IP Library Granted Patent US 7,220,569
Granted Patent B2
US 7,220,569 · App. 10/407,123 · Granted May 22, 2007

Nucleic acids encoding factor X analogues having a modified protease cleavage site

Assignee: Baxter Aktiengesellschaft
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Quick Facts
Patent No.
US 7,220,569
App. No.
10/407,123
Granted
May 22, 2007
Kind
B2
Abstract

Nucleic acids encoding factor X analogues are provided that have a modification in the region of the natural Factor Xa activation cleavage site. The modification results in a processing site for a protease not naturally cleaving in this region of the Factor X sequence.

Claims (22)

1. A recombinant nucleic acid comprising a nucleic acid segment that encodes a Factor X analogue, wherein said analogue is a Factor X that has one or more amino acid modifications in a region between Gly228 and Arg234 of SEQ ID NO:27 that results in a sequence Gly228-R6-R5-R4-R3-R2-Arg234-R1 and wherein

a) R1 is an amino acid selected from the group consisting of Ile, Val, Ser, Thr and Ala;

b) R2 is an amino acid selected from the group consisting of Pro, Gly, Lys and Arg;

c) R3 is an amino acid selected from the group consisting of Phe, Lys, Met, Gln, Glu, Ser, Val, Arg and Pro;

d) R4 is an amino acid selected from the group consisting of Asp, Ile, Ser, Met, Pro, Thr, Arg and Lys;

e) R5 is an amino acid selected from the group consisting of Asn, Lys, Ser, Glu, Ala, Gln, His and Arg; and

f) R6 is an amino acid selected from the group consisting of Asp, Phe, Thr, Arg, Leu and Ser.

2. The recombinant nucleic acid of claim 1 , wherein the Factor X analogue encoded by the recombinant nucleic acid has an exchange of Ile235 of SEQ ID NO:27.

3. The recombinant nucleic acid of claim 1 , wherein the modification in the Factor X analogue encoded by the recombinant nucleic acid results in a processing site for a protease selected from the group consisting of an endoprotease, a serine protease, and a derivative of these proteases.

4. The recombinant nucleic acid of claim 3 , wherein the processing site of the Factor X analogue encoded by the recombinant nucleic acid results in a processing site for an endoprotease selected from the group consisting of kexin/Kex2, furin/PACE, PC1/PC3, PC2, PC4, PACE 4, and LPC/PC7, or a serine protease selected from the group consisting of Factor IIa, Factor XIIa, Factor XIa, Factor Xa and kallikrein.

5. The recombinant nucleic acid of claim 1 , wherein the Factor X analogue encoded by the recombinant nucleic acid has a further modification in a C-terminal region, the further modification occurring at Lys370 and/or within a segment extending from Arg469 to Ser476 of SEQ ID NO:27.

6. The recombinant nucleic acid of claim 5 , wherein the further modification of the Factor X analogue encoded by the recombinant nucleic acid is a substitution at Arg469 or Gly470 of SEQ ID NO:27.

7. The recombinant nucleic acid of claim 5 , wherein the further modification of the Factor X analogue encoded by the recombinant nucleic acid is selected from a mutation, a deletion and an insertion between amino acid positions Arg469 and Ser476 of SEQ ID NO:27.

8. The recombinant nucleic acid of claim 5 , wherein the further modification of the Factor X analogue encoded by the recombinant nucleic acid prevents the β-peptide extending from Gly470 to Lys488 of SEQ ID NO:27 from being cleaved off.

9. The recombinant nucleic acid of claim 1 , wherein the Factor X analogue encoded by the recombinant nucleic acid terminates at Arg469.

10. The recombinant nucleic acid of claim 1 , wherein the modification in the Factor X analogue encoded by the recombinant nucleic acid allows for an activation of the Factor X analogue to native Factor Xa or Factor Xa analogue in vitro.

11. The recombinant nucleic acid of claim 1 , wherein the modification in the Factor X analogue encoded by the recombinant nucleic acid allows for an activation of the Factor X analogue to native Factor Xa or Factor Xa analogue in vivo.

12. The recombinant nucleic acid of claim 1 , wherein the modification in the Factor X analogue encoded by the recombinant nucleic acid allows for activation by a serine protease.

13. The recombinant nucleic acid of claim 1 , wherein the modification in the Factor X analogue encoded by the recombinant nucleic acid allows for activation by a serine protease selected from the group consisting of Factor XIIa, Factor XIa, Factor IIa, Factor Xa and kallikrein.

14. The recombinant nucleic acid of claim 1 , wherein the Factor X analogue encoded by the recombinant nucleic acid has an intact β-peptide, the β-peptide extending from Gly470 to Lys488 of SEQ ID NO:27.

15. A vector comprising the recombinant nucleic acid of claim 1 .

16. An isolated cell comprising the vector of claim 15 .

Assignments (7)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR NAME, EXECUTION DATE, AND ADDRESS OF ASSIGNEE BAXALTA GMBH PREVIOUSLY RECORDED ON REEL 036366 FRAME 0301. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 31, 2016
From: BAXALTA INNOVATIONS GMBH
To: BAXALTA INCORPORATED; BAXALTA GMBH
Reel/Frame 038324/0691 →
CORRECTIVE ASSIGNMENT TO CORRECT THE EXECUTION DATE AND NAME OF ASSIGNEE PREVIOUSLY RECORDED ON REEL 036286 FRAME 0860. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Jan 30, 2016
From: BAXTER AKTIENGESELLSCHAFT
To: BAXTER EASTERN EUROPE VERTRIEBS GMBH
Reel/Frame 037660/0432 →
CHANGE OF NAME Recorded Jan 30, 2016
From: BAXTER TRADING GMBH
To: BAXTER INNOVATIONS GMBH
Reel/Frame 037660/0466 →
CHANGE OF NAME Recorded Jan 30, 2016
From: BAXTER EASTERN EUROPE VERTRIEBS GMBH
To: BAXTER TRADING GMBH
Reel/Frame 037660/0472 →
CHANGE OF NAME Recorded Jan 30, 2016
From: BAXTER INNOVATIONS GMBH
To: BAXALTA INNOVATIONS GMBH
Reel/Frame 037660/0478 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2015
From: BAXTER INNOVATIONS GMBH
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 036366/0301 →
CHANGE OF NAME Recorded Aug 6, 2015
From: BAXTER AKTIENGESELLSCHAFT
To: BAXTER INNOVATIONS GMBH
Reel/Frame 036286/0860 →
Priority Claims (1)
AT A 335/97 · Feb 27, 1997 · national
Continuity (2)
Division 0936779100
Related Publication 20030181381A1 · Sep 25, 2003