IP Library Granted Patent US 9,266,931
Granted Patent B2
US 9,266,931 · App. 14/100,390 · Granted Feb 23, 2016

Modified vitamin K-dependent polypeptides

Inventor: Gary L. Nelsestuen (St. Paul, MN)
Assignee: Regents of the University of Minnesota
C07K14/47A61K38/16A61K38/4846A61K45/00C07K14/00C07K14/745C12N9/647
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Quick Facts
Patent No.
US 9,266,931
App. No.
14/100,390
Granted
Feb 23, 2016
Kind
B2
Abstract

The invention provides vitamin K-dependent polypeptides with enhanced membrane binding affinity. These polypeptides can be used to modulate clot formation in mammals. Methods of modulating clot formation in mammals are also described.

Claims (19)

1. An isolated nucleic acid molecule comprising a nucleic acid sequence encoding a vitamin K-dependent polypeptide that comprises a modified gamma-carboxyglutamic acid (GLA) domain that enhances membrane binding affinity of said vitamin K-dependent polypeptide relative to a corresponding native vitamin K-dependent polypeptide, wherein said modified GLA domain comprises the sequence of SEQ ID NO:3 or SEQ ID NO:4 with one to five amino acid substitutions, wherein the proline residue at position 10 of SEQ ID NO:3 or SEQ ID NO:4 is substituted with a glutamine, aspartic acid, or glutamic acid residue in the modified GLA domain.

2. The isolated nucleic acid molecule of claim 1 , wherein the proline residue at position 10 is substituted with a glutamine residue in the modified GLA domain.

3. The isolated nucleic acid molecule of claim 1 , wherein the modified GLA domain comprises a substitution at position 28 of SEQ ID NO:3 or SEQ ID NO:4.

4. The isolated nucleic acid molecule of claim 3 , wherein a phenylalanine residue is substituted at position 28 in the modified GLA domain.

5. The isolated nucleic acid molecule of claim 4 , wherein the proline residue at position 10 is substituted with a glutamine residue in the modified GLA domain.

6. The isolated nucleic acid molecule of claim 1 , wherein the modified GLA domain comprises a substitution at position 32 of SEQ ID NO:3 or SEQ ID NO:4.

7. The isolated nucleic acid molecule of claim 6 , wherein a glutamic acid residue is substituted at position 32 in the modified GLA domain.

8. The isolated nucleic acid molecule of claim 7 , wherein the proline residue at position 10 is substituted with a glutamine residue in the modified GLA domain.

9. The isolated nucleic acid molecule of claim 6 , wherein an aspartic acid residue is substituted at position 32 in the modified GLA domain.

10. The isolated nucleic acid molecule of claim 9 , wherein the proline residue at position 10 is substituted with a glutamine residue in the modified GLA domain.

11. The isolated nucleic acid molecule of claim 1 , wherein the modified GLA domain comprises a substitution at position 11 of SEQ ID NO:3 or SEQ ID NO:4.

12. The isolated nucleic acid molecule of claim 11 , wherein the proline residue at position 10 is substituted with a glutamine residue in the modified GLA domain.

13. An expression vector comprising the isolated nucleic acid molecule of claim 1 .

14. An isolated host cell comprising the isolated nucleic acid molecule of claim 1 .

15. A method for producing a vitamin K-dependent polypeptide having clotting activity, the method comprising: (a) providing a culture of the host cell of claim 14 in a culture medium, (b) maintaining the culture under conditions that permit expression of the vitamin K-dependent polypeptide, and (c) isolating the mutant vitamin K-dependent polypeptide from the culture medium.

16. An isolated nucleic acid molecule comprising a nucleic acid sequence encoding a vitamin K-dependent polypeptide that comprises a modified GLA domain that enhances membrane binding affinity of the vitamin K-dependent polypeptide relative to a corresponding native vitamin K-dependent polypeptide, wherein said modified GLA domain comprises the amino acid sequence of SEQ ID NO:3 or SEQ ID NO:4 with two amino acid substitutions, wherein a glutamine residue is substituted at amino acid position 10 of SEQ ID NO:3 or SEQ ID NO:4 in the modified GLA domain, and wherein a glutamic acid residue is substituted at position 32 of SEQ ID NO:3 or SEQ ID NO:4 in the modified GLA domain.

17. An expression vector comprising the isolated nucleic acid molecule of claim 16 .

18. An isolated host cell comprising the isolated nucleic acid molecule of claim 16 .

19. A method for producing a vitamin K-dependent polypeptide having clotting activity, the method comprising: (a) providing a culture of the host cell of claim 18 in a culture medium, (b) maintaining the culture under conditions that permit expression of the vitamin K-dependent polypeptide, and (c) isolating the mutant vitamin K-dependent polypeptide from the culture medium.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 28, 2014
From: REGENTS OF THE UNIVERSITY OF MINNESOTA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032128/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2014
From: NELSESTUEN, GARY L.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 031982/0848 →
Continuity (8)
Continuation 13787089 · Mar 6, 2013
Continuation 12770255 · Apr 29, 2010
Division 11555842 · Nov 2, 2006
Continuation 10298330 · Nov 18, 2002
Continuation In Part 09497591 · Feb 3, 2000
Continuation In Part 09302239 · Apr 29, 1999
Continuation In Part 08955636 · Oct 23, 1997
Related Publication 20140113330A1 · Apr 24, 2014