library from the animal to clone out the factor
VIII sequence.
[0074] As an exemplary embodiment, hybrid human/mouse factor VIII
protein can be made as follows. DNA clones corresponding to the
mouse homolog of the human factor VIII gene have been isolated and
sequenced and the amino acid sequence of mouse factor VIII protein
predicted, as described in Elder, G., et al. (1993) Genomics
16(2):374-379, which also includes a comparison of the predicted
amino acid sequences of mouse, human, and part of porcine factor
VIII molecules. The mouse factor VIII cDNA sequence and predicted
amino acid sequence are shown in SEQ ID NO:5 and SEQ ID NO:8,
respectively. In a preferred embodiment, the RNA amplification with
transcript sequencing (RAWTS) methods described in Sarkar, G. et
al. (1989) Science 244:331-334, can be used. Briefly, the steps are
(1) cDNA synthesis with oligo(dT) or an mRNA-specific
oligonucleotide primer; (2) polymerase chain reaction (PCR) in
which one or both oligonucleotides contains a phage promoter
attached to a sequence complementary to the region to be amplified;
(3) transcription with a phage promoter; and (4) reverse
transcriptase-mediated dideoxy sequencing of the transcript, which
is primed with a nested (internal) oligonucleotide. In addition to
revealing sequence information, this method can generate an in
vitro translation product by incorporating a translation initiation
signal into the appropriate PCR primer: and can be used to obtain
novel mRNA sequence information from other species.
Substitution of Amino Acid(s)
[0075] The present invention provides active recombinant hybrid
human/animal and animal/animal factor VIII molecules or fragments
thereof comprising at least one sequence including one or more
unique amino acids of one species substituted for the corresponding
amino acid sequence of the other species or fragments thereof,
nucleic acid sequences encoding these hybrids, methods for
preparing and isolating them, and methods for characterizing their
coagulant, immunogenic and immunoreactive properties.
[0076] The A2 domain is necessary for the procoagulant activity of
the factor VIII molecule. Studies show that porcine factor VIII has
six-fold greater procoagulant activity than human factor VIII
(Lollar, P. et al. (1991) J. Biol. Chem. 266:12481-12486, and that
the difference in coagulant activity between human and porcine
factor VIII appears to be based on a difference in amino acid
sequence between one or more residues in the human and porcine A2
domains (Lollar, P. et al. (1992) J. Biol. Chem. 267:23652-23657.
Further, the A2 and C2 domains and possibly a third light chain
region in the human factor VIII molecule are thought to harbor the
epitopes to which most, if not all, inhibitory antibodies react,
according to Hoyer (1994) Semin. Hematol. 31:1-5.
[0077] Recombinant hybrid human/animal, animal/animal, or
equivalent factor VIII molecules or fragments thereof can be made
by substitution of at least one specific sequence including one or
more unique amino acids from the A2, C2, and/or other domains of
the factor VIII of one species for the corresponding sequence of
the other species, wherein the amino acid sequences differ, as
illustrated in more detail below, between the molecules of the two
species. In an exemplary preferred embodiment described herein, the
present invention provides active recombinant hybrid human/porcine
factor VIII comprising porcine amino acid sequence substituted for
corresponding human amino acid sequence that includes an epitope,
wherein the hybrid factor VIII has decreased or no immunoreactivity
with inhibitory antibodies to factor VIII. In a further embodiment,
active recombinant hybrid factor VIII molecules can also be made
comprising amino acid sequence from more than one species
substituted for the corresponding sequence in a third species.
Recombinant hybrid equivalent molecules can also be made,
comprising human, animal, or hybrid factor VIII including at least
one sequence including one or more amino acids that have no known
sequence identity to factor VIII, as further described below.
[0078] Any hybrid factor VIII construct having specific amino acid
substitution as described can be assayed by standard procedures for
coagulant activity and for reactivity with inhibitory antibodies to
factor VIII for identification of hybrid factor VIII molecules with
enhanced coagulant activity and/or decreased antibody
immunoreactivity. Hybrid molecules may also be identified that have
reduced coagulant activity compared to human or porcine factor VIII
but also have decreased antibody reactivity. One skilled in the art
will recognize that hybrid factor VIII molecules or fragments
thereof having less, equal, or greater coagulant activity, compared
to human or porcine factor VIII, is useful for treating patients
who have a factor VIII deficiency. The methods described herein to
prepare active recombinant hybrid human/porcine factor VIII with
substitution of specific amino acids can be used to prepare active
recombinant hybrid human/non-human, non-porcine mammalian factor
VIII protein, hybrid animal-1/animal-2 factor VIII, and hybrid
equivalent factor VIII or fragments thereof.
Hybrid Factor VIII Molecules with Altered Coagulant Activity
[0079] The present invention provides procoagulant recombinant
hybrid human/animal, animal/animal, or equivalent factor VIII
molecules or fragments thereof comprising at least one specific
sequence including one or more unique amino acids having
procoagulant activity in the factor VIII of one species substituted
for the corresponding amino acid sequence of the factor VIII of the
other species, using established site-directed mutagenesis
techniques as described herein. The specific sequences to be used
in the substitution are selected and the hybrid constructs are
prepared and assayed for coagulant activity, as follows.
Specifically provided as a preferred and exemplary embodiment is a
hybrid human/porcine factor VIII comprising amino acid
substitutions in the A2 domain. It is understood that one skilled
in the art can use these methods to prepare other hybrid
human/animal, animal/animal, and equivalent factor VIII molecules
or fragments thereof having altered coagulant activity, preferably
increased coagulant activity compared to human factor VIII.
[0080] The basis for the greater coagulant activity in porcine
factor VIII appears to be the more rapid spontaneous dissociation
of the A2 subunit of human factor VIIIa than porcine factor VIIIa,
which leads to loss of activity, according to Lollar, P. et al.
(1990) J. Biol. Chem. 265:1688-1692; Lollar, P. et al. (1992) J.
Biol. Chem. 267:23652-23657; Fay, P. J. et al. (1992) J. Biol.
Chem. 267:13246-13250.
[0081] A comparison of the alignment of the amino acid sequences of
the human and porcine factor VIII A2 domains (residue numbering
starts at position 373 with respect to the full length amino acid
sequence of human factor VIII, SEQ ID NO:2) is shown in FIG. 1C.
For preparation of a hybrid human/porcine factor VIII molecule with
altered coagulant activity, the initial target candidates for
mutagenesis, which were revealed upon comparison of the human and
porcine A2 amino acid sequences (SEQ ID NOs: 2 and 6, respectively)
within the human A2 domain, are shown in Table I.
TABLE-US-00001 TABLE I HUMAN AMINO ACID SEQUENCE TARGET CANDIDATES
FOR MUTAGENESIS (SEQ ID NO: 2) Sequence Changes Residues Mismatches
Charge 398-403 6 4 1 434-444 10 4 3 484-496 13 7 3 598-603 6 4 2
536-541 6 4 0 713-722 10 6 2 727-737 11 6 2
[0082] Table I and the bold letters of FIGS. 1A-1B illustrate seven
sequences in the human and pig A2 domain amino acid sequences (SEQ
ID NOs:2 and 4, respectively) that constitute only 17 percent of
the A2 domain but include 70 percent of the sequence differences
between human and porcine A2 domains.
[0083] A recombinant hybrid human/porcine construct is described in
which amino acids Ser373-Glu604 in the A2 domain (Ser373-Arg740) of
human factor VIII have been replaced with the homologous porcine
sequence. This construct does not react with A2 inhibitors and has
the same coagulant activity as human B(-) factor VIII. A
plasma-derived hybrid molecule is described that comprises a
complete porcine A2 domain substitution in the human factor VIII
that has increased coagulant activity compared to human factor
VIII. Comparison of these constructs indicates that a region
between residues Asp605 and Arg740 is responsible for the
difference in activity between human and porcine factor VIII. This
region can be defined more specifically by systematically making
recombinant hybrid human/porcine factor VIII molecules with porcine
substitutions in the region between Asp605 and Arg740 by using
established site-directed mutagenesis techniques, for example, the
"splicing by overlap extension" (SOE) method that has been used
extensively to make hybrid factor VIII molecules containing porcine
substitutions in the NH.sub.2-terminal region of A2. These
molecules can be expressed in COS-7 cells and baby hamster kidney
cells as described above. They can be purified to homogeneity using
methods known in the art, such as heparin-Sepharose.TM. and
immunoaffinity chromatography. Protein concentration can be
estimated by absorption of ultraviolet light at A.sub.280, and the
specific activity of the constructs can be determined by dividing
coagulant activity (measured in units per ml by single stage
clotting assay) by A.sub.280. Human factor VIII has a specific
activity of approximately 3000-4000 U/A.sub.280, whereas porcine
factor VIII has a specific activity of approximately 20,000
U/A.sub.280. In a preferred embodiment, the procoagulant
recombinant hybrid human/porcine factor VIII has a specific
activity of 20,000 U/A.sub.280 and contains a minimal amount of
porcine substitution in the A2 domain.
[0084] As described herein, site-directed mutagenesis techniques
are used to identify hybrid protein with coagulant activity that
can be enhanced, equal to, or reduced, compared to human factor
VIII, but preferably is enhanced. In the hybrid human/porcine
embodiment, specific human sequences are replaced with porcine
sequences, preferably using the splicing by overlap extension
method (SOE), as described by Ho, S. N., et al., (1994) Gene
77:51-59, and in Examples 7 and 8. Oligonucleotide-directed
mutagenesis can also be used, as was done to loop out the amino
acid sequence for part of the human A2 domain (see Example 7). As
functional analysis of the hybrids reveals coagulant activity, the
sequence can be further dissected and mapped for procoagulant
sequence by standard point mutation analysis techniques.
[0085] The present invention contemplates that hybrid factor VIII
cDNA and protein can be characterized by methods that are
established and routine, such as DNA sequencing, coagulant activity
assays, mass by ELISA and by UV absorbance at 280 nm of purified
hybrid factor VIII, specific coagulant activity (U/mg), SDS-PAGE of
purified hybrid factor VIII, and the like. Other known methods of
testing for clinical effectiveness may be required, such as amino
acid, carbohydrate, sulfate, or metal ion analysis.
[0086] A recombinant hybrid factor VIII having superior coagulant
activity, compared to human factor VIII, may be less expensive to
make than plasma-derived factor VIII and may decrease the amount of
factor VIII required for effective treatment of factor VIII
deficiency.
Hybrid Factor VIII Molecules with Reduced Immunoreactivity
[0087] Epitopes that are immunoreactive with antibodies that
inhibit the coagulant activity of factor VIII ("inhibitors" or
"inhibitory antibodies") have been characterized based on known
structure-function relationships in factor VIII. Presumably,
inhibitors could act by disrupting any of the macromolecular
interactions associated with the domain structure of factor VIII or
its associations with von Willebrand factor, thrombin, factor Xa,
factor IXa, or factor X. However, over 90 percent of inhibitory
antibodies to human factor VIII act by binding to epitopes located
in the 40 kDa A2 domain or 20 kDa C2 domain of factor VIII,
disrupting specific functions associated with these domains, as
described by Fulcher et al. (1985) Proc. Natl. Acad. Sci USA
82:7728-7732; and Scandella et al. (1988) Proc. Natl. Acad. Sci.
USA 85:6152-6156. In addition to the A2 and C2 epitopes, there may
be a third epitope in the A3 or C1 domain of the light chain of
factor VIII, according to Scandella et al. (1993) Blood
82:1767-1775. The significance of this putative third epitope is
unknown, but it appears to account for a minor fraction of the
epitope reactivity in factor VIII.
[0088] Anti-A2 antibodies block factor X activation, as shown by
Lollar et al. (1994) J. Clin. Invest. 93:2497-2504. Previous
mapping studies by deletion mutagenesis described by Ware et al.
(1992) Blood Coagul. Fibrinolysis 3:703-716, located the A2 epitope
to within a 20 kDa region of the NH.sub.2-terminal end of the 40
kDa A2 domain. Competition immunoradiometric assays have indicated
that A2 inhibitors recognize either a common epitope or narrowly
clustered epitopes, as described by Scandella et al. (1992) Throm.
Haemostas 67:665-671, and as demonstrated in Example 8.
[0089] The present invention provides active recombinant hybrid and
hybrid equivalent factor VIII molecules or fragments thereof, the
nucleic acid sequences encoding these hybrids, methods of preparing
and isolating them, and methods for characterizing them. These
hybrids comprise human/animal, animal/animal, or equivalent hybrid
factor VIII molecules, further comprising at least one specific
amino acid sequence including one or more unique amino acids of the
factor VIII of one species substituted for the corresponding amino
acid sequence of the factor VIII of the other species; or comprises
at least one sequence including one or more amino acids having no
known sequence identity to factor VIII substituted for specific
amino acid sequence in human, animal, or hybrid factor VIII. The
resulting hybrid factor VIII has reduced or no immunoreactivity to
factor VIII inhibitory antibodies, compared to human or porcine
factor VIII.
[0090] Using the approach described in the previous section for
substitution of amino acids in the factor VIII molecule, mutational
analysis is employed to select corresponding factor VIII amino acid
sequence of one species, preferably porcine, which is substituted
for at least one sequence including one or more amino acids in the
factor VIII of another species, preferably human, or for amino acid
sequence of a hybrid equivalent factor VIII molecule, that includes
one or more critical region(s) in the A2, C2, or any other domain
to which inhibitory antibodies are directed. The methods are
described in more detail below. The resulting procoagulant
recombinant hybrid construct has reduced or no immunoreactivity to
inhibitory antibodies, compared to human factor VIII, using
standard assays. Through systematic substitution of increasingly
smaller amino acid sequences followed by assay of the hybrid
construct for immunoreactivity, as described below, the epitope in
any domain of a factor VIII molecule is mapped, substituted by
amino acid sequence having less or no immunoreactivity, and a
hybrid factor VIII is prepared.
[0091] It is understood that one skilled in the art can use this
approach combining epitope mapping, construction of hybrid factor
VIII molecules, and mutational analysis of the constructs to
identify and replace at least one sequence including one or more
amino acids comprising an epitope in the A2, C2, and/or other
domains to which inhibitory antibodies are directed and to
construct procoagulant recombinant hybrid human/animal,
animal/animal, or equivalent factor VIII or fragments thereof
having decreased or no immunoreactivity compared to human or
porcine factor VIII. This approach is used, as described in Example
8, to prepare a recombinant procoagulant hybrid human/porcine
factor VIII having porcine amino acid substitutions in the human A2
domain and no antigenicity to anti-factor VIII antibodies as an
exemplary embodiment.
[0092] Usually, porcine factor VIII has limited or no reaction with
inhibitory antibodies to human factor VIII. The recombinant hybrid
human/porcine factor VIII molecules having decreased or no
reactivity with inhibitory antibodies based on amino acid
substitution in the A2 domain are prepared, as an example of how
hybrid factor VIII can be prepared using the factor VIII of other
species and substitutions in domains other than A2, as follows. The
porcine A2 domain is cloned by standard cloning techniques, such as
those described above and in Examples 6, 7, and 8, and then cut and
spliced within the A2 domain using routine procedures, such as
using restriction sites to cut the cDNA or splicing by overlap
extension (SOE). The resulting porcine amino acid sequence is
substituted into the human A2 domain to form a hybrid factor VIII
construct, which is inserted into a mammalian expression vector,
preferably ReNeo, stably transfected into cultured cells,
preferably baby hamster kidney cells, and expressed, as described
above. The hybrid factor VIII is assayed for immunoreactivity, for
example with anti-A2 antibodies by the routine Bethesda assay or by
plasma-free chromogenic substrate assay. The Bethesda unit (BU) is
the standard method for measuring inhibitor titers. If the Bethesda
titer is not measurable (<0.7 BU/mg IgG) in the hybrid, then a
human A2 epitope was eliminated in the region of substituted
corresponding porcine sequence. The epitope is progressively
narrowed, and the specific A2 epitope can thus be determined to
produce a hybrid human/porcine molecule with as little porcine
sequence as possible. As described herein, a 25-residue sequence
corresponding to amino acids Arg484-Ile508 that is critical for
inhibitory immunoreactivity has been identified and substituted in
the human A2 domain. Within this sequence are only nine differences
between human and porcine factor VIII. This region can be further
analyzed and substituted.
[0093] Hybrid human/porcine factor VIII molecules having decreased
or no reactivity with inhibitory antibodies based on substitution
of amino acid sequence in the C1, C2 or other domain, with or
without substitution in the A2 domain, can also be prepared. The C2
epitope, for example can be mapped using the homolog scanning
approach combined with site-directed mutagenesis. More
specifically, the procedures can be the same or similar to those
described herein for amino acids substitution in the A2 domain,
including cloning the porcine C2 or other domain, for example by
using RT-PCR or by probing a porcine liver cDNA library with human
C2 or other domain DNA; restriction site techniques and/or
successive SOE to map and simultaneously replace epitopes in the C2
or other domain; substitution for the human C2 or other domain in
B(-) factor VIII; insertion into an expression vector, such as
pBluescript; expression in cultured cells; and routine assay for
immunoreactivity. For the assays, the reactivity of C2 hybrid
factor VIII with a C2-specific inhibitor, MR (Scandella et al.
(1992) Thromb. Haemostasis 67:665-671 and Lubin et al. (1994)),
and/or other C2 specific antibodies prepared by affinity
chromatography can be performed.
[0094] The C2 domain consists of amino acid residues 2173-2332 (SEQ
ID NO:2). Within this 154 amino acid region, inhibitor activity
appears to be directed to a 65 amino acid region between residues
2248 and 2312, according to Shima, M. et al. (1993) Thromb.
Haemostasis 69:240-246. If the C2 sequence of human and porcine
factor VIII is approximately 85 percent identical in this region,
as it is elsewhere in the functionally active regions of factor
VIII, there will be approximately ten differences between human and
porcine factor VIII C2 amino acid sequence, which can be used as
initial targets to construct hybrids with substituted C2
sequence.
[0095] It is likely that clinically significant factor VIII
epitopes are confined to the A2 and C2 domains. However, if
antibodies to other regions (A1, A3, B, or C1 domains) of factor
VIII are identified, the epitopes can be mapped and eliminated by
using the approach described herein for the nonantigenic hybrid
human/porcine factor VIII molecules.
[0096] More specifically, mapping of the putative second light
chain epitope and/or any other epitope in any other animal or human
factor VIII domain can also be accomplished. Initially,
determination of the presence of a third inhibitor epitope in the
A3 or C1 domains can be made as follows. Using human ("H") and
porcine ("p") factor VIII amino acid sequences as a model,
A1.sub.p-A2.sub.p-A3.sub.p-C1.sub.H-C2.sub.p and
A1.sub.p-A2.sub.p-A3.sub.H-C1.sub.p-C2.sub.p B-domainless hybrids
will be constructed. Inhibitor IgG from approximately 20 patient
plasmas (from Dr. Dorothea Scandella, American Red Cross) who have
low or undetectable titers against porcine factor VIII will be
tested against the hybrids. If the third epitope is in the A3
domain, inhibitory IgG is expected to react with
A1.sub.p-A2.sub.p-A3.sub.H-C1.sub.p-C2.sub.p but not
A1.sub.p-A2.sub.p-A3.sub.p-C1.sub.H-C2.sub.p. Conversely, if the
third epitope is in the C1 domain, then inhibitory IgG is expected
to react with A1.sub.p-A2.sub.p-A3.sub.p-C1.sub.H-C2.sub.p but not
A1.sub.p-A2.sub.p-A3.sub.H-C1.sub.p-C2.sub.p. If a third epitope is
identified it will be characterized by the procedures described
herein for the A2 and C2 epitopes.
[0097] For example, antibodies specific for the C1 or A3 domain
epitope can be isolated from total patient IgG by affinity
chromatography using the
A1.sub.p-A2.sub.p-A3.sub.H-C1.sub.p-C2.sub.p and
A1.sub.p-A2.sub.p-A3.sub.p-C1.sub.H-C2.sub.p hybrids, and by
elimination of C2 specific antibodies by passage over recombinant
factor VIII C2-Sepharaose.TM.. The putative third epitope will be
identified by SOE constructs in which, in a preferred embodiment,
portions of the human factor VIII A3 or C1 domain are
systematically replaced with porcine sequence.
Hybrid Factor VIII Molecules with Reduced Immunogenicity:
[0098] A molecule is immunogenic when it can induce the production
of antibodies in human or animal. The present invention provides a
procoagulant recombinant hybrid human/animal or animal/animal
factor VIII molecule, hybrid factor VIII equivalent molecule, or
fragment of either that is less immunogenic than wild-type human
porcine factor VIII in human or animal, comprising at least one
specific amino acid sequence including one or more unique amino
acids of the factor VIII of one species substituted for the
corresponding amino acid sequence that has immunogenic activity of
the factor VIII of the other species; or at least one amino acid
sequence including one or more amino acids having no known identity
to factor VIII substituted for amino acid sequence of the human,
animal, or hybrid factor. This hybrid can be used to lower the
incidence of inhibitor development in an animal or human and to
treat factor VIII deficiency, and would be preferred in treating
previously untreated patients with hemophilia. In a preferred
embodiment, the hybrid factor VIII comprises human factor VIII
amino acid sequence, further comprising one or more alanine
residues substituted for human amino acid sequence having
immunogenic activity, resulting in a procoagulant recombinant
hybrid equivalent molecule or fragment thereof having reduced or no
immunogenicity in human or animal.
[0099] The process described herein of epitope mapping and
mutational analysis combined with substitution of non-antigenic
amino acid sequence in a factor VIII molecule, using hybrid
human/porcine factor VIII, produces hybrid molecules with low
antigenicity. Using this model and the associated methods, any of
the hybrid constructs described herein can be altered by
site-directed mutagenesis techniques to remove as much of any
functional epitope as possible to minimize the ability of the
immune system to recognize the hybrid factor VIII, thereby
decreasing its immunogenicity.
[0100] One method that can be used to further reduce the
antigenicity and to construct a less immunogenic hybrid factor VIII
is alanine scanning mutagenesis, described by Cunningham, B. C. et
al. (1989) Science 244:1081-1085, of selected specific amino acid
sequences in human, animal, or hybrid equivalent factor VIII. In
alanine scanning mutagenesis, amino acid side chains that are
putatively involved in an epitope are replaced by alanine residues
by using site-directed mutagenesis. By comparing antibody binding
of alanine mutants to wild-type protein, the relative contribution
of individual side chains to the binding interaction can be
determined. Alanine substitutions are likely to be especially
useful, since side chain contributions to antibody binding are
eliminated beyond the .beta. carbon, but, unlike glycine
substitution, main chain conformation is not usually altered.
Alanine substitution does not impose major steric, hydrophobic or
electrostatic effects that dominate protein-protein
interactions.
[0101] In protein antigen-antibody interactions, there usually are
about 15-20 antigen side chains in contact with the antibody. Side
chain interactions, as opposed to main chain interactions, dominate
protein-protein interactions. Recent studies have suggested that
only a few (approximately 3 to 5) of these side chain interactions
contribute most of the binding energy. See Clackson, T. et al.
(1995) Science 267:383-386. An extensive analysis of growth hormone
epitopes for several murine monoclonal antibodies revealed the
following hierarchy for side chain contributions to the binding
energy: Arg>Pro>Glu-Asp-Phe-Ile, with Trp, Ala, Gly, and Cys
not tested (Jin, L. et al. (1992) J. Mol. Biol. 226:851-865).
Results with the A2 epitope described herein are consistent with
this, since twelve of the 25 residues in the 484-508 A2 segment
contain these side chains (Table 1).
[0102] The finding that certain amino acid residues are
particularly well recognized by antibodies, indicates that
elimination of these residues from a known epitope can decrease the
ability of the immune system to recognize these epitopes, i.e., can
make a molecule less immunogenic. In the case of the A2 epitope,
immunogenic residues can be replaced without loss of factor VIII
coagulant activity. For example, in HP9, Arg484 is replaced by Ser,
Pro485 is replaced by Ala, Arg489 is replaced by Gly, Pro492 is
replaced by Leu, and Phe501 is replaced by Met. Further, results
from the patient plasmas used to test immunoreactivity in hybrid
human/porcine factor VIII constructs, described in Example 8,
indicate that antibodies from different patients recognize the same
or a very similar structural region in the A2 domain and that the
residues in the A2 domain that participate in binding A2 inhibitors
appear to show little variation. Thus, the A2 epitope included in
human factor VIII residues 484-508 is an immunodominant epitope in
that it is recognized by the human immune system better than other
structural regions of factor VIII. Replacing this structure by
nonantigenic factor VIII sequence from another species or by
non-factor VIII amino acid sequence, while retaining full
procoagulant activity, is expected to alter recognition of hybrid
or hybrid equivalent factor VIII by the immune system.
[0103] It is anticipated that site-directed mutagenesis to replace
bulky and/or charged residues that tend to dominate epitopes with
small, neutral side chains (e.g., alanine) may produce a less
immunogenic region. It is expected that a molecule containing a few
of these substitutions at each significant inhibitor epitope will
be difficult for the immune system to fit by the lock-and-key
mechanism that is typical of antigen-antibody interactions. Because
of its low antigenicity, such a hybrid molecule could be useful in
treating factor VIII deficiency patients with inhibitors, and
because of its low immunogenicity, it could be useful in treating
previously untreated patients with hemophilia A. The POL1212
protein expression product of DNA comprising SEQ ID NO:48 is
especially useful in treatment of hemophilia A patients.
[0104] A general result is that mutation of one of a few key
residues is sufficient to decrease the binding constant for a given
protein-protein interaction by several orders of magnitude. Thus,
it appears likely that all factor VIII epitopes contain a limited
number of amino acids that are critical for inhibitor development.
For each epitope in factor VIII, alanine substitutions for at least
one sequence including one or more specific amino acids having
immunogenic activity, may produce an active molecule that is less
immunogenic than wild-type factor VIII. In a preferred embodiment,
the porcine factor VIII is B-domainless.
[0105] The methods for preparing active recombinant hybrid or
hybrid equivalent factor VIII with substitution of amino acid
sequence having little or no immunogenic activity for amino acid
sequence in the factor VIII having immunogenic activity are as
follows, using hybrid human/porcine factor VIII with amino acid
substitutions in the A2 domain as an exemplary embodiment. There
are 25 residues in the human factor VIII region 484-508.
Site-directed mutagenesis can be used to make single mutants in
which any of these residues is replaced by any of the other 19
amino acids for a total of 475 mutants. Furthermore, hybrid
molecules having more than one mutation can be constructed.
[0106] The hybrid constructs can be assayed for antigenicity by
measuring the binding constant for inhibitor antibodies, as
described by Friguet, B. et al. (1985) J. Immunol. Methods
77:305-319 (1985). In a preferred embodiment, the binding constant
will be reduced by at least three orders of magnitude, which would
lower the Bethesda titer to a level that is clinically
insignificant. For example, the IC.sub.50 (a crude measure of the
binding constant) of inhibition by A2 antibodies was reduced in
hybrid human/porcine factor VIII constructs HP2, HP4, HP5, HP7, and
HP9, described in Example 8, and this was associated with a
reduction in Bethesda titer to an unmeasurable level. It is
anticipated, for example, that a double or triple alanine mutant of
human factor VIII (e.g., a human factor VIII Arg484->A1a,
Arg489->A1a, Phe501->Ala triple mutant) will produce a
molecule with sufficiently low antigenicity for therapeutic use.
Similar mutations can be made in the C2 epitope and the putative
third epitope. An embodiment comprises two or three alanine
substitutions into two or three factor VIII epitopes. Other
substitutions into these regions can also be done.
[0107] In an embodiment of the invention, hybrid equivalent factor
VIII molecules will be identified that are less antigenic and/or
immunogenic in human and animal than either human or porcine factor
VIII. Such hybrid equivalent constructs can be tested in animals
for their reduced antigenicity and/or immunogenicity. For example,
control and factor VIII deficient rabbits, pigs, dogs, mice,
primates, and other mammals can be used as animal models. In one
experimental protocol, the hybrid or hybrid equivalent factor VIII
can be administered systematically over a period of six months to
one year to the animal, preferably by intravenous infusion, and in
a dosage range between 5 and 50 Units/kg body weight, preferably
10-50 Units/kg, and most preferably 40 Units/kg body weight.
Antibodies can be measured in plasma samples taken at intervals
after the infusions over the duration of the testing period by
routine methods, including immunoassay and the Bethesda assay.
Coagulant activity can also be measured in samples with routine
procedures, including a one-stage coagulation assay.
[0108] The hybrid equivalent factor VIII molecules can be tested in
humans for their reduced antigenicity and/or immunogenicity in at
least two types of clinical trials. In one type of trial, designed
to determine whether the hybrid or hybrid equivalent factor VIII is
immunoreactive with inhibitory antibodies, hybrid or hybrid
equivalent factor VIII is administered, preferably by intravenous
infusion, to approximately 25 patients having factor VIII
deficiency who have antibodies to factor VIII that inhibit the
coagulant activity of therapeutic human or porcine factor VIII. The
dosage of the hybrid or hybrid equivalent factor VIII is in a range
between 5 and 50 Units/kg body weight, preferably 10-50 Units/kg,
and most preferably 40 Units/kg body weight. Approximately 1 hour
after each administration, the recovery of factor VIII from blood
samples is measured in a one-stage coagulation assay. Samples are
taken again approximately 5 hours after infusion, and recovery is
measured. Total recovery and the rate of disappearance of factor
VIII from the samples is predictive of the antibody titer and
inhibitory activity. If the antibody titer is high, factor VIII
recovery usually cannot be measured. The recovery results are
compared to the recovery of recovery results in patients treated
with plasma-derived human factor VIII, recombinant human factor
VIII, porcine factor VIII, and other commonly used therapeutic
forms of factor VIII or factor VIII substitutes.
[0109] In a second type of clinical trial, designed to determine
whether the hybrid or hybrid equivalent factor VIII is immunogenic,
i.e., whether patients will develop inhibitory antibodies, hybrid
or hybrid equivalent factor VIII is administered, as described in
the preceding paragraph, to approximately 100 previously untreated
hemophiliac patients who have not developed antibodies to factor
VIII. Treatments are given approximately every 2 weeks over a
period of 6 months to 1 year. At 1 to 3 month intervals during this
period, blood samples are drawn and Bethesda assays or other
antibody assays are performed to determine the presence of
inhibitory antibodies. Recovery assays can also be done, as
described above, after each infusion. Results are compared to
hemophiliac patients who receive plasma-derived human factor VIII,
recombinant human factor VIII, porcine factor VIII, or other
commonly used therapeutic forms of factor VIII or factor VIII
substitutes.
Preparation of Hybrid Factor VIII Molecules Using Human and
Non-Porcine, Non-Human Mammalian Factor VIII Amino Acid
Sequence:
[0110] The methods used to prepare hybrid human/porcine factor VIII
with substitution of specific amino acids can be used to prepare
recombinant hybrid human/non-human, non-porcine mammalian or
animal/animal factor VIII protein that has, compared to human or
porcine factor VIII, altered or the same coagulant activity and/or
equal or reduced immunoreactivity and/or immunogenicity, based on
substitution of one or more amino acids in the A2, C2, and/or other
domains.
[0111] Similar comparisons of amino acid sequence identity can be
made between human and non-human, non-porcine mammalian factor VIII
proteins to determine the amino acid sequences in which
procoagulant activity, anti-A2 and anti-C2 immunoreactivity, and or
immunogenicity, or immunoreactivity and/or immunogenicity in other
domains reside. Similar methods can then be used to prepare hybrid
human/non-human, non-porcine mammalian factor VIII molecules. As
described above, functional analysis of each hybrid will reveal
those with decreased reactivity to inhibitory antibodies, and/or
reduced immunogenicity, and/or increased coagulant activity, and
the sequence can be further dissected by point mutation
analysis.
[0112] For example, hybrid human/mouse factor VIII molecules can be
prepared as described above. The amino acid sequence alignment of
the A2 domain of human (SEQ ID NO:2) and mouse (SEQ ID NO:6) is
shown in FIG. 1C. As reported by Elder et al., the factor VIII
protein encoded by the mouse cDNA (SEQ ID NO:5) has 2319 amino
acids, with 74% sequence identity overall to the human sequence
(SEQ ID NO:2) (87 percent identity when the B domain is excluded
from the comparison), and is 32 amino acids shorter than human
factor VIII. The amino acid sequences in the mouse A and C domains
(SEQ ID NO:6) are highly conserved, with 84-93 percent sequence
identity to the human sequence (SEQ ID NO:2), while the B and the
two short acidic domains have 42-70 percent sequence identity.
Specifically, the A1, A2, and A3 mouse amino acid sequences (SEQ ID
NO: 6) are 85, 85, and 90 percent identical to the corresponding
human amino acid sequences (SEQ ID NO:2). The C1 and C2 mouse amino
acid sequences are 93 and 84 percent identical to the corresponding
human amino acid sequences. In the predicted mouse factor VIII
amino acid sequence (SEQ ID NO: 6), the A1, A2, and A3 domains are
homologous to human factor VIII amino acids 1-372, 373-740, and
1690-2032, respectively, using amino acid sequence identity for
numbering purposes.
[0113] The thrombin/factor Xa and all but one activated protein C
cleavage sites are conserved in mouse factor VIII. The tyrosine
residue for von Willebrand factor binding is also conserved.
[0114] According to Elder et al., the nucleotide sequence (SEQ ID
NO:5) of mouse factor VIII contains 7519 bases and has 67 percent
identity overall with the human nucleotide sequence (SEQ ID NO:1).
The 6957 base pairs of murine coding sequence have 82 percent
sequence identity with the 7053 base pairs of coding sequence in
human factor VIII. When the B domain is not included in the
comparison, there is an 88 percent nucleotide sequence
identity.
[0115] Elder et al. report that human and mouse factor VIII
molecules are 74 percent identical overall, and that 95 percent of
the human residues that lead to hemophilia when altered are
identical in the mouse. These data support the application of the
same techniques used to identify amino acid sequence with coagulant
activity and/or immunoreactivity to antibodies in the porcine
factor VIII molecule to the mouse or other animal factor VIII to
identify similar amino acid sequences and prepare hybrid
molecules.
Preparation of Hybrid Factor VIII Molecules Having Reduced
Cross-Reactivity Using Human and Non-Human, Non-Porcine Mammalian
Factor VIII Amino Acid Sequence and Non-Factor VIII Amino Acid
Sequence:
[0116] Porcine factor VIII is used clinically to treat factor VIII
deficiency patients who have inhibitory antibodies to human factor
VIII. Cross-reactivity, in which human plasma reacts with porcine
factor VIII, can be reduced by preparation of hybrid
porcine/non-human, non-porcine mammalian or hybrid equivalent
factor VIII. In a preferred embodiment, a determination of whether
human A2, C2, or other domain-specific inhibitors react with
non-human, non-porcine mammalian ("other mammalian") factor VIII is
made, using the routine Bethesda assay and the particular other
mammalian plasma as the standard. Inhibitor titers are usually
measured in plasma, so purified other mammalian factor VIII is not
necessary. If the inhibitors do not react with the other mammalian
factor VIII, such as murine factor VIII, the sequence of which is
known, then corresponding other mammalian sequence can be
substituted into the porcine epitope region, as identified by using
human/porcine hybrids. Once the animal sequence is known, site
directed mutagenesis techniques, such as oligonucleotide-mediated
mutagenesis described by Kunkel, T. A. et al. (1991) Meth. Enzymol
204: 125-139, can be used to prepare the hybrid porcine/animal
factor VIII molecule. If other animal plasmas are less reactive
with A2, C2, or other factor VIII inhibitors than murine or porcine
factor VIII, the animal sequence corresponding to the porcine
epitope can be determined by routine procedures, such as RT-PCR,
and a hybrid human/animal or porcine/animal factor VIII constructed
by site-directed mutagenesis. Also, hybrid human/animal or
porcine/non-porcine mammalian factor VIII having reduced
cross-reactivity with human plasma compared to porcine factor VIII
can be prepared that has corresponding amino acid sequence
substitution from one or more other animals. In a further
embodiment, cross-reactivity can be reduced by substitution of
amino acid sequence having no known identity to factor VIII amino
acid sequence, preferably alanine residues using alanine scanning
mutagenesis techniques, for porcine epitope sequence.
[0117] After identification of clinically significant epitopes,
recombinant hybrid factor VIII molecules will be expressed that
have less than or equal cross-reactivity compared with porcine
factor VIII when tested in vitro against a broad survey of
inhibitor plasmas. Preferably these molecules will be combined
A2/C2 hybrids in which immunoreactive amino acid sequence in these
domains is replaced by other mammalian sequence. Additional
mutagenesis in these regions may be done to reduce
cross-reactivity. Reduced cross-reactivity, although desirable, is
not necessary to produce a product that may have advantages over
the existing porcine factor VIII concentrate, which produces side
effects due to contaminant porcine proteins and may produce
untoward effects due to the immunogenicity of porcine factor VIII
sequences. A hybrid human/other mammalian or porcine/other
mammalian factor VIII molecule will not contain foreign porcine
proteins. Additionally, the extensive epitope mapping accomplished
in the porcine A2 domain indicates that greater than 95% of the
therapeutic hybrid human/porcine factor VIII sequence will be
human.
Preparation of Hybrid Factor VIII Equivalents:
[0118] The methods for amino acid substitution in factor VIII
molecules described above and in the examples can also be used to
prepare procoagulant recombinant hybrid factor VIII equivalent
molecules or fragments thereof comprising at least one amino acid
sequence including one or more amino acids having no known amino
acid sequence identity to factor VIII ("non-factor VIII sequence")
substituted for at least one specific amino acid sequence that
includes an antigenic and/or immunogenic site in human, animal, or
hybrid factor VIII. The resulting active hybrid factor VIII
equivalent molecule has equal or less reactivity with factor VIII
inhibitory antibodies and/or less immunogenicity in human and
animals than the unsubstituted human, animal, or hybrid factor
VIII.
[0119] Suitable amino acid residues that can be substituted for
those sequences of amino acids critical to coagulant and/or
antigenic and/or immunogenic activity in human or animal factor
VIII or hybrid human/animal factor VIII to prepare a hybrid
equivalent factor VIII molecule include any amino acids having no
known sequence identity to animal or human factor VIII amino acid
sequence that has coagulant, antigenic, or immunogenic activity. In
a preferred embodiment, the amino acids that can be substituted
include alanine residues using alanine scanning mutagenesis
techniques.
[0120] Hybrid factor VIII equivalent molecules described herein
also include those molecules in which amino acid residues having no
known identity to animal factor VIII sequence are substituted for
amino acid residues not critical to coagulant, antigenic, or
immunogenic activity.
[0121] As described above, in one embodiment of a hybrid factor
VIII equivalent molecule, the molecule has reduced cross-reactivity
with inhibitor plasmas. One or more epitopes in the cross-reactive
factor VIII are identified, as described above, and then replaced
by non-factor VIII amino acid sequence, preferably alanine
residues, using, for example, the alanine scanning mutagenesis
method.
[0122] In a preferred embodiment, a procoagulant recombinant hybrid
factor VIII equivalent molecule is prepared comprising at least one
sequence including one or more amino acids having no known sequence
identity to factor VIII, preferably alanine residues, substituted
for at least one sequence including one or more amino acids
including an epitope, and/or for at least one sequence including
one or more amino acids including an immunogenic site, preferably
in human factor VIII. The resulting hybrid equivalent factor VIII
molecule or fragment thereof has reduced or no immunoreactivity
with inhibitory antibodies to factor VIII and/or reduced or no
immunogenicity in human or animals. The methods for identifying
specific antigenic amino acid sequence in the A2 domain of human
factor VIII for substitution by nonantigenic porcine unique amino
acid sequence are described in Examples 7 and 8 and are exemplary
for identifying antigenic sequence in the A2 and other domains of
human and animal factor VIII and for using site-directed
mutagenesis methods such as alanine scanning mutagenesis to
substitute non-factor VIII amino acid sequence.
[0123] Since the human A2 epitope has been narrowed to 25 or few
amino acids, as described in Example 8, alanine scanning
mutagenesis can be performed on a limited number of hybrid factor
VIII constructs having human amino acid sequence to determine which
are procoagulant, non-immunoreactive and/or nonimmunogenic hybrid
factor VIII constructs based on A2 amino acid substitutions. In the
A2 domain, the most likely candidates for alanine substitutions to
achieve both reduced antigenicity and immunogenicity in the hybrid
construct are Arg484, Pro485, Tyr487, Ser488, Arg489, Pro492,
Va1495, Phe501, and Ile508. The binding affinity of a hybrid
construct comprising each of these mutants for mAb413 and a panel
of A2 specific patient IgGs will be determined by ELISA. Any mutant
that is active and has a binding affinity for A2 inhibitors that is
reduced by more than 2 orders of magnitude is a candidate for the
A2 substituted factor VIII molecule. Constructs having more than
one mutation will be selected, based on the assumption that the
more the epitope is altered, the less immunogenic it will be. It is
possible that there are other candidate residues in the region
between Arg484-Ile508, since there may be key residues for the
epitope that are common to both human and porcine factor VIII. For
example, charged residues are frequently involved in
protein-protein interactions and, in fact, an alanine substitute
for Arg490 produces a factor VIII procoagulated having only 0.2% of
the reactivity to inhibitor of human factor VIII (Table VI).
Similarly, an alanine substitution for Lys493 is a possible
candidate.
[0124] This procedure will be carried out in the C2 epitope and the
putative third epitope, which is thought to be in the A3 or C1
domains, as well as any other epitopes identified in factor VIII,
to prepare hybrid equivalent factor VIII constructs.
Diagnostic Assays.
[0125] The hybrid human/animal, animal/animal, or equivalent factor
VIII cDNA and/or protein expressed therefrom, in whole or in part,
can be used in assays as diagnostic reagents for the detection of
inhibitory antibodies to human or animal factor VIII or to hybrid
human/animal factor or equivalent VIII in substrates, including,
for example, samples of serum and body fluids of human patients
with factor VIII deficiency. These antibody assays include assays
such as ELISA assays, immunoblots, radioimmunoassays,
immunodiffusion assays, and assay of factor VIII biological
activity (e.g., by coagulation assay). Techniques for preparing
these reagents and methods for use thereof are known to those
skilled in the art. For example, an immunoassay for detection of
inhibitory antibodies in a patient serum sample can include
reacting the test sample with a sufficient amount of the hybrid
human/animal factor VIII that contains at least one antigenic site,
wherein the amount is sufficient to form a detectable complex with
the inhibitory antibodies in the sample.
[0126] Nucleic acid and amino acid probes can be prepared based on
the sequence of the hybrid human/porcine, human/non-human,
non-porcine mammalian, animal/animal, or equivalent factor VIII
cDNA or protein molecule or fragments thereof. In some embodiments,
these can be labeled using dyes or enzymatic, fluorescent,
chemiluminescent, or radioactive labels that are commercially
available. The amino acid probes can be used, for example, to
screen sera or other body fluids where the presence of inhibitors
to human, animal, or hybrid human/animal factor VIII is suspected.
Levels of inhibitors can be quantitated in patients and compared to
healthy controls, and can be used, for example, to determine
whether a patient with a factor VIII deficiency can be treated with
a hybrid human/animal or hybrid equivalent factor VIII. The cDNA
probes can be used, for example, for research purposes in screening
DNA libraries.
Pharmaceutical Compositions.
[0127] Pharmaceutical compositions containing hybrid human/animal,
porcine/non-human, non-porcine mammalian, animal-1/animal-2, or
equivalent factor VIII, alone or in combination with appropriate
pharmaceutical stabilization compounds, delivery vehicles, and/or
carrier vehicles, are prepared according to known methods, as
described in Remington's Pharmaceutical Sciences by E. W.
Martin.
[0128] In one preferred embodiment, the preferred carriers or
delivery vehicles for intravenous infusion are physiological saline
or phosphate buffered saline.
[0129] In another preferred embodiment, suitable stabilization
compounds, delivery vehicles, and carrier vehicles include but are
not limited to other human or animal proteins such as albumin.
[0130] Phospholipid vesicles or liposomal suspensions are also
preferred as pharmaceutically acceptable carriers or delivery
vehicles. These can be prepared according to methods known to those
skilled in the art and can contain, for example,
phosphatidylserine/-phosphatidylcholine or other compositions of
phospholipids or detergents that together impart a negative charge
to the surface, since factor VIII binds to negatively charged
phospholipid membranes. Liposomes may be prepared by dissolving
appropriate lipid(s) (such as stearoyl phosphatidyl ethanolamine,
stearoyl phosphatidyl choline, arachadoyl phosphatidyl choline, and
cholesterol) in an inorganic solvent that is then evaporated,
leaving behind a thin film of dried lipid on the surface of the
container. An aqueous solution of the hybrid factor VIII is then
introduced into the container. The container is then swirled by
hand to free lipid material from the sides of the container and to
disperse lipid aggregates, thereby forming the liposomal
suspension.
[0131] The hybrid factor or hybrid equivalent factor VIII can be
combined with other suitable stabilization compounds, delivery
vehicles, and/or carrier vehicles, including vitamin K dependent
clotting factors, tissue factor, and von Willebrand factor (vWf) or
a fragment of vWf that contains the factor VIII binding site, and
polysaccharides such as sucrose.
[0132] Hybrid or hybrid equivalent factor VIII can also be
delivered by gene therapy in the same way that human factor VIII
can be delivered, using delivery means such as retroviral vectors.
This method consists of incorporation of factor VIII cDNA into
human cells that are transplanted directly into a factor VIII
deficient patient or that are placed in an implantable device,
permeable to the factor VIII molecules but impermeable to cells,
that is then transplanted. The preferred method will be
retroviral-mediated gene transfer. In this method, an exogenous
gene (e.g., a factor VIII cDNA) is cloned into the genome of a
modified retrovirus. The gene is inserted into the genome of the
host cell by viral machinery where it will be expressed by the
cell. The retroviral vector is modified so that it will not produce
virus, preventing viral infection of the host. The general
principles for this type of therapy are known to those skilled in
the art and have been reviewed in the literature (e.g., Kohn, D. B.
et al. (1989) Transfusion 29:812-820).
[0133] Hybrid factor VIII can be stored bound to vWf to increase
the half-life and shelf-life of the hybrid molecule. Additionally,
lyophilization of factor VIII can improve the yields of active
molecules in the presence of vWf. Current methods for storage of
human and animal factor VIII used by commercial suppliers can be
employed for storage of hybrid factor VIII. These methods include:
(1) lyophilization of factor VIII in a partially-purified state (as
a factor VIII "concentrate" that is infused without further
purification); (2) immunoaffinity-purification of factor VIII by
the Zimmerman method and lyophilization in the presence of albumin,
which stabilizes the factor VIII; (3) lyophilization of recombinant
factor VIII in the presence of albumin.
[0134] Additionally, hybrid factor VIII has been indefinitely
stable at 4.degree. C. in 0.6 M NaCl, 20 mM MES, and 5 mM
CaCl.sub.2 at pH 6.0 and also can be stored frozen in these buffers
and thawed with minimal loss of activity.
Methods of Treatment.
[0135] Hybrid or hybrid equivalent factor VIII is used to treat
uncontrolled bleeding due to factor VIII deficiency (e.g.,
intraarticular, intracranial, or gastrointestinal hemorrhage) in
hemophiliacs with and without inhibitory antibodies and in patients
with acquired factor VIII deficiency due to the development of
inhibitory antibodies. The active materials are preferably
administered intravenously.
[0136] Additionally, hybrid or hybrid equivalent factor VIII can be
administered by transplant of cells genetically engineered to
produce the hybrid or by implantation of a device containing such
cells, as described above.
[0137] In a preferred embodiment, pharmaceutical compositions of
hybrid or hybrid equivalent factor VIII alone or in combination
with stabilizers, delivery vehicles, and/or carriers are infused
into patients intravenously according to the same procedure that is
used for infusion of human or animal factor VIII.
[0138] The treatment dosages of hybrid or hybrid equivalent factor
VIII composition that must be administered to a patient in need of
such treatment will vary depending on the severity of the factor
VIII deficiency. Generally, dosage level is adjusted in frequency,
duration, and units in keeping with the severity and duration of
each patient's bleeding episode. Accordingly, the hybrid factor
VIII is included in the pharmaceutically acceptable carrier,
delivery vehicle, or stabilizer in an amount sufficient to deliver
to a patient a therapeutically effective amount of the hybrid to
stop bleeding, as measured by standard clotting assays.
[0139] Factor VIII is classically defined as that substance present
in normal blood plasma that corrects the clotting defect in plasma
derived from individuals with hemophilia A. The coagulant activity
in vitro of purified and partially-purified forms of factor VIII is
used to calculate the dose of factor VIII for infusions in human
patients and is a reliable indicator of activity recovered from
patient plasma and of correction of the in vivo bleeding defect.
There are no reported discrepancies between standard assay of novel
factor VIII molecules in vitro and their behavior in the dog
infusion model or in human patients, according to Lusher, J. M. et
al. 328 New Engl. J. Med. 328:453-459; Pittman, D. D. et al. (1992)
Blood 79:389-397; and Brinkhous et al. (1985) Proc. Natl. Acad.
Sci. 82:8752-8755.
[0140] Usually, the desired plasma factor VIII level to be achieved
in the patient through administration of the hybrid or hybrid
equivalent factor VIII is in the range of 30-100% of normal. In a
preferred mode of administration of the hybrid or hybrid equivalent
factor VIII, the composition is given intravenously at a preferred
dosage in the range from about 5 to 50 units/kg body weight, more
preferably in a range of 10-50 units/kg body weight, and most
preferably at a dosage of 20-40 units/kg body weight; the interval
frequency is in the range from about 8 to 24 hours (in severely
affected hemophiliacs); and the duration of treatment in days is in
the range from 1 to 10 days or until the bleeding episode is
resolved. See, e.g., Roberts, H. R., and M. R. Jones, "Hemophilia
and Related Conditions--Congenital Deficiencies of Prothrombin
(Factor II, Factor V, and Factors VII to XII)," Ch. 153, 1453-1474,
1460, in Hematology, Williams, W. J., et al., ed. (1990). Patients
with inhibitors may require more hybrid or hybrid equivalent factor
VIII, or patients may require less hybrid or hybrid equivalent
factor VIII because of its higher specific activity than human
factor VIII or decreased antibody reactivity or immunogenicity. As
in treatment with human or porcine factor VIII, the amount of
hybrid or hybrid equivalent factor VIII infused is defined by the
one-stage factor VIII coagulation assay and, in selected instances,
in vivo recovery is determined by measuring the factor VIII in the
patient's plasma after infusion. It is to be understood that for
any particular subject, specific dosage regimens should be adjusted
over time according to the individual need and the professional
judgment of the person administering or supervising the
administration of the compositions, and that the concentration
ranges set forth herein are exemplary only and are not intended to
limit the scope or practice of the claimed composition.
[0141] For information concerning particular examples of dosages,
formulations and administration regimes of the POL1212 factor VIII
protein, see U.S. Patent Publication No. 2007-0173446.
[0142] Treatment can take the form of a single intravenous
administration of the composition or periodic or continuous
administration over an extended period of time, as required.
Alternatively, hybrid or hybrid equivalent factor VIII can be
administered subcutaneously or orally with liposomes in one or
several doses at varying intervals of time.
[0143] Hybrid or hybrid equivalent factor VIII can also be used to
treat uncontrolled bleeding due to factor VIII deficiency in
hemophiliacs who have developed antibodies to human factor VIII. In
this case, coagulant activity that is superior to that of human or
animal factor VIII alone is not necessary. Coagulant activity that
is inferior to that of human factor VIII (i.e., less than 3,000
units/mg) will be useful if that activity is not neutralized by
antibodies in the patient's plasma.
[0144] The hybrid or hybrid equivalent factor VIII molecule and the
methods for isolation, characterization, making, and using it
generally described above will be further understood with reference
to the following non-limiting examples.
Example 1
Assay of Porcine Factor VIII and Hybrid Human/Porcine Factor
VIII
[0145] Porcine factor VIII has more coagulant activity than human
factor VIII, based on specific activity of the molecule. These
results are shown in Table III in Example 4. This conclusion is
based on the use of appropriate standard curves that allow human
porcine factor VIII to be fairly compared. Coagulation assays are
based on the ability of factor VIII to shorten the clotting time of
plasma derived from a patient with hemophilia A. Two types of
assays were employed: the one-stage and the two stage assay.
[0146] In the one-stage assay, 0.1 ml hemophilia A plasma (George
King Biomedical, Inc.) was incubated with 0.1 ml activated partial
thromboplastin reagent (APTT) (Organon Teknika) and 0.01 ml sample
or standard, consisting of diluted, citrated normal human plasma,
for 5 min at 37.degree. C. in a water bath. Incubation was followed
by addition of 0.1 ml 20 mM CaCl.sub.2, and the time for
development of a fibrin clot was determined by visual
inspection.
[0147] A unit of factor VIII is defined as the amount present in 1
ml of citrated normal human plasma. With human plasma as the
standard, porcine and human factor VIII activity were compared
directly. Dilutions of the plasma standard or purified proteins
were made into 0.15 M NaCl, 0.02 M HEPES, pH 7.4. The standard
curve was constructed based on 3 or 4 dilutions of plasma, the
highest dilution being 1/50, and on log.sub.10 clotting time
plotted against log.sub.10 plasma concentration, which results in a
linear plot. The units of factor VIII in an unknown sample were
determined by interpolation from the standard curve.
[0148] The one-stage assay relies on endogenous activation of
factor VIII by activators formed in the hemophilia A plasma,
whereas the two-stage assay measures the procoagulant activity of
preactivated factor VIII. In the two-stage assay, samples
containing factor VIII that had been reacted with thrombin were
added to a mixture of activated partial thromboplastin and human
hemophilia A plasma that had been preincubated for 5 min at
37.degree. C. The resulting clotting times were then converted to
units/ml, based on the same human standard curve described above.
The relative activity in the two-stage assay was higher than in the
one-stage assay because the factor VIII had been preactivated.
Example 2
Characterization of the Functional Difference Between Human and
Porcine Factor VIII
[0149] The isolation of porcine and human plasma-derived factor
VIII and human recombinant factor VIII have been described in the
literature in Fulcher, C. A. et al. (1982) Proc. Natl. Acad. Sci.
USA 79:1648-1652; Toole et al. (1984) Nature 312:342-347 (Genetics
Institute); Gitschier et al. (1984) Nature 312:326-330 (Genentech);
Wood et al. (1984) Nature 312:330-337 (Genentech); Vehar et al. 312
Nature 312:337-342 (Genentech); Fass et al. (1982) Blood 59:594;
Toole et al. (1986) Proc. Natl. Acad. Sci. USA 83:5939-5942. This
can be accomplished in several ways. All these preparations are
similar in subunit composition, although there is a functional
difference in stability between human and porcine factor VIII.
[0150] For comparison of human recombinant and porcine factor VIII,
preparations of highly-purified human recombinant factor VIII
(Cutter Laboratories, Berkeley, Calif.) and porcine factor VIII
(immunopurified as described in Fass et al. (1982) Blood 59:594)
were subjected to high-pressure liquid chromatography (HPLC) over a
Mono Q.TM. (Pharmacia-LKB, Piscataway, N.J.) anion-exchange column
(Pharmacia, Inc.). The purposes of the Mono Q.TM. HPLC step were
elimination of minor impurities of exchange of human and porcine
factor VIII into a common buffer for comparative purposes. Vials
containing 1000-2000 units of factor VIII were reconstituted with 5
ml H.sub.2O. Hepes (2 M at pH 7.4) was then added to a final
concentration of 0.02 M. Factor VIII was applied to a Mono Q.TM. HR
5/5 column equilibrated in 0.15 M NaCl, 0.02 M HEPES, 5 mM
CaCl.sub.2, at pH 7.4 (Buffer A plus 0.15 M NaCl); washed with 10
ml Buffer A+0.15 M NaCl; and eluted with a 20 ml linear gradient,
0.15 M to 0.90 M NaCl in Buffer A at a flow rate of 1 ml/min.
[0151] For comparison of human plasma-derived factor VIII (purified
by Mono Q.TM. HPLC) and porcine factor VIII,
immunoaffinity-purified, plasma-derived porcine factor VIII was
diluted 1:4 with 0.04 M Hepes, 5 mM CaCl.sub.2, 0.01% Tween-80, at
pH 7.4, and subjected to Mono Q.TM. HPLC under the same conditions
described in the previous paragraph for human factor VIII. These
procedures for the isolation of human and porcine factor VIII are
standard for those skilled in the art.
[0152] Column fractions were assayed for factor VIII activity by a
one-stage coagulation assay. The average results of the assays,
expressed in units of activity per A.sub.280 of material, are given
in Table II, and indicate that porcine factor VIII has at least six
times greater activity than human factor VIII when the one-stage
assay is used.
TABLE-US-00002 TABLE II COMPARISON OF HUMAN AND PORCINE FACTOR VIII
COAGULANT ACTIVITY Activity (U/A.sub.280) Porcine 21,300 Human
plasma-derived 3,600 Human recombinant 2,400
Example 3
Comparison of the Stability of Human and Porcine Factor VIII
[0153] The results of the one-stage assay for factor VIII reflect
activation of factor VIII to factor VIIIa in the sample and
possibly loss of formed factor VIIIa activity. A direct comparison
of the stability of human and porcine factor VIII was made. Samples
from Mono Q.TM. HPLC (Pharmacia, Inc., Piscataway, N.J.) were
diluted to the same concentration and buffer composition and
reacted with thrombin. At various times, samples were removed for
two-stage coagulation assay. Typically, peak activity (at 2 min)
was 10-fold greater for porcine than human factor VIIIa, and the
activities of both porcine and human factor VIIIa subsequently
decreased, with human factor VIIIa activity decreasing more
rapidly.
[0154] Generally, attempts to isolate stable human factor VIIIa are
not successful even when conditions that produce stable porcine
factor VIIIa are used. To demonstrate this, Mono Q.TM.
HPLC-purified human factor VIII was activated with thrombin and
subjected to Mono S.TM. cation-exchange (Pharmacia, Inc.) HPLC
under conditions that produce stable porcine factor VIIIa, as
described by Lollar et al. (1989) Biochemistry 28:666.
[0155] Human factor VIII, 43 .mu.g/ml (0.2 .mu.M) in 0.2 M NaCl,
0.01 M HEPES, 2.5 mM CaCl.sub.2, at pH 7.4, in 10 ml total volume,
was reacted with thrombin (0.036 .mu.M) for 10 min, at which time
FPR-CH.sub.2Cl D-phenyl-prolyl-arginyl-chloromethyl ketone was
added to a concentration of 0.2 .mu.M for irreversible inactivation
of thrombin. The mixture then was diluted 1:1 with 40 mM
2-(N-morpholino) ethane sulfonic acid (MES), 5 mM CaCl.sub.2, at pH
6.0, and loaded at 2 ml/min onto a Mono S.TM. HR 5/5 HPLC column
(Pharmacia, Inc.) equilibrated in 5 mM MES, 5 mM CaCl.sub.2, at pH
6.0 (Buffer B) plus 0.1 M NaCl. Factor VIIIa was eluted without
column washing with a 20 ml gradient from 0.1 M NaCl to 0.9 M NaCl
in Buffer B at 1 ml/min.
[0156] The fraction with coagulant activity in the two-stage assay
eluted as a single peak under these conditions. The specific
activity of the peak fraction was approximately 7,500 U/A.sub.280.
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis
(SDS-PAGE) of the Mono S.TM. factor VIIIa peak, followed by silver
staining of the protein, revealed two bands corresponding to a
heterodimeric (A3-C1-C2/A1) derivative of factor VIII. Although the
A2 fragment was not identified by silver staining under these
conditions because of its low concentration, it was identified as a
trace constituent by .sup.125I-labeling.
[0157] In contrast to the results with human factor VIII, porcine
factor VIIIa isolated by Mono S.TM. HPLC under the same conditions
had a specific activity 1.6.times.10.sup.6 U/A.sub.280. Analysis of
porcine factor VIIIa by SDS-PAGE revealed 3 fragments corresponding
to A1, A2, and A3-C1-C2 subunits, demonstrating that porcine factor
VIIIa possesses three subunits.
[0158] The results of Mono S.TM. HPLC of human thrombin-activated
factor VIII preparations at pH 6.0 indicate that human factor VIIIa
is labile under conditions that yield stable porcine factor VIIIa.
However, although trace amounts of A2 fragment were identified in
the peak fraction, determination of whether the coagulant activity
resulted from small amounts of heterotrimeric factor VIIIa or from
heterodimeric factor VIIIa that has a low specific activity was not
possible from this method alone.
[0159] A way to isolate human factor VIIIa before it loses its A2
subunit is desirable to resolve this question. To this end,
isolation was accomplished in a procedure that involves reduction
of the pH of the Mono S.TM. buffers to pH 5. Mono Q.TM.-purified
human factor VIII (0.5 mg) was diluted with H.sub.2O to give a
final composition of 0.25 mg/ml (1 .mu.m) factor VIII in 0.25 M
NaCl, 0.01 M HEPES, 2.5 mM CaCl.sub.2, 0.005% Tween 80, at pH 7.4
(total volume 7.0 ml). Thrombin was added to a final concentration
of 0.072 .mu.m and allowed to react for 3 min. Thrombin was then
inactivated with FPR-CH.sub.2Cl (0.2 .mu.M). The mixture then was
diluted 1:1 with 40 mM sodium acetate, 5 mM CaCl.sub.2, 0.01%
Tween-80, at pH 5.0, and loaded at 2 ml/min onto a Mono S.TM. HR
5/5 HPLC column equilibrated in 0.01 M sodium acetate, 5 mM
CaCl.sub.2, 0.01% Tween 80, at pH 5.0, plus 0.1 M NaCl. Factor
VIIIa was eluted without column washing with a 20 ml gradient from
0.1 M NaCl to 1.0 M NaCl in the same buffer at 1 ml/min. This
resulted in recovery of coagulant activity in a peak that contained
detectable amounts of the A2 fragment as shown by SDS-PAGE and
silver staining. The specific activity of the peak fraction was
tenfold greater than that recovered at pH 6.0 (75,000 U/A.sub.280
v. 7,500 U/A.sub.280). However, in contrast to porcine factor VIIIa
isolated at pH 6.0, which is indefinitely stable at 4.degree. C.,
human factor VIIIa activity decreased steadily over a period of
several hours after elution from Mono S.TM.. Additionally, the
specific activity of factor VIIIa purified at pH 5.0 and assayed
immediately is only 5% that of porcine factor VIIIa, indicating
that substantial dissociation occurred prior to assay.
[0160] These results demonstrate that both human and porcine factor
VIIIa are composed of three subunits (A1, A2, and A3-C1-C2).
Dissociation of the A2 subunit is responsible for the loss of
activity of both human and porcine factor VIIIa under certain
conditions, such as physiological ionic strength, pH, and
concentration. The relative stability of porcine factor VIIIa under
certain conditions is because of stronger association of the A2
subunit.
Example 4
Preparation of Hybrid Human/Porcine Factor VIII by Reconstitution
with Subunits
[0161] Porcine factor VIII light chains and factor VIII heavy
chains were isolated as follows. A 0.5 M solution of EDTA at pH 7.4
was added to Mono Q.TM.-purified porcine factor VIII to a final
concentration of 0.05 M and was allowed to stand at room
temperature for 18-24 h. An equal volume of 10 mM histidine-Cl, 10
mM EDTA, 0.2% v/v Tween 80, at pH 6.0 (Buffer B), was added, and
the solution was applied at 1 ml/min to a Mono S.TM. HR 5/5 column
previously equilibrated in Buffer A plus 0.25 M NaCl. Factor VIII
heavy chains did not bind the resin, as judged by SDS-PAGE. Factor
VIII light chain was eluted with a linear, 20 ml, 0.1-0.7 M NaCl
gradient in Buffer A at 1 ml/min and was homogeneous by SDS-PAGE.
Factor VIII heavy chains were isolated by Mono Q.TM. HPLC
(Pharmacia, Inc., Piscataway, N.J.) in the following way. Factor
VIII heavy chains do not adsorb to Mono S.TM. during the
purification of factor VIII light chains. The fall-through material
that contained factor VIII heavy chains was adjusted to pH 7.2 by
addition of 0.5 M Hepes buffer, pH 7.4, and applied to a Mono Q.TM.
HR5/5 HPLC column (Pharmacia, Inc.) equilibrated in 0.1 M NaCl,
0.02 M Hepes, 0.01% Tween-80, pH 7.4. The column was washed with 10
ml of this buffer, and factor VIII heavy chains were eluted with a
20 ml 0.1-1.0 M NaCl gradient in this buffer. Human light chains
and heavy chains were isolated in the same manner.
[0162] Human and porcine light and heavy chains were reconstituted
according to the following steps. Ten .mu.l human or porcine factor
VIII light chain, 100 .mu.g/ml, was mixed in 1 M NaCl, 0.02 M
Hepes, 5 mM CaCl.sub.2, 0.01% Tween-80, pH 7.4, with (1) 25 .mu.l
heterologous heavy chain, 60 .mu.g/ml, in the same buffer; (2) 10
.mu.l 0.02 M HEPES, 0.01% Tween-80, pH 7.4; (3) 5 .mu.l 0.6 M
CaCl.sub.2, for 14 hr at room temperature. The mixture was diluted
1/4 with 0.02 M MES, 0.01% Tween-80, 5 mM CaCl.sub.2, pH 6 and
applied to Mono S.TM. Hr5/5 equilibrated in 0.1 M NaCl, 0.02 M MES,
0.01% Tween-80, 5 mM Cacl.sub.2, pH 6.0. A 20 ml gradient was run
from 0.1-1.0 M NaCl in the same buffer at 1 ml/min, and 0.5 ml
fractions were collected. Absorbance was read at 280 nm of
fractions, and fractions were assayed with absorbance for factor
VIII activity by the one-stage clotting assay. Heavy chains were
present in excess, because free light chain (not associated with
heavy chain) also binds Mono S.TM.; excess heavy chains ensure that
free light chains are not part of the preparation. Reconstitution
experiments followed by Mono S.TM. HPLC purification were performed
with all four possible combinations of chains: human light
chain/human heavy chain, human light chain/porcine heavy chain,
porcine light chain/porcine heavy chain, porcine light chain/human
heavy chain. Table III shows that human light chain/porcine heavy
chain factor VIII has activity comparable to native porcine factor
VIII (Table II), indicating that structural elements in the porcine
heavy chain are responsible for the increased coagulant activity of
porcine factor VIII compared to human factor VIII.
TABLE-US-00003 TABLE III COMPARISON OF HYBRID HUMAN/PORCINE FACTOR
VIII COAGULANT ACTIVITY WITH HUMAN AND PORCINE FACTOR VIII Activity
(U/A.sub.280) Porcine light chain/porcine heavy chain 30,600 Human
light chain/porcine heavy chain 44,100 Porcine light chain/human
heavy chain 1,100 Human light chain/human heavy chain 1,000
Example 5
Preparation of Active Hybrid Human/Porcine Factor VIII by
Reconstitution with Domains
[0163] The porcine A1/A3-C1-C2 dimer, the porcine A2 domain, the
human A1/A3-C1-C2 dimer, and the human A2 domain were each isolated
from porcine or human blood, according to the method described in
Lollar et al. (1992) J. Biol. Chem. 267(33):23652-23657. For
example, to isolate the porcine A1/A3-C1-C2 dimer, porcine factor
VIIIa (140 .mu.g) at pH 6.0 was raised to pH 8.0 by addition of 5 N
NaOH for 30 minutes, producing dissociation of the A2 domain and 95
percent inactivation by clotting assay. The mixture was diluted 1:8
with buffer B (20 mM HEPES, 5 mM CaCl.sub.2, 0.01% Tween-80, pH
7.4) and applied to a MonoS.TM. column equilibrated in buffer B.
The A1/A3-C1-C2 dimer eluted as a single sharp peak at
approximately 0.4 M NaCl by using a 0.1-1.0 M NaCl gradient in
buffer B. To isolate the porcine A2 domain, porcine factor VIIIa
was made according to the method of Lollar et al. (1989) Biochem
28:666-674, starting with 0.64 mg of factor VIII. Free porcine A2
domain was isolated as a minor component (50 .mu.g) at 0.3 M NaCl
in the MonoS.TM. chromatogram.
[0164] Hybrid human/porcine factor VIII molecules were
reconstituted from the dimers and domains as follows. The
concentrations and buffer conditions for the purified components
were as follows: porcine A2, 0.63 .mu.M in buffer A (5 mM MES; 5 mM
CaCl.sub.2, 0.01% Tween 80, pH 6.0) plus 0.3 M NaCl; porcine
A1/A3-C1-C2, 0.27 .mu.M in buffer B plus 0.4 M NaCl, pH 7.4; human
A2, 1 .mu.M in 0.3 M NaCl, 10 mM histidine-HCl, 5 mM CaCl.sub.2,
0.01% Tween 20, pH 6.0; human A1/A3-C1-C2, 0.18 .mu.M in 0.5 M
NaCl, 10 mM histidine-C1, 2.5 mM CaCl.sub.2, 0.1% Tween-20, pH 6.0.
Reconstitution experiments were done by mixing equal volumes of A2
domain and A1/A3-C1-C2 dimer. In mixing experiments with porcine
A1/A3-C1-C2 dimer, the pH was lowered to 6.0 by addition of 0.5 M
MES, pH 6.0, to 70 mM.
[0165] The coagulation activities of all four possible hybrid
factor VIIIa molecules, pA2/(hA1/A3-C1-C2), hA2/(pA1/A3-C1-C2),
pA2/(pA1/pA3-C1-C2), and hA2/(hA1/A3-C1-C2), were obtained by a
two-stage clotting assay at various times.
[0166] The generation of activity following mixing the A2 domains
and A1/A3-C1-C2 dimers was nearly complete by one hour and was
stable for at least 24 hours at 37.degree. C. Table IV shows the
activity of reconstituted hybrid factor VIIIa molecules when
assayed at 1 hour. The two-stage assay, by which the specific
activities of factor VIIIa molecules were obtained, differs from
the one-stage assay, and the values cannot be compared to activity
values of factor VIII molecules obtained by a one-stage assay.
TABLE-US-00004 TABLE IV COMPARISON OF COAGULANT ACTIVITIES OF
DOMAIN- SUBSTITUTED HYBRID HUMAN/PORCINE FACTOR VIIIa Hybrid fVIIIa
Specific Activity (U/mg) Porcine A2 + Human 140,000 A1/A3-C1-C2
Porcine A2 + Porcine 70,000 A1/A3-C1-C2 Human A2 + Porcine 40,000
A1/A3-C1-C2 Human A2 + Human 40,000 A1/A3-C1-C2
[0167] Table IV shows that the greatest activity was exhibited by
the porcine A2 domain/human A1/A3-C1-C2 dimer, followed by the
porcine A2 domain/porcine A1/A3-C1-C2 dimer.
[0168] Thus, when the A2 domain of porcine factor VIIIa was mixed
with the A1/A3-C1-C2 dimer of human factor VIIIa, coagulant
activity was obtained. Further, when the A2 domain of human factor
VIIIa was mixed with the A1/A3-C1-C2 dimer of porcine factor VIIIa,
coagulant activity was obtained. By themselves, the A2, A1, and
A3-C1-C2 regions have no coagulant activity.
Example 6
Isolation and Sequencing of the A2 Domain of Porcine Factor
VIII
[0169] Only the nucleotide sequence encoding the B domain and part
of the A2 domain of porcine factor VIII has been sequenced
previously (Toole et al. (1986) Proc. Natl. Acad. Sci. USA
83:5939-5942). The cDNA and predicted amino acid sequences (SEQ ID
NOs: 3 and 4, respectively) for the entire porcine factor VIII A2
domain are disclosed herein.
[0170] The porcine factor VIII A2 domain was cloned by reverse
transcription of porcine spleen total RNA and PCR amplification;
degenerate primers based on the known human factor VIII cDNA
sequence and an exact porcine primer based on a part of the porcine
factor VIII sequence were used. A 1 kb PCR product was isolated and
amplified by insertion into a Bluescript.TM. (Stratagene) phagemid
vector.
[0171] The porcine A2 domain was completely sequenced by dideoxy
sequencing. The cDNA and predicted amino acid sequences are as
described in SEQ ID NOs: 3 and 4, respectively.
Example 7
Preparation of Recombinant Hybrid Human/Animal Factor VIII
[0172] The nucleotide and predicted amino acid sequences (SEQ ID
NOs: 1 and 2, respectively) of human factor VIII have been
described in the literature (Toole et al. (1984) Nature 312:342-347
(Genetics Institute); Gitschier et al. Nature 312:326-330
(Genentech); Wood, et al. (1984) Nature 312:330-337 (Genentech);
Vehar et al. Nature 312:337-342 (Genentech)).
[0173] Making recombinant hybrid human/animal factor VIII requires
that a region of human factor VIII cDNA (Biogen Corp.) be removed
and the animal cDNA sequence having sequence identity be inserted.
Subsequently, the hybrid cDNA is expressed in an appropriate
expression system. As an example, hybrid factor VIII cDNAs were
cloned in which some or all of the porcine A2 domain was
substituted for the corresponding human A2 sequences. Initially,
the entire cDNA sequence corresponding to the A2 domain of human
factor VIII and then a smaller part of the A2 domain was looped out
by oligonucleotide-mediated mutagenesis, a method commonly known to
those skilled in the art (see, e.g., Sambrook, J., E. F. Fritsch,
and T. Maniatis, Molecular Cloning: A Laboratory Manual, Chapter
15, Cold Spring Harbor Press, Cold Spring Harbor, 1989). The steps
were as follows.
Materials
[0174]
Methoxycarbonyl-D-cyclohexylglycyl-glycl-arginine-p-nitroanilide
(Spectrozyme.TM. Xa) and anti-factor VIII monoclonal antibodies
ESH4 and ESH8 were purchased from American Diagnostica (Greenwich,
Conn.). Unilamellar phosphatidylcholine/phosphatidylserine (75/25,
w/w) vesicles were prepared according to the method of Barenholtz,
Y., et al., 16 Biochemistry 2806-2810 (1977)). Recombinant
desulfatohirudin was obtained from Dr. R. B. Wallis, Ciba-Geigy
Pharmaceuticals (Cerritos, Calif.). Porcine factors IXa, X, Xa, and
thrombin were isolated according to the methods of Lollar et al.
(1984) Blood 63:1303-1306, and Duffy, E. J. et al. (1992) J. Biol.
Chem. 207:7621-7827. Albumin-free pure recombinant human factor
VIII was obtained from Baxter-Biotech (Deerfield, Ill.).
Cloning of the Porcine Factor VIII A2 Domain
[0175] The cDNA encoding the porcine A2 domain was obtained
following PCR of reverse-transcribed porcine spleen mRNA isolated
as described by Chomczyneki et al. (1987) Anal. Biochem.
162:156-159. cDNA was prepared using the first-strand cDNA
synthesis kit with random hexamers as primers (Pharmacia,
Piscataway, N.J.). PCR was carried out using a 5'-terminal
degenerate primer 5' AARCAYCCNAARACNTGGG 3' (SEQ ID NO:11), based
on known limited porcine A2 amino acid sequence, and a 3'-terminal
exact primer, 5' GCTCGCACTAGGGGGTCTTGAATTC 3' (SEQ ID NO:12), based
on known porcine DNA sequence immediately 3' of the porcine A2
domain. These oligonucleotides correspond to nucleotides 1186-1203
and 2289-2313 in the human sequence (SEQ ID NO:1). Amplification
was carried out for 35 cycles (1 minute 94.degree. C., 2 minutes
50.degree. C., 2 minutes 72.degree. C.) using Taq DNA polymerase
(Promega Corp., Madison, Wis.). The 1.1-kilobase amplified fragment
was cloned into pBluescript.TM. II KS- (Stratagene) at the EcoRV
site using the T-vector procedure, as described by Murchuk, D. et
al. (1991) Nucl. Acids Res. 19:1154. Escherichia coli
XL1-Blue-competent cells were transformed, and plasmid DNA was
isolated. Sequencing was carried out in both directions using
SequenaseJ version 2.0 (U.S. Biochemical Corp., a Division of
Amersham LifeScience, Inc., Arlington Hts, Ill.). This sequence was
confirmed by an identical sequence that was obtained by direct
sequencing of the PCR product from an independent reverse
transcription of spleen RNA from the same pig (CircumVent.TM., New
England Biolabs, Beverly, Mass.). The region containing the epitope
for autoantibody RC was identified as 373-536 in human factor VIII
(SEQ ID NO:2).
Construction and Expression of a Hybrid Human/Porcine Factor VIII
cDNA
[0176] B-domainless human factor VIII (HB.sup.-, from Biogen, Inc.
Cambridge, Mass.), which lacks sequences encoding for amino acid
residues 741-1648 (SEQ ID NO:2), was used as the starting material
for construction of a hybrid human/porcine factor VIII. HB.sup.-
was cloned into the expression vector ReNeo. To facilitate
manipulation, the cDNA for factor VIII was isolated as a XhoI/HpaI
fragment from ReNeo and cloned into XhoI/EcoRV digested
pBlueScript.TM. II KS. An oligonucleotide, 5'
CCTTCCTTTATCCAAATACGTAGATCAAGAGGAAATTGAC 3' (SEQ ID NO:7), was used
in a site-directed mutagenesis reaction using uracil-containing
phage DNA, as described by Kunkel, T. A. et al. (1991) Meth.
Enzymol 204:125-139, to simultaneously loop-out the human A2
sequence (nucleotides 1169-2304 in SEQ ID NO:1) and introduce a
SnaBI restriction site. The A2-domainless human factor VIII
containing plasmid was digested with SnaBI followed by addition of
ClaI linkers. The porcine A2 domain was then amplified by PCR using
the phosphorylated 5' primer 5' GTAGCGTTGCCAAGAAGCACCCTAAGACG 3'
(SEQ ID NO:8) and 3' primer 5'
GAAGAGTAGTACGAGTTATTTCTCTGGGTTCAATGAC 3' (SEQ ID NO:9),
respectively. ClaI linkers were added to the PCR product followed
by ligation into the human factor VIII-containing vector. The A1/A2
and A2/A3 junctions were corrected to restore the precise thrombin
cleavage and flanking sequences by site-directed mutagenesis using
the oligonucleotide shown in SEQ ID NO:8 and nucleotides 1-22 (5'
GAA . . . TTC in SEQ ID NO:9) to correct the 5'- and 3'-terminal
junctions, respectively. In the resulting construct, designated
HP1, the human A2 domain was exactly substituted with the porcine
A2 domain. A preliminary product contained an unwanted thymine at
the A1-A2 junction as a result of the PCR amplification of the
porcine A2 domain. This single base was looped out by use of the
mutagenic oligonucleotide 5' CCTTTATCCAAATACGTAGCGTTTGCCAAGAAG 3'
(SEQ ID NO:10). The resulting hybrid nucleotide sequence encoded
active factor VIII having human A1, porcine A2 and human A3, C1 and
C2 domains.
[0177] A region containing 63% of the porcine NH.sub.2-terminal A2
domain, which encompasses the putative A2 epitope, was substituted
for the homologous human sequence of B-domainless cDNA by
exchanging SpeI/BamHI fragments between the pBluescript plasmids
containing human factor VIII and human/porcine A2 factor VIII cDNA.
The sequence was confirmed by sequencing the A2 domain and splice
sites. Finally, a SpeI/ApaI fragment, containing the entire A2
sequence, was substituted in place of the corresponding sequence in
HB.sup.-, producing the HP2 construct.
[0178] Preliminary expression of HB.sup.- and HP2 in COS-7 cells
was tested after DEAE-dextran-mediated DNA transfection, as
described by Seldon, R. F., in Current Protocols in Molecular
Biology (Ausubel, F. M., et al., eds), pp. 9.21-9.26, Wiley
Interscience, N.Y. After active factor VIII expression was
confirmed and preliminary antibody inhibition studies were done,
HB.sup.- and HP2 DNA were then stably transfected into baby hamster
kidney cells using liposome-mediated transfection (Lipofectin.TM.
Life Technologies, Inc., Carlsbad, Calif.). Plasmid-containing
clones were selected for G418 resistance in Dulbecco's modified
Eagle's medium-F12, 10% fetal calf serum (DMEM-F12/10% fetal calf
serum) containing 400 .mu.g/ml G418, followed by maintenance in
DMEM-F12/10% fetal calf serum containing 100 .mu.g/ml G418.
Colonies showing maximum expression of HB.sup.- and HP2 factor VIII
activity were selected by ring cloning and expanded for further
characterization.
[0179] HB.sup.- and HP2 factor VIII expression was compared by
plasma-free factor VIII assay, one-stage clotting assay, and
enzyme-linked immunosorbent assay using purified recombinant human
factor VIII as a standard. Specific coagulant activities of 2600
and 2580 units/mg were obtained for HB.sup.- and HP2, respectively.
HB.sup.- and HP2 produced 1.2 and 1.4 units/ml/48 hours/10.sup.7
cells, respectively. This is identical to that of the wild type
construct (2,600.+-.200 units/mg). The specific activities of
HB.sup.- and HP2 were indistinguishable in the plasma-free factor
VIII assay.
[0180] The biological activity of recombinant hybrid human/animal
and equivalent factor VIII with A1, A2, A3, C1, and/or C2 domain
substitutions can be evaluated initially by use of a COS-cell
mammalian transient expression system. Hybrid human/animal and
equivalent cDNA can be transfected into COS cells, and supernatants
can be analyzed for factor VIII activity by use of one-stage and
two-stage coagulation assays as described above. Additionally,
factor VIII activity can be measured by use of a chromogenic
substrate assay, which is more sensitive and allows analysis of
larger numbers of samples. Similar assays are standard in the assay
of factor VIII activity (Wood et al. (1984) Nature 312:330-337;
Toole et al. (1984) Nature 312:342-347). Expression of recombinant
factor VIII in COS cells is also a standard procedure (Toole et al.
(1984) Nature 312:342-347; Pittman et al. (1988) Proc. Natl. Acad.
Sci. USA 85:2429-2433).
[0181] The human factor VIII cDNA used as starting materials for
the recombinant molecules described herein has been expressed in
COS cells yielding a product with biological activity. This
material, as described above, can be used as a standard to compare
hybrid human/animal factor VIII molecules. The activity in the
assays is converted to a specific activity for proper comparison of
the hybrid molecules. For this, a measurement of the mass of factor
VIII produced by the cells is necessary and can be done by
immunoassay with purified human and/or animal factor VIII as
standards. Immunoassays for factor VIII are routine for those
skilled in the art (See, e.g., Lollar et al. (1988) Blood
71:137-143).
Example 8
Determination of Inhibitory Activity in Hybrid Human/Animal and
Equivalent Factor VIII
[0182] Sequences of human and animal factor VIII likely to be
involved as epitopes (i.e., as recognition sites for inhibitory
antibodies that react with factor VIII) can be determined using
routine procedures, for example through use of assay with
antibodies to factor VIII combined with site directed mutagenesis
techniques such as splicing by overlap extension methods (SOE), as
shown below. Sequences of animal factor VIII that are not antigenic
compared to corresponding antigenic human sequences can be
identified, and substitutions can be made to insert animal
sequences and delete human sequences according to standard
recombinant DNA methods. Sequences of amino acids such as alanine
residues having no known sequence identity to factor VIII can also
be substituted by standard recombinant DNA methods or by alanine
scanning mutagenesis. Porcine factor VIII reacts less than human
factor VIII with some inhibitory antibodies; this provides a basis
for current therapy for patients with inhibitors. After the
recombinant hybrids are made, they can be tested in vitro for
reactivity with routine assays, including the Bethesda inhibitor
assay. Those constructs that are less reactive than native human
factor VIII and native animal factor VIII are candidates for
replacement therapy.
[0183] The epitopes to which most, if not all, inhibitory
antibodies reactive with human factor VIII are directed are thought
to reside in two regions in the 2332 amino acid human factor VIII
molecule, the A2 domain (amino acid residues 373-740) and the C2
domain (amino acid residues 2173-2332, both sequences shown in SEQ
ID NO:2). The A2 epitope has been eliminated by making a
recombinant hybrid human-porcine factor VIII molecule in which part
of the human A2 domain is replaced by the porcine sequence having
sequence identity to the replaced human amino acid sequence. This
was accomplished, as described in example 7, by cloning the porcine
A2 domain by standard molecular biology techniques and then cutting
and splicing within the A2 domain using restriction sites. In the
resulting construct, designated HP2, residues 373-604 (SEQ ID NO:4)
of porcine factor VIII were substituted into the human A2 domain.
HP2 was assayed for immunoreactivity with anti-human factor VIII
antibodies using the following methods.
Factor VIII Enzyme-Linked Immunosorbent Assay
[0184] Microtiter plate wells were coated with 0.15 ml of 6
.mu.g/ml ESH4, a human factor VIII light-chain antibody, and
incubated overnight. After the plate was washed three times with
H.sub.2O, the wells were blocked for 1 hour with 0.15 M NaCl, 10 mM
sodium phosphate, 0.05% Tween 20, 0.05% nonfat dry milk, 0.05%
sodium azide, pH 7.4. To increase sensitivity, samples containing
factor VIII were activated with 30 nM thrombin for 15 minutes.
Recombinant desulfatohirudin then was added at 100 nM to inhibit
thrombin. The plate was washed again and 0.1 ml of sample or pure
recombinant human factor VIII (10-600 ng/ml), used as the standard,
were added. Following a 2 hour incubation, the plate was washed and
0.1 ml of biotinylated ESH8, another factor VIII light-chain
antibody, was added to each well. ESH8 was biotinylated using the
Pierce sulfosuccinimidyl-6-(biotinamide)hexanoate biotinylation
kit. After a 1 hour incubation, the plate was washed and 0.1 ml of
streptavidin alkaline phosphatase was added to each well. The plate
was developed using the Bio-Rad alkaline phosphatase substrate
reagent kit, and the resulting absorbance at 405 nm for each well
was determined by using a Vmax microtiter plate reader (Molecular
Devices, Inc., Sunnyville, Calif.). Unknown factor VIII
concentrations were determined from the linear portion of the
factor VIII standard curve.
Factor VIII Assays
[0185] HB.sup.- and HP2 factor VIII were measured in a one-stage
clotting assay, which was performed as described above (Bowie, E.
J. W., and C. A. Owen, in Disorders of Hemostasis (Ratnoff and
Forbes, eds) pp. 43-72, Grunn & Stratton, Inc., Orlando, Fla.
(1984)), or by a plasma-free assay as follows. HB.sup.- or HP2
factor VIII was activated by 40 nM thrombin in 0.15 M NaCl, 20 nM
HEPES, 5 mM CaCl.sub.2, 0.01% Tween 80, pH 7.4, in the presence of
10 nM factor IXa, 425 nM factor X, and 50 .mu.M unilamellar
phosphatidylserine/phosphatidylcholine (25/75, w/w) vesicles. After
5 minutes, the reaction was stopped with 0.05 M EDTA and 100 nM
recombinant desulfatohirudin, and the resultant factor Xa was
measured by chromogenic substrate assay, according to the method of
Hill-Eubanks et al (1990) J. Biol. Chem. 265:17854-17858. Under
these conditions, the amount of factor Xa formed was linearly
proportional to the starting factor VIII concentration as judged by
using purified recombinant human factor VIII (Baxter Biotech,
Deerfield, Ill.) as the standard.
[0186] Prior to clotting assay, HB.sup.- or HP2 factor VIII were
concentrated from 48 hour conditioned medium to 10-15 units/ml by
heparin-Sepharose.TM. chromatography. HB.sup.- or HP2 factor VIII
were added to hemophilia A plasma (George King Biomedical) to a
final concentration of 1 unit/ml. Inhibitor titers in RC or MR
plasma or a stock solution of mAb 413 IgG (4 .mu.M) were measured
by the Bethesda assay as described by Kasper, C. K. et al. (1975)
Thromb. Diath. Haemorrh. 34:869-872. Inhibitor IgG was prepared as
described by Leyte, A. et al. (1991) J. Biol. Chem.
266:740-746.
[0187] HP2 does not react with anti-A2 antibodies. Therefore,
residues 373-603 must contain an epitope for anti-A2
antibodies.
Preparation of Hybrid Human-Porcine Factor VIII and Assay by
Splicing by Overlap Extension (SOE)
[0188] Several more procoagulant recombinant hybrid human/porcine
factor VIII B-domainless molecules with porcine amino acid
substitutions in the human A2 region have been prepared to further
narrow the A2 epitope. Besides restriction site techniques, the
"splicing by overlap extension" method (SOE) as described by Ho et
al. (1989) Gene 77:51-59, has been used to substitute any arbitrary
region of porcine factor VIII cDNA. In SOE, the splice site is
defined by overlapping oligonucleotides that can be amplified to
produce the desired cDNA by PCR. Ten cDNA constructs, designated
HP4 through HP13, have been made. They were inserted into the ReNeo
expression vector, stably transfected into baby hamster kidney
cells, and expressed to high levels (0.5-1 .mu.g (approximately 3-6
units)/10.sup.7 cells/24 hours) as described in Example 7. Factor
VIII coagulant activity was determined in the presence and absence
of a model murine monoclonal inhibitory antibody specific for the
A2 domain, mAb413. In the absence of inhibitor, all of the
constructs had a specific coagulant activity that was
indistinguishable from B(-) human factor VIII.
[0189] The hybrid human/porcine factor VIII constructs were assayed
for reactivity with the anti-A2 inhibitor mAb413 using the Bethesda
assay (Kasper et al. (1975) Thromb. Diath. Haemorrh. 34:869-872).
The Bethesda unit (BU) is the standard method for measuring
inhibitor titers. The results are shown in Table V, and are
compared to recombinant human factor VIII.
TABLE-US-00005 TABLE V COMPARISON OF IMMUNOREACTIVITY OF AMINO
ACID- SUBSTITUTED HYBRID HUMAN/PORCINE FACTOR VIII Porcine
Inhibition Construct Substitution mAb413(BU/mg IgG) Human B(-)
fVIII None 1470 HP4 373-540 <0.7 HP5 373-508 <0.7 HP6 373-444
1450 HP7 445-508 <0.7 HP8 373-483 1250 HP9 484-508 <0.7 HP10
373-403 1170 HP11 404-508 <0.7 HP12 489-508 <0.7 HP13 484-488
<0.7
[0190] The boundaries of porcine substitutions are defined by the
first amino acids that differ between human and porcine factor VIII
at the NH.sub.2-terminal and C-terminal ends of the insertion. As
shown in Table V, if the Bethesda titer is not measurable (<0.7
BU/mg IgG), then an A2 epitope lies in the region of substituted
porcine sequence. The epitope has been progressively narrowed to
residues 484-509 (SEQ ID NO:2), consisting of only 25 residues, as
exemplified by non-reactivity of mAb413 with HP9. Among constructs
HP4 through HP11, HP9 was the most "humanized" construct that did
not react with the inhibitor. This indicates that a critical region
in the A2 epitope is located within the sequence Arg484-Ile508.
[0191] Based on a comparison between human and porcine factor VIII
of the amino acid sequence in this critical region, two more
constructs, HP12 and HP13, were made, in which corresponding
porcine amino acid sequence was substituted for human amino acids
489-508 and 484-488, respectively. Neither reacts with mAb413. This
indicates that residues on each side of the Arg488-Ser489 bond are
important for reaction with A2 inhibitors. In HP12 only 5 residues
are non-human, and in HP13 only 4 residues are non-human. The
484-508, 484-488, and 489-508 porcine substituted hybrids displayed
decreased inhibition by A2 inhibitors from four patient plasmas,
suggesting that there is little variation in the structure of the
A2 epitope according to the inhibitor population response.
[0192] The reactivity of the most humanized constructs, HP9, HP12,
and HP13, with two anti-A2 IgGS preparations prepared from
inhibitor plasmas was determined. Like mAb413, these antibodies did
not react with HP9, HP12, and HP13, but did react with the control
constructs HP(-) and HP8.
[0193] The region between 484-508 can be further analyzed for final
identification of the critical A2 epitope, using the same
procedures.
[0194] The methods described in Examples 7 and 8 can be used to
prepare other hybrid human/non-porcine mammalian factor VIII with
amino acid substitution in the human A2 or other domains, hybrid
human/animal or animal/animal factor VIII with amino acid
substitution in any domain, or hybrid factor VII equivalent
molecules or fragments of any of these, such hybrid factor VIII
having reduced or absent immunoreactivity with anti-factor VIII
antibodies.
Example 9
Elimination of Human Factor VIII A2 Inhibitor Reactivity by
Site-Directed Mutagenesis
[0195] Example 8 showed that substitution of the porcine sequence
bounded by residues 484 and 508 into the human factor VIII A2
domain yields a molecule that has markedly decreased reactivity
with a panel of A2-specific factor VIII inhibitors (see also Healey
et al. (1995) J. Biol. Chem. 270:14505-14509). In this region,
there are 9 amino acid differences between human and porcine factor
VIII. These nine residues in human B-domainless factor VIII, R484,
P485, Y487, P488, R489, P492, V495, F501, and I508 (using the
single letter amino code), were individually changed to alanine by
site-directed mutagenesis. Additionally, MluI and Sac2 restriction
sites were placed in the factor VIII cDNA at sites 5' and 3'
relative to the A2 epitope, without changing the amino acids
corresponding to these sites, to facilitate cloning. The nine
mutants were stably transfected into baby hamster kidney cells and
expressed to high levels. All nine produced biologically active
factor VIII. They were partially purified and concentrated by
heparin-Sepharose chromatography as described by Healey et al.
[0196] The mutants have been characterized by their reactivity with
the murine monoclonal inhibitor MAb413 as in Example 7. This
inhibitor recognizes the same or a very closely clustered epitope
in the A2 domain as all human inhibitors studied to date. Inhibitor
reactivity was measured using the Bethesda assay. Briefly, the
Bethesda titer of an inhibitor is the dilution of inhibitor that
inhibits factor VIII by 50% in a standard one-stage factor VIII
clotting assay. For example, if solution of antibody is diluted
1/420 and it inhibits the recombinant factor VIII test sample by
50%, the Bethesda titer is 420 U. In the case of a pure monoclonal
like MAb413, the mass of antibody is known, so the results are
expressed in Bethesda units (BU) per mg MAb413. To find the 50%
inhibition point, a range of dilutions of MAb413 was made and 50%
inhibition was found by a curve fitting procedure. The results are
as follows:
TABLE-US-00006 TABLE VI MAb413 titer % Mutation (BU/mg) Reactivity*
Wild-type, B(-)fVII 9400 -- 484 .fwdarw. A 160 1.7 P485 .fwdarw. A
4000 42 Y487 .fwdarw. A 50 0.53 P488 .fwdarw. A 3500 37 R489
.fwdarw. A 1.6 0.015 R490 .fwdarw. A <B> <0.2> P492
.fwdarw. A 630 6.7 V495 .fwdarw. A 10700 113 F501 .fwdarw. A 11900
126 I508 .fwdarw. A 5620 60 *Relative to wild-type
[0197] These results indicate that it is possible to reduce the
antigenicity of factor VIII toward the model A2 inhibitor by over a
factor of 10 by making alanine substitutions at positions 484, 487,
489, and 492. The reactivity of R489.fwdarw.A is reduced by nearly
4 orders of magnitude. Any of these alanine substitutions can be
therapeutically useful to reduce the antigenicity and the
immunogenicity of factor VIII.
[0198] The results confirm the efficacy of alanine-scanning
mutagenesis and further demonstrate that biological activity is
retained even though the amino acid sequence has been altered
within an epitope reactive to an inhibitory antibody. Five of the
nine sites where the human and porcine sequences differ are also
sites where the human and murine sequences differ. The factor VIIIs
having alanine substitutions at these positions are therefore
examples of a hybrid factor VIII equivalent molecule having a
sequence with no known sequence identify with any presently known
mammalian factor VIII.
[0199] Further modification, e.g. by combining two alanine
substitutions, can also provide greatly reduced antigenicity for a
wider range of patients, since polyclonal variant antibodies
differing from patient to patient can react with variants of the
factor VIII A2 epitope. In addition, immunogenicity (the capacity
to induce antibodies) is further reduced by incorporation of more
than one amino acid substitution. Such substitutions can include
both alanine, porcine-specific amino acids, or other amino acids
known to have low immunogenic potential. The substitutions at
positions 490, 495 and 501 are likely to be useful in reducing
immunogenicity. In addition, these substitutions are likely to
reduce reactivity to certain patient antibodies.
[0200] Other effective, antigenicity-reducing amino acid
substitutions, besides alanine, can be made as long as care is
taken to avoid those previously noted as being major contributors
to antigen-antibody binding energy, or having bulky or charged side
chains. Amino acids whose substitutions within an epitope reduce
the antigenic reactivity thereof are termed
"immunoreactivity-reducing" amino acids herein. Besides alanine,
other immunoreactivity-reducing amino acids include, without
limitation, methionine, leucine, serine and glycine. It will be
understood that the reduction of immunoreactivity achievable by a
given amino acid will also depend on any effects the substitution
may have on protein conformation, epitope accessibility and the
like.
Example 10
[0201] Klenow fragment, phosphorylated ClaI linkers, NotI linkers,
T4 ligase, and Taq DNA polymerase were purchased from Promega
(Madison, Wis.). Polynucleotide kinase was purchased from Life
Technologies, Inc., Carlsbad Calif. .gamma..sup.32P-ATP (Redivue,
>5000 Ci/mmol) was purchased from Amersham. pBluescript II KS-
and E. coli Epicurean XL1-Blue cells were purchased from Stratagene
(La Jolla, Calif.). Synthetic oligonucleotides were purchased from
Life Technologies, Inc. or Cruachem, Inc. 5'-phosphorylated primers
were used when PCR products were produced for cloning purposes.
Nucleotide (nt) numbering of oligonucleotides used as primers for
polymerase chain reaction (PCR) amplification of porcine fVIII cDNA
or genomic DNA uses the human fVIII cDNA as reference (Wood et al.
(1984) supra).
[0202] Porcine spleen total RNA was isolated by acid guanidinium
thiocyanate-phenol-chloroform extraction (Chomczynski et al. (1987)
Anal. Biochem. 162:156-159). Porcine cDNA was prepared from total
spleen RNA using Moloney murine leukemia virus reverse
transcriptase (RT) and random hexamers to prime the reaction
(First-Strand cDNA Synthesis Kit, Pharmacia Biotech) unless
otherwise indicated. RT reactions contained 45 mM Tris-C1, pH 8.3,
68 mM KCl, 15 mM DTT, 9 mM MgCl.sub.2, 0.08 mg/ml bovine serum
albumin and 1.8 mM deoxynucleotide triphosphate (dNTP). Porcine
genomic DNA was isolated from spleen using a standard procedure
(Strauss, W. M. (1995) In Current Protocols in Molecular Biology,
F. M. Ausubel et al., editors, John Wiley & Sons, pp.
2.2.1-2.2.3). Isolation of DNA from agarose gels was done using
Geneclean.TM. II (Bio 101) or Quiex II Gel Extraction Kit
(Qiagen).
[0203] PCR reactions were done using a Hybaid OmniGene
thermocycler. For PCR reactions employing Taq DNA polymerase,
reactions included 0.6 mM MgCl.sub.2, 0.2 mM dNTPs, 0.5 .mu.M
oligonucleotide primers, 50 U/ml polymerase and 0.1 volume of first
strand cDNA reaction mix. Except where indicated otherwise, PCR
products were gel purified, blunt-ended with Klenow fragment,
precipitated with ethanol, and either ligated to the EcoRV site of
dephosphorylated pBluescript II KS- or ligated with phosphorylated
ClaI linkers using T4 ligase, digested with ClaI, purified by
Sephacryl.TM. 5400 chromatography, and ligated to ClaI-cut,
dephosphorylated pBluescript.TM. II KS-. Ligations were done using
T4 DNA ligase (Rapid DNA ligation kit, Boehringer Mannheim) except
where indicated otherwise. Insert-containing pBluescript.TM. II KS-
plasmids were used to transform E. coli Epicurean XL1-Blue
cells.
[0204] Sequencing of plasmid DNA was done using an Applied Bio
systems 373a automated DNA sequencer and the PRISM dye terminator
kit or manually using Sequenase.TM. v. 2.0 sequencing kit (Amersham
Corporation). Direct sequencing of PCR products, including
.sup.32P-end labeling of oligonucleotides was done using a cycle
sequencing protocol (dsDNA Cycle Sequencing System, Life
Technologies).
Isolation of Porcine fVIII cDNA Clones Containing 5' UTR Sequence,
Signal Peptide and A1 Domain Codons
[0205] The porcine fVIII cDNA 5' to the A2 domain was amplified by
nested RT-PCR of female pig spleen total RNA using a 5' rapid
amplification of cDNA ends (5'-RACE) protocol (Marathon cDNA
Amplification, Clontech, Version PR55453). This included first
strand cDNA synthesis using a lock-docking oligo(dT) primer
(Borson, N. D. et al. (1992) PCR Methods Appl. 2:144-148), second
strand cDNA synthesis using E. coli DNA polymerase I, and ligation
with a 5' extended double stranded adaptor, SEQ ID NO:13 (5'-CTA
ATA CGA CTC ACT ATA GGG CTC GAG CGG CCG CCC GGG CAG GT-3)
(3'-H.sub.2N--CCCGTCCA-PO.sub.4-5') whose short strand was blocked
at the 3' end with an amino group to reduce non-specific PCR
priming and which was complementary to the 8 nucleotides at the 3'
end (Siebert, P. D., et al. (1995) Nucleic. Acids. Res.
23:1087-1088). The first round of PCR was done using an
adaptor-specific oligonucleotide, SEQ ID NO:14 (5'-CCA TCC TAA TAC
GAC TCA CTA TAG GGC-3') (designated AP1) as sense primer, and a
porcine fVIII A2 domain specific oligonucleotide SEQ ID NO:15
(5'-CCA TTG ACA TGA AGA CCG TTT CTC-3') (nt 2081-2104) as antisense
primer. The second round of PCR was done using a nested,
adaptor-specific oligonucleotide, SEQ ID NO:16 (5'-ACT CAC TAT AGG
GCT CGA GCG GC-3') (designated AP2) as sense primer, and a nested,
porcine A2 domain-specific oligonucleotide SEQ ID NO:17 (5'-GGG TGC
AAA GCG CTG ACA TCA GTG-3') (nt 1497-1520) as antisense primer. PCR
was carried out using a commercial kit (Advantage cDNA PCR core
kit) which employs an antibody-mediated hot start protocol
(Kellogg, D. E. et al. (1994) BioTechniques 16:1134-1137). PCR
conditions included denaturation at 94.degree. C. for 60 sec,
followed by 30 cycles (first PCR) or 25 cycles (second PCR) of
denaturation for 30 sec at 94.degree. C., annealing for 30 sec at
60.degree. C. and elongation for 4 min at 68.degree. C. using tube
temperature control. This procedure yielded a prominent.apprxeq.1.6
kb product which was consistent with amplification of a fragment
extending approximately 150 bp into the 5' UTR. The PCR product was
cloned into pBluescript.TM. using ClaI linkers. The inserts of four
clones were sequenced in both directions.
[0206] The sequence of these clones included regions corresponding
to 137 bp of the 5' UTR, the signal peptide, the A1 domain and part
of the A2 domain. A consensus was reached in at least 3 of 4 sites.
However, the clones contained an average of 4 apparent
PCR-generated mutations, presumably due to the multiple rounds of
PCR required to generate a clonable product. Therefore, we used
sequence obtained from the signal peptide region to design a sense
strand phosphorylated PCR primer, SEQ ID NO:18 (5'-CCT CTC GAG CCA
CCA TGT CGA GCC ACC ATG CAG CTA GAG CTC TCC ACC TG-3'), designated
RENEOPIGSP, for synthesis of another PCR product to confirm the
sequence and for cloning into an expression vector. The sequence in
bold represents the translation start codon. The sequence 5' to
this represents sequence identical to that 5' of the insertion site
into the mammalian expression vector ReNeo used for expression of
fVIII (Lubin et al. (1994) supra). This site includes an Xho1
cleavage site (underlined). RENEOPIGSP and the nt 1497-1520
oligonucleotide were used to prime a Taq DNA polymerase-mediated
PCR reaction using porcine female spleen cDNA as a template. DNA
polymerases from several other manufacturers failed to yield a
detectable product. PCR conditions included denaturation at
94.degree. C. for four min, followed by 35 cycles of denaturation
for 1 min at 94.degree. C., annealing for 2 min at 55.degree. C.
and elongation for 2 min at 72.degree. C., followed by a final
elongation step for 5 min at 72.degree. C. The PCR product was
cloned into pBluescript using ClaI linkers. The inserts of two of
these clones were sequenced in both directions and matched the
consensus sequence.
Isolation of Porcine fVIII cDNA Clones Containing A3, C1 and 5'
Half of the C2 Domain Codons
[0207] Initially, two porcine spleen RT-PCR products, corresponding
to a B-A3 domain fragment (nt 4519-5571) and a C1-C2 domain
fragment (nt 6405-6990) were cloned. The 3' end of the C2 domain
that was obtained extended into the exon 26 region, which is the
terminal exon in fVIII. The B-A3 product was made using the
porcine-specific B domain primer, SEQ ID NO:19 (5' CGC GCG GCC GCG
CAT CTG GCA AAG CTG AGT T 3'), where the underlined region
corresponds to a region in porcine fVIII that aligns with nt
4519-4530 in human fVIII. The 5' region of the oligonucleotide
includes a NotI site that was originally intended for cloning
purposes. The antisense primer used in generating the B-A3 product,
SEQ ID NO:20 (5'-GAA ATA AGC CCA GGC TTT GCA GTC RAA-3') was based
on the reverse complement of the human fVIII cDNA sequence at nt
5545-5571. The PCR reaction contained 50 mM KCl, 10 mM Tris-C1, pH
9.0, 0.1% Triton.TM. X-100, 1.5 mM MgCl.sub.2, 2.5 mM dNTPs, 20
.mu.M primers, 25 units/ml Taq DNA polymerase and 1/20 volume of RT
reaction mix. PCR conditions were denaturation at 94EC for 3 min,
followed by 30 cycles of denaturation for 1 min at 94.degree. C.,
annealing for 2 min at 50.degree. C. and elongation for 2 min at
72.degree. C. The PCR products were phosphorylated using T4 DNA
kinase and NotI linkers were added. After cutting with NotI, the
PCR fragments were cloned into the NotI site of BlueScript II KS-
and transformed into XL1-Blue cells.
[0208] The C1-C2 product was made using the known human cDNA
sequence to synthesize sense and antisense primers, SEQ ID NO:21
(5'-AGG AAA TTC CAC TGG AAC CTT N-3') (nt 6405-6426) and SEQ ID
NO:22 (5'-CTG GGG GTG AAT TCG AAG GTA GCG N-3') (reverse complement
of nt 6966-6990), respectively. PCR conditions were identical to
those used to generate the B-A2 product. The resulting fragment was
ligated to the pNOT cloning vector using the Prime PCR Cloner
Cloning System (5 Prime-3 Prime, Inc., Boulder, Colo.) and grown in
JM109 cells.
[0209] The B-A3 and C1-C2 plasmids were partially sequenced to make
the porcine-specific sense and antisense oligonucleotides, SEQ ID
NO:23 (5'-GAG TTC ATC GGG AAG ACC TGT TG-3') (nt 4551-4573) and SEQ
ID NO:24 (5'-ACA GCC CAT CAA CTC CAT GCG AAG-3') (nt 6541-6564),
respectively. These oligonucleotides were used as primers to
generate a 2013 bp RT-PCR product using a Clontech Advantage cDNA
PCR kit. This product, which corresponds to human nt 4551-6564,
includes the region corresponding to the light chain activation
peptide (nt 5002-5124), A3 domain (nt 5125-6114) and most of the C1
domain (nt 6115-6573). The sequence of the C1-C2 clone had
established that human and porcine cDNAs from nt 6565 to the 3' end
of the C1 domain were identical. The PCR product cloned into the
EcoRV site of pBluescript.TM. II KS-. Four clones were completely
sequenced in both directions. A consensus was reached in at least 3
of 4 sites.
Isolation of Porcine fVIII cDNA Clones Containing the 3' Half of
the C2 Domain Codons
[0210] The C2 domain of human fVIII (nucleotides 6574-7053) is
contained within exons 24-26 (Gitschier J. et al. (1984) Nature
312:326-330). Human exon 26 contains 1958 bp, corresponding
nucleotides 6901-8858. It includes 1478 bp of 3' untranslated
sequence. Attempts to clone the exon 26 cDNA corresponding to the
3' end of the C2 domain and the 3'UTR by 3' RACE (Siebert et al.
(1995) supra), inverse PCR (Ochman, H. et al. (1990) Biotechnology
(N.Y). 8:759-760), restriction site PCR (Sarkar, G. et al. (1993)
PCR Meth. Appl. 2:318-322), "unpredictably primed" PCR (Dominguez,
O. et al. (1994) Nucleic. Acids Res. 22:3247-3248) and by screening
a porcine liver cDNA library failed. 3' RACE was attempted using
the same adaptor-ligated double stranded cDNA library that was used
to successfully used to clone the 5' end of the porcine fVIII cDNA.
Thus, the failure of this method was not due to the absence of cDNA
corresponding to exon 26.
[0211] A targeted gene walking PCR procedure (Parker, J. D. et al.
(1991) Nucleic. Acids. Res. 19:3055-3060) was used to clone the 3'
half of the C2 domain. A porcine-specific sense primer, SEQ ID
NO:25 (5'-TCAGGGCAATCAGGACTCC-3') (nt 6904-6924) was synthesized
based on the initial C2 domain sequence and was used in a PCR
reaction with nonspecific "walking" primers selected from
oligonucleotides available in the laboratory. The PCR products were
then targeted by primer extension analysis (Parker et al. (1991)
BioTechniques 10:94-101) using a .sup.32P-end labeled
porcine-specific internal primer, SEQ ID NO:26
(5'-CCGTGGTGAACGCTCTGGACC-3') (nt 6932-6952). Interestingly, of the
40 nonspecific primers tested, only two yielded positive products
on primer extension analysis and these two corresponded to an exact
and a degenerate human sequence at the 3' end of the C2 domain: SEQ
ID NO:27 (5'-GTAGAGGTCCTGTGCCTCGCAGCC-3') (nt 7030-7053) and SEQ ID
NO:28 (5'-GTAGAGSTSCTGKGCCTCRCAKCCYAG-3'), (nt 7027-7053). These
primers had initially been designed to yield a product by
conventional RT-PCR but failed to yield sufficient product that
could be visualized by ethidium bromide dye binding. However, a PCR
product could be identified by the more sensitive primer extension
method. This product was gel-purified and directly sequenced. This
extended the sequence of porcine fVIII 3' to nt 7026.
[0212] Additional sequence was obtained by primer extension
analysis of a nested PCR product generated using the
adaptor-ligated double-stranded cDNA library used in the 5'-RACE
protocol described previously. The first round reaction used the
porcine exact primer SEQ ID NO:29 (5'-CTTCGCATGGAGTTGATGGGCTGT-3')
(nt 6541-6564) and the AP1 primer. The second round reaction used
SEQ ID NO:30 (5'-AATCAGGACTCCTCCACCCCCG-3') (nt 6913-6934) and the
AP2 primer. Direct PCR sequencing extended the sequence 3' to the
end of the C2 domain (nt 7053). The C2 domain sequence was unique
except at nt 7045 near the 3' end of the C2 domain. Analysis of
repeated PCR reactions yielded either A, G or a double read of A/G
at this site.
[0213] Sequencing was extended into the 3'UTR using two additional
primers, SEQ ID NO:31 (5'-GGA TCC ACC CCA CGA GCT GG-3') (nt
6977-6996) and SEQ ID NO:32 (5'-CGC CCT GAG GCT CGA GGT TCT AGG-3')
(nt 7008-7031). Approximately 15 bp of 3' UTR sequence were
obtained, although the sequence was unclear at several sites.
Several antisense primers then were synthesized based on the best
estimates of the 3' untranslated sequence. These primers included
the reverse complement of the TGA stop codon at their 3' termini.
PCR products were obtained from both porcine spleen genomic DNA and
porcine spleen cDNA that were visualized by agarose gel
electrophoresis and ethidium bromide staining using a specific
sense primer SEQ ID NO:33 (5'-AAT CAG GAC TCC TCC ACC CCC G-3') (nt
6913-6934) and the 3' UTR antisense primer, SEQ ID NO:34
(5'-CCTTGCAGGAATTCGATTCA-3'). To obtain sufficient quantities of
material for cloning purposes, a second round of PCR was done using
a nested sense primer, SEQ ID NO:35 (5'-CCGTGGTGAACGCTCTGGACC-3')
(nt 6932-6952) and the same antisense primer. The 141 bp PCR
product was cloned into EcoRV-cut pBluescript.TM. II KS-. Sequence
of three clones derived from genomic DNA and three clones derived
from cDNA was obtained in both directions. The sequence was
unambiguous except at nt 7045, where genomic DNA was always A and
cDNA was always G.
Multiple DNA Sequence Alignments of Human, Porcine, and Mouse fVIII
(FIG. 1A-1H)
[0214] Alignments of the signal peptide, A1, A2, A3, C1, and C2
regions were done using the CLUSTALW program (Thompson, J. D. et
al. (1994) Nucleic. Acids. Res. 22:4673-4680). Gap open and gap
extension penalties were 10 and 0.05 respectively. The alignments
of the human, mouse, and pig B domains have been described
previously (Elder et al. (1993) supra). The human A2 sequence
corresponds to amino acids 373-740 in SEQ ID NO:2. The porcine A2
amino acid sequence is given in SEQ ID NO:4, and the mouse A2
domain amino acid sequence is given in SEQ ID NO:6, amino acids
392-759.
Example 11
Expression of Active, Recombinant B-Domainless Porcine Factor VIII
(PB.sup.-)
[0215] Citrated hemophilia A and normal pooled human plasmas were
purchased from George King Biomedical, Inc. Fetal bovine serum,
geneticin, penicillin, streptomycin, DMEM/F12 medium and AIM-V
medium were purchased from Life Technologies, Inc. Taq DNA
polymerase was purchased from Promega. Vent DNA polymerase was
purchased from New England Biolabs. Pfu DNA polymerase and the
phagemid pBlueScript II KS.sup.- were purchased from Stratagene.
Synthetic oligonucleotides were purchased from Life Technologies or
Cruachem, Inc. Restriction enzymes were purchased from New England
Biolabs or Promega. 5'-phosphorylated primers were used when PCR
products were produced for cloning purposes. Nucleotide (nt)
numbering of oligonucleotides used as primers for polymerase chain
reaction (PCR) amplification of porcine fVIII cDNA or genomic DNA
uses the human fVIII cDNA as reference (Wood et al. (1984) Nature
312:330-337). A fVIII expression vector, designated HB.sup.-/ReNeo,
was obtained from Biogen, Inc. HB.sup.-/ReNeo contains ampicillin
and geneticin resistance genes and a human fVIII cDNA that lacks
the entire B domain, defined as the Ser741-Arg1648 cleavage
fragment produced by thrombin. To simplify mutagenesis of fVIII C2
domain cDNA, which is at the 3' end of the fVIII insert in ReNeo, a
NotI site was introduced two bases 3' to the stop codon of
HB.sup.-/ReNeo by splicing-by-overlap extension (SOE) mutagenesis
(Horton, R. M. et al. (1993) Methods Enzymol. 217:270-279). This
construct is designated HB.sup.-ReNeo/NotI.
[0216] Total RNA was isolated by acid guanidinium
thiocyanate-phenol-chloroform extraction (Chomczynski, P. et al.
(1987) Anal. Biochem. 162:156-159). cDNA was synthesized from mRNA
using Moloney murine leukemia virus reverse transcriptase (RT) and
random hexamers according to instructions supplied by the
manufacturer (First-Strand cDNA Synthesis Kit, Pharmacia Biotech).
Plasmid DNA was purified using a Qiagen Plasmid Maxi Kit (Qiagen,
Inc.). PCR reactions were done using a Hybaid OmniGene thermocycler
using Taq, Vent, or Pfu DNA polymerases. PCR products were gel
purified, precipitated with ethanol, and ligated into plasmid DNA
using T4 DNA ligase (Rapid DNA ligation kit, Boehringer Mannheim).
Insert-containing plasmids were used to transform E. coli Epicurean
XL1-Blue cells. All novel fVIII DNA sequences generated by PCR were
confirmed by dideoxy sequencing using an Applied Biosystems 373a
automated DNA sequencer and the PRISM dye terminator kit.
Construction of a Hybrid fVIII Expression Vector, HP20, Containing
the Porcine C2 Domain
[0217] A porcine fVIII cDNA corresponding to the 3' end of the C1
domain and all of the C2 domain was cloned into pBluescript.TM. by
RT-PCR from spleen total RNA using primers based on known porcine
fVIII cDNA sequence (Healy, J. F. et al. (1996) Blood
88:4209-4214). This construct and HB.sup.-/ReNeo were used as
templates to construct a human C1-porcine C2 fusion product in
pBlueScript.TM. by SOE mutagenesis. The C1-C2 fragment in this
plasmid was removed with ApaI and NotI and ligated into
ApaI/NotI-cut HB.sup.-/ReNeo/NotI to produce HP20/ReNeo/NotI.
Construction of B-Domain Deleted Hybrid Human/Porcine fVIII
Containing the Porcine Light Chain (HP18)
[0218] The human fVIII light chain consists of amino acid residues
Asp1649-Tyr2332. The corresponding residues in the porcine fVIII
cDNA were substituted for this region of HB.sup.- to produce a
hybrid human/porcine fVIII molecule designated HP18. This was done
by substituting a PCR product corresponding to porcine A2 region,
the A3 domain, the C1 domain, and part of the C2 domain for the
corresponding region in HP20. To facilitate constructions, a
synonymous AvrII site was introduced into nt 2273 at the junction
of the A2 and A3 domains of HP20 by SOE mutagenesis.
Construction of B-Domain Deleted Hybrid Human/Porcine fVIII
Containing the Porcine Signal Peptide, A1 Domain and A2 Domain
(HP22)
[0219] The human fVIII signal peptide, A1 domain and A2 domains
consist of amino acid residues Met(-19)-Arg740. The corresponding
residues in the porcine fVIII cDNA were substituted for this region
of HB.sup.- to produce a molecule designated HP22. Additionally, a
synonymous AvrII site was introduced into nt 2273 at the junction
of the A2 and A3 domains of HP22 by SOE mutagenesis. HP22 was
constructed by fusion of a porcine signal peptide-A1-partial A2
fragment in pBlueScript.TM. (Healy et al. (1996) supra) with a
B-domainless hybrid human/porcine fVIII containing the porcine A2
domain, designated HP1 (Lubin et al. (1994) supra).
Construction of Porcine B Domainless fVIII-(PB.sup.-)
[0220] A SpeI/NotI fragment of HP18/BS (+AvrII) was digested with
AvrII/NotI and ligated into AvrII/NotI-digested HP22/BS (+AvrII) to
produce a construct PB.sup.-/BS (+AvrII), which consists of the
porcine fVIII lacking the entire B domain. PB- was cloned into
ReNeo by ligating an Xba/NotI fragment of PB.sup.-/BS (+AvrII) into
HP22/ReNeo/NotI (+AvrII).
Expression of Recombinant fVIII Molecules
[0221] PB.sup.-/ReNeo/NotI (+AvrII) and HP22/ReNeo/NotI (+AvrII)
were transiently transfected into COS cells and expressed as
described previously (Lubin, I. M. et al. (1994) J. Biol. Chem.
269:8639-8641). HB.sup.-/ReNeo/NotI and no DNA (mock) were
transfected as a control.
[0222] The fVIII activity of PB.sup.-, HP22, and HB.sup.- were
measured by a chromogenic assay as follows. Samples of fVIII in COS
cell culture supernatants were activated by 40 nM thrombin in 0.15
M NaCl, 20 mM HEPES, 5 mM CaCl.sub.2, 0.01% Tween 80, pH 7.4 in the
presence of 10 nM factor IXa, 425 nM factor X, and 50 .mu.M
unilamellar phosphatidylserine-phosphatidycholine (25/75 w/w)
vesicles. After 5 min, the reaction was stopped with 0.05 M EDTA
and 100 nM recombinant desulfatohirudin and the resultant factor Xa
was measured by chromogenic substrate assay. In the chromogenic
substrate assay, 0.4 mM Spectrozyme Xa was added and the rate of
para-nitroanilide release was measured by measuring the absorbance
of the solution at 405 nm.
[0223] Results of independently transfected duplicate cell culture
supernatants (absorbance at 405 nm per minute)
[0224] HB.sup.-: 13.9
[0225] PB.sup.-: 139
[0226] HP22: 100
[0227] mock: <0.2
[0228] These results indicate that porcine B-domainless fVIII and a
B-domainless fVIII containing the porcine A1 and A2 subunits are
active and suggest that they have superior activity to human
B-domainless fVIII.
[0229] PB.sup.- was partially purified and concentrated from the
growth medium by heparin-Sepharose.TM. chromatography.
Heparin-Sepharose.TM. (10 ml) was equilibrated with 0.075 M NaCl,
10 mM HEPES, 2.5 mM CaCl.sub.2, 0.005% Tween-80, 0.02% sodium
azide, pH 7.40. Medium (100-200 ml) from expressing cells was
applied to the heparin-Sepharose.TM., which then was washed with 30
ml of equilibration buffer without sodium azide. PB.sup.- was
eluted with 0.65 M NaCl, 20 mM HEPES, 5 mM CaCl.sub.2, 0.01%
Tween-80, pH 7.40 and was stored at -80 EC. The yield of fVIII
coagulant activity was typically 50-75%.
Stable Expression of Porcine B-Domainless fVIII (PB.sup.-)
[0230] Transfected cell lines were maintained in Dulbecco's
modified Eagle's medium-F12 containing 10% fetal bovine serum, 50
U/ml penicillin, 50 .mu.g/ml streptomycin. Fetal bovine serum was
heat inactivated at 50EC for one hour before use. HB.sup.-/ReNeo
and PB.sup.-ReNeo/NotI (+AvrII) were stably transfected into BHK
cells and selected for geneticin resistance using a general
protocol that has been described previously (Lubin et al. (1994)
Biol. Chem. 269:8639-8641) except that expressing cells were
maintained in growth medium containing 600 .mu.g/ml geneticin.
Cells from Corning T-75 flasks grown to confluence were transferred
to Nunc triple flasks in medium containing 600 .mu.g/ml geneticin
and grown to confluence. The medium was removed and replaced with
serum-free, AIM-V medium (Life Technologies, Inc.) without
geneticin. Factor VIII expression was monitored by one-stage factor
VIII coagulant activity (vide supra) and 100-150 ml of medium was
collected once daily for four to five days. Maximum expression
levels in medium for HB.sup.- and PB.sup.- were 1-2 units per ml
and 10-12 units per ml of factor VIII coagulant activity,
respectively.
Purification of PB.sup.-
[0231] PB.sup.- was precipitated from culture supernatant using 60%
saturated ammonium sulfate and then purified by W3-3 immunoaffinity
chromatography and Mono Q.TM. high pressure liquid chromatography
as described previously for the purification of plasma-derived
porcine factor VIII (Lollar et al. (1993) Factor VIII/factor VIIIa.
Methods Enzymol. 222:128-143). The specific coagulant activity of
PB.sup.- was measured by a one-stage coagulation assay (Lollar et
al. (1993) supra) and was similar to plasma-derived porcine factor
VIII.
[0232] When analyzed by SDS-polyacrylamide gel electrophoresis, the
PB- preparation contained three bands of apparent molecular masses
160 kDa, 82 kDa, and 76 kDa. The 82 kDa and 76 kDa bands have been
previously described as heterodimer containing the A1-A2 and
ap-A3-C1-C2 domains (where ap refers to an activation peptide)
(Toole et al. (1984) Nature 312:342-347). The 160 kDa band was
transferred to a polyvinylidene fluoride membrane and subjected to
NH2-terminal sequencing, which yielded Arg-Ile-Xx-Xx-Tyr (where Xx
represents undetermined) which is the NH2-terminal sequence of
single chain factor VIII (Toole et al. (1984) supra). Thus, PB- is
partially processed by cleavage between the A2 and A3 domains, such
that it consists of two forms, a single chain A1-A2-ap-A3-C1-C2
protein and a A1-A2/ap-A3-C1-C2 heterodimer. Similar processing of
recombinant HB- has been reported (Lind et al. (1995) Eur. J.
Biochem. 232:19-27).
Characterization of Porcine Factor VIII
[0233] We have determined the cDNA sequence of porcine fVIII
corresponding to 137 bp of the 5' UTR, the signal peptide coding
region (57 bp), and the A1 (1119 bp), A3 (990 bp), C1 (456 bp), and
C2 (483 bp) domains. Along with previously published sequence of
the B domain and light chain activation peptide regions (Toole et
al. (1986) supra) and the A2 domain (Lubin et al. (1994) supra),
the sequence reported here completes the determination of the
porcine fVIII cDNA corresponding to the translated product. A
fragment that included the 5' UTR region, signal peptide, and A1
domain cDNA was cloned using a 5'-RACE RT-PCR protocol. A primer
based on human C2 sequence was successful in producing an RT-PCR
product that led to cloning of the A3, C1, and 5' half of the C2
domain. The cDNA corresponding to the 3' half of the C2 domain and
3' UTR cDNA proved difficult to clone. The remainder of the C2
domain ultimately was cloned by a targeted gene walking PCR
procedure (Parker et al. (1991) supra).
[0234] The sequence reported herein SEQ ID NO:36 was unambiguous
except at nt 7045 near the 3' end of the C2 domain, which is either
A or G as described hereinabove. The corresponding codon is GAC
(Asp) or AAC (Asn). The human and mouse codons are GAC and CAG
(Gln), respectively. Whether this represents a polymorphism or a
reproducible PCR artifact is unknown. Recombinant hybrid
human/porcine B-domainless fVIII cDNAs containing porcine C2 domain
substitutions corresponding to both the GAC and AAC codons have
been stably expressed with no detectable difference in procoagulant
activity. This indicates that there is not a functional difference
between these two C2 domain variants.
[0235] The alignment of the predicted amino acid sequence of
full-length porcine fVIII SEQ ID NO:37 with the published human
(Wood et al. (1984) supra) and murine (Elder et al. (1993) supra)
sequences is shown in FIG. 1A-1H along with sites for
post-translational modification, proteolytic cleavage, and
recognition by other macromolecules. The degree of identity of the
aligned sequences is shown in Table VII. As noted previously, the B
domains of these species are more divergent than the A or C
domains. This is consistent with the observation that the B domain
has no known function, despite its large size (Elder et al. (1993)
supra; Toole et al. (1986) supra). The results of the present
invention confirm that the B domain or porcine fVIII is not
necessary for activity. Based on the sequence data presented
herein, porcine fVIII having all or part of the B-domain deleted
can be synthesized by expressing the porcine fVIII coding DNA
having deleted therefrom all or part of codons of the porcine B
domain. There is also more divergence of sequences corresponding to
the A1 domain APC/factor IXa cleavage peptide (residues 337-372)
and the light chain activation peptide (Table VII). The thrombin
cleavage site at position 336 to generate the 337-372 peptide is
apparently lost in the mouse since this residue is glutamine
instead of arginine (Elder et al. (1993) supra). The relatively
rapid divergence of thrombin cleavage peptides (or in mouse fVIII a
possibly vestigial 337-372 activation peptide) has been previously
noted for the fibrinopeptides (Creighton, T. E. (1993) In Proteins:
Structures and Molecular Properties, W.H. Freeman, New York, pp.
105-138). Lack of biological function of these peptides once
cleaved has been cited as a possible reason for the rapid
divergence. Arg562 in human fVIII has been proposed to be the more
important cleavage site for activated protein C during the
inactivation of fVIII and fVIIIa (Fay, P. J. et al. (1991) J. Biol.
Chem. 266:20139-20145). This site is conserved in human, porcine
and mouse fVIII.
[0236] Potential N-linked glycosylation sites are also shown in
bold in FIG. 1A-1H. There are eight conserved N-linked
glycosylation sites: one in the A1 domain, one in the A2 domain,
four in the B domain, one in the A3 domain, and one in the C1
domain. The 19 A and C domain cysteines are conserved, whereas
there is divergence of B domain cysteines. Six of the seven
disulfide linkages in fVIII are found at homologous sites in factor
V and ceruloplasmin, and both C domain disulfide linkages are found
in factor V (McMullen, B. A. et al. (1995) Protein Sci. 4:740-746).
Human fVIII contains sulfated tyrosines at positions 346, 718, 719,
723, 1664, and 1680 (Pittman, D. D. et al. (1992) Biochemistry
31:3315-3325; Michnick, D. A. et al. (1994) J. Biol. Chem.
269:20095-20102). These residues are conserved in mouse fVIII and
porcine fVIII (FIG. 1), although the CLUSTALW program failed to
align the mouse tyrosine corresponding to Tyr346 in human
fVIII.
[0237] Mouse and pig plasma can correct the clotting defect in
human hemophilia A plasma, which is consistent with the level of
conservation of residues in the A and C domains of these species.
The procoagulant activity of porcine fVIII is superior to that of
human fVIII (Lollar, P. et al. (1992) J. Biol. Chem.
267:23652-23657). The recombinant porcine factor VIII (B
domain-deleted) expressed and purified as herein described also
displays greater specific coagulant activity than human fVIII,
being comparable to plasma-derived porcine fVIII. This may be due
to a decreased spontaneous dissociation rate of the A2 subunit from
the active A1/A2/A3-C1-C2 fVIIIa heterotrimer. Whether this
difference in procoagulant activity reflects an evolutionary change
in function as an example of species adaptation (Perutz, M. F.
(1996) Adv. Protein Chem. 36:213-244) is unknown. Now that the
porcine fVIII cDNA sequence corresponding to the translated product
is complete, homolog scanning mutagenesis (Cunningham, B. C., et
al. (1989) Science 243:1330-1336) may provide a way to identify
structural differences between human and porcine fVIII that are
responsible for the superior activity of the latter.
[0238] Porcine fVIII is typically less reactive with inhibitory
antibodies that arise in hemophiliacs who have been transfused with
fVIII or which arise as autoantibodies in the general population.
This is the basis for using porcine fVIII concentrate in the
management of patients with inhibitory antibodies (Hay and Lozier
(1995) supra). Most inhibitors are directed against epitopes
located in the A2 domain or C2 domain (Fulcher, C. A. et al. (1985)
Proc. Natl. Acad. Sci. USA 82:7728-7732; Scandella, D. et al.
(1988) Proc. Natl. Acad. Sci. USA 85:6152-6156; Scandella, D. et
al. (1989) Blood 74:1618-1626). Additionally, an epitope of unknown
significance has been identified that is in either the A3 or C1
domain (Scandella et al. (1989) supra; Scandella, D. et al. (1993)
Blood 82:1767-1775; Nakai, H. et al. (1994) Blood 84:224a). The A2
epitope has been mapped to residues 484-508 by homolog scanning
mutagenesis (Healey et al. (1995) supra). In this 25 residue
segment, there is relatively low proportion of identical sequence
(16/25 or 64%). It is interesting that this region, which appears
to be functionally important based on the fact that antibodies to
it are inhibitory, apparently has been subjected to relatively more
rapid genetic drift. Alignment of the porcine A2 domain and A3
domains indicate that the A2 epitope shares no detectable homology
with the corresponding region in the A3 domain.
[0239] The C2 inhibitor epitope of human fVIII has been proposed to
be located to within residues 2248-2312 by deletion mapping
(Scandella, D. et al. (1995) Blood 86:1811-1819). Human and porcine
fVIII are 83% identical in this 65 residue segment. However,
homolog scanning mutagenesis of this region to characterize the C2
epitope has revealed that a major determinant of the C2 epitope was
unexpectedly located in the region corresponding to human amino
acids 2181-2243 (SEQ ID NO:2) and FIG. 1H.
[0240] Human-porcine hybrid factor VIII proteins were made in which
various portions of the C2 domain of human factor VIII were
replaced by the corresponding portions of porcine factor VIII,
using the strategy herein described (Example 8). The synthesis of
the various C2-hybrid factor VIIIs was accomplished by constructing
hybrid coding DNA, using the nucleotide sequence encoding the
porcine C2 region given in SEQ ID NO.37. Each hybrid DNA was
expressed in transfected cells, such that the hybrid factor VIIIs
could be partially purified from the growth medium. Activity, in
the absence of any inhibitor, was measured by the one-stage
clotting assay.
[0241] A battery of five human inhibitors was used to test each
hybrid factor VIII. The inhibitor plasmas containing anti factor
VIII antibody had been previously shown to be directed against
human C2 domain, based on the ability of recombinant human C2
domain to neutralize the inhibition. In all the test plasmas, the
inhibitor titer was neutralized greater than 79% by C2 domain or
light chain but less than 10% by recombinant human A2 domain. In
addition the C2-hybrid factor VIIIs were tested against a murine
monoclonal antibody, which binds the C2 domain, and like human C2
inhibitor antibodies, it inhibited the binding of factor VIII to
phospholipid and to von Willebrand factor.
[0242] By comparing the antibody inhibitor titers against the
C2-hybrid factor VIIIs, the major determinant of the human C2
inhibitor epitope was shown to be the region of residues 2181-2243
(SEQ ID NO:2, see also FIG. 1H). Anti-C2 antibodies directed to a
region COOH-terminal to residue 2253 were not identified in four of
the five patient sera. In comparing hybrids having porcine sequence
corresponding to human amino acid residues numbers 2181-2199 and
2207-2243, it was apparent that both regions contribute to antibody
binding. The porcine amino acid sequence corresponding to human
residues 2181-2243 is numbered 1982-2044 in SEQ ID NO:37. The
sequence of porcine DNA encoding porcine amino acids numbered
1982-2044 is nucleotides numbered 5944-6132 in SEQ ID NO:35.
[0243] Referring to FIG. 1H, it can be seen that in the region
2181-2243, there are 16 amino acid differences between the human
and porcine sequences. The differences are found at residues 2181,
2182, 2188, 2195-2197, 2199, 2207, 2216, 2222, 2224-2227, 2234,
2238 and 2243. Amino acid replacement at one or more of these
numbered residues can be carried out to make a modified human
factor VIII non-reactive to human anti-C2 inhibitor antibodies.
Alanine scanning mutagenesis provides a convenient method for
generating alanine substitutions for naturally-occurring residues,
as previously described. Amino acids other than alanine can be
substituted as well, as described herein. Alanine substitutions for
individual amino acids, especially those which are non-identical
between human/porcine or human/mouse or which are most likely to
contribute to antibody binding, can yield a modified factor VIII
with reduced reactivity to inhibitory antibodies.
[0244] In addition, the strategy of inserting amino acids with
lower potential to be immunogenic in the defined region of residues
2181-2243 yields modified factor VIIIs having reduced
immunogenicity. Reduced immunogenicity factor VIII is useful as a
factor VIII supplement for treatment of hemophilia A patients in
preference to natural-sequence factor VIII. Patients treated with
reduced immunogenicity factor VIII are less likely to develop
inhibitory antibodies, and are therefore less likely to suffer from
reduced effectiveness of treatment over their lifetimes.
[0245] FIGS. 1A-1H taken together provide an aligned sequence
comparison of the human, pig and mouse factor VIII amino acid
sequences. FIG. 1A compares signal peptide regions (human, SEQ ID
NO:40; porcine, SEQ ID NO:37, amino acids 1-19; murine, SEQ ID
NO:6, amino acids 1-19). Note that the amino acids in FIG. 1A-1H
are numbered at the first Alanine of the mature protein as number
1, with amino acids of the signal peptide assigned negative
numbers. The Human fVIII sequence in SEQ ID NO:2 also begins with
the first Alanine of the mature protein as amino acid number 1. In
the amino acid sequences of mouse fVIII (SEQ ID NO:6) and porcine
fVIII (SEQ ID NO:37), the first amino acid (alanine) of the mature
sequence is amino acid number 20. FIG. 1A-1H shows an alignment of
the corresponding sequences of human, mouse and pig fVIII, such
that the regions of greatest amino acid identity are juxtaposed.
The amino acid numbers in FIG. 1A-1H apply to human fVIII only.
FIG. 1B gives the amino acid sequences for the A1 domain of human
(SEQ ID NO:2, amino acids 1-372), porcine (SEQ ID NO:37, amino
acids 20-391), and murine (SEQ ID NO:6, amino acids 20-391). FIG.
1C provides amino acid sequences for the Factor VIII A2 domains
from human (SEQ ID NO:2, amino acids 373-740), pig (SEQ ID NO:37,
amino acids 392-759) and mouse (SEQ ID NO:6, amino acids 392-759).
FIG. 1D provides the amino acid sequences of B domains of human
factor VIII (SEQ ID NO:2, amino acids 741-1648), pig (SEQ ID NO:37,
amino acids 760-1449) and mouse (SEQ ID NO:6, amino acids
760-1640). FIG. 1E compares the amino acid sequences of Factor VIII
light chain activation peptides of human, pig and mouse (SEQ ID
NO:2, amino acids 1649-1689; SEQ ID NO:37, amino acids 1450-1490;
and SEQ ID NO:6, amino acids 1641-1678, respectively). FIG. 1F
provides the sequence comparison for human, pig and mouse Factor
VIII A3 domains (SEQ ID NO:2, amino acids 1690-2019; SEQ ID NO:37,
amino acids 1491-1820; and SEQ ID NO:6, amino acids 1679-2006,
respectively. FIG. 1G provides the amino acid sequences of the
Factor VIII C1 domains of human, pig and mouse (SEQ ID NO:2, amino
acids 2020-2172; SEQ ID NO:37, amino acids 1821-1973; and SEQ ID
NO:6, amino acids 2007-2159, respectively). FIG. 1H provides
sequence data for the C2 domains of the Factor VIII C2 domains of
human, pig and mouse (SEQ ID NO:2, amino acids 2173-2332; SEQ ID
NO:37, amino acids 1974-2133; and SEQ ID NO:6, amino acids
2160-2319, respectively).
[0246] The diamonds represent tyrosine sulfation sites, potential
glycosylation sites are in bold type, proposed binding sites for
Factor IXa, phospholipid and Protein C are double-underlined, and
regions involved in binding anti-A2 and anti-C2 inhibitory
antibodies are italicized. Asterisks highlight amino acid sequences
which are conserved. See also SEQ ID NO:36 (porcine factor VIII
cDNA) and SEQ ID NO:37 (deduced amino acid sequence of porcine
factor VIII). The human numbering system is used as the reference
(Wood et al. (1984) supra). The A1, A2, and B domains are defined
by thrombin cleavage sites at positions 372 and 740 and an unknown
protease cleavage site at 1648 as residues 1-372, 373-740, and
741-1648, respectively (Eaton, D. L. et al. (1986) Biochemistry
25:8343-8347). The A3, C1, and C2 domains are defined as residues
1690-2019, 2020-2172, and 2173-2332, respectively (Vehar et al.
(1984) supra). Cleavage sites for thrombin (factor IIa), factor
IXa, factor Xa and APC (Fay et al. (1991) supra; Eaton, D. et al.
(1986) Biochemistry 25:505-512; Lamphear, B. J. et al. (1992) Blood
80:3120-3128) are shown by placing the enzyme name over the
reactive arginine. An acidic peptide is cleaved from the fVIII
light chain by thrombin or factor Xa at position 1689. Proposed
binding sites for factor IXa (Fay, P. J. et al. (1994) J. Biol.
Chem. 269:20522-20527; Lenting, P. J. et al. (1994) J. Biol. Chem.
269:7150-7155), phospholipid (Foster, P. A. et al. (1990) Blood
75:1999-2004) and protein C (Walker, F. J. et al. (1990) J. Biol.
Chem. 265:1484-1489) are doubly underlined. Regions involved in
binding anti-A2 (Lubin et al. (1994) supra; Healey et al. (1995)
supra); and previously proposed for anti-C2 inhibitory antibodies
are italicized. The C2 inhibitor epitope identified as herein
described (human amino acids 2181-2243) is shown by a single
underline in FIG. 1H. Tyrosine sulfation sites (Pittman et al.
(1992) supra; Michnick et al. (1994) supra) are shown by
.diamond-solid.. Recognition sequences for potential N-linked
glycosylation (NXS/T, where X is not proline) are shown in
bold.
Example 12
Construction of POL1212 and Expression in Baby Hamster Kidney
Cells
[0247] POL1212 is a partially B-domainless porcine factor VIII,
having the B-domain deleted except that 12 amino acids of the NH2
terminus of the B-domain and 12 amino acids of the --COOH terminus
are retained. The cDNAs encoding for the sequences for the porcine
fVIII domains A1, A2, ap-A3-C1, and C2 were obtained as described
in Example 5. The DNA nucleotide sequence and derived amino acid
sequence of porcine factor VIII are presented as SEQ ID NO:36 and
SEQ ID NO:37, respectively. In SEQ ID NO:37, the mature porcine
fVIII protein begins at amino acid 20. The amplified fragments were
separately cloned into the plasmid pBluescript.TM. II KS.sup.-
(pBS).
[0248] POL1212 refers to the cDNA encoding porcine fVIII lacking
most of the B domain and containing DNA sequence encoding a 24
amino acid linker between the A2 and ap domains. POL1212 was
constructed in a mammalian expression vector, ReNeo, which was
obtained from Biogen. ReNeo can replicate in bacteria, replicate as
an episome in COS cells for transient expression of factor VIII, or
be stably integrated into a variety of mammalian cells. It consists
of 1) sequences derived from plasmid pBR322 that include an origin
of replication and ampicillin resistance gene, 2) a neomycin
resistance gene whose expression is under control of the SV40
promoter/enhancer, SV40 small t intron, and the SV40
polyadenylation signal regulatory elements, 3) a site for insertion
of fVIII and its signal peptide, the expression of which is under
control of the SV40 enhancer, adenovirus type 2 major late
promoter, and adenovirus type 2 tripartite leader sequence. Any
vector having similar functional components can be used in place of
the ReNeo vector.
[0249] POL1212/ReNeo was prepared in several steps. First, the
cDNAs encoding for porcine fVIII heavy chain (A1-A2) and the cDNAs
encoding for porcine fVIII light chain (ap-A3-C1-C2) were
separately assembled in pBS. From these constructs, the DNA
encoding for porcine B-domainless fVIII was assembled in pBS
(PB-/pBS). This form of porcine fVIII lacks the entire B domain,
defined as amino acids corresponding to residues 741 B 1648 in
human fVIII (human nucleotides 2278-5001). Next, the DNA encoding
for porcine A2 was substituted for the human A2 domain in the human
B-domainless fVIII expression vector ReNeo (HB-/ReNeo). The DNA
encoding the remainder of the porcine heavy chain and the DNA
encoding the porcine light chain was substituted for the human
domains in two additional steps using the porcine heavy chain/pBS
and PB-/pBS constructs made previously. A fragment of the human B
domain encoding the 5 C-terminal and 9 N-terminal amino acids was
inserted between the A2 and A3 domains producing a construct called
PSQ/ReNeo (Healey et al. (1998) Blood 92:3701-3709). Residues
Glu2181-Val2243 contain a major determinant of the inhibitory
epitope in the C2 domain of human factor VIII). This construct was
used as a template to make a fragment of the porcine B domain
encoding for the 12 C-terminal and 12 N-terminal amino acids. This
fragment was inserted between the A2 and A3 domains resulting in
the final construct, POL1212/ReNeo.
[0250] The POL1212 24 amino acid linker consists of the first 12
and last 12 residues of the porcine fVIII B domain. The POL1212
linker has the following sequence: SFAQNSRPPSASAPKPPVLRRHQR (SEQ ID
NO:41). The nucleotide sequence corresponding to the 1212 linker
(SEQ ID NO:42) and surrounding amino acids (SEQ ID NO:43) is:
TABLE-US-00007 GTC ATT GAA CCT AGG AGC TTT GCC CAG AAT TCA AGA V I
E P R S F A Q N S R CCC CCT AGT GCG AGC GCT CCA AAG CCT CCG GTC CTG
P P S A S A P K P P V L CGA CGG CAT CAG AGG GAC ATA AGC CTT CCT ACT
R R H Q R D I S L P T
[0251] The POL1212 linker was synthesized by splicing-by-overlap
extension (SOE) mutagenesis, as follows:
[0252] PCR reactions used to make SOE products were as follows:
Reaction #1
[0253] Outside primer: Rev 4, which is a porcine A2 primer,
nucleotides 1742-1761. (SEQ ID NO:44) The sequence is:
5'-GAGGAAAACCAGATGATGTCA-3' (SEQ ID NO:44).
[0254] Inside primer: OL12, which is a porcine reverse primer
covering the first (5') 15 amino acids of OL1212 and the last (3')
5 amino acids of porcine A2. The sequence is:
5'-CTTTGGAGCGCTCGCACTAGGGGGTCTTGAATTCTGGGCAAAGCTCCTAGGTTC AATGAC-3'
(SEQ ID NO:45). Template: PSQ/ReNeo. Product: porcine DNA from
nucleotide 1742 in the A2 domain to 2322 in OL1212, 580 bp.
Reaction #2
[0255] Outside primer: P2949 is a porcine reverse A3 primer,
nucleotides 2998-3021 of SEQ ID NO:36. The sequence is:
5'-GGTCACTTGTCTACCGTGAGCAGC-3' (see SEQ ID NO:46).
[0256] Inside primer: OL12+, a porcine primer covering the last
(3') 16 amino acids of OL1212 and the first (5') 6 amino acids of
the activation peptide, nucleotide 2302-2367 of SEQ ID NO:36. The
sequence is:
5'-CCTAGTGCGAGCGCTCCAAAGCCTCCGGTCCTGCGACGGCATCAGAGGGACATA
AGCCTTCCTACT-3' (SEQ ID NO:47). Template: PSQ/ReNeo. Product:
porcine from nucleotide 2302 in POL1212 to nucleotide 3021 in the
A3 domain, 719 bp.
SOE Reaction
[0257] Primers: Rev 4, P2949-
[0258] Templates: Fragment from rxn #1 (bp) and low melt fragment
from rxn #2 (bp).
[0259] Product: porcine DNA from nucleotide 1742 in the A2 domain
to nucleotide 3021 in the A3 domain (SEQ ID NO:36) including
OL1212, 1279 bp. The reaction product was ethanol precipitated.
[0260] The 1212 linker was inserted into PSQ/ReNeo by cutting the
SOE product (insert) and PSQ/ReNeo (vector) with BsaB I. The vector
and insert were ligated using T4 ligase and the product was used to
transform E. coli XL1-Blue cells. Plasmid DNA was prepared from
several colonies and the sequence of the 1212 linker and other
PCR-generated sequence was verified by DNA sequence analysis.
Culture of Baby Hamster Kidney (BHK) CRL-1632 Cells
[0261] A BHK cell line was obtained from the ATCC, accession
identification CRL-1632, and was stored frozen at -20.degree. C.
until further use. The cells were thawed at 37.degree. C. and put
into 10 ml of complete medium, defined as DMEM/F12, 50 U/ml
penicillin, 50 .mu.g/ml streptomycin plus 10% fetal bovine serum
(FBS). FBS was purchased from Hyclone, Logan, Utah. The cells were
centrifuged for 2 minutes at 300 RPM. The medium was aspirated and
the cells were resuspended in two ml complete medium in a T-75
flask containing 20 ml of complete medium.
[0262] POL1212 has been expressed in both baby hamster kidney (BHK)
and Chinese hamster ovary (CHO) cells. Two BHK lines were used, the
CRL-1632 line from ATCC and another BHK line obtained from R.
Mcgillivray, University of British Columbia, (Funk et al. (1990)
Biochemistry 29:1654-1660). The latter were subcultured without
selection in the inventors' lab and designated BHK1632 (Emory), on
deposit with the American Type Culture Collection, Manassas, Va.,
Accession No. PTA-4506. The CHO cell line was CHO-K1, ATCC
accession CCL-61. The expression of the average clone from the
Emory cell line and from CHO-K1 cells was somewhat higher than from
CRL-1632 cells as judged by chromogenic assay activity.
[0263] The cells grown in the T-75 flask formed a confluent
monolayer. A 60 ml culture of E. coli XL1-Blue cells in
LB/ampicillin (50 .mu.g/ml) carrying the POL1212/ReNeo plasmid was
prepared.
Transfection of CRL-1632 BHK cells with POL1212/ReNeo
[0264] DNA from the overnight culture of the POL1212/ReNeo XL1-Blue
cells was prepared using a Qiagen, Valencia, Calif. Spin Miniprep
kit. One flask of CRL-1632 cells was split into a stock flask with
0.2 ml and a flask for transfection with 0.3 ml from 2 ml total.
The other flask was fed fresh medium. Medium was DMEM/F12+10%
Hyclone FBS+50 U/ml penicillin, 50 .mu.g/ml streptomycin. CRL-1632
cells were split into 6 well plates aiming for 50-90% confluence
for transfection (0.3 ml of cells from the T-75 flask in 2 ml
1:5000 Versene, Life Technologies, Gaithersburg, Md., in each well)
using fresh DMEM/F12+10% Hyclone FBS+50 U/ml penicillin, 50
.mu.g/ml streptomycin.
[0265] The following solutions were prepared in sterile 1-2 ml test
tubes;
A) 48 .mu.l (10 .mu.g) Miniprep POL1212/ReNeo DNA plus .mu.l medium
without serum (DMEM/F12) plus 10 .mu.l Lipofectin.TM. (Life
Technologies, Gaithersburg, Md.). B) 10 .mu.l Lipofectin.TM. plus
190 .mu.l medium (mock transfection) was gently mixed and the DNA
and Lipofectin allowed to react for 15 minutes at room temperature.
During this time, the cells were washed twice with 2 ml of
DMEM/F12. 1.8 ml of DMEM/F12 was then added to the cells. The
DNA/Lipofectin complex was added dropwise to the cells and swirled
gently to mix. The cells remained in the incubator overnight.
DNA/Lipofectin was removed, and 3 ml of medium with serum was added
to the cells. The cells were incubated 30-48 hours. Geneticin was
purchased from Life Technologies, Gaithersburg, Md. The cell
cultures were divided 1:20, 1:50 and 1:100, 1:250, 1:500 onto 10 cm
dishes in 10 ml of medium with serum containing 535 .mu.g/ml
geneticin. Over the next several days, cells that did not take up
the POL1212/ReNeo plasmid were killed due to the presence of
geneticin. The remaining cells continued to replicate in geneticin,
forming visible monolayer colonies on the dishes. Expression and
assay of POL1212 from BHK CRL-1632 cells
[0266] Small plastic cylindrical rings were placed around the
colonies. The colonies were aspirated separately using complete
medium and transferred to test tubes. These colonies are referred
to as ring cloned colonies. Ring cloned colonies were plated
separately onto 24 well plates and grown in complete medium.
Chromogenic Substrate Assay for Factor VIII Expression by
Transfected CRL-1632 Cells
[0267] Samples of POL1212 from cell culture supernatants were mixed
with 50 nM purified porcine factor IXa and 0.05 mM
phosphatidylcholine/phosphatidylserine (PCPS) vesicles in 0.15M
NaCl, 20 m HEPES, 5 mM CaCl.sub.2, 0.01% Tween 80, pH 7.4. As a
control, cell culture medium from mock-transfected cells was used.
Thrombin and factor X were added simultaneously to final
concentrations of 40 and 425 nM, respectively. Thrombin activates
factor VIII, which then, along with PCPS, serves as a cofactor for
factor IXa during the activation of factor X.
[0268] After 5 min, the activation of factor X by factor IXa/factor
VIIIa/PCPS was stopped by the addition of EDTA to a final
concentration of 50 mM. At the same time the activation of factor
VIII by thrombin was stopped by the addition of the thrombin
inhibitor, recombinant desulfatohirudin, to a final concentration
of 100 nM. A 25 .mu.l sample of the reaction mix was transferred to
a microtiter well, to which was added 74 .mu.l of Spectrozyme.TM.
Xa (America Diagnostica, Greenwich, Conn.), which is a chromogenic
substrate for factor Xa. The final concentration of Spectrozyme.TM.
Xa was 0.6 mM. The absorbance at 405 nm due to the cleavage of
Spectrozyme.TM. Xa by factor Xa was monitored continuously for 5
minutes with a Vmax Kinetic Plate Reader (Molecular Devices, Inc.,
Menlo Park, Calif.). The results are expressed in terms of
A405/min.
TABLE-US-00008 TABLE VII FACTOR VIII CHROMOGENIC ASSAY OF TEN
RING-CLONED COLONIES A.sub.405/min Colony number (.times.10.sup.3)
Buffer 0.2 1 2.1 2 8.4 3 6.4 4 10.7 5 12.5 6 7.6 7 51.3 8 139.5 9
3.8 10 8.4
These results show that all ten colonies that were selected express
factor VIII activity that is at least ten-fold greater than
background.
[0269] The activity from medium of colony 8, which was the highest
expressing colony, was further examined by one-state factor VIII
clotting assay. In this assay, 50 ml of factor VIII deficient
plasma (George King Biomedical Overland Park, Kans.), 5 ml sample
or standard, and 50 ml of activated particulate thromboplastin time
reagent (Organon Teknika, Durham, N.C.) were incubated 3 min at 37E
C. Samples include colony 8 medium diluted in 0.15 M NaCl, mM
hepes, pH 7.4 (HBS) or, as a control, complete medium. Clotting was
initiated by addition of 50 ml of 20 mM CaCl.sub.2. The clotting
time was measured using an ST4 BIO Coagulation Instrument
(Diagnostica Stago, Parsippany, N.J.). A standard curve was
obtained by making dilutions of pooled, citrated normal human
plasma, lot 0641 (George King Biomedical, Overland Park, Kans.).
The factor VIII concentration of the standard was 0.9 units per
ml.
TABLE-US-00009 TABLE VIII STANDARD CURVE Dilution U/ml Clot Time 1)
Undiluted 0.96 45.2 2) 1/3 (HBS) 0.32 53.7 3) 1/11 (HBS) 0.087 62.5
4) 1/21 (HBS) 0.046 68.9
[0270] Linear regression of the clotting times versus the logarithm
of the concentration of standard yielded a correlation coefficient
of 0.997.
[0271] Test substances gave the following clotting times, which
were converted to units per ml using the standard curve:
TABLE-US-00010 TABLE IX Sample Clot Time (sec) Units/ml 1) Colony 8
(24 h), 1/10 in HBS 40.6 1.74 .times. 10 = 17.4 2) Colony 8 (24 h),
1/10 in HBS 41.1 1.63 .times. 10 = 16.3 3) Colony 8 (24 h), 1/20 in
HBS 47.7 0.69 .times. 20 = 13.8 4) Colony 8 (24 h), 1/20 in HBS
47.2 0.73 .times. 20 = 14.6 5) Complete medium 82.9 0.007 6)
Complete medium 83.3 0.006
These results show that colony 8 clotting activity that is
approximately 2000-fold higher than the control sample.
[0272] The DNA sequence encoding POL1212 (and its 19 amino acid
N-terminal signal peptide) is set forth as SEQ ID NO:48. The
encoded amino acid sequence of POL1212 is set forth as SEQ ID
NO:49. The amino acid sequence of the mature protein after removal
of the signal peptide is provided, as well as the signal peptide
sequence. Further purification of POL1212 can be carried out using
a variety of known methods such as immunoaffinity chromatography
and HPLC chromatography; see Examples 2 and 3 of U.S. Pat. No.
6,458,563.
[0273] For especially advantageous methods of treatment comprising
administration of POL1212 for controlling bleeding a patient in
need of such treatment, see U.S. patent application Ser. No.
11/549,049, filed Oct. 12, 2006, and issued as U.S. Pat. No.
7,576,181 on Aug. 18, 2009, which is incorporated by reference
herein.
[0274] OBI-1 (for recombinant partially B-domainless porcine fVIII)
is also termed POL-1212 in U.S. Pat. No. 6,458,563. Both names,
OBI-1 and POL1212, refer to the same substance, porcine fVIII
having the B-domain deleted except for 12 amino acids at the
N-terminal part of the B-domain and 12 amino acids at the
C-terminal part of the B-domain. The DNA sequence encoding OBI-1 is
given in SEQ ID NO:48. The deduced amino acid sequence of OBI-1
protein is given in SEQ ID NO:49, along with that of the 19 amino
acid leader (signal) peptide. OBI-1 is a protein having a deduced
amino acid sequence of amino acids 1-1448 of SEQ ID NO:49. OBI-1
protein is made by expression of the DNA of SEQ ID NO:48 in a
transformed mammalian host cell, which results in removal of the
signal peptide, amino acids -19 to 1 of SEQ ID NO:49, and secretion
of the protein from the host cell into the cell culture
supernatant. Therefore, OBI-1 is herein defined as the product of
expression of the DNA of SEQ ID NO:48 in a mammalian host cell.
Previous studies (Doering, C. B. et al. (2002) J. Biol. Chem.
277:39345-38349) have documented that the B-domain of porcine fVIII
can be deleted without loss of activity.
[0275] While POL1212 is a particularly preferred Factor VIII
derivative, it will be understood that minor variations of amino
acid sequence or the DNA encoding such sequence relating to POL1212
can be introduced without affecting the essential attributes of
function. For example, the length of B-domain sequence retained as
a linker between the A2 domain and the activation peptide can be
increased or decreased within limits known in the art. Sequence
variants can be introduced in the linker region while retaining the
equivalent functional attributes of POL1212 as taught herein and of
porcine B-domainless factor VIII as taught herein and as known in
the art. Based on comparisons of known factor VIII amino acid
sequences having coagulant activity in human blood, sequence
variants such as individual amino acid substitutions or
substitution of peptide segments with known functional variants can
be made in the basic POL1212 amino acid sequence, while retaining
the equivalent functional attributes thereof. The foregoing types
of variation are not intended as exhaustive, but are merely
exemplary of the sequence modifications that could be made by those
of ordinary skill in the art, without substantially modifying the
functional attributes of the protein. All such variants and
modifications are deemed to fall within the scope of the invention
as claimed or as equivalents thereof.
[0276] The Sequence Listing is incorporated by reference herein.
Sequence CWU 1
1
4919009DNAHomo sapiens 1cagtgggtaa gttccttaaa tgctctgcaa agaaattggg
acttttcatt aaatcagaaa 60ttttactttt ttcccctcct gggagctaaa gatattttag
agaagaatta accttttgct 120tctccagttg aacatttgta gcaataagtc
atgcaaatag agctctccac ctgcttcttt 180ctgtgccttt tgcgattctg
ctttagtgcc accagaagat actacctggg tgcagtggaa 240ctgtcatggg
actatatgca aagtgatctc ggtgagctgc ctgtggacgc aagatttcct
300cctagagtgc caaaatcttt tccattcaac acctcagtcg tgtacaaaaa
gactctgttt 360gtagaattca cggttcacct tttcaacatc gctaagccaa
ggccaccctg gatgggtctg 420ctaggtccta ccatccaggc tgaggtttat
gatacagtgg tcattacact taagaacatg 480gcttcccatc ctgtcagtct
tcatgctgtt ggtgtatcct actggaaagc ttctgaggga 540gctgaatatg
atgatcagac cagtcaaagg gagaaagaag atgataaagt cttccctggt
600ggaagccata catatgtctg gcaggtcctg aaagagaatg gtccaatggc
ctctgaccca 660ctgtgcctta cctactcata tctttctcat gtggacctgg
taaaagactt gaattcaggc 720ctcattggag ccctactagt atgtagagaa
gggagtctgg ccaaggaaaa gacacagacc 780ttgcacaaat ttatactact
ttttgctgta tttgatgaag ggaaaagttg gcactcagaa 840acaaagaact
ccttgatgca ggatagggat gctgcatctg ctcgggcctg gcctaaaatg
900cacacagtca atggttatgt aaacaggtct ctgccaggtc tgattggatg
ccacaggaaa 960tcagtctatt ggcatgtgat tggaatgggc accactcctg
aagtgcactc aatattcctc 1020gaaggtcaca catttcttgt gaggaaccat
cgccaggcgt ccttggaaat ctcgccaata 1080actttcctta ctgctcaaac
actcttgatg gaccttggac agtttctact gttttgtcat 1140atctcttccc
accaacatga tggcatggaa gcttatgtca aagtagacag ctgtccagag
1200gaaccccaac tacgaatgaa aaataatgaa gaagcggaag actatgatga
tgatcttact 1260gattctgaaa tggatgtggt caggtttgat gatgacaact
ctccttcctt tatccaaatt 1320cgctcagttg ccaagaagca tcctaaaact
tgggtacatt acattgctgc tgaagaggag 1380gactgggact atgctccctt
agtcctcgcc cccgatgaca gaagttataa aagtcaatat 1440ttgaacaatg
gccctcagcg gattggtagg aagtacaaaa aagtccgatt tatggcatac
1500acagatgaaa cctttaagac tcgtgaagct attcagcatg aatcaggaat
cttgggacct 1560ttactttatg gggaagttgg agacacactg ttgattatat
ttaagaatca agcaagcaga 1620ccatataaca tctaccctca cggaatcact
gatgtccgtc ctttgtattc aaggagatta 1680ccaaaaggtg taaaacattt
gaaggatttt ccaattctgc caggagaaat attcaaatat 1740aaatggacag
tgactgtaga agatgggcca actaaatcag atcctcggtg cctgacccgc
1800tattactcta gtttcgttaa tatggagaga gatctagctt caggactcat
tggccctctc 1860ctcatctgct acaaagaatc tgtagatcaa agaggaaacc
agataatgtc agacaagagg 1920aatgtcatcc tgttttctgt atttgatgag
aaccgaagct ggtacctcac agagaatata 1980caacgctttc tccccaatcc
agctggagtg cagcttgagg atccagagtt ccaagcctcc 2040aacatcatgc
acagcatcaa tggctatgtt tttgatagtt tgcagttgtc agtttgtttg
2100catgaggtgg catactggta cattctaagc attggagcac agactgactt
cctttctgtc 2160ttcttctctg gatatacctt caaacacaaa atggtctatg
aagacacact caccctattc 2220ccattctcag gagaaactgt cttcatgtcg
atggaaaacc caggtctatg gattctgggg 2280tgccacaact cagactttcg
gaacagaggc atgaccgcct tactgaaggt ttctagttgt 2340gacaagaaca
ctggtgatta ttacgaggac agttatgaag atatttcagc atacttgctg
2400agtaaaaaca atgccattga accaagaagc ttctcccaga attcaagaca
ccctagcact 2460aggcaaaagc aatttaatgc caccacaatt ccagaaaatg
acatagagaa gactgaccct 2520tggtttgcac acagaacacc tatgcctaaa
atacaaaatg tctcctctag tgatttgttg 2580atgctcttgc gacagagtcc
tactccacat gggctatcct tatctgatct ccaagaagcc 2640aaatatgaga
ctttttctga tgatccatca cctggagcaa tagacagtaa taacagcctg
2700tctgaaatga cacacttcag gccacagctc catcacagtg gggacatggt
atttacccct 2760gagtcaggcc tccaattaag attaaatgag aaactgggga
caactgcagc aacagagttg 2820aagaaacttg atttcaaagt ttctagtaca
tcaaataatc tgatttcaac aattccatca 2880gacaatttgg cagcaggtac
tgataataca agttccttag gacccccaag tatgccagtt 2940cattatgata
gtcaattaga taccactcta tttggcaaaa agtcatctcc ccttactgag
3000tctggtggac ctctgagctt gagtgaagaa aataatgatt caaagttgtt
agaatcaggt 3060ttaatgaata gccaagaaag ttcatgggga aaaaatgtat
cgtcaacaga gagtggtagg 3120ttatttaaag ggaaaagagc tcatggacct
gctttgttga ctaaagataa tgccttattc 3180aaagttagca tctctttgtt
aaagacaaac aaaacttcca ataattcagc aactaataga 3240aagactcaca
ttgatggccc atcattatta attgagaata gtccatcagt ctggcaaaat
3300atattagaaa gtgacactga gtttaaaaaa gtgacacctt tgattcatga
cagaatgctt 3360atggacaaaa atgctacagc tttgaggcta aatcatatgt
caaataaaac tacttcatca 3420aaaaacatgg aaatggtcca acagaaaaaa
gagggcccca ttccaccaga tgcacaaaat 3480ccagatatgt cgttctttaa
gatgctattc ttgccagaat cagcaaggtg gatacaaagg 3540actcatggaa
agaactctct gaactctggg caaggcccca gtccaaagca attagtatcc
3600ttaggaccag aaaaatctgt ggaaggtcag aatttcttgt ctgagaaaaa
caaagtggta 3660gtaggaaagg gtgaatttac aaaggacgta ggactcaaag
agatggtttt tccaagcagc 3720agaaacctat ttcttactaa cttggataat
ttacatgaaa ataatacaca caatcaagaa 3780aaaaaaattc aggaagaaat
agaaaagaag gaaacattaa tccaagagaa tgtagttttg 3840cctcagatac
atacagtgac tggcactaag aatttcatga agaacctttt cttactgagc
3900actaggcaaa atgtagaagg ttcatatgag ggggcatatg ctccagtact
tcaagatttt 3960aggtcattaa atgattcaac aaatagaaca aagaaacaca
cagctcattt ctcaaaaaaa 4020ggggaggaag aaaacttgga aggcttggga
aatcaaacca agcaaattgt agagaaatat 4080gcatgcacca caaggatatc
tcctaataca agccagcaga attttgtcac gcaacgtagt 4140aagagagctt
tgaaacaatt cagactccca ctagaagaaa cagaacttga aaaaaggata
4200attgtggatg acacctcaac ccagtggtcc aaaaacatga aacatttgac
cccgagcacc 4260ctcacacaga tagactacaa tgagaaggag aaaggggcca
ttactcagtc tcccttatca 4320gattgcctta cgaggagtca tagcatccct
caagcaaata gatctccatt acccattgca 4380aaggtatcat catttccatc
tattagacct atatatctga ccagggtcct attccaagac 4440aactcttctc
atcttccagc agcatcttat agaaagaaag attctggggt ccaagaaagc
4500agtcatttct tacaaggagc caaaaaaaat aacctttctt tagccattct
aaccttggag 4560atgactggtg atcaaagaga ggttggctcc ctggggacaa
gtgccacaaa ttcagtcaca 4620tacaagaaag ttgagaacac tgttctcccg
aaaccagact tgcccaaaac atctggcaaa 4680gttgaattgc ttccaaaagt
tcacatttat cagaaggacc tattccctac ggaaactagc 4740aatgggtctc
ctggccatct ggatctcgtg gaagggagcc ttcttcaggg aacagaggga
4800gcgattaagt ggaatgaagc aaacagacct ggaaaagttc cctttctgag
agtagcaaca 4860gaaagctctg caaagactcc ctccaagcta ttggatcctc
ttgcttggga taaccactat 4920ggtactcaga taccaaaaga agagtggaaa
tcccaagaga agtcaccaga aaaaacagct 4980tttaagaaaa aggataccat
tttgtccctg aacgcttgtg aaagcaatca tgcaatagca 5040gcaataaatg
agggacaaaa taagcccgaa atagaagtca cctgggcaaa gcaaggtagg
5100actgaaaggc tgtgctctca aaacccacca gtcttgaaac gccatcaacg
ggaaataact 5160cgtactactc ttcagtcaga tcaagaggaa attgactatg
atgataccat atcagttgaa 5220atgaagaagg aagattttga catttatgat
gaggatgaaa atcagagccc ccgcagcttt 5280caaaagaaaa cacgacacta
ttttattgct gcagtggaga ggctctggga ttatgggatg 5340agtagctccc
cacatgttct aagaaacagg gctcagagtg gcagtgtccc tcagttcaag
5400aaagttgttt tccaggaatt tactgatggc tcctttactc agcccttata
ccgtggagaa 5460ctaaatgaac atttgggact cctggggcca tatataagag
cagaagttga agataatatc 5520atggtaactt tcagaaatca ggcctctcgt
ccctattcct tctattctag ccttatttct 5580tatgaggaag atcagaggca
aggagcagaa cctagaaaaa actttgtcaa gcctaatgaa 5640accaaaactt
acttttggaa agtgcaacat catatggcac ccactaaaga tgagtttgac
5700tgcaaagcct gggcttattt ctctgatgtt gacctggaaa aagatgtgca
ctcaggcctg 5760attggacccc ttctggtctg ccacactaac acactgaacc
ctgctcatgg gagacaagtg 5820acagtacagg aatttgctct gtttttcacc
atctttgatg agaccaaaag ctggtacttc 5880actgaaaata tggaaagaaa
ctgcagggct ccctgcaata tccagatgga agatcccact 5940tttaaagaga
attatcgctt ccatgcaatc aatggctaca taatggatac actacctggc
6000ttagtaatgg ctcaggatca aaggattcga tggtatctgc tcagcatggg
cagcaatgaa 6060aacatccatt ctattcattt cagtggacat gtgttcactg
tacgaaaaaa agaggagtat 6120aaaatggcac tgtacaatct ctatccaggt
gtttttgaga cagtggaaat gttaccatcc 6180aaagctggaa tttggcgggt
ggaatgcctt attggcgagc atctacatgc tgggatgagc 6240acactttttc
tggtgtacag caataagtgt cagactcccc tgggaatggc ttctggacac
6300attagagatt ttcagattac agcttcagga caatatggac agtgggcccc
aaagctggcc 6360agacttcatt attccggatc aatcaatgcc tggagcacca
aggagccctt ttcttggatc 6420aaggtggatc tgttggcacc aatgattatt
cacggcatca agacccaggg tgcccgtcag 6480aagttctcca gcctctacat
ctctcagttt atcatcatgt atagtcttga tgggaagaag 6540tggcagactt
atcgaggaaa ttccactgga accttaatgg tcttctttgg caatgtggat
6600tcatctggga taaaacacaa tatttttaac cctccaatta ttgctcgata
catccgtttg 6660cacccaactc attatagcat tcgcagcact cttcgcatgg
agttgatggg ctgtgattta 6720aatagttgca gcatgccatt gggaatggag
agtaaagcaa tatcagatgc acagattact 6780gcttcatcct actttaccaa
tatgtttgcc acctggtctc cttcaaaagc tcgacttcac 6840ctccaaggga
ggagtaatgc ctggagacct caggtgaata atccaaaaga gtggctgcaa
6900gtggacttcc agaagacaat gaaagtcaca ggagtaacta ctcagggagt
aaaatctctg 6960cttaccagca tgtatgtgaa ggagttcctc atctccagca
gtcaagatgg ccatcagtgg 7020actctctttt ttcagaatgg caaagtaaag
gtttttcagg gaaatcaaga ctccttcaca 7080cctgtggtga actctctaga
cccaccgtta ctgactcgct accttcgaat tcacccccag 7140agttgggtgc
accagattgc cctgaggatg gaggttctgg gctgcgaggc acaggacctc
7200tactgagggt ggccactgca gcacctgcca ctgccgtcac ctctccctcc
tcagctccag 7260ggcagtgtcc ctccctggct tgccttctac ctttgtgcta
aatcctagca gacactgcct 7320tgaagcctcc tgaattaact atcatcagtc
ctgcatttct ttggtggggg gccaggaggg 7380tgcatccaat ttaacttaac
tcttacctat tttctgcagc tgctcccaga ttactccttc 7440cttccaatat
aactaggcaa aaagaagtga ggagaaacct gcatgaaagc attcttccct
7500gaaaagttag gcctctcaga gtcaccactt cctctgttgt agaaaaacta
tgtgatgaaa 7560ctttgaaaaa gatatttatg atgttaacat ttcaggttaa
gcctcatacg tttaaaataa 7620aactctcagt tgtttattat cctgatcaag
catggaacaa agcatgtttc aggatcagat 7680caatacaatc ttggagtcaa
aaggcaaatc atttggacaa tctgcaaaat ggagagaata 7740caataactac
tacagtaaag tctgtttctg cttccttaca catagatata attatgttat
7800ttagtcatta tgaggggcac attcttatct ccaaaactag cattcttaaa
ctgagaatta 7860tagatggggt tcaagaatcc ctaagtcccc tgaaattata
taaggcattc tgtataaatg 7920caaatgtgca tttttctgac gagtgtccat
agatataaag ccattggtct taattctgac 7980caataaaaaa ataagtcagg
aggatgcaat tgttgaaagc tttgaaataa aataacatgt 8040cttcttgaaa
tttgtgatgg ccaagaaaga aaatgatgat gacattaggc ttctaaagga
8100catacattta atatttctgt ggaaatatga ggaaaatcca tggttatctg
agataggaga 8160tacaaacttt gtaattctaa taatgcactc agtttactct
ctccctctac taatttcctg 8220ctgaaaataa cacaacaaaa atgtaacagg
ggaaattata taccgtgact gaaaactaga 8280gtcctactta catagttgaa
atatcaagga ggtcagaaga aaattggact ggtgaaaaca 8340gaaaaaacac
tccagtctgc catatcacca cacaatagga tcccccttct tgccctccac
8400ccccataaga ttgtgaaggg tttactgctc cttccatctg cctgcacccc
ttcactatga 8460ctacacagaa ctctcctgat agtaaagggg gctggaggca
aggataagtt atagagcagt 8520tggaggaagc atccaaagac tgcaacccag
ggcaaatgga aaacaggaga tcctaatatg 8580aaagaaaaat ggatcccaat
ctgagaaaag gcaaaagaat ggctactttt ttctatgctg 8640gagtattttc
taataatcct gcttgaccct tatctgacct ctttggaaac tataacatag
8700ctgtcacagt atagtcacaa tccacaaatg atgcaggtgc aaatggttta
tagccctgtg 8760aagttcttaa agtttagagg ctaacttaca gaaatgaata
agttgttttg ttttatagcc 8820cggtagagga gttaacccca aaggtgatat
ggttttattt cctgttatgt ttaacttgat 8880aatcttattt tggcattctt
ttcccattga ctatatacat ctctatttct caaatgttca 8940tggaactagc
tcttttattt tcctgctggt ttcttcagta atgagttaaa taaaacattg
9000acacataca 900922332PRTHomo sapiens 2Ala Thr Arg Arg Tyr Tyr Leu
Gly Ala Val Glu Leu Ser Trp Asp Tyr 1 5 10 15 Met Gln Ser Asp Leu
Gly Glu Leu Pro Val Asp Ala Arg Phe Pro Pro 20 25 30 Arg Val Pro
Lys Ser Phe Pro Phe Asn Thr Ser Val Val Tyr Lys Lys 35 40 45 Thr
Leu Phe Val Glu Phe Thr Val His Leu Phe Asn Ile Ala Lys Pro 50 55
60 Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile Gln Ala Glu Val
65 70 75 80 Tyr Asp Thr Val Val Ile Thr Leu Lys Asn Met Ala Ser His
Pro Val 85 90 95 Ser Leu His Ala Val Gly Val Ser Tyr Trp Lys Ala
Ser Glu Gly Ala 100 105 110 Glu Tyr Asp Asp Gln Thr Ser Gln Arg Glu
Lys Glu Asp Asp Lys Val 115 120 125 Phe Pro Gly Gly Ser His Thr Tyr
Val Trp Gln Val Leu Lys Glu Asn 130 135 140 Gly Pro Met Ala Ser Asp
Pro Leu Cys Leu Thr Tyr Ser Tyr Leu Ser 145 150 155 160 His Val Asp
Leu Val Lys Asp Leu Asn Ser Gly Leu Ile Gly Ala Leu 165 170 175 Leu
Val Cys Arg Glu Gly Ser Leu Ala Lys Glu Lys Thr Gln Thr Leu 180 185
190 His Lys Phe Ile Leu Leu Phe Ala Val Phe Asp Glu Gly Lys Ser Trp
195 200 205 His Ser Glu Thr Lys Asn Ser Leu Met Gln Asp Arg Asp Ala
Ala Ser 210 215 220 Ala Arg Ala Trp Pro Lys Met His Thr Val Asn Gly
Tyr Val Asn Arg 225 230 235 240 Ser Leu Pro Gly Leu Ile Gly Cys His
Arg Lys Ser Val Tyr Trp His 245 250 255 Val Ile Gly Met Gly Thr Thr
Pro Glu Val His Ser Ile Phe Leu Glu 260 265 270 Gly His Thr Phe Leu
Val Arg Asn His Arg Gln Ala Ser Leu Glu Ile 275 280 285 Ser Pro Ile
Thr Phe Leu Thr Ala Gln Thr Leu Leu Met Asp Leu Gly 290 295 300 Gln
Phe Leu Leu Phe Cys His Ile Ser Ser His Gln His Asp Gly Met 305 310
315 320 Glu Ala Tyr Val Lys Val Asp Ser Cys Pro Glu Glu Pro Gln Leu
Arg 325 330 335 Met Lys Asn Asn Glu Glu Ala Glu Asp Tyr Asp Asp Asp
Leu Thr Asp 340 345 350 Ser Glu Met Asp Val Val Arg Phe Asp Asp Asp
Asn Ser Pro Ser Phe 355 360 365 Ile Gln Ile Arg Ser Val Ala Lys Lys
His Pro Lys Thr Trp Val His 370 375 380 Tyr Ile Ala Ala Glu Glu Glu
Asp Trp Asp Tyr Ala Pro Leu Val Leu 385 390 395 400 Ala Pro Asp Asp
Arg Ser Tyr Lys Ser Gln Tyr Leu Asn Asn Gly Pro 405 410 415 Gln Arg
Ile Gly Arg Lys Tyr Lys Lys Val Arg Phe Met Ala Tyr Thr 420 425 430
Asp Glu Thr Phe Lys Thr Arg Glu Ala Ile Gln His Glu Ser Gly Ile 435
440 445 Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu Leu Ile
Ile 450 455 460 Phe Lys Asn Gln Ala Ser Arg Pro Tyr Asn Ile Tyr Pro
His Gly Ile 465 470 475 480 Thr Asp Val Arg Pro Leu Tyr Ser Arg Arg
Leu Pro Lys Gly Val Lys 485 490 495 His Leu Lys Asp Phe Pro Ile Leu
Pro Gly Glu Ile Phe Lys Tyr Lys 500 505 510 Trp Thr Val Thr Val Glu
Asp Gly Pro Thr Lys Ser Asp Pro Arg Cys 515 520 525 Leu Thr Arg Tyr
Tyr Ser Ser Phe Val Asn Met Glu Arg Asp Leu Ala 530 535 540 Ser Gly
Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu Ser Val Asp 545 550 555
560 Gln Arg Gly Asn Gln Ile Met Ser Asp Lys Arg Asn Val Ile Leu Phe
565 570 575 Ser Val Phe Asp Glu Asn Arg Ser Trp Tyr Leu Thr Glu Asn
Ile Gln 580 585 590 Arg Phe Leu Pro Asn Pro Ala Gly Val Gln Leu Glu
Asp Pro Glu Phe 595 600 605 Gln Ala Ser Asn Ile Met His Ser Ile Asn
Gly Tyr Val Phe Asp Ser 610 615 620 Leu Gln Leu Ser Val Cys Leu His
Glu Val Ala Tyr Trp Tyr Ile Leu 625 630 635 640 Ser Ile Gly Ala Gln
Thr Asp Phe Leu Ser Val Phe Phe Ser Gly Tyr 645 650 655 Thr Phe Lys
His Lys Met Val Tyr Glu Asp Thr Leu Thr Leu Phe Pro 660 665 670 Phe
Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro Gly Leu Trp 675 680
685 Ile Leu Gly Cys His Asn Ser Asp Phe Arg Asn Arg Gly Met Thr Ala
690 695 700 Leu Leu Lys Val Ser Ser Cys Asp Lys Asn Thr Gly Asp Tyr
Tyr Glu 705 710 715 720 Asp Ser Tyr Glu Asp Ile Ser Ala Tyr Leu Leu
Ser Lys Asn Asn Ala 725 730 735 Ile Glu Pro Arg Ser Phe Ser Gln Asn
Ser Arg His Pro Ser Thr Arg 740 745 750 Gln Lys Gln Phe Asn Ala Thr
Thr Ile Pro Glu Asn Asp Ile Glu Lys 755 760 765 Thr Asp Pro Trp Phe
Ala His Arg Thr Pro Met Pro Lys Ile Gln Asn 770 775 780 Val Ser Ser
Ser Asp Leu Leu Met Leu Leu Arg Gln Ser Pro Thr Pro 785 790 795 800
His Gly Leu Ser Leu Ser Asp Leu Gln Glu Ala Lys Tyr Glu Thr Phe 805
810 815 Ser Asp Asp Pro Ser Pro Gly Ala Ile Asp Ser Asn Asn Ser Leu
Ser 820 825 830 Glu Met Thr His Phe Arg Pro Gln Leu His His Ser Gly
Asp Met Val 835 840 845 Phe Thr Pro Glu Ser Gly Leu Gln Leu Arg Leu
Asn Glu Lys Leu Gly 850 855 860 Thr Thr Ala Ala Thr Glu Leu Lys Lys
Leu Asp Phe Lys Val Ser Ser 865 870 875 880 Thr Ser Asn Asn Leu Ile
Ser Thr Ile Pro Ser Asp Asn Leu Ala Ala 885 890 895 Gly Thr Asp Asn
Thr Ser Ser Leu Gly Pro Pro Ser Met Pro Val His 900 905 910 Tyr
Asp
Ser Gln Leu Asp Thr Thr Leu Phe Gly Lys Lys Ser Ser Pro 915 920 925
Leu Thr Glu Ser Gly Gly Pro Leu Ser Leu Ser Glu Glu Asn Asn Asp 930
935 940 Ser Lys Leu Leu Glu Ser Gly Leu Met Asn Ser Gln Glu Ser Ser
Trp 945 950 955 960 Gly Lys Asn Val Ser Ser Thr Glu Ser Gly Arg Leu
Phe Lys Gly Lys 965 970 975 Arg Ala His Gly Pro Ala Leu Leu Thr Lys
Asp Asn Ala Leu Phe Lys 980 985 990 Val Ser Ile Ser Leu Leu Lys Thr
Asn Lys Thr Ser Asn Asn Ser Ala 995 1000 1005 Thr Asn Arg Lys Thr
His Ile Asp Gly Pro Ser Leu Leu Ile Glu 1010 1015 1020 Asn Ser Pro
Ser Val Trp Gln Asn Ile Leu Glu Ser Asp Thr Glu 1025 1030 1035 Phe
Lys Lys Val Thr Pro Leu Ile His Asp Arg Met Leu Met Asp 1040 1045
1050 Lys Asn Ala Thr Ala Leu Arg Leu Asn His Met Ser Asn Lys Thr
1055 1060 1065 Thr Ser Ser Lys Asn Met Glu Met Val Gln Gln Lys Lys
Glu Gly 1070 1075 1080 Pro Ile Pro Pro Asp Ala Gln Asn Pro Asp Met
Ser Phe Phe Lys 1085 1090 1095 Met Leu Phe Leu Pro Glu Ser Ala Arg
Trp Ile Gln Arg Thr His 1100 1105 1110 Gly Lys Asn Ser Leu Asn Ser
Gly Gln Gly Pro Ser Pro Lys Gln 1115 1120 1125 Leu Val Ser Leu Gly
Pro Glu Lys Ser Val Glu Gly Gln Asn Phe 1130 1135 1140 Leu Ser Glu
Lys Asn Lys Val Val Val Gly Lys Gly Glu Phe Thr 1145 1150 1155 Lys
Asp Val Gly Leu Lys Glu Met Val Phe Pro Ser Ser Arg Asn 1160 1165
1170 Leu Phe Leu Thr Asn Leu Asp Asn Leu His Glu Asn Asn Thr His
1175 1180 1185 Asn Gln Glu Lys Lys Ile Gln Glu Glu Ile Glu Lys Lys
Glu Thr 1190 1195 1200 Leu Ile Gln Glu Asn Val Val Leu Pro Gln Ile
His Thr Val Thr 1205 1210 1215 Gly Thr Lys Asn Phe Met Lys Asn Leu
Phe Leu Leu Ser Thr Arg 1220 1225 1230 Gln Asn Val Glu Gly Ser Tyr
Glu Gly Ala Tyr Ala Pro Val Leu 1235 1240 1245 Gln Asp Phe Arg Ser
Leu Asn Asp Ser Thr Asn Arg Thr Lys Lys 1250 1255 1260 His Thr Ala
His Phe Ser Lys Lys Gly Glu Glu Glu Asn Leu Glu 1265 1270 1275 Gly
Leu Gly Asn Gln Thr Lys Gln Ile Val Glu Lys Tyr Ala Cys 1280 1285
1290 Thr Thr Arg Ile Ser Pro Asn Thr Ser Gln Gln Asn Phe Val Thr
1295 1300 1305 Gln Arg Ser Lys Arg Ala Leu Lys Gln Phe Arg Leu Pro
Leu Glu 1310 1315 1320 Glu Thr Glu Leu Glu Lys Arg Ile Ile Val Asp
Asp Thr Ser Thr 1325 1330 1335 Gln Trp Ser Lys Asn Met Lys His Leu
Thr Pro Ser Thr Leu Thr 1340 1345 1350 Gln Ile Asp Tyr Asn Glu Lys
Glu Lys Gly Ala Ile Thr Gln Ser 1355 1360 1365 Pro Leu Ser Asp Cys
Leu Thr Arg Ser His Ser Ile Pro Gln Ala 1370 1375 1380 Asn Arg Ser
Pro Leu Pro Ile Ala Lys Val Ser Ser Phe Pro Ser 1385 1390 1395 Ile
Arg Pro Ile Tyr Leu Thr Arg Val Leu Phe Gln Asp Asn Ser 1400 1405
1410 Ser His Leu Pro Ala Ala Ser Tyr Arg Lys Lys Asp Ser Gly Val
1415 1420 1425 Gln Glu Ser Ser His Phe Leu Gln Gly Ala Lys Lys Asn
Asn Leu 1430 1435 1440 Ser Leu Ala Ile Leu Thr Leu Glu Met Thr Gly
Asp Gln Arg Glu 1445 1450 1455 Val Gly Ser Leu Gly Thr Ser Ala Thr
Asn Ser Val Thr Tyr Lys 1460 1465 1470 Lys Val Glu Asn Thr Val Leu
Pro Lys Pro Asp Leu Pro Lys Thr 1475 1480 1485 Ser Gly Lys Val Glu
Leu Leu Pro Lys Val His Ile Tyr Gln Lys 1490 1495 1500 Asp Leu Phe
Pro Thr Glu Thr Ser Asn Gly Ser Pro Gly His Leu 1505 1510 1515 Asp
Leu Val Glu Gly Ser Leu Leu Gln Gly Thr Glu Gly Ala Ile 1520 1525
1530 Lys Trp Asn Glu Ala Asn Arg Pro Gly Lys Val Pro Phe Leu Arg
1535 1540 1545 Val Ala Thr Glu Ser Ser Ala Lys Thr Pro Ser Lys Leu
Leu Asp 1550 1555 1560 Pro Leu Ala Trp Asp Asn His Tyr Gly Thr Gln
Ile Pro Lys Glu 1565 1570 1575 Glu Trp Lys Ser Gln Glu Lys Ser Pro
Glu Lys Thr Ala Phe Lys 1580 1585 1590 Lys Lys Asp Thr Ile Leu Ser
Leu Asn Ala Cys Glu Ser Asn His 1595 1600 1605 Ala Ile Ala Ala Ile
Asn Glu Gly Gln Asn Lys Pro Glu Ile Glu 1610 1615 1620 Val Thr Trp
Ala Lys Gln Gly Arg Thr Glu Arg Leu Cys Ser Gln 1625 1630 1635 Asn
Pro Pro Val Leu Lys Arg His Gln Arg Glu Ile Thr Arg Thr 1640 1645
1650 Thr Leu Gln Ser Asp Gln Glu Glu Ile Asp Tyr Asp Asp Thr Ile
1655 1660 1665 Ser Val Glu Met Lys Lys Glu Asp Phe Asp Ile Tyr Asp
Glu Asp 1670 1675 1680 Glu Asn Gln Ser Pro Arg Ser Phe Gln Lys Lys
Thr Arg His Tyr 1685 1690 1695 Phe Ile Ala Ala Val Glu Arg Leu Trp
Asp Tyr Gly Met Ser Ser 1700 1705 1710 Ser Pro His Val Leu Arg Asn
Arg Ala Gln Ser Gly Ser Val Pro 1715 1720 1725 Gln Phe Lys Lys Val
Val Phe Gln Glu Phe Thr Asp Gly Ser Phe 1730 1735 1740 Thr Gln Pro
Leu Tyr Arg Gly Glu Leu Asn Glu His Leu Gly Leu 1745 1750 1755 Leu
Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val 1760 1765
1770 Thr Phe Arg Asn Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser
1775 1780 1785 Leu Ile Ser Tyr Glu Glu Asp Gln Arg Gln Gly Ala Glu
Pro Arg 1790 1795 1800 Lys Asn Phe Val Lys Pro Asn Glu Thr Lys Thr
Tyr Phe Trp Lys 1805 1810 1815 Val Gln His His Met Ala Pro Thr Lys
Asp Glu Phe Asp Cys Lys 1820 1825 1830 Ala Trp Ala Tyr Phe Ser Asp
Val Asp Leu Glu Lys Asp Val His 1835 1840 1845 Ser Gly Leu Ile Gly
Pro Leu Leu Val Cys His Thr Asn Thr Leu 1850 1855 1860 Asn Pro Ala
His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu 1865 1870 1875 Phe
Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu 1880 1885
1890 Asn Met Glu Arg Asn Cys Arg Ala Pro Cys Asn Ile Gln Met Glu
1895 1900 1905 Asp Pro Thr Phe Lys Glu Asn Tyr Arg Phe His Ala Ile
Asn Gly 1910 1915 1920 Tyr Ile Met Asp Thr Leu Pro Gly Leu Val Met
Ala Gln Asp Gln 1925 1930 1935 Arg Ile Arg Trp Tyr Leu Leu Ser Met
Gly Ser Asn Glu Asn Ile 1940 1945 1950 His Ser Ile His Phe Ser Gly
His Val Phe Thr Val Arg Lys Lys 1955 1960 1965 Glu Glu Tyr Lys Met
Ala Leu Tyr Asn Leu Tyr Pro Gly Val Phe 1970 1975 1980 Glu Thr Val
Glu Met Leu Pro Ser Lys Ala Gly Ile Trp Arg Val 1985 1990 1995 Glu
Cys Leu Ile Gly Glu His Leu His Ala Gly Met Ser Thr Leu 2000 2005
2010 Phe Leu Val Tyr Ser Asn Lys Cys Gln Thr Pro Leu Gly Met Ala
2015 2020 2025 Ser Gly His Ile Arg Asp Phe Gln Ile Thr Ala Ser Gly
Gln Tyr 2030 2035 2040 Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu His
Tyr Ser Gly Ser 2045 2050 2055 Ile Asn Ala Trp Ser Thr Lys Glu Pro
Phe Ser Trp Ile Lys Val 2060 2065 2070 Asp Leu Leu Ala Pro Met Ile
Ile His Gly Ile Lys Thr Gln Gly 2075 2080 2085 Ala Arg Gln Lys Phe
Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile 2090 2095 2100 Met Tyr Ser
Leu Asp Gly Lys Lys Trp Gln Thr Tyr Arg Gly Asn 2105 2110 2115 Ser
Thr Gly Thr Leu Met Val Phe Phe Gly Asn Val Asp Ser Ser 2120 2125
2130 Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile Ile Ala Arg Tyr
2135 2140 2145 Ile Arg Leu His Pro Thr His Tyr Ser Ile Arg Ser Thr
Leu Arg 2150 2155 2160 Met Glu Leu Met Gly Cys Asp Leu Asn Ser Cys
Ser Met Pro Leu 2165 2170 2175 Gly Met Glu Ser Lys Ala Ile Ser Asp
Ala Gln Ile Thr Ala Ser 2180 2185 2190 Ser Tyr Phe Thr Asn Met Phe
Ala Thr Trp Ser Pro Ser Lys Ala 2195 2200 2205 Arg Leu His Leu Gln
Gly Arg Ser Asn Ala Trp Arg Pro Gln Val 2210 2215 2220 Asn Asn Pro
Lys Glu Trp Leu Gln Val Asp Phe Gln Lys Thr Met 2225 2230 2235 Lys
Val Thr Gly Val Thr Thr Gln Gly Val Lys Ser Leu Leu Thr 2240 2245
2250 Ser Met Tyr Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly
2255 2260 2265 His Gln Trp Thr Leu Phe Phe Gln Asn Gly Lys Val Lys
Val Phe 2270 2275 2280 Gln Gly Asn Gln Asp Ser Phe Thr Pro Val Val
Asn Ser Leu Asp 2285 2290 2295 Pro Pro Leu Leu Thr Arg Tyr Leu Arg
Ile His Pro Gln Ser Trp 2300 2305 2310 Val His Gln Ile Ala Leu Arg
Met Glu Val Leu Gly Cys Glu Ala 2315 2320 2325 Gln Asp Leu Tyr 2330
31130DNAporcine 3taagcaccct aagacgtggg tgcactacat ctctgcagag
gaggaggact gggactacgc 60ccccgcggtc cccagcccca gtgacagaag ttataaaagt
ctctacttga acagtggtcc 120tcagcgaatt ggtaggaaat acaaaaaagc
tcgattcgtc gcttacacgg atgtaacatt 180taagactcgt aaagctattc
cgtatgaatc aggaatcctg ggacctttac tttatggaga 240agttggagac
acacttttga ttatatttaa gaataaagcg agccgaccat ataacatcta
300ccctcatgga atcactgatg tcagcgcttt gcacccaggg agacttctaa
aaggttggaa 360acatttgaaa gacatgccaa ttctgccagg agagactttc
aagtataaat ggacagtgac 420tgtggaagat gggccaacca agtccgatcc
tcggtgcctg acccgctact actcgagctc 480cattaatcta gagaaagatc
tggcttcggg actcattggc cctctcctca tctgctacaa 540agaatctgta
gaccaaagag gaaaccagat gatgtcagac aagagaaacg tcatcctgtt
600ttctgtattc gatgagaatc aaagctggta cctcgcagag aatattcagc
gcttcctccc 660caatccggat ggattacagc cccaggatcc agagttccaa
gcttctaaca tcatgcacag 720catcaatggc tatgtttttg atagcttgca
gctgtcggtt tgtttgcacg aggtggcata 780ctggtacatt ctaagtgttg
gagcacagac ggacttcctc tccgtcttct tctctggcta 840caccttcaaa
cacaaaatgg tctatgaaga cacactcacc ctgttcccct tctcaggaga
900aacggtcttc atgtcaatgg aaaacccagg tctctgggtc ctagggtgcc
acaactcaga 960cttgcggaac agagggatga cagccttact gaaggtgtat
agttgtgaca gggacattgg 1020tgattattat gacaacactt atgaagatat
tccaggcttc ttgctgagtg gaaagaatgt 1080cattgaaccc agaagctttg
cccagaattc aagaccccct agtgcgagca 11304368PRTporcine 4Ser Val Ala
Lys Lys His Pro Lys Thr Trp Val His Tyr Ile Ser Ala 1 5 10 15 Glu
Glu Glu Asp Trp Asp Tyr Ala Pro Ala Val Pro Ser Pro Ser Asp 20 25
30 Arg Ser Tyr Lys Ser Leu Tyr Leu Asn Ser Gly Pro Gln Arg Ile Gly
35 40 45 Arg Lys Tyr Lys Lys Ala Arg Phe Val Ala Tyr Thr Asp Val
Thr Phe 50 55 60 Lys Thr Arg Lys Ala Ile Pro Tyr Glu Ser Gly Ile
Leu Gly Pro Leu 65 70 75 80 Leu Tyr Gly Glu Val Gly Asp Thr Leu Leu
Ile Ile Phe Lys Asn Lys 85 90 95 Ala Ser Arg Pro Tyr Asn Ile Tyr
Pro His Gly Ile Thr Asp Val Ser 100 105 110 Ala Leu His Pro Gly Arg
Leu Leu Lys Gly Trp Lys His Leu Lys Asp 115 120 125 Met Pro Ile Leu
Pro Gly Glu Thr Phe Lys Tyr Lys Trp Thr Val Thr 130 135 140 Val Glu
Asp Gly Pro Thr Lys Ser Asp Pro Arg Cys Leu Thr Arg Tyr 145 150 155
160 Tyr Ser Ser Ser Ile Asn Leu Glu Lys Asp Leu Ala Ser Gly Leu Ile
165 170 175 Gly Pro Leu Leu Ile Cys Tyr Lys Glu Ser Val Asp Gln Arg
Gly Asn 180 185 190 Gln Met Met Ser Asp Lys Arg Asn Val Ile Leu Phe
Ser Val Phe Asp 195 200 205 Glu Asn Gln Ser Trp Tyr Leu Ala Glu Asn
Ile Gln Arg Phe Leu Pro 210 215 220 Asn Pro Asp Gly Leu Gln Pro Gln
Asp Pro Glu Phe Gln Ala Ser Asn 225 230 235 240 Ile Met His Ser Ile
Asn Gly Tyr Val Phe Asp Ser Leu Gln Leu Ser 245 250 255 Val Cys Leu
His Glu Val Ala Tyr Trp Tyr Ile Leu Ser Val Gly Ala 260 265 270 Gln
Thr Asp Phe Leu Ser Val Phe Phe Ser Gly Tyr Thr Phe Lys His 275 280
285 Lys Met Val Tyr Glu Asp Thr Leu Thr Leu Phe Pro Phe Ser Gly Glu
290 295 300 Thr Val Phe Met Ser Met Glu Asn Pro Gly Leu Trp Val Leu
Gly Cys 305 310 315 320 His Asn Ser Asp Leu Arg Asn Arg Gly Met Thr
Ala Leu Leu Lys Val 325 330 335 Tyr Ser Cys Asp Arg Asp Ile Gly Asp
Tyr Tyr Asp Asn Thr Tyr Glu 340 345 350 Asp Ile Pro Gly Phe Leu Leu
Ser Gly Lys Asn Val Ile Glu Pro Arg 355 360 365 57493DNAMus
musculus 5tctagagttt ctttgctaca ggtaccaagg aacagtcttt tagaataggc
taggaattta 60aatacacctg aacgcccctc ctcagtattc tgttcctttt cttaaggatt
caaacttgtt 120aggatgcacc cagcaggaaa tgggttaagc cttagctcag
ccactcttcc tattccagtt 180ttcctgtgcc tgcttcctac tacccaaaag
gaagtaatcc ttcagatctg ttttgtgcta 240atgctacttt cactcacagt
agataaactt ccagaaaatc ctctgcaaaa tatttaggac 300tttttactaa
atcattacat ttctttttgt tcttaaaagc taaagttatt ttagagaaga
360gttaaatttt catttcttta gttgaacatt ttctagtaat aaaagccatg
caaatagcac 420tcttcgcttg cttctttctg agccttttca atttctgctc
tagtgccatc agaagatact 480accttggtgc agtggaattg tcctggaact
atattcagag tgatctgctc agtgtgctgc 540atacagactc aagatttctt
cctagaatgt caacatcttt tccattcaac acctccatca 600tgtataaaaa
gactgtgttt gtagagtaca aggaccagct tttcaacatt gccaagccca
660ggccaccctg gatgggtttg ctaggtccta ccatttggac tgaggttcat
gacacagtgg 720tcattacact taaaaacatg gcttctcatc ctgtcagtct
tcatgctgtt ggtgtgtcct 780actggaaagc ttctgaggga gatgaatatg
aagatcagac aagccaaatg gagaaggaag 840atgataaagt tttccctggt
gaaagtcata cttatgtttg gcaagtcctg aaagagaatg 900gtccaatggc
ctctgaccct ccatgtctca cttactcata tatgtctcat gtggatctgg
960tgaaagattt gaattcaggc ctcattggag ctctgctagt atgtaaagaa
ggcagtctct 1020ccaaagaaag aacacagatg ttgtaccaat ttgtactgct
ttttgctgta tttgatgaag 1080ggaagagctg gcactcagaa acaaacgact
cttatacaca gtctatggat tctgcatctg 1140ctagagactg gcctaaaatg
cacacagtca atggctatgt aaacaggtct cttccaggtc 1200tgattggatg
ccataggaaa tcagtctact ggcacgtgat tggaatgggc accactcctg
1260aaatacactc aatattcctc gaaggtcaca cattttttgt gaggaaccac
cgtcaagctt 1320cattggagat atcaccaata actttcctta ctgctcaaac
actcttgata gatcttgggc 1380agttcctact attttgtcat atctcttccc
ataaacatga tggcatggaa gcttatgtca 1440aagtagatag ctgccctgag
gaatcccaat ggcaaaagaa aaataataat gaggaaatgg 1500aagattatga
tgatgatctt tattcagaaa tggatatgtt cacattggat tatgacagct
1560ctccttttat ccaaattcgc tcggttgcta aaaagtaccc taaaacttgg
atacattata 1620tttctgctga ggaggaagac tgggactatg caccttcagt
tcctacctcg gataatggaa 1680gttataaaag ccagtatctg agcaatggtc
ctcatcggat tggtaggaaa tataaaaaag 1740tcagatttat agcatacaca
gatgaaacct ttaagactcg tgaaactatt cagcatgaat 1800caggactctt
gggaccttta ctttatggag aagttggaga cacactgttg attattttta
1860agaatcaagc aagccgacca tataacattt accctcatgg aatcactgat
gtcagtcctc 1920tacatgcaag gagattgcca agaggtataa agcacgtgaa
ggatttgcca attcatccag 1980gagagatatt caagtacaag tggacagtta
cagtagaaga tggaccaact aaatcagatc 2040cacggtgcct gacccgctat
tattcaagtt tcattaaccc tgagagagat ctagcttcag 2100gactgattgg
ccctcttctc atctgctaca aagaatctgt agatcaaagg ggaaaccaga
2160tgatgtcaga caaaagaaat gtcatcctgt tttctatatt tgatgagaac
caaagctggt 2220acatcacaga gaacatgcaa cgcttcctcc ccaatgcagc
taaaacacag ccccaggacc 2280ctgggttcca ggcctccaac atcatgcaca
gcatcaatgg ctatgttttt gatagcttgg 2340agttgacagt ttgtttgcat
gaggtggcat actggcacat tctcagtgtt ggagcacaga 2400cagacttctt
atctatcttc ttctctggat atactttcaa acacaaaatg gtctatgaag
2460atacacttac cctgttccca ttctcaggag aaactgtctt tatgtcgatg
gaaaacccag 2520gtctatgggt cttggggtgt cataattcag actttcggaa
gagaggtatg acagcattgc 2580tgaaagtttc tagttgtgac aagagcacta
gtgattatta tgaagaaata tatgaagata 2640ttccaacaca gttggtgaat
gagaacaatg tcattgatcc cagaagcttc ttccagaata 2700caaatcatcc
taatactagg aaaaagaaat tcaaagattc cacaattcca aaaaatgata
2760tggagaagat tgagcctcag tttgaagaga tagcagagat gcttaaagta
cagagtgtct 2820cagttagtga catgttgatg ctcttgggac agagtcatcc
tactccacat ggcttatttt 2880tatcagatgg ccaagaagcc atctatgagg
ctattcatga tgatcattca ccaaatgcaa 2940tagacagcaa tgaaggccca
tctaaagtga cccaactcag gccagaatcc catcacagtg 3000agaaaatagt
atttactcct cagcccggcc tccagttaag atccaataaa agtttggaga
3060caactataga agtaaagtgg aagaaacttg gtttgcaagt ttctagtttg
ccaagtaatc 3120taatgactac aacaattctg tcagacaatt tgaaagcaac
ttttgaaaag acagattctt 3180caggatttcc agatatgcca gttcactcta
gtagtaaatt aagtactact gcatttggta 3240agaaagcata ttcccttgtt
gggtctcatg tacctttaaa cgcgagtgaa gaaaatagtg 3300attccaacat
attggattca actttaatgt atagtcaaga aagtttacca agagataata
3360tattatcaat agagaatgat agattactca gagagaagag gtttcatgga
attgctttat 3420tgaccaaaga taatacttta ttcaaagaca atgtctcctt
aatgaaaaca aacaaaacat 3480ataatcattc aacaactaat gaaaaactac
acactgagag cccaacatca attgagaata 3540gtacaacaga cttgcaagat
gccatattaa aggtcaatag tgagattcaa gaagtaacag 3600ctttgattca
tgatggaaca cttttaggca aaaattctac atatttgaga ctaaaccata
3660tgctaaatag aactacctca acaaaaaata aagacatatt tcatagaaaa
gatgaagatc 3720ctattccaca agatgaagag aatacaatca tgccattttc
caagatgttg ttcttgtcag 3780aatcttcaaa ttggtttaaa aagaccaatg
gaaataattc cttgaactct gagcaagaac 3840atagtccaaa gcaattagta
tatttaatgt ttaaaaaata tgtaaaaaat caaagtttct 3900tgtcagagaa
aaataaagtc acagtagaac aggatggatt tacaaagaac ataggactta
3960aagacatggc ttttccacat aatatgagca tatttcttac cactttgtct
aacgtacatg 4020aaaatggtag gcacaatcaa gaaaaaaata ttcaggaaga
gatagagaag gaagcactaa 4080ttgaagagaa agtagttttg ccccaggtgc
acgaagcaac tggctctaag aatttcttga 4140aagacatatt gatactaggc
actaggcaaa atataagttt atatgaagta catgtaccag 4200tacttcaaaa
catcacatca ataaacaatt caacaaatac agtacagatt cacatggagc
4260atttctttaa aagaaggaag gacaaggaaa caaattcaga aggcttggta
aataaaacca 4320gagaaatggt aaaaaactat ccaagccaga agaatattac
tactcaacgt agtaaacggg 4380ctttgggaca attcagactg tcaactcaat
ggcttaaaac cataaactgt tcaacacagt 4440gtatcattaa acagatagac
cacagcaagg aaatgaaaaa gttcattact aaatcttcct 4500tatcagattc
ttctgtgatt aaaagcacca ctcagacaaa tagttctgac tcacacattg
4560taaaaacatc agcatttcca ccaatagatc tcaaaaggag tccattccaa
aacaaatttt 4620ctcatgttca agcatcatcc tacatttatg actttaagac
aaaaagttca agaattcaag 4680aaagcaataa tttcttaaaa gaaaccaaaa
taaataaccc ttctttagcc attctaccat 4740ggaatatgtt catagatcaa
ggaaaattta cctccccagg gaaaagtaac acaaactcag 4800tcacatataa
gaaacgtgag aacattattt tcttgaaacc aactttgcct gaagaatctg
4860gcaaaattga attgcttcct caagtttcca ttcaagagga agaaatttta
cctacagaaa 4920ctagccatgg atctcctgga cacttgaatc tcatgaaaga
ggtctttctt cagaaaatac 4980aggggcctac taaatggaat aaagcaaaga
ggcatggaga aagtataaaa ggtaaaacag 5040agagctctaa aaatactcgc
tcaaaactgc taaatcatca tgcttgggat tatcattatg 5100ctgcacagat
accaaaagat atgtggaaat ccaaagagaa gtcaccagaa attatatcca
5160ttaagcaaga ggacaccatt ttgtctctga ggcctcatgg aaacagtcat
tcaatagggg 5220caaatgagaa acaaaattgg cctcaaagag aaaccacttg
ggtaaagcaa ggccaaactc 5280aaaggacatg ctctcaaatc ccaccagtgt
tgaaacgaca tcaaagggaa cttagtgctt 5340ttcaatcaga acaagaagca
actgactatg atgatgccat caccattgaa acaatcgagg 5400attttgacat
ttacagtgag gacataaagc aaggtccccg cagctttcaa cagaaaacaa
5460ggcactattt tattgcagct gtggaacgac tctgggacta tgggatgagt
acatctcatg 5520ttctacgaaa taggtatcaa agtgacaatg tacctcagtt
caagaaagta gttttccagg 5580aatttactga tggctccttt agtcagccct
tatatcgtgg agaattaaat gaacacctgg 5640ggttgttggg cccatatata
agagcagaag ttgaagacaa cattatggta actttcaaaa 5700accaggcctc
ccgtccctac tccttctatt ctagcctcat ttcttataaa gaagatcaga
5760gaggagaaga acctagaaga aactttgtca agcctaatga aaccaaaatt
tatttttgga 5820aagtacaaca tcatatggca cccacagaag atgagtttga
ctgcaaggcc tgggcttatt 5880tctctgatgt tgatcttgaa agagatatgc
actcgggatt aattggaccc cttctgattt 5940gccacgcgaa cacactgaat
cctgctcatg ggagacaagt gtcagtacag gaatttgctc 6000tgcttttcac
tatctttgat gagaccaaga gctggtactt cactgaaaac gtgaaaagga
6060actgcaagac accctgcaat ttccagatgg aagaccccac tttgaaagag
aattatcgct 6120tccatgcaat caatggttat gtaatggata ccctaccagg
cttagtaatg gctcaagatc 6180aaaggattcg atggtatctt ctcagcatgg
gcaacaatga gaacatccaa tctattcatt 6240tcagtggaca tgttttcact
gtacggaaaa aagaggagta taaaatggca gtgtacaacc 6300tctacccagg
tgtttttgag actctggaaa tgataccatc cagagctgga atatggcgag
6360tagaatgcct tattggcgag cacttacagg ctgggatgag cactcttttt
ctggtgtaca 6420gcaagcagtg tcagattcct cttggaatgg cttctggaag
catccgtgat ttccagatta 6480cagcttcagg acattatgga cagtgggccc
caaacctggc aagacttcat tattccggat 6540caatcaatgc ctggagtacc
aaggagccct tttcttggat caaggtagat ctgttggcac 6600caatgattgt
tcatggcatc aagactcagg gtgctcgtca gaaattttcc agcctttata
6660tctctcaatt tatcatcatg tatagcctgg atgggaagaa gtggctgagt
tatcaaggaa 6720attccactgg aaccttaatg gttttctttg gcaatgtgga
ctcatctggg attaagcata 6780atagttttaa tcctccaatt attgctcgat
atatccgttt gcaccccact cattctagca 6840tccgtagtac tcttcgcatg
gagttgatgg gctgtgattt aaacagttgc agcataccat 6900tgggaatgga
aagtaaagta atatcagata cacaaatcac tgcctcatcc tacttcacca
6960acatgtttgc tacttggtct ccttcacaag ctcgacttca cctccaggga
aggactaatg 7020cctggcgacc tcaggtgaat gatccaaaac aatggttgca
agtggactta caaaagacaa 7080tgaaagtcac tggaataata acccagggag
tgaaatctct ctttaccagc atgtttgtga 7140aagagttcct tatttccagc
agtcaagatg gccatcactg gactcaaatt ttatacaatg 7200gcaaggtaaa
ggtttttcag gggaatcagg actcatccac acctatgatg aattctctag
7260acccaccatt actcactcgc tatcttcgaa ttcaccccca gatctgggag
caccaaattg 7320ctctgaggct tgagattcta ggatgtgagg cccagcagca
atactgaggt agcctctgca 7380tcacctgctt attccccttc ctcagctcaa
agattgtctt aatgttttat tgctgtgaag 7440agacactatg accatggcaa
ctctttataa aataaagcat ttaatcaggg ctt 749362319PRTMus musculus 6Met
Gln Ile Ala Leu Phe Ala Cys Phe Phe Leu Ser Leu Phe Asn Phe 1 5 10
15 Cys Ser Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser
20 25 30 Trp Asn Tyr Ile Gln Ser Asp Leu Leu Ser Val Leu His Thr
Asp Ser 35 40 45 Arg Phe Leu Pro Arg Met Ser Thr Ser Phe Pro Phe
Asn Thr Ser Ile 50 55 60 Met Tyr Lys Lys Thr Val Phe Val Glu Tyr
Lys Asp Gln Leu Phe Asn 65 70 75 80 Ile Ala Lys Pro Arg Pro Pro Trp
Met Gly Leu Leu Gly Pro Thr Ile 85 90 95 Trp Thr Glu Val His Asp
Thr Val Val Ile Thr Leu Lys Asn Met Ala 100 105 110 Ser His Pro Val
Ser Leu His Ala Val Gly Val Ser Tyr Trp Lys Ala 115 120 125 Ser Glu
Gly Asp Glu Tyr Glu Asp Gln Thr Ser Gln Met Glu Lys Glu 130 135 140
Asp Asp Lys Val Phe Pro Gly Glu Ser His Thr Tyr Val Trp Gln Val 145
150 155 160 Leu Lys Glu Asn Gly Pro Met Ala Ser Asp Pro Pro Cys Leu
Thr Tyr 165 170 175 Ser Tyr Met Ser His Val Asp Leu Val Lys Asp Leu
Asn Ser Gly Leu 180 185 190 Ile Gly Ala Leu Leu Val Cys Lys Glu Gly
Ser Leu Ser Lys Glu Arg 195 200 205 Thr Gln Met Leu Tyr Gln Phe Val
Leu Leu Phe Ala Val Phe Asp Glu 210 215 220 Gly Lys Ser Trp His Ser
Glu Thr Asn Asp Ser Tyr Thr Gln Ser Met 225 230 235 240 Asp Ser Ala
Ser Ala Arg Asp Trp Pro Lys Met His Thr Val Asn Gly 245 250 255 Tyr
Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Arg Lys Ser 260 265
270 Val Tyr Trp His Val Ile Gly Met Gly Thr Thr Pro Glu Ile His Ser
275 280 285 Ile Phe Leu Glu Gly His Thr Phe Phe Val Arg Asn His Arg
Gln Ala 290 295 300 Ser Leu Glu Ile Ser Pro Ile Thr Phe Leu Thr Ala
Gln Thr Leu Leu 305 310 315 320 Ile Asp Leu Gly Gln Phe Leu Leu Phe
Cys His Ile Ser Ser His Lys 325 330 335 His Asp Gly Met Glu Ala Tyr
Val Lys Val Asp Ser Cys Pro Glu Glu 340 345 350 Ser Gln Trp Gln Lys
Lys Asn Asn Asn Glu Glu Met Glu Asp Tyr Asp 355 360 365 Asp Asp Leu
Tyr Ser Glu Met Asp Met Phe Thr Leu Asp Tyr Asp Ser 370 375 380 Ser
Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys Tyr Pro Lys Thr 385 390
395 400 Trp Ile His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala
Pro 405 410 415 Ser Val Pro Thr Ser Asp Asn Gly Ser Tyr Lys Ser Gln
Tyr Leu Ser 420 425 430 Asn Gly Pro His Arg Ile Gly Arg Lys Tyr Lys
Lys Val Arg Phe Ile 435 440 445 Ala Tyr Thr Asp Glu Thr Phe Lys Thr
Arg Glu Thr Ile Gln His Glu 450 455 460 Ser Gly Leu Leu Gly Pro Leu
Leu Tyr Gly Glu Val Gly Asp Thr Leu 465 470 475 480 Leu Ile Ile Phe
Lys Asn Gln Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495 His Gly
Ile Thr Asp Val Ser Pro Leu His Ala Arg Arg Leu Pro Arg 500 505 510
Gly Ile Lys His Val Lys Asp Leu Pro Ile His Pro Gly Glu Ile Phe 515
520 525 Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser
Asp 530 535 540 Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Phe Ile Asn
Pro Glu Arg 545 550 555 560 Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu
Leu Ile Cys Tyr Lys Glu 565 570 575 Ser Val Asp Gln Arg Gly Asn Gln
Met Met Ser Asp Lys Arg Asn Val 580 585 590 Ile Leu Phe Ser Ile Phe
Asp Glu Asn Gln Ser Trp Tyr Ile Thr Glu 595 600 605 Asn Met Gln Arg
Phe Leu Pro Asn Ala Ala Lys Thr Gln Pro Gln Asp 610 615 620 Pro Gly
Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val 625 630 635
640 Phe Asp Ser Leu Glu Leu Thr Val Cys Leu His Glu Val Ala Tyr Trp
645 650 655 His Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Ile
Phe Phe 660 665 670 Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu
Asp Thr Leu Thr 675 680 685 Leu Phe Pro Phe Ser Gly Glu Thr Val Phe
Met Ser Met Glu Asn Pro 690 695 700 Gly Leu Trp Val Leu Gly Cys His
Asn Ser Asp Phe Arg Lys Arg Gly 705 710 715 720 Met Thr Ala Leu Leu
Lys Val Ser Ser Cys Asp Lys Ser Thr Ser Asp 725 730 735 Tyr Tyr Glu
Glu Ile Tyr Glu Asp Ile Pro Thr Gln Leu Val Asn Glu 740 745 750 Asn
Asn Val Ile Asp Pro Arg Ser Phe Phe Gln Asn Thr Asn His Pro 755 760
765 Asn Thr Arg Lys Lys Lys Phe Lys Asp Ser Thr Ile Pro Lys Asn Asp
770 775 780 Met Glu Lys Ile Glu Pro Gln Phe Glu Glu Ile Ala Glu Met
Leu Lys 785 790 795 800 Val Gln Ser Val Ser Val Ser Asp Met Leu Met
Leu Leu Gly Gln Ser 805 810 815 His Pro Thr Pro His Gly Leu Phe Leu
Ser Asp Gly Gln Glu Ala Ile 820 825 830 Tyr Glu Ala Ile His Asp Asp
His Ser Pro Asn Ala Ile Asp Ser Asn 835 840 845 Glu Gly Pro Ser Lys
Val Thr Gln Leu Arg Pro Glu Ser His His Ser 850 855 860 Glu Lys Ile
Val Phe Thr Pro Gln Pro Gly Leu Gln Leu Arg Ser Asn 865 870 875 880
Lys Ser Leu Glu Thr Thr Ile Glu Val Lys Trp Lys Lys Leu Gly Leu 885
890 895 Gln Val Ser Ser Leu Pro Ser Asn Leu Met Thr Thr Thr Ile Leu
Ser 900 905 910 Asp Asn Leu Lys Ala Thr Phe Glu Lys Thr Asp Ser Ser
Gly Phe Pro 915 920 925 Asp Met Pro Val His Ser Ser Ser Lys Leu Ser
Thr Thr Ala Phe Gly 930 935 940 Lys Lys Ala Tyr Ser Leu Val Gly Ser
His Val Pro Leu Asn Ala Ser 945 950 955 960 Glu Glu Asn Ser Asp Ser
Asn Ile Leu Asp Ser Thr Leu Met Tyr Ser 965 970 975 Gln Glu Ser Leu
Pro Arg Asp Asn Ile Leu Ser Ile Glu Asn Asp Arg 980 985 990 Leu Leu
Arg Glu Lys Arg Phe His Gly Ile Ala Leu Leu Thr Lys Asp 995 1000
1005 Asn Thr Leu Phe Lys Asp Asn Val Ser Leu Met Lys Thr Asn Lys
1010 1015 1020 Thr Tyr Asn His Ser Thr Thr Asn Glu Lys Leu His Thr
Glu Ser 1025 1030 1035 Pro Thr Ser Ile Glu Asn Ser Thr Thr Asp Leu
Gln Asp Ala Ile 1040 1045 1050 Leu Lys Val Asn Ser Glu Ile Gln Glu
Val Thr Ala Leu Ile His 1055 1060 1065 Asp Gly Thr Leu Leu Gly Lys
Asn Ser Thr Tyr Leu Arg Leu Asn 1070 1075 1080 His Met Leu Asn Arg
Thr Thr Ser Thr Lys Asn Lys Asp Ile Phe 1085 1090 1095 His Arg Lys
Asp Glu Asp Pro Ile Pro Gln Asp Glu Glu Asn Thr 1100 1105 1110 Ile
Met Pro Phe Ser Lys Met Leu Phe Leu Ser Glu Ser Ser Asn 1115 1120
1125 Trp Phe Lys Lys Thr Asn Gly Asn Asn Ser Leu Asn Ser Glu Gln
1130 1135 1140 Glu His Ser Pro Lys Gln Leu Val Tyr Leu Met Phe Lys
Lys Tyr 1145 1150 1155 Val Lys Asn Gln Ser Phe Leu Ser Glu Lys Asn
Lys Val Thr Val 1160 1165 1170 Glu Gln Asp Gly Phe Thr Lys Asn Ile
Gly Leu Lys Asp Met Ala 1175 1180 1185 Phe Pro His Asn Met Ser Ile
Phe Leu Thr Thr Leu Ser Asn Val 1190 1195 1200 His Glu Asn Gly Arg
His Asn Gln Glu Lys Asn Ile Gln Glu Glu 1205 1210 1215 Ile Glu Lys
Glu Ala Leu Ile Glu Glu Lys Val Val Leu Pro Gln 1220 1225 1230 Val
His Glu Ala Thr Gly Ser Lys Asn Phe Leu Lys Asp Ile Leu 1235 1240
1245 Ile Leu Gly Thr Arg Gln Asn Ile Ser Leu Tyr Glu Val His Val
1250 1255 1260 Pro Val Leu Gln Asn Ile Thr Ser Ile Asn Asn Ser Thr
Asn Thr 1265 1270 1275 Val Gln Ile His Met Glu His Phe Phe Lys Arg
Arg Lys Asp Lys 1280 1285 1290 Glu Thr Asn Ser Glu Gly Leu Val Asn
Lys Thr Arg Glu Met Val 1295 1300 1305 Lys Asn Tyr Pro Ser Gln Lys
Asn Ile Thr Thr Gln Arg Ser Lys 1310 1315 1320 Arg Ala Leu Gly Gln
Phe Arg Leu Ser Thr Gln Trp Leu Lys Thr 1325 1330 1335 Ile Asn Cys
Ser Thr Gln Cys Ile Ile Lys Gln Ile Asp His Ser 1340 1345 1350 Lys
Glu Met Lys Lys Phe Ile Thr Lys Ser Ser Leu Ser Asp Ser 1355 1360
1365 Ser Val Ile Lys Ser Thr Thr Gln Thr Asn Ser Ser Asp Ser His
1370 1375 1380 Ile Val Lys Thr Ser Ala Phe Pro Pro Ile Asp Leu Lys
Arg Ser 1385 1390 1395 Pro Phe Gln Asn Lys Phe Ser His Val Gln Ala
Ser
Ser Tyr Ile 1400 1405 1410 Tyr Asp Phe Lys Thr Lys Ser Ser Arg Ile
Gln Glu Ser Asn Asn 1415 1420 1425 Phe Leu Lys Glu Thr Lys Ile Asn
Asn Pro Ser Leu Ala Ile Leu 1430 1435 1440 Pro Trp Asn Met Phe Ile
Asp Gln Gly Lys Phe Thr Ser Pro Gly 1445 1450 1455 Lys Ser Asn Thr
Asn Ser Val Thr Tyr Lys Lys Arg Glu Asn Ile 1460 1465 1470 Ile Phe
Leu Lys Pro Thr Leu Pro Glu Glu Ser Gly Lys Ile Glu 1475 1480 1485
Leu Leu Pro Gln Val Ser Ile Gln Glu Glu Glu Ile Leu Pro Thr 1490
1495 1500 Glu Thr Ser His Gly Ser Pro Gly His Leu Asn Leu Met Lys
Glu 1505 1510 1515 Val Phe Leu Gln Lys Ile Gln Gly Pro Thr Lys Trp
Asn Lys Ala 1520 1525 1530 Lys Arg His Gly Glu Ser Ile Lys Gly Lys
Thr Glu Ser Ser Lys 1535 1540 1545 Asn Thr Arg Ser Lys Leu Leu Asn
His His Ala Trp Asp Tyr His 1550 1555 1560 Tyr Ala Ala Gln Ile Pro
Lys Asp Met Trp Lys Ser Lys Glu Lys 1565 1570 1575 Ser Pro Glu Ile
Ile Ser Ile Lys Gln Glu Asp Thr Ile Leu Ser 1580 1585 1590 Leu Arg
Pro His Gly Asn Ser His Ser Ile Gly Ala Asn Glu Lys 1595 1600 1605
Gln Asn Trp Pro Gln Arg Glu Thr Thr Trp Val Lys Gln Gly Gln 1610
1615 1620 Thr Gln Arg Thr Cys Ser Gln Ile Pro Pro Val Leu Lys Arg
His 1625 1630 1635 Gln Arg Glu Leu Ser Ala Phe Gln Ser Glu Gln Glu
Ala Thr Asp 1640 1645 1650 Tyr Asp Asp Ala Ile Thr Ile Glu Thr Ile
Glu Asp Phe Asp Ile 1655 1660 1665 Tyr Ser Glu Asp Ile Lys Gln Gly
Pro Arg Ser Phe Gln Gln Lys 1670 1675 1680 Thr Arg His Tyr Phe Ile
Ala Ala Val Glu Arg Leu Trp Asp Tyr 1685 1690 1695 Gly Met Ser Thr
Ser His Val Leu Arg Asn Arg Tyr Gln Ser Asp 1700 1705 1710 Asn Val
Pro Gln Phe Lys Lys Val Val Phe Gln Glu Phe Thr Asp 1715 1720 1725
Gly Ser Phe Ser Gln Pro Leu Tyr Arg Gly Glu Leu Asn Glu His 1730
1735 1740 Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp
Asn 1745 1750 1755 Ile Met Val Thr Phe Lys Asn Gln Ala Ser Arg Pro
Tyr Ser Phe 1760 1765 1770 Tyr Ser Ser Leu Ile Ser Tyr Lys Glu Asp
Gln Arg Gly Glu Glu 1775 1780 1785 Pro Arg Arg Asn Phe Val Lys Pro
Asn Glu Thr Lys Ile Tyr Phe 1790 1795 1800 Trp Lys Val Gln His His
Met Ala Pro Thr Glu Asp Glu Phe Asp 1805 1810 1815 Cys Lys Ala Trp
Ala Tyr Phe Ser Asp Val Asp Leu Glu Arg Asp 1820 1825 1830 Met His
Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys His Ala Asn 1835 1840 1845
Thr Leu Asn Pro Ala His Gly Arg Gln Val Ser Val Gln Glu Phe 1850
1855 1860 Ala Leu Leu Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp Tyr
Phe 1865 1870 1875 Thr Glu Asn Val Lys Arg Asn Cys Lys Thr Pro Cys
Asn Phe Gln 1880 1885 1890 Met Glu Asp Pro Thr Leu Lys Glu Asn Tyr
Arg Phe His Ala Ile 1895 1900 1905 Asn Gly Tyr Val Met Asp Thr Leu
Pro Gly Leu Val Met Ala Gln 1910 1915 1920 Asp Gln Arg Ile Arg Trp
Tyr Leu Leu Ser Met Gly Asn Asn Glu 1925 1930 1935 Asn Ile Gln Ser
Ile His Phe Ser Gly His Val Phe Thr Val Arg 1940 1945 1950 Lys Lys
Glu Glu Tyr Lys Met Ala Val Tyr Asn Leu Tyr Pro Gly 1955 1960 1965
Val Phe Glu Thr Leu Glu Met Ile Pro Ser Arg Ala Gly Ile Trp 1970
1975 1980 Arg Val Glu Cys Leu Ile Gly Glu His Leu Gln Ala Gly Met
Ser 1985 1990 1995 Thr Leu Phe Leu Val Tyr Ser Lys Gln Cys Gln Ile
Pro Leu Gly 2000 2005 2010 Met Ala Ser Gly Ser Ile Arg Asp Phe Gln
Ile Thr Ala Ser Gly 2015 2020 2025 His Tyr Gly Gln Trp Ala Pro Asn
Leu Ala Arg Leu His Tyr Ser 2030 2035 2040 Gly Ser Ile Asn Ala Trp
Ser Thr Lys Glu Pro Phe Ser Trp Ile 2045 2050 2055 Lys Val Asp Leu
Leu Ala Pro Met Ile Val His Gly Ile Lys Thr 2060 2065 2070 Gln Gly
Ala Arg Gln Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe 2075 2080 2085
Ile Ile Met Tyr Ser Leu Asp Gly Lys Lys Trp Leu Ser Tyr Gln 2090
2095 2100 Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly Asn Val
Asp 2105 2110 2115 Ser Ser Gly Ile Lys His Asn Ser Phe Asn Pro Pro
Ile Ile Ala 2120 2125 2130 Arg Tyr Ile Arg Leu His Pro Thr His Ser
Ser Ile Arg Ser Thr 2135 2140 2145 Leu Arg Met Glu Leu Met Gly Cys
Asp Leu Asn Ser Cys Ser Ile 2150 2155 2160 Pro Leu Gly Met Glu Ser
Lys Val Ile Ser Asp Thr Gln Ile Thr 2165 2170 2175 Ala Ser Ser Tyr
Phe Thr Asn Met Phe Ala Thr Trp Ser Pro Ser 2180 2185 2190 Gln Ala
Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg Pro 2195 2200 2205
Gln Val Asn Asp Pro Lys Gln Trp Leu Gln Val Asp Leu Gln Lys 2210
2215 2220 Thr Met Lys Val Thr Gly Ile Ile Thr Gln Gly Val Lys Ser
Leu 2225 2230 2235 Phe Thr Ser Met Phe Val Lys Glu Phe Leu Ile Ser
Ser Ser Gln 2240 2245 2250 Asp Gly His His Trp Thr Gln Ile Leu Tyr
Asn Gly Lys Val Lys 2255 2260 2265 Val Phe Gln Gly Asn Gln Asp Ser
Ser Thr Pro Met Met Asn Ser 2270 2275 2280 Leu Asp Pro Pro Leu Leu
Thr Arg Tyr Leu Arg Ile His Pro Gln 2285 2290 2295 Ile Trp Glu His
Gln Ile Ala Leu Arg Leu Glu Ile Leu Gly Cys 2300 2305 2310 Glu Ala
Gln Gln Gln Tyr 2315 740DNAArtificialSynthetic construct
oligonucleotide useful as primer. 7ccttccttta tccaaatacg tagatcaaga
ggaaattgac 40829DNAArtificialSynthetic construct oligonucleotide
useful as primer. 8gtagcgttgc caagaagcac cctaagacg
29937DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 9gaagagtagt acgagttatt tctctgggtt caatgac
371033DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 10cctttatcca aatacgtagc gtttgccaag aag
331119DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 11aarcayccna aracntggg 191225DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 12gctcgcacta
gggggtcttg aattc 251344DNAArtificialSynthetic construct
oligonucleotide useful as a primer. 13ctaatacgac tcactatagg
gctcgagcgg ccgcccgggc aggt 441427DNAArtificialSynthetic construct
oligonucleotide useful as a primer. 14ccatcctaat acgactcact atagggc
271524DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 15ccattgacat gaagaccgtt tctc 241623DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 16actcactata
gggctcgagc ggc 231724DNAArtificialSynthetic construct
oligonucleotide useful as a primer. 17gggtgcaaag cgctgacatc agtg
241850DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 18cctctcgagc caccatgtcg agccaccatg cagctagagc tctccacctg
501931DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 19cgcgcggccg cgcatctggc aaagctgagt t
312027DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 20gaaataagcc caggctttgc agtcraa
272122DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 21aggaaattcc actggaacct tn 222225DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 22ctgggggtga
attcgaaggt agcgn 252323DNAArtificialSynthetic construct
oligonucleotide useful as a primer. 23gagttcatcg ggaagacctg ttg
232424DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 24acagcccatc aactccatgc gaag 242519DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 25tcagggcaat
caggactcc 192621DNAArtificialSynthetic construct oligonucleotide
useful as a primer. 26ccgtggtgaa cgctctggac c
212724DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 27gtagaggtcc tgtgcctcgc agcc 242827DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 28gtagagstsc
tgkgcctcrc akccyag 272924DNAArtificialSynthetic construct
oligonucleotide useful as a primer. 29cttcgcatgg agttgatggg ctgt
243022DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 30aatcaggact cctccacccc cg 223120DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 31ggatccaccc
cacgagctgg 203224DNAArtificialSynthetic construct oligonucleotide
useful as a primer. 32cgccctgagg ctcgaggttc tagg
243322DNAArtificialSynthetic construct oligonucleotide useful as a
primer. 33aatcaggact cctccacccc cg 223420DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 34ccttgcagga
attcgattca 203521DNAArtificialSynthetic construct oligonucleotide
useful as a primer. 35ccgtggtgaa cgctctggac c
21366402DNAporcineCDS(1)..(6399) 36atg cag cta gag ctc tcc acc tgt
gtc ttt ctg tgt ctc ttg cca ctc 48Met Gln Leu Glu Leu Ser Thr Cys
Val Phe Leu Cys Leu Leu Pro Leu 1 5 10 15 ggc ttt agt gcc atc agg
aga tac tac ctg ggc gca gtg gaa ctg tcc 96Gly Phe Ser Ala Ile Arg
Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30 tgg gac tac cgg
caa agt gaa ctc ctc cgt gag ctg cac gtg gac acc 144Trp Asp Tyr Arg
Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45 aga ttt
cct gct aca gcg cca gga gct ctt ccg ttg ggc ccg tca gtc 192Arg Phe
Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60
ctg tac aaa aag act gtg ttc gta gag ttc acg gat caa ctt ttc agc
240Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser
65 70 75 80 gtt gcc agg ccc agg cca cca tgg atg ggt ctg ctg ggt cct
acc atc 288Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro
Thr Ile 85 90 95 cag gct gag gtt tac gac acg gtg gtc gtt acc ctg
aag aac atg gct 336Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu
Lys Asn Met Ala 100 105 110 tct cat ccc gtt agt ctt cac gct gtc ggc
gtc tcc ttc tgg aaa tct 384Ser His Pro Val Ser Leu His Ala Val Gly
Val Ser Phe Trp Lys Ser 115 120 125 tcc gaa ggc gct gaa tat gag gat
cac acc agc caa agg gag aag gaa 432Ser Glu Gly Ala Glu Tyr Glu Asp
His Thr Ser Gln Arg Glu Lys Glu 130 135 140 gac gat aaa gtc ctt ccc
ggt aaa agc caa acc tac gtc tgg cag gtc 480Asp Asp Lys Val Leu Pro
Gly Lys Ser Gln Thr Tyr Val Trp Gln Val 145 150 155 160 ctg aaa gaa
aat ggt cca aca gcc tct gac cca cca tgt ctc acc tac 528Leu Lys Glu
Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175 tca
tac ctg tct cac gtg gac ctg gtg aaa gac ctg aat tcg ggc ctc 576Ser
Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185
190 att gga gcc ctg ctg gtt tgt aga gaa ggg agt ctg acc aga gaa agg
624Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg
195 200 205 acc cag aac ctg cac gaa ttt gta cta ctt ttt gct gtc ttt
gat gaa 672Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe
Asp Glu 210 215 220 ggg aaa agt tgg cac tca gca aga aat gac tcc tgg
aca cgg gcc atg 720Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp
Thr Arg Ala Met 225 230 235 240 gat ccc gca cct gcc agg gcc cag cct
gca atg cac aca gtc aat ggc 768Asp Pro Ala Pro Ala Arg Ala Gln Pro
Ala Met His Thr Val Asn Gly 245 250 255 tat gtc aac agg tct ctg cca
ggt ctg atc gga tgt cat aag aaa tca 816Tyr Val Asn Arg Ser Leu Pro
Gly Leu Ile Gly Cys His Lys Lys Ser 260 265 270 gtc tac tgg cac gtg
att gga atg ggc acc agc ccg gaa gtg cac tcc 864Val Tyr Trp His Val
Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 275 280 285 att ttt ctt
gaa ggc cac acg ttt ctc gtg agg cac cat cgc cag gct 912Ile Phe Leu
Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 290 295 300 tcc
ttg gag atc tcg cca cta act ttc ctc act gct cag aca ttc ctg 960Ser
Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu 305 310
315 320 atg gac ctt ggc cag ttc cta ctg ttt tgt cat atc tct tcc cac
cac 1008Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His
His 325 330 335 cat ggt ggc atg gag gct cac gtc aga gta gaa agc tgc
gcc gag gag 1056His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys
Ala Glu Glu 340 345 350 ccc cag ctg cgg agg aaa gct gat gaa gag gaa
gat tat gat gac aat 1104Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu
Asp Tyr Asp Asp Asn 355 360 365 ttg tac gac tcg gac atg gac gtg gtc
cgg ctc gat ggt gac gac gtg 1152Leu Tyr Asp Ser Asp Met Asp Val Val
Arg Leu Asp Gly Asp Asp Val 370 375 380 tct ccc ttt atc caa atc cgc
tcg gtt gcc aag aag cat ccc aaa acc 1200Ser Pro Phe Ile Gln Ile Arg
Ser Val Ala Lys Lys His Pro Lys Thr 385 390 395 400 tgg gtg cac tac
atc tct gca gag gag gag gac tgg gac tac gcc ccc 1248Trp Val His Tyr
Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415 gcg gtc
ccc agc ccc agt gac aga agt tat aaa agt ctc tac ttg aac 1296Ala Val
Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430
agt ggt cct cag cga att ggt agg aaa tac aaa aaa gct cga ttc gtc
1344Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val
435 440 445
gct tac acg gat gta aca ttt aag act cgt aaa gct att ccg tat gaa
1392Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu
450 455 460 tca gga atc ctg gga cct tta ctt tat gga gaa gtt gga gac
aca ctt 1440Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp
Thr Leu 465 470 475 480 ttg att ata ttt aag aat aaa gcg agc cga cca
tat aac atc tac cct 1488Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro
Tyr Asn Ile Tyr Pro 485 490 495 cat gga atc act gat gtc agc gct ttg
cac cca ggg aga ctt cta aaa 1536His Gly Ile Thr Asp Val Ser Ala Leu
His Pro Gly Arg Leu Leu Lys 500 505 510 ggt tgg aaa cat ttg aaa gac
atg cca att ctg cca gga gag act ttc 1584Gly Trp Lys His Leu Lys Asp
Met Pro Ile Leu Pro Gly Glu Thr Phe 515 520 525 aag tat aaa tgg aca
gtg act gtg gaa gat ggg cca acc aag tcc gat 1632Lys Tyr Lys Trp Thr
Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540 cct cgg tgc
ctg acc cgc tac tac tcg agc tcc att aat cta gag aaa 1680Pro Arg Cys
Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys 545 550 555 560
gat ctg gct tcg gga ctc att ggc cct ctc ctc atc tgc tac aaa gaa
1728Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu
565 570 575 tct gta gac caa aga gga aac cag atg atg tca gac aag aga
aac gtc 1776Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg
Asn Val 580 585 590 atc ctg ttt tct gta ttc gat gag aat caa agc tgg
tac ctc gca gag 1824Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp
Tyr Leu Ala Glu 595 600 605 aat att cag cgc ttc ctc ccc aat ccg gat
gga tta cag ccc cag gat 1872Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp
Gly Leu Gln Pro Gln Asp 610 615 620 cca gag ttc caa gct tct aac atc
atg cac agc atc aat ggc tat gtt 1920Pro Glu Phe Gln Ala Ser Asn Ile
Met His Ser Ile Asn Gly Tyr Val 625 630 635 640 ttt gat agc ttg cag
ctg tcg gtt tgt ttg cac gag gtg gca tac tgg 1968Phe Asp Ser Leu Gln
Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655 tac att cta
agt gtt gga gca cag acg gac ttc ctc tcc gtc ttc ttc 2016Tyr Ile Leu
Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670 tct
ggc tac acc ttc aaa cac aaa atg gtc tat gaa gac aca ctc acc 2064Ser
Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680
685 ctg ttc ccc ttc tca gga gaa acg gtc ttc atg tca atg gaa aac cca
2112Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro
690 695 700 ggt ctc tgg gtc cta ggg tgc cac aac tca gac ttg cgg aac
aga ggg 2160Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn
Arg Gly 705 710 715 720 atg aca gcc tta ctg aag gtg tat agt tgt gac
agg gac att ggt gat 2208Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp
Arg Asp Ile Gly Asp 725 730 735 tat tat gac aac act tat gaa gat att
cca ggc ttc ttg ctg agt gga 2256Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile
Pro Gly Phe Leu Leu Ser Gly 740 745 750 aag aat gtc att gaa ccc aga
agc ttt gcc cag aat tca aga ccc cct 2304Lys Asn Val Ile Glu Pro Arg
Ser Phe Ala Gln Asn Ser Arg Pro Pro 755 760 765 agt gcg agc caa aag
caa ttc caa acc atc aca agt cca gaa gat gac 2352Ser Ala Ser Gln Lys
Gln Phe Gln Thr Ile Thr Ser Pro Glu Asp Asp 770 775 780 gtg gag ctt
gac ccg cag tct gga gag aga acc caa gca ctg gaa gaa 2400Val Glu Leu
Asp Pro Gln Ser Gly Glu Arg Thr Gln Ala Leu Glu Glu 785 790 795 800
cta agt gtc ccc tct ggt gat ggg tcg atg ctc ttg gga cag aat cct
2448Leu Ser Val Pro Ser Gly Asp Gly Ser Met Leu Leu Gly Gln Asn Pro
805 810 815 gct cca cat ggc tca tcc tca tct gat ctt caa gaa gcc agg
aat gag 2496Ala Pro His Gly Ser Ser Ser Ser Asp Leu Gln Glu Ala Arg
Asn Glu 820 825 830 gct gat gat tat tta cct gga gca aga gaa aga aac
acg gcc cca tcc 2544Ala Asp Asp Tyr Leu Pro Gly Ala Arg Glu Arg Asn
Thr Ala Pro Ser 835 840 845 gca gcg gca cgt ctc aga cca gag ctg cat
cac agt gcc gaa aga gta 2592Ala Ala Ala Arg Leu Arg Pro Glu Leu His
His Ser Ala Glu Arg Val 850 855 860 ctt act cct gag cca gag aaa gag
ttg aag aaa ctt gat tca aaa atg 2640Leu Thr Pro Glu Pro Glu Lys Glu
Leu Lys Lys Leu Asp Ser Lys Met 865 870 875 880 tct agt tca tca gac
ctt cta aag act tcg cca aca att cca tca gac 2688Ser Ser Ser Ser Asp
Leu Leu Lys Thr Ser Pro Thr Ile Pro Ser Asp 885 890 895 acg ttg tca
gcg gag act gaa agg aca cat tcc tta ggc ccc cca cac 2736Thr Leu Ser
Ala Glu Thr Glu Arg Thr His Ser Leu Gly Pro Pro His 900 905 910 ccg
cag gtt aat ttc agg agt caa tta ggt gcc att gta ctt ggc aaa 2784Pro
Gln Val Asn Phe Arg Ser Gln Leu Gly Ala Ile Val Leu Gly Lys 915 920
925 aat tca tct cac ttt att ggg gct ggt gtc cct ttg ggc tcg act gag
2832Asn Ser Ser His Phe Ile Gly Ala Gly Val Pro Leu Gly Ser Thr Glu
930 935 940 gag gat cat gaa agc tcc ctg gga gaa aat gta tca cca gtg
gag agt 2880Glu Asp His Glu Ser Ser Leu Gly Glu Asn Val Ser Pro Val
Glu Ser 945 950 955 960 gac ggg ata ttt gaa aag gaa aga gct cat gga
cct gct tca ctg acc 2928Asp Gly Ile Phe Glu Lys Glu Arg Ala His Gly
Pro Ala Ser Leu Thr 965 970 975 aaa gac gat gtt tta ttt aaa gtt aat
atc tct ttg gta aag aca aac 2976Lys Asp Asp Val Leu Phe Lys Val Asn
Ile Ser Leu Val Lys Thr Asn 980 985 990 aag gca cga gtt tac tta aaa
act aat aga aag att cac att gat gac 3024Lys Ala Arg Val Tyr Leu Lys
Thr Asn Arg Lys Ile His Ile Asp Asp 995 1000 1005 gca gct tta tta
act gag aat agg gca tct gca acg ttt atg gac 3069Ala Ala Leu Leu Thr
Glu Asn Arg Ala Ser Ala Thr Phe Met Asp 1010 1015 1020 aaa aat act
aca gct tcg gga tta aat cat gtg tca aat tgg ata 3114Lys Asn Thr Thr
Ala Ser Gly Leu Asn His Val Ser Asn Trp Ile 1025 1030 1035 aaa ggg
ccc ctt ggc aag aac ccc cta agc tcg gag cga ggc ccc 3159Lys Gly Pro
Leu Gly Lys Asn Pro Leu Ser Ser Glu Arg Gly Pro 1040 1045 1050 agt
cca gag ctt ctg aca tct tca gga tca gga aaa tct gtg aaa 3204Ser Pro
Glu Leu Leu Thr Ser Ser Gly Ser Gly Lys Ser Val Lys 1055 1060 1065
ggt cag agt tct ggg cag ggg aga ata cgg gtg gca gtg gaa gag 3249Gly
Gln Ser Ser Gly Gln Gly Arg Ile Arg Val Ala Val Glu Glu 1070 1075
1080 gaa gaa ctg agc aaa ggc aaa gag atg atg ctt ccc aac agc gag
3294Glu Glu Leu Ser Lys Gly Lys Glu Met Met Leu Pro Asn Ser Glu
1085 1090 1095 ctc acc ttt ctc act aac tcg gct gat gtc caa gga aac
gat aca 3339Leu Thr Phe Leu Thr Asn Ser Ala Asp Val Gln Gly Asn Asp
Thr 1100 1105 1110 cac agt caa gga aaa aag tct cgg gaa gag atg gaa
agg aga gaa 3384His Ser Gln Gly Lys Lys Ser Arg Glu Glu Met Glu Arg
Arg Glu 1115 1120 1125 aaa tta gtc caa gaa aaa gtc gac ttg cct cag
gtg tat aca gcg 3429Lys Leu Val Gln Glu Lys Val Asp Leu Pro Gln Val
Tyr Thr Ala 1130 1135 1140 act gga act aag aat ttc ctg aga aac att
ttt cac caa agc act 3474Thr Gly Thr Lys Asn Phe Leu Arg Asn Ile Phe
His Gln Ser Thr 1145 1150 1155 gag ccc agt gta gaa ggg ttt gat ggg
ggg tca cat gcg ccg gtg 3519Glu Pro Ser Val Glu Gly Phe Asp Gly Gly
Ser His Ala Pro Val 1160 1165 1170 cct caa gac agc agg tca tta aat
gat tcg gca gag aga gca gag 3564Pro Gln Asp Ser Arg Ser Leu Asn Asp
Ser Ala Glu Arg Ala Glu 1175 1180 1185 act cac ata gcc cat ttc tca
gca att agg gaa gag gca ccc ttg 3609Thr His Ile Ala His Phe Ser Ala
Ile Arg Glu Glu Ala Pro Leu 1190 1195 1200 gaa gcc ccg gga aat cga
aca ggt cca ggt ccg agg agt gcg gtt 3654Glu Ala Pro Gly Asn Arg Thr
Gly Pro Gly Pro Arg Ser Ala Val 1205 1210 1215 ccc cgc cgc gtt aag
cag agc ttg aaa cag atc aga ctc ccg cta 3699Pro Arg Arg Val Lys Gln
Ser Leu Lys Gln Ile Arg Leu Pro Leu 1220 1225 1230 gaa gaa ata aag
cct gaa agg ggg gtg gtt ctg aat gcc acc tca 3744Glu Glu Ile Lys Pro
Glu Arg Gly Val Val Leu Asn Ala Thr Ser 1235 1240 1245 acc cgg tgg
tct gaa agc agt cct atc tta caa gga gcc aaa aga 3789Thr Arg Trp Ser
Glu Ser Ser Pro Ile Leu Gln Gly Ala Lys Arg 1250 1255 1260 aat aac
ctt tct tta cct ttc ctg acc ttg gaa atg gcc gga ggt 3834Asn Asn Leu
Ser Leu Pro Phe Leu Thr Leu Glu Met Ala Gly Gly 1265 1270 1275 caa
gga aag atc agc gcc ctg ggg aaa agt gcc gca ggc ccg ctg 3879Gln Gly
Lys Ile Ser Ala Leu Gly Lys Ser Ala Ala Gly Pro Leu 1280 1285 1290
gcg tcc ggg aag ctg gag aag gct gtt ctc tct tca gca ggc ttg 3924Ala
Ser Gly Lys Leu Glu Lys Ala Val Leu Ser Ser Ala Gly Leu 1295 1300
1305 tct gaa gca tct ggc aaa gct gag ttt ctt cct aaa gtt cga gtt
3969Ser Glu Ala Ser Gly Lys Ala Glu Phe Leu Pro Lys Val Arg Val
1310 1315 1320 cat cgg gaa gac ctg ttg cct caa aaa acc agc aat gtt
tct tgc 4014His Arg Glu Asp Leu Leu Pro Gln Lys Thr Ser Asn Val Ser
Cys 1325 1330 1335 gca cac ggg gat ctc ggc cag gag atc ttc ctg cag
aaa aca cgg 4059Ala His Gly Asp Leu Gly Gln Glu Ile Phe Leu Gln Lys
Thr Arg 1340 1345 1350 gga cct gtt aac ctg aac aaa gta aat aga cct
gga agg act ccc 4104Gly Pro Val Asn Leu Asn Lys Val Asn Arg Pro Gly
Arg Thr Pro 1355 1360 1365 tcc aag ctt ctg ggt ccc ccg atg ccc aaa
gag tgg gaa tcc cta 4149Ser Lys Leu Leu Gly Pro Pro Met Pro Lys Glu
Trp Glu Ser Leu 1370 1375 1380 gag aag tca cca aaa agc aca gct ctc
agg acg aaa gac atc atc 4194Glu Lys Ser Pro Lys Ser Thr Ala Leu Arg
Thr Lys Asp Ile Ile 1385 1390 1395 agt tta ccc ctg gac cgt cac gaa
agc aat cat tca ata gca gca 4239Ser Leu Pro Leu Asp Arg His Glu Ser
Asn His Ser Ile Ala Ala 1400 1405 1410 aaa aat gaa gga caa gcc gag
acc caa aga gaa gcc gcc tgg acg 4284Lys Asn Glu Gly Gln Ala Glu Thr
Gln Arg Glu Ala Ala Trp Thr 1415 1420 1425 aag cag gga ggg cct gga
agg ctg tgc gct cca aag cct ccg gtc 4329Lys Gln Gly Gly Pro Gly Arg
Leu Cys Ala Pro Lys Pro Pro Val 1430 1435 1440 ctg cga cgg cat cag
agg gac ata agc ctt cct act ttt cag ccg 4374Leu Arg Arg His Gln Arg
Asp Ile Ser Leu Pro Thr Phe Gln Pro 1445 1450 1455 gag gaa gac aaa
atg gac tat gat gat atc ttc tca act gaa acg 4419Glu Glu Asp Lys Met
Asp Tyr Asp Asp Ile Phe Ser Thr Glu Thr 1460 1465 1470 aag gga gaa
gat ttt gac att tac ggt gag gat gaa aat cag gac 4464Lys Gly Glu Asp
Phe Asp Ile Tyr Gly Glu Asp Glu Asn Gln Asp 1475 1480 1485 cct cgc
agc ttt cag aag aga acc cga cac tat ttc att gct gcg 4509Pro Arg Ser
Phe Gln Lys Arg Thr Arg His Tyr Phe Ile Ala Ala 1490 1495 1500 gtg
gag cag ctc tgg gat tac ggg atg agc gaa tcc ccc cgg gcg 4554Val Glu
Gln Leu Trp Asp Tyr Gly Met Ser Glu Ser Pro Arg Ala 1505 1510 1515
cta aga aac agg gct cag aac gga gag gtg cct cgg ttc aag aag 4599Leu
Arg Asn Arg Ala Gln Asn Gly Glu Val Pro Arg Phe Lys Lys 1520 1525
1530 gtg gtc ttc cgg gaa ttt gct gac ggc tcc ttc acg cag ccg tcg
4644Val Val Phe Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln Pro Ser
1535 1540 1545 tac cgc ggg gaa ctc aac aaa cac ttg ggg ctc ttg gga
ccc tac 4689Tyr Arg Gly Glu Leu Asn Lys His Leu Gly Leu Leu Gly Pro
Tyr 1550 1555 1560 atc aga gcg gaa gtt gaa gac aac atc atg gta act
ttc aaa aac 4734Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe
Lys Asn 1565 1570 1575 cag gcg tct cgt ccc tat tcc ttc tac tcg agc
ctt att tct tat 4779Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu
Ile Ser Tyr 1580 1585 1590 ccg gat gat cag gag caa ggg gca gaa cct
cga cac aac ttc gtc 4824Pro Asp Asp Gln Glu Gln Gly Ala Glu Pro Arg
His Asn Phe Val 1595 1600 1605 cag cca aat gaa acc aga act tac ttt
tgg aaa gtg cag cat cac 4869Gln Pro Asn Glu Thr Arg Thr Tyr Phe Trp
Lys Val Gln His His 1610 1615 1620 atg gca ccc aca gaa gac gag ttt
gac tgc aaa gcc tgg gcc tac 4914Met Ala Pro Thr Glu Asp Glu Phe Asp
Cys Lys Ala Trp Ala Tyr 1625 1630 1635 ttt tct gat gtt gac ctg gaa
aaa gat gtg cac tca ggc ttg atc 4959Phe Ser Asp Val Asp Leu Glu Lys
Asp Val His Ser Gly Leu Ile 1640 1645 1650 ggc ccc ctt ctg atc tgc
cgc gcc aac acc ctg aac gct gct cac 5004Gly Pro Leu Leu Ile Cys Arg
Ala Asn Thr Leu Asn Ala Ala His 1655 1660 1665 ggt aga caa gtg acc
gtg caa gaa ttt gct ctg ttt ttc act att 5049Gly Arg Gln Val Thr Val
Gln Glu Phe Ala Leu Phe Phe Thr Ile 1670 1675 1680 ttt gat gag aca
aag agc tgg tac ttc act gaa aat gtg gaa agg 5094Phe Asp Glu Thr Lys
Ser Trp Tyr Phe Thr Glu Asn Val Glu Arg 1685 1690 1695 aac tgc cgg
gcc ccc tgc cac ctg cag atg gag gac ccc act ctg 5139Asn Cys Arg Ala
Pro Cys His Leu Gln Met Glu Asp Pro Thr Leu 1700 1705 1710 aaa gaa
aac tat cgc ttc cat gca atc aat ggc tat gtg atg gat 5184Lys Glu Asn
Tyr Arg Phe His Ala Ile Asn Gly Tyr Val Met Asp 1715 1720 1725 aca
ctc cct ggc tta gta atg gct cag aat caa agg atc cga tgg 5229Thr Leu
Pro Gly Leu Val Met Ala Gln Asn Gln Arg Ile Arg Trp
1730 1735 1740 tat ctg ctc agc atg ggc agc aat gaa aat atc cat tcg
att cat 5274Tyr Leu Leu Ser Met Gly Ser Asn Glu Asn Ile His Ser Ile
His 1745 1750 1755 ttt agc gga cac gtg ttc agt gta cgg aaa aag gag
gag tat aaa 5319Phe Ser Gly His Val Phe Ser Val Arg Lys Lys Glu Glu
Tyr Lys 1760 1765 1770 atg gcc gtg tac aat ctc tat ccg ggt gtc ttt
gag aca gtg gaa 5364Met Ala Val Tyr Asn Leu Tyr Pro Gly Val Phe Glu
Thr Val Glu 1775 1780 1785 atg cta ccg tcc aaa gtt gga att tgg cga
ata gaa tgc ctg att 5409Met Leu Pro Ser Lys Val Gly Ile Trp Arg Ile
Glu Cys Leu Ile 1790 1795 1800 ggc gag cac ctg caa gct ggg atg agc
acg act ttc ctg gtg tac 5454Gly Glu His Leu Gln Ala Gly Met Ser Thr
Thr Phe Leu Val Tyr 1805 1810 1815 agc aag gag tgt cag gct cca ctg
gga atg gct tct gga cgc att 5499Ser Lys Glu Cys Gln Ala Pro Leu Gly
Met Ala Ser Gly Arg Ile 1820 1825 1830 aga gat ttt cag atc aca gct
tca gga cag tat gga cag tgg gcc 5544Arg Asp Phe Gln Ile Thr Ala Ser
Gly Gln Tyr Gly Gln Trp Ala 1835 1840 1845 cca aag ctg gcc aga ctt
cat tat tcc gga tca atc aat gcc tgg 5589Pro Lys Leu Ala Arg Leu His
Tyr Ser Gly Ser Ile Asn Ala Trp 1850 1855 1860 agc acc aag gat ccc
cac tcc tgg atc aag gtg gat ctg ttg gca 5634Ser Thr Lys Asp Pro His
Ser Trp Ile Lys Val Asp Leu Leu Ala 1865 1870 1875 cca atg atc att
cac ggc atc atg acc cag ggt gcc cgt cag aag 5679Pro Met Ile Ile His
Gly Ile Met Thr Gln Gly Ala Arg Gln Lys 1880 1885 1890 ttt tcc agc
ctc tac atc tcc cag ttt atc atc atg tac agt ctt 5724Phe Ser Ser Leu
Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu 1895 1900 1905 gac ggg
agg aac tgg cag agt tac cga ggg aat tcc acg ggc acc 5769Asp Gly Arg
Asn Trp Gln Ser Tyr Arg Gly Asn Ser Thr Gly Thr 1910 1915 1920 tta
atg gtc ttc ttt ggc aat gtg gac gca tct ggg att aaa cac 5814Leu Met
Val Phe Phe Gly Asn Val Asp Ala Ser Gly Ile Lys His 1925 1930 1935
aat att ttt aac cct ccg att gtg gct cgg tac atc cgt ttg cac 5859Asn
Ile Phe Asn Pro Pro Ile Val Ala Arg Tyr Ile Arg Leu His 1940 1945
1950 cca aca cat tac agc atc cgc agc act ctt cgc atg gag ttg atg
5904Pro Thr His Tyr Ser Ile Arg Ser Thr Leu Arg Met Glu Leu Met
1955 1960 1965 ggc tgt gat tta aac agt tgc agc atg ccc ctg gga atg
cag aat 5949Gly Cys Asp Leu Asn Ser Cys Ser Met Pro Leu Gly Met Gln
Asn 1970 1975 1980 aaa gcg ata tca gac tca cag atc acg gcc tcc tcc
cac cta agc 5994Lys Ala Ile Ser Asp Ser Gln Ile Thr Ala Ser Ser His
Leu Ser 1985 1990 1995 aat ata ttt gcc acc tgg tct cct tca caa gcc
cga ctt cac ctc 6039Asn Ile Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg
Leu His Leu 2000 2005 2010 cag ggg cgg acg aat gcc tgg cga ccc cgg
gtg agc agc gca gag 6084Gln Gly Arg Thr Asn Ala Trp Arg Pro Arg Val
Ser Ser Ala Glu 2015 2020 2025 gag tgg ctg cag gtg gac ctg cag aag
acg gtg aag gtc aca ggc 6129Glu Trp Leu Gln Val Asp Leu Gln Lys Thr
Val Lys Val Thr Gly 2030 2035 2040 atc acc acc cag ggc gtg aag tcc
ctg ctc agc agc atg tat gtg 6174Ile Thr Thr Gln Gly Val Lys Ser Leu
Leu Ser Ser Met Tyr Val 2045 2050 2055 aag gag ttc ctc gtg tcc agt
agt cag gac ggc cgc cgc tgg acc 6219Lys Glu Phe Leu Val Ser Ser Ser
Gln Asp Gly Arg Arg Trp Thr 2060 2065 2070 ctg ttt ctt cag gac ggc
cac acg aag gtt ttt cag ggc aat cag 6264Leu Phe Leu Gln Asp Gly His
Thr Lys Val Phe Gln Gly Asn Gln 2075 2080 2085 gac tcc tcc acc ccc
gtg gtg aac gct ctg gac ccc ccg ctg ttc 6309Asp Ser Ser Thr Pro Val
Val Asn Ala Leu Asp Pro Pro Leu Phe 2090 2095 2100 acg cgc tac ctg
agg atc cac ccc acg agc tgg gcg cag cac atc 6354Thr Arg Tyr Leu Arg
Ile His Pro Thr Ser Trp Ala Gln His Ile 2105 2110 2115 gcc ctg agg
ctc gag gtt cta gga tgt gag gca cag gat ctc tac 6399Ala Leu Arg Leu
Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 2120 2125 2130 tga
6402372133PRTporcine 37Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu
Cys Leu Leu Pro Leu 1 5 10 15 Gly Phe Ser Ala Ile Arg Arg Tyr Tyr
Leu Gly Ala Val Glu Leu Ser 20 25 30 Trp Asp Tyr Arg Gln Ser Glu
Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45 Arg Phe Pro Ala Thr
Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60 Leu Tyr Lys
Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80 Val
Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90
95 Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala
100 105 110 Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp
Lys Ser 115 120 125 Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln
Arg Glu Lys Glu 130 135 140 Asp Asp Lys Val Leu Pro Gly Lys Ser Gln
Thr Tyr Val Trp Gln Val 145 150 155 160 Leu Lys Glu Asn Gly Pro Thr
Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175 Ser Tyr Leu Ser His
Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190 Ile Gly Ala
Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205 Thr
Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215
220 Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met
225 230 235 240 Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr
Val Asn Gly 245 250 255 Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly
Cys His Lys Lys Ser 260 265 270 Val Tyr Trp His Val Ile Gly Met Gly
Thr Ser Pro Glu Val His Ser 275 280 285 Ile Phe Leu Glu Gly His Thr
Phe Leu Val Arg His His Arg Gln Ala 290 295 300 Ser Leu Glu Ile Ser
Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu 305 310 315 320 Met Asp
Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335
His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340
345 350 Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp
Asn 355 360 365 Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly
Asp Asp Val 370 375 380 Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys
Lys His Pro Lys Thr 385 390 395 400 Trp Val His Tyr Ile Ser Ala Glu
Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415 Ala Val Pro Ser Pro Ser
Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430 Ser Gly Pro Gln
Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445 Ala Tyr
Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460
Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu 465
470 475 480 Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile
Tyr Pro 485 490 495 His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly
Arg Leu Leu Lys 500 505 510 Gly Trp Lys His Leu Lys Asp Met Pro Ile
Leu Pro Gly Glu Thr Phe 515 520 525 Lys Tyr Lys Trp Thr Val Thr Val
Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540 Pro Arg Cys Leu Thr Arg
Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys 545 550 555 560 Asp Leu Ala
Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575 Ser
Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585
590 Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu
595 600 605 Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro
Gln Asp 610 615 620 Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile
Asn Gly Tyr Val 625 630 635 640 Phe Asp Ser Leu Gln Leu Ser Val Cys
Leu His Glu Val Ala Tyr Trp 645 650 655 Tyr Ile Leu Ser Val Gly Ala
Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670 Ser Gly Tyr Thr Phe
Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685 Leu Phe Pro
Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700 Gly
Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly 705 710
715 720 Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly
Asp 725 730 735 Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu
Leu Ser Gly 740 745 750 Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln
Asn Ser Arg Pro Pro 755 760 765 Ser Ala Ser Gln Lys Gln Phe Gln Thr
Ile Thr Ser Pro Glu Asp Asp 770 775 780 Val Glu Leu Asp Pro Gln Ser
Gly Glu Arg Thr Gln Ala Leu Glu Glu 785 790 795 800 Leu Ser Val Pro
Ser Gly Asp Gly Ser Met Leu Leu Gly Gln Asn Pro 805 810 815 Ala Pro
His Gly Ser Ser Ser Ser Asp Leu Gln Glu Ala Arg Asn Glu 820 825 830
Ala Asp Asp Tyr Leu Pro Gly Ala Arg Glu Arg Asn Thr Ala Pro Ser 835
840 845 Ala Ala Ala Arg Leu Arg Pro Glu Leu His His Ser Ala Glu Arg
Val 850 855 860 Leu Thr Pro Glu Pro Glu Lys Glu Leu Lys Lys Leu Asp
Ser Lys Met 865 870 875 880 Ser Ser Ser Ser Asp Leu Leu Lys Thr Ser
Pro Thr Ile Pro Ser Asp 885 890 895 Thr Leu Ser Ala Glu Thr Glu Arg
Thr His Ser Leu Gly Pro Pro His 900 905 910 Pro Gln Val Asn Phe Arg
Ser Gln Leu Gly Ala Ile Val Leu Gly Lys 915 920 925 Asn Ser Ser His
Phe Ile Gly Ala Gly Val Pro Leu Gly Ser Thr Glu 930 935 940 Glu Asp
His Glu Ser Ser Leu Gly Glu Asn Val Ser Pro Val Glu Ser 945 950 955
960 Asp Gly Ile Phe Glu Lys Glu Arg Ala His Gly Pro Ala Ser Leu Thr
965 970 975 Lys Asp Asp Val Leu Phe Lys Val Asn Ile Ser Leu Val Lys
Thr Asn 980 985 990 Lys Ala Arg Val Tyr Leu Lys Thr Asn Arg Lys Ile
His Ile Asp Asp 995 1000 1005 Ala Ala Leu Leu Thr Glu Asn Arg Ala
Ser Ala Thr Phe Met Asp 1010 1015 1020 Lys Asn Thr Thr Ala Ser Gly
Leu Asn His Val Ser Asn Trp Ile 1025 1030 1035 Lys Gly Pro Leu Gly
Lys Asn Pro Leu Ser Ser Glu Arg Gly Pro 1040 1045 1050 Ser Pro Glu
Leu Leu Thr Ser Ser Gly Ser Gly Lys Ser Val Lys 1055 1060 1065 Gly
Gln Ser Ser Gly Gln Gly Arg Ile Arg Val Ala Val Glu Glu 1070 1075
1080 Glu Glu Leu Ser Lys Gly Lys Glu Met Met Leu Pro Asn Ser Glu
1085 1090 1095 Leu Thr Phe Leu Thr Asn Ser Ala Asp Val Gln Gly Asn
Asp Thr 1100 1105 1110 His Ser Gln Gly Lys Lys Ser Arg Glu Glu Met
Glu Arg Arg Glu 1115 1120 1125 Lys Leu Val Gln Glu Lys Val Asp Leu
Pro Gln Val Tyr Thr Ala 1130 1135 1140 Thr Gly Thr Lys Asn Phe Leu
Arg Asn Ile Phe His Gln Ser Thr 1145 1150 1155 Glu Pro Ser Val Glu
Gly Phe Asp Gly Gly Ser His Ala Pro Val 1160 1165 1170 Pro Gln Asp
Ser Arg Ser Leu Asn Asp Ser Ala Glu Arg Ala Glu 1175 1180 1185 Thr
His Ile Ala His Phe Ser Ala Ile Arg Glu Glu Ala Pro Leu 1190 1195
1200 Glu Ala Pro Gly Asn Arg Thr Gly Pro Gly Pro Arg Ser Ala Val
1205 1210 1215 Pro Arg Arg Val Lys Gln Ser Leu Lys Gln Ile Arg Leu
Pro Leu 1220 1225 1230 Glu Glu Ile Lys Pro Glu Arg Gly Val Val Leu
Asn Ala Thr Ser 1235 1240 1245 Thr Arg Trp Ser Glu Ser Ser Pro Ile
Leu Gln Gly Ala Lys Arg 1250 1255 1260 Asn Asn Leu Ser Leu Pro Phe
Leu Thr Leu Glu Met Ala Gly Gly 1265 1270 1275 Gln Gly Lys Ile Ser
Ala Leu Gly Lys Ser Ala Ala Gly Pro Leu 1280 1285 1290 Ala Ser Gly
Lys Leu Glu Lys Ala Val Leu Ser Ser Ala Gly Leu 1295 1300 1305 Ser
Glu Ala Ser Gly Lys Ala Glu Phe Leu Pro Lys Val Arg Val 1310 1315
1320 His Arg Glu Asp Leu Leu Pro Gln Lys Thr Ser Asn Val Ser Cys
1325 1330 1335 Ala His Gly Asp Leu Gly Gln Glu Ile Phe Leu Gln Lys
Thr Arg 1340 1345 1350 Gly Pro Val Asn Leu Asn Lys Val Asn Arg Pro
Gly Arg Thr Pro 1355 1360 1365 Ser Lys Leu Leu Gly Pro Pro Met Pro
Lys Glu Trp Glu Ser Leu 1370 1375 1380 Glu Lys Ser Pro Lys Ser Thr
Ala Leu Arg Thr Lys Asp Ile Ile 1385 1390 1395 Ser Leu Pro Leu Asp
Arg His Glu Ser Asn His Ser Ile Ala Ala 1400 1405 1410 Lys Asn Glu
Gly Gln Ala Glu Thr Gln Arg Glu Ala Ala Trp Thr 1415 1420 1425 Lys
Gln Gly Gly Pro Gly Arg Leu Cys Ala Pro Lys Pro Pro Val 1430 1435
1440 Leu Arg Arg His Gln Arg Asp Ile Ser Leu Pro Thr Phe Gln Pro
1445 1450 1455 Glu Glu Asp Lys Met Asp Tyr Asp Asp Ile Phe Ser Thr
Glu Thr 1460 1465 1470 Lys Gly Glu Asp Phe Asp Ile Tyr Gly Glu Asp
Glu Asn Gln Asp 1475 1480 1485 Pro Arg Ser Phe Gln Lys Arg Thr Arg
His Tyr Phe Ile Ala Ala 1490 1495 1500 Val Glu Gln Leu Trp Asp Tyr
Gly Met Ser Glu Ser Pro Arg Ala 1505 1510 1515 Leu Arg Asn Arg Ala
Gln Asn Gly Glu Val Pro Arg Phe Lys Lys 1520 1525 1530 Val Val Phe
Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln Pro Ser 1535
1540 1545 Tyr Arg Gly Glu Leu Asn Lys His Leu Gly Leu Leu Gly Pro
Tyr 1550 1555 1560 Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr
Phe Lys Asn 1565 1570 1575 Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser
Ser Leu Ile Ser Tyr 1580 1585 1590 Pro Asp Asp Gln Glu Gln Gly Ala
Glu Pro Arg His Asn Phe Val 1595 1600 1605 Gln Pro Asn Glu Thr Arg
Thr Tyr Phe Trp Lys Val Gln His His 1610 1615 1620 Met Ala Pro Thr
Glu Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr 1625 1630 1635 Phe Ser
Asp Val Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile 1640 1645 1650
Gly Pro Leu Leu Ile Cys Arg Ala Asn Thr Leu Asn Ala Ala His 1655
1660 1665 Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe Phe Thr
Ile 1670 1675 1680 Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn
Val Glu Arg 1685 1690 1695 Asn Cys Arg Ala Pro Cys His Leu Gln Met
Glu Asp Pro Thr Leu 1700 1705 1710 Lys Glu Asn Tyr Arg Phe His Ala
Ile Asn Gly Tyr Val Met Asp 1715 1720 1725 Thr Leu Pro Gly Leu Val
Met Ala Gln Asn Gln Arg Ile Arg Trp 1730 1735 1740 Tyr Leu Leu Ser
Met Gly Ser Asn Glu Asn Ile His Ser Ile His 1745 1750 1755 Phe Ser
Gly His Val Phe Ser Val Arg Lys Lys Glu Glu Tyr Lys 1760 1765 1770
Met Ala Val Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr Val Glu 1775
1780 1785 Met Leu Pro Ser Lys Val Gly Ile Trp Arg Ile Glu Cys Leu
Ile 1790 1795 1800 Gly Glu His Leu Gln Ala Gly Met Ser Thr Thr Phe
Leu Val Tyr 1805 1810 1815 Ser Lys Glu Cys Gln Ala Pro Leu Gly Met
Ala Ser Gly Arg Ile 1820 1825 1830 Arg Asp Phe Gln Ile Thr Ala Ser
Gly Gln Tyr Gly Gln Trp Ala 1835 1840 1845 Pro Lys Leu Ala Arg Leu
His Tyr Ser Gly Ser Ile Asn Ala Trp 1850 1855 1860 Ser Thr Lys Asp
Pro His Ser Trp Ile Lys Val Asp Leu Leu Ala 1865 1870 1875 Pro Met
Ile Ile His Gly Ile Met Thr Gln Gly Ala Arg Gln Lys 1880 1885 1890
Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu 1895
1900 1905 Asp Gly Arg Asn Trp Gln Ser Tyr Arg Gly Asn Ser Thr Gly
Thr 1910 1915 1920 Leu Met Val Phe Phe Gly Asn Val Asp Ala Ser Gly
Ile Lys His 1925 1930 1935 Asn Ile Phe Asn Pro Pro Ile Val Ala Arg
Tyr Ile Arg Leu His 1940 1945 1950 Pro Thr His Tyr Ser Ile Arg Ser
Thr Leu Arg Met Glu Leu Met 1955 1960 1965 Gly Cys Asp Leu Asn Ser
Cys Ser Met Pro Leu Gly Met Gln Asn 1970 1975 1980 Lys Ala Ile Ser
Asp Ser Gln Ile Thr Ala Ser Ser His Leu Ser 1985 1990 1995 Asn Ile
Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg Leu His Leu 2000 2005 2010
Gln Gly Arg Thr Asn Ala Trp Arg Pro Arg Val Ser Ser Ala Glu 2015
2020 2025 Glu Trp Leu Gln Val Asp Leu Gln Lys Thr Val Lys Val Thr
Gly 2030 2035 2040 Ile Thr Thr Gln Gly Val Lys Ser Leu Leu Ser Ser
Met Tyr Val 2045 2050 2055 Lys Glu Phe Leu Val Ser Ser Ser Gln Asp
Gly Arg Arg Trp Thr 2060 2065 2070 Leu Phe Leu Gln Asp Gly His Thr
Lys Val Phe Gln Gly Asn Gln 2075 2080 2085 Asp Ser Ser Thr Pro Val
Val Asn Ala Leu Asp Pro Pro Leu Phe 2090 2095 2100 Thr Arg Tyr Leu
Arg Ile His Pro Thr Ser Trp Ala Gln His Ile 2105 2110 2115 Ala Leu
Arg Leu Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 2120 2125 2130
384334DNAArtificialSynthetic construct sequence encoding Factor
VIII lacking B domain. 38ga atg cag cta gag ctc tcc acc tgt gtc ttt
ctg tgt ctc ttg cca 47 Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu
Cys Leu Leu Pro 1 5 10 15 ctc ggc ttt agt gcc atc agg aga tac tac
ctg ggc gca gtg gaa ctg 95Leu Gly Phe Ser Ala Ile Arg Arg Tyr Tyr
Leu Gly Ala Val Glu Leu 20 25 30 tcc tgg gac tac cgg caa agt gaa
ctc ctc cgt gag ctg cac gtg gac 143Ser Trp Asp Tyr Arg Gln Ser Glu
Leu Leu Arg Glu Leu His Val Asp 35 40 45 acc aga ttt cct gct aca
gcg cca gga gct ctt ccg ttg ggc ccg tca 191Thr Arg Phe Pro Ala Thr
Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser 50 55 60 gtc ctg tac aaa
aag act gtg ttc gta gag ttc acg gat caa ctt ttc 239Val Leu Tyr Lys
Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe 65 70 75 agc gtt
gcc agg ccc agg cca cca tgg atg ggt ctg ctg ggt cct acc 287Ser Val
Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr 80 85 90 95
atc cag gct gag gtt tac gac acg gtg gtc gtt acc ctg aag aac atg
335Ile Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met
100 105 110 gct tct cat ccc gtt agt ctt cac gct gtc ggc gtc tcc ttc
tgg aaa 383Ala Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe
Trp Lys 115 120 125 tct tcc gaa ggc gct gaa tat gag gat cac acc agc
caa agg gag aag 431Ser Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser
Gln Arg Glu Lys 130 135 140 gaa gac gat aaa gtc ctt ccc ggt aaa agc
caa acc tac gtc tgg cag 479Glu Asp Asp Lys Val Leu Pro Gly Lys Ser
Gln Thr Tyr Val Trp Gln 145 150 155 gtc ctg aaa gaa aat ggt cca aca
gcc tct gac cca cca tgt ctc acc 527Val Leu Lys Glu Asn Gly Pro Thr
Ala Ser Asp Pro Pro Cys Leu Thr 160 165 170 175 tac tca tac ctg tct
cac gtg gac ctg gtg aaa gac ctg aat tcg ggc 575Tyr Ser Tyr Leu Ser
His Val Asp Leu Val Lys Asp Leu Asn Ser Gly 180 185 190 ctc att gga
gcc ctg ctg gtt tgt aga gaa ggg agt ctg acc aga gaa 623Leu Ile Gly
Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu 195 200 205 agg
acc cag aac ctg cac gaa ttt gta cta ctt ttt gct gtc ttt gat 671Arg
Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp 210 215
220 gaa ggg aaa agt tgg cac tca gca aga aat gac tcc tgg aca cgg gcc
719Glu Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala
225 230 235 atg gat ccc gca cct gcc agg gcc cag cct gca atg cac aca
gtc aat 767Met Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr
Val Asn 240 245 250 255 ggc tat gtc aac agg tct ctg cca ggt ctg atc
gga tgt cat aag aaa 815Gly Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile
Gly Cys His Lys Lys 260 265 270 tca gtc tac tgg cac gtg att gga atg
ggc acc agc ccg gaa gtg cac 863Ser Val Tyr Trp His Val Ile Gly Met
Gly Thr Ser Pro Glu Val His 275 280 285 tcc att ttt ctt gaa ggc cac
acg ttt ctc gtg agg cac cat cgc cag 911Ser Ile Phe Leu Glu Gly His
Thr Phe Leu Val Arg His His Arg Gln 290 295 300 gct tcc ttg gag atc
tcg cca cta act ttc ctc act gct cag aca ttc 959Ala Ser Leu Glu Ile
Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe 305 310 315 ctg atg gac
ctt ggc cag ttc cta ctg ttt tgt cat atc tct tcc cac 1007Leu Met Asp
Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His 320 325 330 335
cac cat ggt ggc atg gag gct cac gtc aga gta gaa agc tgc gcc gag
1055His His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu
340 345 350 gag ccc cag ctg cgg agg aaa gct gat gaa gag gaa gat tat
gat gac 1103Glu Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr
Asp Asp 355 360 365 aat ttg tac gac tcg gac atg gac gtg gtc cgg ctc
gat ggt gac gac 1151Asn Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu
Asp Gly Asp Asp 370 375 380 gtg tct ccc ttt atc caa atc cgc tcg gtt
gcc aag aag cat ccc aaa 1199Val Ser Pro Phe Ile Gln Ile Arg Ser Val
Ala Lys Lys His Pro Lys 385 390 395 acc tgg gtg cac tac atc tct gca
gag gag gag gac tgg gac tac gcc 1247Thr Trp Val His Tyr Ile Ser Ala
Glu Glu Glu Asp Trp Asp Tyr Ala 400 405 410 415 ccc gcg gtc ccc agc
ccc agt gac aga agt tat aaa agt ctc tac ttg 1295Pro Ala Val Pro Ser
Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu 420 425 430 aac agt ggt
cct cag cga att ggt agg aaa tac aaa aaa gct cga ttc 1343Asn Ser Gly
Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe 435 440 445 gtc
gct tac acg gat gta aca ttt aag act cgt aaa gct att ccg tat 1391Val
Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr 450 455
460 gaa tca gga atc ctg gga cct tta ctt tat gga gaa gtt gga gac aca
1439Glu Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr
465 470 475 ctt ttg att ata ttt aag aat aaa gcg agc cga cca tat aac
atc tac 1487Leu Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn
Ile Tyr 480 485 490 495 cct cat gga atc act gat gtc agc gct ttg cac
cca ggg aga ctt cta 1535Pro His Gly Ile Thr Asp Val Ser Ala Leu His
Pro Gly Arg Leu Leu 500 505 510 aaa ggt tgg aaa cat ttg aaa gac atg
cca att ctg cca gga gag act 1583Lys Gly Trp Lys His Leu Lys Asp Met
Pro Ile Leu Pro Gly Glu Thr 515 520 525 ttc aag tat aaa tgg aca gtg
act gtg gaa gat ggg cca acc aag tcc 1631Phe Lys Tyr Lys Trp Thr Val
Thr Val Glu Asp Gly Pro Thr Lys Ser 530 535 540 gat cct cgg tgc ctg
acc cgc tac tac tcg agc tcc att aat cta gag 1679Asp Pro Arg Cys Leu
Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu 545 550 555 aaa gat ctg
gct tcg gga ctc att ggc cct ctc ctc atc tgc tac aaa 1727Lys Asp Leu
Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys 560 565 570 575
gaa tct gta gac caa aga gga aac cag atg atg tca gac aag aga aac
1775Glu Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn
580 585 590 gtc atc ctg ttt tct gta ttc gat gag aat caa agc tgg tac
ctc gca 1823Val Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr
Leu Ala 595 600 605 gag aat att cag cgc ttc ctc ccc aat ccg gat gga
tta cag ccc cag 1871Glu Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly
Leu Gln Pro Gln 610 615 620 gat cca gag ttc caa gct tct aac atc atg
cac agc atc aat ggc tat 1919Asp Pro Glu Phe Gln Ala Ser Asn Ile Met
His Ser Ile Asn Gly Tyr 625 630 635 gtt ttt gat agc ttg cag ctg tcg
gtt tgt ttg cac gag gtg gca tac 1967Val Phe Asp Ser Leu Gln Leu Ser
Val Cys Leu His Glu Val Ala Tyr 640 645 650 655 tgg tac att cta agt
gtt gga gca cag acg gac ttc ctc tcc gtc ttc 2015Trp Tyr Ile Leu Ser
Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe 660 665 670 ttc tct ggc
tac acc ttc aaa cac aaa atg gtc tat gaa gac aca ctc 2063Phe Ser Gly
Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu 675 680 685 acc
ctg ttc ccc ttc tca gga gaa acg gtc ttc atg tca atg gaa aac 2111Thr
Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn 690 695
700 cca ggt ctc tgg gtc cta ggg tgc cac aac tca gac ttg cgg aac aga
2159Pro Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg
705 710 715 ggg atg aca gcc tta ctg aag gtg tat agt tgt gac agg gac
att ggt 2207Gly Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp
Ile Gly 720 725 730 735 gat tat tat gac aac act tat gaa gat att cca
ggc ttc ttg ctg agt 2255Asp Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro
Gly Phe Leu Leu Ser 740 745 750 gga aag aat gtc att gaa ccc aga gac
ata agc ctt cct act ttt cag 2303Gly Lys Asn Val Ile Glu Pro Arg Asp
Ile Ser Leu Pro Thr Phe Gln 755 760 765 ccg gag gaa gac aaa atg gac
tat gat gat atc ttc tca act gaa acg 2351Pro Glu Glu Asp Lys Met Asp
Tyr Asp Asp Ile Phe Ser Thr Glu Thr 770 775 780 aag gga gaa gat ttt
gac att tac ggt gag gat gaa aat cag gac cct 2399Lys Gly Glu Asp Phe
Asp Ile Tyr Gly Glu Asp Glu Asn Gln Asp Pro 785 790 795 cgc agc ttt
cag aag aga acc cga cac tat ttc att gct gcg gtg gag 2447Arg Ser Phe
Gln Lys Arg Thr Arg His Tyr Phe Ile Ala Ala Val Glu 800 805 810 815
cag ctc tgg gat tac ggg atg agc gaa tcc ccc cgg gcg cta aga aac
2495Gln Leu Trp Asp Tyr Gly Met Ser Glu Ser Pro Arg Ala Leu Arg Asn
820 825 830 agg gct cag aac gga gag gtg cct cgg ttc aag aag gtg gtc
ttc cgg 2543Arg Ala Gln Asn Gly Glu Val Pro Arg Phe Lys Lys Val Val
Phe Arg 835 840 845 gaa ttt gct gac ggc tcc ttc acg cag ccg tcg tac
cgc ggg gaa ctc 2591Glu Phe Ala Asp Gly Ser Phe Thr Gln Pro Ser Tyr
Arg Gly Glu Leu 850 855 860 aac aaa cac ttg ggg ctc ttg gga ccc tac
atc aga gcg gaa gtt gaa 2639Asn Lys His Leu Gly Leu Leu Gly Pro Tyr
Ile Arg Ala Glu Val Glu 865 870 875 gac aac atc atg gta act ttc aaa
aac cag gcg tct cgt ccc tat tcc 2687Asp Asn Ile Met Val Thr Phe Lys
Asn Gln Ala Ser Arg Pro Tyr Ser 880 885 890 895 ttc tac tcg agc ctt
att tct tat ccg gat gat cag gag caa ggg gca 2735Phe Tyr Ser Ser Leu
Ile Ser Tyr Pro Asp Asp Gln Glu Gln Gly Ala 900 905 910 gaa cct cga
cac aac ttc gtc cag cca aat gaa acc aga act tac ttt 2783Glu Pro Arg
His Asn Phe Val Gln Pro Asn Glu Thr Arg Thr Tyr Phe 915 920 925 tgg
aaa gtg cag cat cac atg gca ccc aca gaa gac gag ttt gac tgc 2831Trp
Lys Val Gln His His Met Ala Pro Thr Glu Asp Glu Phe Asp Cys 930 935
940 aaa gcc tgg gcc tac ttt tct gat gtt gac ctg gaa aaa gat gtg cac
2879Lys Ala Trp Ala Tyr Phe Ser Asp Val Asp Leu Glu Lys Asp Val His
945 950 955 tca ggc ttg atc ggc ccc ctt ctg atc tgc cgc gcc aac acc
ctg aac 2927Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Arg Ala Asn Thr
Leu Asn 960 965 970 975
gct gct cac ggt aga caa gtg acc gtg caa gaa ttt gct ctg ttt ttc
2975Ala Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe Phe
980 985 990 act att ttt gat gag aca aag agc tgg tac ttc act gaa aat
gtg gaa 3023Thr Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn
Val Glu 995 1000 1005 agg aac tgc cgg gcc ccc tgc cac ctg cag atg
gag gac ccc act 3068Arg Asn Cys Arg Ala Pro Cys His Leu Gln Met Glu
Asp Pro Thr 1010 1015 1020 ctg aaa gaa aac tat cgc ttc cat gca atc
aat ggc tat gtg atg 3113Leu Lys Glu Asn Tyr Arg Phe His Ala Ile Asn
Gly Tyr Val Met 1025 1030 1035 gat aca ctc cct ggc tta gta atg gct
cag aat caa agg atc cga 3158Asp Thr Leu Pro Gly Leu Val Met Ala Gln
Asn Gln Arg Ile Arg 1040 1045 1050 tgg tat ctg ctc agc atg ggc agc
aat gaa aat atc cat tcg att 3203Trp Tyr Leu Leu Ser Met Gly Ser Asn
Glu Asn Ile His Ser Ile 1055 1060 1065 cat ttt agc gga cac gtg ttc
agt gta cgg aaa aag gag gag tat 3248His Phe Ser Gly His Val Phe Ser
Val Arg Lys Lys Glu Glu Tyr 1070 1075 1080 aaa atg gcc gtg tac aat
ctc tat ccg ggt gtc ttt gag aca gtg 3293Lys Met Ala Val Tyr Asn Leu
Tyr Pro Gly Val Phe Glu Thr Val 1085 1090 1095 gaa atg cta ccg tcc
aaa gtt gga att tgg cga ata gaa tgc ctg 3338Glu Met Leu Pro Ser Lys
Val Gly Ile Trp Arg Ile Glu Cys Leu 1100 1105 1110 att ggc gag cac
ctg caa gct ggg atg agc acg act ttc ctg gtg 3383Ile Gly Glu His Leu
Gln Ala Gly Met Ser Thr Thr Phe Leu Val 1115 1120 1125 tac agc aag
gag tgt cag gct cca ctg gga atg gct tct gga cgc 3428Tyr Ser Lys Glu
Cys Gln Ala Pro Leu Gly Met Ala Ser Gly Arg 1130 1135 1140 att aga
gat ttt cag atc aca gct tca gga cag tat gga cag tgg 3473Ile Arg Asp
Phe Gln Ile Thr Ala Ser Gly Gln Tyr Gly Gln Trp 1145 1150 1155 gcc
cca aag ctg gcc aga ctt cat tat tcc gga tca atc aat gcc 3518Ala Pro
Lys Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala 1160 1165 1170
tgg agc acc aag gat ccc cac tcc tgg atc aag gtg gat ctg ttg 3563Trp
Ser Thr Lys Asp Pro His Ser Trp Ile Lys Val Asp Leu Leu 1175 1180
1185 gca cca atg atc att cac ggc atc atg acc cag ggt gcc cgt cag
3608Ala Pro Met Ile Ile His Gly Ile Met Thr Gln Gly Ala Arg Gln
1190 1195 1200 aag ttt tcc agc ctc tac atc tcc cag ttt atc atc atg
tac agt 3653Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr
Ser 1205 1210 1215 ctt gac ggg agg aac tgg cag agt tac cga ggg aat
tcc acg ggc 3698Leu Asp Gly Arg Asn Trp Gln Ser Tyr Arg Gly Asn Ser
Thr Gly 1220 1225 1230 acc tta atg gtc ttc ttt ggc aat gtg gac gca
tct ggg att aaa 3743Thr Leu Met Val Phe Phe Gly Asn Val Asp Ala Ser
Gly Ile Lys 1235 1240 1245 cac aat att ttt aac cct ccg att gtg gct
cgg tac atc cgt ttg 3788His Asn Ile Phe Asn Pro Pro Ile Val Ala Arg
Tyr Ile Arg Leu 1250 1255 1260 cac cca aca cat tac agc atc cgc agc
act ctt cgc atg gag ttg 3833His Pro Thr His Tyr Ser Ile Arg Ser Thr
Leu Arg Met Glu Leu 1265 1270 1275 atg ggc tgt gat tta aac agt tgc
agc atg ccc ctg gga atg cag 3878Met Gly Cys Asp Leu Asn Ser Cys Ser
Met Pro Leu Gly Met Gln 1280 1285 1290 aat aaa gcg ata tca gac tca
cag atc acg gcc tcc tcc cac cta 3923Asn Lys Ala Ile Ser Asp Ser Gln
Ile Thr Ala Ser Ser His Leu 1295 1300 1305 agc aat ata ttt gcc acc
tgg tct cct tca caa gcc cga ctt cac 3968Ser Asn Ile Phe Ala Thr Trp
Ser Pro Ser Gln Ala Arg Leu His 1310 1315 1320 ctc cag ggg cgg acg
aat gcc tgg cga ccc cgg gtg agc agc gca 4013Leu Gln Gly Arg Thr Asn
Ala Trp Arg Pro Arg Val Ser Ser Ala 1325 1330 1335 gag gag tgg ctg
cag gtg gac ctg cag aag acg gtg aag gtc aca 4058Glu Glu Trp Leu Gln
Val Asp Leu Gln Lys Thr Val Lys Val Thr 1340 1345 1350 ggc atc acc
acc cag ggc gtg aag tcc ctg ctc agc agc atg tat 4103Gly Ile Thr Thr
Gln Gly Val Lys Ser Leu Leu Ser Ser Met Tyr 1355 1360 1365 gtg aag
gag ttc ctc gtg tcc agt agt cag gac ggc cgc cgc tgg 4148Val Lys Glu
Phe Leu Val Ser Ser Ser Gln Asp Gly Arg Arg Trp 1370 1375 1380 acc
ctg ttt ctt cag gac ggc cac acg aag gtt ttt cag ggc aat 4193Thr Leu
Phe Leu Gln Asp Gly His Thr Lys Val Phe Gln Gly Asn 1385 1390 1395
cag gac tcc tcc acc ccc gtg gtg aac gct ctg gac ccc ccg ctg 4238Gln
Asp Ser Ser Thr Pro Val Val Asn Ala Leu Asp Pro Pro Leu 1400 1405
1410 ttc acg cgc tac ctg agg atc cac ccc acg agc tgg gcg cag cac
4283Phe Thr Arg Tyr Leu Arg Ile His Pro Thr Ser Trp Ala Gln His
1415 1420 1425 atc gcc ctg agg ctc gag gtt cta gga tgt gag gca cag
gat ctc 4328Ile Ala Leu Arg Leu Glu Val Leu Gly Cys Glu Ala Gln Asp
Leu 1430 1435 1440 tac tga 4334Tyr 391443PRTArtificialSynthetic
Construct 39Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu
Pro Leu 1 5 10 15 Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala
Val Glu Leu Ser 20 25 30 Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg
Glu Leu His Val Asp Thr 35 40 45 Arg Phe Pro Ala Thr Ala Pro Gly
Ala Leu Pro Leu Gly Pro Ser Val 50 55 60 Leu Tyr Lys Lys Thr Val
Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80 Val Ala Arg Pro
Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95 Gln Ala
Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 100 105 110
Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 115
120 125 Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys
Glu 130 135 140 Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val
Trp Gln Val 145 150 155 160 Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp
Pro Pro Cys Leu Thr Tyr 165 170 175 Ser Tyr Leu Ser His Val Asp Leu
Val Lys Asp Leu Asn Ser Gly Leu 180 185 190 Ile Gly Ala Leu Leu Val
Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205 Thr Gln Asn Leu
His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220 Gly Lys
Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met 225 230 235
240 Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly
245 250 255 Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys
Lys Ser 260 265 270 Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro
Glu Val His Ser 275 280 285 Ile Phe Leu Glu Gly His Thr Phe Leu Val
Arg His His Arg Gln Ala 290 295 300 Ser Leu Glu Ile Ser Pro Leu Thr
Phe Leu Thr Ala Gln Thr Phe Leu 305 310 315 320 Met Asp Leu Gly Gln
Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335 His Gly Gly
Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340 345 350 Pro
Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 355 360
365 Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val
370 375 380 Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro
Lys Thr 385 390 395 400 Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp
Trp Asp Tyr Ala Pro 405 410 415 Ala Val Pro Ser Pro Ser Asp Arg Ser
Tyr Lys Ser Leu Tyr Leu Asn 420 425 430 Ser Gly Pro Gln Arg Ile Gly
Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445 Ala Tyr Thr Asp Val
Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460 Ser Gly Ile
Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu 465 470 475 480
Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485
490 495 His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu Leu
Lys 500 505 510 Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro Gly
Glu Thr Phe 515 520 525 Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly
Pro Thr Lys Ser Asp 530 535 540 Pro Arg Cys Leu Thr Arg Tyr Tyr Ser
Ser Ser Ile Asn Leu Glu Lys 545 550 555 560 Asp Leu Ala Ser Gly Leu
Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575 Ser Val Asp Gln
Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590 Ile Leu
Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 595 600 605
Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp 610
615 620 Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr
Val 625 630 635 640 Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu
Val Ala Tyr Trp 645 650 655 Tyr Ile Leu Ser Val Gly Ala Gln Thr Asp
Phe Leu Ser Val Phe Phe 660 665 670 Ser Gly Tyr Thr Phe Lys His Lys
Met Val Tyr Glu Asp Thr Leu Thr 675 680 685 Leu Phe Pro Phe Ser Gly
Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700 Gly Leu Trp Val
Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly 705 710 715 720 Met
Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp 725 730
735 Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu Ser Gly
740 745 750 Lys Asn Val Ile Glu Pro Arg Asp Ile Ser Leu Pro Thr Phe
Gln Pro 755 760 765 Glu Glu Asp Lys Met Asp Tyr Asp Asp Ile Phe Ser
Thr Glu Thr Lys 770 775 780 Gly Glu Asp Phe Asp Ile Tyr Gly Glu Asp
Glu Asn Gln Asp Pro Arg 785 790 795 800 Ser Phe Gln Lys Arg Thr Arg
His Tyr Phe Ile Ala Ala Val Glu Gln 805 810 815 Leu Trp Asp Tyr Gly
Met Ser Glu Ser Pro Arg Ala Leu Arg Asn Arg 820 825 830 Ala Gln Asn
Gly Glu Val Pro Arg Phe Lys Lys Val Val Phe Arg Glu 835 840 845 Phe
Ala Asp Gly Ser Phe Thr Gln Pro Ser Tyr Arg Gly Glu Leu Asn 850 855
860 Lys His Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp
865 870 875 880 Asn Ile Met Val Thr Phe Lys Asn Gln Ala Ser Arg Pro
Tyr Ser Phe 885 890 895 Tyr Ser Ser Leu Ile Ser Tyr Pro Asp Asp Gln
Glu Gln Gly Ala Glu 900 905 910 Pro Arg His Asn Phe Val Gln Pro Asn
Glu Thr Arg Thr Tyr Phe Trp 915 920 925 Lys Val Gln His His Met Ala
Pro Thr Glu Asp Glu Phe Asp Cys Lys 930 935 940 Ala Trp Ala Tyr Phe
Ser Asp Val Asp Leu Glu Lys Asp Val His Ser 945 950 955 960 Gly Leu
Ile Gly Pro Leu Leu Ile Cys Arg Ala Asn Thr Leu Asn Ala 965 970 975
Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe Phe Thr 980
985 990 Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn Val Glu
Arg 995 1000 1005 Asn Cys Arg Ala Pro Cys His Leu Gln Met Glu Asp
Pro Thr Leu 1010 1015 1020 Lys Glu Asn Tyr Arg Phe His Ala Ile Asn
Gly Tyr Val Met Asp 1025 1030 1035 Thr Leu Pro Gly Leu Val Met Ala
Gln Asn Gln Arg Ile Arg Trp 1040 1045 1050 Tyr Leu Leu Ser Met Gly
Ser Asn Glu Asn Ile His Ser Ile His 1055 1060 1065 Phe Ser Gly His
Val Phe Ser Val Arg Lys Lys Glu Glu Tyr Lys 1070 1075 1080 Met Ala
Val Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr Val Glu 1085 1090 1095
Met Leu Pro Ser Lys Val Gly Ile Trp Arg Ile Glu Cys Leu Ile 1100
1105 1110 Gly Glu His Leu Gln Ala Gly Met Ser Thr Thr Phe Leu Val
Tyr 1115 1120 1125 Ser Lys Glu Cys Gln Ala Pro Leu Gly Met Ala Ser
Gly Arg Ile 1130 1135 1140 Arg Asp Phe Gln Ile Thr Ala Ser Gly Gln
Tyr Gly Gln Trp Ala 1145 1150 1155 Pro Lys Leu Ala Arg Leu His Tyr
Ser Gly Ser Ile Asn Ala Trp 1160 1165 1170 Ser Thr Lys Asp Pro His
Ser Trp Ile Lys Val Asp Leu Leu Ala 1175 1180 1185 Pro Met Ile Ile
His Gly Ile Met Thr Gln Gly Ala Arg Gln Lys 1190 1195 1200 Phe Ser
Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu 1205 1210 1215
Asp Gly Arg Asn Trp Gln Ser Tyr Arg Gly Asn Ser Thr Gly Thr 1220
1225 1230 Leu Met Val Phe Phe Gly Asn Val Asp Ala Ser Gly Ile Lys
His 1235 1240 1245 Asn Ile Phe Asn Pro Pro Ile Val Ala Arg Tyr Ile
Arg Leu His 1250 1255 1260 Pro Thr His Tyr Ser Ile Arg Ser Thr Leu
Arg Met Glu Leu Met 1265 1270 1275 Gly Cys Asp Leu Asn Ser Cys Ser
Met Pro Leu Gly Met Gln Asn 1280 1285 1290 Lys Ala Ile Ser Asp Ser
Gln Ile Thr Ala Ser Ser His Leu Ser 1295 1300 1305 Asn Ile Phe Ala
Thr Trp Ser Pro Ser Gln Ala Arg Leu His Leu 1310 1315 1320 Gln Gly
Arg Thr Asn Ala Trp Arg Pro Arg Val Ser Ser Ala Glu 1325 1330 1335
Glu Trp Leu Gln Val Asp Leu Gln Lys Thr Val Lys Val Thr Gly 1340
1345 1350 Ile Thr Thr Gln Gly Val Lys Ser Leu Leu Ser Ser Met Tyr
Val 1355 1360 1365 Lys Glu Phe Leu Val Ser Ser Ser Gln Asp Gly Arg
Arg Trp Thr 1370 1375 1380 Leu Phe Leu Gln Asp Gly His Thr Lys Val
Phe Gln Gly Asn Gln 1385 1390 1395 Asp Ser Ser Thr Pro Val Val Asn
Ala Leu Asp Pro Pro Leu Phe 1400
1405 1410 Thr Arg Tyr Leu Arg Ile His Pro Thr Ser Trp Ala Gln His
Ile 1415 1420 1425 Ala Leu Arg Leu Glu Val Leu Gly Cys Glu Ala Gln
Asp Leu Tyr 1430 1435 1440 4019PRTHomo sapiens 40Met Gln Ile Glu
Leu Ser Thr Cys Phe Phe Leu Cys Leu Leu Arg Phe 1 5 10 15 Cys Phe
Ser 4124PRTArtificialSynthetic peptide linker in POL 1212. 41Ser
Phe Ala Gln Asn Ser Arg Pro Pro Ser Ala Ser Ala Pro Lys Pro 1 5 10
15 Pro Val Leu Arg Arg His Gln Arg 20 42105DNAArtificialSynthetic
construct oligonucleotide encoding linker sequence 42gtc att gaa
cct agg agc ttt gcc cag aat tca aga ccc cct agt gcg 48Val Ile Glu
Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro Ser Ala 1 5 10 15 agc
gct cca aag cct ccg gtc ctg cga cgg cat cag agg gac ata agc 96Ser
Ala Pro Lys Pro Pro Val Leu Arg Arg His Gln Arg Asp Ile Ser 20 25
30 ctt cct act 105Leu Pro Thr 35 4335PRTArtificialSynthetic
Construct 43Val Ile Glu Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro
Ser Ala 1 5 10 15 Ser Ala Pro Lys Pro Pro Val Leu Arg Arg His Gln
Arg Asp Ile Ser 20 25 30 Leu Pro Thr 35 4421DNAArtificialSynthetic
construct oligonucleotide useful as a primer. 44gaggaaaacc
agatgatgtc a 214560DNAArtificialSynthetic construct oligonucleotide
useful as a primer. 45ctttggagcg ctcgcactag ggggtcttga attctgggca
aagctcctag gttcaatgac 604624DNAArtificialSynthetic construct
oligonucleotide useful as a pirmer. 46ggtcacttgt ctaccgtgag cagc
244766DNAArtificialSynthetic construct sequence encoding linker in
POL 1212 protein. 47cctagtgcga gcgctccaaa gcctccggtc ctgcgacggc
atcagaggga cataagcctt 60cctact 66484404DNAArtificialSynthetic
construct coding sequence for POL 1212 Factor VIII derivative.
48atg cag cta gag ctc tcc acc tgt gtc ttt ctg tgt ctc ttg cca ctc
48Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu Pro Leu
-15 -10 -5 ggc ttt agt gcc atc agg aga tac tac ctg ggc gca gtg gaa
ctg tcc 96Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu
Leu Ser -1 1 5 10 tgg gac tac cgg caa agt gaa ctc ctc cgt gag ctg
cac gtg gac acc 144Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu
His Val Asp Thr 15 20 25 aga ttt cct gct aca gcg cca gga gct ctt
ccg ttg ggc ccg tca gtc 192Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu
Pro Leu Gly Pro Ser Val 30 35 40 45 ctg tac aaa aag act gtg ttc gta
gag ttc acg gat caa ctt ttc agc 240Leu Tyr Lys Lys Thr Val Phe Val
Glu Phe Thr Asp Gln Leu Phe Ser 50 55 60 gtt gcc agg ccc agg cca
cca tgg atg ggt ctg ctg ggt cct acc atc 288Val Ala Arg Pro Arg Pro
Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 65 70 75 cag gct gag gtt
tac gac acg gtg gtc gtt acc ctg aag aac atg gct 336Gln Ala Glu Val
Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 80 85 90 tct cat
ccc gtt agt ctt cac gct gtc ggc gtc tcc ttc tgg aaa tct 384Ser His
Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 95 100 105
tcc gaa ggc gct gaa tat gag gat cac acc agc caa agg gag aag gaa
432Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys Glu
110 115 120 125 gac gat aaa gtc ctt ccc ggt aaa agc caa acc tac gtc
tgg cag gtc 480Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val
Trp Gln Val 130 135 140 ctg aaa gaa aat ggt cca aca gcc tct gac cca
cca tgt ctt acc tac 528Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro
Pro Cys Leu Thr Tyr 145 150 155 tca tac ctg tct cac gtg gac ctg gtg
aaa gac ctg aat tcg ggc ctc 576Ser Tyr Leu Ser His Val Asp Leu Val
Lys Asp Leu Asn Ser Gly Leu 160 165 170 att gga gcc ctg ctg gtt tgt
aga gaa ggg agt ctg acc aga gaa agg 624Ile Gly Ala Leu Leu Val Cys
Arg Glu Gly Ser Leu Thr Arg Glu Arg 175 180 185 acc cag aac ctg cac
gaa ttt gta cta ctt ttt gct gtc ttt gat gaa 672Thr Gln Asn Leu His
Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 190 195 200 205 ggg aaa
agt tgg cac tca gca aga aat gac tcc tgg aca cgg gcc atg 720Gly Lys
Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met 210 215 220
gat ccc gca cct gcc agg gcc cag cct gca atg cac aca gtc aat ggc
768Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly
225 230 235 tat gtc aac agg tct ctg cca ggt ctg atc gga tgt cat aag
aaa tca 816Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys
Lys Ser 240 245 250 gtc tac tgg cac gtg att gga atg ggc acc agc ccg
gaa gtg cac tcc 864Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro
Glu Val His Ser 255 260 265 att ttt ctt gaa ggc cac acg ttt ctc gtg
agg cac cat cgc cag gct 912Ile Phe Leu Glu Gly His Thr Phe Leu Val
Arg His His Arg Gln Ala 270 275 280 285 tcc ttg gag atc tcg cca cta
act ttc ctc act gct cag aca ttc ctg 960Ser Leu Glu Ile Ser Pro Leu
Thr Phe Leu Thr Ala Gln Thr Phe Leu 290 295 300 atg gac ctt ggc cag
ttc cta ctg ttt tgt cat atc tct tcc cac cac 1008Met Asp Leu Gly Gln
Phe Leu Leu Phe Cys His Ile Ser Ser His His 305 310 315 cat ggt ggc
atg gag gct cac gtc aga gta gaa agc tgc gcc gag gag 1056His Gly Gly
Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 320 325 330 ccc
cag ctg cgg agg aaa gct gat gaa gag gaa gat tat gat gac aat 1104Pro
Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 335 340
345 ttg tac gac tcg gac atg gac gtg gtc cgg ctc gat ggt gac gac gtg
1152Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val
350 355 360 365 tct ccc ttt atc caa atc cgc tcg gtt gcc aag aag cat
ccc aaa acc 1200Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His
Pro Lys Thr 370 375 380 tgg gtg cac tac atc tct gca gag gag gag gac
tgg gac tac gcc ccc 1248Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp
Trp Asp Tyr Ala Pro 385 390 395 gcg gtc ccc agc ccc agt gac aga agt
tat aaa agt ctc tac ttg aac 1296Ala Val Pro Ser Pro Ser Asp Arg Ser
Tyr Lys Ser Leu Tyr Leu Asn 400 405 410 agt ggt cct cag cga att ggt
agg aaa tac aaa aaa gct cga ttc gtc 1344Ser Gly Pro Gln Arg Ile Gly
Arg Lys Tyr Lys Lys Ala Arg Phe Val 415 420 425 gct tac acg gat gta
aca ttt aag act cgt aaa gct att ccg tat gaa 1392Ala Tyr Thr Asp Val
Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 430 435 440 445 tca gga
atc ctg gga cct tta ctt tat gga gaa gtt gga gac aca ctt 1440Ser Gly
Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu 450 455 460
ttg att ata ttt aag aat aaa gcg agc cga cca tat aac atc tac cct
1488Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro
465 470 475 cat gga atc act gat gtc agc gct ttg cac cca ggg aga ctt
cta aaa 1536His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu
Leu Lys 480 485 490 ggt tgg aaa cat ttg aaa gac atg cca att ctg cca
gga gag act ttc 1584Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro
Gly Glu Thr Phe 495 500 505 aag tat aaa tgg aca gtg act gtg gaa gat
ggg cca acc aag tcc gat 1632Lys Tyr Lys Trp Thr Val Thr Val Glu Asp
Gly Pro Thr Lys Ser Asp 510 515 520 525 cct cgg tgc ctg acc cgc tac
tac tcg agc tcc att aat cta gag aaa 1680Pro Arg Cys Leu Thr Arg Tyr
Tyr Ser Ser Ser Ile Asn Leu Glu Lys 530 535 540 gat ctg gct tcg gga
ctc att ggc cct ctc ctc atc tgc tac aaa gaa 1728Asp Leu Ala Ser Gly
Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 545 550 555 tct gta gac
caa aga gga aac cag atg atg tca gac aag aga aac gtc 1776Ser Val Asp
Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 560 565 570 atc
ctg ttt tct gta ttc gat gag aat caa agc tgg tac ctc gca gag 1824Ile
Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 575 580
585 aat att cag cgc ttc ctc ccc aat ccg gat gga tta cag ccc cag gat
1872Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp
590 595 600 605 cca gag ttc caa gct tct aac atc atg cac agc atc aat
ggc tat gtt 1920Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn
Gly Tyr Val 610 615 620 ttt gat agc ttg cag ctg tcg gtt tgt ttg cac
gag gtg gca tac tgg 1968Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His
Glu Val Ala Tyr Trp 625 630 635 tac att cta agt gtt gga gca cag acg
gac ttc ctc tcc gtc ttc ttc 2016Tyr Ile Leu Ser Val Gly Ala Gln Thr
Asp Phe Leu Ser Val Phe Phe 640 645 650 tct ggc tac acc ttc aaa cac
aaa atg gtc tat gaa gac aca ctc acc 2064Ser Gly Tyr Thr Phe Lys His
Lys Met Val Tyr Glu Asp Thr Leu Thr 655 660 665 ctg ttc ccc ttc tca
gga gaa acg gtc ttc atg tca atg gaa aac cca 2112Leu Phe Pro Phe Ser
Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 670 675 680 685 ggt ctc
tgg gtc ctt ggg tgc cac aac tca gac ttg cgg aac aga ggg 2160Gly Leu
Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly 690 695 700
atg aca gcc tta ctg aag gtg tat agt tgt gac agg gac att ggt gat
2208Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp
705 710 715 tat tat gac aac act tat gaa gat att cca ggc ttc ttg ctg
agt gga 2256Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu
Ser Gly 720 725 730 aag aat gtc att gaa cct agg agc ttt gcc cag aat
tca aga ccc cct 2304Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln Asn
Ser Arg Pro Pro 735 740 745 agt gcg agc gct cca aag cct ccg gtc ctg
cga cgg cat cag agg gac 2352Ser Ala Ser Ala Pro Lys Pro Pro Val Leu
Arg Arg His Gln Arg Asp 750 755 760 765 ata agc ctt cct act ttt cag
ccg gag gaa gac aaa atg gac tat gat 2400Ile Ser Leu Pro Thr Phe Gln
Pro Glu Glu Asp Lys Met Asp Tyr Asp 770 775 780 gat atc ttc tca act
gaa acg aag gga gaa gat ttt gac att tac ggt 2448Asp Ile Phe Ser Thr
Glu Thr Lys Gly Glu Asp Phe Asp Ile Tyr Gly 785 790 795 gag gat gaa
aat cag gac cct cgc agc ttt cag aag aga acc cga cac 2496Glu Asp Glu
Asn Gln Asp Pro Arg Ser Phe Gln Lys Arg Thr Arg His 800 805 810 tat
ttc att gct gcg gtg gag cag ctc tgg gat tac ggg atg agc gaa 2544Tyr
Phe Ile Ala Ala Val Glu Gln Leu Trp Asp Tyr Gly Met Ser Glu 815 820
825 tcc ccc cgg gcg cta aga aac agg gct cag aac gga gag gtg cct cgg
2592Ser Pro Arg Ala Leu Arg Asn Arg Ala Gln Asn Gly Glu Val Pro Arg
830 835 840 845 ttc aag aag gtg gtc ttc cgg gaa ttt gct gac ggc tcc
ttc acg cag 2640Phe Lys Lys Val Val Phe Arg Glu Phe Ala Asp Gly Ser
Phe Thr Gln 850 855 860 ccg tcg tac cgc ggg gaa ctc aac aaa cac ttg
ggg ctc ttg gga ccc 2688Pro Ser Tyr Arg Gly Glu Leu Asn Lys His Leu
Gly Leu Leu Gly Pro 865 870 875 tac atc aga gcg gaa gtt gaa gac aac
atc atg gta act ttc aaa aac 2736Tyr Ile Arg Ala Glu Val Glu Asp Asn
Ile Met Val Thr Phe Lys Asn 880 885 890 cag gcg tct cgt ccc tat tcc
ttc tac tcg agc ctt att tct tat ccg 2784Gln Ala Ser Arg Pro Tyr Ser
Phe Tyr Ser Ser Leu Ile Ser Tyr Pro 895 900 905 gat gat cag gag caa
ggg gca gaa cct cga cac aac ttc gtc cag cca 2832Asp Asp Gln Glu Gln
Gly Ala Glu Pro Arg His Asn Phe Val Gln Pro 910 915 920 925 aat gaa
acc aga act tac ttt tgg aaa gtg cag cat cac atg gca ccc 2880Asn Glu
Thr Arg Thr Tyr Phe Trp Lys Val Gln His His Met Ala Pro 930 935 940
aca gaa gac gag ttt gac tgc aaa gcc tgg gcc tac ttt tct gat gtt
2928Thr Glu Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr Phe Ser Asp Val
945 950 955 gac ctg gaa aaa gat gtg cac tca ggc ttg atc ggc ccc ctt
ctg atc 2976Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile Gly Pro Leu
Leu Ile 960 965 970 tgc cgc gcc aac acc ctg aac gct gct cac ggt aga
caa gtg acc gtg 3024Cys Arg Ala Asn Thr Leu Asn Ala Ala His Gly Arg
Gln Val Thr Val 975 980 985 caa gaa ttt gct ctg ttt ttc act att ttt
gat gag aca aag agc tgg 3072Gln Glu Phe Ala Leu Phe Phe Thr Ile Phe
Asp Glu Thr Lys Ser Trp 990 995 1000 1005 tac ttc act gaa aat gtg
gaa agg aac tgc cgg gcc ccc tgc cat 3117Tyr Phe Thr Glu Asn Val Glu
Arg Asn Cys Arg Ala Pro Cys His 1010 1015 1020 ctg cag atg gag gac
ccc act ctg aaa gaa aac tat cgc ttc cat 3162Leu Gln Met Glu Asp Pro
Thr Leu Lys Glu Asn Tyr Arg Phe His 1025 1030 1035 gca atc aat ggc
tat gtg atg gat aca ctc cct ggc tta gta atg 3207Ala Ile Asn Gly Tyr
Val Met Asp Thr Leu Pro Gly Leu Val Met 1040 1045 1050 gct cag aat
caa agg atc cga tgg tat ctg ctc agc atg ggc agc 3252Ala Gln Asn Gln
Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Ser 1055 1060 1065 aat gaa
aat atc cat tcg att cat ttt agc gga cac gtg ttc agt 3297Asn Glu Asn
Ile His Ser Ile His Phe Ser Gly His Val Phe Ser 1070 1075 1080 gta
cgg aaa aag gag gag tat aaa atg gcc gtg tac aat ctc tat 3342Val Arg
Lys Lys Glu Glu Tyr Lys Met Ala Val Tyr Asn Leu Tyr 1085 1090 1095
ccg ggt gtc ttt gag aca gtg gaa atg cta ccg tcc aaa gtt gga 3387Pro
Gly Val Phe Glu Thr Val Glu Met Leu Pro Ser Lys Val Gly 1100 1105
1110 att tgg cga ata gaa tgc ctg att ggc gag cac ctg caa gct ggg
3432Ile Trp Arg Ile Glu Cys Leu Ile Gly Glu His Leu Gln Ala Gly
1115 1120 1125
atg agc acg act ttc ctg gtg tac agc aag gag tgt cag gct cca 3477Met
Ser Thr Thr Phe Leu Val Tyr Ser Lys Glu Cys Gln Ala Pro 1130 1135
1140 ctg gga atg gct tct gga cgc att aga gat ttt cag atc aca gct
3522Leu Gly Met Ala Ser Gly Arg Ile Arg Asp Phe Gln Ile Thr Ala
1145 1150 1155 tca gga cag tat gga cag tgg gcc cca aag ctg gcc aga
ctt cat 3567Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu
His 1160 1165 1170 tat tcc gga tca atc aat gcc tgg agc acc aag gat
ccc cac tcc 3612Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr Lys Asp Pro
His Ser 1175 1180 1185 tgg atc aag gtg gat ctg ttg gca cca atg atc
att cac ggc atc 3657Trp Ile Lys Val Asp Leu Leu Ala Pro Met Ile Ile
His Gly Ile 1190 1195 1200 atg acc cag ggt gcc cgt cag aag ttt tcc
agc ctc tac atc tcc 3702Met Thr Gln Gly Ala Arg Gln Lys Phe Ser Ser
Leu Tyr Ile Ser 1205 1210 1215 cag ttt atc atc atg tac agt ctt gac
ggg agg aac tgg cag agt 3747Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly
Arg Asn Trp Gln Ser 1220 1225 1230 tac cga ggg aat tcc acg ggc acc
tta atg gtc ttc ttt ggc aat 3792Tyr Arg Gly Asn Ser Thr Gly Thr Leu
Met Val Phe Phe Gly Asn 1235 1240 1245 gtg gac gca tct ggg att aaa
cac aat att ttt aac cct ccg att 3837Val Asp Ala Ser Gly Ile Lys His
Asn Ile Phe Asn Pro Pro Ile 1250 1255 1260 gtg gct cgg tac atc cgt
ttg cac cca aca cat tac agc atc cgc 3882Val Ala Arg Tyr Ile Arg Leu
His Pro Thr His Tyr Ser Ile Arg 1265 1270 1275 agc act ctt cgc atg
gag ttg atg ggc tgt gat tta aac agt tgc 3927Ser Thr Leu Arg Met Glu
Leu Met Gly Cys Asp Leu Asn Ser Cys 1280 1285 1290 agc atg ccc ctg
gga atg cag aat aaa gcg ata tca gac tca cag 3972Ser Met Pro Leu Gly
Met Gln Asn Lys Ala Ile Ser Asp Ser Gln 1295 1300 1305 atc acg gcc
tcc tcc cac cta agc aat ata ttt gcc acc tgg tct 4017Ile Thr Ala Ser
Ser His Leu Ser Asn Ile Phe Ala Thr Trp Ser 1310 1315 1320 cct tca
caa gcc cga ctt cac ctc cag ggg cgg acg aat gcc tgg 4062Pro Ser Gln
Ala Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp 1325 1330 1335 cga
ccc cgg gtg agc agc gca gag gag tgg ctg cag gtg gac ctg 4107Arg Pro
Arg Val Ser Ser Ala Glu Glu Trp Leu Gln Val Asp Leu 1340 1345 1350
cag aag acg gtg aag gtc aca ggc atc acc acc cag ggc gtg aag 4152Gln
Lys Thr Val Lys Val Thr Gly Ile Thr Thr Gln Gly Val Lys 1355 1360
1365 tcc ctg ctc agc agc atg tat gtg aag gag ttc ctc gtg tcc agt
4197Ser Leu Leu Ser Ser Met Tyr Val Lys Glu Phe Leu Val Ser Ser
1370 1375 1380 agt cag gac ggc cgc cgc tgg acc ctg ttt ctt cag gac
ggc cac 4242Ser Gln Asp Gly Arg Arg Trp Thr Leu Phe Leu Gln Asp Gly
His 1385 1390 1395 acg aag gtt ttt cag ggc aat cag gac tcc tcc acc
ccc gtg gtg 4287Thr Lys Val Phe Gln Gly Asn Gln Asp Ser Ser Thr Pro
Val Val 1400 1405 1410 aac gct ctg gac ccc ccg ctg ttc acg cgc tac
ctg agg atc cac 4332Asn Ala Leu Asp Pro Pro Leu Phe Thr Arg Tyr Leu
Arg Ile His 1415 1420 1425 ccc acg agc tgg gcg cag cac atc gcc ctg
agg ctc gag gtt cta 4377Pro Thr Ser Trp Ala Gln His Ile Ala Leu Arg
Leu Glu Val Leu 1430 1435 1440 gga tgt gag gca cag gat ctc tac tga
4404Gly Cys Glu Ala Gln Asp Leu Tyr 1445
491467PRTArtificialSynthetic Construct 49Met Gln Leu Glu Leu Ser
Thr Cys Val Phe Leu Cys Leu Leu Pro Leu -15 -10 -5 Gly Phe Ser Ala
Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser -1 1 5 10 Trp Asp
Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 15 20 25
Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 30
35 40 45 Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu
Phe Ser 50 55 60 Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu
Gly Pro Thr Ile 65 70 75 Gln Ala Glu Val Tyr Asp Thr Val Val Val
Thr Leu Lys Asn Met Ala 80 85 90 Ser His Pro Val Ser Leu His Ala
Val Gly Val Ser Phe Trp Lys Ser 95 100 105 Ser Glu Gly Ala Glu Tyr
Glu Asp His Thr Ser Gln Arg Glu Lys Glu 110 115 120 125 Asp Asp Lys
Val Leu Pro Gly Lys Ser Gln Thr Tyr Val Trp Gln Val 130 135 140 Leu
Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 145 150
155 Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu
160 165 170 Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg
Glu Arg 175 180 185 Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala
Val Phe Asp Glu 190 195 200 205 Gly Lys Ser Trp His Ser Ala Arg Asn
Asp Ser Trp Thr Arg Ala Met 210 215 220 Asp Pro Ala Pro Ala Arg Ala
Gln Pro Ala Met His Thr Val Asn Gly 225 230 235 Tyr Val Asn Arg Ser
Leu Pro Gly Leu Ile Gly Cys His Lys Lys Ser 240 245 250 Val Tyr Trp
His Val Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 255 260 265 Ile
Phe Leu Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 270 275
280 285 Ser Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe
Leu 290 295 300 Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser
Ser His His 305 310 315 His Gly Gly Met Glu Ala His Val Arg Val Glu
Ser Cys Ala Glu Glu 320 325 330 Pro Gln Leu Arg Arg Lys Ala Asp Glu
Glu Glu Asp Tyr Asp Asp Asn 335 340 345 Leu Tyr Asp Ser Asp Met Asp
Val Val Arg Leu Asp Gly Asp Asp Val 350 355 360 365 Ser Pro Phe Ile
Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr 370 375 380 Trp Val
His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 385 390 395
Ala Val Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 400
405 410 Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe
Val 415 420 425 Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile
Pro Tyr Glu 430 435 440 445 Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly
Glu Val Gly Asp Thr Leu 450 455 460 Leu Ile Ile Phe Lys Asn Lys Ala
Ser Arg Pro Tyr Asn Ile Tyr Pro 465 470 475 His Gly Ile Thr Asp Val
Ser Ala Leu His Pro Gly Arg Leu Leu Lys 480 485 490 Gly Trp Lys His
Leu Lys Asp Met Pro Ile Leu Pro Gly Glu Thr Phe 495 500 505 Lys Tyr
Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 510 515 520
525 Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys
530 535 540 Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr
Lys Glu 545 550 555 Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp
Lys Arg Asn Val 560 565 570 Ile Leu Phe Ser Val Phe Asp Glu Asn Gln
Ser Trp Tyr Leu Ala Glu 575 580 585 Asn Ile Gln Arg Phe Leu Pro Asn
Pro Asp Gly Leu Gln Pro Gln Asp 590 595 600 605 Pro Glu Phe Gln Ala
Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val 610 615 620 Phe Asp Ser
Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 625 630 635 Tyr
Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 640 645
650 Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr
655 660 665 Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu
Asn Pro 670 675 680 685 Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp
Leu Arg Asn Arg Gly 690 695 700 Met Thr Ala Leu Leu Lys Val Tyr Ser
Cys Asp Arg Asp Ile Gly Asp 705 710 715 Tyr Tyr Asp Asn Thr Tyr Glu
Asp Ile Pro Gly Phe Leu Leu Ser Gly 720 725 730 Lys Asn Val Ile Glu
Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro 735 740 745 Ser Ala Ser
Ala Pro Lys Pro Pro Val Leu Arg Arg His Gln Arg Asp 750 755 760 765
Ile Ser Leu Pro Thr Phe Gln Pro Glu Glu Asp Lys Met Asp Tyr Asp 770
775 780 Asp Ile Phe Ser Thr Glu Thr Lys Gly Glu Asp Phe Asp Ile Tyr
Gly 785 790 795 Glu Asp Glu Asn Gln Asp Pro Arg Ser Phe Gln Lys Arg
Thr Arg His 800 805 810 Tyr Phe Ile Ala Ala Val Glu Gln Leu Trp Asp
Tyr Gly Met Ser Glu 815 820 825 Ser Pro Arg Ala Leu Arg Asn Arg Ala
Gln Asn Gly Glu Val Pro Arg 830 835 840 845 Phe Lys Lys Val Val Phe
Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln 850 855 860 Pro Ser Tyr Arg
Gly Glu Leu Asn Lys His Leu Gly Leu Leu Gly Pro 865 870 875 Tyr Ile
Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe Lys Asn 880 885 890
Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu Ile Ser Tyr Pro 895
900 905 Asp Asp Gln Glu Gln Gly Ala Glu Pro Arg His Asn Phe Val Gln
Pro 910 915 920 925 Asn Glu Thr Arg Thr Tyr Phe Trp Lys Val Gln His
His Met Ala Pro 930 935 940 Thr Glu Asp Glu Phe Asp Cys Lys Ala Trp
Ala Tyr Phe Ser Asp Val 945 950 955 Asp Leu Glu Lys Asp Val His Ser
Gly Leu Ile Gly Pro Leu Leu Ile 960 965 970 Cys Arg Ala Asn Thr Leu
Asn Ala Ala His Gly Arg Gln Val Thr Val 975 980 985 Gln Glu Phe Ala
Leu Phe Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp 990 995 1000 1005
Tyr Phe Thr Glu Asn Val Glu Arg Asn Cys Arg Ala Pro Cys His 1010
1015 1020 Leu Gln Met Glu Asp Pro Thr Leu Lys Glu Asn Tyr Arg Phe
His 1025 1030 1035 Ala Ile Asn Gly Tyr Val Met Asp Thr Leu Pro Gly
Leu Val Met 1040 1045 1050 Ala Gln Asn Gln Arg Ile Arg Trp Tyr Leu
Leu Ser Met Gly Ser 1055 1060 1065 Asn Glu Asn Ile His Ser Ile His
Phe Ser Gly His Val Phe Ser 1070 1075 1080 Val Arg Lys Lys Glu Glu
Tyr Lys Met Ala Val Tyr Asn Leu Tyr 1085 1090 1095 Pro Gly Val Phe
Glu Thr Val Glu Met Leu Pro Ser Lys Val Gly 1100 1105 1110 Ile Trp
Arg Ile Glu Cys Leu Ile Gly Glu His Leu Gln Ala Gly 1115 1120 1125
Met Ser Thr Thr Phe Leu Val Tyr Ser Lys Glu Cys Gln Ala Pro 1130
1135 1140 Leu Gly Met Ala Ser Gly Arg Ile Arg Asp Phe Gln Ile Thr
Ala 1145 1150 1155 Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala
Arg Leu His 1160 1165 1170 Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr
Lys Asp Pro His Ser 1175 1180 1185 Trp Ile Lys Val Asp Leu Leu Ala
Pro Met Ile Ile His Gly Ile 1190 1195 1200 Met Thr Gln Gly Ala Arg
Gln Lys Phe Ser Ser Leu Tyr Ile Ser 1205 1210 1215 Gln Phe Ile Ile
Met Tyr Ser Leu Asp Gly Arg Asn Trp Gln Ser 1220 1225 1230 Tyr Arg
Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly Asn 1235 1240 1245
Val Asp Ala Ser Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile 1250
1255 1260 Val Ala Arg Tyr Ile Arg Leu His Pro Thr His Tyr Ser Ile
Arg 1265 1270 1275 Ser Thr Leu Arg Met Glu Leu Met Gly Cys Asp Leu
Asn Ser Cys 1280 1285 1290 Ser Met Pro Leu Gly Met Gln Asn Lys Ala
Ile Ser Asp Ser Gln 1295 1300 1305 Ile Thr Ala Ser Ser His Leu Ser
Asn Ile Phe Ala Thr Trp Ser 1310 1315 1320 Pro Ser Gln Ala Arg Leu
His Leu Gln Gly Arg Thr Asn Ala Trp 1325 1330 1335 Arg Pro Arg Val
Ser Ser Ala Glu Glu Trp Leu Gln Val Asp Leu 1340 1345 1350 Gln Lys
Thr Val Lys Val Thr Gly Ile Thr Thr Gln Gly Val Lys 1355 1360 1365
Ser Leu Leu Ser Ser Met Tyr Val Lys Glu Phe Leu Val Ser Ser 1370
1375 1380 Ser Gln Asp Gly Arg Arg Trp Thr Leu Phe Leu Gln Asp Gly
His 1385 1390 1395 Thr Lys Val Phe Gln Gly Asn Gln Asp Ser Ser Thr
Pro Val Val 1400 1405 1410 Asn Ala Leu Asp Pro Pro Leu Phe Thr Arg
Tyr Leu Arg Ile His 1415 1420 1425 Pro Thr Ser Trp Ala Gln His Ile
Ala Leu Arg Leu Glu Val Leu 1430 1435 1440 Gly Cys Glu Ala Gln Asp
Leu Tyr 1445
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