Highly sensitive proteomic analysis methods, and kits and systems for practicing the same

• US 7,354,721 B2
• Filed: 09/21/2001
• Issued: 04/08/2008
• Est. Priority Date: 09/22/2000
• Status: Expired due to Fees

• Current Assignee: Clontech Laboratories Incorporated
• Original Assignee: Clontech Laboratories Incorporated
• Inventors: Tchaga, Grigoriy S.
• Primary Examiner(s): Lam; Ann Y.
• Application Number:
  US09/960,716
• Publication Number:
  US 20030036095A1
• Time in Patent Office: 2,391 Days
• Field of Search: 435/7.1, 435/7.2, 435/7.4, 435/7.5, 435/7.6, 435/7.7, 435/7.71, 435/7.72, 435/7.8, 435/7.9, 435/7.91, 435/7.92, 435/7.93, 435/7.94, 435/7.95, 436/518, 436/523, 436/524, 436529-535, 436/546, 436/172, 436/177
• US Class Current: 435/7.1
• CPC Class Codes: B01J 2219/00585 Parallel processes
• CPC Class Codes: B01J 2219/00596 Solid-phase processes
• CPC Class Codes: B01J 2219/00605 the compounds being directly bound or immobilised to solid supports
• CPC Class Codes: B01J 2219/00612 the surface being inorganic
• CPC Class Codes: B01J 2219/00626 Covalent
• CPC Class Codes: B01J 2219/0063 Other, e.g. van der Waals forces, hydrogen bonding
• CPC Class Codes: B01J 2219/00637 by coating it with another layer
• CPC Class Codes: B01J 2219/00659 Two-dimensional arrays
• CPC Class Codes: B01J 2219/0072 Organic compounds
• CPC Class Codes: C03C 17/30 with silicon-containing compounds
• CPC Class Codes: C03C 17/3405 with at least two coatings of organic materials C03C17/36, C03C17/42 take precedence
• CPC Class Codes: G01N 2400/46 Pectin
• CPC Class Codes: G01N 33/54353 with ligand attached to the carrier via a chemical coupling agent coatings G01N33/54393
• CPC Class Codes: G01N 33/552 Glass or silica
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: G01N 33/6803 General methods of protein analysis not limited to specific proteins or families of proteins

Abstract

Methods of determining whether a sample includes one or more analytes, particularly proteinaceous analytes, of interest are provided. In the subject methods, an array of binding agents, where each binding agent includes an epitope binding domain of an antibody, is contacted with the sample. In many embodiments, contact occurs in the presence of a metal ion chelating polysaccharide, e.g., a pectin. Following contact, the presence of binding complexes on the array surface are detected and the resultant data is employed to determine whether the sample includes the one or more analytes of interest. Also provided are kits, systems and other compositions of matter for practicing the subject methods. The subject methods and compositions find use in a variety of applications, including proteomic applications such as protein expression analysis, e.g., differential protein expression profiling.

Claims

1. A method of determining whether a sample includes at least one analyte of interest, said method comprising:

(a) pre-incubating said sample with a first buffer composition comprising a metal ion chelating polysaccharide, wherein said metal ion chelating polysaccharide comprises polygalactouronate domains;

(b) contacting said pre-incubated sample with a planar array of a plurality of distinct binding agents displayed on a surface of a solid support, wherein each of said binding agents at least comprises a specific epitope binding domain of an antibody;

(c) detecting the presence of any resultant binding complexes on said surface to obtain analyte binding data; and

(d) employing said analyte binding data to determine whether said sample includes said at least one analyte of interest.

2. The method according to claim 1, wherein said metal ion chelating polysaccharide is a pectin.

3. The method according to claim 2, wherein said pectin is apple pectin.

4. The method according to claim 1, wherein said method further comprises extracting said at least one analyte from a cellular source and labeling said extracted at least one analyte, wherein said extracting and labeling steps employ a second buffer composition that is the same.

5. The method according to claim 4, wherein said second buffer composition is free of components that include primary amine moieties.

6. The method according to claim 5, wherein said second buffer composition has a pH ranging from about 7 to about 12.

7. The method according to claim 6, wherein said second buffer composition is capable of extracting at least about 95% of the proteins of an initial cellular source.

8. The method according to claim 1, wherein said at least one analyte is a protein.

9. The method according to claim 1, wherein said method comprises determining the presence of at least two distinct analytes in said sample.

10. The method according to claim 1, wherein said method comprises a plurality of washing steps between said contacting and detecting steps.

11. The method according to claim 1, wherein:

(a) said method comprises quantitatively detecting at least two different protein analytes in said sample;

(b) said method further comprises extracting said at least one analyte from a cellular source in an extraction buffer and labeling said extracted at least one analyte in a buffer that is the same as said extraction buffer; and

(c) wherein said method comprises a plurality of washing steps between said contacting and detecting steps.

12. The method according to claim 11, wherein said metal ion chelating polysaccharide is a pectin.

13. The method according to claim 12, wherein said pectin is apple pectin.

14. The method according to claim 11, wherein said method is a method of determining a protein expression profile for said sample.

15. The method according to claim 1, wherein said method further comprises a sample fractionating step prior to said contacting step.

16. The method according to claim 15, wherein said fractionating step comprises contacting said sample with at least one affinity column.