IP Library Granted Patent US 7,964,184
Granted Patent B2
US 7,964,184 · App. 11/929,478 · Granted Jun 21, 2011

Cysteine variants of interferon-gamma

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Quick Facts
Patent No.
US 7,964,184
App. No.
11/929,478
Granted
Jun 21, 2011
Kind
B2
Abstract

The growth hormone supergene family comprises greater than 20 structurally related cytokines and growth factors. A general method is provided for creating site-specific, biologically active conjugates of these proteins. The method involves adding cysteine residues to non-essential regions of the proteins or substituting cysteine residues for non-essential amino acids in the proteins using site-directed mutagenesis and then covalently coupling a cysteine-reactive polymer or other type of cysteine-reactive moiety to the proteins via the added cysteine residue. Disclosed herein are preferred sites for adding cysteine residues or introducing cysteine substitutions into the proteins, and the proteins and protein derivatives produced thereby.

Claims (12)

1. A recombinant cysteine variant of gamma interferon, wherein said variant is selected from the group consisting of the mature gamma interferon protein with a single cysteine residue added proximal to the first amino acid, and the mature gamma interferon protein with a single cysteine residue added distal to the last amino acid, wherein said cysteine variant has gamma interferon biological activity in vitro comparable to gamma interferon wild-type activity in vitro.

2. The recombinant cysteine variant of claim 1 , wherein a single cysteine residue is added proximal to the first amino acid of the mature gamma interferon protein.

3. The recombinant cysteine variant of claim 1 , wherein a single cysteine residue is added distal to the last amino acid of the gamma interferon protein.

4. The recombinant cysteine variant of claim 1 , wherein said cysteine variant is modified with a cysteine-reactive moiety.

5. The recombinant cysteine variant of claim 1 , wherein said variant is modified with a cysteine-reactive polyethylene glycol.

6. The recombinant cysteine variant of claim 1 , wherein said variant is modified with polyethylene glycol.

7. The recombinant cysteine variant of claim 2 , wherein said cysteine variant is modified with a cysteine-reactive moiety.

8. The recombinant cysteine variant of claim 2 , wherein said variant is modified with a cysteine-reactive polyethylene glycol.

9. The recombinant cysteine variant of claim 2 , wherein said variant is modified with polyethylene glycol.

10. The recombinant cysteine variant of claim 3 , wherein said cysteine variant is modified with a cysteine-reactive moiety.

11. The recombinant cysteine variant of claim 3 , wherein said variant is modified with a cysteine-reactive polyethylene glycol.

12. The recombinant cysteine variant of claim 3 , wherein said variant is modified with polyethylene glycol.

Assignments (1)
CONFIRMATORY LICENSE Recorded Feb 21, 2014
From: BOLDER BIOTECHNOLOGY, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032319/0050 →
Continuity (5)
Continuation 10773530 · Feb 5, 2004
Continuation 10400377 · Mar 26, 2003
Division 09462941
Provisional Application 60052516 · Jul 14, 1997
Related Publication 20080219950A1 · Sep 11, 2008