PEPTIDE REAGENTS AND METHOD FOR INHIBITING AUTOANTIBODY ANTIGEN BINDING

• US 20110136141A1
• Filed: 12/03/2009
• Published: 06/09/2011
• Est. Priority Date: 12/03/2009
• Status: Abandoned Application

• Current Assignee: Abbott Laboratories Incorporated
• Original Assignee: Abbott Laboratories Incorporated
• Inventors: Brashear, Jefffrey R., Adamczyk, Maciej, Mattingly, Phillip G.
• Application Number:
  US12/630,671
• Publication Number:
  US 20110136141A1
• Time in Patent Office: Days
• US Class Current: 435/7.9
• CPC Class Codes: G01N 33/5306 Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding

Abstract

The present disclosure provides immunoassays and kits for detection or quantification of an protein of interest in a test sample that potentially contains endogenously produced autoantibodies reactive with the analyte.

Claims

1. A reagent for use in an immunoassay for determining the presence or amount of at least one protein in a test sample, the reagent comprising:

at least one peptide comprising at least 5 consecutive amino acid residues wherein the peptide is derived from said protein and further wherein said reagent is used to block the interaction between an endogenous antibody and said protein in the test sample.

2. The reagent of claim 1, wherein the protein is selected from the group consisting of:

cardiac troponin I (SEQ ID NO;

1), cardiac troponin T (SEQ ID NO;

2), thyroid stimulating hormone (TSH) (SEQ ID NO;

3), beta-human chorionic gonadotropin (beta-HCG) (SEQ ID NO;

4), myeloperoxidase (MPO) (SEQ ID NO;

5), prostate specific antigen (PSA) (SEQ ID NO;

6), human B-type natriuretic peptide (hBNP) (SEQ ID NO;

7), myosin light chain 2 (SEQ ID NO;

8), myosin-6 (SEQ ID NO;

9) and myosin-7 (SEQ ID NO;

10).

3. The reagent of claim 1, wherein the peptide has a length of 5 consecutive amino acids to 15 consecutive amino acids.

4. The reagent of claim 1, wherein the protein is cardiac troponin I, and the peptide has a sequence comprising at least five consecutive amino acid residues from a sequence selected from the group consisting of SSDAAREPRPAPAPI (SEQ ID NO:

11), VDEERYDIEAKVTKN (SEQ ID NO;

12), DIEAKVTKNITEIAD (SEQ ID NO;

13), LDLRAHLKQVKKEDT (SEQ ID NO;

14), and ALSGMEGRKKKFES (SEQ ID NO;

15).

20. A kit for detecting and/or quantifying at least one protein of interest in a test sample, the kit comprising:

the reagent of claim 1;

a capture reagent comprising an antibody that binds to the protein of interest; and

instructions for detecting and/or quantifying at least one protein of interest in a test sample.

21. The kit of claim 20, wherein the kit further comprises a conjugate comprising an antibody conjugated to a detectable label.

22. The kit of claim 21, wherein the detectable label is selected from the group consisting of a radioactive label, an enzymatic label, a chemiluminescent label, a fluorescence label, a thermometric label, and an immuno-polymerase chain reaction label.

23. The kit of claim 22, wherein the detectable label is an acridinium compound.

24. The kit of claim 23, wherein the acridinium compound is an acridinium-9-carboxamide having a structure according to formula I:

25. The kit of claim 23, wherein the acridinium compound is an acridinium-9-carboxylate aryl ester having a structure according to formula II:

26. The kit of claim 23, further comprising a basic solution.

27. The kit of claim 26, wherein the basic solution is a solution having a pH of at least about 10.

28. The kit of claim 23, further comprising a hydrogen peroxide source.

29. The kit of claim 28, wherein the hydrogen peroxide source comprises a buffer or a solution containing hydrogen peroxide.

30. The kit of claim 28, wherein the hydrogen peroxide source comprises a hydrogen peroxide generating enzyme.

31. The kit of claim 30, wherein the hydrogen peroxide generating enzyme is selected from the group consisting of:

(R)-6-hydroxynicotine oxidase, (S)-2-hydroxy acid oxidase, (S)-6-hydroxynicotine oxidase, 3-aci-nitropropanoate oxidase, 3-hydroxyanthranilate oxidase, 4-hydroxymandelate oxidase, 6-hydroxynicotinate dehydrogenase, abscisic-aldehyde oxidase, acyl-CoA oxidase, alcohol oxidase, aldehyde oxidase, amine oxidase, amine oxidase (copper-containing), amine oxidase (flavin-containing), aryl-alcohol oxidase, aryl-aldehyde oxidase, catechol oxidase, cholesterol oxidase, choline oxidase, columbamine oxidase, cyclohexylamine oxidase, cytochrome c oxidase, D-amino-acid oxidase, D-arabinono-1,4-lactone oxidase, D-arabinono-1,4-lactone oxidase, D-aspartate oxidase, D-glutamate oxidase, D-glutamate(D-aspartate) oxidase, dihydrobenzophenanthridine oxidase, dihydroorotate oxidase, dihydrouracil oxidase, dimethylglycine oxidase, D-mannitol oxidase, ecdysone oxidase, ethanolamine oxidase, galactose oxidase, glucose oxidase, glutathione oxidase, glycerol-3-phosphate oxidase, glycine oxidase, glyoxylate oxidase, hexose oxidase, hydroxyphytanate oxidase, indole-3-acetaldehyde oxidase, lactic acid oxidase, L-amino-acid oxidase, L-aspartate oxidase, L-galactonolactone oxidase, L-glutamate oxidase, L-gulonolactone oxidase, L-lysine 6-oxidase, L-lysine oxidase, long-chain-alcohol oxidase, L-pipecolate oxidase, L-sorbose oxidase, malate oxidase, methanethiol oxidase, monoamino acid oxidase, N⁶-methyl-lysine oxidase, N-acylhexosamine oxidase, NAD(P)H oxidase, nitroalkane oxidase, N-methyl-L-amino-acid oxidase, nucleoside oxidase, oxalate oxidase, polyamine oxidase, polyphenol oxidase, polyvinyl-alcohol oxidase, prenylcysteine oxidase, protein-lysine 6-oxidase, putrescine oxidase, pyranose oxidase, pyridoxal 5′

-phosphate synthase, pyridoxine 4-oxidase, pyrroloquinoline-quinone synthase, pyruvate oxidase, pyruvate oxidase (CoA-acetylating), reticuline oxidase, retinal oxidase, rifamycin-B oxidase, sarcosine oxidase, secondary-alcohol oxidase, sulfite oxidase, superoxide dismutase, superoxide reductase, tetrahydroberberine oxidase, thiamine oxidase, tryptophan α

,β

-oxidase, urate oxidase (uricase, uric acid oxidase), vanillyl-alcohol oxidase, xanthine oxidase, xylitol oxidase and combinations thereof.

32. The kit of claim 20, wherein the protein is cardiac troponin I, cardiac troponin T, thyroid stimulating hormone (TSH), beta-human chorionic gonadotropin (beta-HCG), myeloperoxidase (MPO), prostate specific antigen (PSA), human B-type natriuretic peptide (hBNP), myosin light chain 2, myosin-6 or myosin-7.

33. The kit of claim 20, wherein the reagent is a peptide having a length of 5 consecutive amino acids to 15 consecutive amino acids.

34. The kit of claim 33, wherein the protein is cardiac troponin I, and the peptide has a sequence comprising at least five consecutive amino acid residues from a sequence selected from the group consisting of SSDAAREPRPAPAPI (SEQ ID NO:

11), VDEERYDIEAKVTKN (SEQ ID NO;

12), DIEAKVTKNITEIAD (SEQ ID NO;

13), LDLRAHLKQVKKEDT (SEQ ID NO;

14), and ALSGMEGRKKKFES (SEQ ID NO;

15).

5. A reagent for use in an immunoassay for determining the presence or amount of at cardiac troponin I in a test sample, the reagent comprising a peptide having a sequence comprising at least five consecutive amino acid residues from a sequence selected from the group consisting of SSDAAREPRPAPAPI (SEQ ID NO:

11), VDEERYDIEAKVTKN (SEQ ID NO;

12), DIEAKVTKNITEIAD (SEQ ID NO;

13), LDLRAHLKQVKKEDT (SEQ ID NO;

14), and ALSGMEGRKKKFES (SEQ ID NO;

15).

6. A method of detecting at least one protein of interest in a test sample, the method comprising the steps of:

a. preparing a first mixture comprising a test sample suspected of containing at least one protein of interest and at least one reagent, wherein said reagent (1) is at least one peptide comprising at least 5 consecutive amino acid residues derived from said protein that binds to the antibody of interest; and

(2) disrupts the interaction between an endogenous antibody in the test sample and the antigen;

b. preparing a second mixture comprising the first mixture and a first specific binding partner, wherein the first specific binding partner comprises an antibody, wherein the antibody binds with the protein of interest to form a first specific binding partner-protein complex; and

c. contacting the second mixture with a second specific binding partner, wherein the second specific binding partner comprises an antibody that has been conjugated to a detectable label and further wherein the second specific binding partner binds to the first specific binding partner-protein complex to form a first specific binding partner-protein-second specific binding partner complex; and

d. measuring the signal generated by or emitted from the detectable label and detecting the protein of interest in the test sample.

7. The method of claim 6, wherein the protein is selected from the group consisting of:

cardiac troponin I, cardiac troponin T, thyroid stimulating hormone (TSH), beta-human chorionic gonadotropin (beta-HCG), myeloperoxidase (MPO), prostate specific antigen (PSA), human B-type natriuretic peptide (hBNP), myosin light chain 2, myosin-6 and myosin-7.

8. The method of claim 6, wherein the test sample is whole blood, serum or plasma.

9. The method of claim 6, wherein the first specific binding partner is immobilized to a solid phase either before or after the formation of the first specific binding partner-protein complex.

10. The method of claim 6, wherein the second specific binding partner is immobilized to a solid phase either before or after formation of the first specific binding partner-protein-second specific binding partner complex.

11. The method of claim 6, wherein the detectable label is selected from the group consisting of a radioactive label, an enzymatic label, a chemiluminescent label, a fluorescence label, a thermometric label, and an immuno-polymerase chain reaction label.

12. The method of claim 6, wherein said detectable label is an acridinium compound.

13. The method of claim 12 further comprising:

a. generating or providing a source of hydrogen peroxide to the second mixture contacted with a second specific binding partner;

b. adding a basic solution to the mixture of step (a);

c. measuring the light signal generated or emitted in step (b) and detecting the protein of interest in the sample.

14. The method of claim 12, wherein the acridinium compound is an acridinium-9-carboxamide having a structure according to formula I:

15. The method of claim 12, wherein the acridinium compound is an acridinium-9-carboxylate aryl ester having a structure according to formula II:

16. The method of claim 6, wherein the reagent is a peptide having a length of 5 consecutive amino acids to 15 consecutive amino acids.

17. The method of claim 6, wherein the protein is cardiac troponin I, and the peptide has a sequence comprising at least five consecutive amino acid residues from a sequence selected from the group consisting of SSDAAREPRPAPAPI (SEQ ID NO:

11), VDEERYDIEAKVTKN (SEQ ID NO;

12), DIEAKVTKNITEIAD (SEQ ID NO;

13), LDLRAHLKQVKKEDT (SEQ ID NO;

14), and ALSGMEGRKKKFES (SEQ ID NO;

15).

18. The method of claim 6, further comprising the step of quantifying the amount of protein of interest in the test sample by relating the amount of signal in step (d) to the amount of the one or more proteins of interest in the test sample either by use of a standard curve for the protein of interest or by comparison to a reference standard.

19. The method of claim 7, wherein the method is adapted for use in an automated system or semi-automated system.