Chaperonin 10 variants
The invention relates generally to chaperonin 10 N-terminal variants. More specifically, the invention relates to chaperonin 10 N-terminal variants with enhanced immunomodulatory capacity and/or enhanced binding affinity for pathogen-associated molecular patterns (PAMPs) and/or damage-associated molecular patterns (DAMPs).
1. An isolated chaperonin 10 (Cpn10) variant polypeptide derived from human Cpn10 sharing at least 90% sequence identity with a wild-type human Cpn10 polypeptide and comprising an N-terminus extended by two to five additional amino acid residues compared to said wild-type polypeptide, wherein the polypeptide has increased binding affinity for a pathogen-associated molecular pattern (PAMP) compared to the binding affinity of Ala-Cpn10 (SEQ ID NO: 3) for said PAMP, wherein the isolated Cpn10 polypeptide possesses a conserved core antiparallel β-barrel flanked by a β-hairpin roof loop region and a mobile loop region.
2. The isolated human Cpn10 variant polypeptide of claim 1 , wherein the N-terminus of said human variant polypeptide commences with a methionine residue.
3. The isolated human Cpn10 variant polypeptide of claim 2 , wherein said methionine residue precedes an amino acid residue selected from the group consisting of arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, tyrosine, and valine.
4. An isolated chaperonin 10 (Cpn10) variant polypeptide sharing at least 90% sequence identity with a wild-type Cpn10 polypeptide and comprising an N-terminus extended by at least two additional amino acid residues compared to said wild-type polypeptide, wherein the polypeptide has increased binding affinity for a pathogen-associated molecular pattern (PAMP) compared to the binding affinity of Ala-Cpn10 (SEQ ID NO: 3) for said PAMP, wherein the N-terminus of said variant polypeptide commences with a methionine residue, and wherein said methionine residue precedes an amino acid residue selected from the group consisting of arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, tyrosine, and valine, wherein said polypeptide comprises the amino acid sequence as set forth in SEQ ID NOs: 29.
5. The isolated Cpn10 variant polypeptide of claim 1 , wherein said polypeptide comprises the amino acid sequence as set forth in any one of SEQ ID NOs: 52, 55, 60, 81, 84, 87, or 96.
6. An isolated human chaperonin 10 (Cpn10) variant polypeptide sharing at least 80% sequence identity with a wild-type human Cpn10 polypeptide and comprising an N-terminus extended by one additional amino acid residue compared to said wild-type human polypeptide, wherein said additional amino acid residue is a serine or proline residue, and wherein said variant polypeptide has increased immunomodulatory function compared to human Ala-Cpn10, wherein the isolated Cpn10 polypeptide possesses a conserved core antiparallel β-barrel flanked by a β-hairpin roof loop region and a mobile loop region.
7. An isolated human Cpn10 variant polypeptide sharing at least 80% sequence identity with a wild-type human Cpn10 polypeptide and comprising an N-terminus extended by one additional amino acid residue compared to said wild-type human polypeptide, wherein said additional amino acid residue is a serine or proline residue, and wherein said variant polypeptide has increased immunomodulatory function compared to human Ala-Cpn10, wherein the isolated Cpn10 polypeptide possesses a core antiparallel β-barrel flanked by a β-hairpin roof loop region and a mobile loop region, wherein said polypeptide comprises the amino acid sequence as set forth in SEQ ID NO: 21 or 35.
8. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutically acceptable excipient, diluent or carrier.
9. A method for treating an inflammatory disease in a subject wherein the inflammatory disease is selected from the group consisting of rheumatoid arthritis and psoriasis, said method comprising administering to the subject a therapeutically effective amount of the polypeptide of claim 1 .
10. The isolated variant Cpn10 polypeptide of claim 1 wherein the N-terminus is extended by two to three amino acids.
11. The isolated variant Cpn10 polypeptide of claim 1 wherein the polypeptide shares at least 95% sequence identity with a wild-type human Cpn10 polypeptide.
12. The isolated variant Cpn10 polypeptide of claim 10 wherein the N-terminus of the polypeptide begins with a methionine residue.
13. The isolated variant Cpn10 polypeptide of claim 12 wherein said methionine residue precedes an amino acid residue selected from the group consisting of arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, tyrosine, and valine.
14. The isolated variant Cpn10 polypeptide of claim 13 wherein said methionine residue precedes an amino acid residue selected from the group consisting of isoleucine, leucine, lysine, phenylalanine, tryptophan, tyrosine, and valine.
15. The isolated variant Cpn10 polypeptide of claim 10 wherein the two to three amino acids extending the amino-terminus are selected from the group consisting of lysine, arginine, and histidine.
16. The isolated variant Cpn10 polypeptide of claim 10 wherein the two to three amino acids extending the amino-terminus are selected from the group consisting of aspartic acid and glutamic acid.