FGF21 polypeptides comprising two or more mutations and uses thereof
The invention provides nucleic acid molecules encoding FGF21 mutant polypeptides, FGF21 mutant polypeptides, pharmaceutical compositions comprising FGF21 mutant polypeptides, wherein the FGF 21 mutant polypeptides comprise two or more mutations, and methods for treating metabolic disorders using such nucleic acids, polypeptides, or pharmaceutical compositions.
1. An isolated polypeptide comprising an amino acid sequence of SEQ ID NO: 4 and further comprising at least one amino acid substitution at position 180; and a substitution at position 171, wherein the substituted residue at position 180 is a glutamic acid residue and the substituted residue at position 171 is a glycine reidue.
2. A fusion polypeptide comprising the isolated polypeptide of claim 1 , fused to a heterologous amino acid sequence.
3. The fusion polypeptide of claim 2 , wherein the heterologous amino acid sequence is an Fc domain or fragment thereof.
4. The fusion polypeptide of claim 3 , wherein the Fc domain comprises the amino acid sequence of SEQ ID NO:11.
5. The fusion polypeptide of claim 4 , wherein the polypeptide is fused to the Fc domain via a linker.
6. The fusion polypeptide of claim 5 , wherein the linker comprises GGGGSGGGGSGGGGS (SEQ ID NO:31).
7. The fusion polypeptide of claim 6 , wherein the polypeptide comprises SEQ ID NO:47.
8. A multimer comprising two or more fusion polypeptides of claim 7 .
9. A pharmaceutical composition comprising the isolated polypeptide of claim 7 and a pharmaceutically acceptable formulation agent.
10. The pharmaceutical composition of claim 9 , wherein the pharmaceutically acceptable formulation agent is a hydrogel.
11. 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 12 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.
12. The isolated polypeptide of claim 1 , wherein the polypeptide is covalently linked to one or more polymers.
13. The isolated polypeptide of claim 12 , wherein the polymer is PEG.
14. The isolated polypeptide of claim 1 , wherein the polypeptide comprises a substitution at position 98, a substitution at position 171 and a substitution at position 180 of SEQ ID NO:4 and wherein:
(a) the substitution at position 171 is selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, lysine, serine, threonine, tryptophan, or tyrosine;
(b) the substitution at position 98 is selected from the group consisting of arginine, cysteine, glutamic acid, glutamine, lysine, or threonine; and
(c) the substitution at position 180 is selected from the group consisting of glycine, proline, serine or glutamic acid;
and combinations thereof.
15. The isolated polypeptide of claim 14 , wherein the residue at position 98 is arginine, the residue at position 171 is glycine and the residue at position 180 is glutamic acid.
16. A fusion polypeptide comprising the isolated polypeptide of claim 15 fused to a heterologous amino acid sequence.
17. The fusion polypeptide of claim 16 , wherein the heterologous amino acid sequence is an Fc domain or fragment thereof.
18. The fusion polypeptide of claim 17 , wherein the IgG constant domain comprises the amino acid sequence of SEQ ID NO:11.
19. The fusion polypeptide of claim 18 , wherein the polypeptide is fused to the Fc domain via a linker.
20. The fusion polypeptide of claim 19 , wherein the linker comprises GGGGSGGGGSGGGGS (SEQ ID NO:31).
21. The fusion polypeptide of claim 20 , wherein the polypeptide comprises SEQ ID NO:47.
22. A multimer comprising two or more fusion polypeptides of claim 21 .
23. An isolated nucleic acid encoding a polypeptide comprising an amino acid sequence of SE ID NO: 4 and further comprising an amino acid substitution at position 180; and a substitution at position 171, wherein the substituted residue at position 180 is a glycine residue and the substituted residue at position 171 is a, glutamic acid residue.
24. The isolated nucleic acid of claim 23 , wherein the nucleic acid comprises SEQ ID NO:46.
25. A vector comprising the nucleic acid molecule claim 24 .
26. A host cell comprising the nucleic acid molecule of claim 25 .