FGF21 mutants and uses thereof
The invention provides nucleic acid molecules encoding FGF21 mutant polypeptides, FGF21 mutant polypeptides, pharmaceutical compositions comprising FGF21 mutant polypeptides, and methods for treating metabolic disorders using such nucleic acids, polypeptides, or pharmaceutical compositions.
1. A polypeptide comprising an amino acid sequence of SEQ ID NO:4, further comprising the substitution of a lysine residue for the alanine residue at position 45, an arginine residue for the leucine residue at position 98, a glutamic acid residue for the glycine residue at position 170, or a glycine or serine residue for the proline residue at position 171 and combinations thereof.
2. The isolated polypeptide of claim 1 further comprising at least one amino acid substitution that is:
(a) a phenylalanine, proline, alanine, serine or glycine at position 179;
(b) a glutamic acid, glycine, proline, or serine at position 180; or
(c) a lysine, glycine, threonine, alanine, leucine, or proline at position 181.
3. The isolated polypeptide of claim 1 further comprising 1 to 10 amino acid residues fused to the C-terminus of the polypeptide.
4. The isolated polypeptide of claim 1 wherein the polypeptide comprises:
(a) an amino-terminal truncation of no more than 8 amino acid residues, wherein the polypeptide is capable of lowering blood glucose in a mammal;
(b) a carboxyl-terminal truncation of no more than 10 amino acid residues, wherein the polypeptide is capable of lowering blood glucose in a mammal; or
(c) an amino-terminal truncation of no more than 8 amino acid residues and a carboxyl-terminal truncation of no more than 12 amino acid residues, wherein the polypeptide is capable of lowering blood glucose in a mammal.
5. The isolated polypeptide of claim 1 wherein the polypeptide is covalently linked to one or more polymers.
6. The isolated polypeptide of claim 5 , wherein the polymer is PEG.
7. A fusion polypeptide comprising the isolated polypeptide of claim 1 fused to a heterologous amino acid sequence.
8. The fusion polypeptide of claim 7 , wherein the polypeptide is fused to the heterologous amino acid sequence via a linker.
9. The fusion polypeptide of claim 8 , wherein the linker comprises GGGGGSGGGSGGGGS (SEQ ID NO: 23).
10. The fusion polypeptide of claim 8 , wherein the heterologous amino acid sequence is an IgG constant domain or fragment thereof.
11. The fusion polypeptide of claim 10 , wherein the IgG constant domain comprises the amino acid sequence of SEQ ID NO:13.
12. A multimer comprising two or more copies of the fusion polypeptide of claim 11 .
13. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutically acceptable formulation agent.
14. A method of treating type 2 diabetes comprising administering to a human patient in need thereof the pharmaceutical composition of claim 13 .
15. A method of reducing triglyceride levels in a patient comprising administering to a human patient in need thereof the pharmaceutical composition of claim 13 .
16. A method of improving glucose tolerance in a patient comprising administering to a human patient in need thereof the pharmaceutical composition of claim 13 .
17. A method of lowering body weight in a patient comprising administering to a human patient in need thereof the pharmaceutical composition of claim 13 .
18. A method of lowering insulin levels in a patient comprising administering to a human patient in need thereof the pharmaceutical composition of claim 13 .
19. A nucleic acid molecule encoding a polypeptide comprising an amino acid sequence of SEQ ID NO:4, further comprising the substitution of a lysine residue for the alanine residue at position 45, an arqinine residue for the leucine residue at position 98, a glutamic acid residue for the qlycine residue at position 170, or a glycine or serine residue for the proline residue at position 171, and combinations thereof.
20. A vector comprising the nucleic acid molecule claim 19 .
21. A host cell comprising the nucleic acid molecule of claim 19 .