Modified human interferon-beta polypeptides
The invention provides compositions and methods of identifying, modifying and producing modified target molecules, including therapeutic molecules by modification with non-natural amino acids. Certain aspects of the invention include methods of adding a chemical moiety to a target molecule, and the compositions resulting therefrom. Certain aspects of the invention also relate to kits for identifying, modifying and producing modified target molecules described herein.
1. A modified human interferon-β polypeptide having at least 90% identity to human interferon-β, and comprising the following amino acid alterations: methionine at position 1 to azidohomoalanine, serine at position 2 to glutamic acid, cysteine at position 17 to serine, methionine at position 36 to isoleucine, isoleucine at position 40 to phenylalanine, isoleucine at position 44 to leucine, methionine at position 62 to isoleucine, and methionine at position 117 to threonine.
2. The polypeptide of claim 1 , wherein said azidohomoalanine is conjugated to a polyalkylene glycol.
3. The polypeptide of claim 2 , wherein the polyalkylene glycol has a molecular weight of from about 1,000 Daltons to about 100 kDa.
4. The polypeptide of claim 2 , wherein the polyalkylene glycol has a molecular weight of from about 2 kDa to about 60 kDa.
5. The polypeptide of claim 2 , wherein the polyalkylene glycol has a molecular weight of from about 10 kDa to about 40 kDa.
6. The polypeptide of claim 2 , wherein the polyalkylene glycol is polyethylene glycol and has a molecular weight of about 40 kDa.
7. The polypeptide of claim 2 , wherein the polyalkylene glycol is unbranched.
8. The polypeptide of claim 2 , wherein the polyalkylene glycol is branched.
9. The polypeptide of claim 8 , wherein the branched polyalkylene glycol comprises two branches each with a molecular weight of about 18 kDa to about 22 kDa.
10. The polypeptide of claim 9 , wherein the branched polyalkylene glycol is a branched polyethylene glycol.
11. The polypeptide of claim 2 , wherein the polyalkylene glycol is conjugated to the polypeptide through a triazole linkage, wherein said triazole linkage is formed by a [3+2] cycloaddition reaction.
12. A composition comprising the polypeptide of claim 1 , and a pharmaceutically acceptable diluent or excipient.