Sequential analysis of biological samples

• US 7,629,125 B2
• Filed: 11/16/2006
• Issued: 12/08/2009
• Est. Priority Date: 11/16/2006
• Status: Active Grant

• Current Assignee: Leica Microsystems Gmbh (Danaher Corporation)
• Original Assignee: General Electric Company
• Inventors: Filkins, Robert John, Sood, Anup, Gerdes, Michael, Seel, Maximilian Lewis, Montalto, Michael Christopher
• Primary Examiner(s): Horlick; Kenneth R.
• Assistant Examiner(s): Thomas; David C
• Application Number:
  US11/560,599
• Publication Number:
  US 20080118916A1
• Time in Patent Office: 1,118 Days
• Field of Search: None
• US Class Current: 435/6.16
• CPC Class Codes: C12Q 1/68 involving nucleic acids
• CPC Class Codes: G01N 33/53 Immunoassay; Biospecific binding assay; Materials therefor
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

Methods for detecting multiple targets in a biological sample are provided. The methods includes contacting the sample with a first probe; physically binding the first probe to a first target; observing a first signal from the first probe; applying a chemical agent to modify the first signal; contacting the sample with a second probe; physically binding the second probe to a second target; and observing a second signal from the second probe. The methods disclosed herein also provide for multiple iterations of binding, observing, signal modification for deriving information about multiple targets in a single sample. An associated kit and device are also provided.

Claims

1. A method of detecting multiple targets in a biological sample, comprising:

(a) contacting the sample with a first probe;

(b) physically binding the first probe to a first target;

(c) observing a first signal from the first probe;

(d) applying a chemical agent after step (c) to modify the observed first signal;

(e) contacting the sample with a second probe;

(f) physically binding the second probe to a second target; and

(g) observing a second signal from the second probe.

2. The method of claim 1, wherein the target is selected from the group consisting of a nucleic acid, a peptide, a protein, a polysaccharide, a lipid, an enzyme, an enzyme substrate, a ligand, a receptor, an antigen, and a hapten.

3. The method of claim 1, wherein the probe comprises a binder and a signal generator.

4. The method of claim 3, wherein the signal generator is associated with the binder.

5. The method of claim 4, wherein the signal generator is associated with the binder though a cleavable linker.

6. The method of claim 3, wherein the binder is selected from a nucleic acid, a peptide, a protein, a polysaccharide, a lipid, an enzyme, an enzyme substrate, an enzyme inhibitor, a ligand, a receptor, an antigen, or a hapten.

7. The method of claim 3, wherein the signal generator is selected from a chromophore, a fluorophore, a Raman-active tag, a radioactive label, an enzyme, or an enzyme substrate.

8. The method of claim 1, wherein the chemical agent comprises an acid, a base, a nucleophile, an electrophile, an oxidizing agent, or a reducing agent.

9. The method of claim 1, wherein the chemical agent is selected from sodium hydroxide, hydrogen peroxide, or sodium periodate.

10. The method of claim 1, wherein modification of the signal comprises a decrease in intensity of signal, a shift in the signal peak, a change in the resonant frequency, or cleavage of the signal generator.

11. The method of claim 1, comprising observing the signal after the signal modification step.

12. The method of claim 1, wherein one or both of the contacting steps comprises contacting the sample with a plurality of probes each comprising a different binder and a different signal generator.

13. The method of claim 12, wherein at least one, but not all of the signals from the said plurality of probes in step (a) or step (e) remains unaltered in step (d).

14. The method of claim 1, comprising repeating steps (d) to (g) at least once using one or more probe in step (e).

15. The method of claim 1, wherein the biological sample comprises a whole cell or a tissue sample.

16. The method of claim 14, wherein the probe comprises an antibody and a fluorophore.

17. The method of claim 16, further comprising contacting the sample with a primary antibody prior to step (a).

18. The method of claim 17, wherein the probe comprises a secondary antibody and a fluorophore.

19. The method of claim 1, further comprising contacting the biological sample with a morphological stain.

20. The method of claim 19, wherein the morphological stain comprises 4′

,6-diamidino-2-phenylindole, esoin, or hematoxylin.

21. The method of claim 1, further comprising observing an intensity value of the first signal, the second signal, or both the first signal and the second signal.

22. The method of claim 1, comprising correlating the intensity value to an amount of target in the biological sample.

23. The method of claim 1, further comprising observing a location of the first signal, the second signal, or both the first signal and the second signal in the biological sample.

24. The method of claim 23, comprising correlating the location of the signal to a location of the target in the biological sample.

25. The method of claim 1, further comprising applying a chemical reagent to modify the observed second signal.

26. The method of claim 25, further comprising repeating the steps (a) to (d) using a third probe, a fourth probe, and so forth.

27. The method of claim 26, wherein the multiple targets consist of multiple proteins.

28. A method of detecting multiple targets in a biological sample, comprising:

(a) contacting the sample with a first probe;

(b) physically binding the first probe to a first target;

(c) observing a first signal from the first probe;

(d) coffelating the observed first signal to the detection of the first target;

(e) applying a chemical agent after step (d) to modify the observed first signal in step (c) ; and

(f) repeating the steps (a) to (e) with a second probe, a third probe, or an n^th probe to detect a second target, a third target, or an n^th target.

29. The method of claim 28, wherein the multiple targets consist of multiple proteins.

31. The method of claim 29, wherein the steps (a) to (e) are repeated up to about 9 times.

30. A method of detecting multiple targets in a biological sample, comprising:

(a) contacting the biological sample with a first probe, wherein the first probe is capable of binding a first target;

(b) physically binding the first probe to the first target to form a first target-bound probe;

(c) observing a first signal from the first target-bound probe;

(d) applying a chemical agent after step (c) to decrease the observed first signal;

(e) correlating the observed first signal to the detection of the first target; and

(f) repeating the steps (a) to (e) with a subsequent probe to detect a subsequent target.