U.S. patent application number 13/101434 was filed with the patent office on 2011-08-25 for antibodies specific for sclerostin and methods for increasing bone mineralization.
This patent application is currently assigned to UCB Manufacturing, Inc.. Invention is credited to John Latham, Jiye Shi, David G. Winkler.
Application Number | 20110206677 13/101434 |
Document ID | / |
Family ID | 34135049 |
Filed Date | 2011-08-25 |
United States Patent
Application |
20110206677 |
Kind Code |
A1 |
Winkler; David G. ; et
al. |
August 25, 2011 |
ANTIBODIES SPECIFIC FOR SCLEROSTIN AND METHODS FOR INCREASING BONE
MINERALIZATION
Abstract
Compositions and methods relating to antibodies that
specifically bind to TGF-beta binding proteins are provided. These
methods and compositions relate to altering bone mineral density by
interfering with the interaction between a TGF-beta binding protein
sclerostin and a TGF-beta superfamily member, particularly a bone
morphogenic protein. Increasing bone mineral density has uses in
diseases and conditions in which low bone mineral density typifies
the condition, such as osteopenia, osteoporosis, and bone
fractures.
Inventors: |
Winkler; David G.;
(Arlington, MA) ; Shi; Jiye; (Rochester, NY)
; Latham; John; (Seattle, WA) |
Assignee: |
UCB Manufacturing, Inc.
Rochester
NY
|
Family ID: |
34135049 |
Appl. No.: |
13/101434 |
Filed: |
May 5, 2011 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12958195 |
Dec 1, 2010 |
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13101434 |
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12109029 |
Apr 24, 2008 |
7868134 |
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12958195 |
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10868497 |
Jun 15, 2004 |
7381409 |
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12109029 |
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60478977 |
Jun 16, 2003 |
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Current U.S.
Class: |
424/139.1 ;
435/243; 435/320.1; 435/331; 435/419; 435/69.6; 530/387.3;
530/387.9; 536/23.53 |
Current CPC
Class: |
C07K 14/475 20130101;
A61K 47/646 20170801; A61P 19/10 20180101; A61K 47/643 20170801;
C07K 16/22 20130101; G01N 33/6854 20130101; A61P 19/08 20180101;
C07K 14/51 20130101; C07K 2317/76 20130101; G01N 2333/4704
20130101; C07K 16/18 20130101; A61P 1/02 20180101 |
Class at
Publication: |
424/139.1 ;
530/387.9; 530/387.3; 536/23.53; 435/331; 435/243; 435/419;
435/320.1; 435/69.6 |
International
Class: |
A61K 39/395 20060101
A61K039/395; C07K 16/18 20060101 C07K016/18; C07H 21/00 20060101
C07H021/00; A61P 19/08 20060101 A61P019/08; C12N 5/16 20060101
C12N005/16; C12N 5/10 20060101 C12N005/10; C12N 1/00 20060101
C12N001/00; C12N 15/63 20060101 C12N015/63; C12P 21/02 20060101
C12P021/02; A61P 19/10 20060101 A61P019/10 |
Claims
1.-51. (canceled)
52. An isolated antibody, or antigen-binding fragment thereof, that
binds to a sclerostin polypeptide comprising an amino acid sequence
set forth in SEQ ID NO: 1, wherein said antibody or fragment binds
to the sequence of SEQ ID NO: 53.
53. The antibody or antigen-binding fragment of claim 52 that is
capable of increasing bone mineral content in a mammal.
54. The antibody or antigen-binding fragment of claim 52, wherein
the antibody is a monoclonal antibody.
55. The antibody or antigen-binding fragment of claim 52, wherein
the antibody is a human antibody, a humanized antibody or a
chimeric antibody.
56. The antibody or antigen-binding fragment of claim 52 that
comprises an antigen-binding fragment.
57. The antibody or antigen-binding fragment of claim 56, wherein
the antigen-binding fragment is selected from the group consisting
of F(ab')2, Fab, Fab', Fd, and Fv.
58. A hybridoma cell producing the antibody or antigen-binding
fragment of claim 52.
59. A nucleic acid comprising a nucleic acid sequence encoding the
antibody or antigen-binding fragment of claim 52.
60. An isolated host cell comprising the nucleic acid of claim
59.
61. A vector comprising the nucleic acid of claim 59.
62. An isolated host cell comprising the vector of claim 61.
63. A method of producing an antibody or antigen-binding fragment
thereof comprising the step of culturing the host cell of claim 60
and isolating the antibody produced therefrom.
64. A method of producing an antibody or antigen-binding fragment
thereof comprising the step of culturing the host cell of claim 62
and isolating the antibody produced therefrom.
65. A composition comprising the antibody or antigen-binding
fragment of claim 52 and a pharmaceutically acceptable carrier.
66. A method for increasing bone mineral content in a warm-blooded
animal, the method comprising administering to the warm-blooded
animal the antibody or antigen-binding fragment of claim 52.
67. The method of claim 66, wherein the warm-blooded animal is a
human.
68. The method of claim 67, wherein the human has a condition
selected from the group consisting of achondroplasia,
cleidrocranial dysostosise, echondromatosis, fibrous dysplasia,
Gaucher's hypophosphatemic rickets, Marfan's, multiple hereditary
exotoses, neurofibromatosis, osteogenesis inperfecta,
osteopetrosis, osteopoikilosis sclerotic lesions, fractures,
periodontal disease, pseudoarthosis and pyogenic
osteolmyelitis.
69. A method of treating bone fracture, dysplasia associated with
abnormal growth or development of bone, osteoporosis, or osteopenia
in a human wherein the method comprises administering to the human
the antibody or antigen-binding fragment of claim 52.
70. The method of claim 69, wherein the osteopenia is caused by an
anaemic state, steroids, heparin, a bone morrow disorder, scurvy,
malnutrition, calcium deficiency, idiopathic osteoporosis,
congenital osteopenia or osteoporosis, alcoholism, chronic liver
disease, senility, post menstrual state, oligomenorrhea,
amenorrhea, pregnancy, diabetes mellitus, hyperthyroidism,
Cushing's disease, acromegaly, hypogonadism, immobilization or
disuse, reflex sympathetic dystrophy syndrome, transient regional
osteoporosis or osteomalacia.
71. An isolated antibody, or antigen binding fragment thereof, that
binds to the amino acid sequence of SEQ ID NO: 53 within SEQ ID NO:
1 with an affinity K.sub.D of less than or equal to about 10.sup.-6
M.
72. The antibody or antigen-binding fragment of claim 71 that binds
to a second amino acid sequence of SEQ ID NO: 1, wherein said
second amino acid sequence is SEQ ID NO: 22 or SEQ ID NO: 33.
73. The antibody or antigen-binding fragment of claim 71 that is
capable of increasing bone mineral content in a mammal.
74. The antibody or antigen-binding fragment of claim 71, herein
the antibody is a monoclonal antibody.
75. The antibody or antigen-binding fragment of claim 71, wherein
the antibody is a human antibody, a humanized antibody or a
chimeric antibody.
76. The antibody or antigen-binding fragment of claim 71 that
comprises an antigen-binding fragment.
77. The antibody or antigen-binding fragment of claim 76, wherein
the antigen-binding fragment is selected from the group consisting
of F(ab').sub.2, Fab, Fab', Fd, and Fv.
78. A hybridoma cell producing the antibody or antigen-binding
fragment of claim 71.
79. A nucleic acid comprising a nucleic acid sequence encoding the
antibody or antigen-binding fragment of claim 71.
80. An isolated host cell comprising the nucleic acid of claim
79.
81. A vector comprising the nucleic acid of claim 79.
82. An isolated host cell comprising the vector of claim 81.
83. A method of producing an antibody comprising the step of
culturing the host cell of claim 80 and isolating the antibody
produced therefrom.
84. A method of producing an antibody comprising the step of
culturing the host cell of claim 82 and isolating the antibody
produced therefrom.
85. A composition comprising the antibody or antigen-binding
fragment of claim 71 and a pharmaceutically acceptable carrier.
86. A method for increasing bone mineral content in a warm-blooded
animal, the method comprising administering to the warm-blooded
animal the antibody or antigen-binding fragment of claim 71.
87. The method of claim 86, wherein the warm-blooded animal is a
human.
88. The method of claim 87, wherein the human has a condition
selected from the group consisting of achondroplasia,
cleidrocranial dysostosise, echondromatosis, fibrous dysplasia,
Gaucher's hypophosphatemic rickets, Marfan's, multiple hereditary
exotoses, neurofibromatosis, osteogenesis inperfecta,
osteopetrosis, osteopoikilosis sclerotic lesions, fractures,
periodontal disease, pseudoarthosis and pyogenic osteomyelitis.
89. A method of treating bone fracture, dysplasia associated with
abnormal growth or development of bone, osteoporosis, or osteopenia
in a human wherein the method comprises administering to the human
the antibody or antigen-binding fragment of claim 71.
90. The method of claim 89, wherein the osteopenia is caused by an
anaemic state, steroids, heparin, a bone morrow disorder, scurvy,
malnutrition, calcium deficiency, idiopathic osteoporosis,
congenital osteopenia or osteoporosis, alcoholism, chronic liver
disease, senility, post menstrual state, oligomenorrhea,
amenorrhea, pregnancy, diabetes mellitus, hyperthyroidism,
Cushing's disease, acromegaly, hypogonadism, immobilization or
disuse, reflex sympathetic dystrophy syndrome, transient regional
osteoporosis or osteomalacia.
Description
CROSS REFERENCE TO RELATED APPLICATION(S)
[0001] This application claims the benefit of U.S. Provisional
Application Ser. No. 60/478,977 filed Jun. 16, 2003.
TECHNICAL FIELD
[0002] The present invention relates generally to pharmaceutical
products and methods and, more specifically, to methods and
sclerostin-specific antibodies suitable for increasing the mineral
content of bone. Such compositions and methods may be used to treat
a wide variety of conditions including, for example, osteopenia,
osteoporosis, fractures, and other disorders in which low bone
mineral density is a hallmark of the disease.
BACKGROUND OF THE INVENTION
[0003] Two or three distinct phases of changes to bone mass occur
over the life of an individual (see Riggs, West J. Med. 154:63-77
(1991)). The first phase occurs in both men and women and proceeds
to attainment of a peak bone mass. This first phase is achieved
through linear growth of the endochondral growth plates and radial
growth due to a rate of periosteal apposition. The second phase
begins around age 30 for trabecular bone (flat bones such as the
vertebrae and pelvis) and about age 40 for cortical bone (e.g.,
long bones found in the limbs) and continues to old age. This phase
is characterized by slow bone loss and occurs in both men and
women. In women, a third phase of bone loss also occurs, most
likely due to postmenopausal estrogen deficiencies. During this
phase alone, women may lose an additional 10% of bone mass from the
cortical bone and 25% from the trabecular compartment (see Riggs,
supra).
[0004] Loss of bone mineral content can be caused by a wide variety
of conditions and may result in significant medical problems. For
example, osteoporosis is a debilitating disease in humans and is
characterized by marked decreases in skeletal bone mass and mineral
density, structural deterioration of bone, including degradation of
bone microarchitecture and corresponding increases in bone
fragility, and susceptibility to fracture in afflicted individuals.
Osteoporosis in humans is preceded by clinical osteopenia (bone
mineral density that is greater than one standard deviation but
less than 2.5 standard deviations below the mean value for young
adult bone), a condition found in approximately 25 million people
in the United States. Another 7-8 million patients in the United
States have been diagnosed with clinical osteoporosis (defined as
bone mineral content greater than 2.5 standard deviations below
that of mature young adult bone). Osteoporosis is one of the most
expensive diseases for the health care system, costing tens of
billions of dollars annually in the United States. In addition to
health care-related costs, long-term residential care, and lost
working days add to the financial and social costs of this disease.
Worldwide, approximately 75 million people are at risk for
osteoporosis.
[0005] The frequency of osteoporosis in the human population
increases with age. Among Caucasians, osteporosis is predominant in
women who, in the United States, comprise 80% of the osteoporosis
patient pool. The increased fragility and susceptibility to
fracture of skeletal bone in the aged is aggravated by the greater
risk of accidental falls in this population. More than 1.5 million
osteoporosis-related bone fractures are reported in the United
States each year. Fractured hips, wrists, and vertebrae are among
the most common injuries associated with osteoporosis. Hip
fractures in particular are extremely uncomfortable and expensive
for the patient, and for women, correlate with high rates of
mortality and morbidity.
[0006] Although osteoporosis has been regarded as an increase in
the risk of fracture due to decreased bone mass, none of the
presently available treatments for skeletal disorders can
substantially increase the bone density of adults. A strong
perception among many physicians is that drugs are needed that
could increase bone density in adults, particularly in the bones of
the wrist, spinal column, and hip that are at risk in osteopenia
and osteoporosis.
[0007] Current strategies for the prevention of osteoporosis may
offer some benefit to individuals but cannot ensure resolution of
the disease. These strategies include moderating physical activity
(particularly in weight-bearing activities) with the onset of
advanced age, providing adequate calcium in the diet, and avoiding
consumption of products containing alcohol or tobacco. For patients
presenting clinical osteopenia or osteoporosis, the prevalent
current therapeutic drugs and strategies are directed to reducing
further loss of bone mass by inhibiting the process of bone
absorption, a natural aspect of the bone remodeling process that
occurs constitutively.
[0008] For example, estrogen is now being prescribed to retard bone
loss. However, some controversy exists over whether patients gain
any long-term benefit and whether estrogen has any effect at all on
patients over 75 years old. Moreover, use of estrogen is believed
to increase the risk of breast and endometrial cancer. Calcitonin,
osteocalcin with vitamin K, or high doses of dietary calcium, with
or without vitamin D, have also been suggested for postmenopausal
women. High doses of calcium, however, can often have unpleasant
gastrointestinal side effects, and serum and urinary calcium levels
must be continuously monitored (e.g., Khosla and Rigss, Mayo Clin.
Proc. 70:978-982, 1995).
[0009] Other therapeutic approaches to osteoporosis include
bisphosphonates (e.g., Fosamax.TM., Actonel.TM., Bonviva.TM.,
Zometa.TM., olpadronate, neridronate, skelid, bonefos), parathyroid
hormone, calcilytics, calcimimetics (e.g., cinacalcet), statins,
anabolic steroids, lanthanum and strontium salts, and sodium
fluoride. Such therapeutics, however, are often associated with
undesirable side effects (for example, calcitonin and steroids may
cause nausea and provoke an immune reaction, bisphosphonates and
sodium fluoride may inhibit repair of fractures, even though bone
density increases modestly) that may preclude their efficacious use
(see Khosla and Rigss, supra).
[0010] No currently practiced therapeutic strategy for treating a
condition associated with excessive or insufficient bone
mineralization, such as osteoporosis or other disorders
characterized by loss of bone mineralization, involves a drug that
alters (i.e., increases or decreases in a statistically significant
manner) bone mass. In particular, no current strategy
therapeutically stimulates or enhances the growth of new bone mass.
The present invention provides compositions and methods which can
be used to increase bone mineralization, and which therefore may be
used to treat a wide variety of conditions in which an increase in
bone mass is desirable. The present invention also offers other
related advantages.
BRIEF SUMMARY OF THE INVENTION
[0011] Briefly stated, the present invention provides antibodies
that specifically bind to a TGF-beta binding protein, sclerostin
(SOST), and provides immunogens comprising SOST peptides derived
from regions of SOST that interact with a member of the TGF-beta
superfamily such as a bone morphogenic protein. In one embodiment,
the invention provides an isolated antibody, or an antigen-binding
fragment thereof, that binds specifically to a SOST polypeptide,
which comprises an amino acid sequence set forth in SEQ ID NO:1,
20, 58, 60, 62, or 68, wherein the antibody competitively inhibits
binding of the SOST polypeptide to at least one of (i) a bone
morphogenic protein (BMP) Type I Receptor binding site and (ii) a
BMP Type II Receptor binding site, wherein the BMP Type I Receptor
binding site is capable of binding to a BMP Type I Receptor
polypeptide comprising an amino acid sequence set forth in GenBank
Acc. Nos. NM.sub.--004329 (SEQ ID NO:71); D89675 (SEQ ID NO:72);
NM.sub.--001203 (SEQ ID NO:73); S75359 (SEQ ID NO:74);
NM.sub.--030849 (SEQ ID NO:75); D38082 (SEQ ID NO:76);
NP.sub.--001194 (SEQ ID NO:77); BAA19765 (SEQ ID NO:78); or
AAB33865 (SEQ ID NO:79), and wherein the BMP Type II Receptor
binding site is capable of binding to a BMP Type II Receptor
polypeptide comprising the amino acid sequence set forth in GenBank
Acc. NOs. U25110 (SEQ ID NO:80); NM.sub.--033346 (SEQ ID NO:81);
Z48923 (SEQ ID NO:83); CAA88759 (SEQ ID NO:84); or NM.sub.--001204
(SEQ ID NO:82). In a particular embodiment, the antibody, or the
antigen-binding fragment thereof, binds specifically to a
polypeptide that comprises an amino acid sequence set forth in SEQ
ID NO:2-6, 12-15, 21, 22, 25, 26, 47, 48, 49, or 50, and in other
particular embodiments, the antibody binds specifically to a
polypeptide that comprises an amino acid sequence set forth in SEQ
ID NO: 5, 6, or 14.
[0012] In one embodiment, the invention provides an isolated
antibody, or an antigen-binding fragment thereof, that is produced
by immunizing a non-human animal with a peptide of at least 20
amino acids and no more than 75 amino acids that comprises an amino
acid sequence of SEQ ID NOs:2-19, 21-28, or 47-50, wherein the
antibody binds specifically to a SOST polypeptide, which comprises
an amino acid sequence set forth in SEQ ID NOs:1, 20, 58, 60, 62,
or 68, and wherein the antibody competitively inhibits binding of
the SOST polypeptide to at least one of (i) a bone morphogenic
protein (BMP) Type I Receptor binding site and (ii) a BMP Type II
Receptor binding site, wherein the BMP Type I Receptor binding site
is capable of binding to a BMP Type I Receptor polypeptide (set
forth in any one of GenBank sequences provided herein), and wherein
the BMP Type II Receptor binding sites is capable of binding to a
BMP Type II Receptor polypeptide (set forth in any one of GenBank
sequences provided herein). In certain preferred embodiments, an
antibody is produced by immunizing a non-human animal with a
peptide of at least 20 amino acids and no more than 75 amino acids
that comprises an amino acid sequence of SEQ ID NO:5, 6, 10, 11,
14, or 18.
[0013] The present invention further provides an antibody, or an
antigen-binding fragment thereof, that binds specifically to a SOST
polypeptide and that impairs formation of a SOST homodimer, wherein
the SOST polypeptide comprises an amino acid sequence set forth in
SEQ ID NOs:1, 20, 58, 60, 62, or 68, and wherein the antibody binds
to a polypeptide that comprises an amino acid sequence of SEQ ID
NOs:29-31, 33-36, 41-43, or 51-54.
[0014] In another embodiment, the invention provides an isolated
antibody, or an antigen-binding fragment thereof, that is produced
by immunizing a non-human animal with a peptide of at least 20
amino acids and no more than 75 amino acids comprising an amino
acid sequence of SEQ ID NOs: 29-46, 51, 52, 53, or 54, wherein the
antibody, or the antigen-binding fragment thereof, binds
specifically to a SOST polypeptide that comprises an amino acid
sequence set forth in SEQ ID NO:1, 20, 58, 60, 62, or 68, and
wherein the antibody impairs formation of a SOST homodimer.
[0015] In certain particular embodiments of the invention, the
antibody is a polyclonal antibody. In other embodiments, the
antibody is a monoclonal antibody, which is a mouse, human, rat, or
hamster monoclonal antibody. The invention also provides a
hybridoma cell or a host cell that is capable of producing the
monoclonal antibody. In other embodiments of the invention, the
antibody is a humanized antibody or a chimeric antibody. The
invention further provides a host cell that produces the humanized
or chimeric antibody. In certain embodiments the antigen-binding
fragment of the antibody is a F(ab').sub.2, Fab', Fab, Fd, or Fv
fragment. The invention also provides an antibody that is a single
chain antibody and provides a host cell that is capable of
expressing the single chain antibody. In another embodiment, the
invention provides a composition comprising such antibodies and a
physiologically acceptable carrier.
[0016] The invention provides an immunogen comprising a peptide
comprising 6, 7, 8, 9, 10, 11, or 12 consecutive amino acids of a
SOST polypeptide, which SOST polypeptide comprises an amino acid
sequence set forth in SEQ ID NOs:1, 20, 58, 60, 62, or 68, and
wherein the peptide is capable of eliciting in a non-human animal
an antibody that binds specifically to the SOST polypeptide and
that competitively inhibits binding of the SOST polypeptide to at
least one of (i) a bone morphogenic protein (BMP) Type I Receptor
binding site and (ii) a BMP Type II Receptor binding site, wherein
the BMP Type I Receptor binding site is capable of binding to a BMP
Type I Receptor polypeptide, wherein the BMP Type I Receptor
binding site is capable of binding to a BMP Type I Receptor
polypeptide comprising an amino acid sequence set forth in GenBank
Acc. Nos. NM.sub.--004329 (SEQ ID NO:71); D89675 (SEQ ID NO:72);
NM.sub.--001203 (SEQ ID NO:73); S75359 (SEQ ID NO:74);
NM.sub.--030849 (SEQ ID NO:75); D38082 (SEQ ID NO:76);
NP.sub.--001194 (SEQ ID NO:77); BAA19765 (SEQ ID NO:78); or
AAB33865 (SEQ ID NO:79), and wherein the BMP Type II Receptor
binding site is capable of binding to a BMP Type II Receptor
polypeptide comprising the amino acid sequence set forth in GenBank
Acc. NOs. U25110 (SEQ ID NO:80); NM.sub.--033346 (SEQ ID NO:81);
Z48923 (SEQ ID NO:83); CAA88759 (SEQ ID NO:84); or NM.sub.--001204
(SEQ ID NO:82).
[0017] In another embodiment, an immunogen comprises a peptide
comprising at least 21 consecutive amino acids and no more than 50
consecutive amino acids of a SOST polypeptide, said SOST
polypeptide comprising an amino acid sequence set forth in SEQ ID
NOs:1, 20, 58, 60, 62, or 68, wherein the peptide is capable of
eliciting in a non-human animal an antibody that binds specifically
to the SOST polypeptide and that competitively inhibits binding of
the SOST polypeptide to at least one of (i) a bone morphogenic
protein (BMP) Type I Receptor binding site and (ii) a BMP Type II
Receptor binding site, wherein the BMP Type I Receptor binding site
is capable of binding to a BMP Type I Receptor polypeptide (set
forth in any one of GenBank sequences provided herein), and wherein
the BMP Type II Receptor binding site is capable of binding to a
BMP Type II Receptor polypeptide (set forth in any one of GenBank
sequences provided herein).
[0018] In certain embodiments the invention provides an immunogen
comprising a peptide of at least 20 amino acids and no more than 75
amino acids comprising an amino acid sequence of SEQ ID NOs: 2-19,
21-28, 47, 48, 49, or 50, wherein the peptide is capable of
eliciting in a non-human animal an antibody that binds specifically
to a SOST polypeptide, which comprises an amino acid sequence set
forth in SEQ ID NO:1, 20, 58, 60, 62, or 68, wherein the antibody
competitively inhibits binding of the SOST polypeptide to at least
one of (i) a bone morphogenic protein (BMP) Type I Receptor binding
site and (ii) a BMP Type II Receptor binding site, wherein the BMP
Type I Receptor binding site is capable of binding to a BMP Type I
Receptor polypeptide comprising an amino acid sequence set forth in
GenBank Acc. Nos. NM.sub.--004329 (SEQ ID NO:71); D89675 (SEQ ID
NO:72); NM.sub.--001203 (SEQ ID NO:73); S75359 (SEQ ID NO:74);
NM.sub.--030849 (SEQ ID NO:75); D38082 (SEQ ID NO:76);
NP.sub.--001194 (SEQ ID NO:77); BAA19765 (SEQ ID NO:78); or
AAB33865 (SEQ ID NO:79), and wherein the BMP Type II Receptor
binding site is capable of binding to a BMP Type II Receptor
polypeptide comprising the amino acid sequence set forth in GenBank
Acc. NOs. U25110 (SEQ ID NO:80); NM.sub.--033346 (SEQ ID NO:81);
Z48923 (SEQ ID NO:83); CAA88759 (SEQ ID NO:84); or NM.sub.--001204
(SEQ ID NO:82). In a particular embodiment, the invention provides
an immunogen comprising a peptide of at least 20 amino acids and no
more than 75 amino acids comprising an amino acid sequence of SEQ
ID NO:5, 6, 10, 11, 14, or 18.
[0019] The invention also provides an immunogen comprising a
peptide of at least 20 amino acids and no more than 75 amino acids
comprising an amino acid sequence of SEQ ID NOs: 29-46, 51, 52, 53,
or 54, wherein the peptide is capable of eliciting in a non-human
animal an antibody that binds specifically to a SOST polypeptide,
which comprises an amino acid sequence set forth in SEQ ID NO:1,
20, 58, 60, 62, or 68, and wherein the antibody impairs formation
of a SOST homodimer. In another embodiment, an immunogen comprises
a peptide comprising 6, 7, 8, 9, 10, 11, or 12 consecutive amino
acids of a SOST polypeptide, wherein the SOST polypeptide comprises
an amino acid sequence set forth in SEQ ID NO:1, 20, 58, 60, 62, or
68, and wherein the peptide is capable of eliciting in a non-human
animal an antibody that binds specifically to the SOST polypeptide
and that impairs formation of a SOST homodimer. In certain
embodiments, the invention provides an immunogen that comprises a
peptide comprising at least 21 consecutive amino acids and no more
than 50 consecutive amino acids of a SOST polypeptide, which
polypeptide comprises SEQ ID NO:1, 20, 58, 60, 62, or 68, and
wherein the peptide is capable of eliciting in a non-human animal
an antibody that binds specifically to the SOST polypeptide and
that impairs formation of a SOST homodimer.
[0020] In certain particular embodiments, the subject invention
immunogens are associated with a carrier molecule. In certain
embodiments, the carrier molecule is a carrier polypeptide, and in
particular embodiments, the carrier polypeptide is keyhole limpet
hemocyanin.
[0021] The present invention also provides a method for producing
an antibody that specifically binds to a SOST polypeptide,
comprising immunizing a non-human animal with an immunogen
comprising a peptide of 6, 7, 8, 9, 10, 11, or 12 consecutive amino
acids or at least 21 and no more than 50 consecutive amino acids of
a SOST polypeptide having the sequence set forth in SEQ ID NO:1,
20, 58, 60, 62, or 68, that is capable of eliciting in a non-human
animal an antibody that binds specifically to the SOST polypeptide
and that competitively inhibits binding of the SOST polypeptide to
at least one of (i) a bone morphogenic protein (BMP) Type I
Receptor binding site and (ii) a BMP Type II Receptor binding site,
wherein the BMP Type I Receptor binding site is capable of binding
to a BMP Type I Receptor polypeptide, wherein the BMP Type I
Receptor binding site is capable of binding to a BMP Type I
Receptor polypeptide comprising an amino acid sequence set forth in
GenBank Acc. Nos. NM.sub.--004329 (SEQ ID NO:71); D89675 (SEQ ID
NO:72); NM.sub.--001203 (SEQ ID NO:73); S75359 (SEQ ID NO:74);
NM.sub.--030849 (SEQ ID NO:75); D38082 (SEQ ID NO:76);
NP.sub.--001194 (SEQ ID NO:77); BAA19765 (SEQ ID NO:78); or
AAB33865 (SEQ ID NO:79), and wherein the BMP Type II Receptor
binding site is capable of binding to a BMP Type II Receptor
polypeptide comprising the amino acid sequence set forth in GenBank
Acc. NOs. U25110 (SEQ ID NO:80); NM.sub.--033346 (SEQ ID NO:81);
Z48923 (SEQ ID NO:83); CAA88759 (SEQ ID NO:84); or NM.sub.--001204
(SEQ ID NO:82). In another embodiment, the present invention
provides a method for producing an antibody that specifically binds
to a SOST polypeptide, comprising immunizing a non-human animal
with an immunogen comprising a peptide at least 20 amino acids and
no more than 75 amino acids comprising an amino acid sequence of
SEQ ID NO: 2-19, 21-28, 47, 48, 49, or 50, wherein the peptide is
capable of eliciting in a non-human animal an antibody that binds
specifically to a SOST polypeptide, which comprises an amino acid
sequence set forth in SEQ ID NO:1, 20, 58, 60, 62, or 68, wherein
the antibody competitively inhibits binding of the SOST polypeptide
to at least one of (i) a bone morphogenic protein (BMP) Type I
Receptor binding site and (ii) a BMP Type II Receptor binding site,
wherein the BMP Type I Receptor binding site is capable of binding
to a BMP Type I Receptor polypeptide. In a particular embodiment,
the immunogen comprises a peptide at least 20 amino acids and no
more than 75 amino acids comprising an amino acid sequence of SEQ
ID NO:5, 6, 10, 11, 14, or 18.
[0022] In other preferred embodiments, the invention provides a
method for producing an antibody that specifically binds to a SOST
polypeptide, comprising immunizing a non-human animal with an
immunogen comprising a peptide of 6, 7, 8, 9, 10, 11, or 12
consecutive amino acids or at least 21 and no more than 50
consecutive amino acids of a SOST polypeptide having the sequence
set forth in SEQ ID NO:1, 20, 58, 60, 62, or 68, that is capable of
eliciting in a non-human animal an antibody that binds specifically
to the SOST polypeptide and that is capable of impairing formation
of a SOST homodimer. In another embodiment, the invention provides
a method for producing an antibody that specifically binds to a
SOST polypeptide, comprising immunizing a non-human animal with an
immunogen comprising a peptide at least 20 amino acids and no more
than 75 amino acids comprising an amino acid sequence of SEQ ID NO:
29-46, 51, 52, 53, or 54, wherein the peptide is capable of
eliciting in a non-human animal an antibody that binds specifically
to a SOST polypeptide and impairs formation of a SOST
homodimer.
[0023] The present invention also provides a method for identifying
an antibody that modulates a TGF-beta signaling pathway, comprising
contacting an antibody that specifically binds to a SOST
polypeptide which comprises an amino acid sequence set forth in any
one of SEQ ID NOS: 1, 20, 58, 60, 62, or 68 with at least one SOST
peptide comprising an amino acid sequence of SEQ ID NO: 2-19, or
21-54, under conditions and for a time sufficient to permit
formation of an antibody/SOST peptide complex; and detecting a
level of antibody/SOST peptide complex, and thereby detecting the
presence of an antibody that modulates a TGF-beta signaling
pathway. In another embodiment, the invention provides a method for
identifying an antibody that impairs binding of a BMP to a SOST
polypeptide, comprising contacting (i) an antibody that
specifically binds to a SOST polypeptide which comprises an amino
acid sequence set forth in any one of SEQ ID NOS: 1, 20, 58, 60,
62, or 68 with (ii) at least one SOST peptide comprising an amino
acid sequence of SEQ ID NO: 2-19, 21-28, or 47-50 under conditions
and for a time sufficient to permit formation of an antibody/SOST
peptide complex; and detecting a level of antibody/SOST peptide
complex, and thereby detecting the presence of an antibody that
impairs binding of a BMP to a SOST polypeptide. In particular
embodiments of the method for identifying an antibody that
modulates a TGF-beta signaling pathway and for identifying an
antibody that impairs binding of a BMP to a SOST polypeptide, the
SOST peptide comprises an amino acid sequence of SEQ ID NO:5, 6,
10, 11, 14, or 18.
[0024] In another embodiment, the invention provides a method for
identifying an antibody that impairs SOST homodimer formation,
comprising contacting (i) an antibody that specifically binds to a
SOST polypeptide which comprises an amino acid sequence set forth
in any one of SEQ ID NOS: 1, 20, 58, 60, 62, or 68, with (ii) at
least one SOST peptide comprising an amino acid sequence of SEQ ID
NO: 29-46 or 51-54 under conditions and for a time sufficient to
permit formation of an antibody/SOST peptide complex; and detecting
a level of antibody/SOST peptide complex, and thereby detecting the
presence of an antibody that that impairs SOST homodimer
formation.
[0025] In another embodiment, the invention provides a method for
identifying an antibody that increases bone mineral content,
comprising contacting (i) an antibody that specifically binds to a
SOST polypeptide which comprises an amino acid sequence set forth
in any one of SEQ ID NOS: 1, 20, 58, 60, 62, or 68 with (ii) at
least one SOST peptide comprising an amino acid sequence of SEQ ID
NO: 2-19, or 21-54 under conditions and for a time sufficient to
permit formation of an antibody/SOST peptide complex; and detecting
a level of antibody/SOST peptide complex, and thereby detecting the
presence of an antibody that increases bone mineral content. In a
particular embodiment, the peptide comprises an amino acid sequence
of SEQ ID NO:5, 6, 10, 11, 14, or 18.
[0026] In certain particular embodiments for identifying an
antibody that modulates a TGF-beta signaling pathway, for
identifying an antibody that impairs binding of a BMP to a SOST
polypeptide, for identifying an antibody that impairs SOST
homodimer formation, or for identifying an antibody that increases
bone mineral content, the antibody is present in a biological
sample or the antibody is a purified antibody. In certain
embodiments the purified antibody is a polyclonal antibody, a
monoclonal antibody, a chimeric antibody, a humanized antibody, or
an antigen-binding fragment of any of these antibodies.
[0027] These and other embodiments of the present invention will
become apparent upon reference to the following detailed
description and attached drawings. All references disclosed herein
are hereby incorporated by reference in their entireties as if each
was incorporated individually.
BRIEF DESCRIPTION OF THE DRAWINGS
[0028] FIG. 1 presents an alignment of the region containing the
characteristic cystine-knot of a SOST polypeptide and its closest
homologues. Three disulphide bonds that form the cystine-knot are
illustrated as solid lines. An extra disulphide bond, shown by a
dotted line, is unique to this family, which connects two
.beta.-hairpin tips in the 3D structure. The polypeptides depicted
are SOST: sclerostin (SEQ ID NO:95); CGHB: Human Chorionic
Gonadotropin .beta. (SEQ ID NO:96); FSHB: follicle-stimulating
hormone beta subunit (SEQ ID NO:97); TSHB: thyrotropin beta chain
precursor (SEQ ID NO:98); VWF: Von Willebrand factor (SEQ ID
NO:99); MUC2: human mucin 2 precursor (SEQ ID NO:100); CER1:
Cerberus 1 (Xenopus laevis homolog) (SEQ ID NO:101); DRM: gremlin
(SEQ ID NO:102); DAN: (SEQ ID NO:103); CTGF: connective tissue
growth factor precursor (SEQ ID NO:104); NOV: NovH (nephroblastoma
overexpressed gene protein homolog) (SEQ ID NO:105); CYR6: (SEQ ID
NO:106).
[0029] FIG. 2 illustrates a 3D model of the core region of SOST
(SOST_Core).
[0030] FIG. 3 presents a 3D model of the core region of SOST
homodimer.
[0031] FIGS. 4A and B provides an amino acid sequence alignment of
Noggin from five different animals: human (NOGG_HUMAN (SEQ ID
NO:107); chicken (NOGG_CHICK, SEQ ID NO:108); African clawed frog
(NOGG_XENLA, SEQ ID NO:109); NOGG_FUGRU, SEQ ID NO:110); and
zebrafish (NOGG_ZEBRA, SEQ ID NO:111); and SOST from human
(SOST_HUMAN, SEQ ID NO:1), rat (SOST_RAT, SEQ ID NO:20), and mouse
(SOST_Mouse, SEQ ID NO:112).
[0032] FIG. 5 illustrates the Noggin/BMP-7 complex structure. The
BMP homodimer is shown on the bottom portion of the figure in
surface mode. The Noggin homodimer is shown on top of the BMP dimer
in cartoon mode. The circles outline the N-terminal binding region,
the core region, and the linker between the N-terminal and core
regions.
[0033] FIG. 6 depicts a 3D model of the potential BMP-binding
fragment located at the SOST N-terminal region. A BMP dimer is
shown in surface mode, and the potential BMP-binding fragment is
shown in stick mode. A phenylalanine residue fitting into a
hydrophobic pocket on the BMP surface is noted.
DETAILED DESCRIPTION OF THE INVENTION
[0034] The present invention provides antibodies that specifically
bind to a SOST polypeptide methods for using such antibodies. The
present invention also provides SOST polypeptide immunogens that
may be used for generation and analysis of these antibodies. The
antibodies may be useful to block or impair binding of a SOST
polypeptide, which is a TGF-beta binding protein, to a ligand,
particularly a bone morphogenic protein, and may also block or
impair binding of the SOST polypeptide to one or more other
ligands.
[0035] The invention relates in part to the surprising discovery,
within the sclerostin polypeptide sequence, of specific short
peptide sequences that are specifically recognized by
anti-sclerostin antibodies capable of competitively inhibiting
binding of sclerostin polypeptides to BMP, where such
sclerostin-BMP binding otherwise would occur via a BMP Type I
Receptor binding site and/or a BMP Type II Receptor binding site. A
molecule such as an antibody that inhibits the binding of the
TGF-beta binding protein to one or more members of the TGF-beta
family of proteins, including one or more bone morphogenic proteins
(BMPs), should be understood to include, for example, a molecule
that allows the activation of a TGF-beta family member or BMP, or
allows binding of TGF-beta family members including one or more
BMPs to their respective receptors by removing or preventing the
TGF-beta member from binding to the TGF-binding-protein.
[0036] The present invention also provides peptide and polypeptide
immunogens that, unexpectedly, may be used to generate and/or
identify antibodies or fragments thereof that are capable of
inhibiting, preventing, or impairing (e.g., decreasing in a
statistically significant manner) binding of the TGF-beta binding
protein SOST to one or more BMPs. Exemplary peptide immunogens may
comprise 6, 7, 8, 9, 10, 11, 12, 20-25, 21-50, 26-30, 31-40, 41-50,
51-60, 61-70, or 71-75 consecutive amino acids of a sclerostin
polypeptide as provided herein (or of a variant thereof), such
peptides comprising, for instance, amino acid sequences as set
forth in SEQ ID NOS:2-19, 21-53, and 54. The present invention also
provides peptide and polypeptide immunogens that may be used to
generate and/or identify antibodies or fragments thereof that are
capable of inhibiting, preventing, or impairing the formation of
SOST homodimers. The antibodies of the present invention are useful
for increasing the mineral content and mineral density of bone,
thereby ameliorating numerous conditions that result in the loss of
bone mineral content, including for example, disease, genetic
predisposition, accidents that result in the lack of use of bone
(e.g., due to fracture), therapeutics that effect bone resorption
or that kill bone forming cells, and normal aging.
Sclerosteosis
[0037] Sclerosteosis is a disease related to abnormal bone mineral
density in humans. Sclerosteosis is a term that was applied by
Hansen (Hansen, H. G., Sklerosteose in: Opitz et al., eds. Handbuch
der Kinderheilkunde, (Berlin: Springer 1967) 351-355) to a disorder
similar to van Buchem hyperostosis corticalis generalisata but
possibly differing in radiologic appearance of the bone changes and
in the presence of asymmetric cutaneous syndactyly of the index and
middle fingers in many cases. Sclerosteosis is now understood to be
an autosomal semi-dominant disorder that is characterized by widely
disseminated sclerotic lesions of the bone in the adult. The
condition is progressive. Sclerosteosis also has a developmental
aspect that is associated with syndactyly (two or more fingers
fused together). Sclerosteosis Syndrome is associated with large
stature, and many affected individuals attain a height of six feet
or more. In addition, the jaw of persons with this condition has an
unusually square appearance. The bone mineral content of
homozygotes can be 1 to 6 fold greater than normal individuals, and
bone mineral density can be 1 to 4 fold above normal values (e.g.,
in comparison to unaffected siblings).
[0038] Sclerosteosis Syndrome occurs primarily in Afrikaaners of
Dutch descent in South Africa. Approximately 1 of every 140
individuals in the Afrikaaner population is a carrier of the
mutated gene (heterozygotes). The mutation shows 100% penetrance.
Anecdotal reports indicate that increased bone mineral density has
been observed in heterozygotes but they have no associated
pathologies (e.g., syndactyly or skull overgrowth).
[0039] No abnormality of the pituitary-hypothalamus axis has been
observed in patients with sclerosteosis. In particular, no
over-production of growth hormone and cortisone occurs, and sex
hormone levels are normal in affected individuals. Bone turnover
markers (such as osteoblast specific alkaline phosphatase,
osteocalcin, type 1 procollagen C' propeptide (PICP), and total
alkaline phosphatase (see Comier, Curr. Opin. in Rheu. 7:243
(1995)) indicate that hyperosteoblastic activity is associated with
the disease but normal to slightly decreased osteoclast activity is
observed as measured by markers of bone resorption (pyridinoline,
deoxypryridinoline, N-telopeptide, urinary hydroxyproline, plasma
tartrate-resistant acid phosphatases, and galactosyl hydroxylysine
(see Comier, supra)).
[0040] Sclerosteosis is characterized by the continual deposition
of bone throughout the skeleton during the lifetime of the affected
individuals. In homozygotes the continual deposition of bone
mineral leads to an overgrowth of bone in areas of the skeleton
where mechanoreceptors are absent (e.g., skull, jaw, cranium). In
homozygotes with Sclerosteosis, the overgrowth of the bones of the
skull leads to cranial compression and eventually to death due to
excessive hydrostatic pressure on the brain stem. A generalized and
diffuse sclerosis is observed in all other parts of the skeleton.
Cortical areas of the long bones are greatly thickened resulting in
a substantial increase in bone strength. Trabecular connections are
increased in thickness, which in turn increases the strength of the
trabecular bone. Sclerotic bones appear unusually opaque to
x-rays.
[0041] The rare genetic mutation that is responsible for
Sclerosteosis Syndrome has been localized to the region of human
chromosome 17. A gene within this region encodes a novel member of
the TGF-beta binding-protein family (see, e.g., U.S. Pat. Nos.
6,395,511, 6,489,445, and 6,495,736; Brunkow et al., Am. J. Hum.
Genet. 68:577-89 (2001)). Therapeutics related to altering or
modulating the level of sclerostin may therefore be useful in
treating conditions and diseases related to abnormal bone
development or deterioration. As described in more detail below,
antibodies that specifically bind to this TGF-beta binding-protein,
sclerostin (also referred to herein as Beer or as SOST), may be
used to increase bone mineral content thus treating, preventing,
retarding progression, or ameliorating the symptoms of a number of
diseases.
TGF-Beta Superfamily
[0042] Among significant molecules to which reference is made
herein include any known or novel members of the Transforming
Growth Factor-beta (TGF-beta) superfamily, which includes bone
morphogenic proteins (BMPs). Also included in the TGF-beta
superfamily are TGF-beta receptors, which should be understood to
refer to one or more receptors that are specific for a particular
member of the TGF-beta superfamily (including BMPs), and TGF-beta
binding proteins, which should be understood to refer to one or
more polypeptides with specific binding affinity for a particular
member or subset of members of the TGF-beta superfamily (including
BMPs). A specific example of a TGF-beta binding protein includes
sclerostin or SOST. Polynucleotide sequences encoding SOST and SOST
variants in various animals, including humans, are provided herein
in SEQ ID NOs: 55, 56, 57, 59, 61, 63, 65, and 67 and 69 (the
encoded polypeptide sequences are provided in SEQ ID NOs: 1, 20,
58, 60, 62, 64, 66, 68, and 70, respectively). (See, e.g., U.S.
Pat. Nos. 6,395,511; 6,489,445; and 6,495,736. See also e.g.,
Balemans et al., 2002 Dev. Biol. 250:231; Schmitt et al., 1999J.
Orthopaed. Res. 17:269; Khalil, 1999 Microbes Infect. 1:1255;
Miyazono et al., 1993 Growth Factors 8:11; von Bubnoff et al., 2001
Dev. Biol. 239:1; Koli et al., 2001 Microsc. Res. Tech. 52:354;
Ebara et al., 2002 Spine 27(16 Suppl. 1):S10; Bondestam, 2002,
Ligands & Signaling Components of the Transforming Growth
Factor .beta. Family, Helsinki University Biomedical Dissertations
No. 17).
[0043] The TGF-beta superfamily contains a variety of growth
factors that share common sequence elements and structural motifs
at both secondary and tertiary levels. This protein family exerts a
wide spectrum of biological responses that affect a large variety
of cell types. Many of the members of the TGF-beta family have
important functions in pattern formation and tissue specification
during embryonal development. In adults, TGF-beta family members
are involved, for example, in wound healing, bone repair and bone
remodeling, and in modulation of the immune system. In addition to
the TGF-beta polypeptides, this superfamily includes BMPs,
activins, inhibins, Growth and Differentiation Factors (GDFs), and
Glial-Derived Neurotrophic Factors (GDNFs). Primary classification
is established through general sequence features that bin a
specific protein into a general subfamily. Additional
stratification within the sub-family is possible due to stricter
sequence conservation between members of the smaller group. In
certain instances, such as with BMP-5, BMP-6, and BMP-7, the amino
acid percent identity may be as high as 75% among members of the
smaller group. This level of identity enables a single
representative sequence to illustrate the key biochemical elements
of the sub-group that separates it from other members of the larger
family.
[0044] The crystal structure of TGF-beta2 has been determined. The
general fold of the TGF-beta2 monomer contains a stable, compact,
cysteine knotlike structure formed by three disulphide bridges.
Dimerization, which is stabilized by one disulphide bridge, is
antiparallel.
[0045] TGF-beta family members signal by inducing the formation of
hetero-oligomeric receptor complexes. Transduction of TGF-beta
signals involves two distinct subfamilies of transmembrane
serine/threonine kinase receptors, type I and type II. At least
seven type I receptors and five type II receptors have been
identified (see Kawabata et al., Cytokine Growth Factor Rev.
9:49-61 (1998); Miyazono et al., Adv. Immunol. 75:115-57 (2000).
Each member of the TGF-beta family binds to a characteristic
combination of type I and type II receptors, both of which are
needed for signaling. In the current model for TGF-beta receptor
activation, a TGF-beta ligand first binds to the type II receptor
(TbR-II), which then recruits a type I receptor (TbR-I) to form a
ligand/type II/type I ternary complex. The type I receptor, cannot
bind ligand in the absence of TbR-II. TbR-II then phosphorylates
TbR-I predominantly in a domain rich in glycine and serine residues
(GS domain) in the juxtamembrane region, thereby activating TbR-I.
The activated type I receptor kinase then phosphorylates particular
members of the Smad family of proteins that translocate to the
nucleus where they modulate transcription of specific genes.
Bone Morphogenic Proteins (BMPs): Key Regulatory Proteins of Bone
Mineral Density
[0046] A major advance in the understanding of bone formation was
the identification of the BMPs, also known as osteogenic proteins
(OPs), which regulate cartilage and bone differentiation in vivo.
BMPs/OPs induce endochondral bone differentiation through a cascade
of events by which mesenchymal stem cells differentiate into
chondrocytes that lay down a cartilage structure that is reabsorbed
and replaced by bone tissue (see Balemans et al., Dev. Biol.
250:231-50 (2002)). Thus, this process involves formation of
cartilage, hypertrophy and calcification of the cartilage, vascular
invasion, differentiation of osteoblasts, and formation of bone. As
described above, the BMPs/OPs (BMP 2-14, and osteogenic protein 1
and -2, OP-1 and OP-2) (see, e.g., GenBank P12643 (BMP-2); GenBank
P12645 (BMP3); GenBank P55107 (BMP-3b, Growth/differentiation
factor 10) (GDF-10)); GenBank P12644 (BMP4); GenBank P22003 (BMP5);
GenBank P22004 (BMP6); GenBank P18075 (BMP7); GenBank P34820
(BMP8); GenBank Q9UK05 (BMP9); GenBank 095393 (BM10); GenBank
095390 (BMP11, Growth/differentiation factor 11 precursor
(GDF-11)); GenBank 095972 (BM15)) are members of the TGF-beta
superfamily. The striking evolutionary conservation among members
of the BMP/OP sub-family suggests that they are important in the
normal development and function of animals. In addition to
postfetal chondrogenesis and osteogenesis, the BMPs/OPs play
multiple roles in skeletogenesis, including the development of
craniofacial and dental tissues. Different BMP family members also
have biological activities in various other cell types, including
monocytes, epithelial cells, mesenchymal cells, and neuronal cells.
BMPs regulate cell proliferation and differentiation, chemotaxis
and apoptosis, and also control fundamental roles, for example,
left-right asymmetry, neurogenesis, mesoderm patterning, and
embryonic development and organogenesis of a number of organs
including the kidney, gut, lung, teeth, limb, amnion, and testis
(see Balemans, supra).
[0047] BMPs are synthesized as large precursor proteins. Upon
dimerization, the BMPs are proteolyically cleaved within the cell
to yield carboxy-terminal mature proteins that are then secreted
from the cell. BMPs, like other TGF-beta family members, initiate
signal transduction by binding cooperatively to both type I and
type II serine/threonine kinase receptors. Type I receptors for
which BMPs may act as ligands include BMPR-IA (also known as
ALK-3), BMPR-IB (also known as ALK-6), ALK-1, and ALK-2 (also known
as ActR-I). Of the type II receptors, BMPs bind to BMP type II
receptor (BMPR-II), Activin type II (ActR-II), and Activin type IIB
(ActR-IIB). (See Balemans et al., supra, and references cited
therein). Polynucleotide sequences and the encoded amino acid
sequence of BMP type I receptor polypeptides are provided in the
GenBank database, for example, GenBank NM.sub.--004329 (SEQ ID
NO:71 encoded by SEQ ID NO:85); D89675 (SEQ ID NO:72 encoded by SEQ
ID NO:86); NM.sub.--001203 (SEQ ID NO:73 encoded by SEQ ID NO:87);
S75359 (SEQ ID NO:74 encoded by SEQ ID NO:88); NM.sub.--030849 (SEQ
ID NO:75 encoded by SEQ ID NO:89); and D38082 (SEQ ID NO:76 encoded
by SEQ ID NO:90). Other polypeptide sequences of type I receptors
are provided in the GenBank database, for example, NP.sub.--001194
(SEQ ID NO:77); BAA19765 (SEQ ID NO:78); and AAB33865 (SEQ ID
NO:79). Polynucleotide sequences and the encoded amino acid
sequence of BMP type II receptor polypeptides are provided in the
GenBank database and include, for example, U25110 (SEQ ID NO:80
encoded by SEQ ID NO:91); NM.sub.--033346 (SEQ ID NO:81 encoded by
SEQ ID NO:92); NM.sub.--001204 (SEQ ID NO:82 encoded by SEQ ID
NO:93); and Z48923 (SEQ ID NO:83 encoded by SEQ ID NO:94).
Additional polypeptide sequences of type II receptors are also
provided in the GenBank database, for example, CAA88759 (SEQ ID
NO:84).
[0048] BMPs, similar to other cystine-knot proteins, form a
homodimer structure (Scheufler et al., J. Mol. Biol. 287:103-15
(1999)). According to evolutionary trace analysis performed on the
BMP/TGF-.beta. family, the BMP type I receptor binding site and
type II receptor binding site were mapped to the surface of the BMP
structure (Innis et al., Protein Eng. 13:839-47 (2000)). The
location of the type I receptor binding site on BMP was later
confirmed by the x-ray structure of BMP-2/BMP Receptor IA complex
(Nickel et al., J. Joint Surg. Am. 83A(Suppl 1(Pt 1)):S7-S14
(2001)). The predicted type II receptor binding site is in good
agreement with the x-ray structure of TGF-.beta.3/TGF-.beta. Type
II receptor complex (Hart et al., Nat. Struct. Biol. 9:203-208
(2002)), which is highly similar to the BMP/BMP Receptor IIA
system.
[0049] The BMP and Activin sub-families are subject to significant
post-translational regulation by TGF-beta binding proteins. An
intricate extracellular control system exists, whereby a high
affinity antagonist is synthesized and exported, and subsequently
forms a complex selectively with BMPs or activins to disrupt their
biological activity (Smith, Trends Genet. 15:3-6 (1999)). A number
of such TGF-beta binding proteins have been identified, and on the
basis of sequence divergence, the antagonists appear to have
evolved independently because of the lack of primary sequence
conservation. In vertebrates, antagonists include noggin, chordin,
chordin-like, follistatin, FSRP, the DAN/Cerberus protein family,
and sclerostin (SOST) (see Balemans et al., supra, and references
cited therein). The mechanism of antagonism seems to differ for the
different antagonists (Iemura et al. (1998) Proc. Natl. Acad. Sci.
USA 95:9337-9342).
[0050] The type I and type II receptor binding sites on the BMP
antagonist noggin have also been mapped. Noggin binds to BMPs with
high affinity (Zimmerman et al., 1996). A study of the noggin/BMP-7
complex structure revealed the binding interactions between the two
proteins (Groppe et al., Nature 420:636-42 (2002)). Superposition
of the noggin-BMP-7 structure onto a model of the BMP signaling
complex showed that noggin binding effectively masks both pairs of
binding epitopes (i.e., BMP Type I and Type II receptor binding
sites) on BMP-7. The cysteine-rich scaffold sequence of noggin is
preceded by an N-terminal segment of about 20 amino acid residues
that are referred to as the "clip" (residues 28-48). The type I
receptor-binding site is occluded by the N-terminal portion of the
clip domain of Noggin, and the type II receptor binding site is
occluded by the carboxy terminal portion of the clip domain. Two
.beta.-strands in the core region near the C-terminus of noggin
also contact BMP-7 at the type II receptor binding site. This
binding mode enables a Noggin dimer to efficiently block all the
receptor binding sites (two type I and two type II receptor binding
sites) on a BMP dimer.
[0051] Sclerostin Polypeptides and Encoding Polynucleotides The BMP
antagonist sclerostin (U.S. Pat. Nos. 67,395,511, 6,489,445, and
6,495,736; see also SEQ ID NOs: 1, 20, 58, 60, 62, 64, 66, 68, and
70), possesses a nearly identical cysteine (disulfide) scaffold
when compared with Human DAN, Human Gremlin, and Human Cerberus,
and SCGF (U.S. Pat. No. 5,780,263) but almost no homology at the
nucleotide level (for background information, see generally Hsu et
al., Mol. Cell. 1:673-683 (1998)). Sclerostin should also be
understood to include variants of this TGF-beta binding-protein
(e.g., SEQ ID NOs. 60 and 62). As used herein, a TGF-beta
binding-protein variant polynucleotide refers to nucleic acid
molecule that encodes a polypeptide having an amino acid sequence
that is a modification (insertion, deletion, or substitution of one
or more nucleotides) of SEQ ID NOs: 55-57, 59, 61, 63, 65, 67, or
69. Such variants include naturally-occurring polymorphisms or
allelic variants of TGF-beta binding-protein encoding
polynucleotides, as well as synthetic polynucleotides that encode
conservative amino acid substitutions of these amino acid
sequences. A variety of criteria known to those skilled in the art
indicate whether amino acids at a particular position in a peptide
or polypeptide are similar. For example, a similar amino acid or a
conservative amino acid substitution is one in which an amino acid
residue is replaced with an amino acid residue having a similar
side chain, which include amino acids with basic side chains (e.g.,
lysine, arginine, histidine); acidic side chains (e.g., aspartic
acid, glutamic acid); uncharged polar side chains (e.g., glycine,
asparagine, glutamine, serine, threonine, tyrosine, cysteine,
histidine); nonpolar side chains (e.g., alanine, valine, leucine,
isoleucine, proline, phenylalanine, methionine, tryptophan);
beta-branched side chains (e.g., threonine, valine, isoleucine),
and aromatic side chains (e.g., tyrosine, phenylalanine,
tryptophan). Proline, which is considered more difficult to
classify, shares properties with amino acids that have aliphatic
side chains (e.g., Leu, Val, Ile, and Ala). In certain
circumstances, substitution of glutamine for glutamic acid or
asparagine for aspartic acid may be considered a similar
substitution in that glutamine and asparagine are amide derivatives
of glutamic acid and aspartic acid, respectively.
[0052] Additional variant forms of a TGF-beta binding protein
encoding polynucleotide are nucleic acid molecules that contain
substitutions, insertions or deletions of one or more nucleotides
found within the nucleotide sequences described herein. A variant
or mutant of a TGF-beta binding protein may be constructed or
identified so that the altered version of the TGF-beta binding
protein competes with the wildtype TGF-beta binding protein. Such
competition would preferably block the activity of the wildtype
TGF-beta binding protein and thus lead to increased bone
density.
[0053] An isolated polynucleotide is a nucleic acid molecule
(polynucleotide or oligonucleotide) that is not integrated in the
genomic DNA of an organism. A polynucleotide is considered to be
isolated if, for example, it is cloned into a vector that is not a
part of the natural environment. For example, a DNA molecule that
encodes a TGF-binding protein that has been separated from the
genomic DNA of a eukaryotic cell is an isolated DNA molecule.
Another example of an isolated nucleic acid molecule is a
chemically-synthesized nucleic acid molecule that is not integrated
into the genome of an organism. The isolated nucleic acid molecule
may be DNA, cDNA, RNA, or composed at least in part of nucleic acid
analogs.
[0054] TGF-beta binding-protein variant polynucleotides can be
identified by determining whether the polynucleotides hybridize
with a nucleic acid molecule having the nucleotide sequence of SEQ
ID NOs: 55-57, 59, 61, 63, 65, 67, or 69 under stringent
conditions. In addition, TGF-beta binding-protein variant
polynucleotides encode a protein having a cysteine backbone.
TGF-beta binding-protein variant polynucleotides may also be
identified by sequence comparison. As used herein, two amino acid
sequences have "100% amino acid sequence identity" if the amino
acid residues of the two amino acid sequences are the same when
aligned for maximal correspondence. Similarly, two nucleotide
sequences have "100% nucleotide sequence identity" if the
nucleotides of the two nucleotide sequences are the same when
aligned for maximal correspondence. Sequence comparisons can be
performed using standard software programs such as those included
in the LASERGENE bioinformatics computing suite, which is produced
by DNASTAR (Madison, Wis.), or the BLAST algorithm available at the
NCBI web site ([Internet]<:http:www.ncbi.nlm.nih.gov>). Other
methods for comparing two or more nucleotide or amino acid
sequences by determining optimal alignment are well-known to those
of skill in the art (see, for example, Peruski and Peruski, The
Internet and the New Biology: Tools for Genomic and Molecular
Research (ASM Press, Inc. 1997), Wu et al. (eds.), "Information
Superhighway and Computer Databases of Nucleic Acids and Proteins,"
in Methods in Gene Biotechnology, pages 123-151 (CRC Press, Inc.
1997), and Bishop (ed.), Guide to Human Genome Computing, 2nd
Edition (Academic Press, Inc. 1998)).
[0055] A variant TGF-beta binding protein should have at least a
50% amino acid sequence identity to SEQ ID NOs: 1, 20, 58, 60, 62,
64, 66, and 68, and preferably greater than 60%, 65%, 70%, 75%,
80%, 85%, 90%, 95%, or 98% identity. Alternatively, TGF-beta
binding-protein variants can be identified by having at least a 70%
nucleotide sequence identity to SEQ ID NOs: 55-57, 59, 61, 63, 65,
67, or 69. Moreover, the present invention contemplates TGF-beta
binding-protein polynucleotide variants having greater than 75%,
80%, 85%, 90%, or 95% identity to SEQ ID NO:55 or 57. Regardless of
the particular method used to identify a TGF-beta binding-protein
variant polynucleotide or variant TGF-beta binding protein, such a
variant can be functionally characterized by, for example, its
ability to bind to and/or inhibit the signaling of a selected
member of the TGF-beta family of proteins, or by its ability to
bind specifically to an anti-TGF-beta binding-protein antibody.
[0056] Within the context of this invention, a "functional
fragment" of a TGF-beta binding-protein polynucleotide refers to a
nucleic acid molecule that encodes a portion of a TGF-beta
binding-protein polypeptide that either (1) possesses a functional
activity as described herein or (2) specifically binds to an
anti-TGF-beta binding protein antibody. For example, a functional
fragment of a TGF-beta binding protein encoding polynucleotide
described herein comprises a portion of the nucleotide sequence of
SEQ ID Nos: 55-57, 59, 61, 63, 65, 67, or 69.
[0057] An "isolated polypeptide" referred to herein is a
polypeptide that is removed from its natural environment. For
example, a naturally-occurring protein is isolated if it is
separated from some or all of the coexisting materials in the
natural system, such as carbohydrate, lipid, nucleic acids, or
proteinaceous impurities associated with the polypeptide in nature.
Preferably, such isolated polypeptides are at least about 90% pure,
more preferably at least about 95% pure, and most preferably at
least about 99% pure.
Antibodies Specific for TGF-Beta Binding Proteins
[0058] The present invention provides antibodies that specifically
bind to SOST and also provides SOST polypeptide immunogens that may
be used for generation and analysis of these antibodies and also
provides methods for using such antibodies. The antibodies of the
present invention as described herein specifically bind to a SOST
polypeptide and thereby block or inhibit the binding of a BMP to
the SOST polypeptide, that is, prevent or impair the interaction
between the BMP and SOST. The effect of blocking this interaction
is to alter (increase or decrease in a statistically significant
manner) bone mineral density, preferably to increase bone mineral
density.
[0059] Polypeptides or peptides useful for immunization and/or
analysis of SOST-specific antibodies may also be selected by
analyzing the primary, secondary, and tertiary structure of a
TGF-beta binding protein according to methods known to those
skilled in the art and described herein, in order to determine
amino acid sequences more likely to generate an antigenic response
in a host animal. See, e.g., Novotny, Mol. Immunol. 28:201-207
(1991); Berzofsky, Science 229:932-40 (1985)). Modeling and x-ray
crystallography data may also be used to predict and/or identify
which portions or regions of a TGF-beta binding protein interact
with which portions of a TGF-beta binding protein ligand, such as a
BMP. TGF-beta binding protein peptide immunogens may be designed
and prepared that include amino acid sequences within or
surrounding the portions or regions of interaction. These
antibodies may be useful to block or impair binding of the TGF-beta
binding protein to the same ligand and may also block or impair
binding of the TGF-beta binding protein to one or more other
ligands.
[0060] Antibodies or antigen binding fragments thereof contemplated
by the present invention include antibodies that are capable of
specifically binding to SOST and competitively inhibiting binding
of a TGF-beta polypeptide, such as a BMP, to SOST. For example, the
antibodies contemplated by the present invention competitively
inhibit binding of the SOST polypeptide to the BMP Type I receptor
site on a BMP, or to the BMP Type II receptor binding site, or may
competitively inhibit binding of SOST to both the Type I and Type
II receptor binding sites on a BMP. Without wishing to be bound by
theory, when an anti-SOST antibody competitively inhibits binding
of the Type I and/or Type II binding sites of the BMP polypeptide
to SOST, thus blocking the antagonistic activity of SOST, the
receptor binding sites on BMP are available to bind to the Type I
and Type II receptors, thereby increasing bone mineralization. The
binding interaction between a TGF-beta binding protein such as SOST
and a TGF-beta polypeptide such as a BMP generally occurs when each
of the ligand pairs forms a homodimer. Therefore instead of or in
addition to using an antibody specific for SOST to block, impair,
or prevent binding of SOST to a BMP by competitively inhibiting
binding of SOST to BMP, a SOST specific antibody may be used to
block or impair SOST homodimer formation.
[0061] By way of example, one dimer of human Noggin, which is a BMP
antagonist that has the ability to bind a BMP with high affinity
(Zimmerman et al., supra), was isolated in complex with one dimer
of human BMP-7 and analyzed by multiwavelength anomalous
diffraction (MAD) (Groppe et al., Nature 420:636-42 (2002)). As
discussed herein, this study revealed that Noggin dimer may
efficiently block all the receptor binding sites (two type I and
two type II receptor binding sites) on a BMP dimer. The location of
the amino acids of Noggin that contact BMP-7 may be useful in
modeling the interaction between other TGF-beta binding proteins,
such as sclerostin (SOST), and BMPs, and thus aiding the design of
peptides that may be used as immunogens to generate antibodies that
block or impair such an interaction.
[0062] In one embodiment of the present invention, an antibody, or
an antigen-binding fragment thereof, that binds specifically to a
SOST polypeptide competitively inhibits binding of the SOST
polypeptide to at least one or both of a bone morphogenic protein
(BMP) Type I Receptor binding site and a BMP Type II Receptor
binding site that are located on a BMP. The epitopes on SOST to
which these antibodies bind may include or be included within
contiguous amino acid sequences that are located at the N-terminus
of the SOST polypeptide (amino acids at about positions 1-56 of SEQ
ID NO:1). The polypeptides may also include a short linker peptide
sequence that connects the N-terminal region to the core region,
for example, polypeptides as provided in SEQ ID NO:47 (human) and
SEQ ID NO:48 (rat). Shorter representative N-terminus peptide
sequences of human SOST (e.g., SEQ ID NO:1) include SEQ ID NOS:2-6,
and representative rat SOST (e.g., SEQ ID NO:20) peptide sequences
include SEQ ID NOS:12-15.
[0063] Antibodies that specifically bind to a SOST polypeptide and
block or competitively inhibit binding of the SOST polypeptide to a
BMP, for example, by blocking or inhibiting binding to amino acids
of a BMP corresponding to one or more of the Type I and Type II
receptor binding sites may also specifically bind to peptides that
comprise an amino acid sequence corresponding to the core region of
SOST (amino acids at about positions 57-146 of SEQ ID NO:1).
Polypeptides that include the core region may also include
additional amino acids extending at either or both the N-terminus
and C-terminus, for example, to include cysteine residues that may
be useful for conjugating the polypeptide to a carrier molecule.
Representative core polypeptides of human and rat SOST, for
example, comprise the amino acid sequences set forth in SEQ ID
NO:49 and SEQ ID NO:50, respectively. Such antibodies may also bind
shorter polypeptide sequences. Representative human SOST core
peptide sequences are provided in SEQ ID NOs:21-24 and
representative rat SOST core sequences are provided in SEQ ID
NOs:25-28.
[0064] In another embodiment, antibodies that specifically bind to
a SOST polypeptide impair (inhibit, prevent, or block, e.g.,
decrease in a statistically significant manner) formation of a SOST
homodimer. Because the interaction between SOST and a BMP may
involve a homodimer of SOST and a homodimer of the BMP, an antibody
that prevents or impairs homodimer formation of SOST may thereby
alter bone mineral density, preferably increasing bone mineral
density. In one embodiment, antibodies that bind to the core region
of SOST prevent homodimer formation. Such antibodies may also bind
to peptides that comprise contiguous amino acid sequences
corresponding the core region, for example, SEQ ID NOs: 29, 30 and
53 (human SOST) and SEQ ID NOs:31 and 54 (rat SOST). Antibodies
that bind to an epitope located on the C-terminal region of a SOST
polypeptide (at about amino acid positions 147-190 of either SEQ ID
NO:1 or 20) may also impair homodimer formation. Representative
C-terminal polypeptides of human and rat SOST, for example,
comprise the amino acid sequences set forth in SEQ ID NO:51 and SEQ
ID NO:52, respectively. Such antibodies may also bind shorter
polypeptide sequences. Representative human SOST C-terminal peptide
sequences are provided in SEQ ID NOs:33-36 and representative rat
SOST C-terminal sequences are provided in SEQ ID NOs:41-43.
[0065] The SOST polypeptides and peptides disclosed herein to which
antibodies may specifically bind are useful as immunogens. These
immunogens of the present invention may be used for immunizing an
animal to generate a humoral immune response that results in
production of antibodies that specifically bind to a Type I or Type
II receptor binding site or both located on a BMP include peptides
derived from the N-terminal region of SOST or that may prevent SOST
homodimer formation.
[0066] Such SOST polypeptides and peptides that are useful as
immunogens may also be used in methods for screening samples
containing antibodies, for example, samples of purified antibodies,
antisera, or cell culture supernatants or any other biological
sample that may contain one or more antibodies specific for SOST.
These peptides may also be used in methods for identifying and
selecting from a biological sample one or more B cells that are
producing an antibody that specifically binds to SOST (e.g., plaque
forming assays and the like). The B cells may then be used as
source of a SOST specific antibody-encoding polynucleotide that can
be cloned and/or modified by recombinant molecular biology
techniques known in the art and described herein.
[0067] A "biological sample" as used herein refers in certain
embodiments to a sample containing at least one antibody specific
for a SOST polypeptide, and a biological sample may be provided by
obtaining a blood sample (from which serum or plasma may be
prepared), biopsy specimen, tissue explant, organ culture, or any
other tissue or cell preparation from a subject or a biological
source. A sample may further refer to a tissue or cell preparation
in which the morphological integrity or physical state has been
disrupted, for example, by dissection, dissociation,
solubilization, fractionation, homogenization, biochemical or
chemical extraction, pulverization, lyophilization, sonication, or
any other means for processing a sample derived from a subject or
biological source. The subject or biological source may be a human
or non-human animal, a primary cell culture (e.g., B cells
immunized in vitro), or culture adapted cell line including but not
limited to genetically engineered cell lines that may contain
chromosomally integrated or episomal recombinant nucleic acid
sequences, immortalized or immortalizable cell lines, somatic cell
hybrid cell lines, differentiated or differentiatable cell lines,
transformed cell lines, and the like.
[0068] SOST peptide immunogens may also be prepared by synthesizing
a series of peptides that, in total, represent the entire
polypeptide sequence of a SOST polypeptide and that each have a
portion of the SOST amino acid sequence in common with another
peptide in the series. This overlapping portion would preferably be
at least four amino acids, and more preferably 5, 6, 7, 8, 9, or 10
amino acids. Each peptide may be used to immunize an animal, the
sera collected from the animal, and tested in an assay to identify
which animal is producing antibodies that impair or block binding
of SOST to a TGF-beta protein. Antibodies are then prepared from
such identified immunized animals according to methods known in the
art and described herein.
[0069] Peptides, polypeptides, and other non-peptide molecules that
specifically bind to a TGF-beta binding protein such as SOST are
contemplated by this invention. As used herein, a molecule is said
to "specifically bind" to a TGF-beta binding protein if it reacts
at a detectable level with the TGF-beta binding protein, but does
not react detectably with peptides and polypeptides containing an
unrelated sequence, or a sequence of a different TGF-beta binding
protein. Preferred binding molecules include antibodies, which may
be, for example, polyclonal, monoclonal, single chain, chimeric,
anti-idiotypic, or CDR-grafted immunoglobulins, or fragments
thereof, such as proteolytically generated or recombinantly
produced immunoglobulin F(ab').sub.2, Fab, Fab' Fv, and Fd
fragments.
[0070] Particularly useful are anti-TGF-beta binding-protein
antibodies that "specifically bind" TGF-beta binding-protein of SEQ
ID NOs: 1, 20, 58, 60, 62, 64, 66, or 68, but not to other TGF-beta
binding-proteins such as Dan, Cerberus, SCGF, or Gremlin.
Antibodies are understood to specifically bind a TGF-beta
binding-protein, or a specific TGF-beta family member, if they bind
with a K.sub.a of greater than or equal to 10.sup.4 M.sup.-1, more
preferably greater than or equal to about 10.sup.5 M.sup.-1, more
preferably greater than or equal to about 10.sup.6 M.sup.-1, still
more preferably greater than or equal to 10.sup.7 M.sup.-1, and
still more preferably greater than or equal to 10.sup.8 M.sup.-1,
and do not bind to other TGF-beta binding-proteins. Affinity of an
antibody for its cognate antigen is also commonly expressed as a
dissociation constant K.sub.D, and an anti-SOST antibody
specifically binds to a TGF-beta family member if it binds with a
K.sub.D of less than or equal to 10.sup.-4 M, more preferably less
than or equal to about 10.sup.-5 M, more preferably less than or
equal to about 10.sup.-6 M, still more preferably less than or
equal to 10.sup.-7 M, and still more preferably less than or equal
to 10.sup.-8 M. Furthermore, antibodies of the present invention
preferably block, impair, or inhibit (e.g., decrease with
statistical significance) binding of a TGF-beta binding-protein to
a TGF-beta family member.
[0071] The affinity of an antibody or binding partner, as well as
the extent to which an antibody inhibits binding can be readily
determined by one of ordinary skill in the art using conventional
techniques, for example those described by Scatchard et al. (Ann.
N.Y. Acad. Sci. 51:660-672, (1949)) or by surface plasmon resonance
(SPR; BIAcore, Biosensor, Piscataway, N.J.). For surface plasmon
resonance, target molecules are immobilized on a solid phase and
exposed to ligands in a mobile phase running along a flow cell. If
ligand binding to the immobilized target occurs, the local
refractive index changes, leading to a change in SPR angle, which
can be monitored in real time by detecting changes in the intensity
of the reflected light. The rates of change of the SPR signal can
be analyzed to yield apparent rate constants for the association
and dissociation phases of the binding reaction. The ratio of these
values gives the apparent equilibrium constant (affinity) (see,
e.g., Wolff et al., Cancer Res. 53:2560-65 (1993)).
[0072] An antibody according to the present invention may belong to
any immunoglobulin class, for example IgG, IgE, IgM, IgD, or IgA.
It may be obtained from or derived from an animal, for example,
fowl (e.g., chicken) and mammals, which includes but is not limited
to a mouse, rat, hamster, rabbit, or other rodent, a cow, horse,
sheep, goat, camel, human, or other primate. The antibody may be an
internalising antibody.
[0073] Methods well known in the art may be used to generate
antibodies, polyclonal antisera, or monoclonal antibodies that are
specific for a TGF-beta binding protein such as SOST. Antibodies
also may be produced as genetically engineered immunoglobulins (Ig)
or Ig fragments designed to have desirable properties. For example,
by way of illustration and not limitation, antibodies may include a
recombinant IgG that is a chimeric fusion protein having at least
one variable (V) region domain from a first mammalian species and
at least one constant region domain from a second, distinct
mammalian species. Most commonly, a chimeric antibody has murine
variable region sequences and human constant region sequences. Such
a murine/human chimeric immunoglobulin may be "humanized" by
grafting the complementarity determining regions (CDRs) derived
from a murine antibody, which confer binding specificity for an
antigen, into human-derived V region framework regions and
human-derived constant regions. Fragments of these molecules may be
generated by proteolytic digestion, or optionally, by proteolytic
digestion followed by mild reduction of disulfide bonds and
alkylation. Alternatively, such fragments may also be generated by
recombinant genetic engineering techniques.
[0074] Certain preferred antibodies are those antibodies that
inhibit or block a TGF-beta binding protein activity within an in
vitro assay, as described herein. Binding properties of an antibody
to a TGF-beta binding protein may generally be assessed using
immunodetection methods including, for example, an enzyme-linked
immunosorbent assay (ELISA), immunoprecipitation, immunoblotting,
countercurrent immunoelectrophoresis, radioimmunoassays, dot blot
assays, inhibition or competition assays, and the like, which may
be readily performed by those having ordinary skill in the art
(see, e.g., U.S. Pat. Nos. 4,376,110 and 4,486,530; Harlow et al.,
Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory
(1988)).
[0075] An immunogen may be comprised of cells expressing a TGF-beta
binding protein such as a SOST polypeptide, purified or partially
purified SOST polypeptide, or variants or fragments (i.e.,
peptides) thereof, or peptides derived from a SOST polypeptide.
Such peptides may be generated by proteolytic cleavage of a larger
polypeptide, by recombinant molecular methodologies, or may be
chemically synthesized. For instance, nucleic acid sequences
encoding SOST polypeptide are provided herein, such that those
skilled in the art may routinely prepare SOST polypeptide for use
as immunogens. Peptides may be chemically synthesized by methods as
described herein and known in the art. Alternatively, peptides may
be generated by proteolytic cleavage of a SOST polypeptide, and
individual peptides isolated by methods known in the art such as
polyacrylamide gel electrophoresis or any number of liquid
chromatography or other separation methods. Peptides useful as
immunogens typically may have an amino acid sequence of at least 4
or 5 consecutive amino acids from a SOST polypeptide amino acid
sequence such as those described herein, and preferably have at
least 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 18, 19 or 20 consecutive
amino acids of a SOST polypeptide. Certain other preferred peptide
immunogens comprise at least 6 but no more than 12 or more
consecutive amino acids of a SOST polypeptide sequence, and other
preferred peptide immunogens comprise at least 20 but no more than
75 consecutive amino acids, and other preferred peptide immunogens
comprise at least 21 but no more than 50 consecutive amino acids of
a SOST polypeptide. Other preferred peptide immunogens comprise
21-25, 26-30, 31-35, 36-40, 41-50, or any whole integer number of
amino acids between and including 21 and 100 consecutive amino
acids, and between 100 and 190 consecutive amino acids of a SOST
polypeptide sequence.
[0076] Polyclonal antibodies that bind specifically to SOST can be
prepared using methods described herein and well-known to persons
skilled in the art (see, for example, Green et al., "Production of
Polyclonal Antisera," in Immunochemical Protocols (Manson, ed.),
pages 1-5 (Humana Press 1992); Harlow et al., Antibodies: A
Laboratory Manual, Cold Spring Harbor Laboratory (1988); Williams
et al., "Expression of foreign proteins in E. coli using plasmid
vectors and purification of specific polyclonal antibodies," in DNA
Cloning 2: Expression Systems, 2nd Edition, Glover et al. (eds.),
page 15 (Oxford University Press 1995)). Antibodies to a TGF-beta
binding-protein can be obtained, for example, by immunizing an
animal with the TGF-beta binding-protein product of an expression
vector, or by immunizing with an isolated TGF-beta binding protein
or a peptide fragment thereof, as described herein. Although
polyclonal antibodies are typically raised in animals such as rats,
mice, rabbits, goats, cattle, or sheep, an anti-TGF-beta
binding-protein antibody of the present invention may also be
obtained from a subhuman primate. General techniques for raising
diagnostically and therapeutically useful antibodies in baboons may
be found, for example, in WO 91/11465 (1991) and in Losman et al.,
Int. J. Cancer 46:310, 1990.
[0077] Preparation of an Immunogen for Injection into Animals May
Include covalent coupling of the TGF-beta binding protein (or
variant or fragment thereof), to another immunogenic protein, for
example, a carrier protein such as keyhole limpet hemocyanin (KLH)
or bovine serum albumin (BSA) or the like. A polypeptide or peptide
immunogen may include one or more additional amino acids at either
the N-terminal or C-terminal end that facilitate the conjugation
procedure (e.g., the addition of a cysteine to facilitate
conjugation of a peptide to KLH). Other amino acid residues within
a polypeptide or peptide may be substituted to prevent conjugation
at that particular amino acid position to a carrier polypeptide
(e.g., substituting a serine residue for cysteine at internal
positions of a polypeptide/peptide) or may be substituted to
facilitate solubility or to increase immunogenicity.
[0078] TGF-beta binding protein peptide, polypeptide, or TGF-beta
binding protein-expressing cells to be used as an immunogen may be
emulsified in an adjuvant, for example, Freund's complete or
incomplete adjuvant or the Ribi Adjuvant System (Corixa
Corporation, Seattle, Wash.). See also, e.g., Harlow et al., supra.
The immunogen may be injected into the animal via any number of
different routes, including intraperitoneally, intramuscularly,
intraocularly, intradermally, or subcutaneously. In general, after
the first injection, animals receive one or more booster
immunizations according to a preferred schedule that may vary
according to, inter alia, the antigen, the adjuvant (if any),
and/or the particular animal species. The immune response may be
monitored by periodically bleeding the animal and preparing and
analyzing sera in an immunoassay, such as an ELISA or Ouchterlony
diffusion assay, or the like, to determine the specific antibody
titer. Once an adequate antibody titer is established, the animals
may be bled periodically to accumulate the polyclonal antisera or
may be exsanguinated. Polyclonal antibodies that bind specifically
to the TGF-beta binding protein or peptide may then be purified
from such antisera, for example, by affinity chromatography using
protein A. Alternatively, affinity chromatography may be performed
wherein the TGF-beta binding protein or peptide or an antibody
specific for an Ig constant region of the particular immunized
animal species is immobilized on a suitable solid support.
[0079] Antibodies for use in the invention include monoclonal
antibodies that are prepared by conventional immunization and cell
fusion procedures as described herein an known in the art.
Monoclonal anti-TGF-beta binding-protein antibodies may be
generated using a variety of techniques. Monoclonal antibodies that
bind to specific antigens may be obtained by methods known to those
skilled in the art (see, for example, Kohler et al., Nature
256:495, 1975; Coligan et al. (eds.), Current Protocols in
Immunology, 1:2.5.1-2.6.7 (John Wiley & Sons 1991); U.S. Pat.
Nos. RE 32,011, 4,902,614, 4,543,439, and 4,411,993; Monoclonal
Antibodies, Hybridomas: A New Dimension in Biological Analyses,
Plenum Press, Kennett, McKeam, and Bechtol (eds.) (1980); and
Antibodies: A Laboratory Manual, Harlow and Lane (eds.), Cold
Spring Harbor Laboratory Press (1988); Picksley et al., "Production
of monoclonal antibodies against proteins expressed in E. coli," in
DNA Cloning 2: Expression Systems, 2nd Edition, Glover et al.
(eds.), page 93 (Oxford University Press 1995)). Antibody fragments
may be derived therefrom using any suitable standard technique such
as proteolytic digestion, or optionally, by proteolytic digestion
(for example, using papain or pepsin) followed by mild reduction of
disulfide bonds and alkylation. Alternatively, such fragments may
also be generated by recombinant genetic engineering
techniques.
[0080] Briefly, monoclonal antibodies can be obtained by injecting
an animal, for example, a rat, hamster, or preferably a mouse, with
an immunogen comprising a TGF-beta binding-protein gene product, or
peptide fragment thereof, according to methods known in the art and
described herein. The presence of specific antibody production may
be monitored after the initial injection (injections may be
administered by any one of several routes as described herein for
generation of polyclonal antibodies) and/or after a booster
injection by obtaining a serum sample and detecting the presence of
an antibody that binds to a TGF-beta binding-protein or peptide
using any one of several immunodetection methods known in the art
and described herein. From animals producing antibodies that bind
to the TGF-beta binding protein, lymphoid cells, most commonly
cells from the spleen or lymph node, are removed to obtain
B-lymphocytes. The B-lymphocytes are then fused with a
drug-sensitized myeloma cell fusion partner, preferably one that is
syngeneic with the immunized animal and that optionally has other
desirable properties (e.g., inability to express endogenous Ig gene
products, e.g., P3.times.63-Ag 8.653 (ATCC No. CRL 1580); NS0,
SP20) to produce hybridomas, which are immortal eukaryotic cell
lines. The lymphoid (e.g., spleen) cells and the myeloma cells may
be combined for a few minutes with a membrane fusion-promoting
agent, such as polyethylene glycol or a nonionic detergent, and
then plated at low density on a selective medium that supports the
growth of hybridoma cells but not unfused myeloma cells. A
preferred selection media is HAT (hypoxanthine, aminopterin,
thymidine). After a sufficient time, usually about one to two
weeks, colonies of cells are observed. Single colonies are
isolated, and antibodies produced by the cells may be tested for
binding activity to the TGF-beta binding protein, or variant or
fragment thereof, using any one of a variety of immunoassays known
in the art and described herein. Hybridomas producing monoclonal
antibodies with high affinity and specificity for SOST are
preferred. Hybridomas that produce monoclonal antibodies that
specifically bind to a TGF-beta binding protein or variant or
fragment thereof are therefore contemplated by the present
invention. The hybridomas are cloned (e.g., by limited dilution
cloning or by soft agar plaque isolation) and positive clones that
produce an antibody specific to the antigen are selected and
cultured. Antibodies that block, inhibit, or impair binding of the
TGF-beta binding protein to a TGF-beta family member are
preferred.
[0081] The monoclonal antibodies from the hybridoma cultures may be
isolated from the supernatants of hybridoma cultures. An
alternative method for production of a murine monoclonal antibody
is to inject the hybridoma cells into the peritoneal cavity of a
syngeneic mouse, for example, a mouse that has been treated (e.g.,
pristane-primed) to promote formation of ascites fluid containing
the monoclonal antibody. Monoclonal antibodies can be isolated and
purified by a variety of well-established techniques. Such
isolation techniques include affinity chromatography with Protein-A
Sepharose, size-exclusion chromatography, and ion-exchange
chromatography (see, for example, Coligan at pages 2.7.1-2.7.12 and
pages 2.9.1-2.9.3; Baines et al., "Purification of Immunoglobulin G
(IgG)," in Methods in Molecular Biology, Vol. 10, pages 79-104 (The
Humana Press, Inc. 1992)). Monoclonal antibodies may be purified by
affinity chromatography using an appropriate ligand selected based
on particular properties of the antibody (e.g., heavy or light
chain isotype, binding specificity, etc.). Examples of a suitable
ligand, immobilized on a solid support, include Protein A, Protein
G, an anti-constant region (light chain or heavy chain) antibody,
an anti-idiotype antibody, and a TGF-beta binding protein, or
fragment or variant thereof.
[0082] In addition, an anti-TGF-beta binding-protein antibody of
the present invention may be a human monoclonal antibody. Human
monoclonal antibodies may be generated by any number of techniques
with which those having ordinary skill in the art will be familiar.
Such methods include, but are not limited to, Epstein Barr Virus
(EBV) transformation of human peripheral blood cells (e.g.,
containing B lymphocytes), in vitro immunization of human B cells,
fusion of spleen cells from immunized transgenic mice carrying
inserted human immunoglobulin genes, isolation from human
immunoglobulin V region phage libraries, or other procedures as
known in the art and based on the disclosure herein. For example,
human monoclonal antibodies may be obtained from transgenic mice
that have been engineered to produce specific human antibodies in
response to antigenic challenge. Methods for obtaining human
antibodies from transgenic mice are described, for example, by
Green et al., Nature Genet. 7:13, 1994; Lonberg et al., Nature
368:856, 1994; Taylor et al., Int. Immun. 6:579, 1994; U.S. Pat.
No. 5,877,397; Bruggemann et al., 1997 Curr. Opin. Biotechnol.
8:455-58; Jakobovits et al., 1995 Ann. N.Y. Acad. Sci. 764:525-35.
In this technique, elements of the human heavy and light chain
locus are introduced into strains of mice derived from embryonic
stem cell lines that contain targeted disruptions of the endogenous
heavy chain and light chain loci. (See also Bruggemann et al.,
Curr. Opin. Biotechnol. 8:455-58 (1997)). For example, human
immunoglobulin transgenes may be mini-gene constructs, or transloci
on yeast artificial chromosomes, which undergo B cell-specific DNA
rearrangement and hypermutation in the mouse lymphoid tissue. Human
monoclonal antibodies may be obtained by immunizing the transgenic
mice, which may then produce human antibodies specific for the
antigen. Lymphoid cells of the immunized transgenic mice can be
used to produce human antibody-secreting hybridomas according to
the methods described herein. Polyclonal sera containing human
antibodies may also be obtained from the blood of the immunized
animals.
[0083] Another method for generating human TGF-beta binding protein
specific monoclonal antibodies includes immortalizing human
peripheral blood cells by EBV transformation. See, e.g., U.S. Pat.
No. 4,464,456. Such an immortalized B cell line (or lymphoblastoid
cell line) producing a monoclonal antibody that specifically binds
to a TGF-beta binding protein (or a variant or fragment thereof)
can be identified by immunodetection methods as provided herein,
for example, an ELISA, and then isolated by standard cloning
techniques. The stability of the lymphoblastoid cell line producing
an anti-TGF-beta binding protein antibody may be improved by fusing
the transformed cell line with a murine myeloma to produce a
mouse-human hybrid cell line according to methods known in the art
(see, e.g., Glasky et al., Hybridoma 8:377-89 (1989)). Still
another method to generate human monoclonal antibodies is in vitro
immunization, which includes priming human splenic B cells with
antigen, followed by fusion of primed B cells with a heterohybrid
fusion partner. See, e.g., Boerner et al., 1991 J. Immunol.
147:86-95.
[0084] In certain embodiments, a B cell that is producing an
anti-SOST antibody is selected and the light chain and heavy chain
variable regions are cloned from the B cell according to molecular
biology techniques known in the art (WO 92/02551; U.S. Pat. No.
5,627,052; Babcook et al., Proc. Natl. Acad. Sci. USA 93:7843-48
(1996)) and described herein. Preferably B cells from an immunized
animal are isolated from the spleen, lymph node, or peripheral
blood sample by selecting a cell that is producing an antibody that
specifically binds to SOST. B cells may also be isolated from
humans, for example, from a peripheral blood sample. Methods for
detecting single B cells that are producing an antibody with the
desired specificity are well known in the art, for example, by
plaque formation, fluorescence-activated cell sorting, in vitro
stimulation followed by detection of specific antibody, and the
like. Methods for selection of specific antibody producing B cells
include, for example, preparing a single cell suspension of B cells
in soft agar that contains SOST or a peptide fragment thereof.
Binding of the specific antibody produced by the B cell to the
antigen results in the formation of a complex, which may be visible
as an immunoprecipitate. After the B cells producing the specific
antibody are selected, the specific antibody genes may be cloned by
isolating and amplifying DNA or mRNA according to methods known in
the art and described herein.
[0085] For particular uses, fragments of anti-TGF-beta binding
protein antibodies may be desired. Antibody fragments,
F(ab').sub.2, Fab, Fab', Fv, Fc, Fd, retain the antigen binding
site of the whole antibody and therefore bind to the same epitope.
These antigen-binding fragments derived from an antibody can be
obtained, for example, by proteolytic hydrolysis of the antibody,
for example, pepsin or papain digestion of whole antibodies
according to conventional methods. As an illustration, antibody
fragments can be produced by enzymatic cleavage of antibodies with
pepsin to provide a 5S fragment denoted F(ab').sub.2. This fragment
can be further cleaved using a thiol reducing agent to produce 3.5S
Fab' monovalent fragments. Optionally, the cleavage reaction can be
performed using a blocking group for the sulfhydryl groups that
result from cleavage of disulfide linkages. As an alternative, an
enzymatic cleavage using papain produces two monovalent Fab
fragments and an Fc fragment directly. These methods are described,
for example, by Goldenberg, U.S. Pat. No. 4,331,647, Nisonoff et
al., Arch. Biochem. Biophys. 89:230, 1960; Porter, Biochem. J.
73:119, 1959; Edelman et al., in Methods in Enzymology 1:422
(Academic Press 1967); and by Coligan at pages 2.8.1-2.8.10 and
2.10.-2.10.4. Other methods for cleaving antibodies, such as
separating heavy chains to form monovalent light-heavy chain
fragments (Fd), further cleaving of fragments, or other enzymatic,
chemical, or genetic techniques may also be used, so long as the
fragments bind to the antigen that is recognized by the intact
antibody.
[0086] An antibody fragment may also be any synthetic or
genetically engineered protein that acts like an antibody in that
it binds to a specific antigen to form a complex. For example,
antibody fragments include isolated fragments consisting of the
light chain variable region, "Fv" fragments consisting of the
variable regions of the heavy and light chains, recombinant single
chain polypeptide molecules in which light and heavy variable
regions are connected by a peptide linker (scFv proteins), and
minimal recognition units consisting of the amino acid residues
that mimic the hypervariable region. The antibody of the present
invention preferably comprises at least one variable region domain.
The variable region domain may be of any size or amino acid
composition and will generally comprise at least one hypervariable
amino acid sequence responsible for antigen binding and which is
adjacent to or in frame with one or more framework sequences. In
general terms, the variable (V) region domain may be any suitable
arrangement of immunoglobulin heavy (V.sub.H) and/or light
(V.sub.L) chain variable domains. Thus, for example, the V region
domain may be monomeric and be a V.sub.H or V.sub.L domain, which
is capable of independently binding antigen with acceptable
affinity. Alternatively, the V region domain may be dimeric and
contain V.sub.H-V.sub.H, V.sub.H-V.sub.L, or V.sub.L-V.sub.L,
dimers. Preferably, the V region dimer comprises at least one
V.sub.H and at least one V.sub.L chain that are non-covalently
associated (hereinafter referred to as F.sub.V). If desired, the
chains may be covalently coupled either directly, for example via a
disulfide bond between the two variable domains, or through a
linker, for example a peptide linker, to form a single chain Fv
(scF.sub.V).
[0087] The variable region domain may be any naturally occurring
variable domain or an engineered version thereof. By engineered
version is meant a variable region domain that has been created
using recombinant DNA engineering techniques. Such engineered
versions include those created, for example, from a specific
antibody variable region by insertions, deletions, or changes in or
to the amino acid sequences of the specific antibody. Particular
examples include engineered variable region domains containing at
least one CDR and optionally one or more framework amino acids from
a first antibody and the remainder of the variable region domain
from a second antibody.
[0088] The variable region domain may be covalently attached at a
C-terminal amino acid to at least one other antibody domain or a
fragment thereof. Thus, for example, a V.sub.H domain that is
present in the variable region domain may be linked to an
immunoglobulin C.sub.H1 domain, or a fragment thereof. Similarly a
V.sub.L domain may be linked to a C.sub.K domain or a fragment
thereof. In this way, for example, the antibody may be a Fab
fragment wherein the antigen binding domain contains associated
V.sub.H and V.sub.L domains covalently linked at their C-termini to
a CH1 and C.sub.K domain, respectively. The CH1 domain may be
extended with further amino acids, for example to provide a hinge
region or a portion of a hinge region domain as found in a Fab'
fragment, or to provide further domains, such as antibody CH2 and
CH3 domains.
[0089] Another form of an antibody fragment is a peptide comprising
for a single complementarity-determining region (CDR). CDR peptides
("minimal recognition units") can be obtained by constructing
polynucleotides that encode the CDR of an antibody of interest.
Such polynucleotides are prepared, for example, by using the
polymerase chain reaction to synthesize the variable region using
mRNA of antibody-producing cells as a template (see, for example,
Larrick et al., Methods: A Companion to Methods in Enzymology
2:106, 1991; Courtenay-Luck, "Genetic Manipulation of Monoclonal
Antibodies," in Monoclonal Antibodies: Production, Engineering and
Clinical Application, Ritter et al. (eds.), page 166 (Cambridge
University Press 1995); and Ward et al., "Genetic Manipulation and
Expression of Antibodies," in Monoclonal Antibodies: Principles and
Applications, Birch et al., (eds.), page 137 (Wiley-Liss, Inc.
1995)).
[0090] Alternatively, the antibody may be a recombinant or
engineered antibody obtained by the use of recombinant DNA
techniques involving the manipulation and re-expression of DNA
encoding antibody variable and/or constant regions. Such DNA is
known and/or is readily available from DNA libraries including for
example phage-antibody libraries (see Chiswell and McCafferty,
Tibtech. 10:80-84 (1992)) or if desired can be synthesized.
Standard molecular biology and/or chemistry procedures may be used
to sequence and manipulate the DNA, for example, to introduce
codons to create cysteine residues, or to modify, add or delete
other amino acids or domains as desired.
[0091] Chimeric antibodies, specific for a TGF-beta binding
protein, and which include humanized antibodies, may also be
generated according to the present invention. A chimeric antibody
has at least one constant region domain derived from a first
mammalian species and at least one variable region domain derived
from a second, distinct mammalian species (see, e.g., Morrison et
al., Proc. Natl. Acad. Sci. USA, 81:6851-55 (1984)). In preferred
embodiments, a chimeric antibody may be constructed by cloning the
polynucleotide sequence that encodes at least one variable region
domain derived from a non-human monoclonal antibody, such as the
variable region derived from a murine, rat, or hamster monoclonal
antibody, into a vector containing a nucleotide sequence that
encodes at least one human constant region (see, e.g., Shin et al.,
Methods Enzymol. 178:459-76 (1989); Walls et al., Nucleic Acids
Res. 21:2921-29 (1993)). By way of example, the polynucleotide
sequence encoding the light chain variable region of a murine
monoclonal antibody may be inserted into a vector containing a
nucleotide sequence encoding the human kappa light chain constant
region sequence. In a separate vector, the polynucleotide sequence
encoding the heavy chain variable region of the monoclonal antibody
may be cloned in frame with sequences encoding a human IgG constant
region, for example, the human IgG1 constant region. The particular
human constant region selected may depend upon the effector
functions desired for the particular antibody (e.g., complement
fixing, binding to a particular Fc receptor, etc.). Preferably, the
constructed vectors will be transfected into eukaryotic cells for
stable expression of the chimeric antibody. Another method known in
the art for generating chimeric antibodies is homologous
recombination (e.g., U.S. Pat. No. 5,482,856).
[0092] A non-human/human chimeric antibody may be further
genetically engineered to create a "humanized" antibody. Such a
humanized antibody may comprise a plurality of CDRs derived from an
immunoglobulin of a non-human mammalian species, at least one human
variable framework region, and at least one human immunoglobulin
constant region. Useful strategies for designing humanized
antibodies may include, for example by way of illustration and not
limitation, identification of human variable framework regions that
are most homologous to the non-human framework regions of the
chimeric antibody. Without wishing to be bound by theory, such a
strategy may increase the likelihood that the humanized antibody
will retain specific binding affinity for a TGF-beta binding
protein, which in some preferred embodiments may be substantially
the same affinity for a TGF-beta binding protein or variant or
fragment thereof, and in certain other preferred embodiments may be
a greater affinity for TGF-beta binding protein. See, e.g., Jones
et al., 1986 Nature 321:522-25; Riechmann et al., 1988 Nature
332:323-27. Designing such a humanized antibody may therefore
include determining CDR loop conformations and structural
determinants of the non-human variable regions, for example, by
computer modeling, and then comparing the CDR loops and
determinants to known human CDR loop structures and determinants.
See, e.g., Padlan et al., 1995 FASEB 9:133-39; Chothia et al., 1989
Nature, 342:377-383. Computer modeling may also be used to compare
human structural templates selected by sequence homology with the
non-human variable regions. See, e.g., Bajorath et al., 1995 Ther.
Immunol. 2:95-103; EP-0578515-A3. If humanization of the non-human
CDRs results in a decrease in binding affinity, computer modeling
may aid in identifying specific amino acid residues that could be
changed by site-directed or other mutagenesis techniques to
partially, completely or supra-optimally (i.e., increase to a level
greater than that of the non-humanized antibody) restore affinity.
Those having ordinary skill in the art are familiar with these
techniques, and will readily appreciate numerous variations and
modifications to such design strategies.
[0093] One such method for preparing a humanized antibody is called
veneering. As used herein, the terms "veneered FRs" and
"recombinantly veneered FRs" refer to the selective replacement of
FR residues from, e.g., a rodent heavy or light chain V region,
with human FR residues in order to provide a xenogeneic molecule
comprising an antigen-binding site that retains substantially all
of the native FR polypeptide folding structure. Veneering
techniques are based on the understanding that the ligand binding
characteristics of an antigen-binding site are determined primarily
by the structure and relative disposition of the heavy and light
chain CDR sets within the antigen-binding surface. Davies et al.,
Ann. Rev. Biochem. 59:439-73, 1990. Thus, antigen binding
specificity can be preserved in a humanized antibody only wherein
the CDR structures, their interaction with each other, and their
interaction with the rest of the V region domains are carefully
maintained. By using veneering techniques, exterior (e.g.,
solvent-accessible) FR residues that are readily encountered by the
immune system are selectively replaced with human residues to
provide a hybrid molecule that comprises either a weakly
immunogenic, or substantially non-immunogenic veneered surface.
[0094] The process of veneering makes use of the available sequence
data for human antibody variable domains compiled by Kabat et al.,
in Sequences of Proteins of Immunological Interest, 4th ed., (U.S.
Dept. of Health and Human Services, U.S. Government Printing
Office, 1987), updates to the Kabat database, and other accessible
U.S. and foreign databases (both nucleic acid and protein). Solvent
accessibilities of V region amino acids can be deduced from the
known three-dimensional structure for human and murine antibody
fragments. Initially, the FRs of the variable domains of an
antibody molecule of interest are compared with corresponding FR
sequences of human variable domains obtained from the
above-identified sources. The most homologous human V regions are
then compared residue by residue to corresponding murine amino
acids. The residues in the murine FR that differ from the human
counterpart are replaced by the residues present in the human
moiety using recombinant techniques well known in the art. Residue
switching is only carried out with moieties which are at least
partially exposed (solvent accessible), and care is exercised in
the replacement of amino acid residues that may have a significant
effect on the tertiary structure of V region domains, such as
proline, glycine, and charged amino acids.
[0095] In this manner, the resultant "veneered" antigen-binding
sites are thus designed to retain the rodent CDR residues, the
residues substantially adjacent to the CDRs, the residues
identified as buried or mostly buried (solvent inaccessible), the
residues believed to participate in non-covalent (e.g.,
electrostatic and hydrophobic) contacts between heavy and light
chain domains, and the residues from conserved structural regions
of the FRs which are believed to influence the "canonical" tertiary
structures of the CDR loops. These design criteria are then used to
prepare recombinant nucleotide sequences that combine the CDRs of
both the heavy and light chain of a antigen-binding site into
human-appearing FRs that can be used to transfect mammalian cells
for the expression of recombinant human antibodies that exhibit the
antigen specificity of the rodent antibody molecule.
[0096] An additional method for selecting antibodies that
specifically bind to a TGF-beta binding protein or variant or
fragment thereof is by phage display. See, e.g., Winter et al.,
1994 Annu. Rev. Immunol. 12:433-55; Burton et al., 1994 Adv.
Immunol. 57:191-280. Human or murine immunoglobulin variable region
gene combinatorial libraries may be created in phage vectors that
can be screened to select Ig fragments (Fab, Fv, sFv, or multimers
thereof) that bind specifically to TGF-beta binding protein or
variant or fragment thereof. See, e.g., U.S. Pat. No. 5,223,409;
Huse et al., 1989 Science 246:1275-81; Sastry et al., Proc. Natl.
Acad. Sci. USA 86:5728-32 (1989); Alting-Mees et al., Strategies in
Molecular Biology 3:1-9 (1990); Kang et al., 1991 Proc. Natl. Acad.
Sci. USA 88:4363-66; Hoogenboom et al., 1992 J. Molec. Biol.
227:381-388; Schlebusch et al., 1997 Hybridoma 16:47-52 and
references cited therein. For example, a library containing a
plurality of polynucleotide sequences encoding Ig variable region
fragments may be inserted into the genome of a filamentous
bacteriophage, such as M13 or a variant thereof, in frame with the
sequence encoding a phage coat protein. A fusion protein may be a
fusion of the coat protein with the light chain variable region
domain and/or with the heavy chain variable region domain.
According to certain embodiments, immunoglobulin Fab fragments may
also be displayed on a phage particle (see, e.g., U.S. Pat. No.
5,698,426).
[0097] Heavy and light chain immunoglobulin cDNA expression
libraries may also be prepared in lambda phage, for example, using
.lamda.ImmunoZap.TM.(H) and .lamda. ImmunoZap.TM.(L) vectors
(Stratagene, La Jolla, Calif.). Briefly, mRNA is isolated from a B
cell population, and used to create heavy and light chain
immunoglobulin cDNA expression libraries in the .lamda.ImmunoZap(H)
and .lamda.ImmunoZap(L) vectors. These vectors may be screened
individually or co-expressed to form Fab fragments or antibodies
(see Huse et al., supra; see also Sastry et al., supra). Positive
plaques may subsequently be converted to a non-lytic plasmid that
allows high level expression of monoclonal antibody fragments from
E. coli.
[0098] Similarly, portions or fragments, such as Fab and Fv
fragments, of antibodies may also be constructed using conventional
enzymatic digestion or recombinant DNA techniques to incorporate
the variable regions of a gene that encodes a antibody specific for
a TGF-beta binding protein. Within one embodiment, in a hybridoma
the variable regions of a gene expressing a monoclonal antibody of
interest are amplified using nucleotide primers. These primers may
be synthesized by one of ordinary skill in the art, or may be
purchased from commercially available sources. (See, e.g.,
Stratagene (La Jolla, Calif.), which sells primers for mouse and
human variable regions including, among others, primers for
V.sub.Ha, V.sub.Hb, V.sub.Hc, V.sub.Hd, C.sub.H1, V.sub.L and
C.sub.L regions.) These primers may be used to amplify heavy or
light chain variable regions, which may then be inserted into
vectors such as ImmunoZAP.TM. H or ImmunoZAP.TM. L (Stratagene),
respectively. These vectors may then be introduced into E. coli,
yeast, or mammalian-based systems for expression. Large amounts of
a single-chain protein containing a fusion of the V.sub.H and
V.sub.L domains may be produced using these methods (see Bird et
al., Science 242:423-426, 1988). In addition, such techniques may
be used to humanize a non-human antibody V region without altering
the binding specificity of the antibody.
[0099] In certain particular embodiments of the invention,
combinatorial phage libraries may also be used for humanization of
non-human variable regions. See, e.g., Rosok et al., 1996 J. Biol.
Chem. 271:22611-18; Rader et al., 1998 Proc. Natl. Acad. Sci. USA
95:8910-15. A phage library may be screened to select an Ig
variable region fragment of interest by immunodetection methods
known in the art and described herein, and the DNA sequence of the
inserted immunoglobulin gene in the phage so selected may be
determined by standard techniques. See, Sambrook et al., 2001
Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press.
The selected Ig-encoding sequence may then be cloned into another
suitable vector for expression of the Ig fragment or, optionally,
may be cloned into a vector containing Ig constant regions, for
expression of whole immunoglobulin chains.
[0100] In certain other embodiments, the invention contemplates
SOST-specific antibodies that are multimeric antibody fragments.
Useful methodologies are described generally, for example in Hayden
et al. 1997, Curr Opin. Immunol. 9:201-12; Coloma et al., 1997 Nat.
Biotechnol. 15:159-63. For example, multimeric antibody fragments
may be created by phage techniques to form miniantibodies (U.S.
Pat. No. 5,910,573) or diabodies (Holliger et al., 1997, Cancer
Immunol. Immunother. 45:128-130).
[0101] In certain embodiments of the invention, an antibody
specific for SOST may be an antibody that is expressed as an
intracellular protein. Such intracellular antibodies are also
referred to as intrabodies and may comprise an Fab fragment, or
preferably comprise a scFv fragment (see, e.g., Lecerf et al.,
Proc. Natl. Acad. Sci. USA 98:4764-49 (2001). The framework regions
flanking the CDR regions can be modified to improve expression
levels and solubility of an intrabody in an intracellular reducing
environment (see, e.g., Worn et al., J. Biol. Chem. 275:2795-803
(2000). An intrabody may be directed to a particular cellular
location or organelle, for example by constructing a vector that
comprises a polynucleotide sequence encoding the variable regions
of an intrabody that may be operatively fused to a polynucleotide
sequence that encodes a particular target antigen within the cell
(see, e.g., Graus-Porta et al., Mol. Cell. Biol. 15:1182-91 (1995);
Lener et al., Eur. J. Biochem. 267:1196-205 (2000)). An intrabody
may be introduced into a cell by a variety of techniques available
to the skilled artisan including via a gene therapy vector, or a
lipid mixture (e.g., Provectin.TM. manufactured by Imgenex
Corporation, San Diego, Calif.), or according to photochemical
internalization methods.
[0102] Introducing amino acid mutations into an immunoglobulin
molecule specific for a TGF-beta binding protein may be useful to
increase the specificity or affinity for TGF-beta binding protein
or to alter an effector function. Immunoglobulins with higher
affinity for TGF-beta binding protein may be generated by
site-directed mutagenesis of particular residues. Computer assisted
three-dimensional molecular modeling may be employed to identify
the amino acid residues to be changed, in order to improve affinity
for the TGF-beta binding protein. See, e.g., Mountain et al., 1992,
Biotechnol. Genet. Eng. Rev. 10:1-142. Alternatively, combinatorial
libraries of CDRs may be generated in M13 phage and screened for
immunoglobulin fragments with improved affinity. See, e.g., Glaser
et al., 1992, J. Immunol. 149:3903-3913; Barbas et al., 1994 Proc.
Natl. Acad. Sci. USA 91:3809-13; U.S. Pat. No. 5,792,456.
[0103] Effector functions may also be altered by site-directed
mutagenesis. See, e.g., Duncan et al., 1988 Nature 332:563-64;
Morgan et al., 1995 Immunology 86:319-24; Eghtedarzedeh-Kondri et
al., 1997 Biotechniques 23:830-34. For example, mutation of the
glycosylation site on the Fc portion of the immunoglobulin may
alter the ability of the immunoglobulin to fix complement. See,
e.g., Wright et al., 1997 Trends Biotechnol. 15:26-32. Other
mutations in the constant region domains may alter the ability of
the immunoglobulin to fix complement, or to effect
antibody-dependent cellular cytotoxicity. See, e.g., Duncan et al.,
1988 Nature 332:563-64; Morgan et al., 1995 Immunology 86:319-24;
Sensel et al., 1997 Mol. Immunol. 34:1019-29.
[0104] According to certain embodiments, non-human, human, or
humanized heavy chain and light chain variable regions of any of
the Ig molecules described herein may be constructed as single
chain Fv (scFv) polypeptide fragments (single chain antibodies).
See, e.g., Bird et al., 1988 Science 242:423-426; Huston et al.,
1988 Proc. Natl. Acad. Sci. USA 85:5879-5883. Multi-functional scFv
fusion proteins may be generated by linking a polynucleotide
sequence encoding an scFv polypeptide in-frame with at least one
polynucleotide sequence encoding any of a variety of known effector
proteins. These methods are known in the art, and are disclosed,
for example, in EP-BI-0318554, U.S. Pat. No. 5,132,405, U.S. Pat.
No. 5,091,513, and U.S. Pat. No. 5,476,786. By way of example,
effector proteins may include immunoglobulin constant region
sequences. See, e.g., Hollenbaugh et al., 1995 J. Immunol. Methods
188:1-7. Other examples of effector proteins are enzymes. As a
non-limiting example, such an enzyme may provide a biological
activity for therapeutic purposes (see, e.g., Siemers et al., 1997
Bioconjug. Chem. 8:510-19), or may provide a detectable activity,
such as horseradish peroxidase-catalyzed conversion of any of a
number of well-known substrates into a detectable product, for
diagnostic uses. Still other examples of scFv fusion proteins
include Ig-toxin fusions, or immunotoxins, wherein the scFv
polypeptide is linked to a toxin.
[0105] The scFv or any antibody fragment described herein may, in
certain embodiments, be fused to peptide or polypeptide domains
that permits detection of specific binding between the fusion
protein and antigen (e.g., a TGF-beta binding protein). For
example, the fusion polypeptide domain may be an affinity tag
polypeptide for detecting binding of the scFv fusion protein to a
TGF-beta binding protein by any of a variety of techniques with
which those skilled in the art will be familiar. Examples of a
peptide tag, include avidin, streptavidin or His (e.g.,
polyhistidine). Detection techniques may also include, for example,
binding of an avidin or streptavidin fusion protein to biotin or to
a biotin mimetic sequence (see, e.g., Luo et al., 1998 J.
Biotechnol. 65:225 and references cited therein), direct covalent
modification of a fusion protein with a detectable moiety (e.g., a
labeling moiety), non-covalent binding of the fusion protein to a
specific labeled reporter molecule, enzymatic modification of a
detectable substrate by a fusion protein that includes a portion
having enzyme activity, or immobilization (covalent or
non-covalent) of the fusion protein on a solid-phase support. Other
useful affinity polypeptides for construction of scFv fusion
proteins may include streptavidin fusion proteins, as disclosed,
for example, in WO 89/03422, U.S. Pat. No. 5,489,528, U.S. Pat. No.
5,672,691, WO 93/24631, U.S. Pat. No. 5,168,049, U.S. Pat. No.
5,272,254; avidin fusion proteins (see, e.g., EP 511,747); an
enzyme such as glutathione-S-transferase; and Staphylococcus aureus
protein A polypeptide.
[0106] The polynucleotides encoding an antibody or fragment thereof
that specifically bind a TGF-beta binding protein, as described
herein, may be propagated and expressed according to any of a
variety of well-known procedures for nucleic acid excision,
ligation, transformation, and transfection using any number of
known expression vectors. Thus, in certain embodiments expression
of an antibody fragment may be preferred in a prokaryotic host,
such as Escherichia coli (see, e.g., Pluckthun et al., 1989 Methods
Enzymol. 178:497-515). In certain other embodiments, expression of
the antibody or a fragment thereof may be preferred in a eukaryotic
host cell, including yeast (e.g., Saccharomyces cerevisiae,
Schizosaccharomyces pombe, and Pichia pastoris), animal cells
(including mammalian cells) or plant cells. Examples of suitable
animal cells include, but are not limited to, myeloma (such as a
mouse NSO line), COS, CHO, or hybridoma cells. Examples of plant
cells include tobacco, corn, soybean, and rice cells.
[0107] One or more replicable expression vectors containing DNA
encoding a variable and/or constant region may be prepared and used
to transform an appropriate cell line, for example, a non-producing
myeloma cell line, such as a mouse NSO line or a bacteria, such as
E. coli, in which production of the antibody will occur. In order
to obtain efficient transcription and translation, the DNA sequence
in each vector should include appropriate regulatory sequences,
particularly a promoter and leader sequence operatively linked to
the variable domain sequence. Particular methods for producing
antibodies in this way are generally well known and routinely used.
For example, basic molecular biology procedures are described by
Maniatis et al. (Molecular Cloning, A Laboratory Manual, 2nd ed.,
Cold Spring Harbor Laboratory, New York, 1989; see also Maniatis et
al, 3rd ed., Cold Spring Harbor Laboratory, New York, (2001)). DNA
sequencing can be performed as described in Sanger et al (PNAS
74:5463, (1977)) and the Amersham International plc sequencing
handbook, and site directed mutagenesis can be carried out
according to methods known in the art (Kramer et al., Nucleic Acids
Res. 12:9441, (1984); Kunkel Proc. Natl. Acad. Sci. USA 82:488-92
(1985); Kunkel et al., Methods in Enzymol. 154:367-82 (1987); the
Anglian Biotechnology Ltd handbook). Additionally, numerous
publications describe techniques suitable for the preparation of
antibodies by manipulation of DNA, creation of expression vectors,
and transformation of appropriate cells (Mountain A and Adair, J R
in Biotechnology and Genetic Engineering Reviews (ed. Tombs, M P.
10, Chapter 1, 1992, Intercept, Andover, UK); International Patent
Specification No. WO 91/09967).
[0108] In certain embodiments, the antibody according to the
invention may have one or more effector or reporter molecules
attached to it. A reporter molecule may be a detectable moiety or
label such as an enzyme, cytotoxic agent or other reporter
molecule, including a dye, radionuclide, luminescent group,
fluorescent group, or biotin, or the like. The TGF-beta binding
protein-specific immunoglobulin or fragment thereof may be
radiolabeled for diagnostic or therapeutic applications. Techniques
for radiolabeling of antibodies are known in the art. See, e.g.,
Adams 1998 In Vivo 12:11-21; Hiltunen 1993 Acta Oncol. 32:831-9.
Therapeutic applications are described in greater detail below and
may include use of the TGF-beta binding protein specific antibody
(or fragment thereof) in conjunction with other therapeutic agents.
The effector or reporter molecules may be attached to the antibody
through any available amino acid side-chain, terminal amino acid,
or carbohydrate functional group located in the antibody, provided
that the attachment or attachment process does not adversely affect
the binding properties such that the usefulness of the molecule is
abrogated. Particular functional groups include, for example any
free amino, imino, thiol, hydroxyl, carboxyl, or aldehyde group.
Attachment of the antibody and the effector and/or reporter
molecule(s) may be achieved via such groups and an appropriate
functional group in the effector or reporter molecule. The linkage
may be direct or indirect through spacing or bridging groups.
[0109] Effector molecules include, for example, antineoplastic
agents, toxins (such as enzymatically active toxins of bacterial
(such as Pseudomonas aeruginosa exotoxin A) or plant origin and
fragments thereof (e.g., ricin and fragments thereof, plant
gelonin, bryodin from Byonia dioica, or the like. See, e.g., Thrush
et al., 1996 Annu. Rev. Immunol. 14:49-71; Frankel et al., 1996
Cancer Res. 56:926-32). Additional effector molecules include
biologically active proteins (for example, enzymes), nucleic acids
and fragments thereof, naturally occurring and synthetic polymers,
for example, polysaccharides and polyalkylene polymers such as
poly(ethylene glycol) and derivatives thereof, radionuclides,
particularly radioiodide, and chelated metals. Suitable reporter
groups include chelated metals, fluorescent compounds or compounds
that may be detected by NMR or ESR spectroscopy. Particularly
useful effector groups are calichaemicin and derivatives thereof
(see, for example, South African Patent Specifications Nos.
85/8794, 88/8127 and 90/2839).
[0110] Numerous other toxins, including chemotherapeutic agents,
anti-mitotic agents, antibiotics, inducers of apoptosis (or
"apoptogens", see, e.g., Green and Reed, 1998, Science
281:1309-1312), or the like, are known to those familiar with the
art, and the examples provided herein are intended to be
illustrative without limiting the scope and spirit of the
invention. Particular antineoplastic agents include cytotoxic and
cytostatic agents, for example alkylating agents, such as nitrogen
mustards (e.g., chlorambucil, melphalan, mechlorethamine,
cyclophosphamide, or uracil mustard) and derivatives thereof,
triethylenephosphoramide, triethylenethiophosphor-amide, busulphan,
or cisplatin; antimetabolites, such as methotrexate, fluorouracil,
floxuridine, cytarabine, mercaptopurine, thioguanine, fluoroacetic
acid or fluorocitric acid, antibiotics, such as bleomycins (e.g.,
bleomycin sulphate), doxorubicin, daunorubicin, mitomycins (e.g.,
mitomycin C), actinomycins (e.g., dactinomycin) plicamycin,
calichaemicin and derivatives thereof, or esperamicin and
derivatives thereof; mitotic inhibitors, such as etoposide,
vincristine or vinblastine and derivatives thereof; alkaloids, such
as ellipticine; polyols such as taxicin-I or taxicin-II; hormones,
such as androgens (e.g., dromostanolone or testolactone),
progestins (e.g., megestrol acetate or medroxyprogesterone
acetate), estrogens (e.g., dimethylstilbestrol diphosphate,
polyestradiol phosphate or estramustine phosphate) or antiestrogens
(e.g., tamoxifen); anthraquinones, such as mitoxantrone, ureas,
such as hydroxyurea; hydrazines, such as procarbazine; or
imidazoles, such as dacarbazine.
[0111] Chelated metals useful as effector molecules include
chelates of di- or tripositive metals having a coordination number
from 2 to 8 inclusive. Particular examples of such metals include
technetium (Tc), rhenium (Re), cobalt (Co), copper (Cu), gold (Au),
silver (Ag), lead (Pb), bismuth (Bi), indium (In), gallium (Ga),
yttrium (Y), terbium (Tb), gadolinium (Gd), and scandium (Sc). In
general the metal is preferably a radionuclide. Particular
radionuclides include .sup.99mTc, .sup.186Re, .sup.188R, .sup.58C,
.sup.60Co, .sup.67Cu, .sup.195Au, .sup.199Au, .sup.110Ag, .sup.203
Pb, .sup.206 Bi, .sup.207Bi, .sup.111In, .sup.67Ga, .sup.68Ga,
.sup.88Y, .sup.90Y, .sup.160Tb, .sup.153Gd, and .sup.47Sc. The
chelated metal may be for example one of the above types of metal
chelated with any suitable polydentate chelating agent, for example
acyclic or cyclic polyamines, polyethers, (e.g., crown ethers and
derivatives thereof), polyamides; porphyrins; and carbocyclic
derivatives. In general, the type of chelating agent will depend on
the metal in use. One particularly useful group of chelating agents
in conjugates according to the invention, however, comprises
acyclic and cyclic polyamines, especially polyaminocarboxylic
acids, for example diethylenetriaminepentaacetic acid and
derivatives thereof, and macrocyclic amines, e.g. cyclic tri-aza
and tetra-aza derivatives (for example, as described in
International Patent Specification No. WO 92/22583); and
polyamides, especially desferrioxamine and derivatives thereof.
[0112] When a thiol group in the antibody is used as the point of
attachment, the effector molecule may be attached according to a
reaction that occurs with a thiol-reactive group present in the
effector or reporter molecule. Examples of such groups include an
a-halocarboxylic acid or ester, such as iodoacetamide, an imide,
such as maleimide, a vinyl sulphone, or a disulphide. These and
other suitable linking procedures are generally and more
particularly described in International Patent Specifications Nos.
WO 93/06231, WO 92/22583, WO 90/091195, and WO 89/01476.
[0113] The invention also contemplates the generation of
anti-idiotype antibodies that recognize an antibody (or
antigen-binding fragment thereof) that specifically binds to a SOST
polypeptide as provided herein, or a variant or fragment thereof.
Anti-idiotype antibodies may be generated as polyclonal antibodies
or as monoclonal antibodies by the methods described herein, using
an anti-TGF-beta binding protein antibody (or antigen-binding
fragment thereof) as immunogen. Anti-idiotype antibodies or
fragments thereof may also be generated by any of the recombinant
genetic engineering methods described above, or by phage display
selection. An anti-idiotype antibody may react with the antigen
binding site of the anti-SOST antibody such that binding of the
antibody to a SOST polypeptide is competitively inhibited.
Alternatively, an anti-idiotype antibody as provided herein may not
competitively inhibit binding of an anti-TGF-beta binding protein
antibody to a TGF-beta binding protein.
[0114] In certain embodiments of the invention, an antibody that
specifically binds to SOST may be used to detect expression of the
SOST polypeptide. In certain particular embodiments, one antibody
or a panel of antibodies may be exposed to cells that express a
SOST polypeptide and expression of the SOST polypeptide may be
determined by detection using another SOST specific antibody that
binds to a different epitope than the antibody or antibodies first
used in the assay.
Assays for Selecting Agents that Increase Bone Density
[0115] As discussed above, the present invention provides methods
for selecting and/or isolating agents that are capable of
increasing bone density. In certain preferred embodiments, the
agent is an antibody that specifically binds to SOST (a TGF-beta
binding protein) or a variant or a fragment thereof. For example,
within one embodiment of the present invention, methods are
provided for determining whether an agent is capable of increasing
bone mineral content, comprising the steps of (a) contacting or
mixing a candidate agent with a TGF-beta binding protein and a
member of the TGF-beta family of proteins and (b) determining
whether the candidate agent stimulates signaling by the TGF-beta
family of proteins, or impairs or inhibits the binding of the
TGF-beta binding protein to one or more members of the TGF-beta
family of proteins. Within certain embodiments, the agent enhances
the ability of TGF-beta to function as a positive regulator of
mesenchymal cell differentiation.
[0116] In a preferred embodiment of the invention, a method is
provided for identifying an antibody that modulates a TGF-beta
signaling pathway comprising contacting an antibody that
specifically binds to a SOST polypeptide with a SOST peptide,
including but not limited to the peptides disclosed herein, under
conditions and for a time sufficient to permit formation of an
antibody plus (+) SOST (antibody/SOST) complex and then detecting
the level (e.g., quantifying the amount) of the SOST/antibody
complex to determine the presence of an antibody that modulates a
TGF-beta signaling pathway. The method may be performed using SPR
or any number of different immunoassays known in the art and
disclosed herein, including an ELISA, immunoblot, or the like. A
TGF-beta signaling pathway includes a signaling pathway by which a
BMP binds to a type I and a type II receptor on a cell to stimulate
or induce the pathway that modulates bone mineral content. In
certain preferred embodiments of the invention, an antibody that
specifically binds to SOST stimulates or enhances the pathway for
increasing bone mineral content. Such an antibody may be identified
using the methods disclosed herein to detect binding of an antibody
to SOST specific peptides.
[0117] The subject invention methods may also be used for
identifying antibodies that impair, inhibit (including
competitively inhibit), or prevent binding of a BMP to a SOST
polypeptide by detecting whether an antibody binds to SOST peptides
that are located in regions or portions of regions on SOST to which
a BMP binds, such as peptides at the amino terminal end of SOST and
peptides that include amino terminal amino acid residues and a
portion of the core region (docking core) of SOST (e.g., SEQ ID
NOs:2-19, 21-28, and 47-50). The methods of the present invention
may also be used to identify an antibody that impairs, prevents, or
inhibits, formation of SOST homodimers. Such an antibody that binds
specifically to SOST may be identified by detecting binding of the
antibody to peptides that are derived from the core or the carboxy
terminal region of SOST (e.g., SEQ ID NOs: 29-46 and 51-54).
[0118] Within other embodiments of the invention, methods are
provided for determining whether an agent is capable of increasing
bone mineral content, comprising the steps of (a) contacting a
candidate agent to cells that express a TGF-beta binding-protein
and (b) determining whether the expression of the TGF-beta
binding-protein in the exposed cells decreases or whether an
activity of the TGF-beta binding protein decreases, and thereby
determining whether the compound is capable of increasing bone
mineral content. Within one embodiment, the cells may include
spontaneously transformed or untransformed normal human bone from
bone biopsies or rat parietal bone osteoblasts.
[0119] Immunoassays may be used for detecting and quantifying the
expression of a TGF-beta binding protein and include, for example,
Countercurrent Immuno-Electrophoresis (CIEP), radioimmunoassays,
radioimmunoprecipitations, Enzyme-Linked Immuno-Sorbent Assays
(ELISA), immunoblot assays such as dot blot assays and Western
blots, inhibition or competition assays, and sandwich assays (see
U.S. Pat. Nos. 4,376,110 and 4,486,530; see also Antibodies: A
Laboratory Manual, supra). Such immunoassays may use an antibody
that is specific for a TGF-beta binding protein such as the
anti-sclerostin antibodies described herein, or may use an antibody
that is specific for a reporter molecule that is attached to the
TGF-beta binding protein. The level of polypeptide expression may
also be determined by quantifying the amount of TGF-beta binding
protein that binds to a TGF-beta binding protein ligand. By way of
example, binding of sclerostin in a sample to a BMP may be detected
by surface plasmon resonance. Alternatively, the level of
expression of mRNA encoding the specific TGF-beta binding protein
may be quantified.
[0120] In other embodiments, an antibody specific for SOST may be
used in a method, such as a competition assay, in which candidate
agents are screened to identify an agent that will compete with the
antibody for binding to the TGF-binding protein. The interaction
between an antibody and a TGF-beta protein may be determined using
immunoassay methods known in the art and described herein.
[0121] By way of example, a family member of the TGF-beta
superfamily, such as a TGF-beta binding protein or a TGF-beta
superfamily member that is a ligand of TGF-beta binding protein, is
first bound to a solid phase, followed by addition of a candidate
agent. A ligand of the TGF-beta superfamily member that is bound to
the solid phase is added concurrently or added in a subsequent
step, the solid phase washed, and the quantity of ligand that bound
to the family member determined, which indicates whether the
candidate agent blocks binding of the ligand to the TGF-beta
member. Alternatively, the ligand of the TGF-beta superfamily
member may be attached to the solid phase, and the TGF-beta
superfamily member may be added concurrently or subsequently to the
addition of the candidate molecule. The amount of ligand that binds
to the TGF-beta superfamily member can be measured by labeling the
ligand with a detectable molecule according to methods known in the
art and described herein. Alternatively, the binding of the ligand
to the TGF-beta superfamily member may be measured by adding one or
more detecting molecules, such as an antibody or fragment thereof
that specifically binds to the ligand and quantifying the amount of
the molecule that binds to the ligand. Agents that are suitable for
use in increasing bone mineral content as described herein are
those agents that decrease the binding of TGF-beta binding protein
to its ligand that is a member of the TGF-beta superfamily in a
statistically significant manner.
[0122] Within other embodiments of the invention, methods are
provided for determining whether an agent is capable of increasing
bone mineral content, comprising the steps of (a) contacting a
candidate agent to cells that express a TGF-beta protein and (b)
determining whether the activity of TGF-beta protein from the
exposed cells is altered, and therefrom determining whether the
compound is capable of increasing bone mineral content. Similar to
the methods described herein, a wide variety of methods may be used
to assess changes in TGF-beta binding-protein expression when a
cell producing the TGF-beta binding protein is exposed to a
selected test compound.
[0123] Within another embodiment of the present invention, methods
are provided for determining whether an agent is capable of
increasing bone mineral content, comprising the steps of (a)
contacting a candidate agent with a TGF-beta-binding-protein and a
selected member of the TGF-beta family of proteins, and (b)
determining whether the selected agent up-regulates the signaling
of the TGF-beta family of proteins or inhibits the binding of the
TGF-beta binding-protein to the TGF-beta family member. Within
certain embodiments, the molecule enhances the ability of a
TGF-beta family member to function as a positive regulator of
mesenchymal cell differentiation.
[0124] Similar to the above-described methods, a variety of methods
may be used to assess stimulation of a TGF-beta family member by a
test compound, such as an antibody that specifically binds to SOST.
One such representative method (see also Durham et al., Endo.
136:1374-1380) comprises attaching a TGF-beta family member, such
as a BMP (e.g., BMP-2, BMP-4, BMP-5, BMP-6, BMP-7) to the solid
phase at a concentration that is equivalent to its Kd. The
dissociation constant (Kd) may be determined according to methods
for measuring binding rate constants known in the art, such as
surface plasmon resonance using a BIAcore instrument according to
techniques known in the art and described by the manufacturer
(Biosensor, Piscataway, N.J.). A collection of antagonist candidate
agents is then added at a fixed concentration (typically, 20 .mu.M
for small organic molecule collections (an isolated organic small
molecule as used herein means that the molecule is greater than 90%
pure as determined according to methods well known in the art
(e.g., NMR, melting point) and 1 .mu.M for candidate antibodies).
An agent is considered an antagonist of this interaction when the
agent inhibits binding of the BMP to SOST, that is, a decrease in
the level of binding is observed, by at least 40%, preferably 50%
or 60%, and more preferably 80% or 90% compared to the level of BMP
binding to SOST that is observed in the absence of the agent. Such
an agent may be further evaluated as a potential inhibitor on the
basis of titration studies according to which its inhibition
constant and its influence on TGF-beta binding-protein binding
affinity is determined. Comparable specificity control assays may
also be conducted to establish the selectivity profile for the
identified antagonist according to studies using assays dependent
on the BMP ligand action (e.g. BMP/BMP receptor competition
study).
[0125] Within yet other embodiments of the present invention,
methods are provided for determining whether a candidate agent is
capable of increasing bone mineral content, comprising the step of
determining whether a candidate agent inhibits the binding of
TGF-beta binding-protein to bone, or an analogue thereof. As used
herein, it should be understood that bone or analogues thereof
refers to hydroxyapatite, or a surface composed of a powdered form
of bone, crushed bone or intact bone. Similar to the methods
described herein, a wide variety of methods may be used to assess
the inhibition of TGF-beta binding-protein localization to bone
matrix (see, e.g., Nicolas et al., Calcif Tissue Int. 47:206-12
(1995)).
[0126] While the methods described herein may refer to the analysis
of an individual candidate agent, the present invention should not
be so limited. In particular, the agent may be contained within a
mixture of candidate agents. As described herein, the candidate
agents may be small organic molecules or may be antibodies or
fragments thereof or other peptides or polypeptides. Antibodies or
fragments may be identified by screening a library of antibodies or
antibody fragments or prepared by methods described herein. Hence,
the recited methods may further comprise the step of isolating an
agent that inhibits the binding of TGF-beta binding-protein to a
TGF-beta family member.
[0127] In one embodiment of the invention, an antibody or
antigen-binding fragment thereof that specifically binds to a SOST
polypeptide is capable of competitively inhibiting binding of a
TGF-beta family member to the SOST polypeptide. The capability of
the antibody or antibody fragment to impair or blocking binding of
a TGF-beta family member, such as a BMP, to SOST may be determined
according to any of the methods described herein. The antibody or
fragment thereof that specifically binds to SOST may impair, block,
or prevent binding of a TGF-beta family member to SOST by impairing
SOST homodimer formation. An antibody that specifically binds to
SOST may also be used to identify an activity of SOST by inhibiting
or impairing SOST from binding to a BMP. Alternatively, the
antibody or fragment thereof may be incorporated in a cell-based
assay or in an animal model in which SOST has a defined activity to
determine whether the antibody alters (increases or decreases in a
statistically significant manner) that activity. An antibody or
fragment thereof that specifically binds to SOST may be used to
examine the effect of such an antibody in a signal transduction
pathway and thereby modulate (stimulate or inhibit) the signaling
pathway. Preferably, binding of an antibody to SOST results in a
stimulation or induction of a signaling pathway.
Production of Proteins
[0128] Polypeptides described herein include the TGF binding
protein sclerostin and variants thereof and antibodies or fragments
thereof that specifically bind to sclerostin. The polynucleotides
that encode these polypeptides include derivatives that are
substantially similar to the polynucleotides (and, when
appropriate, to the proteins including peptides and polypeptides
that are encoded by the polynucleotides and their derivatives). As
used herein, a nucleotide sequence is deemed to be "substantially
similar" if (a) the nucleotide sequence is derived from the coding
region of the polynucleotides described herein and includes, for
example, portions of the sequence or allelic variations of the
sequences discussed above, or alternatively, encodes a molecule
that inhibits the binding of TGF-beta binding-protein to a member
of the TGF-beta family; (b) the polynucleotide is capable of
hybridizing to polynucleotide as provided herein under moderate,
high or very high stringency (see Sambrook et al., Molecular
Cloning: A Laboratory Manual, 3nd ed., Cold Spring Harbor
Laboratory Press, NY, 2001); and/or (c) the polynucleotide
sequences are degenerate with respect to codon sequences for a
particular amino acid of the polynucleotide sequences described in
(a) or (b). Further, the nucleic acid molecule disclosed herein
includes both complementary and non-complementary sequences,
provided the sequences otherwise meet the criteria set forth
herein. Within the context of the present invention, high
stringency means standard hybridization conditions (e.g.,
5.times.SSPE, 0.5% SDS at 55-65.degree. C., or the equivalent;
5.times.SSPE (1.times.SSPE=180 mM sodium chloride; 10 mM sodium
phosphate; 1 mM EDTA (pH 7.7); 5.times.Denhardt's solution
(100.times.Denhardt's=2% (w/v) bovine serum albumin, 2% (w/v)
Ficoll, 2% (w/v) polyvinylpyrrolidone); and 0.5% SDS).
Post-hybridization washes at high stringency are typically
performed in 0.5.times.SSC (1.times.SSC=150 mM sodium chloride, 15
mM trisodium citrate) or in 0.5.times.SSPE at 55-60.degree.
C.).
[0129] Polynucleotides encoding SOST may be isolated from genomic
or cDNA libraries, from cells in a biological sample, tissues, or
cell lines, and prepared using any variety of techniques (see,
e.g., Sambrook, supra). For example, a polynucleotide may be
amplified from cDNA prepared from a suitable cell or tissue. These
polynucleotides may be amplified by polymerase chain reaction (PCR)
using sequence specific primers that are designed on the basis of
the sequences provided herein, and which may be purchased or
synthesized. Polynucleotides may also be obtained by screening cDNA
or genomic DNA libraries using sequence specific probes and
primers. General methods for screening libraries by PCR are
provided by, for example, Yu et al., "Use of the Polymerase Chain
Reaction to Screen Phage Libraries," in Methods in Molecular
Biology, Vol. 15: PCR Protocols: Current Methods and Applications,
White (ed.), pages 211-215 (Humana Press, Inc. 1993). Moreover,
techniques for using PCR to isolate related genes are described by,
for example, Preston, "Use of Degenerate Oligonucleotide Primers
and the Polymerase Chain Reaction to Clone Gene Family Members," in
Methods in Molecular Biology, Vol. 15: PCR Protocols: Current
Methods and Applications, White (ed.), pages 317-337 (Humana Press,
Inc. 1993).
[0130] The sequence of a TGF-beta binding-protein cDNA or TGF-beta
binding-protein genomic fragment can be determined using standard
methods. Moreover, the identification of genomic fragments
containing a TGF-beta binding-protein promoter or regulatory
element can be achieved using well-established techniques, such as
deletion analysis (see, generally, Ausubel (1995)).
[0131] As an alternative, a polynucleotide encoding a TGF-beta
binding-protein can be obtained by synthesizing DNA molecules using
mutually priming long oligonucleotides and the nucleotide sequences
described herein (see, e.g., Ausubel (1995) at pages 8-8 to 8-9).
If PCR is incorporated into the method DNA molecules at least two
kilobases in length can be synthesized (Adang et al., Plant Molec.
Biol. 21:1131, 1993; Bambot et al., PCR Methods and Applications
2:266, 1993; Dillon et al., "Use of the Polymerase Chain Reaction
for the Rapid Construction of Synthetic Genes," in Methods in
Molecular Biology, Vol. 15: PCR Protocols: Current Methods and
Applications, White (ed.), pages 263-268, (Humana Press, Inc.
1993); Holowachuk et al., PCR Methods Appl. 4:299, 1995).
[0132] Nucleic acid molecules encoding a variant TGF-beta
binding-protein can be obtained by screening various cDNA or
genomic libraries with polynucleotide probes having nucleotide
sequences based upon SEQ ID NO:55-57, 59, 61, 63, 65, 67, and 69,
using procedures described herein. TGF-beta binding-protein
polynucleotide variants can also be constructed synthetically. For
example, a nucleic acid molecule can be designed that encodes a
polypeptide having a conservative amino acid change when compared
with the amino acid sequence of SEQ ID NOs: 1, 20, 58, 60, 62, 64,
66, 68, or 70. That is, variants can be obtained that contain one
or more amino acid substitutions of SEQ ID NOs: 1, 20, 58, 60, 62,
64, 66, 68, or 70, in which an alkyl amino acid is substituted for
an alkyl amino acid in a TGF-beta binding-protein amino acid
sequence; an aromatic amino acid is substituted for an aromatic
amino acid in a TGF-beta binding-protein amino acid sequence; a
sulfur-containing amino acid is substituted for a sulfur-containing
amino acid in a TGF-beta binding-protein amino acid sequence; a
hydroxy-containing amino acid is substituted for a
hydroxy-containing amino acid in a TGF-beta binding-protein amino
acid sequence; an acidic amino acid is substituted for an acidic
amino acid in a TGF-beta binding-protein amino acid sequence; a
basic amino acid is substituted for a basic amino acid in a
TGF-beta binding-protein amino acid sequence; or a dibasic
monocarboxylic amino acid is substituted for a dibasic
monocarboxylic amino acid in a TGF-beta binding-protein amino acid
sequence.
[0133] Among the common amino acids, for example, a conservative
amino acid substitution is illustrated by a substitution among
amino acids within each of the following groups: (1) glycine,
alanine, valine, leucine, and isoleucine (non-polar alkyl
group-containing side chain); (2) phenylalanine, tyrosine, and
tryptophan (aromatic side chain) (3) serine and threonine (hydroxyl
group side chain), (4) aspartate and glutamate (carboxylic acid
group side chain); (5) glutamine and asparagines (amide
group-containing side chain) and (6) lysine, arginine and histidine
(amino group side chain). In making such substitutions, it is
important to, where possible, maintain the cysteine backbone
outlined in FIG. 1.
[0134] Conservative amino acid changes in SOST can be introduced by
substituting nucleotides for the nucleotides recited in any one of
SEQ ID NOs: 55-57, 59, 61, 63, 65, 67, or 69. Such conservative
amino acid variants can be obtained, for example, by
oligonucleotide-directed mutagenesis, linker-scanning mutagenesis,
mutagenesis using the polymerase chain reaction, and the like (see
Ausubel (1995) at pages 8-10 to 8-22; and McPherson (ed.), Directed
Mutagenesis: A Practical Approach (IRL Press 1991)). The functional
activity of such variants can be determined using standard methods
and assays described herein. Alternatively, a variant TGF-beta
binding-protein polypeptide retains the ability to specifically
bind to anti-SOST antibodies.
[0135] Routine deletion analyses of nucleic acid molecules can be
performed to obtain "functional fragments" of a nucleic acid
molecule that encodes a TGF-beta binding-protein polypeptide. By
way of illustration, DNA molecules having the nucleotide sequence
of any one of SEQ ID NOs:55-57, 59, 61, 63, 65, 67, or 69 can be
digested with Bal31 nuclease to obtain a series of nested
deletions. The fragments are then inserted into expression vectors
in proper reading frame, and the expressed polypeptides are
isolated and tested for activity, or for the ability to bind
anti-TGF-beta binding-protein antibodies. One alternative to
exonuclease digestion is to use oligonucleotide-directed
mutagenesis to introduce deletions or stop codons to specify
production of a desired fragment. Alternatively, particular
fragments of a TGF-beta binding-protein encoding polynucleotide can
be synthesized using the polymerase chain reaction. In addition to
assays and methods disclosed herein, standard techniques for
functional analysis of proteins are described by, for example,
Treuter et al., Molec. Gen. Genet. 240:113, 1993; Content et al.,
"Expression and preliminary deletion analysis of the 42 kDa 2-5A
synthetase induced by human interferon," in Biological Interferon
Systems, Proceedings of ISIR-TNO Meeting on Interferon Systems,
Cantell (ed.), pages 65-72 (Nijhoff 1987); Herschman, "The EGF
Receptor," in Control of Animal Cell Proliferation, Vol. 1, Boynton
et al., (eds.) pages 169-199 (Academic Press 1985); Coumailleau et
al., J. Biol. Chem. 270:29270, 1995; Fukunaga et al., J. Biol.
Chem. 270:25291, 1995; Yamaguchi et al., Biochem. Pharmacol.
50:1295, 1995; and Meisel et al., Plant Molec. Biol. 30:1,
1996.
[0136] The structure of the polypeptides encoded by the nucleic
acid molecules described herein may be predicted from the primary
translation products using the hydrophobicity plot function of, for
example, P/C Gene or Intelligenetics Suite (Intelligenetics,
Mountain View, Calif.), or according to the methods described by
Kyte and Doolittle (J. Mol. Biol. 157:105-132, 1982). Polypeptides
may be prepared in the form of acidic or basic salts or in neutral
form. In addition, individual amino acid residues may be modified
by oxidation or reduction. Furthermore, various substitutions,
deletions, or additions may be made to the amino acid or nucleic
acid sequences, the net effect of which is to retain or further
enhance or decrease the biological activity of the mutant or
wild-type protein. Preferably, a SOST variant, or a fragment
thereof retains or has enhanced ability to bind to a SOST specific
antibody. Moreover, due to degeneracy in the genetic code, for
example, the nucleotide sequences encoding the same amino acid
sequence may vary considerably.
[0137] Other derivatives of the proteins provided herein include
conjugates of the proteins with other proteins or polypeptides.
This may be accomplished, for example, by the synthesis of
N-terminal or C-terminal fusion proteins that may be added to
facilitate purification or identification of proteins (see U.S.
Pat. No. 4,851,341, see also, Hopp et al., Bio/Technology 6:1204,
1988.) Alternatively, fusion proteins such as FLAG.RTM./TGF-beta
binding-protein may be constructed in order to assist in the
identification, expression, and analysis of the protein.
[0138] Proteins described herein may be constructed using a wide
variety of techniques described herein. Further, mutations may be
introduced at particular loci by synthesizing oligonucleotides that
contain a mutant sequence that are flanked by restriction sites,
enabling ligation to fragments of the native sequence. Following
ligation, the resulting reconstructed sequence encodes a derivative
having the desired amino acid insertion, substitution, or
deletion.
[0139] Alternatively, oligonucleotide-directed site-specific (or
segment specific) mutagenesis procedures may be employed to provide
an altered polynucleotide having particular codons altered
according to the substitution, deletion, or insertion. Exemplary
methods of making the alterations set forth above are disclosed by
Walder et al. (Gene 42:133, 1986); Bauer et al. (Gene 37:73, 1985);
Craik (BioTechniques, January 1985, 12-19); Smith et al. (Genetic
Engineering: Principles and Methods, Plenum Press, 1981); and
Sambrook et al. (supra). Deletion or truncation derivatives of
proteins (e.g., a soluble extracellular portion) may also be
constructed by using convenient restriction endonuclease sites
adjacent to the desired deletion. Subsequent to restriction,
overhangs may be filled in and the DNA religated. Exemplary methods
of making the alterations set forth above are disclosed by Sambrook
et al. (Molecular Cloning: A Laboratory Manual, 3d Ed., Cold Spring
Harbor Laboratory Press (2001)).
[0140] Mutations that are made in the nucleic acid molecules
preferably preserve the reading frame of the coding sequences.
Furthermore, the mutations will preferably not create complementary
regions that when transcribed could hybridize to produce secondary
mRNA structures, such as loops or hairpins, which would adversely
affect translation of the mRNA. Although a mutation site may be
predetermined, it is not necessary that the nature of the mutation
per se be predetermined. For example, in order to select for
optimum characteristics of mutants at a given site, random
mutagenesis may be conducted at the target codon and the expressed
mutants screened for gain, loss, or retention of biological
activity. Alternatively, mutations may be introduced at particular
loci by synthesizing oligonucleotides containing a mutant sequence,
flanked by restriction sites enabling ligation to fragments of the
native sequence. Following ligation, the resulting reconstructed
sequence encodes a derivative having the desired amino acid
insertion, substitution, or deletion. Nucleic acid molecules that
encode proteins of the present invention may also be constructed
using techniques such as polymerase chain reaction (PCR)
mutagenesis, chemical mutagenesis (Drinkwater and Klinedinst, PNAS
83:3402-3406, 1986), forced nucleotide misincorporation (e.g., Liao
and Wise Gene 88:107-111, 1990), or use of randomly mutagenized
oligonucleotides (Horwitz et al., Genome 3:112-117, 1989).
[0141] The present invention also provides for the manipulation and
expression of the polynucleotides provided herein and of
polynucleotides encoding the subject invention antibodies by
culturing host cells containing a vector capable of expressing such
polynucleotides. An expression vector refers to recombinant nucleic
acid construct that is capable of directing the expression of
desired protein. The vector may be composed of deoxyribonucleic
acids (DNA), synthetic or cDNA-derived, ribonucleic acids (RNA), or
a combination of the two (e.g., a DNA-RNA chimera). A cDNA
polynucleotide is generally understood to mean a DNA polynucleotide
prepared by transcribing an RNA molecule, such as mRNA. These
vectors or vector constructs that include a polynucleotide sequence
encoding the desired protein preferably are operably linked to
suitable transcriptional or translational regulatory elements.
Suitable regulatory elements may be derived from a variety of
sources, including bacterial, fungal, viral, mammalian, insect, or
plant genes. Selection of appropriate regulatory elements is
dependent on the host cell chosen, and may be readily accomplished
by one of ordinary skill in the art. Examples of regulatory
elements include a transcriptional promoter and enhancer or RNA
polymerase binding sequence, a transcriptional terminator, and a
ribosomal binding sequence including a translation initiation
signal. Optionally, the vector may include a polyadenylation
sequence, one or more restriction sites, as well as one or more
selectable markers such as neomycin phosphotransferase or
hygromycin phosphotransferase or any other markers known in the
art. Additionally, depending on the host cell chosen and the vector
employed, other genetic elements such as an origin of replication,
additional nucleic acid restriction sites, enhancers, sequences
conferring inducibility of transcription, and selectable markers,
may also be incorporated into the vectors described herein.
[0142] Nucleic acid molecules that encode any of the proteins
described above may be readily expressed by a wide variety of
prokaryotic and eukaryotic host cells, including bacterial,
mammalian, yeast or other fungi, viral, insect, or plant cells.
Methods for transforming or transfecting such cells to express
foreign DNA are well known in the art (see, e.g., Itakura et al.,
U.S. Pat. No. 4,704,362; Hinnen et al., Proc. Natl. Acad. Sci. USA
75:1929-1933, 1978; Murray et al., U.S. Pat. No. 4,801,542; Upshall
et al., U.S. Pat. No. 4,935,349; Hagen et al., U.S. Pat. No.
4,784,950; Axel et al., U.S. Pat. No. 4,399,216; Goeddel et al.,
U.S. Pat. No. 4,766,075; and Sambrook et al. Molecular Cloning: A
Laboratory Manual, 3nd ed., Cold Spring Harbor Laboratory Press,
2001; for plant cells see Czako and Marton, Plant Physiol.
104:1067-1071, 1994; and Paszkowski et al., Biotech. 24:387-392,
1992).
[0143] Bacterial host cells suitable for carrying out the present
invention include E. coli BL21(DE3), BL21(DE3)pLysS,
BL21(DE3)pLysE, DH1, DH4I, DH5, DH5I, DH51F', DH51MCR, DH10B,
DH10B/p3, DH11S, C600, HB11, JM11, JM105, JM109, JM110, K38, RR1,
Y1088, Y1089, CSH18, ER1451, and ER1647 (see, for example, Brown
(Ed.), Molecular Biology Labfax (Academic Press 1991)); B. subtilis
(BR151, YB886, M1119, M1120, and B170 (see, for example, Hardy,
"Bacillus Cloning Methods," in DNA Cloning: A Practical Approach,
Glover (Ed.) (IRL Press 1985)); Salmonella typhimurium; and various
species within the genera Pseudomonas, Streptomyces, and
Staphylococcus, as well as many other bacterial species well known
to one of ordinary skill in the art. A representative example of a
bacterial host cell includes E. coli DH50.alpha. (Stratagene,
LaJolla, Calif.).
[0144] Bacterial expression vectors preferably comprise a promoter
that functions in the host cell, one or more selectable phenotypic
markers, and a bacterial origin of replication. Representative
promoters include the .beta.-lactamase (penicillinase) and lactose
promoter system (see Chang et al., Nature 275:615, 1978), the T7
RNA polymerase promoter (Studier et al., Meth. Enzymol. 185:60-89,
1990), the lambda promoter (Elvin et al., Gene 87:123-126, 1990),
the trp promoter (Nichols and Yanofsky, Meth. in Enzymology
101:155, 1983), and the tac promoter (Russell et al., Gene 20:231,
1982). Additional promoters include promoters capable of
recognizing the T4, T3, Sp6 and T7 polymerases, the P.sub.R and
P.sub.L promoters of bacteriophage lambda, the recA, heat shock,
lacUV5, tac, lpp-lacSpr, phoA, and lacZ promoters of E. coli,
promoters of B. subtilis, the promoters of the bacteriophages of
Bacillus, Streptomyces promoters, the int promoter of bacteriophage
lambda, the bla promoter of pBR322, and the CAT promoter of the
chloramphenicol acetyl transferase gene. Prokaryotic promoters have
been reviewed by Glick, J. Ind. Microbiol. 1:277, 1987, Watson et
al., Molecular Biology of the Gene, 4th Ed. (Benjamin Cummins
1987), and by Ausubel et al. (1995). Representative selectable
markers include various antibiotic resistance markers such as the
kanamycin or ampicillin resistance genes. Many plasmids suitable
for transforming host cells are well known in the art, including
among others, pBR322 (see Bolivar et al., Gene 2:95, 1977), the pUC
plasmids pUC18, pUC19, pUC118, pUC119 (see Messing, Meth. in
Enzymology 101:20-77, 1983 and Vieira and Messing, Gene 19:259-268,
1982), and pNH8A, pNH16a, pNH18a, and Bluescript M13 (Stratagene,
La Jolla, Calif.).
[0145] Yeast and fungi host cells suitable for carrying out the
present invention include, among others, Saccharomyces pombe,
Saccharomyces cerevisiae, the genera Pichia or Kluyveromyces and
various species of the genus Aspergillus (McKnight et al., U.S.
Pat. No. 4,935,349). Suitable expression vectors for yeast and
fungi include, among others, YCp50 (ATCC No. 37419) for yeast, and
the amdS cloning vector pV3 (Turnbull, Bio/Technology 7:169, 1989),
YRp7 (Struhl et al., Proc. Natl. Acad. Sci. USA 76:1035-1039,
1978), YEp13 (Broach et al., Gene 8:121-133, 1979), pJDB249 and
pJDB219 (Beggs, Nature 275:104-108, 1978) and derivatives
thereof.
[0146] Preferred promoters for use in yeast include promoters from
yeast glycolytic genes (Hitzeman et al., J. Biol. Chem.
255:12073-12080, 1980; Alber and Kawasaki, J. Mol. Appl. Genet.
1:419-434, 1982) or alcohol dehydrogenase genes (Young et al., in
Genetic Engineering of Microorganisms for Chemicals, Hollaender et
al. (eds.), p. 355, Plenum, New York, 1982; Ammerer, Meth. Enzymol.
101:192-201, 1983). Examples of useful promoters for fungi vectors
include those derived from Aspergillus nidulans glycolytic genes,
such as the adh3 promoter (McKnight et al., EMBO J. 4:2093-2099,
1985). The expression units may also include a transcriptional
terminator. An example of a suitable terminator is the adh3
terminator (McKnight et al., supra, 1985).
[0147] As with bacterial vectors, the yeast vectors will generally
include a selectable marker, which may be one of any number of
genes that exhibit a dominant phenotype for which a phenotypic
assay exists to enable transformants to be selected. Preferred
selectable markers are those that complement host cell auxotrophy,
provide antibiotic resistance, or enable a cell to utilize specific
carbon sources, and include leu2 (Broach et al., ibid.), ura3
(Botstein et al., Gene 8:17, 1979), or his3 (Struhl et al., ibid.).
Another suitable selectable marker is the cat gene, which confers
chloramphenicol resistance on yeast cells. Many yeast cloning
vectors have been designed and are readily available. These vectors
include YIp-based vectors such as YIp5, YRp vectors such as YRp17,
YEp vectors such as YEp13, and YCp vectors such as YCp19. One
skilled in the art will appreciate that a wide variety of suitable
vectors are available for expression in yeast cells.
[0148] Techniques for transforming fungi are well known in the
literature and have been described, for instance, by Beggs (ibid.),
Hinnen et al. (Proc. Natl. Acad. Sci. USA 75:1929-1933, 1978),
Yelton et al. (Proc. Natl. Acad. Sci. USA 81:1740-1747, 1984), and
Russell (Nature 301:167-169, 1983). The genotype of the host cell
may contain a genetic defect that is complemented by the selectable
marker present on the expression vector. Choice of a particular
host and selectable marker is well within the level of ordinary
skill in the art.
[0149] Protocols for the transformation of yeast are also well
known to those of ordinary skill in the art. For example,
transformation may be readily accomplished either by preparation of
spheroplasts of yeast with DNA (see Hinnen et al., PNAS USA
75:1929, 1978) or by treatment with alkaline salts such as LiCl
(see Itoh et al., J. Bacteriology 153:163, 1983). Transformation of
fungi may also be carried out using polyethylene glycol as
described by Cullen et al. (Bio/Technology 5:369, 1987).
[0150] Viral vectors include those that comprise a promoter that
directs the expression of an isolated nucleic acid molecule
encoding a desired protein as described above. A wide variety of
promoters may be used within the context of the present invention,
including for example, promoters such as MoMLV LTR; RSV LTR (e.g.,
Gorman et al., Proc. Natl. Acad. Sci. USA 79:6777, 1982); Friend
MuLV LTR; adenoviral promoter (Ohno et al., Science 265:781-784,
1994); neomycin phosphotransferase promoter/enhancer; late
parvovirus promoter (Koering et al., Hum. Gene Therap. 5:457-463,
1994); Herpes TK promoter (see, e.g., McKnight, Cell 31:355, 1982);
SV40 promoter (e.g., SV40 early promoter (Benoist et al., Nature
290:304, 1981); metallothionein IIa gene enhancer/promoter; mouse
metallothionein I gene (Hamer et al., J. Molec. Appl. Genet. 1:273,
1982); mouse mammary tumor virus promoter (see, generally,
Etcheverry, "Expression of Engineered Proteins in Mammalian Cell
Culture," in Protein Engineering: Principles and Practice, Cleland
et al. (eds.), pages 163-181 (John Wiley & Sons, Inc. 1996));
cytomegalovirus immediate early promoter, and the cytomegalovirus
immediate late promoter. Alternatively, a prokaryotic promoter,
such as the bacteriophage T3 RNA polymerase promoter, can be used
to control TGF-beta binding-protein gene expression in mammalian
cells if the prokaryotic promoter is regulated by a eukaryotic
promoter (Zhou et al., Mol. Cell. Biol. 10:4529, 1990; Kaufman et
al., Nuc. Acids Res. 19:4485, 1991).
[0151] Within particularly preferred embodiments of the invention,
the promoter is a tissue-specific promoter (see e.g., WO 91/02805;
EP 0,415,731; and WO 90/07936). Representative examples of suitable
tissue specific promoters include neural specific enolase promoter,
platelet derived growth factor beta promoter, bone morphogenic
protein promoter, human alpha1-chimaerin promoter, synapsin I
promoter and synapsin II promoter. In addition to the above-noted
promoters, other viral-specific promoters (e.g., retroviral
promoters (including those noted above, as well as others such as
HIV promoters), hepatitis, herpes (e.g., EBV), and bacterial,
fungal or parasitic (e.g., malarial) -specific promoters may be
utilized in order to target a specific cell or tissue that is
infected with a virus, bacteria, fungus, or parasite.
[0152] Mammalian cells suitable for carrying out the present
invention include, among others COS, CHO, SaOS, osteosarcomas,
KS483, MG-63, primary osteoblasts, and human or mammalian bone
marrow stroma. Additional mammalian host cells include African
green monkey kidney cells (Vero; ATCC CRL 1587), human embryonic
kidney cells (293-HEK; ATCC CRL 1573), baby hamster kidney cells
(BHK-21; ATCC CRL 8544), canine kidney cells (MDCK; ATCC CCL 34),
Chinese hamster ovary cells (CHO-K1; ATCC CCL61), rat pituitary
cells (GH1; ATCC CCL82), HeLa S3 cells (ATCC CCL2.2), rat hepatoma
cells (H-4-II-E; ATCC CRL 1548) SV40-transformed monkey kidney
cells (COS-1; ATCC CRL 1650) and murine embryonic cells (NIH-3T3;
ATCC CRL 1658).
[0153] Mammalian expression vectors for use in carrying out the
present invention will include a promoter capable of directing the
transcription of a cloned gene or cDNA. Preferred promoters include
viral promoters and cellular promoters. Bone specific promoters
include the promoter for bone sialo-protein and the promoter for
osteocalcin. Viral promoters include the cytomegalovirus immediate
early promoter (Boshart et al., Cell 41:521-530, 1985),
cytomegalovirus immediate late promoter, SV40 promoter (Subramani
et al., Mol. Cell. Biol. 1:854-864, 1981), MMTV LTR, RSV LTR,
metallothionein-1, adenovirus E1a. Cellular promoters include the
mouse metallothionein-1 promoter (Palmiter et al., U.S. Pat. No.
4,579,821), a mouse V.sub..kappa. promoter (Bergman et al., Proc.
Natl. Acad. Sci. USA 81:7041-7045, 1983; Grant et al., Nucleic
Acids Res. 15:5496, 1987) and a mouse V.sub.H promoter (Loh et al.,
Cell 33:85-93, 1983). The choice of promoter will depend, at least
in part, upon the level of expression desired or the recipient cell
line to be transfected.
[0154] Such expression vectors may also contain a set of RNA splice
sites located downstream from the promoter and upstream from the
DNA sequence encoding the peptide or protein of interest. Preferred
RNA splice sites may be obtained from adenovirus and/or
immunoglobulin genes. Also contained in the expression vectors is a
polyadenylation signal located downstream of the coding sequence of
interest. Suitable polyadenylation signals include the early or
late polyadenylation signals from SV40 (Kaufman and Sharp, ibid.),
the polyadenylation signal from the Adenovirus 5 E1B region and the
human growth hormone gene terminator (DeNoto et al., Nucleic Acids
Res. 9:3719-3730, 1981). The expression vectors may include a
noncoding viral leader sequence, such as the Adenovirus 2
tripartite leader, located between the promoter and the RNA splice
sites. Preferred vectors may also include enhancer sequences, such
as the SV40 enhancer. Expression vectors may also include sequences
encoding the adenovirus VA RNAs. Suitable expression vectors can be
obtained from commercial sources (e.g., Stratagene, La Jolla,
Calif.).
[0155] Vector constructs comprising cloned DNA sequences can be
introduced into cultured mammalian cells by, for example,
liposome-mediated transfection, calcium phosphate-mediated
transfection (Wigler et al., Cell 14:725, 1978; Corsaro and
Pearson, Somatic Cell Genetics 7:603, 1981; Graham and Van der Eb,
Virology 52:456, 1973), electroporation (Neumann et al., EMBO J.
1:841-845, 1982), or DEAE-dextran mediated transfection (Ausubel et
al. (eds.), Current Protocols in Molecular Biology, John Wiley and
Sons, Inc., NY, 1987); retroviral, adenoviral and protoplast
fusion-mediated transfection (see Sambrook et al., supra). Naked
vector constructs can also be taken up by muscular cells or other
suitable cells subsequent to injection into the muscle of a mammal
(or other animal). To identify cells that have been stably
transfected with the vector containing the cloned DNA, a selectable
marker is generally introduced into the cells along with the gene
or cDNA of interest. Preferred selectable markers for use in
cultured mammalian cells include genes that confer resistance to
drugs, such as neomycin, hygromycin, and methotrexate. The
selectable marker may be an amplifiable selectable marker.
Preferred amplifiable selectable markers are the DHFR gene and the
neomycin resistance gene. Selectable markers are reviewed by Thilly
(Mammalian Cell Technology, Butterworth Publishers, Stoneham,
Mass.).
[0156] Mammalian cells containing a suitable vector are allowed to
grow for a period of time, typically 1-2 days, to begin expressing
the DNA sequence(s) of interest. Drug selection is then applied to
select for growth of cells that are expressing the selectable
marker in a stable fashion. For cells that have been transfected
with an amplifiable, selectable marker, the drug concentration may
be increased in a stepwise manner to select for increased copy
number of the cloned sequences, thereby increasing expression
levels. Cells expressing the introduced sequences are selected and
screened for production of the protein of interest in the desired
form or at the desired level. Cells that satisfy these criteria can
then be cloned and scaled up for production.
[0157] Numerous insect host cells known in the art can also be
useful within the present invention. For example, baculoviruses as
vectors for expressing heterologous DNA sequences in insect cells
may be used (Atkinson et al., Pestic. Sci. 28:215-224 (1990)). The
baculovirus system provides an efficient means to introduce cloned
TGF-beta binding-protein encoding polynucleotides into insect
cells. Suitable expression vectors are based upon the Autographa
californica multiple nuclear polyhedrosis virus (AcMNPV), which
contain well known promoters such as Drosophila heat shock protein
(hsp) 70 promoter, Autographa californica nuclear polyhedrosis
virus immediate-early gene promoter (ie-1), and the delayed early
39K promoter, baculovirus p10 promoter, and the Drosophila
metallothionein promoter. Suitable insect host cells include cell
lines derived from IPLB-Sf-21, a Spodoptera frugiperda pupal
ovarian cell line, such as Sf9 (ATCC CRL 1711), Sf21AE, and Sf21
(Invitrogen Corporation; San Diego, Calif.), as well as Drosophila
Schneider-2 cells. Established techniques for producing recombinant
proteins in baculovirus systems are provided by Bailey et al.,
"Manipulation of Baculovirus Vectors," in Methods in Molecular
Biology, Volume 7: Gene Transfer and Expression Protocols, Murray
(ed.), pages 147-168 (The Humana Press, Inc. 1991); Patel et al.,
"The baculovirus expression system," in DNA Cloning 2: Expression
Systems, 2nd Edition, Glover et al. (eds.), pages 205-244 (Oxford
University Press 1995); Ausubel (1995) at pages 16-37 to 16-57, by
Richardson (ed.), Baculovirus Expression Protocols (The Humana
Press, Inc. 1995); and Lucknow, "Insect Cell Expression
Technology," in Protein Engineering Principles and Practice,
Cleland et al. (eds.), pages 183-218 (John Wiley & Sons, Inc.
1996).
[0158] Alternatively, numerous plant host cells are known in the
art and can also be useful for expressing polynucleotides, for
example, Agrobacterium rhizogenes (Sinkar et al. J. Biosci.
(Bangalore) 11:47-58, 1987). Expression vectors can also be
introduced into plant protoplasts, intact plant tissues, or
isolated plant cells. General methods of culturing plant tissues
are provided, for example, by Miki et al., "Procedures for
Introducing Foreign DNA into Plants," in Methods in Plant Molecular
Biology and Biotechnology, Glick et al. (eds.), pages 67-88 (CRC
Press, 1993).
[0159] Within related embodiments of the present invention,
proteins of the present invention may be expressed in a transgenic
animal whose germ cells and somatic cells contain a gene that
encodes the desired protein and that is operatively linked to a
promoter effective for the expression of the gene. Alternatively,
in a similar manner, transgenic animals may be prepared that lack
the desired gene (e.g., "knock-out" mice). Such transgenics may be
prepared in a variety of non-human animals, including mice, rats,
rabbits, sheep, dogs, goats, and pigs (see Hammer et al., Nature
315:680-683, 1985, Palmiter et al., Science 222:809-814, 1983,
Brinster et al., Proc. Natl. Acad. Sci. USA 82:4438-4442, 1985,
Palmiter and Brinster, Cell 41:343-345, 1985, and U.S. Pat. Nos.
5,175,383, 5,087,571, 4,736,866, 5,387,742, 5,347,075, 5,221,778,
and 5,175,384). Briefly, an expression vector, including a nucleic
acid molecule to be expressed together with appropriately
positioned expression control sequences, is introduced into
pronuclei of fertilized eggs, for example, by microinjection.
Integration of the injected DNA is detected by blot analysis of DNA
from tissue samples. It is preferred that the introduced DNA be
incorporated into the germ line of the animal so that it is passed
on to the animal's progeny. Tissue-specific expression may be
achieved through the use of a tissue-specific promoter, or through
the use of an inducible promoter, such as the metallothionein gene
promoter (Palmiter et al., 1983, supra), which allows regulated
expression of the transgene.
[0160] Proteins can be isolated by, among other methods, culturing
suitable host and vector systems to produce the recombinant
translation products of the present invention. Supernatants from
such cell lines, or protein inclusion bodies, or whole cells from
which the protein is not secreted into the supernatant, can then be
treated by a variety of purification procedures in order to isolate
the desired proteins. For example, the supernatant may be first
concentrated using commercially available protein concentration
filters, such as an Amicon or Millipore Pellicon ultrafiltration
unit. Following concentration, the concentrate may be applied to a
suitable purification matrix such as an affinity matrix, for
example, a specific antibody bound to a suitable support.
Alternatively, anion or cation exchange resins or size-exclusion
matrices may be employed in order to purify the protein. As a
further alternative, one or more reverse-phase high performance
liquid chromatography (RP-HPLC) steps may be used to further purify
the protein. Other methods of isolating the proteins of the present
invention are well known in the art. The purity of an isolated
protein or polypeptide may be determined by SDS-PAGE analysis
followed by Coomassie blue staining or by silver staining.
[0161] General methods for expressing and recovering foreign
protein produced by a mammalian cell system is provided by, for
example, Etcheverry, "Expression of Engineered Proteins in
Mammalian Cell Culture," in Protein Engineering: Principles and
Practice, Cleland et al. (eds.), pages 163 (Wiley-Liss, Inc. 1996).
Standard techniques for recovering protein produced by a bacterial
system is provided by, for example, Grisshammer et al.,
"Purification of over-produced proteins from E. coli cells," in DNA
Cloning 2: Expression Systems, 2nd Edition, Glover et al. (eds.),
pages 59-92 (Oxford University Press 1995). Established methods for
isolating recombinant proteins from a baculovirus system are
described by Richardson (ed.), Baculovirus Expression Protocols
(The Humana Press, Inc., 1995).
[0162] More generally, a TGF-beta binding-protein can be isolated
by standard techniques, such as affinity chromatography, size
exclusion chromatography, ion exchange chromatography, HPLC, and
the like. Additional variations in TGF-beta binding-protein
isolation and purification can be devised by those of skill in the
art. For example, anti-TGF-beta binding-protein antibodies,
obtained as described herein, can be used to isolate large
quantities of protein by immunoaffinity purification. Purification
of antibodies of the present invention are further described
herein.
Detectable Labels
[0163] A detectable label is a molecule or atom that can be
conjugated to a polypeptide (including an antibody or fragment
thereof) or a polynucleotide to produce a molecule useful for
diagnosis. Examples of detectable labels include chelators,
photoactive agents, radioisotopes, fluorescent agents, paramagnetic
ions, enzymes, and other marker moieties. A TGF binding protein or
an antibody that specifically binds to the TGF binding protein or
candidate molecules described above may be labeled with a variety
of compounds including, for example, fluorescent molecules, toxins,
and radionuclides. Representative examples of fluorescent molecules
include fluorescein, Phycobili proteins, such as phycoerythrin,
rhodamine, Texas red, and luciferase. Representative examples of
toxins include ricin, abrin diphtheria toxin, cholera toxin,
gelonin, pokeweed antiviral protein, tritin, Shigella toxin, and
Pseudomonas exotoxin A. Representative examples of radionuclides
include Cu-64, Ga-67, Ga-68, Zr-89, Ru-97, Tc-99m, Rh-105, Pd-109,
In-111, I-123, I-125, I-131, Re-186, Re-188, Au-198, Au-199,
Pb-203, At-211, Pb-212 and Bi-212. In addition, the antibodies
described above may also be labeled or conjugated to one partner of
a ligand binding pair. Representative examples include
avidin-biotin, streptavidin-biotin, and riboflavin-riboflavin
binding protein.
[0164] Methods for conjugating or labeling the molecules described
herein with the representative labels set forth above may be
readily accomplished by one of ordinary skill in the art (see
Trichothecene Antibody Conjugate, U.S. Pat. No. 4,744,981; Antibody
Conjugate, U.S. Pat. No. 5,106,951; Fluorogenic Materials and
Labeling Techniques, U.S. Pat. No. 4,018,884; Metal Radionuclide
Labeled Proteins for Diagnosis and Therapy, U.S. Pat. No.
4,897,255; and Metal Radionuclide Chelating Compounds for Improved
Chelation Kinetics, U.S. Pat. No. 4,988,496; see also Inman,
Methods In Enzymology, Vol. 34, Affinity Techniques, Enzyme
Purification: Part B, Jakoby and Wilchek (eds.), Academic Press,
New York, p. 30, 1974; see also Wilchek and Bayer, "The
Avidin-Biotin Complex in Bioanalytical Applications," Anal.
Biochem. 171:1-32, 1988). An immunoconjugate is a composition
comprising an antibody, such as an anti-TGF-beta binding protein
antibody, or an antibody fragment thereof, and a detectable label.
Preferably the antibody moiety of the immunoconjugate specifically
binds to its cognate antigen with the same or slightly reduced
binding affinity after conjugation as before conjugation.
Pharmaceutical Compositions
[0165] As noted above, the present invention also provides a
variety of pharmaceutical compositions, comprising one of the
above-described molecules that inhibits binding of the TGF-beta
binding-protein to a member of the TGF-beta family along with a
pharmaceutically or physiologically acceptable carrier, excipient,
or diluent. Any suitable carrier known to those of ordinary skill
in the art may be employed in the pharmaceutical compositions of
the present invention. Carriers for therapeutic use are well known,
and are described, for example, in Remingtons Pharmaceutical
Sciences, Mack Publishing Co. (A. R. Gennaro ed. (1985)).
Generally, such carriers should be nontoxic to recipients at the
dosages and concentrations employed. Ordinarily, the preparation of
such compositions entails combining the therapeutic agent with
buffers; antioxidants such as ascorbic acid, low molecular weight
(less than about 10 residues) polypeptides; proteins; amino acids;
carbohydrates including maltose, glucose, sucrose, or dextrins;
chelating agents such as EDTA; glutathione; and other stabilizers
and excipients. Neutral buffered saline or saline mixed with
nonspecific serum albumin are exemplary diluents. Alternatively,
compositions of the present invention may be formulated as a
lyophilizate.
[0166] In general, the type of carrier is selected based on the
mode of administration. Pharmaceutical compositions may be
formulated for any appropriate manner of administration, including,
for example, topical, oral, nasal, intrathecal, rectal, vaginal,
sublingual or parenteral administration, including subcutaneous,
intravenous, intramuscular, intrasternal, intracavernous,
intrameatal, or intraurethral injection or infusion. A
pharmaceutical composition (e.g., for oral administration or
delivery by injection) may be in the form of a liquid (e.g., an
elixir, syrup, solution, emulsion or suspension). A liquid
pharmaceutical composition may include, for example, one or more of
the following: sterile diluents such as water for injection, saline
solution, preferably physiological saline, Ringer's solution,
isotonic sodium chloride, fixed oils that may serve as the solvent
or suspending medium, polyethylene glycols, glycerin, propylene
glycol or other solvents; antibacterial agents; antioxidants;
chelating agents; buffers such as acetates, citrates or phosphates
and agents for the adjustment of tonicity such as sodium chloride
or dextrose. A parenteral preparation can be enclosed in ampoules,
disposable syringes or multiple dose vials made of glass or
plastic. The use of physiological saline is preferred, and an
injectable pharmaceutical composition is preferably sterile.
[0167] The compositions described herein may be formulated for
sustained release (i.e., a formulation such as a capsule or sponge
that effects a slow release of compound following administration).
Such compositions may generally be prepared using well known
technology and administered by, for example, oral, rectal or
subcutaneous implantation, or by implantation at the desired target
site. Sustained-release formulations may contain an agent dispersed
in a carrier matrix and/or contained within a reservoir surrounded
by a rate controlling membrane. Carriers for use within such
formulations are biocompatible, and may also be biodegradable;
preferably the formulation provides a relatively constant level of
active component release. The amount of active compound contained
within a sustained release formulation depends upon the site of
implantation, the rate and expected duration of release and the
nature of the condition to be treated or prevented. Illustrative
carriers useful in this regard include microparticles of
poly(lactide-co-glycolide), polyacrylate, latex, starch, cellulose,
dextran and the like. Other illustrative delayed-release carriers
include supramolecular biovectors, which comprise a non-liquid
hydrophilic core (e.g., a cross-linked polysaccharide or
oligosaccharide) and, optionally, an external layer comprising an
amphiphilic compound, such as a phospholipid (see e.g., U.S. Pat.
No. 5,151,254 and PCT applications WO 94/20078, WO/94/23701 and WO
96/06638).
[0168] In another illustrative embodiment, biodegradable
microspheres (e.g., polylactate polyglycolate) are employed as
carriers for the compositions of this invention. Suitable
biodegradable microspheres are disclosed, for example, in U.S. Pat.
Nos. 4,897,268; 5,075,109; 5,928,647; 5,811,128; 5,820,883;
5,853,763; 5,814,344, 5,407,609 and 5,942,252. Modified hepatitis B
core protein carrier systems, such as described in WO/99 40934, and
references cited therein, will also be useful for many
applications. Another illustrative carrier/delivery system employs
a carrier comprising particulate-protein complexes, such as those
described in U.S. Pat. No. 5,928,647, which are capable of inducing
a class I-restricted cytotoxic T lymphocyte responses in a
host.
[0169] In another illustrative embodiment, calcium phosphate core
particles are employed as carriers or as controlled release
matrices for the compositions of this invention. Exemplary calcium
phosphate particles are disclosed, for example, in published patent
application No. WO/0046147.
[0170] For pharmaceutical compositions comprising a polynucleotide
encoding an anti-SOST antibody and/or modulating agent (such that
the polypeptide and/or modulating agent is generated in situ), the
polynucleotide may be present within any of a variety of delivery
systems known to those of ordinary skill in the art, including
nucleic acid, and bacterial, viral and mammalian expression
systems. Techniques for incorporating DNA into such expression
systems are well known to those of ordinary skill in the art. The
DNA may also be "naked," as described, for example, in Ulmer et
al., Science 259:1745-1749, 1993 and reviewed by Cohen, Science
259:1691-1692, 1993. The uptake of naked DNA may be increased by
coating the DNA onto biodegradable beads, which are efficiently
transported into the cells.
[0171] The development of suitable dosing and treatment regimens
for using the particular compositions described herein in a variety
of treatment regimens, including e.g., oral, parenteral,
intravenous, intranasal, and intramuscular administration and
formulation, is well known in the art, some of which are briefly
discussed below for general purposes of illustration.
[0172] In certain applications, the pharmaceutical compositions
disclosed herein may be delivered via oral administration to an
animal. As such, these compositions may be formulated with an inert
diluent or with an assimilable edible carrier, or they may be
enclosed in hard- or soft-shell gelatin capsule, or they may be
compressed into tablets, or they may be incorporated directly with
the food of the diet.
[0173] In certain circumstances it will be desirable to deliver the
pharmaceutical compositions disclosed herein parenterally,
intravenously, intramuscularly, or even intraperitoneally. Such
approaches are well known to the skilled artisan, some of which are
further described, for example, in U.S. Pat. No. 5,543,158; U.S.
Pat. No. 5,641,515 and U.S. Pat. No. 5,399,363. In certain
embodiments, solutions of the active compounds as free base or
pharmacologically acceptable salts may be prepared in water
suitably mixed with a surfactant, such as hydroxypropylcellulose.
Dispersions may also be prepared in glycerol, liquid polyethylene
glycols, and mixtures thereof and in oils. Under ordinary
conditions of storage and use, these preparations generally will
contain a preservative to prevent the growth of microorganisms.
[0174] Illustrative pharmaceutical forms suitable for injectable
use include sterile aqueous solutions or dispersions and sterile
powders for the extemporaneous preparation of sterile injectable
solutions or dispersions (for example, see U.S. Pat. No.
5,466,468). In all cases the form must be sterile and must be fluid
to the extent that easy syringability exists. It must be stable
under the conditions of manufacture and storage and must be
preserved against the contaminating action of microorganisms, such
as bacteria and fungi. The carrier can be a solvent or dispersion
medium containing, for example, water, ethanol, polyol (e.g.,
glycerol, propylene glycol, and liquid polyethylene glycol, and the
like), suitable mixtures thereof, and/or vegetable oils. Proper
fluidity may be maintained, for example, by the use of a coating,
such as lecithin, by the maintenance of the required particle size
in the case of dispersion and/or by the use of surfactants. The
prevention of the action of microorganisms can be facilitated by
various antibacterial and antifungal agents, for example, parabens,
chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In
many cases, it will be preferable to include isotonic agents, for
example, sugars or sodium chloride. Prolonged absorption of the
injectable compositions can be brought about by the use in the
compositions of agents delaying absorption, for example, aluminum
monostearate and gelatin.
[0175] In one embodiment, for parenteral administration in an
aqueous solution, the solution should be suitably buffered if
necessary and the liquid diluent first rendered isotonic with
sufficient saline or glucose. These particular aqueous solutions
are especially suitable for intravenous, intramuscular,
subcutaneous and intraperitoneal administration. In this
connection, a sterile aqueous medium that can be employed will be
known to those of skill in the art in light of the present
disclosure. For example, one dosage may be dissolved in 1 ml of
isotonic NaCl solution and either added to 1000 ml of
hypodermoclysis fluid or injected at the proposed site of infusion,
(see for example, Remington's Pharmaceutical Sciences, 15th ed.,
pp. 1035-1038 and 1570-1580). Some variation in dosage will
necessarily occur depending on the condition of the subject being
treated. Moreover, for human administration, preparations will of
course preferably meet sterility, pyrogenicity, and the general
safety and purity standards as required by FDA Office of Biologics
standards.
[0176] In another embodiment of the invention, the compositions
disclosed herein may be formulated in a neutral or salt form.
Illustrative pharmaceutically-acceptable salts include the acid
addition salts (formed with the free amino groups of the protein)
and which are formed with inorganic acids such as, for example,
hydrochloric or phosphoric acids, or such organic acids as acetic,
oxalic, tartaric, mandelic, and the like. Salts formed with the
free carboxyl groups can also be derived from inorganic bases such
as, for example, sodium, potassium, ammonium, calcium, or ferric
hydroxides, and such organic bases as isopropylamine,
trimethylamine, histidine, procaine and the like. Upon formulation,
solutions will be administered in a manner compatible with the
dosage formulation and in such amount as is therapeutically
effective.
[0177] The carriers can further comprise any and all solvents,
dispersion media, vehicles, coatings, diluents, antibacterial and
antifungal agents, isotonic and absorption delaying agents,
buffers, carrier solutions, suspensions, colloids, and the like.
The use of such media and agents for pharmaceutical active
substances is well known in the art. Except insofar as any
conventional media or agent is incompatible with the active
ingredient, its use in the therapeutic compositions is
contemplated. Supplementary active ingredients can also be
incorporated into the compositions. The phrase
"pharmaceutically-acceptable" refers to molecular entities and
compositions that do not produce an allergic or similar untoward
reaction when administered to a human.
[0178] In certain embodiments, liposomes, nanocapsules,
microparticles, lipid particles, vesicles, and the like, are used
for the introduction of the compositions of the present invention
into suitable host cells/organisms. In particular, the compositions
of the present invention may be formulated for delivery either
encapsulated in a lipid particle, a liposome, a vesicle, a
nanosphere, or a nanoparticle or the like. Alternatively,
compositions of the present invention can be bound, either
covalently or non-covalently, to the surface of such carrier
vehicles.
[0179] The formation and use of liposome and liposome-like
preparations as potential drug carriers is generally known to those
of skill in the art (see for example, Lasic, Trends Biotechnol.
16(7):307-21, 1998; Takakura, Nippon Rinsho 56(3):691-95, 1998;
Chandran et al., Indian J. Exp. Biol. 35(8):801-09, 1997; Margalit,
Crit. Rev. Ther. Drug Carrier Syst. 12(2-3):233-61, 1995; U.S. Pat.
No. 5,567,434; U.S. Pat. No. 5,552,157; U.S. Pat. No. 5,565,213;
U.S. Pat. No. 5,738,868 and U.S. Pat. No. 5,795,587, each
specifically incorporated herein by reference in its entirety).
Liposomes have been used successfully with a number of cell types
that are normally difficult to transfect by other procedures,
including T cell suspensions, primary hepatocyte cultures and PC 12
cells (Renneisen et al., J. Biol. Chem. 265(27):16337-42, 1990;
Muller et al., DNA Cell Biol. 9(3):221-29, 1990). In addition,
liposomes are free of the DNA length constraints that are typical
of viral-based delivery systems. Liposomes have been used
effectively to introduce genes, various drugs, radiotherapeutic
agents, enzymes, viruses, transcription factors, allosteric
effectors and the like, into a variety of cultured cell lines and
animals. Furthermore, he use of liposomes does not appear to be
associated with autoimmune responses or unacceptable toxicity after
systemic delivery. In certain embodiments, liposomes are formed
from phospholipids that are dispersed in an aqueous medium and
spontaneously form multilamellar concentric bilayer vesicles (also
termed multilamellar vesicles (MLVs).
[0180] Alternatively, in other embodiments, the invention provides
for pharmaceutically-acceptable nanocapsule formulations of the
compositions of the present invention. Nanocapsules can generally
entrap compounds in a stable and reproducible way (see, for
example, Quintanar-Guerrero et al., Drug Dev. Ind. Pharm.
24(12):1113-28, 1998). To avoid side effects due to intracellular
polymeric overloading, such ultrafine particles (sized around 0.1
.mu.m) may be designed using polymers able to be degraded in vivo.
Such particles can be made as described, for example, by Couvreur
et al., Crit. Rev. Ther. Drug Carrier Syst. 5(1):1-20, 1988; zur
Muhlen et al., Eur. J. Pharm. Biopharm. 45(2):149-55, 1998; Zambaux
et al., J. Controlled Release 50(1-3):31-40, 1998; and U.S. Pat.
No. 5,145,684.
[0181] In addition, pharmaceutical compositions of the present
invention may be placed within containers, along with packaging
material that provides instructions regarding the use of such
pharmaceutical compositions. Generally, such instructions will
include a tangible expression describing the reagent concentration,
as well as within certain embodiments, relative amounts of
excipient ingredients or diluents (e.g., water, saline or PBS) that
may be necessary to reconstitute the pharmaceutical
composition.
Methods of Treatment
[0182] The present invention also provides methods for increasing
the mineral content and mineral density of bone. Briefly, numerous
conditions result in the loss of bone mineral content, including
for example, disease, genetic predisposition, accidents that result
in the lack of use of bone (e.g., due to fracture), therapeutics
that effect bone resorption or that kill bone forming cells, and
normal aging. Through use of the molecules described herein that
inhibit binding of the TGF-beta binding-protein to a TGF-beta
family member, such conditions may be treated or prevented. As used
herein, that bone mineral content is understood to have increased
if bone mineral content has increased in a statistically
significant manner at a selected site.
[0183] A wide variety of conditions that result in loss of bone
mineral content may be treated with the molecules described herein.
Patients with such conditions may be identified through clinical
diagnosis using well known techniques (see, e.g., Harrison's
Principles of Internal Medicine, McGraw-Hill, Inc.). Representative
examples of diseases that may be treated included dysplasias,
wherein growth or development of bone is abnormal. Representative
examples of such conditions include achondroplasia, cleidocranial
dysostosis, enchondromatosis, fibrous dysplasia, Gaucher's Disease,
hypophosphatemic rickets, Marfan's syndrome, multiple hereditary
exotoses, neurofibromatosis, osteogenesis imperfecta,
osteopetrosis, osteopoikilosis, sclerotic lesions, fractures,
periodontal disease, pseudoarthrosis, and pyogenic
osteomyelitis.
[0184] Other conditions that may be treated or prevented include a
wide variety of causes of osteopenia (i.e., a condition that causes
greater than one standard deviation of bone mineral content or
density below peak skeletal mineral content at youth).
Representative examples of such conditions include anemic states,
conditions caused by steroids, conditions caused by heparin, bone
marrow disorders, scurvy, malnutrition, calcium deficiency,
idiopathic osteoporosis, congenital osteopenia or osteoporosis,
alcoholism, chronic liver disease, senility, postmenopausal state,
oligomenorrhea, amenorrhea, pregnancy, diabetes mellitus,
hyperthyroidism, Cushing's disease, acromegaly, hypogonadism,
immobilization or disuse, reflex sympathetic dystrophy syndrome,
transient regional osteoporosis, and osteomalacia.
[0185] Within one embodiment of the present invention, bone mineral
content or density may be increased by administering to a
warm-blooded animal a therapeutically effective amount of a
molecule that inhibits a SOST polypeptide from binding to a
TGF-beta family member. Examples of warm-blooded animals that may
be treated include both vertebrates and mammals, including for
example humans, horses, cows, pigs, sheep, dogs, cats, rats, and
mice. Representative examples of therapeutic molecules include
ribozymes, ribozyme genes, antisense oligonucleotides, and
antibodies as described herein.
[0186] Within other embodiments of the present invention, methods
are provided for increasing bone density comprising the steps of
introducing into cells that home to bone, a vector that directs the
expression of a molecule that inhibits binding of SOST to a member
of the TGF-beta family, and administering the vector containing
cells to a warm-blooded animal. Briefly, cells that home to bone
may be obtained directly from the bone of patients (e.g., cells
obtained from the bone marrow such as CD34+, osteoblasts,
osteocytes, and the like), from peripheral blood, or from cultures.
Representative examples of suitable vectors include viral vectors
such as herpes viral vectors (e.g., U.S. Pat. No. 5,288,641);
adenoviral vectors (e.g., WO 94/26914, WO 93/9191; Kolls et al.,
Proc. Natl. Acad. Sci. USA 91(1):215-219, 1994; Kass-Eisler et al.,
Proc. Natl. Acad. Sci. USA 90(24):11498-502, 1993; Guzman et al.,
Circulation 88(6):2838-48, 1993; Guzman et al., Cir. Res.
73(6):1202-1207, 1993; Zabner et al., Cell 75(2):207-216, 1993; Li
et al., Hum. Gene Ther. 4(4):403-409, 1993; Caillaud et al., Eur.
J. Neurosci. 5(10:1287-1291, 1993; Vincent et al., Nat. Genet.
5(2):130-134, 1993; Jaffe et al., Nat. Genet. 1(5):372-378, 1992;
and Levrero et al., Gene 101(2):195-202, 1991); adeno-associated
viral vectors (WO 95/13365; Flotte et al., PNAS 90(22):10613-10617,
1993); baculovirus vectors; parvovirus vectors (Koering et al.,
Hum. Gene Therap. 5:457-463, 1994); pox virus vectors (Panicali and
Paoletti, Proc. Natl. Acad. Sci. USA 79:4927-4931, 1982; and Ozaki
et al., Biochem. Biophys. Res. Comm. 193(2):653-660, 1993), and
retroviruses (e.g., EP 0,415,731; WO 90/07936; WO 91/0285, WO
94/03622; WO 93/25698; WO 93/25234; U.S. Pat. No. 5,219,740; WO
93/11230; WO 93/10218). Viral vectors may likewise be constructed
that contain a mixture of different elements (e.g., promoters,
envelope sequences, and the like) from different viruses or from
non-viral sources. Within various embodiments, either the viral
vector itself, or a viral particle that contains the viral vector
may be used in the methods and compositions described below.
[0187] Within other embodiments of the invention, nucleic acid
molecules that encode a molecule that inhibits binding of a SOST
polypeptide to a member of the TGF-beta family themselves may be
administered by a variety of techniques including, for example,
administration of asialoosomucoid (ASOR) conjugated with
poly-L-lysine DNA complexes (Cristano et al., PNAS 92122-92126,
1993); DNA linked to killed adenovirus (Curiel et al., Hum. Gene
Ther. 3(2):147-154, 1992); cytofectin-mediated introduction
(DMRIE-DOPE, Vical, Calif.); direct DNA injection (Acsadi et al.,
Nature 352:815-818, 1991); DNA ligand (Wu et al., J. of Biol. Chem.
264:16985-16987, 1989); lipofection (Felgner et al., Proc. Natl.
Acad. Sci. USA 84:7413-7417, 1989); liposomes (Pickering et al.,
Circ. 89(1):13-21, 1994; and Wang et al., PNAS 84:7851-7855, 1987);
microprojectile bombardment (Williams et al., Proc. Natl. Acad.
Sci. USA 88:2726-2730, 1991); and direct delivery of nucleic acids
which encode the protein itself either alone (Vile and Hart, Cancer
Res. 53: 3860-3864, 1993), or utilizing PEG-nucleic acid
complexes.
[0188] Determination of increased bone mineral content may be
determined directly through the use of X-rays (e.g., Dual Energy
X-ray Absorptometry or "DEXA"), or by inference through bone
turnover markers such as osteoblast specific alkaline phosphatase,
osteocalcin, type 1 procollagen C' propeptide (PICP), and total
alkaline phosphatase (see Comier, Curr. Opin. in Rheu. 7:243
(1995)), or by markers of bone resorption including, but not
limited to, pyridinoline, deoxypryridinoline, N-telopeptide,
urinary hydroxyproline, plasma tartrate-resistant acid
phosphatases, and galactosyl hydroxylysine (see Comier, id.). The
amount of bone mass may also be calculated from body weights or by
using other methods (see Guinness-Hey, Metab. Bone Dis. Relat. Res.
5:177-181, 1984).
[0189] As will be evident to one of skill in the art, the amount
and frequency of administration will depend, of course, on such
factors as the nature and severity of the indication being treated,
the desired response, the condition of the patient, and so forth.
Typically, the compositions may be administered by a variety of
techniques, as noted above.
[0190] The following examples are offered by way of illustration,
and not by way of limitation.
EXAMPLES
Example 1
Modeling of Sclerostin Core Region
[0191] Homology recognition techniques (e.g., PSI-BLAST (Altschul
et al., Nucleic Acids Res. 25:3389-402 (1997)), FUGUE (Shi et al.,
J. Mol. Biol. 310:243-57 (2001)) suggested that the core region of
SOST (SOST_Core) adopts a cystine-knot fold. FUGUE is a sensitive
method for detecting homology between sequences and structures.
Human Chorionic Gonadotropin .beta. (hCG-.beta.), for which an
experimentally determined 3D structure is known, was identified by
FUGUE (Shi et al., supra) as the closest homologue of SOST_Core.
Therefore, hCG-.beta. was used as the structural template to build
3D models for SOST_Core.
[0192] An alignment of SOST_Core and its close homologues is shown
in FIG. 1. Among the homologues shown in the alignment, only
hCG-.beta. (CGHB) had known 3D structure. The sequence identity
between SOST_Core and hCG-.beta. was approximately 25%. Eight CYS
residues were conserved throughout the family, emphasizing the
overall structural similarity between SOST_Core and hCG-.beta..
Three pairs of cystines (1-5, 3-7, 4-8) formed disulfide bonds
(shown with solid lines in FIG. 1) in a "knot" configuration, which
is characteristic to the cystine-knot fold. An extra disulfide bond
(2-6), shown as a dotted line in FIG. 1, was unique to this family
and distinguished the family of proteins from other cystine-knot
families (e.g., TGF-.beta., BMP).
[0193] SOST_Core was modeled using PDB (Berman et al., Acta
Crystallogr. D. Biol. Cystallogr. 58(Pt 6 Pt1):899-907 (2002))
entry 1HCN, the 3D structure of hCG-.beta. (Wu et al., Structure
2:545-58 (1994)), as the structural template. Models were
calculated with MODELER (Sali & Blundell, J. Mol. Biol.
234:779-815 (1993)). A snapshot of the best model is shown in FIG.
2.
[0194] Most of the cystine-knot proteins form dimers because of the
lack of hydrophobic core in a monomer (Scheufler et al., supra;
Schlunegger and Grutter, J. Mol. Biol. 231:445-58 (1993)); Wu et
al., supra). SOST likely follows the same rule and forms a
homodimer to increase its stability. Constructing a model for the
dimerized SOST_Core region presented several challenges because (1)
the sequence similarity between SOST_Core and hCG-.beta. was low
(25%); (2) instead of a homodimer, hCG-.beta. formed a heterodimer
with hCG-.alpha.; and (3) a number of different relative
conformations of monomers have been observed in dimerized
cystine-knot proteins from different families (e.g., PDGF,
TGF-.beta., Neurotrophin, IL-17F, Gonadotropin), which suggested
that the dimer conformation of SOST could deviate significantly
from the hCG-.alpha./.beta. heterodimer conformation. In
constructing the model, hCG-.alpha. was replaced with hCG-.beta.
from the heterodimer structure (1HCN) using structure
superimposition techniques combined with manual adjustment, and
then a SOST_Core homodimer model was built according to the pseudo
hCG-.beta. homodimer structure. The final model is shown in FIG.
3.
Example 2
Modeling SOST-BMP Interaction
[0195] This example describes protein modeling of type I and type
II receptor binding sites on BMP that are involved with interaction
between BMP and SOST.
[0196] Competition studies demonstrated that SOST competed with
both type I and type II receptors for binding to BMP. In an
ELISA-based competition assay, BMP-6 selectively interacted with
the sclerostin-coated surface (300 ng/well) with high affinity
(K.sub.D=3.4 nM). Increasing amounts of BMP receptor IA (FC fusion
construct) competed with sclerostin for binding to BMP-6 (11 nM)
(IC.sub.50=114 nM). A 10-fold molar excess of the BMP receptor was
sufficient to reduce binding of sclerostin to BMP-6 by
approximately 50%. This competition was also observed with a BMP
receptor II-FC fusion protein (IC.sub.50=36 nM) and DAN
(IC.sub.50=43 nM). Specificity of the assay was shown by lack of
competition for binding to BMP-6 between sclerostin and a rActivin
R1B-FC fusion protein, a TGF-.beta. receptor family member that did
not bind BMP.
[0197] The type I and type II receptor binding sites on a BMP
polypeptide have been mapped and were spatially separated
(Scheufler et al., supra; Innis et al., supra; Nickel et al.,
supra; Hart et al. supra). Noggin, another BMP antagonist that
binds to BMP with high affinity, contacts BMP at both type I and
type II receptor binding sites via the N-terminal portion of Noggin
(Groppe et al., supra). The two .beta.-strands in the core region
near the C-terminal also contact BMP at the type II receptor
binding site.
[0198] A manually tuned alignment of Noggin and SOST indicated that
the two polypeptides shared sequence similarity between the
N-terminal portions of the proteins and between the core regions.
An amino acid sequence alignment is presented in FIG. 4. The
cysteine residues that form the characteristic cys-knot were
conserved between Noggin and SOST. The overall sequence identity
was 24%, and the sequence identity within the N-terminal binding
region (alignment positions 1-45) was 33%. Two residues in the
Noggin N-terminal binding region, namely Leu (L) at alignment
position 21 and Glu (E) at position 23, were reported to play
important roles in BMP binding (Groppe et al., supra). Both
residues were conserved in SOST as well. The sequence similarity
within the core region (alignment positions 131-228) was about 20%,
but the cys-knot scaffold was maintained and a sufficient number of
key residues was conserved, supporting the homology between Noggin
and SOST.
[0199] The Noggin structure was compared to SOST also to understand
how two SOST monomers dimerize. As shown in FIG. 5, the Noggin
structure suggested that the linker between the N-terminal region
and the core region not only played a role in connecting the two
regions, but also formed part of the dimerization interface between
two Noggin monomers. One major difference between Noggin and SOST
was that the linker between the N-terminal region and the core
region was much shorter in SOST.
[0200] The C-terminal region of SOST may play a role in SOST
dimerization. The sequence of Noggin ended with the core region,
while SOST had an extra C-terminal region. In the Noggin structure
a disulfide bond connected the C-termini of two Noggin monomers.
Thus, the C-terminal region of SOST started close to the interface
of two monomers and could contribute to dimerization. In addition,
secondary structure prediction shows that some portions of the
C-terminal region of SOST had a tendency to form helices. This
region in SOST may be responsible for the dimerization activity,
possibly through helix-helix packing, which mimicked the function
of the longer linker in Noggin. Another difference between the
structure of Noggin and SOST was the amino acid insertion in the
SOST core region at alignment positions 169-185 (see FIG. 4). This
insertion extended a .beta.-hairpin, which pointed towards the
dimerization interface in the Noggin structure (shown in FIG. 5 as
a loop region in the middle of the monomers and above the
C-terminal Cys residue). This elongated .beta.-hairpin could also
contribute to SOST dimerization.
Example 3
Design and Preparation of SOST Peptide Immunogens
[0201] This Example describes the design of SOST peptide immunogens
that are used for immunizing animals and generating antibodies that
block interactions between BMP and SOST and prevent dimer formation
of SOST monomers.
BMP Binding Fragments
[0202] The overall similarity between SOST and Noggin and the
similarity between the N-terminal regions of the two polypeptides
suggest that SOST may interact with BMP in a similar manner to
Noggin. That is, the N-terminal region of SOST may interact with
both the type I and type II receptor binding sites on BMP, and a
portion of the core region (amino acid alignment positions 190-220
in FIG. 4) may interact with the type II receptor binding site such
that antibodies specific for these SOST regions may block or impair
binding of BMP to SOST.
[0203] The amino acid sequences of these SOST polypeptide fragments
for rat and human SOST are provided as follows.
[0204] SOST_N_Linker: The N-terminal region (includes the short
linker that connects to the core region)
TABLE-US-00001 Human: (SEQ ID NO: 47)
QGWQAFKNDATEIIPELGEYPEPPPELENNKTMNRAENGGRPPHHPFET KDVSEYS Rat: (SEQ
ID NO: 48) QGWQAFKNDATEIIPGLREYPEPPQELENNQTMNRAENGGRPPHHPYDT
KDVSEYS
[0205] SOST_Core_Bind: Portion of the core region that is likely to
contact BMP at its type II receptor binding site (extended slightly
at both termini to include the CYS residue anchors):
TABLE-US-00002 Human: (SEQ ID NO: 49)
CIPDRYRAQRVQLLCPGGEAPRARKVRLVASC Rat: (SEQ ID NO: 50)
CIPDRYRAQRVQLLCPGGAAPRSRKVRLVASC
SOST Dimerization Fragments
[0206] The C-terminal region of SOST is likely to be involved in
the formation of SOST homodimers (see Example 2). The elongated
.beta.-hairpin may also play a role in homodimer formation.
Antibodies that specifically bind to such regions may prevent or
impair dimerization of SOST monomers, which may in turn interfere
with interaction between SOST and BMP. Polypeptide fragments in rat
and human SOST corresponding to these regions are as follows.
[0207] SOST_C: the C-terminal Region
TABLE-US-00003 Human: (SEQ ID NO: 51)
LTRFHNQSELKDFGTEAARPQKGRKPRPRARSAKANQAELENAY Rat: (SEQ ID NO: 52)
LTRFHNQSELKDFGPETARPQKGRKPRPRARGAKANQAELENAY
[0208] SOST_Core_Dimer: Portion of the core region that is likely
involved in SOST dimerization (extended slightly at both termini to
include the Cys residue anchors):
TABLE-US-00004 Human: CGPARLLPNAIGRGKWWRPSGPDFRC (SEQ ID NO: 53)
Rat: CGPARLLPNAIGRVKWWRPNGPDFRC (SEQ ID NO: 54)
BMP Binding Fragment at SOST N-terminus
[0209] The key N-terminal binding region of SOST (alignment
positions 1-35 in FIG. 4) was modeled on the basis of the
Noggin/BMP-7 complex structure (Protein Data Bank Entry No: 1M4U)
and the amino acid sequence alignment (see FIG. 4) to identify
amino acid residues of the SOST N-terminus that likely interact
with BMP. The model of SOST is presented in FIG. 6. In the
comparative model, phenylalanine (Phe, F) at alignment position 8
(see arrow and accompanying text) in the SOST sequence projects
into a hydrophobic pocket on the surface of the BMP dimer. The same
"knob-into-hole" feature has been observed in the BMP and type I
receptor complex structure (Nickel et al., supra), where Phe85 of
the receptor fits into the same pocket, which is a key feature in
ligand-type I receptor recognition for TGF-.beta. superfamily
members (including, for example, TGF-.beta. family, BMP family, and
the like). According to the model, a proline (Pro) directed turn is
also conserved, which allows the N-terminal binding fragment to
thread along the BMP dimer surface, traveling from type I receptor
binding site to type II receptor binding site on the other side of
the complex. Also conserved is another Pro-directed turn near the
carboxy end of the binding fragment, which then connects to the
linker region. Extensive contacts between SOST and BMP are evident
in FIG. 6.
Peptide Immunogens
[0210] Peptides were designed to encompass the SOST N-terminal
region predicted to make contact with BMP proteins. The peptide
sequences are presented below. For immunizing animals, the peptide
sequences were designed to overlap, and an additional cysteine was
added to the C-terminal end to facilitate crosslinking to KLH. The
peptides were then used for immunization. The peptide sequences of
the immunogens are as follows.
[0211] Human SOST:
TABLE-US-00005 QGWQAFKNDATEIIPELGEY (SEQ ID NO: 2)
TEIIPELGEYPEPPPELENN (SEQ ID NO: 3) PEPPPELENNKTMNRAENGG (SEQ ID
NO: 4) KTMNRAENGGRPPHHPFETK (SEQ ID NO: 5) RPPHHPFETKDVSEYS (SEQ ID
NO: 6)
[0212] Human SOST Peptides with Additional Cys:
TABLE-US-00006 QGWQAFKNDATEIIPELGEY-C (SEQ ID NO: 7)
TEIIPELGEYPEPPPELENN-C (SEQ ID NO: 8) PEPPPELENNKTMNRAENGG-C (SEQ
ID NO: 9) KTMNRAENGGRPPHHPFETK-C (SEQ ID NO: 10) RPPHHPFETKDVSEYS-C
(SEQ ID NO: 11)
[0213] Rat SOST:
TABLE-US-00007 QGWQAFKNDATEIIPGLREYPEPP (SEQ ID NO: 12)
PEPPQELENNQTMNRAENGG (SEQ ID NO: 13) ENGGRPPHHPYDTKDVSEYS (SEQ ID
NO: 14) TEIIPGLREYPEPPQELENN (SEQ ID NO: 15)
[0214] Rat SOST Peptides with Additional Cys:
TABLE-US-00008 QGWQAFKNDATEIIPGLREYPEPP-C (SEQ ID NO: 16)
PEPPQELENNQTMNRAENGG-C (SEQ ID NO: 17) ENGGRPPHHPYDTKDVSEYS-C (SEQ
ID NO: 18) TEIIPGLREYPEPPQELENN-C (SEQ ID NO: 19)
[0215] The following peptides were designed to contain the amino
acid portion of core region that was predicted to make contact with
BMP proteins. Cysteine was added at the C-terminal end of each
peptide for conjugation to KLH, and the conjugated peptides were
used for immunization. In the Docking Core N-terminal Peptide an
internal cysteine was changed to a serine to avoid double
conjugation to KLH.
[0216] For Human SOST:
[0217] Amino acid sequence without Cys residues added:
TABLE-US-00009 Docking_Core_N-terminal_Peptide: (SEQ ID NO: 21)
IPDRYRAQRVQLLCPGGEAP Docking_Core_Cterm_Peptide: (SEQ ID NO: 22)
QLLCPGGEAPRARKVRLVAS Docking_Core_N-terminal_Peptide: (SEQ ID NO:
23) IPDRYRAQRVQLLCPGGEAP-C Docking_Core_Cterm_Peptide: (SEQ ID NO:
24) QLLCPGGEAPRARKVRLVAS-C
[0218] For Rat SOST:
[0219] Amino acid sequence without Cys residues added or
substituted:
TABLE-US-00010 Docking_Core_N-terminal_Peptide: (SEQ ID NO: 25)
IPDRYRAQRVQLLCPGG Docking_Core_Cterm_Peptide: (SEQ ID NO: 26)
PGGAAPRSRKVRLVAS Peptide immunogens with Cys added and substituted:
Docking_Core_N-terminal_Peptide: (SEQ ID NO: 27)
IPDRYRAQRVQLLSPGG-C Docking_Core_Cterm_Peptide: (SEQ ID NO: 28)
PGGAAPRSRKVRLVAS-C
[0220] Two regions within SOST that potentially interact to form
SOST homodimers include the amino acids with the SOST core region
that are not present in Noggin. Human SOST peptides designed to
contain this sequence had a C-terminal or N-terminal Cys that was
conjugated to KLH. For the rat SOST peptide, a cysteine was added
to the carboxy terminus of the sequence (SEQ ID NO:31). The KLH
conjugated peptides were used for immunization.
[0221] For Human SOST:
TABLE-US-00011 CGPARLLPNAIGRGKWWRPS (SEQ ID NO: 29)
IGRGKWWRPSGPDFRC (SEQ ID NO: 30)
[0222] For Rat SOST:
TABLE-US-00012 PNAIGRVKWWRPNGPDFR (SEQ ID NO: 31) Rat SOST peptide
with cysteine added PNAIGRVKWWRPNGPDFR-C (SEQ ID NO: 32)
[0223] The second region within SOST that potentially interacts to
form SOST homodimers includes the C-terminal region. Peptide
immunogens were designed to include amino acid sequences within
this region (see below). For conjugation to KLH, a cysteine residue
was added to the C-terminal end, and the conjugated peptides were
used for immunization.
[0224] For Human SOST:
TABLE-US-00013 KRLTRFHNQS ELKDFGTEAA (SEQ ID NO: 33) ELKDFGTEAA
RPQKGRKPRP (SEQ ID NO: 34) RPQKGRKPRP RARSAKANQA (SEQ ID NO: 35)
RARSAKANQA ELENAY (SEQ ID NO: 36)
[0225] Peptide Immunogens with Cys Added at C-terminus:
TABLE-US-00014 KRLTRFHNQS ELKDFGTEAA-C (SEQ ID NO: 37) ELKDFGTEAA
RPQKGRKPRP-C (SEQ ID NO: 38) RPQKGRKPRP RARSAKANQA-C (SEQ ID NO:
39) RARSAKANQA ELENAY-C (SEQ ID NO: 40)
[0226] For Rat SOST:
TABLE-US-00015 KRLTRFHNQSELKDFGPETARPQ (SEQ ID NO: 41)
KGRKPRPRARGAKANQAELENAY (SEQ ID NO: 42) SELKDFGPETARPQKGRKPRPRAR
(SEQ ID NO: 43)
[0227] Peptide Immunogens with Cys Added at C-terminus:
TABLE-US-00016 KRLTRFHNQSELKDFGPETARPQ-C (SEQ ID NO: 44)
KGRKPRPRARGAKANQAELENAY-C (SEQ ID NO: 45)
SELKDFGPETARPQKGRKPRPRAR-C (SEQ ID NO: 46)
Example 4
Assay for Detecting Binding of Antibodies to a TGF-Beta
Binding-Protein
[0228] This example describes an assay for detecting binding of a
ligand, for example, an antibody or antibody fragment thereof, to
sclerostin.
[0229] A FLAG.RTM.-sclerostin fusion protein was prepared according
to protocols provided by the manufacturer (Sigma Aldrich, St.
Louis, Mo.) and as described in U.S. Pat. No. 6,395,511. Each well
of a 96 well microtiter plate is coated with anti-FLAG.RTM.
monoclonal antibody (Sigma Aldrich) and then blocked with 10% BSA
in PBS. The fusion protein (20 ng) is added to 100 .mu.l PBS/0.2%
BSA and adsorbed onto the 96-well plate for 60 minutes at room
temperature. This protein solution is removed and the wells are
washed to remove unbound fusion protein. A BMP, for example, BMP-4,
BMP-5, BMP-6, or BMP-7, is diluted in PBS/0.2% BSA and added to
each well at concentrations ranging from 10 .mu.M to 500 nM. After
an incubation for 2 hours at room temperature, the binding solution
is removed and the plate is washed three times with 200 .mu.l
volumes of PBS/0.2% BSA. Binding of the BMP to sclerostin is
detected using polyclonal antiserum or monoclonal antibody specific
for the BMP and an appropriate enzyme-conjugated second step
reagent according to standard ELISA techniques (see, e.g., Ausubel
et al., Current Protocols in Mol. Biol. Vol 2 11.2.1-11.2.22
(1998)). Specific binding is calculated by subtracting non-specific
binding from total binding and analyzed using the LIGAND program
(Munson and Podbard, Anal. Biochem. 107:220-39 (1980)).
[0230] Binding of sclerostin to a BMP is also detected by
homogeneous time resolved fluorescence detection (Mellor et al., J.
Biomol. Screening, 3:91-99 (1998)). A polynucleotide sequence
encoding sclerostin is operatively linked to a human immunoglobulin
constant region in a recombinant nucleic acid construct and
expressed as a human Fc-sclerostin fusion protein according to
methods known in the art and described herein. Similarly, a BMP
ligand is engineered and expressed as a BMP-mouse Fc fusion
protein. These two fusion proteins are incubated together and the
assay conducted as described by Mellor et al.
Example 5
Screening Assay for Antibodies that Inhibit Binding of TGF-Beta
Family Members to TGF-Beta Binding Protein
[0231] This example describes a method for detecting an antibody
that inhibits binding of a TGF-beta family member to sclerostin. An
ELISA is performed essentially as described in Example 4 except
that the BMP concentration is held fixed at its Kd (determined, for
example, by BIAcore analysis). In addition, an antibody or a
library or collection of antibodies is added to the wells to a
concentration of 1 .mu.M. Antibodies are incubated for 2 hours at
room temperature with the BMP and sclerostin, the solution removed,
and the bound BMP is quantified as described (see Example 4).
Antibodies that inhibit 40% of the BMP binding observed in the
absence of antibody are considered antagonists of this interaction.
These antibodies are further evaluated as potential inhibitors by
performing titration studies to determine their inhibition
constants and their effect on TGF-beta binding-protein binding
affinity. Comparable specificity control assays may also be
conducted to establish the selectivity profile for the identified
antagonist using assays dependent on the BMP ligand action (e.g., a
BMP/BMP receptor competition study).
Example 6
Inhibition of TGF-Beta Binding-Protein Localization to Bone
Matrix
[0232] Evaluation of inhibition of localization to bone matrix
(hydroxyapatite) is conducted using modifications to the method of
Nicolas (Calcif Tissue Int. 57:206-12 (1995)). Briefly,
.sup.125I-labelled TGF-beta binding-protein is prepared as
described by Nicolas (supra). Hydroxyapatite is added to each well
of a 96-well microtiter plate equipped with a polypropylene
filtration membrane (Polyfiltroninc, Weymouth Mass.). TGF-beta
binding-protein diluted in 0.2% albumin in PBS buffer is then added
to the wells. The wells containing matrix are washed 3 times with
0.2% albumin in PBS buffer. Adsorbed TGF-beta binding-protein is
eluted using 0.3 M NaOH and then quantified.
[0233] An antibody or other agent that inhibits or impairs binding
of the sclerostin TGF-beta binding protein to the hydroxyapatite is
identified by incubating the TGF-beta binding protein with the
antibody and applying the mixture to the matrix as described above.
The matrix is washed 3 times with 0.2% albumin in PBS buffer.
Adsorbed sclerostin is eluted with 0.3 M NaOH and then quantified.
An antibody that inhibits the level of binding of sclerostin to the
hydroxyapatite by at least 40% compared to the level of binding
observed in the absence of antibody is considered a bone
localization inhibitor. Such an antibody is further characterized
in dose response studies to determine its inhibition constant and
its effect on TGF-beta binding-protein binding affinity.
[0234] From the foregoing, although specific embodiments of the
invention have been described herein for purposes of illustration,
various modifications may be made without deviating from the spirit
and scope of the invention. Accordingly, the invention is not
limited except as by the appended claims.
Sequence CWU 1
1
1121190PRTHomo sapiens 1Gln Gly Trp Gln Ala Phe Lys Asn Asp Ala Thr
Glu Ile Ile Pro Glu1 5 10 15Leu Gly Glu Tyr Pro Glu Pro Pro Pro Glu
Leu Glu Asn Asn Lys Thr 20 25 30Met Asn Arg Ala Glu Asn Gly Gly Arg
Pro Pro His His Pro Phe Glu 35 40 45Thr Lys Asp Val Ser Glu Tyr Ser
Cys Arg Glu Leu His Phe Thr Arg 50 55 60Tyr Val Thr Asp Gly Pro Cys
Arg Ser Ala Lys Pro Val Thr Glu Leu65 70 75 80Val Cys Ser Gly Gln
Cys Gly Pro Ala Arg Leu Leu Pro Asn Ala Ile 85 90 95Gly Arg Gly Lys
Trp Trp Arg Pro Ser Gly Pro Asp Phe Arg Cys Ile 100 105 110Pro Asp
Arg Tyr Arg Ala Gln Arg Val Gln Leu Leu Cys Pro Gly Gly 115 120
125Glu Ala Pro Arg Ala Arg Lys Val Arg Leu Val Ala Ser Cys Lys Cys
130 135 140Lys Arg Leu Thr Arg Phe His Asn Gln Ser Glu Leu Lys Asp
Phe Gly145 150 155 160Thr Glu Ala Ala Arg Pro Gln Lys Gly Arg Lys
Pro Arg Pro Arg Ala 165 170 175Arg Ser Ala Lys Ala Asn Gln Ala Glu
Leu Glu Asn Ala Tyr 180 185 190220PRTHomo sapiens 2Gln Gly Trp Gln
Ala Phe Lys Asn Asp Ala Thr Glu Ile Ile Pro Glu1 5 10 15Leu Gly Glu
Tyr 20320PRTHomo sapiens 3Thr Glu Ile Ile Pro Glu Leu Gly Glu Tyr
Pro Glu Pro Pro Pro Glu1 5 10 15Leu Glu Asn Asn 20420PRTHomo
sapiens 4Pro Glu Pro Pro Pro Glu Leu Glu Asn Asn Lys Thr Met Asn
Arg Ala1 5 10 15Glu Asn Gly Gly 20520PRTHomo sapiens 5Lys Thr Met
Asn Arg Ala Glu Asn Gly Gly Arg Pro Pro His His Pro1 5 10 15Phe Glu
Thr Lys 20616PRTHomo sapiens 6Arg Pro Pro His His Pro Phe Glu Thr
Lys Asp Val Ser Glu Tyr Ser1 5 10 15721PRTArtificial SequenceHuman
SOST peptide fragment with additional cysteine added 7Gln Gly Trp
Gln Ala Phe Lys Asn Asp Ala Thr Glu Ile Ile Pro Glu1 5 10 15Leu Gly
Glu Tyr Cys 20821PRTArtificial SequenceHuman SOST peptide fragment
with additional cysteine added 8Thr Glu Ile Ile Pro Glu Leu Gly Glu
Tyr Pro Glu Pro Pro Pro Glu1 5 10 15Leu Glu Asn Asn Cys
20921PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 9Pro Glu Pro Pro Pro Glu Leu Glu Asn Asn
Lys Thr Met Asn Arg Ala1 5 10 15Glu Asn Gly Gly Cys
201021PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 10Lys Thr Met Asn Arg Ala Glu Asn Gly Gly
Arg Pro Pro His His Pro1 5 10 15Phe Glu Thr Lys Cys
201117PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 11Arg Pro Pro His His Pro Phe Glu Thr Lys
Asp Val Ser Glu Tyr Ser1 5 10 15Cys 1224PRTRattus norvegicus 12Gln
Gly Trp Gln Ala Phe Lys Asn Asp Ala Thr Glu Ile Ile Pro Gly1 5 10
15Leu Arg Glu Tyr Pro Glu Pro Pro 201320PRTRattus morvegicus 13Pro
Glu Pro Pro Gln Glu Leu Glu Asn Asn Gln Thr Met Asn Arg Ala1 5 10
15Glu Asn Gly Gly 201420PRTRattus norvegicus 14Glu Asn Gly Gly Arg
Pro Pro His His Pro Tyr Asp Thr Lys Asp Val1 5 10 15Ser Glu Tyr Ser
201520PRTRattus norvegicus 15Thr Glu Ile Ile Pro Gly Leu Arg Glu
Tyr Pro Glu Pro Pro Gln Glu1 5 10 15Leu Glu Asn Asn
201625PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 16Gln Gly Trp Gln Ala Phe Lys Asn Asp Ala
Thr Glu Ile Ile Pro Gly1 5 10 15Leu Arg Glu Tyr Pro Glu Pro Pro Cys
20 251721PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 17Pro Glu Pro Pro Gln Glu Leu Glu Asn Asn
Gln Thr Met Asn Arg Ala1 5 10 15Glu Asn Gly Gly Cys
201821PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 18Glu Asn Gly Gly Arg Pro Pro His His Pro
Tyr Asp Thr Lys Asp Val1 5 10 15Ser Glu Tyr Ser Cys
201921PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 19Thr Glu Ile Ile Pro Gly Leu Arg Glu Tyr
Pro Glu Pro Pro Gln Glu1 5 10 15Leu Glu Asn Asn Cys
2020190PRTRattus norvegicus 20Gln Gly Trp Gln Ala Phe Lys Asn Asp
Ala Thr Glu Ile Ile Pro Gly1 5 10 15Leu Arg Glu Tyr Pro Glu Pro Pro
Gln Glu Leu Glu Asn Asn Gln Thr 20 25 30Met Asn Arg Ala Glu Asn Gly
Gly Arg Pro Pro His His Pro Tyr Asp 35 40 45Thr Lys Asp Val Ser Glu
Tyr Ser Cys Arg Glu Leu His Tyr Thr Arg 50 55 60Phe Val Thr Asp Gly
Pro Cys Arg Ser Ala Lys Pro Val Thr Glu Leu65 70 75 80Val Cys Ser
Gly Gln Cys Gly Pro Ala Arg Leu Leu Pro Asn Ala Ile 85 90 95Gly Arg
Val Lys Trp Trp Arg Pro Asn Gly Pro Asp Phe Arg Cys Ile 100 105
110Pro Asp Arg Tyr Arg Ala Gln Arg Val Gln Leu Leu Cys Pro Gly Gly
115 120 125Ala Ala Pro Arg Ser Arg Lys Val Arg Leu Val Ala Ser Cys
Lys Cys 130 135 140Lys Arg Leu Thr Arg Phe His Asn Gln Ser Glu Leu
Lys Asp Phe Gly145 150 155 160Pro Glu Thr Ala Arg Pro Gln Lys Gly
Arg Lys Pro Arg Pro Arg Ala 165 170 175Arg Gly Ala Lys Ala Asn Gln
Ala Glu Leu Glu Asn Ala Tyr 180 185 1902120PRTHomo sapiens 21Ile
Pro Asp Arg Tyr Arg Ala Gln Arg Val Gln Leu Leu Cys Pro Gly1 5 10
15Gly Glu Ala Pro 202220PRTHomo sapiens 22Gln Leu Leu Cys Pro Gly
Gly Glu Ala Pro Arg Ala Arg Lys Val Arg1 5 10 15Leu Val Ala Ser
202321PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 23Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val
Gln Leu Leu Cys Pro Gly1 5 10 15Gly Glu Ala Pro Cys
202421PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 24Gln Leu Leu Cys Pro Gly Gly Glu Ala Pro
Arg Ala Arg Lys Val Arg1 5 10 15Leu Val Ala Ser Cys 202517PRTRattus
Norvegicus 25Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val Gln Leu Leu
Cys Pro Gly1 5 10 15Gly2616PRTRattus norvegicus 26Pro Gly Gly Ala
Ala Pro Arg Ser Arg Lys Val Arg Leu Val Ala Ser1 5 10
152718PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 27Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val
Gln Leu Leu Ser Pro Gly1 5 10 15Gly Cys2817PRTArtificial
SequenceRat SOST peptide fragment with additional cysteine added
28Pro Gly Gly Ala Ala Pro Arg Ser Arg Lys Val Arg Leu Val Ala Ser1
5 10 15Cys2920PRTHomo sapiens 29Cys Gly Pro Ala Arg Leu Leu Pro Asn
Ala Ile Gly Arg Gly Lys Trp1 5 10 15Trp Arg Pro Ser 203016PRTHomo
sapiens 30Ile Gly Arg Gly Lys Trp Trp Arg Pro Ser Gly Pro Asp Phe
Arg Cys1 5 10 153118PRTRattus norvegicus 31Pro Asn Ala Ile Gly Arg
Val Lys Trp Trp Arg Pro Asn Gly Pro Asp1 5 10 15Phe
Arg3219PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 32Pro Asn Ala Ile Gly Arg Val Lys Trp Trp
Arg Pro Asn Gly Pro Asp1 5 10 15Phe Arg Cys3320PRTHomo sapiens
33Lys Arg Leu Thr Arg Phe His Asn Gln Ser Glu Leu Lys Asp Phe Gly1
5 10 15Thr Glu Ala Ala 203420PRTHomo sapiens 34Glu Leu Lys Asp Phe
Gly Thr Glu Ala Ala Arg Pro Gln Lys Gly Arg1 5 10 15Lys Pro Arg Pro
203520PRTHomo sapiens 35Arg Pro Gln Lys Gly Arg Lys Pro Arg Pro Arg
Ala Arg Ser Ala Lys1 5 10 15Ala Asn Gln Ala 203616PRTHomo sapiens
36Arg Ala Arg Ser Ala Lys Ala Asn Gln Ala Glu Leu Glu Asn Ala Tyr1
5 10 153721PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 37Lys Arg Leu Thr Arg Phe His Asn Gln Ser
Glu Leu Lys Asp Phe Gly1 5 10 15Thr Glu Ala Ala Cys
203821PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 38Glu Leu Lys Asp Phe Gly Thr Glu Ala Ala
Arg Pro Gln Lys Gly Arg1 5 10 15Lys Pro Arg Pro Cys
203921PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 39Arg Pro Gln Lys Gly Arg Lys Pro Arg Pro
Arg Ala Arg Ser Ala Lys1 5 10 15Ala Asn Gln Ala Cys
204017PRTArtificial SequenceHuman SOST peptide fragment with
additional cysteine added 40Arg Ala Arg Ser Ala Lys Ala Asn Gln Ala
Glu Leu Glu Asn Ala Tyr1 5 10 15Cys4123PRTRattus norvegicus 41Lys
Arg Leu Thr Arg Phe His Asn Gln Ser Glu Leu Lys Asp Phe Gly1 5 10
15Pro Glu Thr Ala Arg Pro Gln 204223PRTRattus norvegicus 42Lys Gly
Arg Lys Pro Arg Pro Arg Ala Arg Gly Ala Lys Ala Asn Gln1 5 10 15Ala
Glu Leu Glu Asn Ala Tyr204324PRTRattus norvegicus 43Ser Glu Leu Lys
Asp Phe Gly Pro Glu Thr Ala Arg Pro Gln Lys Gly1 5 10 15Arg Lys Pro
Arg Pro Arg Ala Arg 204424PRTArtificial SequenceRat SOST peptide
fragment with additional cysteine added 44Lys Arg Leu Thr Arg Phe
His Asn Gln Ser Glu Leu Lys Asp Phe Gly1 5 10 15Pro Glu Thr Ala Arg
Pro Gln Cys 204524PRTArtificial SequenceRat SOST peptide fragment
with additional cysteine added 45Lys Gly Arg Lys Pro Arg Pro Arg
Ala Arg Gly Ala Lys Ala Asn Gln1 5 10 15Ala Glu Leu Glu Asn Ala Tyr
Cys 204625PRTArtificial SequenceRat SOST peptide fragment with
additional cysteine added 46Ser Glu Leu Lys Asp Phe Gly Pro Glu Thr
Ala Arg Pro Gln Lys Gly1 5 10 15Arg Lys Pro Arg Pro Arg Ala Arg Cys
20 254756PRTHomo sapiens 47Gln Gly Trp Gln Ala Phe Lys Asn Asp Ala
Thr Glu Ile Ile Pro Glu1 5 10 15Leu Gly Glu Tyr Pro Glu Pro Pro Pro
Glu Leu Glu Asn Asn Lys Thr 20 25 30Met Asn Arg Ala Glu Asn Gly Gly
Arg Pro Pro His His Pro Phe Glu 35 40 45Thr Lys Asp Val Ser Glu Tyr
Ser 50 554856PRTRattus norvegicus 48Gln Gly Trp Gln Ala Phe Lys Asn
Asp Ala Thr Glu Ile Ile Pro Gly1 5 10 15Leu Arg Glu Tyr Pro Glu Pro
Pro Gln Glu Leu Glu Asn Asn Gln Thr 20 25 30Met Asn Arg Ala Glu Asn
Gly Gly Arg Pro Pro His His Pro Tyr Asp 35 40 45Thr Lys Asp Val Ser
Glu Tyr Ser 50 554932PRTHomo sapiens 49Cys Ile Pro Asp Arg Tyr Arg
Ala Gln Arg Val Gln Leu Leu Cys Pro1 5 10 15Gly Gly Glu Ala Pro Arg
Ala Arg Lys Val Arg Leu Val Ala Ser Cys 20 25 305032PRTRattus
norvegicus 50Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val Gln Leu
Leu Cys Pro1 5 10 15Gly Gly Ala Ala Pro Arg Ser Arg Lys Val Arg Leu
Val Ala Ser Cys 20 25 305144PRTHomo sapiens 51Leu Thr Arg Phe His
Asn Gln Ser Glu Leu Lys Asp Phe Gly Thr Glu1 5 10 15Ala Ala Arg Pro
Gln Lys Gly Arg Lys Pro Arg Pro Arg Ala Arg Ser 20 25 30Ala Lys Ala
Asn Gln Ala Glu Leu Glu Asn Ala Tyr 35 405244PRTRattus norvegicus
52Leu Thr Arg Phe His Asn Gln Ser Glu Leu Lys Asp Phe Gly Pro Glu1
5 10 15Thr Ala Arg Pro Gln Lys Gly Arg Lys Pro Arg Pro Arg Ala Arg
Gly 20 25 30Ala Lys Ala Asn Gln Ala Glu Leu Glu Asn Ala Tyr 35
405326PRTHomo sapiens 53Cys Gly Pro Ala Arg Leu Leu Pro Asn Ala Ile
Gly Arg Gly Lys Trp1 5 10 15Trp Arg Pro Ser Gly Pro Asp Phe Arg Cys
20 255426PRTRattus norvegicus 54Cys Gly Pro Ala Arg Leu Leu Pro Asn
Ala Ile Gly Arg Val Lys Trp1 5 10 15Trp Arg Pro Asn Gly Pro Asp Phe
Arg Cys 20 2555570DNAHomo sapiens 55caggggtggc aggcgttcaa
gaatgatgcc acggaaatca tccccgagct cggagagtac 60cccgagcctc caccggagct
ggagaacaac aagaccatga accgggcgga gaacggaggg 120cggcctcccc
accacccctt tgagaccaaa gacgtgtccg agtacagctg ccgcgagctg
180cacttcaccc gctacgtgac cgatgggccg tgccgcagcg ccaagccggt
caccgagctg 240gtgtgctccg gccagtgcgg cccggcgcgc ctgctgccca
acgccatcgg ccgcggcaag 300tggtggcgac ctagtgggcc cgacttccgc
tgcatccccg accgctaccg cgcgcagcgc 360gtgcagctgc tgtgtcccgg
tggtgaggcg ccgcgcgcgc gcaaggtgcg cctggtggcc 420tcgtgcaagt
gcaagcgcct cacccgcttc cacaaccagt cggagctcaa ggacttcggg
480accgaggccg ctcggccgca gaagggccgg aagccgcggc cccgcgcccg
gagcgccaaa 540gccaaccagg ccgagctgga gaacgcctac 57056570DNARattus
norvegicus 56caggggtggc aagccttcaa gaatgatgcc acagaaatca tcccgggact
cagagagtac 60ccagagcctc ctcaggaact agagaacaac cagaccatga accgggccga
gaacggaggc 120agaccccccc accatcctta tgacaccaaa gacgtgtccg
agtacagctg ccgcgagctg 180cactacaccc gcttcgtgac cgacggcccg
tgccgcagtg ccaagccggt caccgagttg 240gtgtgctcgg gccagtgcgg
ccccgcgcgg ctgctgccca acgccatcgg gcgcgtgaag 300tggtggcgcc
cgaacggacc cgacttccgc tgcatcccgg atcgctaccg cgcgcagcgg
360gtgcagctgc tgtgccccgg cggcgcggcg ccgcgctcgc gcaaggtgcg
tctggtggcc 420tcgtgcaagt gcaagcgcct cacccgcttc cacaaccagt
cggagctcaa ggacttcgga 480cctgagaccg cgcggccgca gaagggtcgc
aagccgcggc cccgcgcccg gggagccaaa 540gccaaccagg cggagctgga
gaacgcctac 570572301DNAHomo sapiens 57agagcctgtg ctactggaag
gtggcgtgcc ctcctctggc tggtaccatg cagctcccac 60tggccctgtg tctcgtctgc
ctgctggtac acacagcctt ccgtgtagtg gagggccagg 120ggtggcaggc
gttcaagaat gatgccacgg aaatcatccc cgagctcgga gagtaccccg
180agcctccacc ggagctggag aacaacaaga ccatgaaccg ggcggagaac
ggagggcggc 240ctccccacca cccctttgag accaaagacg tgtccgagta
cagctgccgc gagctgcact 300tcacccgcta cgtgaccgat gggccgtgcc
gcagcgccaa gccggtcacc gagctggtgt 360gctccggcca gtgcggcccg
gcgcgcctgc tgcccaacgc catcggccgc ggcaagtggt 420ggcgacctag
tgggcccgac ttccgctgca tccccgaccg ctaccgcgcg cagcgcgtgc
480agctgctgtg tcccggtggt gaggcgccgc gcgcgcgcaa ggtgcgcctg
gtggcctcgt 540gcaagtgcaa gcgcctcacc cgcttccaca accagtcgga
gctcaaggac ttcgggaccg 600aggccgctcg gccgcagaag ggccggaagc
cgcggccccg cgcccggagc gccaaagcca 660accaggccga gctggagaac
gcctactaga gcccgcccgc gcccctcccc accggcgggc 720gccccggccc
tgaacccgcg ccccacattt ctgtcctctg cgcgtggttt gattgtttat
780atttcattgt aaatgcctgc aacccagggc agggggctga gaccttccag
gccctgagga 840atcccgggcg ccggcaaggc ccccctcagc ccgccagctg
aggggtccca cggggcaggg 900gagggaattg agagtcacag acactgagcc
acgcagcccc gcctctgggg ccgcctacct 960ttgctggtcc cacttcagag
gaggcagaaa tggaagcatt ttcaccgccc tggggtttta 1020agggagcggt
gtgggagtgg gaaagtccag ggactggtta agaaagttgg ataagattcc
1080cccttgcacc tcgctgccca tcagaaagcc tgaggcgtgc ccagagcaca
agactggggg 1140caactgtaga tgtggtttct agtcctggct ctgccactaa
cttgctgtgt aaccttgaac 1200tacacaattc tccttcggga cctcaatttc
cactttgtaa aatgagggtg gaggtgggaa 1260taggatctcg aggagactat
tggcatatga ttccaaggac tccagtgcct tttgaatggg 1320cagaggtgag
agagagagag agaaagagag agaatgaatg cagttgcatt gattcagtgc
1380caaggtcact tccagaattc agagttgtga tgctctcttc tgacagccaa
agatgaaaaa 1440caaacagaaa aaaaaaagta aagagtctat ttatggctga
catatttacg gctgacaaac 1500tcctggaaga agctatgctg cttcccagcc
tggcttcccc ggatgtttgg ctacctccac 1560ccctccatct caaagaaata
acatcatcca ttggggtaga aaaggagagg gtccgagggt 1620ggtgggaggg
atagaaatca catccgcccc aacttcccaa agagcagcat ccctcccccg
1680acccatagcc atgttttaaa gtcaccttcc gaagagaagt gaaaggttca
aggacactgg 1740ccttgcaggc ccgagggagc agccatcaca aactcacaga
ccagcacatc ccttttgaga 1800caccgccttc tgcccaccac tcacggacac
atttctgcct agaaaacagc ttcttactgc 1860tcttacatgt
gatggcatat cttacactaa aagaatatta ttgggggaaa aactacaagt
1920gctgtacata tgctgagaaa ctgcagagca taatagctgc cacccaaaaa
tctttttgaa 1980aatcatttcc agacaacctc ttactttctg tgtagttttt
aattgttaaa aaaaaaaagt 2040tttaaacaga agcacatgac atatgaaagc
ctgcaggact ggtcgttttt ttggcaattc 2100ttccacgtgg gacttgtcca
caagaatgaa agtagtggtt tttaaagagt taagttacat 2160atttattttc
tcacttaagt tatttatgca aaagtttttc ttgtagagaa tgacaatgtt
2220aatattgctt tatgaattaa cagtctgttc ttccagagtc cagagacatt
gttaataaag 2280acaatgaatc atgaccgaaa g 230158213PRTHomo sapiens
58Met Gln Leu Pro Leu Ala Leu Cys Leu Val Cys Leu Leu Val His Thr1
5 10 15Ala Phe Arg Val Val Glu Gly Gln Gly Trp Gln Ala Phe Lys Asn
Asp 20 25 30Ala Thr Glu Ile Ile Pro Glu Leu Gly Glu Tyr Pro Glu Pro
Pro Pro 35 40 45Glu Leu Glu Asn Asn Lys Thr Met Asn Arg Ala Glu Asn
Gly Gly Arg 50 55 60Pro Pro His His Pro Phe Glu Thr Lys Asp Val Ser
Glu Tyr Ser Cys65 70 75 80Arg Glu Leu His Phe Thr Arg Tyr Val Thr
Asp Gly Pro Cys Arg Ser 85 90 95Ala Lys Pro Val Thr Glu Leu Val Cys
Ser Gly Gln Cys Gly Pro Ala 100 105 110Arg Leu Leu Pro Asn Ala Ile
Gly Arg Gly Lys Trp Trp Arg Pro Ser 115 120 125Gly Pro Asp Phe Arg
Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val 130 135 140Gln Leu Leu
Cys Pro Gly Gly Glu Ala Pro Arg Ala Arg Lys Val Arg145 150 155
160Leu Val Ala Ser Cys Lys Cys Lys Arg Leu Thr Arg Phe His Asn Gln
165 170 175Ser Glu Leu Lys Asp Phe Gly Thr Glu Ala Ala Arg Pro Gln
Lys Gly 180 185 190Arg Lys Pro Arg Pro Arg Ala Arg Ser Ala Lys Ala
Asn Gln Ala Glu 195 200 205Leu Glu Asn Ala Tyr 210592301DNAHomo
sapiens 59agagcctgtg ctactggaag gtggcgtgcc ctcctctggc tggtaccatg
cagctcccac 60tggccctgtg tctcatctgc ctgctggtac acacagcctt ccgtgtagtg
gagggccagg 120ggtggcaggc gttcaagaat gatgccacgg aaatcatccg
cgagctcgga gagtaccccg 180agcctccacc ggagctggag aacaacaaga
ccatgaaccg ggcggagaac ggagggcggc 240ctccccacca cccctttgag
accaaagacg tgtccgagta cagctgccgc gagctgcact 300tcacccgcta
cgtgaccgat gggccgtgcc gcagcgccaa gccggtcacc gagctggtgt
360gctccggcca gtgcggcccg gcgcgcctgc tgcccaacgc catcggccgc
ggcaagtggt 420ggcgacctag tgggcccgac ttccgctgca tccccgaccg
ctaccgcgcg cagcgcgtgc 480agctgctgtg tcccggtggt gaggcgccgc
gcgcgcgcaa ggtgcgcctg gtggcctcgt 540gcaagtgcaa gcgcctcacc
cgcttccaca accagtcgga gctcaaggac ttcgggaccg 600aggccgctcg
gccgcagaag ggccggaagc cgcggccccg cgcccggagc gccaaagcca
660accaggccga gctggagaac gcctactaga gcccgcccgc gcccctcccc
accggcgggc 720gccccggccc tgaacccgcg ccccacattt ctgtcctctg
cgcgtggttt gattgtttat 780atttcattgt aaatgcctgc aacccagggc
agggggctga gaccttccag gccctgagga 840atcccgggcg ccggcaaggc
ccccctcagc ccgccagctg aggggtccca cggggcaggg 900gagggaattg
agagtcacag acactgagcc acgcagcccc gcctctgggg ccgcctacct
960ttgctggtcc cacttcagag gaggcagaaa tggaagcatt ttcaccgccc
tggggtttta 1020agggagcggt gtgggagtgg gaaagtccag ggactggtta
agaaagttgg ataagattcc 1080cccttgcacc tcgctgccca tcagaaagcc
tgaggcgtgc ccagagcaca agactggggg 1140caactgtaga tgtggtttct
agtcctggct ctgccactaa cttgctgtgt aaccttgaac 1200tacacaattc
tccttcggga cctcaatttc cactttgtaa aatgagggtg gaggtgggaa
1260taggatctcg aggagactat tggcatatga ttccaaggac tccagtgcct
tttgaatggg 1320cagaggtgag agagagagag agaaagagag agaatgaatg
cagttgcatt gattcagtgc 1380caaggtcact tccagaattc agagttgtga
tgctctcttc tgacagccaa agatgaaaaa 1440caaacagaaa aaaaaaagta
aagagtctat ttatggctga catatttacg gctgacaaac 1500tcctggaaga
agctatgctg cttcccagcc tggcttcccc ggatgtttgg ctacctccac
1560ccctccatct caaagaaata acatcatcca ttggggtaga aaaggagagg
gtccgagggt 1620ggtgggaggg atagaaatca catccgcccc aacttcccaa
agagcagcat ccctcccccg 1680acccatagcc atgttttaaa gtcaccttcc
gaagagaagt gaaaggttca aggacactgg 1740ccttgcaggc ccgagggagc
agccatcaca aactcacaga ccagcacatc ccttttgaga 1800caccgccttc
tgcccaccac tcacggacac atttctgcct agaaaacagc ttcttactgc
1860tcttacatgt gatggcatat cttacactaa aagaatatta ttgggggaaa
aactacaagt 1920gctgtacata tgctgagaaa ctgcagagca taatagctgc
cacccaaaaa tctttttgaa 1980aatcatttcc agacaacctc ttactttctg
tgtagttttt aattgttaaa aaaaaaaagt 2040tttaaacaga agcacatgac
atatgaaagc ctgcaggact ggtcgttttt ttggcaattc 2100ttccacgtgg
gacttgtcca caagaatgaa agtagtggtt tttaaagagt taagttacat
2160atttattttc tcacttaagt tatttatgca aaagtttttc ttgtagagaa
tgacaatgtt 2220aatattgctt tatgaattaa cagtctgttc ttccagagtc
cagagacatt gttaataaag 2280acaatgaatc atgaccgaaa g 230160213PRTHomo
sapiens 60Met Gln Leu Pro Leu Ala Leu Cys Leu Ile Cys Leu Leu Val
His Thr1 5 10 15Ala Phe Arg Val Val Glu Gly Gln Gly Trp Gln Ala Phe
Lys Asn Asp 20 25 30Ala Thr Glu Ile Ile Arg Glu Leu Gly Glu Tyr Pro
Glu Pro Pro Pro 35 40 45Glu Leu Glu Asn Asn Lys Thr Met Asn Arg Ala
Glu Asn Gly Gly Arg 50 55 60Pro Pro His His Pro Phe Glu Thr Lys Asp
Val Ser Glu Tyr Ser Cys65 70 75 80Arg Glu Leu His Phe Thr Arg Tyr
Val Thr Asp Gly Pro Cys Arg Ser 85 90 95Ala Lys Pro Val Thr Glu Leu
Val Cys Ser Gly Gln Cys Gly Pro Ala 100 105 110Arg Leu Leu Pro Asn
Ala Ile Gly Arg Gly Lys Trp Trp Arg Pro Ser 115 120 125Gly Pro Asp
Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val 130 135 140Gln
Leu Leu Cys Pro Gly Gly Glu Ala Pro Arg Ala Arg Lys Val Arg145 150
155 160Leu Val Ala Ser Cys Lys Cys Lys Arg Leu Thr Arg Phe His Asn
Gln 165 170 175Ser Glu Leu Lys Asp Phe Gly Thr Glu Ala Ala Arg Pro
Gln Lys Gly 180 185 190Arg Lys Pro Arg Pro Arg Ala Arg Ser Ala Lys
Ala Asn Gln Ala Glu 195 200 205Leu Glu Asn Ala Tyr 210612301DNAHomo
sapiens 61agagcctgtg ctactggaag gtggcgtgcc ctcctctggc tggtaccatg
cagctcccac 60tggccctgtg tctcgtctgc ctgctggtac acacagcctt ccgtgtagtg
gagggccagg 120ggtggcaggc gttcaagaat gatgccacgg aaatcatccg
cgagctcgga gagtaccccg 180agcctccacc ggagctggag aacaacaaga
ccatgaaccg ggcggagaac ggagggcggc 240ctccccacca cccctttgag
accaaagacg tgtccgagta cagctgccgc gagctgcact 300tcacccgcta
cgtgaccgat gggccgtgcc gcagcgccaa gccggtcacc gagctggtgt
360gctccggcca gtgcggcccg gcgcgcctgc tgcccaacgc catcggccgc
ggcaagtggt 420ggcgacctag tgggcccgac ttccgctgca tccccgaccg
ctaccgcgcg cagcgcgtgc 480agctgctgtg tcccggtggt gaggcgccgc
gcgcgcgcaa ggtgcgcctg gtggcctcgt 540gcaagtgcaa gcgcctcacc
cgcttccaca accagtcgga gctcaaggac ttcgggaccg 600aggccgctcg
gccgcagaag ggccggaagc cgcggccccg cgcccggagc gccaaagcca
660accaggccga gctggagaac gcctactaga gcccgcccgc gcccctcccc
accggcgggc 720gccccggccc tgaacccgcg ccccacattt ctgtcctctg
cgcgtggttt gattgtttat 780atttcattgt aaatgcctgc aacccagggc
agggggctga gaccttccag gccctgagga 840atcccgggcg ccggcaaggc
ccccctcagc ccgccagctg aggggtccca cggggcaggg 900gagggaattg
agagtcacag acactgagcc acgcagcccc gcctctgggg ccgcctacct
960ttgctggtcc cacttcagag gaggcagaaa tggaagcatt ttcaccgccc
tggggtttta 1020agggagcggt gtgggagtgg gaaagtccag ggactggtta
agaaagttgg ataagattcc 1080cccttgcacc tcgctgccca tcagaaagcc
tgaggcgtgc ccagagcaca agactggggg 1140caactgtaga tgtggtttct
agtcctggct ctgccactaa cttgctgtgt aaccttgaac 1200tacacaattc
tccttcggga cctcaatttc cactttgtaa aatgagggtg gaggtgggaa
1260taggatctcg aggagactat tggcatatga ttccaaggac tccagtgcct
tttgaatggg 1320cagaggtgag agagagagag agaaagagag agaatgaatg
cagttgcatt gattcagtgc 1380caaggtcact tccagaattc agagttgtga
tgctctcttc tgacagccaa agatgaaaaa 1440caaacagaaa aaaaaaagta
aagagtctat ttatggctga catatttacg gctgacaaac 1500tcctggaaga
agctatgctg cttcccagcc tggcttcccc ggatgtttgg ctacctccac
1560ccctccatct caaagaaata acatcatcca ttggggtaga aaaggagagg
gtccgagggt 1620ggtgggaggg atagaaatca catccgcccc aacttcccaa
agagcagcat ccctcccccg 1680acccatagcc atgttttaaa gtcaccttcc
gaagagaagt gaaaggttca aggacactgg 1740ccttgcaggc ccgagggagc
agccatcaca aactcacaga ccagcacatc ccttttgaga 1800caccgccttc
tgcccaccac tcacggacac atttctgcct agaaaacagc ttcttactgc
1860tcttacatgt gatggcatat cttacactaa aagaatatta ttgggggaaa
aactacaagt 1920gctgtacata tgctgagaaa ctgcagagca taatagctgc
cacccaaaaa tctttttgaa 1980aatcatttcc agacaacctc ttactttctg
tgtagttttt aattgttaaa aaaaaaaagt 2040tttaaacaga agcacatgac
atatgaaagc ctgcaggact ggtcgttttt ttggcaattc 2100ttccacgtgg
gacttgtcca caagaatgaa agtagtggtt tttaaagagt taagttacat
2160atttattttc tcacttaagt tatttatgca aaagtttttc ttgtagagaa
tgacaatgtt 2220aatattgctt tatgaattaa cagtctgttc ttccagagtc
cagagacatt gttaataaag 2280acaatgaatc atgaccgaaa g 230162213PRTHomo
sapiens 62Met Gln Leu Pro Leu Ala Leu Cys Leu Val Cys Leu Leu Val
His Thr1 5 10 15Ala Phe Arg Val Val Glu Gly Gln Gly Trp Gln Ala Phe
Lys Asn Asp 20 25 30Ala Thr Glu Ile Ile Arg Glu Leu Gly Glu Tyr Pro
Glu Pro Pro Pro 35 40 45Glu Leu Glu Asn Asn Lys Thr Met Asn Arg Ala
Glu Asn Gly Gly Arg 50 55 60Pro Pro His His Pro Phe Glu Thr Lys Asp
Val Ser Glu Tyr Ser Cys65 70 75 80Arg Glu Leu His Phe Thr Arg Tyr
Val Thr Asp Gly Pro Cys Arg Ser 85 90 95Ala Lys Pro Val Thr Glu Leu
Val Cys Ser Gly Gln Cys Gly Pro Ala 100 105 110Arg Leu Leu Pro Asn
Ala Ile Gly Arg Gly Lys Trp Trp Arg Pro Ser 115 120 125Gly Pro Asp
Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg Val 130 135 140Gln
Leu Leu Cys Pro Gly Gly Glu Ala Pro Arg Ala Arg Lys Val Arg145 150
155 160Leu Val Ala Ser Cys Lys Cys Lys Arg Leu Thr Arg Phe His Asn
Gln 165 170 175Ser Glu Leu Lys Asp Phe Gly Thr Glu Ala Ala Arg Pro
Gln Lys Gly 180 185 190Arg Lys Pro Arg Pro Arg Ala Arg Ser Ala Lys
Ala Asn Gln Ala Glu 195 200 205Leu Glu Asn Ala Tyr
21063642DNACercopithecus pygerythrus 63atgcagctcc cactggccct
gtgtcttgtc tgcctgctgg tacacgcagc cttccgtgta 60gtggagggcc aggggtggca
ggccttcaag aatgatgcca cggaaatcat ccccgagctc 120ggagagtacc
ccgagcctcc accggagctg gagaacaaca agaccatgaa ccgggcggag
180aatggagggc ggcctcccca ccaccccttt gagaccaaag acgtgtccga
gtacagctgc 240cgagagctgc acttcacccg ctacgtgacc gatgggccgt
gccgcagcgc caagccagtc 300accgagttgg tgtgctccgg ccagtgcggc
ccggcacgcc tgctgcccaa cgccatcggc 360cgcggcaagt ggtggcgccc
gagtgggccc gacttccgct gcatccccga ccgctaccgc 420gcgcagcgtg
tgcagctgct gtgtcccggt ggtgccgcgc cgcgcgcgcg caaggtgcgc
480ctggtggcct cgtgcaagtg caagcgcctc acccgcttcc acaaccagtc
ggagctcaag 540gacttcggtc ccgaggccgc tcggccgcag aagggccgga
agccgcggcc ccgcgcccgg 600ggggccaaag ccaatcaggc cgagctggag
aacgcctact ag 64264213PRTCercopithecus pygerythrus 64Met Gln Leu
Pro Leu Ala Leu Cys Leu Val Cys Leu Leu Val His Ala1 5 10 15Ala Phe
Arg Val Val Glu Gly Gln Gly Trp Gln Ala Phe Lys Asn Asp 20 25 30Ala
Thr Glu Ile Ile Pro Glu Leu Gly Glu Tyr Pro Glu Pro Pro Pro 35 40
45Glu Leu Glu Asn Asn Lys Thr Met Asn Arg Ala Glu Asn Gly Gly Arg
50 55 60Pro Pro His His Pro Phe Glu Thr Lys Asp Val Ser Glu Tyr Ser
Cys65 70 75 80Arg Glu Leu His Phe Thr Arg Tyr Val Thr Asp Gly Pro
Cys Arg Ser 85 90 95Ala Lys Pro Val Thr Glu Leu Val Cys Ser Gly Gln
Cys Gly Pro Ala 100 105 110Arg Leu Leu Pro Asn Ala Ile Gly Arg Gly
Lys Trp Trp Arg Pro Ser 115 120 125Gly Pro Asp Phe Arg Cys Ile Pro
Asp Arg Tyr Arg Ala Gln Arg Val 130 135 140Gln Leu Leu Cys Pro Gly
Gly Ala Ala Pro Arg Ala Arg Lys Val Arg145 150 155 160Leu Val Ala
Ser Cys Lys Cys Lys Arg Leu Thr Arg Phe His Asn Gln 165 170 175Ser
Glu Leu Lys Asp Phe Gly Pro Glu Ala Ala Arg Pro Gln Lys Gly 180 185
190Arg Lys Pro Arg Pro Arg Ala Arg Gly Ala Lys Ala Asn Gln Ala Glu
195 200 205Leu Glu Asn Ala Tyr 21065638DNAMus musculus 65atgcagccct
cactagcccc gtgcctcatc tgcctacttg tgcacgctgc cttctgtgct 60gtggagggcc
aggggtggca agccttcagg aatgatgcca cagaggtcat cccagggctt
120ggagagtacc ccgagcctcc tcctgagaac aaccagacca tgaaccgggc
ggagaatgga 180ggcagacctc cccaccatcc ctatgacgcc aaaggtgtgt
ccgagtacag ctgccgcgag 240ctgcactaca cccgcttcct gacagacggc
ccatgccgca gcgccaagcc ggtcaccgag 300ttggtgtgct ccggccagtg
cggccccgcg cggctgctgc ccaacgccat cgggcgcgtg 360aagtggtggc
gcccgaacgg accggatttc cgctgcatcc cggatcgcta ccgcgcgcag
420cgggtgcagc tgctgtgccc cgggggcgcg gcgccgcgct cgcgcaaggt
gcgtctggtg 480gcctcgtgca agtgcaagcg cctcacccgc ttccacaacc
agtcggagct caaggacttc 540gggccggaga ccgcgcggcc gcagaagggt
cgcaagccgc ggcccggcgc ccggggagcc 600aaagccaacc aggcggagct
ggagaacgcc tactagag 63866211PRTMus musculus 66Met Gln Pro Ser Leu
Ala Pro Cys Leu Ile Cys Leu Leu Val His Ala1 5 10 15Ala Phe Cys Ala
Val Glu Gly Gln Gly Trp Gln Ala Phe Arg Asn Asp 20 25 30Ala Thr Glu
Val Ile Pro Gly Leu Gly Glu Tyr Pro Glu Pro Pro Pro 35 40 45Glu Asn
Asn Gln Thr Met Asn Arg Ala Glu Asn Gly Gly Arg Pro Pro 50 55 60His
His Pro Tyr Asp Ala Lys Asp Val Ser Glu Tyr Ser Cys Arg Glu65 70 75
80Leu His Tyr Thr Arg Phe Leu Thr Asp Gly Pro Cys Arg Ser Ala Lys
85 90 95Pro Val Thr Glu Leu Val Cys Ser Gly Gln Cys Gly Pro Ala Arg
Leu 100 105 110Leu Pro Asn Ala Ile Gly Arg Val Lys Trp Trp Arg Pro
Asn Gly Pro 115 120 125Asp Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala
Gln Arg Val Gln Leu 130 135 140Leu Cys Pro Gly Gly Ala Ala Pro Arg
Ser Arg Lys Val Arg Leu Val145 150 155 160Ala Ser Cys Lys Cys Lys
Arg Leu Thr Arg Phe His Asn Gln Ser Glu 165 170 175Leu Lys Asp Phe
Gly Pro Glu Thr Ala Arg Pro Gln Lys Gly Arg Lys 180 185 190Pro Arg
Pro Gly Ala Arg Gly Ala Lys Ala Asn Gln Ala Glu Leu Glu 195 200
205Asn Ala Tyr 21067674DNARattus norvegicus 67gaggaccgag tgcccttcct
ccttctggca ccatgcagct ctcactagcc ccttgccttg 60cctgcctgct tgtacatgca
gccttcgttg ctgtggagag ccaggggtgg caagccttca 120agaatgatgc
cacagaaatc atcccgggac tcagagagta cccagagcct cctcaggaac
180tagagaacaa ccagaccatg aaccgggccg agaacggagg cagacccccc
caccatcctt 240atgacaccaa agacgtgtcc gagtacagct gccgcgagct
gcactacacc cgcttcgtga 300ccgacggccc gtgccgcagt gccaagccgg
tcaccgagtt ggtgtgctcg ggccagtgcg 360gccccgcgcg gctgctgccc
aacgccatcg ggcgcgtgaa gtggtggcgc ccgaacggac 420ccgacttccg
ctgcatcccg gatcgctacc gcgcgcagcg ggtgcagctg ctgtgccccg
480gcggcgcggc gccgcgctcg cgcaaggtgc gtctggtggc ctcgtgcaag
tgcaagcgcc 540tcacccgctt ccacaaccag tcggagctca aggacttcgg
acctgagacc gcgcggccgc 600agaagggtcg caagccgcgg ccccgcgccc
ggggagccaa agccaaccag gcggagctgg 660agaacgccta ctag
67468213PRTRattus norvegicus 68Met Gln Leu Ser Leu Ala Pro Cys Leu
Ala Cys Leu Leu Val His Ala1 5 10 15Ala Phe Val Ala Val Glu Ser Gln
Gly Trp Gln Ala Phe Lys Asn Asp 20 25 30Ala Thr Glu Ile Ile Pro Gly
Leu Arg Glu Tyr Pro Glu Pro Pro Gln 35 40 45Glu Leu Glu Asn Asn Gln
Thr Met Asn Arg Ala Glu Asn Gly Gly Arg 50 55 60Pro Pro His His Pro
Tyr Asp Thr Lys Asp Val Ser Glu Tyr Ser Cys65 70 75 80Arg Glu Leu
His Tyr Thr Arg Phe Val Thr Asp Gly Pro Cys Arg Ser 85 90 95Ala Lys
Pro Val Thr Glu Leu Val Cys Ser Gly Gln Cys Gly Pro Ala 100 105
110Arg Leu Leu Pro Asn Ala Ile Gly Arg Val Lys Trp Trp Arg Pro Asn
115 120 125Gly Pro Asp Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala Gln
Arg Val 130 135 140Gln Leu Leu Cys Pro Gly Gly Ala Ala Pro Arg Ser
Arg Lys Val Arg145 150 155 160Leu Val Ala Ser Cys Lys Cys Lys Arg
Leu Thr Arg Phe His Asn Gln 165 170 175Ser Glu Leu Lys Asp Phe Gly
Pro Glu Thr Ala Arg Pro Gln Lys Gly 180 185 190Arg Lys Pro Arg Pro
Arg Ala Arg Gly Ala Lys Ala
Asn Gln Ala Glu 195 200 205Leu Glu Asn Ala Tyr 21069532DNABos torus
69agaatgatgc cacagaaatc atccccgagc tgggcgagta ccccgagcct ctgccagagc
60tgaacaacaa gaccatgaac cgggcggaga acggagggag acctccccac cacccctttg
120agaccaaaga cgcctccgag tacagctgcc gggagctgca cttcacccgc
tacgtgaccg 180atgggccgtg ccgcagcgcc aagccggtca ccgagctggt
gtgctcgggc cagtgcggcc 240cggcgcgcct gctgcccaac gccatcggcc
gcggcaagtg gtggcgccca agcgggcccg 300acttccgctg catccccgac
cgctaccgcg cgcagcgggt gcagctgttg tgtcctggcg 360gcgcggcgcc
gcgcgcgcgc aaggtgcgcc tggtggcctc gtgcaagtgc aagcgcctca
420ctcgcttcca caaccagtcc gagctcaagg acttcgggcc cgaggccgcg
cggccgcaaa 480cgggccggaa gctgcggccc cgcgcccggg gcaccaaagc
cagccgggcc ga 53270176PRTBos torus 70Asn Asp Ala Thr Glu Ile Ile
Pro Glu Leu Gly Glu Tyr Pro Glu Pro1 5 10 15Leu Pro Glu Leu Asn Asn
Lys Thr Met Asn Arg Ala Glu Asn Gly Gly 20 25 30Arg Pro Pro His His
Pro Phe Glu Thr Lys Asp Ala Ser Glu Tyr Ser 35 40 45Cys Arg Glu Leu
His Phe Thr Arg Tyr Val Thr Asp Gly Pro Cys Arg 50 55 60Ser Ala Lys
Pro Val Thr Glu Leu Val Cys Ser Gly Gln Cys Gly Pro65 70 75 80Ala
Arg Leu Leu Pro Asn Ala Ile Gly Arg Gly Lys Trp Trp Arg Pro 85 90
95Ser Gly Pro Asp Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg
100 105 110Val Gln Leu Leu Cys Pro Gly Gly Ala Ala Pro Arg Ala Arg
Lys Val 115 120 125Arg Leu Val Ala Ser Cys Lys Cys Lys Arg Leu Thr
Arg Phe His Asn 130 135 140Gln Ser Glu Leu Lys Asp Phe Gly Pro Glu
Ala Ala Arg Pro Gln Thr145 150 155 160Gly Arg Lys Leu Arg Pro Arg
Ala Arg Gly Thr Lys Ala Ser Arg Ala 165 170 17571532PRTHomo sapiens
71Met Thr Gln Leu Tyr Ile Tyr Ile Arg Leu Leu Gly Ala Tyr Leu Phe1
5 10 15Ile Ile Ser Arg Val Gln Gly Gln Asn Leu Asp Ser Met Leu His
Gly 20 25 30Thr Gly Met Lys Ser Asp Ser Asp Gln Lys Lys Ser Glu Asn
Gly Val 35 40 45Thr Leu Ala Pro Glu Asp Thr Leu Pro Phe Leu Lys Cys
Tyr Cys Ser 50 55 60Gly His Cys Pro Asp Asp Ala Ile Asn Asn Thr Cys
Ile Thr Asn Gly65 70 75 80His Cys Phe Ala Ile Ile Glu Glu Asp Asp
Gln Gly Glu Thr Thr Leu 85 90 95Ala Ser Gly Cys Met Lys Tyr Glu Gly
Ser Asp Phe Gln Cys Lys Asp 100 105 110Ser Pro Lys Ala Gln Leu Arg
Arg Thr Ile Glu Cys Cys Arg Thr Asn 115 120 125Leu Cys Asn Gln Tyr
Leu Gln Pro Thr Leu Pro Pro Val Val Ile Gly 130 135 140Pro Phe Phe
Asp Gly Ser Ile Arg Trp Leu Val Leu Leu Ile Ser Met145 150 155
160Ala Val Cys Ile Ile Ala Met Ile Ile Phe Ser Ser Cys Phe Cys Tyr
165 170 175Lys His Tyr Cys Lys Ser Ile Ser Ser Arg Arg Arg Tyr Asn
Arg Asp 180 185 190Leu Glu Gln Asp Glu Ala Phe Ile Pro Val Gly Glu
Ser Leu Lys Asp 195 200 205Leu Ile Asp Gln Ser Gln Ser Ser Gly Ser
Gly Ser Gly Leu Pro Leu 210 215 220Leu Val Gln Arg Thr Ile Ala Lys
Gln Ile Gln Met Val Arg Gln Val225 230 235 240Gly Lys Gly Arg Tyr
Gly Glu Val Trp Met Gly Lys Trp Arg Gly Glu 245 250 255Lys Val Ala
Val Lys Val Phe Phe Thr Thr Glu Glu Ala Ser Trp Phe 260 265 270Arg
Glu Thr Glu Ile Tyr Gln Thr Val Leu Met Arg His Glu Asn Ile 275 280
285Leu Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr Gly Ser Trp Thr Gln
290 295 300Leu Tyr Leu Ile Thr Asp Tyr His Glu Asn Gly Ser Leu Tyr
Asp Phe305 310 315 320Leu Lys Cys Ala Thr Leu Asp Thr Arg Ala Leu
Leu Lys Leu Ala Tyr 325 330 335Ser Ala Ala Cys Gly Leu Cys His Leu
His Thr Glu Ile Tyr Gly Thr 340 345 350Gln Gly Lys Pro Ala Ile Ala
His Arg Asp Leu Lys Ser Lys Asn Ile 355 360 365Leu Ile Lys Lys Asn
Gly Ser Cys Cys Ile Ala Asp Leu Gly Leu Ala 370 375 380Val Lys Phe
Asn Ser Asp Thr Asn Glu Val Asp Val Pro Leu Asn Thr385 390 395
400Arg Val Gly Thr Lys Arg Tyr Met Ala Pro Glu Val Leu Asp Glu Ser
405 410 415Leu Asn Lys Asn His Phe Gln Pro Tyr Ile Met Ala Asp Ile
Tyr Ser 420 425 430Phe Gly Leu Ile Ile Trp Glu Met Ala Arg Arg Cys
Ile Thr Gly Gly 435 440 445Ile Val Glu Glu Tyr Gln Leu Pro Tyr Tyr
Asn Met Val Pro Ser Asp 450 455 460Pro Ser Tyr Glu Asp Met Arg Glu
Val Val Cys Val Lys Arg Leu Arg465 470 475 480Pro Ile Val Ser Asn
Arg Trp Asn Ser Asp Glu Cys Leu Arg Ala Val 485 490 495Leu Lys Leu
Met Ser Glu Cys Trp Ala His Asn Pro Ala Ser Arg Leu 500 505 510Thr
Ala Leu Arg Ile Lys Lys Thr Leu Ala Lys Met Val Glu Ser Gln 515 520
525Asp Val Lys Ile 53072502PRTHomo sapiens 72Met Leu Leu Arg Ser
Ala Gly Lys Leu Asn Val Gly Thr Lys Lys Glu1 5 10 15Asp Gly Glu Ser
Thr Ala Pro Thr Pro Arg Pro Lys Val Leu Arg Cys 20 25 30Lys Cys His
His His Cys Pro Glu Asp Ser Val Asn Asn Ile Cys Ser 35 40 45Thr Asp
Gly Tyr Cys Phe Thr Met Ile Glu Glu Asp Asp Ser Gly Leu 50 55 60Pro
Val Val Thr Ser Gly Cys Leu Gly Leu Glu Gly Ser Asp Phe Gln65 70 75
80Cys Arg Asp Thr Pro Ile Pro His Gln Arg Arg Ser Ile Glu Cys Cys
85 90 95Thr Glu Arg Asn Glu Cys Asn Lys Asp Leu His Pro Thr Leu Pro
Pro 100 105 110Leu Lys Asn Arg Asp Phe Val Asp Gly Pro Ile His His
Arg Ala Leu 115 120 125Leu Ile Ser Val Thr Val Cys Ser Leu Leu Leu
Val Leu Ile Ile Leu 130 135 140Phe Cys Tyr Phe Arg Tyr Lys Arg Gln
Glu Thr Arg Pro Arg Tyr Ser145 150 155 160Ile Gly Leu Glu Gln Asp
Glu Thr Tyr Ile Pro Pro Gly Glu Ser Leu 165 170 175Arg Asp Leu Ile
Glu Gln Ser Gln Ser Ser Gly Ser Gly Ser Gly Leu 180 185 190Pro Leu
Leu Val Gln Arg Thr Ile Ala Lys Gln Ile Gln Met Val Lys 195 200
205Gln Ile Gly Lys Gly Arg Tyr Gly Glu Val Trp Met Gly Lys Trp Arg
210 215 220Gly Glu Lys Val Ala Val Lys Val Phe Phe Thr Thr Glu Glu
Ala Ser225 230 235 240Trp Phe Arg Glu Thr Glu Ile Tyr Gln Thr Val
Leu Met Arg His Glu 245 250 255Asn Ile Leu Gly Phe Ile Ala Ala Asp
Ile Lys Gly Thr Gly Ser Trp 260 265 270Thr Gln Leu Tyr Leu Ile Thr
Asp Tyr His Glu Asn Gly Ser Leu Tyr 275 280 285Asp Tyr Leu Lys Ser
Thr Thr Leu Asp Ala Lys Ser Met Leu Lys Leu 290 295 300Ala Tyr Ser
Ser Val Ser Gly Leu Cys His Leu His Thr Glu Ile Phe305 310 315
320Ser Thr Gln Gly Lys Pro Ala Ile Ala His Arg Asp Leu Lys Ser Lys
325 330 335Asn Ile Leu Val Lys Lys Asn Gly Thr Cys Cys Ile Ala Asp
Leu Gly 340 345 350Leu Ala Val Lys Phe Ile Ser Asp Thr Asn Glu Val
Asp Ile Pro Pro 355 360 365Asn Thr Arg Val Gly Thr Lys Arg Tyr Met
Pro Pro Glu Val Leu Asp 370 375 380Glu Ser Leu Asn Arg Asn His Phe
Gln Ser Tyr Ile Met Ala Asp Met385 390 395 400Tyr Ser Phe Gly Leu
Ile Leu Trp Glu Val Ala Arg Arg Cys Val Ser 405 410 415Gly Gly Ile
Val Glu Glu Tyr Gln Leu Pro Tyr His Asp Leu Val Pro 420 425 430Ser
Asp Pro Ser Tyr Glu Asp Met Arg Glu Ile Val Cys Ile Lys Lys 435 440
445Leu Arg Pro Ser Phe Pro Asn Arg Trp Ser Ser Asp Glu Cys Leu Arg
450 455 460Gln Met Gly Lys Leu Met Thr Glu Cys Trp Ala His Asn Pro
Ala Ser465 470 475 480Arg Leu Thr Ala Leu Arg Val Lys Lys Thr Leu
Ala Lys Met Ser Glu 485 490 495Ser Gln Asp Ile Lys Leu
50073502PRTHomo sapiens 73Met Leu Leu Arg Ser Ala Gly Lys Leu Asn
Val Gly Thr Lys Lys Glu1 5 10 15Asp Gly Glu Ser Thr Ala Pro Thr Pro
Arg Pro Lys Val Leu Arg Cys 20 25 30Lys Cys His His His Cys Pro Glu
Asp Ser Val Asn Asn Ile Cys Ser 35 40 45Thr Asp Gly Tyr Cys Phe Thr
Met Ile Glu Glu Asp Asp Ser Gly Leu 50 55 60Pro Val Val Thr Ser Gly
Cys Leu Gly Leu Glu Gly Ser Asp Phe Gln65 70 75 80Cys Arg Asp Thr
Pro Ile Pro His Gln Arg Arg Ser Ile Glu Cys Cys 85 90 95Thr Glu Arg
Asn Glu Cys Asn Lys Asp Leu His Pro Thr Leu Pro Pro 100 105 110Leu
Lys Asn Arg Asp Phe Val Asp Gly Pro Ile His His Arg Ala Leu 115 120
125Leu Ile Ser Val Thr Val Cys Ser Leu Leu Leu Val Leu Ile Ile Leu
130 135 140Phe Cys Tyr Phe Arg Tyr Lys Arg Gln Glu Thr Arg Pro Arg
Tyr Ser145 150 155 160Ile Gly Leu Glu Gln Asp Glu Thr Tyr Ile Pro
Pro Gly Glu Ser Leu 165 170 175Arg Asp Leu Ile Glu Gln Ser Gln Ser
Ser Gly Ser Gly Ser Gly Leu 180 185 190Pro Leu Leu Val Gln Arg Thr
Ile Ala Lys Gln Ile Gln Met Val Lys 195 200 205Gln Ile Gly Lys Gly
Arg Tyr Gly Glu Val Trp Met Gly Lys Trp Arg 210 215 220Gly Glu Lys
Val Ala Val Lys Val Phe Phe Thr Thr Glu Glu Ala Ser225 230 235
240Trp Phe Arg Glu Thr Glu Ile Tyr Gln Thr Val Leu Met Arg His Glu
245 250 255Asn Ile Leu Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr Gly
Ser Trp 260 265 270Thr Gln Leu Tyr Leu Ile Thr Asp Tyr His Glu Asn
Gly Ser Leu Tyr 275 280 285Asp Tyr Leu Lys Ser Thr Thr Leu Asp Ala
Lys Ser Met Leu Lys Leu 290 295 300Ala Tyr Ser Ser Val Ser Gly Leu
Cys His Leu His Thr Glu Ile Phe305 310 315 320Ser Thr Gln Gly Lys
Pro Ala Ile Ala His Arg Asp Leu Lys Ser Lys 325 330 335Asn Ile Leu
Val Lys Lys Asn Gly Thr Cys Cys Ile Ala Asp Leu Gly 340 345 350Leu
Ala Val Lys Phe Ile Ser Asp Thr Asn Glu Val Asp Ile Pro Pro 355 360
365Asn Thr Arg Val Gly Thr Lys Arg Tyr Met Pro Pro Glu Val Leu Asp
370 375 380Glu Ser Leu Asn Arg Asn His Phe Gln Ser Tyr Ile Met Ala
Asp Met385 390 395 400Tyr Ser Phe Gly Leu Ile Leu Trp Glu Val Ala
Arg Arg Cys Val Ser 405 410 415Gly Gly Ile Val Glu Glu Tyr Gln Leu
Pro Tyr His Asp Leu Val Pro 420 425 430Ser Asp Pro Ser Tyr Glu Asp
Met Arg Glu Ile Val Cys Ile Lys Lys 435 440 445Leu Arg Pro Ser Phe
Pro Asn Arg Trp Ser Ser Asp Glu Cys Leu Arg 450 455 460Gln Met Gly
Lys Leu Met Thr Glu Cys Trp Ala His Asn Pro Ala Ser465 470 475
480Arg Leu Thr Ala Leu Arg Val Lys Lys Thr Leu Ala Lys Met Ser Glu
485 490 495Ser Gln Asp Ile Lys Leu 50074532PRTRattus sp. 74Met Thr
Gln Leu Tyr Thr Tyr Ile Arg Leu Leu Gly Ala Cys Leu Phe1 5 10 15Ile
Ile Ser His Val Gln Gly Gln Asn Leu Asp Ser Met Leu His Gly 20 25
30Thr Gly Met Lys Ser Asp Val Asp Gln Lys Lys Pro Glu Asn Gly Val
35 40 45Thr Leu Ala Pro Glu Asp Thr Leu Pro Phe Leu Lys Cys Tyr Cys
Ser 50 55 60Gly His Cys Pro Asp Asp Ala Ile Asn Asn Thr Cys Ile Thr
Asn Gly65 70 75 80His Cys Phe Ala Ile Ile Glu Glu Asp Asp Gln Gly
Glu Thr Thr Leu 85 90 95Thr Ser Gly Cys Met Lys Tyr Glu Gly Ser Asp
Phe Gln Cys Lys Asp 100 105 110Ser Pro Lys Ala Gln Leu Arg Arg Thr
Ile Glu Cys Cys Arg Thr Asn 115 120 125Leu Cys Asn Gln Tyr Leu Gln
Pro Thr Leu Pro Pro Val Val Ile Gly 130 135 140Pro Phe Phe Asp Gly
Ser Val Arg Trp Leu Ala Val Leu Ile Ser Met145 150 155 160Ala Val
Cys Ile Val Ala Met Ile Val Phe Ser Ser Cys Phe Cys Tyr 165 170
175Lys His Tyr Cys Lys Ser Ile Ser Ser Arg Gly Arg Tyr Asn Arg Asp
180 185 190Leu Glu Gln Asp Glu Ala Phe Ile Pro Val Gly Glu Ser Leu
Lys Asp 195 200 205Leu Ile Asp Gln Ser Gln Ser Ser Gly Ser Gly Ser
Gly Leu Pro Leu 210 215 220Leu Val Gln Arg Thr Ile Ala Lys Gln Ile
Gln Met Val Arg Gln Val225 230 235 240Gly Lys Gly Arg Tyr Gly Glu
Val Trp Met Gly Lys Trp Arg Gly Glu 245 250 255Lys Val Ala Val Lys
Val Phe Phe Thr Thr Glu Glu Ala Ser Trp Phe 260 265 270Arg Glu Thr
Glu Ile Tyr Gln Thr Val Leu Met Arg His Glu Asn Ile 275 280 285Leu
Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr Gly Ser Trp Thr Gln 290 295
300Leu Tyr Leu Ile Thr Asp Tyr His Glu Asn Gly Ser Leu Tyr Asp
Phe305 310 315 320Leu Lys Cys Ala Thr Leu Asp Thr Arg Ala Leu Leu
Lys Leu Ala Tyr 325 330 335Ser Ala Ala Cys Gly Leu Cys His Leu His
Thr Glu Ile Tyr Gly Thr 340 345 350Gln Gly Lys Pro Ala Ile Ala His
Arg Asp Leu Lys Ser Lys Asn Ile 355 360 365Leu Ile Lys Lys Asn Gly
Ser Cys Cys Ile Ala Asp Leu Gly Leu Ala 370 375 380Val Lys Phe Asn
Ser Asp Thr Asn Glu Val Asp Ile Pro Leu Asn Thr385 390 395 400Arg
Val Gly Thr Arg Arg Tyr Met Ala Pro Glu Val Leu Asp Glu Ser 405 410
415Leu Ser Lys Asn His Phe Gln Pro Tyr Ile Met Ala Asp Ile Tyr Ser
420 425 430Phe Gly Leu Ile Ile Trp Glu Met Ala Arg Arg Cys Ile Thr
Gly Gly 435 440 445Ile Val Glu Glu Tyr Gln Leu Pro Tyr Tyr Asn Met
Val Pro Ser Asp 450 455 460Pro Ser Tyr Glu Asp Met Arg Glu Val Val
Cys Val Lys Arg Leu Arg465 470 475 480Pro Ile Val Ser Asn Arg Trp
Asn Ser Asp Glu Cys Leu Arg Ala Val 485 490 495Leu Lys Leu Met Ser
Glu Cys Trp Ala His Asn Pro Ala Ser Arg Leu 500 505 510Thr Ala Leu
Arg Ile Lys Lys Thr Leu Ala Lys Met Val Glu Ser Gln 515 520 525Asp
Val Lys Ile 53075532PRTRattus norvegicus 75Met Thr Gln Leu Tyr Thr
Tyr Ile Arg Leu Leu Gly Ala Cys Leu Phe1 5 10 15Ile Ile Ser His Val
Gln Gly Gln Asn Leu Asp Ser Met Leu His Gly 20 25 30Thr Gly Met Lys
Ser Asp Val Asp Gln Lys Lys Pro Glu Asn Gly Val 35 40 45Thr Leu Ala
Pro Glu Asp Thr Leu Pro Phe Leu Lys Cys Tyr Cys Ser 50 55 60Gly His
Cys Pro Asp Asp Ala Ile Asn Asn Thr Cys Ile Thr Asn Gly65 70 75
80His Cys Phe Ala Ile Ile Glu Glu Asp Asp Gln Gly Glu Thr Thr Leu
85 90 95Thr Ser Gly Cys Met Lys Tyr Glu Gly Ser Asp Phe Gln Cys Lys
Asp 100 105 110Ser Pro
Lys Ala Gln Leu Arg Arg Thr Ile Glu Cys Cys Arg Thr Asn 115 120
125Leu Cys Asn Gln Tyr Leu Gln Pro Thr Leu Pro Pro Val Val Ile Gly
130 135 140Pro Phe Phe Asp Gly Ser Val Arg Trp Leu Ala Val Leu Ile
Ser Met145 150 155 160Ala Val Cys Ile Val Ala Met Ile Val Phe Ser
Ser Cys Phe Cys Tyr 165 170 175Lys His Tyr Cys Lys Ser Ile Ser Ser
Arg Gly Arg Tyr Asn Arg Asp 180 185 190Leu Glu Gln Asp Glu Ala Phe
Ile Pro Val Gly Glu Ser Leu Lys Asp 195 200 205Leu Ile Asp Gln Ser
Gln Ser Ser Gly Ser Gly Ser Gly Leu Pro Leu 210 215 220Leu Val Gln
Arg Thr Ile Ala Lys Gln Ile Gln Met Val Arg Gln Val225 230 235
240Gly Lys Gly Arg Tyr Gly Glu Val Trp Met Gly Lys Trp Arg Gly Glu
245 250 255Lys Val Ala Val Lys Val Phe Phe Thr Thr Glu Glu Ala Ser
Trp Phe 260 265 270Arg Glu Thr Glu Ile Tyr Gln Thr Val Leu Met Arg
His Glu Asn Ile 275 280 285Leu Gly Phe Ile Ala Ala Asp Ile Lys Gly
Thr Gly Ser Trp Thr Gln 290 295 300Leu Tyr Leu Ile Thr Asp Tyr His
Glu Asn Gly Ser Leu Tyr Asp Phe305 310 315 320Leu Lys Cys Ala Thr
Leu Asp Thr Arg Ala Leu Leu Lys Leu Ala Tyr 325 330 335Ser Ala Ala
Cys Gly Leu Cys His Leu His Thr Glu Ile Tyr Gly Thr 340 345 350Gln
Gly Lys Pro Ala Ile Ala His Arg Asp Leu Lys Ser Lys Asn Ile 355 360
365Leu Ile Lys Lys Asn Gly Ser Cys Cys Ile Ala Asp Leu Gly Leu Ala
370 375 380Val Lys Phe Asn Ser Asp Thr Asn Glu Val Asp Ile Pro Leu
Asn Thr385 390 395 400Arg Val Gly Thr Arg Arg Tyr Met Ala Pro Glu
Val Leu Asp Glu Ser 405 410 415Leu Ser Lys Asn His Phe Gln Pro Tyr
Ile Met Ala Asp Ile Tyr Ser 420 425 430Phe Gly Leu Ile Ile Trp Glu
Met Ala Arg Arg Cys Ile Thr Gly Gly 435 440 445Ile Val Glu Glu Tyr
Gln Leu Pro Tyr Tyr Asn Met Val Pro Ser Asp 450 455 460Pro Ser Tyr
Glu Asp Met Arg Glu Val Val Cys Val Lys Arg Leu Arg465 470 475
480Pro Ile Val Ser Asn Arg Trp Asn Ser Asp Glu Cys Leu Arg Ala Val
485 490 495Leu Lys Leu Met Ser Glu Cys Trp Ala His Asn Pro Ala Ser
Arg Leu 500 505 510Thr Ala Leu Arg Ile Lys Lys Thr Leu Ala Lys Met
Val Glu Ser Gln 515 520 525Asp Val Lys Ile 53076532PRTRattus
norvegicus 76Met Thr Gln Leu Tyr Thr Tyr Ile Arg Leu Leu Gly Ala
Cys Leu Phe1 5 10 15Ile Ile Ser His Val Gln Gly Gln Asn Leu Asp Ser
Met Leu His Gly 20 25 30Thr Gly Met Lys Ser Asp Val Asp Gln Lys Lys
Pro Glu Asn Gly Val 35 40 45Thr Leu Ala Pro Glu Asp Thr Leu Pro Phe
Leu Lys Cys Tyr Cys Ser 50 55 60Gly His Cys Pro Asp Asp Ala Ile Asn
Asn Thr Cys Ile Thr Asn Gly65 70 75 80His Cys Phe Ala Ile Ile Glu
Glu Asp Asp Gln Gly Glu Thr Thr Leu 85 90 95Thr Ser Gly Cys Met Lys
Tyr Glu Gly Ser Asp Phe Gln Cys Lys Asp 100 105 110Ser Pro Lys Ala
Gln Leu Arg Arg Thr Ile Glu Cys Cys Arg Thr Asn 115 120 125Leu Cys
Asn Gln Tyr Leu Gln Pro Thr Leu Pro Pro Val Val Ile Gly 130 135
140Pro Phe Phe Asp Gly Ser Val Arg Trp Leu Ala Val Leu Ile Ser
Met145 150 155 160Ala Val Cys Ile Val Ala Met Ile Val Phe Ser Ser
Cys Phe Cys Tyr 165 170 175Lys His Tyr Cys Lys Ser Ile Ser Ser Arg
Gly Arg Tyr Asn Arg Asp 180 185 190Leu Glu Gln Asp Glu Ala Phe Ile
Pro Val Gly Glu Ser Leu Lys Asp 195 200 205Leu Ile Asp Gln Ser Gln
Ser Ser Gly Ser Gly Ser Gly Leu Pro Leu 210 215 220Leu Val Gln Arg
Thr Ile Ala Lys Gln Ile Gln Met Val Arg Gln Val225 230 235 240Gly
Lys Gly Arg Tyr Gly Glu Val Trp Met Gly Lys Trp Arg Gly Glu 245 250
255Lys Val Ala Val Lys Val Phe Phe Thr Thr Glu Glu Ala Ser Trp Phe
260 265 270Arg Glu Thr Glu Ile Tyr Gln Thr Val Leu Met Arg His Glu
Asn Ile 275 280 285Leu Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr Gly
Ser Trp Thr Gln 290 295 300Leu Tyr Leu Ile Thr Asp Tyr His Glu Asn
Gly Ser Leu Tyr Asp Phe305 310 315 320Leu Lys Cys Ala Thr Leu Asp
Thr Arg Ala Leu Leu Lys Leu Ala Tyr 325 330 335Ser Ala Ala Cys Gly
Leu Cys His Leu His Thr Glu Ile Tyr Gly Thr 340 345 350Gln Gly Lys
Pro Ala Ile Ala His Arg Asp Leu Lys Ser Lys Asn Ile 355 360 365Leu
Ile Lys Lys Asn Gly Ser Cys Cys Ile Ala Asp Leu Gly Leu Ala 370 375
380Val Lys Phe Asn Ser Asp Thr Asn Glu Val Asp Ile Pro Leu Asn
Thr385 390 395 400Arg Val Gly Thr Arg Arg Tyr Met Ala Pro Glu Val
Leu Asp Glu Ser 405 410 415Leu Ser Lys Asn His Phe Gln Pro Tyr Ile
Met Ala Asp Ile Tyr Ser 420 425 430Phe Gly Leu Ile Ile Trp Glu Met
Ala Arg Arg Cys Ile Thr Gly Gly 435 440 445Ile Val Glu Glu Tyr Gln
Leu Pro Tyr Tyr Asn Met Val Pro Ser Asp 450 455 460Pro Ser Tyr Glu
Asp Met Arg Glu Val Val Cys Val Lys Arg Leu Arg465 470 475 480Pro
Ile Val Ser Asn Arg Trp Asn Ser Asp Glu Cys Leu Arg Ala Val 485 490
495Leu Lys Leu Met Ser Glu Cys Trp Ala His Asn Pro Ala Ser Arg Leu
500 505 510Thr Ala Leu Arg Ile Lys Lys Thr Leu Ala Lys Met Val Glu
Ser Gln 515 520 525Asp Val Lys Ile 53077502PRTHomo sapiens 77Met
Leu Leu Arg Ser Ala Gly Lys Leu Asn Val Gly Thr Lys Lys Glu1 5 10
15Asp Gly Glu Ser Thr Ala Pro Thr Pro Arg Pro Lys Val Leu Arg Cys
20 25 30Lys Cys His His His Cys Pro Glu Asp Ser Val Asn Asn Ile Cys
Ser 35 40 45Thr Asp Gly Tyr Cys Phe Thr Met Ile Glu Glu Asp Asp Ser
Gly Leu 50 55 60Pro Val Val Thr Ser Gly Cys Leu Gly Leu Glu Gly Ser
Asp Phe Gln65 70 75 80Cys Arg Asp Thr Pro Ile Pro His Gln Arg Arg
Ser Ile Glu Cys Cys 85 90 95Thr Glu Arg Asn Glu Cys Asn Lys Asp Leu
His Pro Thr Leu Pro Pro 100 105 110Leu Lys Asn Arg Asp Phe Val Asp
Gly Pro Ile His His Arg Ala Leu 115 120 125Leu Ile Ser Val Thr Val
Cys Ser Leu Leu Leu Val Leu Ile Ile Leu 130 135 140Phe Cys Tyr Phe
Arg Tyr Lys Arg Gln Glu Thr Arg Pro Arg Tyr Ser145 150 155 160Ile
Gly Leu Glu Gln Asp Glu Thr Tyr Ile Pro Pro Gly Glu Ser Leu 165 170
175Arg Asp Leu Ile Glu Gln Ser Gln Ser Ser Gly Ser Gly Ser Gly Leu
180 185 190Pro Leu Leu Val Gln Arg Thr Ile Ala Lys Gln Ile Gln Met
Val Lys 195 200 205Gln Ile Gly Lys Gly Arg Tyr Gly Glu Val Trp Met
Gly Lys Trp Arg 210 215 220Gly Glu Lys Val Ala Val Lys Val Phe Phe
Thr Thr Glu Glu Ala Ser225 230 235 240Trp Phe Arg Glu Thr Glu Ile
Tyr Gln Thr Val Leu Met Arg His Glu 245 250 255Asn Ile Leu Gly Phe
Ile Ala Ala Asp Ile Lys Gly Thr Gly Ser Trp 260 265 270Thr Gln Leu
Tyr Leu Ile Thr Asp Tyr His Glu Asn Gly Ser Leu Tyr 275 280 285Asp
Tyr Leu Lys Ser Thr Thr Leu Asp Ala Lys Ser Met Leu Lys Leu 290 295
300Ala Tyr Ser Ser Val Ser Gly Leu Cys His Leu His Thr Glu Ile
Phe305 310 315 320Ser Thr Gln Gly Lys Pro Ala Ile Ala His Arg Asp
Leu Lys Ser Lys 325 330 335Asn Ile Leu Val Lys Lys Asn Gly Thr Cys
Cys Ile Ala Asp Leu Gly 340 345 350Leu Ala Val Lys Phe Ile Ser Asp
Thr Asn Glu Val Asp Ile Pro Pro 355 360 365Asn Thr Arg Val Gly Thr
Lys Arg Tyr Met Pro Pro Glu Val Leu Asp 370 375 380Glu Ser Leu Asn
Arg Asn His Phe Gln Ser Tyr Ile Met Ala Asp Met385 390 395 400Tyr
Ser Phe Gly Leu Ile Leu Trp Glu Val Ala Arg Arg Cys Val Ser 405 410
415Gly Gly Ile Val Glu Glu Tyr Gln Leu Pro Tyr His Asp Leu Val Pro
420 425 430Ser Asp Pro Ser Tyr Glu Asp Met Arg Glu Ile Val Cys Ile
Lys Lys 435 440 445Leu Arg Pro Ser Phe Pro Asn Arg Trp Ser Ser Asp
Glu Cys Leu Arg 450 455 460Gln Met Gly Lys Leu Met Thr Glu Cys Trp
Ala His Asn Pro Ala Ser465 470 475 480Arg Leu Thr Ala Leu Arg Val
Lys Lys Thr Leu Ala Lys Met Ser Glu 485 490 495Ser Gln Asp Ile Lys
Leu 50078502PRTHomo sapiens 78Met Leu Leu Arg Ser Ala Gly Lys Leu
Asn Val Gly Thr Lys Lys Glu1 5 10 15Asp Gly Glu Ser Thr Ala Pro Thr
Pro Arg Pro Lys Val Leu Arg Cys 20 25 30Lys Cys His His His Cys Pro
Glu Asp Ser Val Asn Asn Ile Cys Ser 35 40 45Thr Asp Gly Tyr Cys Phe
Thr Met Ile Glu Glu Asp Asp Ser Gly Leu 50 55 60Pro Val Val Thr Ser
Gly Cys Leu Gly Leu Glu Gly Ser Asp Phe Gln65 70 75 80Cys Arg Asp
Thr Pro Ile Pro His Gln Arg Arg Ser Ile Glu Cys Cys 85 90 95Thr Glu
Arg Asn Glu Cys Asn Lys Asp Leu His Pro Thr Leu Pro Pro 100 105
110Leu Lys Asn Arg Asp Phe Val Asp Gly Pro Ile His His Arg Ala Leu
115 120 125Leu Ile Ser Val Thr Val Cys Ser Leu Leu Leu Val Leu Ile
Ile Leu 130 135 140Phe Cys Tyr Phe Arg Tyr Lys Arg Gln Glu Thr Arg
Pro Arg Tyr Ser145 150 155 160Ile Gly Leu Glu Gln Asp Glu Thr Tyr
Ile Pro Pro Gly Glu Ser Leu 165 170 175Arg Asp Leu Ile Glu Gln Ser
Gln Ser Ser Gly Ser Gly Ser Gly Leu 180 185 190Pro Leu Leu Val Gln
Arg Thr Ile Ala Lys Gln Ile Gln Met Val Lys 195 200 205Gln Ile Gly
Lys Gly Arg Tyr Gly Glu Val Trp Met Gly Lys Trp Arg 210 215 220Gly
Glu Lys Val Ala Val Lys Val Phe Phe Thr Thr Glu Glu Ala Ser225 230
235 240Trp Phe Arg Glu Thr Glu Ile Tyr Gln Thr Val Leu Met Arg His
Glu 245 250 255Asn Ile Leu Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr
Gly Ser Trp 260 265 270Thr Gln Leu Tyr Leu Ile Thr Asp Tyr His Glu
Asn Gly Ser Leu Tyr 275 280 285Asp Tyr Leu Lys Ser Thr Thr Leu Asp
Ala Lys Ser Met Leu Lys Leu 290 295 300Ala Tyr Ser Ser Val Ser Gly
Leu Cys His Leu His Thr Glu Ile Phe305 310 315 320Ser Thr Gln Gly
Lys Pro Ala Ile Ala His Arg Asp Leu Lys Ser Lys 325 330 335Asn Ile
Leu Val Lys Lys Asn Gly Thr Cys Cys Ile Ala Asp Leu Gly 340 345
350Leu Ala Val Lys Phe Ile Ser Asp Thr Asn Glu Val Asp Ile Pro Pro
355 360 365Asn Thr Arg Val Gly Thr Lys Arg Tyr Met Pro Pro Glu Val
Leu Asp 370 375 380Glu Ser Leu Asn Arg Asn His Phe Gln Ser Tyr Ile
Met Ala Asp Met385 390 395 400Tyr Ser Phe Gly Leu Ile Leu Trp Glu
Val Ala Arg Arg Cys Val Ser 405 410 415Gly Gly Ile Val Glu Glu Tyr
Gln Leu Pro Tyr His Asp Leu Val Pro 420 425 430Ser Asp Pro Ser Tyr
Glu Asp Met Arg Glu Ile Val Cys Ile Lys Lys 435 440 445Leu Arg Pro
Ser Phe Pro Asn Arg Trp Ser Ser Asp Glu Cys Leu Arg 450 455 460Gln
Met Gly Lys Leu Met Thr Glu Cys Trp Ala His Asn Pro Ala Ser465 470
475 480Arg Leu Thr Ala Leu Arg Val Lys Lys Thr Leu Ala Lys Met Ser
Glu 485 490 495Ser Gln Asp Ile Lys Leu 50079532PRTRattus sp. 79Met
Thr Gln Leu Tyr Thr Tyr Ile Arg Leu Leu Gly Ala Cys Leu Phe1 5 10
15Ile Ile Ser His Val Gln Gly Gln Asn Leu Asp Ser Met Leu His Gly
20 25 30Thr Gly Met Lys Ser Asp Val Asp Gln Lys Lys Pro Glu Asn Gly
Val 35 40 45Thr Leu Ala Pro Glu Asp Thr Leu Pro Phe Leu Lys Cys Tyr
Cys Ser 50 55 60Gly His Cys Pro Asp Asp Ala Ile Asn Asn Thr Cys Ile
Thr Asn Gly65 70 75 80His Cys Phe Ala Ile Ile Glu Glu Asp Asp Gln
Gly Glu Thr Thr Leu 85 90 95Thr Ser Gly Cys Met Lys Tyr Glu Gly Ser
Asp Phe Gln Cys Lys Asp 100 105 110Ser Pro Lys Ala Gln Leu Arg Arg
Thr Ile Glu Cys Cys Arg Thr Asn 115 120 125Leu Cys Asn Gln Tyr Leu
Gln Pro Thr Leu Pro Pro Val Val Ile Gly 130 135 140Pro Phe Phe Asp
Gly Ser Val Arg Trp Leu Ala Val Leu Ile Ser Met145 150 155 160Ala
Val Cys Ile Val Ala Met Ile Val Phe Ser Ser Cys Phe Cys Tyr 165 170
175Lys His Tyr Cys Lys Ser Ile Ser Ser Arg Gly Arg Tyr Asn Arg Asp
180 185 190Leu Glu Gln Asp Glu Ala Phe Ile Pro Val Gly Glu Ser Leu
Lys Asp 195 200 205Leu Ile Asp Gln Ser Gln Ser Ser Gly Ser Gly Ser
Gly Leu Pro Leu 210 215 220Leu Val Gln Arg Thr Ile Ala Lys Gln Ile
Gln Met Val Arg Gln Val225 230 235 240Gly Lys Gly Arg Tyr Gly Glu
Val Trp Met Gly Lys Trp Arg Gly Glu 245 250 255Lys Val Ala Val Lys
Val Phe Phe Thr Thr Glu Glu Ala Ser Trp Phe 260 265 270Arg Glu Thr
Glu Ile Tyr Gln Thr Val Leu Met Arg His Glu Asn Ile 275 280 285Leu
Gly Phe Ile Ala Ala Asp Ile Lys Gly Thr Gly Ser Trp Thr Gln 290 295
300Leu Tyr Leu Ile Thr Asp Tyr His Glu Asn Gly Ser Leu Tyr Asp
Phe305 310 315 320Leu Lys Cys Ala Thr Leu Asp Thr Arg Ala Leu Leu
Lys Leu Ala Tyr 325 330 335Ser Ala Ala Cys Gly Leu Cys His Leu His
Thr Glu Ile Tyr Gly Thr 340 345 350Gln Gly Lys Pro Ala Ile Ala His
Arg Asp Leu Lys Ser Lys Asn Ile 355 360 365Leu Ile Lys Lys Asn Gly
Ser Cys Cys Ile Ala Asp Leu Gly Leu Ala 370 375 380Val Lys Phe Asn
Ser Asp Thr Asn Glu Val Asp Ile Pro Leu Asn Thr385 390 395 400Arg
Val Gly Thr Arg Arg Tyr Met Ala Pro Glu Val Leu Asp Glu Ser 405 410
415Leu Ser Lys Asn His Phe Gln Pro Tyr Ile Met Ala Asp Ile Tyr Ser
420 425 430Phe Gly Leu Ile Ile Trp Glu Met Ala Arg Arg Cys Ile Thr
Gly Gly 435 440 445Ile Val Glu Glu Tyr Gln Leu Pro Tyr Tyr Asn Met
Val Pro Ser Asp 450 455 460Pro Ser Tyr Glu Asp Met Arg Glu Val Val
Cys Val Lys Arg Leu Arg465 470 475 480Pro Ile Val Ser Asn Arg Trp
Asn Ser Asp Glu Cys Leu Arg Ala Val 485 490 495Leu Lys Leu Met Ser
Glu Cys Trp Ala His Asn Pro Ala Ser Arg Leu 500 505 510Thr
Ala Leu Arg Ile Lys Lys Thr Leu Ala Lys Met Val Glu Ser Gln 515 520
525Asp Val Lys Ile 53080530PRTHomo sapiens 80Met Thr Ser Ser Leu
Gln Arg Pro Trp Arg Val Pro Trp Leu Pro Trp1 5 10 15Thr Ile Leu Leu
Val Ser Thr Ala Ala Ala Ser Gln Asn Gln Glu Arg 20 25 30Leu Cys Ala
Phe Lys Asp Pro Tyr Gln Gln Asp Leu Gly Ile Gly Glu 35 40 45Ser Arg
Ile Ser His Glu Asn Gly Thr Ile Leu Cys Ser Lys Gly Ser 50 55 60Thr
Cys Tyr Gly Leu Trp Glu Lys Ser Lys Gly Asp Ile Asn Leu Val65 70 75
80Lys Gln Gly Cys Trp Ser His Ile Gly Asp Pro Gln Glu Cys His Tyr
85 90 95Glu Glu Cys Val Val Thr Thr Thr Pro Pro Ser Ile Gln Asn Gly
Thr 100 105 110Tyr Arg Phe Cys Cys Cys Ser Thr Asp Leu Cys Asn Val
Asn Phe Thr 115 120 125Glu Asn Phe Pro Pro Pro Asp Thr Thr Pro Leu
Ser Pro Pro His Ser 130 135 140Phe Asn Arg Asp Glu Thr Ile Ile Ile
Ala Leu Ala Ser Val Ser Val145 150 155 160Leu Ala Val Leu Ile Val
Ala Leu Cys Phe Gly Tyr Arg Met Leu Thr 165 170 175Gly Asp Arg Lys
Gln Gly Leu His Ser Met Asn Met Met Glu Ala Ala 180 185 190Ala Ser
Glu Pro Ser Leu Asp Leu Asp Asn Leu Lys Leu Leu Glu Leu 195 200
205Ile Gly Arg Gly Arg Tyr Gly Ala Val Tyr Lys Gly Ser Leu Asp Glu
210 215 220Arg Pro Val Ala Val Lys Val Phe Ser Phe Ala Asn Arg Gln
Asn Phe225 230 235 240Ile Asn Glu Lys Asn Ile Tyr Arg Val Pro Leu
Met Glu His Asp Asn 245 250 255Ile Ala Arg Phe Ile Val Gly Asp Glu
Arg Val Thr Ala Asp Gly Arg 260 265 270Met Glu Tyr Leu Leu Val Met
Glu Tyr Tyr Pro Asn Gly Ser Leu Cys 275 280 285Lys Tyr Leu Ser Leu
His Thr Ser Asp Trp Val Ser Ser Cys Arg Leu 290 295 300Ala His Ser
Val Thr Arg Gly Leu Ala Tyr Leu His Thr Glu Leu Pro305 310 315
320Arg Gly Asp His Tyr Lys Pro Ala Ile Ser His Arg Asp Leu Asn Ser
325 330 335Arg Asn Val Leu Val Lys Asn Asp Gly Thr Cys Val Ile Ser
Asp Phe 340 345 350Gly Leu Ser Met Arg Leu Thr Gly Asn Arg Leu Val
Arg Pro Gly Glu 355 360 365Glu Asp Asn Ala Ala Ile Ser Glu Val Gly
Thr Ile Arg Tyr Met Ala 370 375 380Pro Glu Val Leu Glu Gly Ala Val
Asn Leu Arg Asp Cys Glu Ser Ala385 390 395 400Leu Lys Gln Val Asp
Met Tyr Ala Leu Gly Leu Ile Tyr Trp Glu Ile 405 410 415Phe Met Arg
Cys Thr Asp Leu Phe Pro Gly Glu Ser Val Pro Glu Tyr 420 425 430Gln
Met Ala Phe Gln Thr Glu Val Gly Asn His Pro Thr Phe Glu Asp 435 440
445Met Gln Val Leu Val Ser Arg Glu Lys Gln Arg Pro Lys Phe Pro Glu
450 455 460Ala Trp Lys Glu Asn Ser Leu Ala Val Arg Ser Leu Lys Glu
Thr Ile465 470 475 480Glu Asp Cys Trp Asp Gln Asp Ala Glu Ala Arg
Leu Thr Ala Gln Cys 485 490 495Ala Glu Glu Arg Met Ala Glu Leu Met
Met Ile Trp Glu Arg Asn Lys 500 505 510Ser Val Ser Pro Thr Val Asn
Pro Met Ser Thr Ala Met Gln Asn Glu 515 520 525Arg Arg
53081530PRTHomo sapiens 81Met Thr Ser Ser Leu Gln Arg Pro Trp Arg
Val Pro Trp Leu Pro Trp1 5 10 15Thr Ile Leu Leu Val Ser Thr Ala Ala
Ala Ser Gln Asn Gln Glu Arg 20 25 30Leu Cys Ala Phe Lys Asp Pro Tyr
Gln Gln Asp Leu Gly Ile Gly Glu 35 40 45Ser Arg Ile Ser His Glu Asn
Gly Thr Ile Leu Cys Ser Lys Gly Ser 50 55 60Thr Cys Tyr Gly Leu Trp
Glu Lys Ser Lys Gly Asp Ile Asn Leu Val65 70 75 80Lys Gln Gly Cys
Trp Ser His Ile Gly Asp Pro Gln Glu Cys His Tyr 85 90 95Glu Glu Cys
Val Val Thr Thr Thr Pro Pro Ser Ile Gln Asn Gly Thr 100 105 110Tyr
Arg Phe Cys Cys Cys Ser Thr Asp Leu Cys Asn Val Asn Phe Thr 115 120
125Glu Asn Phe Pro Pro Pro Asp Thr Thr Pro Leu Ser Pro Pro His Ser
130 135 140Phe Asn Arg Asp Glu Thr Ile Ile Ile Ala Leu Ala Ser Val
Ser Val145 150 155 160Leu Ala Val Leu Ile Val Ala Leu Cys Phe Gly
Tyr Arg Met Leu Thr 165 170 175Gly Asp Arg Lys Gln Gly Leu His Ser
Met Asn Met Met Glu Ala Ala 180 185 190Ala Ser Glu Pro Ser Leu Asp
Leu Asp Asn Leu Lys Leu Leu Glu Leu 195 200 205Ile Gly Arg Gly Arg
Tyr Gly Ala Val Tyr Lys Gly Ser Leu Asp Glu 210 215 220Arg Pro Val
Ala Val Lys Val Phe Ser Phe Ala Asn Arg Gln Asn Phe225 230 235
240Ile Asn Glu Lys Asn Ile Tyr Arg Val Pro Leu Met Glu His Asp Asn
245 250 255Ile Ala Arg Phe Ile Val Gly Asp Glu Arg Val Thr Ala Asp
Gly Arg 260 265 270Met Glu Tyr Leu Leu Val Met Glu Tyr Tyr Pro Asn
Gly Ser Leu Cys 275 280 285Lys Tyr Leu Ser Leu His Thr Ser Asp Trp
Val Ser Ser Cys Arg Leu 290 295 300Ala His Ser Val Thr Arg Gly Leu
Ala Tyr Leu His Thr Glu Leu Pro305 310 315 320Arg Gly Asp His Tyr
Lys Pro Ala Ile Ser His Arg Asp Leu Asn Ser 325 330 335Arg Asn Val
Leu Val Lys Asn Asp Gly Thr Cys Val Ile Ser Asp Phe 340 345 350Gly
Leu Ser Met Arg Leu Thr Gly Asn Arg Leu Val Arg Pro Gly Glu 355 360
365Glu Asp Asn Ala Ala Ile Ser Glu Val Gly Thr Ile Arg Tyr Met Ala
370 375 380Pro Glu Val Leu Glu Gly Ala Val Asn Leu Arg Asp Cys Glu
Ser Ala385 390 395 400Leu Lys Gln Val Asp Met Tyr Ala Leu Gly Leu
Ile Tyr Trp Glu Ile 405 410 415Phe Met Arg Cys Thr Asp Leu Phe Pro
Gly Glu Ser Val Pro Glu Tyr 420 425 430Gln Met Ala Phe Gln Thr Glu
Val Gly Asn His Pro Thr Phe Glu Asp 435 440 445Met Gln Val Leu Val
Ser Arg Glu Lys Gln Arg Pro Lys Phe Pro Glu 450 455 460Ala Trp Lys
Glu Asn Ser Leu Ala Val Arg Ser Leu Lys Glu Thr Ile465 470 475
480Glu Asp Cys Trp Asp Gln Asp Ala Glu Ala Arg Leu Thr Ala Gln Cys
485 490 495Ala Glu Glu Arg Met Ala Glu Leu Met Met Ile Trp Glu Arg
Asn Lys 500 505 510Ser Val Ser Pro Thr Val Asn Pro Met Ser Thr Ala
Met Gln Asn Glu 515 520 525Arg Arg 530821038PRTHomo sapiens 82Met
Thr Ser Ser Leu Gln Arg Pro Trp Arg Val Pro Trp Leu Pro Trp1 5 10
15Thr Ile Leu Leu Val Ser Thr Ala Ala Ala Ser Gln Asn Gln Glu Arg
20 25 30Leu Cys Ala Phe Lys Asp Pro Tyr Gln Gln Asp Leu Gly Ile Gly
Glu 35 40 45Ser Arg Ile Ser His Glu Asn Gly Thr Ile Leu Cys Ser Lys
Gly Ser 50 55 60Thr Cys Tyr Gly Leu Trp Glu Lys Ser Lys Gly Asp Ile
Asn Leu Val65 70 75 80Lys Gln Gly Cys Trp Ser His Ile Gly Asp Pro
Gln Glu Cys His Tyr 85 90 95Glu Glu Cys Val Val Thr Thr Thr Pro Pro
Ser Ile Gln Asn Gly Thr 100 105 110Tyr Arg Phe Cys Cys Cys Ser Thr
Asp Leu Cys Asn Val Asn Phe Thr 115 120 125Glu Asn Phe Pro Pro Pro
Asp Thr Thr Pro Leu Ser Pro Pro His Ser 130 135 140Phe Asn Arg Asp
Glu Thr Ile Ile Ile Ala Leu Ala Ser Val Ser Val145 150 155 160Leu
Ala Val Leu Ile Val Ala Leu Cys Phe Gly Tyr Arg Met Leu Thr 165 170
175Gly Asp Arg Lys Gln Gly Leu His Ser Met Asn Met Met Glu Ala Ala
180 185 190Ala Ser Glu Pro Ser Leu Asp Leu Asp Asn Leu Lys Leu Leu
Glu Leu 195 200 205Ile Gly Arg Gly Arg Tyr Gly Ala Val Tyr Lys Gly
Ser Leu Asp Glu 210 215 220Arg Pro Val Ala Val Lys Val Phe Ser Phe
Ala Asn Arg Gln Asn Phe225 230 235 240Ile Asn Glu Lys Asn Ile Tyr
Arg Val Pro Leu Met Glu His Asp Asn 245 250 255Ile Ala Arg Phe Ile
Val Gly Asp Glu Arg Val Thr Ala Asp Gly Arg 260 265 270Met Glu Tyr
Leu Leu Val Met Glu Tyr Tyr Pro Asn Gly Ser Leu Cys 275 280 285Lys
Tyr Leu Ser Leu His Thr Ser Asp Trp Val Ser Ser Cys Arg Leu 290 295
300Ala His Ser Val Thr Arg Gly Leu Ala Tyr Leu His Thr Glu Leu
Pro305 310 315 320Arg Gly Asp His Tyr Lys Pro Ala Ile Ser His Arg
Asp Leu Asn Ser 325 330 335Arg Asn Val Leu Val Lys Asn Asp Gly Thr
Cys Val Ile Ser Asp Phe 340 345 350Gly Leu Ser Met Arg Leu Thr Gly
Asn Arg Leu Val Arg Pro Gly Glu 355 360 365Glu Asp Asn Ala Ala Ile
Ser Glu Val Gly Thr Ile Arg Tyr Met Ala 370 375 380Pro Glu Val Leu
Glu Gly Ala Val Asn Leu Arg Asp Cys Glu Ser Ala385 390 395 400Leu
Lys Gln Val Asp Met Tyr Ala Leu Gly Leu Ile Tyr Trp Glu Ile 405 410
415Phe Met Arg Cys Thr Asp Leu Phe Pro Gly Glu Ser Val Pro Glu Tyr
420 425 430Gln Met Ala Phe Gln Thr Glu Val Gly Asn His Pro Thr Phe
Glu Asp 435 440 445Met Gln Val Leu Val Ser Arg Glu Lys Gln Arg Pro
Lys Phe Pro Glu 450 455 460Ala Trp Lys Glu Asn Ser Leu Ala Val Arg
Ser Leu Lys Glu Thr Ile465 470 475 480Glu Asp Cys Trp Asp Gln Asp
Ala Glu Ala Arg Leu Thr Ala Gln Cys 485 490 495Ala Glu Glu Arg Met
Ala Glu Leu Met Met Ile Trp Glu Arg Asn Lys 500 505 510Ser Val Ser
Pro Thr Val Asn Pro Met Ser Thr Ala Met Gln Asn Glu 515 520 525Arg
Asn Leu Ser His Asn Arg Arg Val Pro Lys Ile Gly Pro Tyr Pro 530 535
540Asp Tyr Ser Ser Ser Ser Tyr Ile Glu Asp Ser Ile His His Thr
Asp545 550 555 560Ser Ile Val Lys Asn Ile Ser Ser Glu His Ser Met
Ser Ser Thr Pro 565 570 575Leu Thr Ile Gly Glu Lys Asn Arg Asn Ser
Ile Asn Tyr Glu Arg Gln 580 585 590Gln Ala Gln Ala Arg Ile Pro Ser
Pro Glu Thr Ser Val Thr Ser Leu 595 600 605Ser Thr Asn Thr Thr Thr
Thr Asn Thr Thr Gly Leu Thr Pro Ser Thr 610 615 620Gly Met Thr Thr
Ile Ser Glu Met Pro Tyr Pro Asp Glu Thr Asn Leu625 630 635 640His
Thr Thr Asn Val Ala Gln Ser Ile Gly Pro Thr Pro Val Cys Leu 645 650
655Gln Leu Thr Glu Glu Asp Leu Glu Thr Asn Lys Leu Asp Pro Lys Glu
660 665 670Val Asp Lys Asn Leu Lys Glu Ser Ser Asp Glu Asn Leu Met
Glu His 675 680 685Ser Leu Lys Gln Phe Ser Gly Pro Asp Pro Leu Ser
Ser Thr Ser Ser 690 695 700Ser Leu Leu Tyr Pro Leu Ile Lys Leu Ala
Val Glu Ala Thr Gly Gln705 710 715 720Gln Asp Phe Thr Gln Thr Ala
Asn Gly Gln Ala Cys Leu Ile Pro Asp 725 730 735Val Leu Pro Thr Gln
Ile Tyr Pro Leu Pro Lys Gln Gln Asn Leu Pro 740 745 750Lys Arg Pro
Thr Ser Leu Pro Leu Asn Thr Lys Asn Ser Thr Lys Glu 755 760 765Pro
Arg Leu Lys Phe Gly Ser Lys His Lys Ser Asn Leu Lys Gln Val 770 775
780Glu Thr Gly Val Ala Lys Met Asn Thr Ile Asn Ala Ala Glu Pro
His785 790 795 800Val Val Thr Val Thr Met Asn Gly Val Ala Gly Arg
Asn His Ser Val 805 810 815Asn Ser His Ala Ala Thr Thr Gln Tyr Ala
Asn Gly Thr Val Leu Ser 820 825 830Gly Gln Thr Thr Asn Ile Val Thr
His Arg Ala Gln Glu Met Leu Gln 835 840 845Asn Gln Phe Ile Gly Glu
Asp Thr Arg Leu Asn Ile Asn Ser Ser Pro 850 855 860Asp Glu His Glu
Pro Leu Leu Arg Arg Glu Gln Gln Ala Gly His Asp865 870 875 880Glu
Gly Val Leu Asp Arg Leu Val Asp Arg Arg Glu Arg Pro Leu Glu 885 890
895Gly Gly Arg Thr Asn Ser Asn Asn Asn Asn Ser Asn Pro Cys Ser Glu
900 905 910Gln Asp Val Leu Ala Gln Gly Val Pro Ser Thr Ala Ala Asp
Pro Gly 915 920 925Pro Ser Lys Pro Arg Arg Ala Gln Arg Pro Asn Ser
Leu Asp Leu Ser 930 935 940Ala Thr Asn Val Leu Asp Gly Ser Ser Ile
Gln Ile Gly Glu Ser Thr945 950 955 960Gln Asp Gly Lys Ser Gly Ser
Gly Glu Lys Ile Lys Lys Arg Val Lys 965 970 975Thr Pro Tyr Ser Leu
Lys Arg Trp Arg Pro Ser Thr Trp Val Ile Ser 980 985 990Thr Glu Ser
Leu Asp Cys Glu Val Asn Asn Asn Gly Ser Asn Arg Ala 995 1000
1005Val His Ser Lys Ser Ser Thr Ala Val Tyr Leu Ala Glu Gly Gly
1010 1015 1020Thr Ala Thr Thr Met Val Ser Lys Asp Ile Gly Met Asn
Cys Leu 1025 1030 1035831038PRTHomo sapiens 83Met Thr Ser Ser Leu
Gln Arg Pro Trp Arg Val Pro Trp Leu Pro Trp1 5 10 15Thr Ile Leu Leu
Val Ser Thr Ala Ala Ala Ser Gln Asn Gln Glu Arg 20 25 30Leu Cys Ala
Phe Lys Asp Pro Tyr Gln Gln Asp Leu Gly Ile Gly Glu 35 40 45Ser Arg
Ile Ser His Glu Asn Gly Thr Ile Leu Cys Ser Lys Gly Ser 50 55 60Thr
Cys Tyr Gly Leu Trp Glu Lys Ser Lys Gly Asp Ile Asn Leu Val65 70 75
80Lys Gln Gly Cys Trp Ser His Ile Gly Asp Pro Gln Glu Cys His Tyr
85 90 95Glu Glu Cys Val Val Thr Thr Thr Pro Pro Ser Ile Gln Asn Gly
Thr 100 105 110Tyr Arg Phe Cys Cys Cys Ser Thr Asp Leu Cys Asn Val
Asn Phe Thr 115 120 125Glu Asn Phe Pro Pro Pro Asp Thr Thr Pro Leu
Ser Pro Pro His Ser 130 135 140Phe Asn Arg Asp Glu Thr Ile Ile Ile
Ala Leu Ala Ser Val Ser Val145 150 155 160Leu Ala Val Leu Ile Val
Ala Leu Cys Phe Gly Tyr Arg Met Leu Thr 165 170 175Gly Asp Arg Lys
Gln Gly Leu His Ser Met Asn Met Met Glu Ala Ala 180 185 190Ala Ser
Glu Pro Ser Leu Asp Leu Asp Asn Leu Lys Leu Leu Glu Leu 195 200
205Ile Gly Arg Gly Arg Tyr Gly Ala Val Tyr Lys Gly Ser Leu Asp Glu
210 215 220Arg Pro Val Ala Val Lys Val Phe Ser Phe Ala Asn Arg Gln
Asn Phe225 230 235 240Ile Asn Glu Lys Asn Ile Tyr Arg Val Pro Leu
Met Glu His Asp Asn 245 250 255Ile Ala Arg Phe Ile Val Gly Asp Glu
Arg Val Thr Ala Asp Gly Arg 260 265 270Met Glu Tyr Leu Leu Val Met
Glu Tyr Tyr Pro Asn Gly Ser Leu Cys 275 280 285Lys Tyr Leu Ser Leu
His Thr Ser Asp Trp Val Ser Ser Cys Arg Leu 290 295 300Ala His Ser
Val Thr Arg Gly Leu Ala Tyr Leu His Thr Glu Leu Pro305 310 315
320Arg Gly Asp His Tyr Lys Pro Ala Ile Ser His Arg Asp Leu Asn Ser
325 330 335Arg Asn Val Leu Val Lys Asn Asp Gly Thr Cys Val
Ile Ser Asp Phe 340 345 350Gly Leu Ser Met Arg Leu Thr Gly Asn Arg
Leu Val Arg Pro Gly Glu 355 360 365Glu Asp Asn Ala Ala Ile Ser Glu
Val Gly Thr Ile Arg Tyr Met Ala 370 375 380Pro Glu Val Leu Glu Gly
Ala Val Asn Leu Arg Asp Cys Glu Ser Ala385 390 395 400Leu Lys Gln
Val Asp Met Tyr Ala Leu Gly Leu Ile Tyr Trp Glu Ile 405 410 415Phe
Met Arg Cys Thr Asp Leu Phe Pro Gly Glu Ser Val Pro Glu Tyr 420 425
430Gln Met Ala Phe Gln Thr Glu Val Gly Asn His Pro Thr Phe Glu Asp
435 440 445Met Gln Val Leu Val Ser Arg Glu Lys Gln Arg Pro Lys Phe
Pro Glu 450 455 460Ala Trp Lys Glu Asn Ser Leu Ala Val Arg Ser Leu
Lys Glu Thr Ile465 470 475 480Glu Asp Cys Trp Asp Gln Asp Ala Glu
Ala Arg Leu Thr Ala Gln Cys 485 490 495Ala Glu Glu Arg Met Ala Glu
Leu Met Met Ile Trp Glu Arg Asn Lys 500 505 510Ser Val Ser Pro Thr
Val Asn Pro Met Ser Thr Ala Met Gln Asn Glu 515 520 525Arg Asn Leu
Ser His Asn Arg Arg Val Pro Lys Ile Gly Pro Tyr Pro 530 535 540Asp
Tyr Ser Ser Ser Ser Tyr Ile Glu Asp Ser Ile His His Thr Asp545 550
555 560Ser Ile Val Lys Asn Ile Ser Ser Glu His Ser Met Ser Ser Thr
Pro 565 570 575Leu Thr Ile Gly Glu Lys Asn Arg Asn Ser Ile Asn Tyr
Glu Arg Gln 580 585 590Gln Ala Gln Ala Arg Ile Pro Ser Pro Glu Thr
Ser Val Thr Ser Leu 595 600 605Ser Thr Asn Thr Thr Thr Thr Asn Thr
Thr Gly Leu Thr Pro Ser Thr 610 615 620Gly Met Thr Thr Ile Ser Glu
Met Pro Tyr Pro Asp Glu Thr Asn Leu625 630 635 640His Thr Thr Asn
Val Ala Gln Ser Ile Gly Pro Thr Pro Val Cys Leu 645 650 655Gln Leu
Thr Glu Glu Asp Leu Glu Thr Asn Lys Leu Asp Pro Lys Glu 660 665
670Val Asp Lys Asn Leu Lys Glu Ser Ser Asp Glu Asn Leu Met Glu His
675 680 685Ser Leu Lys Gln Phe Ser Gly Pro Asp Pro Leu Ser Ser Thr
Ser Ser 690 695 700Ser Leu Leu Tyr Pro Leu Ile Lys Leu Ala Val Glu
Ala Thr Gly Gln705 710 715 720Gln Asp Phe Thr Gln Thr Ala Asn Gly
Gln Ala Cys Leu Ile Pro Asp 725 730 735Val Leu Pro Thr Gln Ile Tyr
Pro Leu Pro Lys Gln Gln Asn Leu Pro 740 745 750Lys Arg Pro Thr Ser
Leu Pro Leu Asn Thr Lys Asn Ser Thr Lys Glu 755 760 765Pro Arg Leu
Lys Phe Gly Ser Lys His Lys Ser Asn Leu Lys Gln Val 770 775 780Glu
Thr Gly Val Ala Lys Met Asn Thr Ile Asn Ala Ala Glu Pro His785 790
795 800Val Val Thr Val Thr Met Asn Gly Val Ala Gly Arg Asn His Ser
Val 805 810 815Asn Ser His Ala Ala Thr Thr Gln Tyr Ala Asn Arg Thr
Val Leu Ser 820 825 830Gly Gln Thr Thr Asn Ile Val Thr His Arg Ala
Gln Glu Met Leu Gln 835 840 845Asn Gln Phe Ile Gly Glu Asp Thr Arg
Leu Asn Ile Asn Ser Ser Pro 850 855 860Asp Glu His Glu Pro Leu Leu
Arg Arg Glu Gln Gln Ala Gly His Asp865 870 875 880Glu Gly Val Leu
Asp Arg Leu Val Asp Arg Arg Glu Arg Pro Leu Glu 885 890 895Gly Gly
Arg Thr Asn Ser Asn Asn Asn Asn Ser Asn Pro Cys Ser Glu 900 905
910Gln Asp Val Leu Ala Gln Gly Val Pro Ser Thr Ala Ala Asp Pro Gly
915 920 925Pro Ser Lys Pro Arg Arg Ala Gln Arg Pro Asn Ser Leu Asp
Leu Ser 930 935 940Ala Thr Asn Val Leu Asp Gly Ser Ser Ile Gln Ile
Gly Glu Ser Thr945 950 955 960Gln Asp Gly Lys Ser Gly Ser Gly Glu
Lys Ile Lys Lys Arg Val Lys 965 970 975Thr Pro Tyr Ser Leu Lys Arg
Trp Arg Pro Ser Thr Trp Val Ile Ser 980 985 990Thr Glu Ser Leu Asp
Cys Glu Val Asn Asn Asn Gly Ser Asn Arg Ala 995 1000 1005Val His
Ser Lys Ser Ser Thr Ala Val Tyr Leu Ala Glu Gly Gly 1010 1015
1020Thr Ala Thr Thr Met Val Ser Lys Asp Ile Gly Met Asn Cys Leu
1025 1030 1035841038PRTHomo sapiens 84Met Thr Ser Ser Leu Gln Arg
Pro Trp Arg Val Pro Trp Leu Pro Trp1 5 10 15Thr Ile Leu Leu Val Ser
Thr Ala Ala Ala Ser Gln Asn Gln Glu Arg 20 25 30Leu Cys Ala Phe Lys
Asp Pro Tyr Gln Gln Asp Leu Gly Ile Gly Glu 35 40 45Ser Arg Ile Ser
His Glu Asn Gly Thr Ile Leu Cys Ser Lys Gly Ser 50 55 60Thr Cys Tyr
Gly Leu Trp Glu Lys Ser Lys Gly Asp Ile Asn Leu Val65 70 75 80Lys
Gln Gly Cys Trp Ser His Ile Gly Asp Pro Gln Glu Cys His Tyr 85 90
95Glu Glu Cys Val Val Thr Thr Thr Pro Pro Ser Ile Gln Asn Gly Thr
100 105 110Tyr Arg Phe Cys Cys Cys Ser Thr Asp Leu Cys Asn Val Asn
Phe Thr 115 120 125Glu Asn Phe Pro Pro Pro Asp Thr Thr Pro Leu Ser
Pro Pro His Ser 130 135 140Phe Asn Arg Asp Glu Thr Ile Ile Ile Ala
Leu Ala Ser Val Ser Val145 150 155 160Leu Ala Val Leu Ile Val Ala
Leu Cys Phe Gly Tyr Arg Met Leu Thr 165 170 175Gly Asp Arg Lys Gln
Gly Leu His Ser Met Asn Met Met Glu Ala Ala 180 185 190Ala Ser Glu
Pro Ser Leu Asp Leu Asp Asn Leu Lys Leu Leu Glu Leu 195 200 205Ile
Gly Arg Gly Arg Tyr Gly Ala Val Tyr Lys Gly Ser Leu Asp Glu 210 215
220Arg Pro Val Ala Val Lys Val Phe Ser Phe Ala Asn Arg Gln Asn
Phe225 230 235 240Ile Asn Glu Lys Asn Ile Tyr Arg Val Pro Leu Met
Glu His Asp Asn 245 250 255Ile Ala Arg Phe Ile Val Gly Asp Glu Arg
Val Thr Ala Asp Gly Arg 260 265 270Met Glu Tyr Leu Leu Val Met Glu
Tyr Tyr Pro Asn Gly Ser Leu Cys 275 280 285Lys Tyr Leu Ser Leu His
Thr Ser Asp Trp Val Ser Ser Cys Arg Leu 290 295 300Ala His Ser Val
Thr Arg Gly Leu Ala Tyr Leu His Thr Glu Leu Pro305 310 315 320Arg
Gly Asp His Tyr Lys Pro Ala Ile Ser His Arg Asp Leu Asn Ser 325 330
335Arg Asn Val Leu Val Lys Asn Asp Gly Thr Cys Val Ile Ser Asp Phe
340 345 350Gly Leu Ser Met Arg Leu Thr Gly Asn Arg Leu Val Arg Pro
Gly Glu 355 360 365Glu Asp Asn Ala Ala Ile Ser Glu Val Gly Thr Ile
Arg Tyr Met Ala 370 375 380Pro Glu Val Leu Glu Gly Ala Val Asn Leu
Arg Asp Cys Glu Ser Ala385 390 395 400Leu Lys Gln Val Asp Met Tyr
Ala Leu Gly Leu Ile Tyr Trp Glu Ile 405 410 415Phe Met Arg Cys Thr
Asp Leu Phe Pro Gly Glu Ser Val Pro Glu Tyr 420 425 430Gln Met Ala
Phe Gln Thr Glu Val Gly Asn His Pro Thr Phe Glu Asp 435 440 445Met
Gln Val Leu Val Ser Arg Glu Lys Gln Arg Pro Lys Phe Pro Glu 450 455
460Ala Trp Lys Glu Asn Ser Leu Ala Val Arg Ser Leu Lys Glu Thr
Ile465 470 475 480Glu Asp Cys Trp Asp Gln Asp Ala Glu Ala Arg Leu
Thr Ala Gln Cys 485 490 495Ala Glu Glu Arg Met Ala Glu Leu Met Met
Ile Trp Glu Arg Asn Lys 500 505 510Ser Val Ser Pro Thr Val Asn Pro
Met Ser Thr Ala Met Gln Asn Glu 515 520 525Arg Asn Leu Ser His Asn
Arg Arg Val Pro Lys Ile Gly Pro Tyr Pro 530 535 540Asp Tyr Ser Ser
Ser Ser Tyr Ile Glu Asp Ser Ile His His Thr Asp545 550 555 560Ser
Ile Val Lys Asn Ile Ser Ser Glu His Ser Met Ser Ser Thr Pro 565 570
575Leu Thr Ile Gly Glu Lys Asn Arg Asn Ser Ile Asn Tyr Glu Arg Gln
580 585 590Gln Ala Gln Ala Arg Ile Pro Ser Pro Glu Thr Ser Val Thr
Ser Leu 595 600 605Ser Thr Asn Thr Thr Thr Thr Asn Thr Thr Gly Leu
Thr Pro Ser Thr 610 615 620Gly Met Thr Thr Ile Ser Glu Met Pro Tyr
Pro Asp Glu Thr Asn Leu625 630 635 640His Thr Thr Asn Val Ala Gln
Ser Ile Gly Pro Thr Pro Val Cys Leu 645 650 655Gln Leu Thr Glu Glu
Asp Leu Glu Thr Asn Lys Leu Asp Pro Lys Glu 660 665 670Val Asp Lys
Asn Leu Lys Glu Ser Ser Asp Glu Asn Leu Met Glu His 675 680 685Ser
Leu Lys Gln Phe Ser Gly Pro Asp Pro Leu Ser Ser Thr Ser Ser 690 695
700Ser Leu Leu Tyr Pro Leu Ile Lys Leu Ala Val Glu Ala Thr Gly
Gln705 710 715 720Gln Asp Phe Thr Gln Thr Ala Asn Gly Gln Ala Cys
Leu Ile Pro Asp 725 730 735Val Leu Pro Thr Gln Ile Tyr Pro Leu Pro
Lys Gln Gln Asn Leu Pro 740 745 750Lys Arg Pro Thr Ser Leu Pro Leu
Asn Thr Lys Asn Ser Thr Lys Glu 755 760 765Pro Arg Leu Lys Phe Gly
Ser Lys His Lys Ser Asn Leu Lys Gln Val 770 775 780Glu Thr Gly Val
Ala Lys Met Asn Thr Ile Asn Ala Ala Glu Pro His785 790 795 800Val
Val Thr Val Thr Met Asn Gly Val Ala Gly Arg Asn His Ser Val 805 810
815Asn Ser His Ala Ala Thr Thr Gln Tyr Ala Asn Arg Thr Val Leu Ser
820 825 830Gly Gln Thr Thr Asn Ile Val Thr His Arg Ala Gln Glu Met
Leu Gln 835 840 845Asn Gln Phe Ile Gly Glu Asp Thr Arg Leu Asn Ile
Asn Ser Ser Pro 850 855 860Asp Glu His Glu Pro Leu Leu Arg Arg Glu
Gln Gln Ala Gly His Asp865 870 875 880Glu Gly Val Leu Asp Arg Leu
Val Asp Arg Arg Glu Arg Pro Leu Glu 885 890 895Gly Gly Arg Thr Asn
Ser Asn Asn Asn Asn Ser Asn Pro Cys Ser Glu 900 905 910Gln Asp Val
Leu Ala Gln Gly Val Pro Ser Thr Ala Ala Asp Pro Gly 915 920 925Pro
Ser Lys Pro Arg Arg Ala Gln Arg Pro Asn Ser Leu Asp Leu Ser 930 935
940Ala Thr Asn Val Leu Asp Gly Ser Ser Ile Gln Ile Gly Glu Ser
Thr945 950 955 960Gln Asp Gly Lys Ser Gly Ser Gly Glu Lys Ile Lys
Lys Arg Val Lys 965 970 975Thr Pro Tyr Ser Leu Lys Arg Trp Arg Pro
Ser Thr Trp Val Ile Ser 980 985 990Thr Glu Ser Leu Asp Cys Glu Val
Asn Asn Asn Gly Ser Asn Arg Ala 995 1000 1005Val His Ser Lys Ser
Ser Thr Ala Val Tyr Leu Ala Glu Gly Gly 1010 1015 1020Thr Ala Thr
Thr Met Val Ser Lys Asp Ile Gly Met Asn Cys Leu 1025 1030
1035852932DNAHomo sapiens 85gctccgcgcc gagggctgga ggatgcgttc
cctggggtcc ggacttatga aaatatgcat 60cagtttaata ctgtcttgga attcatgaga
tggaagcata ggtcaaagct gtttggagaa 120aatcagaagt acagttttat
ctagccacat cttggaggag tcgtaagaaa gcagtgggag 180ttgaagtcat
tgtcaagtgc ttgcgatctt ttacaagaaa atctcactga atgatagtca
240tttaaattgg tgaagtagca agaccaatta ttaaaggtga cagtacacag
gaaacattac 300aattgaacaa tgactcagct atacatttac atcagattat
tgggagccta tttgttcatc 360atttctcgtg ttcaaggaca gaatctggat
agtatgcttc atggcactgg gatgaaatca 420gactccgacc agaaaaagtc
agaaaatgga gtaaccttag caccagagga taccttgcct 480tttttaaagt
gctattgctc agggcactgt ccagatgatg ctattaataa cacatgcata
540actaatggac attgctttgc catcatagaa gaagatgacc agggagaaac
cacattagct 600tcagggtgta tgaaatatga aggatctgat tttcagtgca
aagattctcc aaaagcccag 660ctacgccgga caatagaatg ttgtcggacc
aatttatgta accagtattt gcaacccaca 720ctgccccctg ttgtcatagg
tccgtttttt gatggcagca ttcgatggct ggttttgctc 780atttctatgg
ctgtctgcat aattgctatg atcatcttct ccagctgctt ttgttacaaa
840cattattgca agagcatctc aagcagacgt cgttacaatc gtgatttgga
acaggatgaa 900gcatttattc cagttggaga atcactaaaa gaccttattg
accagtcaca aagttctggt 960agtgggtctg gactaccttt attggttcag
cgaactattg ccaaacagat tcagatggtc 1020cggcaagttg gtaaaggccg
atatggagaa gtatggatgg gcaaatggcg tggcgaaaaa 1080gtggcggtga
aagtattctt taccactgaa gaagccagct ggtttcgaga aacagaaatc
1140taccaaactg tgctaatgcg ccatgaaaac atacttggtt tcatagcggc
agacattaaa 1200ggtacaggtt cctggactca gctctatttg attactgatt
accatgaaaa tggatctctc 1260tatgacttcc tgaaatgtgc tacactggac
accagagccc tgcttaaatt ggcttattca 1320gctgcctgtg gtctgtgcca
cctgcacaca gaaatttatg gcacccaagg aaagcccgca 1380attgctcatc
gagacctaaa gagcaaaaac atcctcatca agaaaaatgg gagttgctgc
1440attgctgacc tgggccttgc tgttaaattc aacagtgaca caaatgaagt
tgatgtgccc 1500ttgaatacca gggtgggcac caaacgctac atggctcccg
aagtgctgga cgaaagcctg 1560aacaaaaacc acttccagcc ctacatcatg
gctgacatct acagcttcgg cctaatcatt 1620tgggagatgg ctcgtcgttg
tatcacagga gggatcgtgg aagaatacca attgccatat 1680tacaacatgg
taccgagtga tccgtcatac gaagatatgc gtgaggttgt gtgtgtcaaa
1740cgtttgcggc caattgtgtc taatcggtgg aacagtgatg aatgtctacg
agcagttttg 1800aagctaatgt cagaatgctg ggcccacaat ccagcctcca
gactcacagc attgagaatt 1860aagaagacgc ttgccaagat ggttgaatcc
caagatgtaa aaatctgatg gttaaaccat 1920cggaggagaa actctagact
gcaagaactg tttttaccca tggcatgggt ggaattagag 1980tggaataagg
atgttaactt ggttctcaga ctctttcttc actacgtgtt cacaggctgc
2040taatattaaa cctttcagta ctcttattag gatacaagct gggaacttct
aaacacttca 2100ttctttatat atggacagct ttattttaaa tgtggttttt
gatgcctttt tttaagtggg 2160tttttatgaa ctgcatcaag acttcaatcc
tgattagtgt ctccagtcaa gctctgggta 2220ctgaattgcc tgttcataaa
acggtgcttt ctgtgaaagc cttaagaaga taaatgagcg 2280cagcagagat
ggagaaatag actttgcctt ttacctgaga cattcagttc gtttgtattc
2340tacctttgta aaacagccta tagatgatga tgtgtttggg atactgctta
ttttatgata 2400gtttgtcctg tgtccttagt gatgtgtgtg tgtctccatg
cacatgcacg ccgggattcc 2460tctgctgcca tttgaattag aagaaaataa
tttatatgca tgcacaggaa gatattggtg 2520gccggtggtt ttgtgcttta
aaaatgcaat atctgaccaa gattcgccaa tctcatacaa 2580gccatttact
ttgcaagtga gatagcttcc ccaccagctt tattttttaa catgaaagct
2640gatgccaagg ccaaaagaag tttaaagcat ctgtaaattt ggactgtttt
ccttcaacca 2700ccattttttt tgtggttatt atttttgtca cggaaagcat
cctctccaaa gttggagctt 2760ctattgccat gaaccatgct tacaaagaaa
gcacttctta ttgaagtgaa ttcctgcatt 2820tgatagcaat gtaagtgcct
ataaccatgt tctatattct ttattctcag taacttttaa 2880aagggaagtt
atttatattt tgtgtataat gtgctttatt tgcaaatcac cc 2932861575DNAHomo
sapiens 86gcaaacttcc ttgataacat gcttttgcga agtgcaggaa aattaaatgt
gggcaccaag 60aaagaggatg gtgagagtac agcccccacc ccccgtccaa aggtcttgcg
ttgtaaatgc 120caccaccatt gtccagaaga ctcagtcaac aatatttgca
gcacagacgg atattgtttc 180acgatgatag aagaggatga ctctgggttg
cctgtggtca cttctggttg cctaggacta 240gaaggctcag attttcagtg
tcgggacact cccattcctc atcaaagaag atcaattgaa 300tgctgcacag
aaaggaacga atgtaataaa gacctacacc ctacactgcc tccattgaaa
360aacagagatt ttgttgatgg acctatacac cacagggctt tacttatatc
tgtgactgtc 420tgtagtttgc tcttggtcct tatcatatta ttttgttact
tccggtataa aagacaagaa 480accagacctc gatacagcat tgggttagaa
caggatgaaa cttacattcc tcctggagaa 540tccctgagag acttaattga
gcagtctcag agctcaggaa gtggatcagg cctccctctg 600ctggtccaaa
ggactatagc taagcagatt cagatggtga aacagattgg aaaaggtcgc
660tatggggaag tttggatggg aaagtggcgt ggcgaaaagg tagctgtgaa
agtgttcttc 720accacagagg aagccagctg gttcagagag acagaaatat
atcagacagt gttgatgagg 780catgaaaaca ttttgggttt cattgctgca
gatatcaaag ggacagggtc ctggacccag 840ttgtacctaa tcacagacta
tcatgaaaat ggttcccttt atgattatct gaagtccacc 900accctagacg
ctaaatcaat gctgaagtta gcctactctt ctgtcagtgg cttatgtcat
960ttacacacag aaatctttag tactcaaggc aaaccagcaa ttgcccatcg
agatctgaaa 1020agtaaaaaca ttctggtgaa gaaaaatgga acttgctgta
ttgctgacct gggcctggct 1080gttaaattta ttagtgatac aaatgaagtt
gacataccac ctaacactcg agttggcacc 1140aaacgctata tgcctccaga
agtgttggac gagagcttga acagaaatca cttccagtct 1200tacatcatgg
ctgacatgta tagttttggc ctcatccttt gggaggttgc taggagatgt
1260gtatcaggag gtatagtgga agaataccag cttccttatc atgacctagt
gcccagtgac 1320ccctcttatg aggacatgag ggagattgtg tgcatcaaga
agttacgccc ctcattccca 1380aaccggtgga gcagtgatga gtgtctaagg
cagatgggaa aactcatgac agaatgctgg 1440gctcacaatc ctgcatcaag
gctgacagcc ctgcgggtta agaaaacact tgccaaaatg
1500tcagagtccc aggacattaa actctgatag gagaggaaaa gtaagcatct
ctgcagaaag 1560ccaacaggta ccctt 1575872032DNAHomo sapiens
87cgcggggcgc ggagtcggcg gggcctcgcg ggacgcgggc agtgcggaga ccgcggcgct
60gaggacgcgg gagccgggag cgcacgcgcg gggtggagtt cagcctactc tttcttagat
120gtgaaaggaa aggaagatca tttcatgcct tgttgataaa ggttcagact
tctgctgatt 180cataaccatt tggctctgag ctatgacaag agaggaaaca
aaaagttaaa cttacaagcc 240tgccataagt gagaagcaaa cttccttgat
aacatgcttt tgcgaagtgc aggaaaatta 300aatgtgggca ccaagaaaga
ggatggtgag agtacagccc ccaccccccg tccaaaggtc 360ttgcgttgta
aatgccacca ccattgtcca gaagactcag tcaacaatat ttgcagcaca
420gacggatatt gtttcacgat gatagaagag gatgactctg ggttgcctgt
ggtcacttct 480ggttgcctag gactagaagg ctcagatttt cagtgtcggg
acactcccat tcctcatcaa 540agaagatcaa ttgaatgctg cacagaaagg
aacgaatgta ataaagacct acaccctaca 600ctgcctccat tgaaaaacag
agattttgtt gatggaccta tacaccacag ggctttactt 660atatctgtga
ctgtctgtag tttgctcttg gtccttatca tattattttg ttacttccgg
720tataaaagac aagaaaccag acctcgatac agcattgggt tagaacagga
tgaaacttac 780attcctcctg gagaatccct gagagactta attgagcagt
ctcagagctc aggaagtgga 840tcaggcctcc ctctgctggt ccaaaggact
atagctaagc agattcagat ggtgaaacag 900attggaaaag gtcgctatgg
ggaagtttgg atgggaaagt ggcgtggcga aaaggtagct 960gtgaaagtgt
tcttcaccac agaggaagcc agctggttca gagagacaga aatatatcag
1020acagtgttga tgaggcatga aaacattttg ggtttcattg ctgcagatat
caaagggaca 1080gggtcctgga cccagttgta cctaatcaca gactatcatg
aaaatggttc cctttatgat 1140tatctgaagt ccaccaccct agacgctaaa
tcaatgctga agttagccta ctcttctgtc 1200agtggcttat gtcatttaca
cacagaaatc tttagtactc aaggcaaacc agcaattgcc 1260catcgagatc
tgaaaagtaa aaacattctg gtgaagaaaa atggaacttg ctgtattgct
1320gacctgggcc tggctgttaa atttattagt gatacaaatg aagttgacat
accacctaac 1380actcgagttg gcaccaaacg ctatatgcct ccagaagtgt
tggacgagag cttgaacaga 1440aatcacttcc agtcttacat catggctgac
atgtatagtt ttggcctcat cctttgggag 1500gttgctagga gatgtgtatc
aggaggtata gtggaagaat accagcttcc ttatcatgac 1560ctagtgccca
gtgacccctc ttatgaggac atgagggaga ttgtgtgcat caagaagtta
1620cgcccctcat tcccaaaccg gtggagcagt gatgagtgtc taaggcagat
gggaaaactc 1680atgacagaat gctgggctca caatcctgca tcaaggctga
cagccctgcg ggttaagaaa 1740acacttgcca aaatgtcaga gtcccaggac
attaaactct gataggagag gaaaagtaag 1800catctctgca gaaagccaac
aggtactctt ctgtttgtgg gcagagcaaa agacatcaaa 1860taagcatcca
cagtacaagc cttgaacatc gtcctgcttc ccagtgggtt cagacctcac
1920ctttcaggga gcgacctggg caaagacaga gaagctccca gaaggagaga
ttgatccgtg 1980tctgtttgta ggcggagaaa ccgttgggta acttgttcaa
gatatgatgc at 2032883167DNARattus sp. 88gaattcatga gatggaaaca
taggtcaaag ctgtttggag aaattggaac tacagtttta 60tctagccaca tctctgagaa
gtctgaagaa agcagcaggt gaaagtcatt gtcaagtgat 120tttgttcttc
tgtaaggaaa cctcgttcag taaggccgtt tacttcagtg aaacagcagg
180accagtaatc aaggtggccc ggacaggaca cgtgcgaatt ggacaatgac
tcagctatac 240acttacatca gattactggg agcctgtctg ttcatcattt
ctcatgttca agggcagaat 300ctagatagta tgctccatgg tactggtatg
aaatcagacg tggaccagaa gaagccggaa 360aatggagtga cgttagcacc
agaggacacc ttacctttct taaaatgcta ttgctcagga 420cactgcccag
atgacgctat taataacaca tgcataacta atggccattg ctttgccatt
480atagaagaag atgatcaggg agaaaccacg ttaacttctg ggtgtatgaa
gtatgaaggc 540tctgattttc aatgcaagga ttcaccaaaa gcccagctac
gcaggacaat agaatgttgt 600cggaccaatt tgtgcaacca atatttgcag
cctacactgc cccctgtcgt tataggccca 660ttctttgatg gcagcgtccg
atggctggct gtgctcatct ctatggctgt ctgtattgtc 720gccatgatcg
tcttctccag ctgcttctgt tacaaacatt actgtaagag tatctcaagc
780agaggtcgtt acaaccgtga cttggaacag gatgaagcat ttattccagt
aggagaatca 840ctgaaagacc tgattgacca gtcacaaagc tctggtagtg
gatctggatt acctttattg 900gttcagcgaa ctattgccaa acagattcag
atggttcggc aggttggtaa aggccggtat 960ggagaagtat ggatgggtaa
atggcgtggt gaaaaagtgg ctgtcaaagt attttttacc 1020actgaagaag
ctagctggtt tagagaaaca gaaatctacc agacggtgtt aatgcgtcat
1080gaaaatatac ttggttttat agctgcagac attaaaggca ccggttcctg
gactcagctg 1140tatttgatta ctgattacca tgagaatggg tctctctatg
acttcctgaa atgtgccacc 1200ctggacacca gagccctact caagttagct
tattctgctg cctgtggtct gtgccacctc 1260cacacagaaa tttatggcac
gcaaggcaag cctgcaattg ctcatcgaga cctgaagagc 1320aaaaacatcc
ttattaagaa aaatggtagt tgctgtattg ctgacctggg cctagctgtt
1380aaattcaaca gtgacacaaa tgaagttgac atacccttga acaccagggt
gggcaccagg 1440cggtacatgg ctccagaagt gctggacgag agcctgagta
aaaaccattt ccagccctac 1500atcatggctg acatctacag ctttggtttg
atcatttggg agatggcccg tcgctgtatt 1560acaggaggaa tcgtggagga
atatcaatta ccatattaca acatggtgcc tagtgaccca 1620tcttatgaag
acatgcgtga ggtcgtgtgt gtgaaacgct tgcggccaat cgtctctaac
1680cgctggaaca gtgatgaatg tcttcgagcc gttttgaagc tgatgtcaga
atgctgggcc 1740cataatccag catccagact cacagctttg agaatcaaga
agacgctcgc aaagatggtt 1800gaatcccagg atgtaaagat ttgacaaaca
gttttgagaa agaatttaga ctgcaagaaa 1860ttcacccgag gaagggtgga
gttagcatgg actaggatgt cggcttggtt tccagactct 1920ctcctctaca
tcttcacagg ctgctaacag taaactttca ggactctgca gaatgcaggg
1980ttggagcttc agacatagga cttcagacat gctgttcttt gcgtatggac
agctttgttt 2040taaatgtggg cttttgatgc ctttttggtt tttatgaatt
gcatcaagac tccaatcctg 2100ataagaagtc tctggtcaaa ctctggttac
tcactatcct gtccataaag tggtgctttc 2160tgtgaaagcc ttaaggaaat
tagtgagctc agcagagatg gagaaaggca tatttgccct 2220ctacagagaa
aatatctgtc tgtgttctgt ctctgtaaac agcctggact atgatctctt
2280tgggatgctg cctggttgat gatggtgcat catgcctctg atatgcatac
cagacttcct 2340ctgctgccat gggcttacaa gacaagaatg tgaaggttgc
acaggacggt atttgtggcc 2400agtggtttaa atatgcaata tctaatcgac
attcgccaat ctcataaaag ccatctacct 2460tgtaactgaa gtaacttctc
taccaacttt atttttagca taatagttgt aaaggccaaa 2520ctatgtataa
agtgtccata gactcgaact gttttcctcc agtcaccatt ttgttttcct
2580tttggtaatt atttttgtta tataattcct cctatccaga attggcgctc
actgtcttga 2640accatacttt gaaagaaatg cctcttcctg gagtctgcct
tactgcatct gatcaccatg 2700tgcatacctc tgatcaaatt ctggagtctt
tgttctcggt acctcttaaa aagggaaatt 2760gtgtatcatg tgtagtgtgc
ttttattttc aaaatcttca tagcctttat tctagccatt 2820tttacctaca
tactcattct gtacaaaaca gctcactcgg tctcacggct gatcctcagt
2880ggaaatgatt taaagtagag ctgtgtacga atttcagaat tcatgtattt
aaaaacttca 2940cactaacact ttactaagat attgtctcat atcttttatg
aggatgtcag ctgattttca 3000atgactataa atgtatctta gctatctaaa
tcttttgaaa tttggtttta taatttctgg 3060tccctaactt gtgaagacaa
agaggcagaa gtacccagtc taccacattt acactgtaca 3120ttattaaata
aaaaaatgta tattttaaaa aaaaaaaaaa aaaaaaa 3167893167DNARattus
norvegicus 89gaattcatga gatggaaaca taggtcaaag ctgtttggag aaattggaac
tacagtttta 60tctagccaca tctctgagaa gtctgaagaa agcagcaggt gaaagtcatt
gtcaagtgat 120tttgttcttc tgtaaggaaa cctcgttcag taaggccgtt
tacttcagtg aaacagcagg 180accagtaatc aaggtggccc ggacaggaca
cgtgcgaatt ggacaatgac tcagctatac 240acttacatca gattactggg
agcctgtctg ttcatcattt ctcatgttca agggcagaat 300ctagatagta
tgctccatgg tactggtatg aaatcagacg tggaccagaa gaagccggaa
360aatggagtga cgttagcacc agaggacacc ttacctttct taaaatgcta
ttgctcagga 420cactgcccag atgacgctat taataacaca tgcataacta
atggccattg ctttgccatt 480atagaagaag atgatcaggg agaaaccacg
ttaacttctg ggtgtatgaa gtatgaaggc 540tctgattttc aatgcaagga
ttcaccaaaa gcccagctac gcaggacaat agaatgttgt 600cggaccaatt
tgtgcaacca atatttgcag cctacactgc cccctgtcgt tataggccca
660ttctttgatg gcagcgtccg atggctggct gtgctcatct ctatggctgt
ctgtattgtc 720gccatgatcg tcttctccag ctgcttctgt tacaaacatt
actgtaagag tatctcaagc 780agaggtcgtt acaaccgtga cttggaacag
gatgaagcat ttattccagt aggagaatca 840ctgaaagacc tgattgacca
gtcacaaagc tctggtagtg gatctggatt acctttattg 900gttcagcgaa
ctattgccaa acagattcag atggttcggc aggttggtaa aggccggtat
960ggagaagtat ggatgggtaa atggcgtggt gaaaaagtgg ctgtcaaagt
attttttacc 1020actgaagaag ctagctggtt tagagaaaca gaaatctacc
agacggtgtt aatgcgtcat 1080gaaaatatac ttggttttat agctgcagac
attaaaggca ccggttcctg gactcagctg 1140tatttgatta ctgattacca
tgagaatggg tctctctatg acttcctgaa atgtgccacc 1200ctggacacca
gagccctact caagttagct tattctgctg cctgtggtct gtgccacctc
1260cacacagaaa tttatggcac gcaaggcaag cctgcaattg ctcatcgaga
cctgaagagc 1320aaaaacatcc ttattaagaa aaatggtagt tgctgtattg
ctgacctggg cctagctgtt 1380aaattcaaca gtgacacaaa tgaagttgac
atacccttga acaccagggt gggcaccagg 1440cggtacatgg ctccagaagt
gctggacgag agcctgagta aaaaccattt ccagccctac 1500atcatggctg
acatctacag ctttggtttg atcatttggg agatggcccg tcgctgtatt
1560acaggaggaa tcgtggagga atatcaatta ccatattaca acatggtgcc
tagtgaccca 1620tcttatgaag acatgcgtga ggtcgtgtgt gtgaaacgct
tgcggccaat cgtctctaac 1680cgctggaaca gtgatgaatg tcttcgagcc
gttttgaagc tgatgtcaga atgctgggcc 1740cataatccag catccagact
cacagctttg agaatcaaga agacgctcgc aaagatggtt 1800gaatcccagg
atgtaaagat ttgacaaaca gttttgagaa agaatttaga ctgcaagaaa
1860ttcacccgag gaagggtgga gttagcatgg actaggatgt cggcttggtt
tccagactct 1920ctcctctaca tcttcacagg ctgctaacag taaactttca
ggactctgca gaatgcaggg 1980ttggagcttc agacatagga cttcagacat
gctgttcttt gcgtatggac agctttgttt 2040taaatgtggg cttttgatgc
ctttttggtt tttatgaatt gcatcaagac tccaatcctg 2100ataagaagtc
tctggtcaaa ctctggttac tcactatcct gtccataaag tggtgctttc
2160tgtgaaagcc ttaaggaaat tagtgagctc agcagagatg gagaaaggca
tatttgccct 2220ctacagagaa aatatctgtc tgtgttctgt ctctgtaaac
agcctggact atgatctctt 2280tgggatgctg cctggttgat gatggtgcat
catgcctctg atatgcatac cagacttcct 2340ctgctgccat gggcttacaa
gacaagaatg tgaaggttgc acaggacggt atttgtggcc 2400agtggtttaa
atatgcaata tctaatcgac attcgccaat ctcataaaag ccatctacct
2460tgtaactgaa gtaacttctc taccaacttt atttttagca taatagttgt
aaaggccaaa 2520ctatgtataa agtgtccata gactcgaact gttttcctcc
agtcaccatt ttgttttcct 2580tttggtaatt atttttgtta tataattcct
cctatccaga attggcgctc actgtcttga 2640accatacttt gaaagaaatg
cctcttcctg gagtctgcct tactgcatct gatcaccatg 2700tgcatacctc
tgatcaaatt ctggagtctt tgttctcggt acctcttaaa aagggaaatt
2760gtgtatcatg tgtagtgtgc ttttattttc aaaatcttca tagcctttat
tctagccatt 2820tttacctaca tactcattct gtacaaaaca gctcactcgg
tctcacggct gatcctcagt 2880ggaaatgatt taaagtagag ctgtgtacga
atttcagaat tcatgtattt aaaaacttca 2940cactaacact ttactaagat
attgtctcat atcttttatg aggatgtcag ctgattttca 3000atgactataa
atgtatctta gctatctaaa tcttttgaaa tttggtttta taatttctgg
3060tccctaactt gtgaagacaa agaggcagaa gtacccagtc taccacattt
acactgtaca 3120ttattaaata aaaaaatgta tattttaaaa aaaaaaaaaa aaaaaaa
3167903003DNARattus norvegicus 90cgttcagtaa ggccgtttac ttcagtgaaa
cagcaggacc agtaatcaag gtggcccgga 60caggacacgt gcgaattgga caatgactca
gctatacact tacatcagat tactgggagc 120ctgtctgttc atcatttctc
atgttcaagg gcagaatcta gatagtatgc tccatggtac 180tggtatgaaa
tcagacgtgg accagaagaa gccggaaaat ggagtgacgt tagcaccaga
240ggacacctta cctttcttaa aatgctattg ctcaggacac tgcccagatg
acgctattaa 300taacacatgc ataactaatg gccattgctt tgccattata
gaagaagatg atcagggaga 360aaccacgtta acttctgggt gtatgaagta
tgaaggctct gattttcaat gcaaggattc 420accaaaagcc cagctacgca
ggacaataga atgttgtcgg accaatttgt gcaaccaata 480tttgcagcct
acactgcccc ctgtcgttat aggcccattc tttgatggca gcgtccgatg
540gctggctgtg ctcatctcta tggctgtctg tattgtcgcc atgatcgtct
tctccagctg 600cttctgttac aaacattact gtaagagtat ctcaagcaga
ggtcgttaca accgtgactt 660ggaacaggat gaagcattta ttccagtagg
agaatcactg aaagacctga ttgaccagtc 720acaaagctct ggtagtggat
ctggattacc tttattggtt cagcgaacta ttgccaaaca 780gattcagatg
gttcggcagg ttggtaaagg ccggtatgga gaagtatgga tgggtaaatg
840gcgtggtgaa aaagtggctg tcaaagtatt ttttaccact gaagaagcta
gctggtttag 900agaaacagaa atctaccaga cggtgttaat gcgtcatgaa
aatatacttg gttttatagc 960tgcagacatt aaaggcaccg gttcctggac
tcagctgtat ttgattactg attaccatga 1020gaatgggtct ctctatgact
tcctgaaatg tgccaccctg gacaccagag ccctactcaa 1080gttagcttat
tctgctgcct gtggtctgtg ccacctccac acagaaattt atggcacgca
1140aggcaagcct gcaattgctc atcgagacct gaagagcaaa aacatcctta
ttaagaaaaa 1200tggtagttgc tgtattgctg acctgggcct agctgttaaa
ttcaacagtg acacaaatga 1260agttgacata cccttgaaca ccagggtggg
caccaggcgg tacatggctc cagaagtgct 1320ggacgagagc ctgagtaaaa
accatttcca gccctacatc atggctgaca tctacagctt 1380tggtttgatc
atttgggaga tggcccgtcg ctgtattaca ggaggaatcg tggaggaata
1440tcaattacca tattacaaca tggtgcctag tgacccatct tatgaagaca
tgcgtgaggt 1500cgtgtgtgtg aaacgcttgc ggccaatcgt ctctaaccgc
tggaacagtg atgaatgtct 1560tcgagccgtt ttgaagctga tgtcagaatg
ctgggcccat aatccagcat ccagactcac 1620agctttgaga atcaagaaga
cgctcgcaaa gatggttgaa tcccaggatg taaagatttg 1680acaaacagtt
ttgagaaaga atttagactg caagaaattc acccgaggaa gggtggagtt
1740agcatggact aggatgtcgg cttggtttcc agactctctc ctctacatct
tcacaggctg 1800ctaacagtaa actttcagga ctctgcagaa tgcagggttg
gagcttcaga cataggactt 1860cagacatgct gttctttgcg tatggacagc
tttgttttaa atgtgggctt ttgatgcctt 1920tttggttttt atgaattgca
tcaagactcc aatcctgata agaagtctct ggtcaaactc 1980tggttactca
ctatcctgtc cataaagtgg tgctttctgt gaaagcctta aggaaattag
2040tgagctcagc agagatggag aaaggcatat ttgccctcta cagagaaaat
atctgtctgt 2100gttctgtctc tgtaaacagc ctggactatg atctctttgg
gatgctgcct ggttgatgat 2160ggtgcatcat gcctctgata tgcataccag
acttcctctg ctgccatggg cttacaagac 2220aagaatgtga aggttgcaca
ggacggtatt tgtggccagt ggtttaaata tgcaatatct 2280aatcgacatt
cgccaatctc ataaaagcca tctaccttgt aactgaagta acttctctac
2340caactttatt tttagcataa tagttgtaaa ggccaaacta tgtataaagt
gtccatagac 2400tcgaactgtt ttcctccagt caccattttg ttttcctttt
ggtaattatt tttgttatat 2460aattcctcct atccagaatt ggcgctcact
gtcttgaacc atactttgaa agaaatgcct 2520cttcctggag tctgccttac
tgcatctgat caccatgtgc atacctctga tcaaattctg 2580gagtctttgt
tctcggtacc tcttaaaaag ggaaattgtg tatcatgtgt agtgtgcttt
2640tattttcaaa atcttcatag cctttattct agccattttt acctacatac
tcattctgta 2700caaaacagct cactcggtct cacggctgat cctcagtgga
aatgatttaa agtagagctg 2760tgtacgaatt tcagaattca tgtatttaaa
aacttcacac taacacttta ctaagatatt 2820gtctcatatc ttttatgagg
atgtcagctg attttcaatg actataaatg tatcttagct 2880atctaaatct
tttgaaattt ggttttataa tttctggtcc ctaacttgtg aagacaaaga
2940ggcagaagta cccagtctac cacatttaca ctgtacatta ttaaataaaa
aaatgtatat 3000ttt 3003912063DNAHomo sapiens 91gaattccggt
gatgatgatg gtgatggtga tgatggtgat gaggatgatg gtgatgatga 60tgatggtgtt
ggtgatggtt tttgcatctt ccattcatga actaagtact cttattagtg
120aatttctttt ctttgccctc ctgattcttg gctggcccag ggatgacttc
ctcgctgcag 180cggccctggc gggtgccctg gctaccatgg accatcctgc
tggtcagcac tgcggctgct 240tcgcagaatc aagaacggct atgtgcgttt
aaagatccgt atcagcaaga ccttgggata 300ggtgagagta gaatctctca
tgaaaatggg acaatattat gctcgaaagg tagcacctgc 360tatggccttt
gggagaaatc aaaaggggac ataaatcttg taaaacaagg atgttggtct
420cacattggag atccccaaga gtgtcactat gaagaatgtg tagtaactac
cactcctccc 480tcaattcaga atggaacata ccgtttctgc tgttgtagca
cagatttatg taatgtcaac 540tttactgaga attttccacc tcctgacaca
acaccactca gtccacctca ttcatttaac 600cgagatgaga caataatcat
tgctttggca tcagtctctg tattagctgt tttgatagtt 660gccttatgct
ttggatacag aatgttgaca ggagaccgta aacaaggtct tcacagtatg
720aacatgatgg aggcagcagc atccgaaccc tctcttgatc tagataatct
gaaactgttg 780gagctgattg gccgaggtcg atatggagca gtatataaag
gctccttgga tgagcgtcca 840gttgctgtaa aagtgttttc ctttgcaaac
cgtcagaatt ttatcaacga aaagaacatt 900tacagagtgc ctttgatgga
acatgacaac attgcccgct ttatagttgg agatgagaga 960gtcactgcag
atggacgcat ggaatatttg cttgtgatgg agtactatcc caatggatct
1020ttatgcaagt atttaagtct ccacacaagt gactgggtaa gctcttgccg
tcttgctcat 1080tctgttacta gaggactggc ttatcttcac acagaattac
cacgaggaga tcattataaa 1140cctgcaattt cccatcgaga tttaaacagc
agaaatgtcc tagtgaaaaa tgatggaacc 1200tgtgttatta gtgactttgg
actgtccatg aggctgactg gaaatagact ggtgcgccca 1260ggggaggaag
ataatgcagc cataagcgag gttggcacta tcagatatat ggcaccagaa
1320gtgctagaag gagctgtgaa cttgagggac tgtgaatcag ctttgaaaca
agtagacatg 1380tatgctcttg gactaatcta ttgggagata tttatgagat
gtacagacct cttcccaggg 1440gaatccgtac cagagtacca gatggctttt
cagacagagg ttggaaacca tcccactttt 1500gaggatatgc aggttctcgt
gtctagggaa aaacagagac ccaagttccc agaagcctgg 1560aaagaaaata
gcctggcagt gaggtcactc aaggagacaa tcgaagactg ttgggaccag
1620gatgcagagg ctcggcttac tgcacagtgt gctgaggaaa ggatggctga
acttatgatg 1680atttgggaaa gaaacaaatc tgtgagccca acagtcaatc
caatgtctac tgctatgcag 1740aatgaacgta ggtgagtcaa cacaagatgg
caaatcagga tcaggtgaaa agatcaagaa 1800acgtgtgaaa actccctatt
ctcttaagcg gtggcgcccc tccacctggg tcatctccac 1860tgaatcgctg
gactgtgaag tcaacaataa tggcagtaac agggcagttc attccaaatc
1920cagcactgct gtttaccttg cagaaggagg cactgctaca accatggtgt
ctaaagatat 1980aggaatgaac tgtctgtgaa atgttttcaa gcctatggag
tgaaattatt ttttgcatca 2040tttaaacatg cagaagatgt tta
2063921964DNAHomo sapiens 92atttcttttc tttgccctcc tgattcttgg
ctggcccagg gatgacttcc tcgctgcagc 60ggccctggcg ggtgccctgg ctaccatgga
ccatcctgct ggtcagcact gcggctgctt 120cgcagaatca agaacggcta
tgtgcgttta aagatccgta tcagcaagac cttgggatag 180gtgagagtag
aatctctcat gaaaatggga caatattatg ctcgaaaggt agcacctgct
240atggcctttg ggagaaatca aaaggggaca taaatcttgt aaaacaagga
tgttggtctc 300acattggaga tccccaagag tgtcactatg aagaatgtgt
agtaactacc actcctccct 360caattcagaa tggaacatac cgtttctgct
gttgtagcac agatttatgt aatgtcaact 420ttactgagaa ttttccacct
cctgacacaa caccactcag tccacctcat tcatttaacc 480gagatgagac
aataatcatt gctttggcat cagtctctgt attagctgtt ttgatagttg
540ccttatgctt tggatacaga atgttgacag gagaccgtaa acaaggtctt
cacagtatga 600acatgatgga ggcagcagca tccgaaccct ctcttgatct
agataatctg aaactgttgg 660agctgattgg ccgaggtcga tatggagcag
tatataaagg ctccttggat gagcgtccag 720ttgctgtaaa agtgttttcc
tttgcaaacc gtcagaattt tatcaacgaa aagaacattt 780acagagtgcc
tttgatggaa catgacaaca ttgcccgctt tatagttgga gatgagagag
840tcactgcaga tggacgcatg gaatatttgc ttgtgatgga gtactatccc
aatggatctt 900tatgcaagta tttaagtctc cacacaagtg actgggtaag
ctcttgccgt cttgctcatt 960ctgttactag aggactggct tatcttcaca
cagaattacc acgaggagat cattataaac 1020ctgcaatttc ccatcgagat
ttaaacagca gaaatgtcct agtgaaaaat gatggaacct 1080gtgttattag
tgactttgga ctgtccatga ggctgactgg aaatagactg gtgcgcccag
1140gggaggaaga taatgcagcc ataagcgagg ttggcactat cagatatatg
gcaccagaag 1200tgctagaagg agctgtgaac ttgagggact gtgaatcagc
tttgaaacaa gtagacatgt 1260atgctcttgg actaatctat tgggagatat
ttatgagatg tacagacctc ttcccagggg 1320aatccgtacc agagtaccag
atggcttttc agacagaggt tggaaaccat cccacttttg 1380aggatatgca
ggttctcgtg tctagggaaa aacagagacc caagttccca gaagcctgga
1440aagaaaatag cctggcagtg aggtcactca aggagacaat cgaagactgt
tgggaccagg 1500atgcagaggc tcggcttact gcacagtgtg ctgaggaaag
gatggctgaa cttatgatga 1560tttgggaaag aaacaaatct gtgagcccaa
cagtcaatcc aatgtctact gctatgcaga 1620atgaacgtag gtgagtcaac
acaagatggc aaatcaggat caggtgaaaa gatcaagaaa 1680cgtgtgaaaa
ctccctattc tcttaagcgg tggcgcccct ccacctgggt catctccact
1740gaatcgctgg actgtgaagt caacaataat ggcagtaaca gggcagttca
ttccaaatcc 1800agcactgctg tttaccttgc agaaggaggc actgctacaa
ccatggtgtc taaagatata 1860ggaatgaact gtctgtgaaa tgttttcaag
cctatggagt gaaattattt tttgcatcat 1920ttaaacatgc agaagatgtt
taaaaataaa aaaaaaactg cttt 1964933611DNAHomo sapiens 93cgccccccga
ccccggatcg aatccccgcc ctccgcaccc tggatatgtt ttctcccaga 60cctggatatt
tttttgatat cgtgaaacta cgagggaaat aatttggggg atttcttctt
120ggctccctgc tttccccaca gacatgcctt ccgtttggag ggccgcggca
ccccgtccga 180ggcgaaggaa cccccccagc cgcgagggag agaaatgaag
ggaatttctg cagcggcatg 240aaagctctgc agctaggtcc tctcatcagc
catttgtcct ttcaaactgt attgtgatac 300gggcaggatc agtccacggg
agagaagacg agcctcccgg ctgtttctcc gccggtctac 360ttcccatatt
tcttttcttt gccctcctga ttcttggctg gcccagggat gacttcctcg
420ctgcagcggc cctggcgggt gccctggcta ccatggacca tcctgctggt
cagcactgcg 480gctgcttcgc agaatcaaga acggctatgt gcgtttaaag
atccgtatca gcaagacctt 540gggataggtg agagtagaat ctctcatgaa
aatgggacaa tattatgctc gaaaggtagc 600acctgctatg gcctttggga
gaaatcaaaa ggggacataa atcttgtaaa acaaggatgt 660tggtctcaca
ttggagatcc ccaagagtgt cactatgaag aatgtgtagt aactaccact
720cctccctcaa ttcagaatgg aacataccgt ttctgctgtt gtagcacaga
tttatgtaat 780gtcaacttta ctgagaattt tccacctcct gacacaacac
cactcagtcc acctcattca 840tttaaccgag atgagacaat aatcattgct
ttggcatcag tctctgtatt agctgttttg 900atagttgcct tatgctttgg
atacagaatg ttgacaggag accgtaaaca aggtcttcac 960agtatgaaca
tgatggaggc agcagcatcc gaaccctctc ttgatctaga taatctgaaa
1020ctgttggagc tgattggccg aggtcgatat ggagcagtat ataaaggctc
cttggatgag 1080cgtccagttg ctgtaaaagt gttttccttt gcaaaccgtc
agaattttat caacgaaaag 1140aacatttaca gagtgccttt gatggaacat
gacaacattg cccgctttat agttggagat 1200gagagagtca ctgcagatgg
acgcatggaa tatttgcttg tgatggagta ctatcccaat 1260ggatctttat
gcaagtattt aagtctccac acaagtgact gggtaagctc ttgccgtctt
1320gctcattctg ttactagagg actggcttat cttcacacag aattaccacg
aggagatcat 1380tataaacctg caatttccca tcgagattta aacagcagaa
atgtcctagt gaaaaatgat 1440ggaacctgtg ttattagtga ctttggactg
tccatgaggc tgactggaaa tagactggtg 1500cgcccagggg aggaagataa
tgcagccata agcgaggttg gcactatcag atatatggca 1560ccagaagtgc
tagaaggagc tgtgaacttg agggactgtg aatcagcttt gaaacaagta
1620gacatgtatg ctcttggact aatctattgg gagatattta tgagatgtac
agacctcttc 1680ccaggggaat ccgtaccaga gtaccagatg gcttttcaga
cagaggttgg aaaccatccc 1740acttttgagg atatgcaggt tctcgtgtct
agggaaaaac agagacccaa gttcccagaa 1800gcctggaaag aaaatagcct
ggcagtgagg tcactcaagg agacaatcga agactgttgg 1860gaccaggatg
cagaggctcg gcttactgca cagtgtgctg aggaaaggat ggctgaactt
1920atgatgattt gggaaagaaa caaatctgtg agcccaacag tcaatccaat
gtctactgct 1980atgcagaatg aacgcaacct gtcacataat aggcgtgtgc
caaaaattgg tccttatcca 2040gattattctt cctcctcata cattgaagac
tctatccatc atactgacag catcgtgaag 2100aatatttcct ctgagcattc
tatgtccagc acacctttga ctatagggga aaaaaaccga 2160aattcaatta
actatgaacg acagcaagca caagctcgaa tccccagccc tgaaacaagt
2220gtcaccagcc tctccaccaa cacaacaacc acaaacacca caggactcac
gccaagtact 2280ggcatgacta ctatatctga gatgccatac ccagatgaaa
caaatctgca taccacaaat 2340gttgcacagt caattgggcc aacccctgtc
tgcttacagc tgacagaaga agacttggaa 2400accaacaagc tagacccaaa
agaagttgat aagaacctca aggaaagctc tgatgagaat 2460ctcatggagc
actctcttaa acagttcagt ggcccagacc cactgagcag tactagttct
2520agcttgcttt acccactcat aaaacttgca gtagaagcaa ctggacagca
ggacttcaca 2580cagactgcaa atggccaagc atgtttgatt cctgatgttc
tgcctactca gatctatcct 2640ctccccaagc agcagaacct tcccaagaga
cctactagtt tgcctttgaa caccaaaaat 2700tcaacaaaag agccccggct
aaaatttggc agcaagcaca aatcaaactt gaaacaagtc 2760gaaactggag
ttgccaagat gaatacaatc aatgcagcag aacctcatgt ggtgacagtc
2820accatgaatg gtgtggcagg tagaaaccac agtgttaact cccatgctgc
cacaacccaa 2880tatgccaatg ggacagtact atctggccaa acaaccaaca
tagtgacaca tagggcccaa 2940gaaatgttgc agaatcagtt tattggtgag
gacacccggc tgaatattaa ttccagtcct 3000gatgagcatg agcctttact
gagacgagag caacaagctg gccatgatga aggtgttctg 3060gatcgtcttg
tggacaggag ggaacggcca ctagaaggtg gccgaactaa ttccaataac
3120aacaacagca atccatgttc agaacaagat gttcttgcac agggtgttcc
aagcacagca 3180gcagatcctg ggccatcaaa gcccagaaga gcacagaggc
ctaattctct ggatctttca 3240gccacaaatg tcctggatgg cagcagtata
cagataggtg agtcaacaca agatggcaaa 3300tcaggatcag gtgaaaagat
caagaaacgt gtgaaaactc cctattctct taagcggtgg 3360cgcccctcca
cctgggtcat ctccactgaa tcgctggact gtgaagtcaa caataatggc
3420agtaacaggg cagttcattc caaatccagc actgctgttt accttgcaga
aggaggcact 3480gctacaacca tggtgtctaa agatatagga atgaactgtc
tgtgaaatgt tttcaagcct 3540atggagtgaa attatttttt gcatcattta
aacatgcaga agatgtttaa aaataaaaaa 3600aaaactgctt t 3611943871DNAHomo
sapiens 94ggcctccgca ccctggatat gttttctccc agacctggat atttttttga
tatcgtgaaa 60ctacgaggga aataatttgg gggatttctt cttggctccc tgctttcccc
acagacatac 120cttccgtttg gagggccgcg gcaccccgtc cgaggcgaag
gaaccccccc atccgcgagg 180gagagaaatg aagggaattt ctgcagcggc
atgaaagctc tgcagctagg tcctctcatc 240agccatttgt cctttcaaac
tgtattgtga tacgggcagg atcagtccac gggagagaag 300acgagcctcc
cggctgtttc tccgccggtc tacttcccat atttcttttc tttgccctcc
360tgattcttgg ctggcccagg gatgacttcc tcgctgcagc ggccctggcg
ggtgccctgg 420ctaccatgga ccatcctgct ggtcagcact gcggctgctt
cgcagaatca agaacggcta 480tgtgcgttta aagatccgta tcagcaagac
cttgggatag gtgagagtag aatctctcat 540gaaaatggga caatattatg
ctcgaaaggt agcacctgct atggcctttg ggagaaatca 600aaaggggaca
taaatcttgt aaaacaagga tgttggtctc acattggaga tccccaagag
660tgtcactatg aagaatgtgt agtaactacc actcctccct caattcagaa
tggaacatac 720cgtttctgct gttgtagcac agatttatgt aatgtcaact
ttactgagaa ttttccacct 780cctgacacaa caccactcag tccacctcat
tcatttaacc gagatgagac aataatcatt 840gctttggcat cagtctctgt
attagctgtt ttgatagttg ccttatgctt tggatacaga 900atgttgacag
gagaccgtaa acaaggtctt cacagtatga acatgatgga ggcagcagca
960tccgaaccct ctcttgatct agataatctg aaactgttgg agctgattgg
ccgaggtcga 1020tatggagcag tatataaagg ctccttggat gagcgtccag
ttgctgtaaa agtgttttcc 1080tttgcaaacc gtcagaattt tatcaacgaa
aagaacattt acagagtgcc tttgatggaa 1140catgacaaca ttgcccgctt
tatagttgga gatgagagag tcactgcaga tggacgcatg 1200gaatatttgc
ttgtgatgga gtactatccc aatggatctt tatgcaagta tttaagtctc
1260cacacaagtg actgggtaag ctcttgccgt cttgctcatt ctgttactag
aggactggct 1320tatcttcaca cagaattacc acgaggagat cattataaac
ctgcaatttc ccatcgagat 1380ttaaacagca gaaatgtcct agtgaaaaat
gatggaacct gtgttattag tgactttgga 1440ctgtccatga ggctgactgg
aaatagactg gtgcgcccag gggaggaaga taatgcagcc 1500ataagcgagg
ttggcactat cagatatatg gcaccagaag tgctagaagg agctgtgaac
1560ttgagggact gtgaatcagc tttgaaacaa gtagacatgt atgctcttgg
actaatctat 1620tgggagatat ttatgagatg tacagacctc ttcccagggg
aatccgtacc agagtaccag 1680atggcttttc agacagaggt tggaaaccat
cccacttttg aggatatgca ggttctcgtg 1740tctagggaaa aacagagacc
caagttccca gaagcctgga aagaaaatag cctggcagtg 1800aggtcactca
aggagacaat cgaagactgt tgggaccagg atgcagaggc tcggcttact
1860gcacagtgtg ctgaggaaag gatggctgaa cttatgatga tttgggaaag
aaacaaatct 1920gtgagcccaa cagtcaatcc aatgtctact gctatgcaga
atgaacgcaa cctgtcacat 1980aataggcgtg tgccaaaaat tggtccttat
ccagattatt cttcctcctc atacattgaa 2040gactctatcc atcatactga
cagcatcgtg aagaatattt cctctgagca ttctatgtcc 2100agcacacctt
tgactatagg ggaaaaaaac cgaaattcaa ttaactatga acgacagcaa
2160gcacaagctc gaatccccag ccctgaaaca agtgtcacca gcctctccac
caacacaaca 2220accacaaaca ccacaggact cacgccaagt actggcatga
ctactatatc tgagatgcca 2280tacccagatg aaacaaatct gcataccaca
aatgttgcac agtcaattgg gccaacccct 2340gtctgcttac agctgacaga
agaagacttg gaaaccaaca agctagaccc aaaagaagtt 2400gataagaacc
tcaaggaaag ctctgatgag aatctcatgg agcactctct taaacagttc
2460agtggcccag acccactgag cagtactagt tctagcttgc tttacccact
cataaaactt 2520gcagtagaag caactggaca gcaggacttc acacagactg
caaatggcca agcatgtttg 2580attcctgatg ttctgcctac tcagatctat
cctctcccca agcagcagaa ccttcccaag 2640agacctacta gtttgccttt
gaacaccaaa aattcaacaa aagagccccg gctaaaattt 2700ggcagcaagc
acaaatcaaa cttgaaacaa gtcgaaactg gagttgccaa gatgaataca
2760atcaatgcag cagaacctca tgtggtgaca gtcaccatga atggtgtggc
aggtagaaac 2820cacagtgtta actcccatgc tgccacaacc caatatgcca
ataggacagt actatctggc 2880caaacaacca acatagtgac acatagggcc
caagaaatgt tgcagaatca gtttattggt 2940gaggacaccc ggctgaatat
taattccagt cctgatgagc atgagccttt actgagacga 3000gagcaacaag
ctggccatga tgaaggtgtt ctggatcgtc ttgtggacag gagggaacgg
3060ccactagaag gtggccgaac taattccaat aacaacaaca gcaatccatg
ttcagaacaa 3120gatgttcttg cacagggtgt tccaagcaca gcagcagatc
ctgggccatc aaagcccaga 3180agagcacaga ggcctaattc tctggatctt
tcagccacaa atgtcctgga tggcagcagt 3240atacagatag gtgagtcaac
acaagatggc aaatcaggat caggtgaaaa gatcaagaaa 3300cgtgtgaaaa
ctccctattc tcttaagcgg tggcgcccct ccacctgggt catctccact
3360gaatcgctgg actgtgaagt caacaataat ggcagtaaca gggcagttca
ttccaaatcc 3420agcactgctg tttaccttgc agaaggaggc actgctacaa
ccatggtgtc taaagatata 3480ggaatgaact gtctgtgaaa tgttttcaag
cctatggagt gaaattattt tttgcatcat 3540ttaaacatgc agaagatgtt
taccgggcgg ggtgacagga gagagcgtca gcggcaagct 3600gtggaggatg
gggctcagaa tgcagacctg ggctggccgc atggcctctc cctgagccct
3660gatttgtggt agggaagcag tatgggtgca gtcccctcct aggcctccct
ctggggtccc 3720ccgatcctat cccacctctt cagggtgagc cagcctcacc
tcttcctagt cctgagggtg 3780agggcaggct gaggcaacga gtgggaggtt
caaacaagag tgggctggag ccaagggaaa 3840atagagatga tgtaatttct
ttccggaatt c 38719588PRTHomo sapiens 95Cys Arg Glu Leu His Phe Thr
Arg Tyr Val Thr Asp Gly Pro Cys Arg1 5 10 15Ser Ala Lys Pro Val Thr
Glu Leu Val Cys Ser Gly Gln Cys Gly Pro 20 25 30Ala Arg Leu Leu Pro
Asn Ala Ile Gly Arg Gly Lys Trp Trp Arg Pro 35 40 45Ser Gly Pro Asp
Phe Arg Cys Ile Pro Asp Arg Tyr Arg Ala Gln Arg 50 55 60Val Gln Leu
Leu Cys Pro Gly Gly Glu Ala Pro Arg Ala Arg Lys Val65 70 75 80Arg
Leu Val Ala Ser Cys Lys Cys 859682PRTHomo sapiens 96Cys Arg Pro Ile
Asn Ala Thr Leu Ala Val Glu Lys Glu Gly Cys Pro1 5 10 15Val Cys Ile
Thr Val Asn Thr Thr Ile Cys Ala Gly Tyr Cys Pro Thr 20 25 30Met Thr
Arg Val Leu Gln Gly Val Leu Pro Ala Leu Pro Gln Val Val 35 40 45Cys
Asn Tyr Arg Asp Val Arg Phe Glu Ser Ile Arg Leu Pro Gly Cys 50 55
60Pro Arg Gly Val Asn Pro Val Val Ser Tyr Ala Val Ala Leu Ser Cys65
70 75 80Gln Cys9782PRTHomo sapiens 97Cys Glu Leu Thr Asn Ile Thr
Ile Ala Ile Glu Lys Glu Glu Cys Arg1 5 10 15Phe Cys Ile Ser Ile Asn
Thr Thr Trp Cys Ala Gly Tyr Cys Tyr Thr 20 25 30Arg Asp Leu Val Tyr
Lys Asp Pro Ala Arg Pro Lys Ile Gln Lys Thr 35 40 45Cys Thr Phe Lys
Glu Leu Val Tyr Glu Thr Val Arg Val Pro Gly Cys 50 55 60Ala His His
Ala Asp Ser Leu Tyr Thr Tyr Pro Val Ala Thr Gln Cys65 70 75 80His
Cys9884PRTHomo sapiens 98Cys Ile Pro Thr Glu Tyr Thr Met His Ile
Glu Arg Arg Glu Cys Ala1 5 10 15Tyr Cys Leu Thr Ile Asn Thr Thr Ile
Cys Ala Gly Tyr Cys Met Thr 20 25 30Arg Asp Ile Asn Gly Lys Leu Phe
Leu Pro Lys Tyr Ala Leu Ser Gln 35 40 45Asp Val Cys Thr Tyr Arg Asp
Phe Ile Tyr Arg Thr Val Glu Ile Pro 50 55 60Gly Cys Pro Leu His Val
Ala Pro Tyr Phe Ser Tyr Pro Val Ala Leu65 70 75 80Ser Cys Lys
Cys9983PRTHomo sapiens 99Cys Asn Asp Ile Thr Ala Arg Leu Gln Tyr
Val Lys Val Gly Ser Cys1 5 10 15Lys Ser Glu Val Glu Val Asp Ile His
Tyr Cys Gln Gly Lys Cys Ala 20 25 30Ser Lys Ala Met Tyr Ser Ile Asp
Ile Asn Asp Val Gln Asp Gln Cys 35 40 45Ser Cys Cys Ser Pro Thr Arg
Thr Glu Pro Met Gln Val Ala Leu His 50 55 60Cys Thr Asn Gly Ser Val
Val Tyr His Glu Val Leu Asn Ala Met Glu65 70 75 80Cys Lys
Cys10080PRTHomo sapiens 100Cys Ser Thr Val Pro Val Thr Thr Glu Val
Ser Tyr Ala Gly Cys Thr1 5 10 15Lys Thr Val Leu Met Asn His Cys Ser
Gly Ser Cys Gly Thr Phe Val 20 25 30Met Tyr Ser Ala Lys Ala Gln Ala
Leu Asp His Ser Cys Ser Cys Cys 35 40 45Lys Glu Glu Lys Thr Ser Gln
Arg Glu Val Val Leu Ser Cys Pro Asn 50 55 60Gly Gly Ser Leu Thr His
Thr Tyr Thr His Ile Glu Ser Cys Gln Cys65 70 75 8010180PRTHomo
sapiens 101Cys Arg Thr Val Pro Phe Ser Gln Thr Ile Thr His Glu Gly
Cys Glu1 5 10 15Lys Val Val Val Gln Asn Asn Leu Cys Phe Gly Lys Cys
Gly Ser Val 20 25 30His Phe Pro Gly Ala Ala Gln His Ser His Thr Ser
Cys Ser His Cys 35 40 45Leu Pro Ala Lys Phe Thr Thr Met His Leu Pro
Leu Asn Cys Thr Glu 50 55 60Leu Ser Ser Val Ile Lys Val Val Met Leu
Val Glu Glu Cys Gln Cys65 70 75 8010285PRTHomo sapiens 102Cys Lys
Thr Gln Pro Leu Lys Gln Thr Ile His Glu Glu Gly Cys Asn1 5 10 15Ser
Arg Thr Ile Ile Asn Arg Phe Cys Tyr Gly Gln Cys Asn Ser Phe 20 25
30Tyr Ile Pro Arg His Ile Arg Lys Glu Glu Gly Ser Phe Gln Ser Cys
35 40 45Ser Phe Cys Lys Pro Lys Lys Phe Thr Thr Met Met Val Thr Leu
Asn 50 55 60Cys Pro Glu Leu Gln Pro Pro Thr Lys Lys Lys Arg Val Thr
Arg Val65 70 75 80Lys Gln Cys Arg Cys 8510386PRTHomo sapiens 103Cys
Glu Ala Lys Asn Ile Thr Gln Ile Val Gly His Ser Gly Cys Glu1 5 10
15Ala Lys Ser Ile Gln Asn Arg Ala Cys Leu Gly Gln Cys Phe Ser Tyr
20 25 30Ser Val Pro Asn Thr Phe Pro Gln Ser Thr Glu Ser Leu Val His
Cys 35 40 45Asp Ser Cys Met Pro Ala Gln Ser Met Trp Glu Ile Val Thr
Leu Glu 50 55 60Cys Pro Gly His Glu Glu Val Pro Arg Val Asp Lys Leu
Val Glu Lys65 70 75 80Ile Leu His Cys Ser Cys 8510470PRTHomo sapies
104Cys Ile Arg Thr Pro Lys Ile Ser Lys Pro Ile Lys Phe Glu Leu Ser1
5 10 15Gly Cys Thr Ser Met Lys Thr Tyr Arg Ala Lys Phe Cys Gly Val
Cys 20 25 30Thr Asp Gly Arg Cys Cys Thr Pro His Arg Thr Thr Thr Leu
Pro Val 35 40 45Glu Phe Lys Cys Pro Asp Gly Glu Val Met Lys Lys Asn
Met Met Phe 50 55 60Ile Lys Thr Cys Ala Cys65 7010570PRTHomo
sapiens 105Cys Leu Arg Thr Lys Lys Ser Leu Lys Ala Ile His Leu Gln
Phe Lys1 5 10 15Asn Cys Thr Ser Leu His Thr Tyr Lys Pro Arg Phe Cys
Gly Val Cys 20 25 30Ser Asp Gly Arg Cys Cys Thr Pro His Asn Thr Lys
Thr Ile Gln Ala 35 40 45Glu Phe Gln Cys Ser Pro Gly Gln Ile Val Lys
Lys Pro Val Met Val 50 55 60Ile Gly Thr Cys Thr Cys65
7010670PRTHomo sapiens 106Cys Ser Lys Thr Lys Lys Ser Pro Glu Pro
Val Arg Phe Thr Tyr Ala1 5 10 15Gly Cys Leu Ser Val Lys Lys Tyr Arg
Pro Lys Tyr Cys Gly Ser Cys 20 25 30Val Asp Gly Arg Cys Cys Thr Pro
Gln Leu Thr Arg Thr Val Lys Met 35 40 45Arg Phe Arg Cys Glu Asp Gly
Glu Thr Phe Ser Lys Asn Val Met Met 50 55 60Ile Gln Ser Cys Lys
Cys65 70107205PRTHomo sapiens 107Gln His Tyr Leu His Ile Arg Pro
Ala Pro Ser Asp Asn Leu Pro Leu1 5 10 15Val Asp Leu Ile Glu His Pro
Asp Pro Ile Phe Asp Pro Lys Glu Lys 20 25 30Asp Leu Asn Glu Thr Leu
Leu Arg Ser Leu Leu Gly Gly His Tyr Asp 35 40 45Pro Gly Phe Met Ala
Thr Ser Pro Pro Glu Asp Arg Pro Gly Gly Gly 50 55 60Gly Gly Ala Ala
Gly Gly Ala Glu Asp Leu Ala Glu Leu Asp Gln Leu65 70 75 80Leu Arg
Gln Arg Pro Ser Gly Ala Met Pro Ser Glu Ile Lys Gly Leu 85 90 95Glu
Phe Ser Glu Gly Leu Ala Gln Gly Lys Lys Gln Arg Leu Ser Lys 100 105
110Lys Leu Arg Arg Lys Leu Gln Met Trp Leu Trp Ser
Gln Thr Phe Cys 115 120 125Pro Val Leu Tyr Ala Trp Asn Asp Leu Gly
Ser Arg Phe Trp Pro Arg 130 135 140Tyr Val Lys Val Gly Ser Cys Phe
Ser Lys Arg Ser Cys Ser Val Pro145 150 155 160Glu Gly Met Val Cys
Lys Pro Ser Lys Ser Val His Leu Thr Val Leu 165 170 175Arg Trp Arg
Cys Gln Arg Arg Gly Gly Gln Arg Cys Gly Trp Ile Pro 180 185 190Ile
Gln Tyr Pro Ile Ile Ser Glu Cys Lys Cys Ser Cys 195 200
205108197PRTGallus gallus 108Gln His Tyr Leu His Ile Arg Pro Ala
Pro Ser Asp Asn Leu Pro Leu1 5 10 15Val Asp Leu Ile Glu His Pro Asp
Pro Ile Phe Asp Pro Lys Glu Lys 20 25 30Asp Leu Asn Glu Thr Leu Leu
Arg Ser Leu Met Gly Gly His Phe Asp 35 40 45Pro Asn Phe Met Ala Met
Ser Leu Pro Glu Asp Arg Leu Gly Val Asp 50 55 60Asp Leu Ala Glu Leu
Asp Leu Leu Leu Arg Gln Arg Pro Ser Gly Ala65 70 75 80Met Pro Gly
Glu Ile Lys Gly Leu Glu Phe Tyr Asp Gly Leu Gln Pro 85 90 95Gly Lys
Lys His Arg Leu Ser Lys Lys Leu Arg Arg Lys Leu Gln Met 100 105
110Trp Leu Trp Ser Gln Thr Phe Cys Pro Val Leu Tyr Thr Trp Asn Asp
115 120 125Leu Gly Ser Arg Phe Trp Pro Arg Tyr Val Lys Val Gly Ser
Cys Tyr 130 135 140Ser Lys Arg Ser Cys Ser Val Pro Glu Gly Met Val
Cys Lys Pro Ala145 150 155 160Lys Ser Val His Leu Thr Ile Leu Arg
Trp Arg Cys Gln Arg Arg Gly 165 170 175Gly Gln Arg Cys Thr Trp Ile
Pro Ile Gln Tyr Pro Ile Ile Ala Glu 180 185 190Cys Lys Cys Ser Cys
195109196PRTXenopus laevis 109Gln His Tyr Leu His Ile Arg Pro Ala
Pro Ser Glu Asn Leu Pro Leu1 5 10 15Val Asp Leu Ile Glu His Pro Asp
Pro Ile Tyr Asp Pro Lys Glu Lys 20 25 30Asp Leu Asn Glu Thr Leu Leu
Arg Thr Leu Met Val Gly His Phe Asp 35 40 45Pro Asn Phe Met Ala Thr
Ile Leu Pro Glu Glu Arg Leu Gly Val Glu 50 55 60Asp Leu Gly Glu Leu
Asp Leu Leu Leu Arg Gln Lys Pro Ser Gly Ala65 70 75 80Met Pro Ala
Glu Ile Lys Gly Leu Glu Phe Tyr Glu Gly Leu Gln Ser 85 90 95Lys Lys
His Arg Leu Ser Lys Lys Leu Arg Arg Lys Leu Gln Met Trp 100 105
110Leu Trp Ser Gln Thr Phe Cys Pro Val Leu Tyr Thr Trp Asn Asp Leu
115 120 125Gly Thr Arg Phe Trp Pro Arg Tyr Val Lys Val Gly Ser Cys
Tyr Ser 130 135 140Lys Arg Ser Cys Ser Val Pro Glu Gly Met Val Cys
Lys Ala Ala Lys145 150 155 160Ser Met His Leu Thr Ile Leu Arg Trp
Arg Cys Gln Arg Arg Val Gln 165 170 175Gln Lys Cys Ala Trp Ile Thr
Ile Gln Tyr Pro Val Ile Ser Glu Cys 180 185 190Lys Cys Ser Cys
195110195PRTTakifugu rubripes 110Gln Pro Tyr Tyr Leu Leu Arg Pro
Ile Pro Ser Asp Ser Leu Pro Ile1 5 10 15Val Glu Leu Lys Glu Asp Pro
Gly Pro Val Phe Asp Pro Lys Glu Arg 20 25 30Asp Leu Asn Glu Thr Glu
Leu Lys Ser Val Leu Gly Asp Phe Asp Ser 35 40 45Arg Phe Leu Ser Val
Leu Pro Pro Ala Glu Asp Gly His Ala Gly Asn 50 55 60Asp Glu Leu Asp
Asp Phe Asp Ala Gln Arg Trp Gly Gly Ala Leu Pro65 70 75 80Lys Glu
Ile Arg Ala Val Asp Phe Asp Ala Pro Gln Leu Gly Lys Lys 85 90 95His
Lys Pro Ser Lys Lys Leu Lys Arg Arg Leu Gln Gln Trp Leu Trp 100 105
110Ala Tyr Ser Phe Cys Pro Leu Ala His Ala Trp Thr Asp Leu Gly Ser
115 120 125Arg Phe Trp Pro Arg Phe Val Arg Ala Gly Ser Cys Leu Ser
Lys Arg 130 135 140Ser Cys Ser Val Pro Glu Gly Met Thr Cys Lys Pro
Ala Thr Ser Thr145 150 155 160His Leu Thr Ile Leu Arg Trp Arg Cys
Val Gln Arg Lys Val Gly Leu 165 170 175Lys Cys Ala Trp Ile Pro Met
Gln Tyr Pro Val Ile Thr Asp Cys Lys 180 185 190Cys Ser Cys
195111196PRTDanio rerio 111Gln His Tyr Tyr Leu Leu Arg Pro Ile Pro
Ser Asp Ser Leu Pro Ile1 5 10 15Val Glu Leu Lys Glu Asp Pro Asp Pro
Val Leu Asp Pro Lys Glu Arg 20 25 30Asp Leu Asn Glu Thr Glu Leu Arg
Ala Ile Leu Gly Ser His Phe Glu 35 40 45Gln Asn Phe Met Ser Ile Asn
Pro Pro Glu Asp Lys His Ala Gly Gln 50 55 60Asp Glu Leu Asn Glu Ser
Glu Leu Met Lys Gln Arg Pro Asn Gly Ile65 70 75 80Met Pro Lys Glu
Ile Lys Ala Met Glu Phe Asp Ile Gln His Gly Lys 85 90 95Lys His Lys
Pro Ser Lys Lys Leu Arg Arg Arg Leu Gln Leu Trp Leu 100 105 110Trp
Ser Tyr Thr Phe Cys Pro Val Val His Thr Trp Gln Asp Leu Gly 115 120
125Asn Arg Phe Trp Pro Arg Tyr Leu Lys Val Gly Ser Cys Tyr Asn Lys
130 135 140Arg Ser Cys Ser Val Pro Glu Gly Met Val Cys Lys Pro Pro
Lys Ser145 150 155 160Ser His Leu Thr Val Leu Arg Trp Arg Cys Val
Gln Arg Lys Gly Gly 165 170 175Leu Lys Cys Ala Trp Ile Pro Val Gln
Tyr Pro Val Ile Ser Glu Cys 180 185 190Lys Cys Ser Cys
195112188PRTMus musculus 112Gln Gly Trp Gln Ala Phe Arg Asn Asp Ala
Thr Glu Val Ile Pro Gly1 5 10 15Leu Gly Glu Tyr Pro Glu Pro Pro Pro
Glu Asn Asn Gln Thr Met Asn 20 25 30Arg Ala Glu Asn Gly Gly Arg Pro
Pro His His Pro Tyr Asp Ala Lys 35 40 45Gly Val Ser Glu Tyr Ser Cys
Arg Glu Leu His Tyr Thr Arg Phe Leu 50 55 60Thr Asp Gly Pro Cys Arg
Ser Ala Lys Pro Val Thr Glu Leu Val Cys65 70 75 80Ser Gly Gln Cys
Gly Pro Ala Arg Leu Leu Pro Asn Ala Ile Gly Arg 85 90 95Val Lys Trp
Trp Arg Pro Asn Gly Pro Asp Phe Arg Cys Ile Pro Asp 100 105 110Arg
Tyr Arg Ala Gln Arg Val Gln Leu Leu Cys Pro Gly Gly Ala Ala 115 120
125Pro Arg Ser Arg Lys Val Arg Leu Val Ala Ser Cys Lys Cys Lys Arg
130 135 140Leu Thr Arg Phe His Asn Gln Ser Glu Leu Lys Asp Phe Gly
Pro Glu145 150 155 160Thr Ala Arg Pro Gln Lys Gly Arg Lys Pro Arg
Pro Gly Ala Arg Gly 165 170 175Ala Lys Ala Asn Gln Ala Glu Leu Glu
Asn Ala Tyr 180 185
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