Immunoaffinity isolation of modified peptides from complex mixtures

• US 7,198,896 B2
• Filed: 06/19/2002
• Issued: 04/03/2007
• Est. Priority Date: 09/04/1998
• Status: Expired due to Term

• Current Assignee: Cell Signaling Technology Incorporated
• Original Assignee: Cell Signaling Technology Incorporated
• Inventors: Comb, Michael J., Zhang, Hui, Tan, Yi, Rush, John, Zha, Xiangming
• Primary Examiner(s): Le; Long V.
• Assistant Examiner(s): Do; Pensee T.
• Application Number:
  US10/175,486
• Publication Number:
  US 20030044848A1
• Time in Patent Office: 1,749 Days
• Field of Search: 435/6, 435/4, 435/69.1, 435/29, 435/144, 436/518, 436/89, 436/501, 210/601, 210/656, 210/661
• US Class Current: 435/7.23
• CPC Class Codes: C07K 16/44 against material not provided for elsewhere , e.g. haptens, metals, DNA, RNA, amino acids

Abstract

The invention provides methods for isolating a modified peptide from a complex mixture of peptides, the method comprising the steps of: (a) obtaining a proteinaceous preparation from an organism, wherein the preparation comprises modified peptides from two or more different proteins; (b) contacting the preparation with at least one immobilized modification-specific antibody; and (c) isolating at least one modified peptide specifically bound by the immobilized modification-specific antibody in step (b). The method may further comprise the step of (d) characterizing the modified peptide isolated in step (c) by mass spectrometry (MS), tandem mass spectrometry (MS—MS), and/or MS³ analysis, or the step of (e) utilizing a search program to substantially match the spectra obtained for the modified peptide during the characterization of step (d) with the spectra for a known peptide sequence, thereby identifying the parent protein(s) of the modified peptide. Also provided are an immunoaffinity isolation device comprising a modification-specific antibody, and antibodies against novel UFD1 and PTN6 phosphorylation sites.

Claims

1. A method for isolating a target population of naturally-occurring post-translationally modified peptides from a complex mixture of peptides, said method comprising the steps of:

(a) obtaining a digested proteinaceous preparation from an organism, wherein said digested proteinaceous preparation comprises a complex in mixture of peptides comprising naturally-occurring post-translationally modified peptides from two or more different proteins;

(b) contacting said digested proteinaceous preparation with at least one immobilized post-translational modification-specific antibody; and

(c) isolating said target population of naturally-occurring post-translationally modified peptides specifically bound by said immobilized modification-specific antibody in step (b).

2. The method of claim 1, further comprising the step of (d) characterizing said population of modified peptides isolated in step (c) by mass spectrometry (MS), tandem mass spectrometry (MS=MS), and/or MS³ analysis.

3. The method of claim 2, wherein said mass spectrometry comprises matrix-assisted laser desorption time-of-flight (MALDI-TOF) MS, wherein said tandem mass spectrometry comprises liquid chromatography (LC)-MS/MS, and wherein said MS³ analysis comprises LC-MS³.

4. The method of claim 2, wherein said immobilized antibody of step (b) is immobilized in chromatography resin within a column, said column being coupled to a mass spectrometer for said characterization of step (d).

5. The method of claims 2 or 3, further comprising the step of (c) utilizing a search program to substantially match the spectra obtained for said modified peptides during the characterization of step (d) with the spectra for known peptide sequences, thereby identifying the parent protein(s) of said modified peptides.

6. The method of claim 5, wherein at least one modified peptide characterized in step (d) comprises an unknown post-translational modification site of said parent protein.

7. The method of claims 2 or 3, further comprising the step of (e) comparing the modification state of at least one modified peptide characterized in step (d) with the modification state of a corresponding peptide in a reference sample, thereby to compare protein activation in said proteinaceous preparation with protein activation in said reference sample.

8. The method of claim 7, wherein said proteinaceous preparation corresponds to a diseased organism and said reference sample corresponds to a normal organism, whereby comparison of protein activation provides information on activation changes resulting from said disease.

9. The method of claim 8, wherein the comparison of protein activation identifies at least one modified peptide characterized in step (d) as corresponding to a parent protein not previously reported as so modified in said disease.

10. The method of claim 7, wherein said proteinaceous preparation is obtained from a tissue biopsy cell or a clinical fluid sample and said reference sample corresponds to a diseased organism, whereby the comparison of protein activation provides information useful for diagnosis of said disease.

11. The method of claim 7, wherein said protein preparation corresponds with an organism or preparation treated with at least one test compound and said reference sample corresponds with an untreated organism or preparation, whereby the comparison of protein activation provides information on activation changes resulting from treatment with said test compound.

12. The method of claim 10 or 11, wherein said disease is cancer.

13. The method of claim 11, wherein said test compound comprises a cancer.

14. The method of claim 11, wherein said test compound comprises a kinase inhibitor.

15. The method of claim 1, wherein said proteinaceous preparation comprises a digested biological sample selected from the group consisting of a digested crude cell extract, a digested tissue sample, a digested serum sample, a digested urine sample, a digested synovial fluid sample, and a digested spinal fluid sample.

16. The method of claim 15, wherein said digested preparation is obtained using at least one proteolytic enzyme or chemical cleavage.

17. The method of claim 16, wherein said proteolytic enzyme is immobilized.

18. The method of claim 16, wherein said proteolytic enzyme is soluble, and wherein said digested preparation is treated with a proteolysis inhibitor prior to said contacting step (b).

19. The method of claim 1, wherein step (a) further comprises pre-purifying said proteinaceous preparation by immobilized metal affinity chromatography (IMAC).

20. The method of claim 1, wherein said immobilized antibody of step (b) is covalently-linked to a chromatography resin or noncovalently-linked to protein-A-or protein-G-agarose.

21. The method of claim 20, wherein said resin is contained within a column or micropipette tip.

22. The method of claim 1, wherein said modification comprises phosphorylation.

23. The method of claim 1, wherein said modified peptide(s) comprise(s) a phosphopeptide.

24. The method of claim 1, wherein said post-translational modification-specific antibody comprises a motif-specific, context-independent antibody that specifically binds a motif comprising at least one phosphorylated amino acid.

25. The method of claim 24, wherein said motif consists of a single phosphorylated amino acid.

26. The method of claim 24, wherein said motif consists of all or part of a kinase consensus substrate motif or a protein-protein binding motif.

27. The method of claim 26, wherein said kinase consensus substrate motif is selected from the group consisting of mitogen-activated protein kinase (MAPK) consensus substrate motifs, cyclin-dependent kinase (CDK) consensus substrate motifs, protein kinase A (PKA) consensus substrate motifs, AKT consensus substrate motifs, protein kinase C (PKC) consensus substrate motifs, phosphothreonine-X-arginine, and ATM (ataxia telangiecstasia mutated) consensus substrate motifs, and wherein said protein-protein binding is a 14-3-3 binding motif or a 3-phosphoinositide-dependent kinase 1 (PDK1) docking motif.

28. The method of claim 1, wherein said post-translational modification-specific antibody is a monoclonal antibody or a polyclonal antibody.

29. The method of claim 1, wherein at least one modified peptide isolated in step (c) corresponds to a known marker of disease.

30. The method of claim 1, wherein said modification comprises acetylation, glycosylation, or methylation.

31. The method of claim 1, wherein said immobilized post-translational modification-specific antibody of step (b) comprises an antibody that specifically binds a single acetylated amino acid or a single phosphorylated amino acid.

32. A method for isolating a target population of phosphopeptides from a complex mixture of peptides, said method comprising the steps of:

(a) obtaining a digested proteinaceous preparation from an organism, wherein said digested proteinaceous preparation comprises a complex mixture of peptides comprising phosphopeptides from two or more different proteins;

(b) contacting said digested proteinaceous preparation with at least one immobilized motif-specific, context-independent antibody that binds a motif comprising at least one phosphorylated amino acid;

(c) isolating said target population of phosphopeptides specifically bound by said immobilized antibody in step (b); and

(d) characterizing said phosphopeptides isolated in step (c) by mass spectrometry (MS), tandem mass spectrometry (MS—

MS), and/or MS³ analysis.

33. The method of claim 32, further comprising the step of (e) utilizing a search program to substantially match the mass spectra obtained for said phosphopeptides during the characterization of step (d) with the mass spectra for a peptide of one or more known protein(s), thereby identifying the parent protein(s) of said phosphopeptides.

34. The method of claim 32, wherein said mass spectrometry comprises matrix-assisted laser desorption time-of-flight (MALDI-TOF) MS, wherein said tandem mass spectrometry comprises liquid chromatography (LC)-MS/MS, and wherein said MS³ analysis comprises LC-MS³.

35. The method of claim 32, wherein step (a) further comprises digesting said proteinaceous preparation to produce a complex mixture of peptides.

36. The method of claim 32, wherein said motif of step (b) comprises all or part of a kinase consensus substrate motif or a protein-protein binding motif, or consists of a single phosphorylated amino acid.

37. The method of claim 32, wherein said immobilized motif-specific, context-independent antibody of step (b) comprises an antibody that specifically binds a single phosphorylated amino acid selected from the group consisting of phosphotyrosine, phosphoserine, and phosphothreonine.