IP Library Granted Patent US 8,114,633
Granted Patent B2
US 8,114,633 · App. 12/341,098 · Granted Feb 14, 2012

Methods for differentiating plasma-derived protein from recombinant protein in a sample

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Quick Facts
Patent No.
US 8,114,633
App. No.
12/341,098
Granted
Feb 14, 2012
Kind
B2
Abstract

The present invention relates, in general, to methods for detecting and quantitating plasma-derived protein and recombinant protein in a sample based on the difference in protein glycosylation, when the plasma protein and the recombinant protein are essentially the same protein.

Claims (19)

1. A method to quantitate the amount of recombinant protein (rP) in a sample containing both plasma-derived protein (pdP) and recombinant protein (rP) from an individual, wherein the plasma-derived protein and recombinant protein are the same protein having different glycosylation patterns, said different glycosylation patterns giving rise to different degrees of binding to lectin, wherein the combined amount of plasma-derived protein and recombinant protein is equal to total protein (pdP+rP=tP), said total protein being pre-determined, said method comprising the steps of:

(a) contacting the sample from the individual with a lectin composition and detecting differential protein binding of the plasma-derived protein and recombinant protein to the lectin composition,

(b) calculating a difference between lectin binding to the total protein in said sample from said individual and expected lectin binding to a total protein in a reference sample of equal volume having an amount of the plasma-derived protein equal to the total protein (tP) in the sample from the individual, wherein the difference in lectin binding correlates to the amount of recombinant protein in the sample from the individual.

2. The method of claim 1 wherein the lectin is labeled with a detectable label.

3. The method of claim 2 wherein the label is biotin.

4. The method of claim 1 wherein the lectin is Sambucus Nigra agglutinin (SNA).

5. The method of claim 1 wherein the sample is serum.

6. The method of claim 1 wherein the protein is a blood clotting factor.

7. The method of claim 1 wherein the blood clotting factor is selected from the group consisting of von Willebrand factor (vWF), Factor VIII (FVIII), Factor VII (FVII), and Factor IX (FIX).

8. The method of claim 1 wherein the recombinant protein is produced by Chinese hamster ovary (CHO) cells.

9. The method of claim 1 wherein the recombinant protein is produced in insect cells.

10. The method of claim 1 wherein the plasma-derived protein comprises ÿ,6-neuraminic acid and the recombinant protein lacks α,2,6-neuraminic acid.

11. The method of claim 1 wherein the sample is contacted with a binding agent specific for the protein prior to contacting with the lectin composition.

12. The method of claim 11 wherein the protein binding agent is bound on a solid support.

13. The method of claim 11 wherein the protein binding agent is in solution.

14. The method of claim 11 wherein the protein binding agent is an antibody.

15. The method of claim 14 wherein the antibody is a monoclonal antibody.

16. The method of claim 1 further comprising, after contacting with the binding agent, contacting the sample with a periodate solution.

17. The method of claim 1 wherein the recombinant protein is a fragment, variant or analog of the plasma-derived protein.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2015
From: BAXTER HEALTHCARE SA
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 036367/0652 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2015
From: BAXTER INTERNATIONAL INC.
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 036375/0542 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2009
From: WEBER, ALFRED; TURECEK, PETER; SCHWARZ, HANS-PETER
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE S.A.
Reel/Frame 022859/0760 →