Methods and reagents for multiplexed analyses

• US 20040197841A1
• Filed: 04/02/2003
• Published: 10/07/2004
• Est. Priority Date: 04/02/2003
• Status: Abandoned Application

• Current Assignee: Agilent Technologies, Inc.
• Original Assignee: Agilent Technologies, Inc.
• Inventors: Apffel, James Alexander Jr.
• Application Number:
  US10/405,438
• Publication Number:
  US 20040197841A1
• Time in Patent Office: Days
• US Class Current: 435/7.92
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: G16B 25/00 ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
• CPC Class Codes: G16B 25/10 Gene or protein expression profiling; Expression-ratio estimation or normalisation

Abstract

Methods, devices and kits are disclosed for detecting one or more target proteins in a sample suspected of containing a plurality of the target proteins. An assay medium comprising the sample is incubated with a surface of a substrate comprising a plurality of capture agents bound to the surface in a predetermined arrangement or pattern. For each target protein, at least two capture agents specific for different binding sites on the target protein are employed. The two capture agents are disposed on the surface of the substrate in a spatial relationship so that both bind to a molecule of the target protein, preferably the same molecule of the target protein. The binding to the molecule of the target protein is usually substantially simultaneous. The assay medium is incubated under conditions for binding of the capture agents to the target proteins. The substrate is then examined for the presence of the target proteins.

Claims

1. A method for detecting one or more target proteins in a sample suspected of containing a plurality of said target proteins, said method comprising:

(a) incubating an assay medium comprising said sample with a surface of a substrate comprising a plurality of capture agents bound thereto in a predetermined pattern, wherein for each target protein at least two capture agents specific for different binding sites on said target protein are employed and wherein said two capture agents bind to said target protein, said assay medium being incubated under conditions for binding of said capture agents to said target proteins, and

(b) examining said substrate surface for the presence of said target proteins.

2. A method according to claim 1 wherein each of said capture agents is independently selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagents.

3. A method according to claim 1 wherein each of said capture agents is independently an antibody or an antibody fragment.

4. A method according to claim 1 wherein said examining of said substrate comprises contacting said substrate with a specific binding partner for each of said proteins.

5. A method according to claim 4 wherein said specific binding partners for said target proteins are selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagents.

6. A method according to claim 4 wherein said specific binding partners for said target proteins comprise a detectable moiety.

7. A method according to claim 6 wherein said detectable moiety is selected from the group consisting of luminescers, enzymes, enzyme substrates, radioactive group, particles, and promoters.

8. A method according to claim 1 wherein said examining of said substrate comprises contacting said substrate surface with a wash fluid and observing said substrate surface or said wash fluid for the presence of said target proteins.

9. A method according to claim 4 wherein said specific binding partners are antibodies.

10. A method according to claim 1 wherein said substrate surface comprises an array of said capture agents.

11. A method according to claim 10 wherein said examining comprises observing a binding pattern on said array and evaluating the presence of the target proteins based on the observed binding pattern

12. A method according to claim 1 wherein said two capture agents bind to different epitopes on the same molecule of said target protein.

13. A method for determining one or more different target proteins in a sample suspected of containing a plurality of said target proteins, said method comprising:

(a) incubating an assay medium comprising said sample with a surface of a substrate comprising an array of capture agents bound thereto, wherein at least two capture agents specific for different binding sites on each of said different target proteins are employed and wherein said two capture agents bind to said target protein, said assay medium being incubated under conditions for binding of said capture agents to said target proteins, and

(b) examining said substrate surface for the presence of said target proteins.

14. A method according to claim 13 wherein each of said capture agents is independently selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagent.

15. A method according to claim 13 wherein each of said capture agents is an antibody or an antibody fragment.

16. A method according to claim 13 wherein said substrate is examined for the presence of said target proteins by contacting said substrate with a specific binding partner for each of said proteins.

17. A method according to claim 16 wherein said specific binding partners for said target proteins are selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagents.

18. A method according to claim 16 wherein said specific binding partners for said target proteins comprise a detectable moiety.

19. A method according to claim 18 wherein said detectable moiety is selected from the group consisting of luminescers, enzymes, enzyme substrates, radioactive group, particles, and promoters.

20. A method according to claim 13 wherein said examining of said substrate comprises contacting said substrate surface with a wash fluid and observing said substrate surface or said wash fluid for the presence of said target proteins.

21. A method according to claim 13 wherein said examining comprises observing a binding pattern on said array and evaluating the presence of the target proteins based on the observed binding pattern

22. A method according to claim 13 wherein said two capture agents bind to different epitopes on the same molecule of said target protein.

23. A device for determining one or more different target proteins in a sample suspected of containing a plurality of said target proteins, said apparatus comprising:

(a) a solid substrate comprising a surface, and

(b) a plurality of capture agents bound to said surface in a predetermined pattern, wherein at least two capture agents specific for different binding sites on each of said target proteins are present and wherein said two capture agents are spatially disposed to both bind to a single molecule of said target protein.

24. A device according to claim 23 wherein each of said capture agents is independently selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagent.

25. A device according to claim 23 wherein each of said capture agents is an antibody or an antibody fragment.

26. A device according to claim 23 wherein said capture agents are present on said surface in an array.

27. A kit comprising in packaged combination a device according to claim 23 and a plurality of specific binding partners, one for each of said proteins.

28. A kit according to claim 27 wherein said specific binding partners for said target proteins are selected from the group consisting of synthetic proteins, natural proteins, aptamers, synthetic peptides, natural peptides and synthetic affinity reagents.

29. A kit according to claim 27 wherein said specific binding partners for said target proteins comprise a detectable moiety.

30. A kit according to claim 29 wherein said detectable moiety is selected from the group consisting of luminescers, enzymes, enzyme substrates, radioactive group, particles, and promoters.