Method for detection or quantitation of an analyte using an analyte dependent enzyme activation system

• US 5,583,001 A
• Filed: 05/04/1994
• Issued: 12/10/1996
• Est. Priority Date: 03/29/1989
• Status: Expired due to Term

• Current Assignee: NEN Life Science Products Inc (Revvity, Inc.)
• Original Assignee: E. I. du Pont de Nemours and Company (Corteva, Inc.)
• Inventors: Bobrow, Mark N., Litt, Gerald J.
• Primary Examiner(s): Nucker, Christine M.
• Assistant Examiner(s): STUCKER, JEFFREY J
• Application Number:
  US08/238,186
• Time in Patent Office: 951 Days
• Field of Search: 435/7.91, 435/7.7, 435/7.71, 435/7.72, 435/7.6, 435/7.8, 435/7.1, 435/15, 435/18, 435/21, 435/25, 435/28, 435/7.9, 435/7.5, 436/501, 436/518
• US Class Current: 435/7.5
• CPC Class Codes: G01N 33/532 Production of labelled immunochemicals
• CPC Class Codes: G01N 33/535 with enzyme label or co-enzymes, co-factors, enzyme inhibitors or enzyme substrates
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: G01N 33/581 with enzyme label (including co-enzymes, co-factors, enzyme inhibitors or substrates)

Abstract

The present invention concerns a method to catalyze reporter deposition to improve detection or quantitation of an analyte in a sample by amplifying the detector signal which comprises reacting an analyte dependent enzyme activation system with a conjugate consisting of a detectably labeled substrate specific for the enzyme system, said conjugate reacts with the analyte dependent enzyme activation system to form an activated conjugate which deposits substantially wherever receptor for the activated conjugate is immobilized, said receptor not being reactive with the analyte dependent enzyme activation system.

In another embodiment the invention concerns an assay for detecting or quantitating the presence or absence of an analyte in a sample using catalyzed reporter deposition to amplify the reporter signal.

Claims

1. An assay for detecting or quantitating the presence or absence of an analyte in a sample which comprises

a) immobilizing the analyte on a solid phase;

b) reacting the product of step (a) with an analyte-dependent enzyme activation system wherein the analyte-dependent enzyme activation system is a member of a specific binding pair coupled to an enzyme or is an enzyme;

c) reacting the product of step (b) with a conjugate consisting of a detectably labeled substrate specific for the enzyme system to form an activated conjugate which is a first member of a specific binding pair wherein the activated conjugate deposits covalently on the solid phase by binding to the second member of the specific binding pair on the surface of the solid phase, said second member, not being reactive with the analyte dependent enzyme activation system wherein deposited detectable labels either directly or indirectly generate a signal which can be detected or quantitated; and

d) detecting or quantitating the presence or absence of the analyte in the sample from the signal generated in step (c).

2. An assay according to claim 1 wherein the analyte dependent enzyme activation system has at least one enzyme selected from the group consisting of oxidoreductases, hydrolases, lyases, transferases, isomerases, and ligases.

3. An assay according to claim 2 wherein the enzyme is selected from the group consisting of peroxidases, oxidases, phosphatases, esterases and glycosidases.

4. An assay according to claim 3 wherein the enzyme is selected from the group consisting of horseradish peroxidase, glucose oxidase, alkaline phosphatase, and beta-galactosidase.

5. An assay according to claim 1 wherein the detectable label is selected from the group consisting of enzymes, radioactive isotopes, fluorogenic, chemiluminescent, or electrochemical or a member of a specific binding pair.

6. An assay according to claim 4 wherein the enzyme is horseradish peroxidase.

7. An assay according to claim 6 wherein the conjugate is selected from the group consisting of biotin tyramine, p-hydroxyphenylpropionyl-biocytin or fluorescein-tyramine.

8. An assay according to claim 1 wherein the conjugate in step (c) is reacted with a detectably labeled member of a specific binding pair.

9. An assay according to claim 1 wherein the activated conjugate in step (c) is reacted with a detectably labeled antibody.

10. An assay according to claim 1 wherein the activated conjugate in step (c) is biotinylated and is reacted with a detectably labeled streptavidin.

11. An assay according to claim 1 wherein said assay is an immunoassay.

13. An assay for detecting or quantitating the presence or absence of an analyte in a sample which comprises

a) reacting analyte which is at least one component of an analyte dependent enzyme activation system wherein said analyte-dependent enzyme activation system is a member of a specific binding pair coupled to an enzyme or is an enzyme with a conjugate consisting of a detectably labeled substrate specific for the enzyme system to form an activated conjugate which is a first member of a specific binding pair wherein the activated conjugate deposits on the solid phase by binding to the second member of the specific binding pair on the surface of the solid phase, said second member not being reactive with the analyte dependent enzyme activation system wherein deposited detectable labels either directly or indirectly generate a signal which can be detected or quantitated;

and

b) detecting or quantitating the presence or absence of the analyte in the sample from the signal generated in step (a).

12. An assay according to claim 16 wherein the conjugate is a detectably labelled phenol.

14. An assay according to claim 13 wherein the analyte dependent enzyme activation system has at least one enzyme selected from the group consisting of oxidoreductases, hydrolases, lyases, transferases, isomerases, and ligases.

15. An assay according to claim 14 wherein the enzyme is selected from the group consisting of peroxidases, oxidases, phosphatases, esterases and glycosidases.

16. An assay according to claim 15 wherein the enzyme is selected from the group consisting of horseradish peroxidase, glucose oxidase, alkaline phosphatase, and beta-galactosidase.

17. An assay according to claim 13 wherein the detectable label is selected from the group consisting of enzymes, radioactive isotopes, fluorogenic, chemiluminescent, or electrochemical or a member of a specific binding pair.

18. An assay according to claim 13 wherein the activated conjugate in step (b) is reacted with a detectably labeled member of a specific binding pair.

19. An assay according to claim 13 wherein the activated conjugate step (b) is biotinylated and is reacted with a detectably labeled streptavidin.

20. An assay according to claim 13 wherein the activated conjugate in step (b) is reacted with a detectably labeled antibody.

21. An assay according to claim 13 wherein said assay is an immunoassay.

22. An assay according to claim 16 wherein the enzyme is horseradish peroxidase.

23. An assay according to claim 22 wherein the conjugate is a detectably labelled phenol.

24. An assay according to claim 23 wherein the detectably labelled phenol is selected from the group consisting of biotin tyramine, p-hydroxyphenylpropionyl-biocytin or fluorescein-tryamine.