INDIRECTLY LABELLED ASSAY CONJUGATES AND METHODS OF PREPARING AND USING SAME

• US 20090068635A1
• Filed: 09/06/2007
• Published: 03/12/2009
• Est. Priority Date: 09/06/2007
• Status: Abandoned Application

• Current Assignee: Abbott Laboratories Incorporated
• Original Assignee: Abbott Laboratories Incorporated
• Inventors: Gutierrez, Robin A., Desai, Suresh M., Muerhoff, Anthony S., Dawson, George J., Leary, Thomas P.
• Application Number:
  US11/851,050
• Publication Number:
  US 20090068635A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: C07K 1/13 Labelling of peptides
• CPC Class Codes: G01N 2333/186 Hepatitis C; Hepatitis NANB
• CPC Class Codes: G01N 33/532 Production of labelled immunochemicals
• CPC Class Codes: G01N 33/56983 Viruses

Abstract

Indirectly labelled assay conjugates prepared by a method that includes the step of submitting the binding member comprised by the conjugate to denaturing conditions prior to labelling the binding member. The indirectly labelled assay conjugates demonstrate an increased sensitivity when employed in diagnostic assays compared to assay conjugates prepared by methods that do not include a step of submitting the binding member to denaturing conditions prior to labelling. Processes for the preparation of the indirectly labelled assay conjugates, methods of detecting an analyte comprising the use of the indirectly labelled assay conjugate and kits comprising the indirectly labelled conjugates are also provided.

Claims

1. A process for preparing a protein conjugate, said process comprising the steps of:

(a) subjecting a protein to denaturing conditions to provide a treated protein; and

(b) conjugating said treated protein to a label moiety to provide said indirectly labelled protein conjugate, said label moiety comprising a carrier molecule coupled to one or more detectable labels.

2. The process according to claim 17 wherein said denaturing conditions comprise treatment of said protein with a protein denaturing agent.

3. The process according to claim 2, further comprising submitting the treated protein to a purification or dilution step to reduce the concentration of the protein denaturing agent prior to step (b).

4. The process according to claim 2, wherein said protein denaturing agent is urea.

5. The process according to claim 4, wherein said urea is at a concentration between about 5M and about 9M.

6. The process according to claim 1, further comprising submitting said treated protein to a reduction step prior to step (b).

7. The process according to claim 6, wherein said reduction step comprises treatment with dithiothreitol (DTT), dithioerythritol, mercaptoethanol, cysteine, or tris(2-carboxyethyl)phosphine (TCEP).

8. The process according to claim 1, wherein said carrier moiety comprises at least one detectable label.

9. The process according to claim 17 wherein said carrier molecule is a protein molecule.

10. The process according to claim 9, wherein said protein molecule is bovine serum albumin, thyroglobulin, haemocyanin, myosin, apoferritin, ovalbumin or α

₂-macroglobulin.

11. The process according to claim 9, wherein said protein molecule is bovine serum albumin.

12. The process according to claim 1, wherein said protein comprises a viral antigen.

13. The process according to claim 1 wherein said protein comprises a hepatitis C viral antigen.

14. The process according to claim 13, wherein said hepatitis C viral antigen comprises a NS3 antigen.

15. The process according to claim 1, wherein said detectable label is a chemiluminescent label.

16. The process according to claim 15, wherein said chemiluminescent label is an acridinium ester.

17. A protein conjugate prepared by the process of claim 1.

18. The protein conjugate according to claim 17, wherein said carrier molecule is a protein molecule.

19. The protein conjugate according to claim 18, wherein said protein molecule is bovine serum albumin, thyroglobulin, haemocyanin, myosin, apoferritin, ovalbumin or α

₂-macroglobulin.

20. The protein conjugate according to claim 18, wherein said protein molecule is bovine serum albumin.

21. The protein conjugate according to claim 17, wherein said protein comprises a viral antigen.

22. The protein conjugate according to claim 17, wherein said protein comprises a hepatitis C viral antigen.

23. The protein conjugate according to claim 22, wherein said hepatitis C viral antigen comprises a NS3 antigen.

24. The protein conjugate according to claim 17, wherein said detectable label is a chemiluminescent label.

25. The protein conjugate according to claim 24, wherein said chemiluminescent label is an acridinium ester.

26. A method of detecting a target analyte in a sample comprising utilizing the protein conjugate of claim 17, wherein said protein specifically binds to said target analyte.

27. The method according to claim 26, comprising the steps of:

contacting said sample with the protein conjugate under conditions that allow the binding of the assay conjugate to the target analyte to form a complex, and detecting the complex as an indication of the presence of target analyte in the sample.

28. The method according to claim 27, comprising the steps of:

contacting an immobilized capture agent which specifically binds to the target analyte with said sample under conditions that allow the binding of the target analyte to the capture agent to form a first complex;

contacting said first complex with the assay conjugate under conditions that allow binding of the assay conjugate to the target analyte such that a second complex comprising the binding member, target analyte and assay conjugate is formed, and detecting the second complex as an indication of the presence of target analyte in the sample.

29. The method according to claim 26, wherein said protein comprises a viral antigen and said target analyte is a viral antibody.

30. The method according to claim 29, wherein said protein comprises a hepatitis C viral antigen and said target analyte is a hepatitis C virus antibody.

31. The method according to claim 30, wherein said hepatitis C viral antigen comprises a NS3 antigen and said hepatitis C virus antibody is an antibody against NS3.

32. A kit comprising the protein conjugate according to claim 17 and optionally instructions for use.

34. The protein conjugate according to claim 33, wherein said protein conjugate is produced by the process according to claim 1.

33. A protein conjugate comprising a hepatitis C virus NS3 antigen conjugated to a label moiety, said label moiety comprising a carrier moiety coupled to at least one detectable label.

35. The protein conjugate according to claim 33, wherein said label moiety is conjugated to said NS3 antigen via a linker.

36. The protein conjugate according to claim 33, wherein said carrier moiety is bovine serum albumin.

37. The protein conjugate according to claim 33, wherein said at least one detectable label is an acridinium ester.

38. The protein conjugate according to claim 33, wherein said NS3 antigen comprises SEQ ID NO:

1.