Stabilized activin IIB receptor polypeptides and uses thereof
The present invention provides stabilized activin IIB receptor polypeptides and proteins capable of binding and inhibiting the activities of activin A, myostatin, or GDF-11. The present invention also provides polynucleotides, vectors and host cells capable of producing the stabilized polypeptides and proteins. Compositions and methods for treating muscle-wasting diseases and metabolic disorders are also provided.
1. An isolated protein comprising a stabilized activin IIB receptor polypeptide (svActRIIB) wherein said polypeptide is selected from the group consisting of:
(a) a polypeptide consisting of the sequence set forth in SEQ ID NO: 2, except for a single amino acid substitution at position 28, and a single amino acid substitution at position 44, wherein the substitution at position 28 is selected from the group consisting of W and Y, and the substitution at position 44 is T;
(b) a polypeptide consisting of the sequence set forth in amino acids 19 through 134 of SEQ ID NO: 2, except for a single amino acid substitution at position 28, and a single amino acid substitution at position 44, wherein the substitution at position 28 is selected from the group consisting of W and Y, and the substitution at position 44 is T;
(c) a polypeptide consisting of the sequence set forth in amino acids 23 through 134 of SEQ ID NO: 2, except for a single amino acid substitution at position 28, and a single amino acid substitution at position 44, wherein the substitution at position 28 is selected from the group consisting of W and Y, and the substitution at position 44 is T;
(d) a polypeptide consisting of the sequence set forth in amino acids 25 through 134 of SEQ ID NO: 2, except for a single amino acid substitution at position 28, and a single amino acid substitution at position 44, wherein the substitution at position 28 is selected from the group consisting of W and Y, and the substitution at position 44 is T;
(e) a polypeptide of any one of (a) through (d), except for a single amino acid substitution at position 28, and a single amino acid substitution at position 44, wherein the substitution at position 28 is selected from the group consisting of W and Y, and the substitution at position 44 is T, wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11.
2. An isolated protein comprising a stabilized activin IIB receptor polypeptide, wherein said polypeptide is selected from a polypeptide consisting of the sequence set forth in the group consisting of SEQ ID NO: 4, 6, 12 and 14.
3. The protein of claim 2 , wherein the polypeptide is connected to at least one heterologous protein.
4. The protein of claim 3 , wherein the heterologous polypeptide is an IgG Fc domain.
5. The protein of claim 3 , wherein the heterologous polypeptide is connected to the polypeptide by a linker sequence.
6. The protein of claim 5 , wherein the linker is selected from the group consisting of: SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 49 and SEQ ID NO: 50.
7. The protein of claim 2 , wherein the amino acid residue at position 64 is alanine.
8. A pharmaceutical composition comprising an effective amount of the protein of claim 1 or 2 in admixture with a pharmaceutically acceptable carrier.
9. A method of inhibiting myostatin activity or activin activity in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 8 to the subject.
10. A method of increasing lean muscle mass or increasing the ratio of lean muscle mass to fat mass in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 8 to the subject.
11. A method of treating a muscle-wasting disease or metabolic disorder in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 8 to the subject.
12. The method of claim 11 , wherein the muscle-wasting disease is selected from muscular dystrophy, amyotrophic lateral sclerosis, congestive obstructive pulmonary disease, chronic heart failure, cancer cachexia, AIDS, renal failure, uremia, rheumatoid arthritis, age-related sarcopenia, organ atrophy, carpal tunnel syndrome, androgen deprivation, burn injury, diabetes, and muscle-wasting due to prolonged bed rest, spinal chord injury, stroke, bone fracture, aging or exposure to micro-gravity.
13. The method of claim 11 , wherein the metabolic disorder is selected from diabetes, obesity, hyperglycemia, and bone loss.
14. A method of treating a disease in which activin is overexpressed in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 8 to said subject.
15. The method of claim 14 , wherein the disease is cancer.