IP Library Patent Application 11771400
Patent Application
App. No. 11/771,400

Method of Producing Factor VIII Proteins by Recombinant Methods

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/771,400
Abstract

Provided herein are methods and compositions for producing Factor VIII proteins. Such methods include introducing into a cell a nucleic acid molecule encoding a Factor VIII protein operably linked to a promoter, wherein the promoter is characterized by the ability to produce commercially viable Factor VIII protein; and incubating the cell under conditions for producing commercially viable Factor VIII protein. Also provided are nucleic acid molecules which encode a Factor VIII protein operably linked to a Chinese hamster elongation factor 1-α (CHEF1) promoter, which may be used in the methods provided herein.

Claims (43)

1 . A method for producing a recombinant Factor VIII protein, comprising the steps of:

introducing into a cell a nucleic acid molecule encoding a Factor VIII protein operably linked to a promoter, wherein the promoter is characterized by the ability to produce commercially viable Factor VIII protein; and

incubating the cell under conditions for producing Factor VIII protein.

2 . The method of claim 1 , wherein the cell is a mammalian cell.

3 . The method of claim 2 , wherein the mammalian cell is selected from the group consisting of a COS-1, CHO, and HEK 293 cell.

4 . The method of claim 1 , wherein the nucleic acid molecule comprises a cDNA which encodes the Factor VIII protein.

5 . The method of claim 1 , wherein the nucleic acid molecule is operably linked to a Chinese hamster elongation factor 1-α (CHEF1) promoter.

6 . The method of claim 1 , wherein the Factor VIII protein comprises a deletion of the B-domain starting at Arg 740 when the protein is aligned with the wild-type Factor VIII, followed by an addition of an amino acid spacer containing at least one N-linked glycosylation site, wherein the amino acid spacer containing the at least one N-linked glycosylation site facilitates the secretion or expression of the B-domain-deletion Factor VIII protein.

7 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 750 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 226 amino acid spacer containing 6 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

8 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 769 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 29 amino acid spacer containing one N-linked glycosylation site, thereby partially replacing the B domain of the modified Factor VIII protein.

9 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 794 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 55 amino acid spacer containing 2 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

10 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 857 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 117 amino acid spacer containing 3 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

11 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 903 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 163 amino acid spacer containing 4 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

12 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 946 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 206 amino acid spacer containing 5 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

13 . The method of claim 6 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 1009 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 269 amino acid spacer containing 8 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

14 . The method of claim 1 wherein the Factor VIII protein comprises a heterologous sequence.

15 . A method for identifying a cell expressing commercially viable Factor VIII protein, comprising:

a) introducing into cells a nucleic acid molecule encoding a Factor VIII protein operably linked to a promoter, wherein the promoter is characterized by the ability to produce commercially viable Factor VIII protein;

b) incubating the cells under conditions for producing Factor VIII protein;

c) selecting clones expressing high levels of FVIII relative to the other clones;

d) recloning the cells selected in step c); and

e) identifying at least one subclone expressing a higher level of FVIII relative to those selected in step c).

16 . A nucleic acid molecule encoding a Factor VIII protein operably linked to a Chinese hamster elongation factor 1-α (CHEF1) promoter.

17 . The nucleic acid molecule of claim 16 , wherein the nucleic acid molecule comprises a cDNA which encodes the Factor VIII protein.

18 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises a deletion of the B-domain starting at Arg 740 when the protein is aligned with the wild-type Factor VIII, followed by an addition of an amino acid spacer containing at least one N-linked glycosylation site, wherein the amino acid spacer containing the at least one N-linked glycosylation site facilitates the secretion or expression of the B-domain-deletion Factor VIII protein.

19 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 750 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 226 amino acid spacer containing 6 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

20 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 769 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 29 amino acid spacer containing one N-linked glycosylation site, thereby partially replacing the B domain of the modified Factor VIII protein.

21 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 794 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 55 amino acid spacer containing 2 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

22 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 857 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 117 amino acid spacer containing 3 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

23 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 903 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 163 amino acid spacer containing 4 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

24 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 946 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 206 amino acid spacer containing 5 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

25 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises an amino acid sequence inserted at position 1009 when the protein is aligned with the wild-type Factor VIII, the inserted amino acid sequence consisting of a 269 amino acid spacer containing 8 N-linked glycosylation sites, thereby partially replacing the B domain of the modified Factor VIII protein.

26 . The nucleic acid molecule of claim 16 , which encodes a heterologous protein.

27 . The method of claim 15 further comprising:

f) recloning the at least one subclone identified in step e); and

g) identifying at least one subclone expressing a higher level of FVIII relative to the at least one subclone selected in step e).

28 . The method of claim 1 , wherein the Factor VIII protein comprises a deletion of the B-domain starting at Arg 740 when the protein is aligned with the wild-type Factor VIII.

29 . The method of claim 1 , wherein the Factor VIII protein comprises a substitution of phenylalanine at position 309 to serine when the protein is aligned with the wild-type Factor VIII.

30 . The method of claim 28 , wherein the Factor VIII protein comprises a substitution of phenylalanine at position 309 to serine when the protein is aligned with the wild-type Factor VIII.

31 . The nucleic acid molecule of claim 16 , wherein the Factor VIII protein comprises a deletion of the B-domain starting at Arg 740 when the protein is aligned with the wild-type Factor VIII.

32 . The nucleic acid molecule of claim 16 wherein the Factor VIII protein comprises a substitution of phenylalanine at position 309 to serine when the protein is aligned with the wild-type Factor VIII.

33 . The nucleic acid molecule of claim 31 wherein the Factor VIII protein comprises a substitution of phenylalanine at position 309 to serine when the protein is aligned with the wild-type Factor VIII.

34 . The method of claim 1 wherein the Factor VIII protein is produced at a level selected from the group consisting of at least about 20 IU/mL, at least about 30 IU/mL, at least about 40 IU/mL, at least about 50 IU/mL, at least about 60 IU/mL, at least about 70 IU/mL, at least about 80 IU/mL, at least about 90 IU/mL, at least about 100 IU/mL, at least about 110 IU/mL, at least about 120 IU/mL, at least about 130 IU/mL, at least about 140 IU/mL, at least about 150 IU/mL, at least about 160 IU/mL, at least about 170 IU/mL, at least about 180 IU/mL, at least about 190 IU/mL, at least about 200 IU/mL, and at least about 210 IU/mL.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2011
From: DROHAN, WILLIAM
To: INSPIRATION BIOPHARMACEUTICALS
Reel/Frame 026211/0108 →
CONFIRMATORY LICENSE Recorded Jan 27, 2010
From: UNIVERISTY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023856/0301 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2009
From: GRIFFITH, MICHAEL
To: INSPIRATION BIOPHARMACEUTICALS
Reel/Frame 023655/0178 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2007
From: KAUFMAN, RANDAL J; PIPE, STEVEN W
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 020278/0471 →