RAGE protein derivatives
View Patent ↗The present invention is drawn to fusion proteins comprising a Receptor for Advanced Glycation Endproducts (RAGE) and an immunoglobulin element. The invention also encompasses methods of treating a condition characterized by activation of an inflammatory cytokine cascade comprising administering such fusion proteins. The invention is also drawn to nucleic acids encoding the fusion proteins, as well as vectors and cells comprising such nucleic acids.
1. A fusion protein comprising at least a first and a second polypeptide, wherein:
said first polypeptide consists of a fragment of a Receptor for Advanced Glycation End Product (RAGE) extracellular domain wherein said fragment consists of amino acid residue 1 to amino acid residue 305 of SEQ ID NO:2; and
said second polypeptide comprises an immunoglobulin element, wherein said immunoglobulin element comprises from about amino acid residue 101 to about amino acid residue 329 of SEQ ID NO:4.
2. A fusion protein comprising at least a first and a second polypeptide, wherein:
said first polypeptide consists of a fragment of a Receptor for Advanced Glycation End Product (RAGE) extracellular domain, said fragment of a RAGE extracellular domain is a human RAGE extracellular domain and comprises from about amino acid residue 19 to about amino acid residue 305 of SEQ ID NO:2; and
said second polypeptide comprises an immunoglobulin element, wherein said immunoglobulin element comprises from about amino acid residue 101 to about amino acid residue 329 of SEQ ID NO:4.
3. A fusion protein comprising the amino acid sequence depicted in SEQ ID NO:6.
4. The fusion protein of claim 1 , wherein said immunoglobulin element comprises an Fc domain.
5. The fusion protein of claim 1 , wherein said immunoglobulin element comprises an immunoglobulin heavy chain.
6. The fusion protein of claim 1 , wherein said immunoglobulin element comprises a C H 1 domain and a Fc domain.
7. A pharmaceutical composition comprising the fusion protein of claim 1 in a pharmaceutically-acceptable excipient.
8. The pharmaceutical composition of claim 7 further comprising an antibody or antigen-binding fragment thereof that binds to an HMGB1 polypeptide or an antigenic fragment of said HMGB1 polypeptide.
9. A nucleic acid encoding a fusion protein, wherein said fusion protein comprises at least a first and a second polypeptide, wherein:
said first polypeptide consists of a fragment of a Receptor for Advanced Glycation End Product (RAGE) extracellular domain, wherein said fragment consists of amino acid residue 1 to amino acid residue 305 of SEQ ID NO:2; and
said second polypeptide comprises an immunoglobulin element, wherein said immunoglobulin element comprises from about amino acid residue 101 to about amino acid residue 329 of SEQ ID NO:4.
10. An expression vector comprising the nucleic acid of claim 9 .
11. A cell transfected with the expression vector of claim 10 .
12. A method of producing a fusion protein comprising culturing the cell of claim 11 in a cell culture medium suitable for expression of the fusion protein and expressing said fusion protein.
13. A nucleic acid encoding a fusion protein, wherein said fusion protein comprises at least a first and a second polypeptide, wherein:
said first polypeptide consists of a fragment of a Receptor for Advanced Glycation End Product (RAGE) extracellular domain, said fragment of a RAGE extracellular domain is a human RAGE extracellular domain and comprises from about amino acid residue 19 to about amino acid residue 305 of SEQ ID NO:2; and
said second polypeptide comprises an immunogloublin element, wherein said immunoglobulin element comprises from about amino acid residue 101 to about amino acid residue 329 of SEQ ID NO:4.
14. An expression vector comprising the nucleic acid of claim 13 .
15. A cell transfected with the expression vector of claim 14 .
16. A method of producing a fusion protein, comprising culturing the cell of claim 15 in a cell culture medium suitable for expression of the fusion protein and expressing said fusion protein.
17. A nucleic acid encoding a fusion protein, wherein said fusion protein comprises the amino acid sequence depicted in SEQ ID NO:6.
18. An expression vector comprising the nucleic acid of claim 17 .
19. A cell transfected with the expression vector of claim 18 .
20. A method of producing a fusion protein, comprising culturing the cell of claim 19 in a cell culture medium suitable for expression of the fusion protein and expressing said fusion protein.
21. The fusion protein of claim 2 wherein said immunoglobulin element comprises an Fc domain.
22. The fusion protein of claim 2 , wherein said immunoglobulin element comprises an immunoglobulin heavy chain.
23. The fusion protein of claim 2 wherein said immunoglobulin element comprises a C H 1 domain and a Fe domain.
24. A pharmaceutical composition comprising the fusion protein of claim 2 in a pharmaceutically-acceptable excipient.