Hyaluronic acid binding domain-growth factor fusion protein cDNAs and fusion proteins for cartilage matrix preservation and repair
The present invention provides fusion proteins including a hyaluronic acid-binding domain of a cartilage matrix protein and a conserved region of a growth factor protein. Certain embodiments provide nucleic nucleic acid sequences encoding a fusion protein and compositions thereof. Methods for using fusion polypeptides and nucleic acid molecules discloses herein are also provided. In certain embodiments, the fusion proteins and/or nucleic acid molecules can be used to treat a cartilage matrix protein-related condition in a subject.
1. A fusion protein, comprising:
a hyaluronic acid-binding (HAB) polypeptide, wherein the HAB polypeptide is a polypeptide having the sequence of amino acids 1-178 of SEQ ID NO: 72; and
a conserved region of a growth factor (GF) protein,
wherein said fusion protein upregulates glycosaminoglycan (GAG) expression in chondrocytes.
2. The fusion protein of claim 1 , further comprising at least one additional element selected from the group consisting of: a signal peptide (SP); a linker peptide (linker); a protease cleavage site; and an E peptide.
3. The fusion protein of claim 1 , wherein the HAB polypeptide is linked to the amino (N)-terminus of the conserved region of the GF protein.
4. The fusion protein of claim 2 , further comprising at least one of a linker peptide (linker) positioned between the HAB polypeptide and the conserved region of the GF protein and a protease cleavage site positioned between the HAB and the conserved region of the GF protein.
5. The fusion protein of claim 2 , wherein the SP is selected from the group consisting of: aggrecan signal peptide; CD44 signal peptide; link protein signal peptide; TSG-6 signal peptide; and versican signal peptide.
6. The fusion protein of claim 2 , wherein the linker is selected from the group consisting of: Linker 1: GGSG (SEQ ID NO: 1); Linker 2: GGSGGGSG (SEQ ID NO: 2); Linker 3: GGSGGGSGGGSG (SEQ ID NO: 3); Linker 4: GGGGS (SEQ ID NO: 4); Linker 5: GGGGSGGGGS (SEQ ID NO: 5); Linker 6: GGGGSGGGGSGGGGS (SEQ ID NO: 6); Linker 7: GGSGGS (SEQ ID NO: 7); and Linker 8: VIGHPIDSE (SEQ ID NO: 8).
7. The fusion protein of claim 2 , wherein the protease cleavage site is selected from the group consisting of: SEQ ID NO: 9; SEQ ID NO: 10; SEQ ID NO: 11; SEQ ID NO: 12; and SEQ ID NO: 13.
8. The fusion protein of claim 1 , wherein the GF protein is selected from the group consisting of: IGF-1; BMP2; BMP4; BMP7; FGF2; FGF18; GDF5; TGF-β1; and TGF-β3.
9. The fusion protein of claim 1 , further comprising: flanking amino acids to the HAB polypeptide, wherein the number of flanking amino acids is selected from the group consisting of: 5 amino acids; 10 amino acids; 15 amino acids; 20 amino acids; 25 amino acids; 30 amino acids; 35 amino acids; 40 amino acids; 45 amino acids; 50 amino acids; 55 amino acids; and 60 amino acids.
10. The fusion protein of claim 9 , wherein the flanking amino acids are at the N terminus of HAB polypeptide.
11. The fusion protein of claim 9 , wherein the flanking amino acids are at the C terminus of HAB polypeptide.
12. A nucleic acid molecule comprising a nucleic acid sequence that encodes the fusion protein of claim 1 .
13. The nucleic acid molecule of claim 12 , wherein the nucleic acid molecule further comprises at least one additional nucleic acid sequence, wherein the additional nucleic acid sequence is selected from the group consisting of: a nucleic acid sequence that encodes at least one signal peptide (SP); a nucleic acid sequence that encodes at least one linker sequence (linker); a nucleic acid sequence that encodes at least one protease cleavage site; a nucleic acid sequence that encodes at least one E peptide; and a nucleic acid sequence that encodes at least one additional functional peptide; wherein the nucleic acids are operably linked so as to express a functional fusion protein.
14. The nucleic acid molecule of claim 13 , wherein the SP is selected from the group consisting of: aggrecan signal peptide; CD44 signal peptide; link protein signal peptide; TSG-6 signal peptide; and versican signal peptide.
15. The nucleic acid molecule of claim 13 , wherein the linker is selected from the group consisting of: Linker 1: GGSG (SEQ ID NO: 1); Linker 2: GGSGGGSG (SEQ ID NO: 2); Linker 3: GGSGGGSGGGSG (SEQ ID NO: 3); Linker 4: GGGGS (SEQ ID NO: 4); Linker 5: GGGGSGGGGS (SEQ ID NO: 5); Linker 6: GGGGSGGGGSGGGGS (SEQ ID NO: 6); Linker 7: GGSGGS (SEQ ID NO: 7); and Linker 8: VIGHPIDSE (SEQ ID NO: 8).
16. The nucleic acid molecule of claim 13 , comprising a nucleic acid sequence that encodes a cleavage site for a protease selected from the group consisting of: enterokinase (EK); Furin; Factor Xa; Matrix metalloproteinase (MMP); and Aggrecanase.
17. The nucleic acid molecule of claim 12 , wherein the GF is selected from the group consisting of: IGF-1; BMP2; BMP4; BMP7; FGF2; FGF18; GDF5; TGF-β1; and TGF-β3.
18. The nucleic acid molecule of claim 12 , wherein the fusion protein further comprises flanking amino acids to the HAB polypeptide, wherein the number of flanking amino acids is selected from the group consisting of: at least 60 amino acids, at least 50 amino acids, at least 40 amino acids, at least 30 amino acids, at least 20 amino acids, fewer than 20 amino acids; fewer than 15 amino acids; fewer than 10 amino acids; and fewer than 5 amino acids.
19. A composition comprising the nucleic acid molecule of claim 12 and a pharmaceutically-acceptable carrier.
20. A composition comprising the fusion protein of claim 1 and a pharmaceutically-acceptable carrier.
21. An expression vector encoding the fusion protein of claim 1 , wherein the expression vector is a plasmid or a virus.
22. The expression vector of claim 21 , wherein the expression vector is an adeno-associated virus plasmid (pAAV).
23. An isolated cell transformed, transfected, or transduced by a vector of claim 21 .
24. The cell of claim 23 , wherein the cell is a chondrocyte.
25. A non-human animal comprising the cell of claim 23 .
26. A method of producing a fusion protein comprising, expressing a nucleic acid molecule in the cell of claim 23 .
27. A method to upregulate glycosaminoglycan expression in at least one chondrocyte, comprising: expressing the nucleic acid molecule of claim 12 in at least one chondrocyte.
28. A method for treating a cartilage matrix protein-related condition in a subject, the method comprising administering to the subject a composition of claim 20 .
29. The method of claim 28 , wherein the GF protein is IGF-I.
30. The method of claim 28 , wherein the fusion protein is introduced to at least one chondrocyte in vivo.
31. The method of claim 28 , wherein the fusion protein is administered to the subject intra-articularly.
32. The method of claim 28 , wherein the cartilage matrix protein-related condition is selected from the group consisting of: joint stiffness; joint pain; intervertebral disc pain; degenerative disease; facet disease; traumatic cartilage injury; surgical cartilage injury; osteoarthritis; and rheumatoid arthritis.
33. The fusion protein of claim 1 , wherein the GF protein is IGF-1.
34. The fusion protein of claim 1 , wherein the fusion protein comprises an amino acid sequence that is at least 90 percent identical to SEQ ID NO: 72.
35. A fusion protein comprising IGF-1 and a polypeptide having an amino acid sequence at least 90 percent identical to amino acids 1-357 of SEQ ID NO: 44.
36. A fusion protein, comprising:
a hyaluronic acid-binding (HAB) polypeptide, wherein the HAB polypeptide is a polypeptide having at least 90 percent identity to a polypeptide of amino acids 1-178 of SEQ ID NO: 72;
a conserved region of a growth factor (GF) protein; and
at least one additional element selected from the group consisting of: aggrecan signal peptide; Linker 8: VIGHPIDSE (SEQ ID NO: 8); and the protease cleavage site of SEQ ID NO: 13,
wherein the fusion protein upregulates glycosaminoglycan (GAG) expression in chondrocytes.