Detecting or quantifying multiple analytes using labelling techniques

• US 5,656,207 A
• Filed: 05/11/1995
• Issued: 08/12/1997
• Est. Priority Date: 06/24/1989
• Status: Expired due to Term

• Current Assignee: Gen-Probe Incorporated (Hologic Incorporated)
• Original Assignee: Gen-Probe Incorporated (Hologic Incorporated)
• Inventors: Weeks, Ian, Woodhead, James Stuart, Batmanghelich, Shariar
• Primary Examiner(s): TUCKER, PHILIP C
• Application Number:
  US08/439,311
• Time in Patent Office: 824 Days
• Field of Search: 252/700, 435/5, 435/6, 435/7.1, 435/7.92-7.95, 435/8, 435/26, 435/968, 435/973
• US Class Current: 252/700
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin
• CPC Class Codes: G01N 21/76 Chemiluminescence; Bioluminescence
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: Y10S 435/968 High energy substrates, e.g. fluorescent, chemiluminescent, radioactive
• CPC Class Codes: Y10S 435/973 Simultaneous determination of more than one analyte

Abstract

A method for the assay, detection etc. of each of a plurality of substances of interest in a sample comprises labelling each of the substances with one or more components each capable of taking part in a respective distinguishable chemiluminescent reaction. Luminescent reagents for use in the method are also disclosed.

Claims

1. A specific binding assay for two or more individual analytes in a liquid test sample which assay comprises:

a) contacting the sample with two or more specific labeled reagents, wherein each such reagent comprises

i) a member of a specific binding pair to which an individual analyte is a member, and

ii) a different, specific light-emitting label covalently or non-covalently joined to said member, in order to form at least one labeled said specific binding pair,

b) physically or chemically differentiating each said labeled specific binding pair from said labeled reagents,

c) generating and measuring light emission from each specifically labeled specific binding pair, as a measure of the presence or amount of each said analyte,

wherein each of the labels emit light at distinguishable emission maxima, or emit peak energy at distinguishable times after the generation of said emission, from at least one other of said labels.

2. The method of claim 1 wherein at least one of said labels is selected from the group consisting of acridinium compounds, phenanthridium compounds, phthalhydrazides, oxalate esters, dioxetanes and dioxetanones.

3. The method of claim 2 wherein at least one label forms an acridone before light is emitted from said label.

4. The method of claim 2 wherein at least one of said labels is an aryl acridinium ester.

5. The method of claim 4 wherein the aryl ring of at least one said label or labels is substituted at one or more position with a chemical group, each independently selected from the group consisting of an electron-withdrawing group and an electron-donating group such that emission of light occurs over said distinguishable times.

6. The method of claim 4 wherein the acridinium ring of at least one said label or labels is substituted at one or more position with a chemical group, each independently selected from the group consisting of an electron-withdrawing group and an electron-donating group such that emission of light occurs over said distinguishable times.

7. The method of claim 5 or 6 wherein said electron-withdrawing group is a halogen.

8. The method of claim 5 or 6 wherein said electron-donating group is selected from the group consisting of a methyl group and a methoxy group.

9. The method of claim 2 wherein at least one of said labels is an optionally substituted diphenylanthracene.

10. The method of claim 1 wherein at least one of said labels is a fluorescent molecule which is able to emit light by energy transfer from another molecule.

11. The method of claim 1, 4, 5, or 6 wherein each said specific binding partner is selected from the group consisting of hormones, vitamins, co-factors, nucleic acids, antigens, antibodies, haptens, ligands, enzymes, and enzyme substrates.

12. The method of claim 1, 4, 5 or 6 wherein the labels comprised in at least two of said different specific labeled specific binding pairs are caused to emit light at substantially the same time.

13. The method of claim 1 or 4 wherein the intensity of the light emitted from said labeled specific binding pairs is detected over different time intervals which may overlap in relation to the starting point of said detection and the duration of said light emission.

14. The method of claim 1 or 4 wherein the light emitted from at least two said labeled specific binding pairs is detected over different wavelength ranges.

15. The method of claim 1 or 4 wherein said sample is contacted with at least three specific labeled reagents, wherein light emitted by labels joined to at least two said reagents can be distinguished by detection over different wavelength ranges, and light emitted by labels joined to at least two said reagents can be distinguished by variation of light intensity over time.

16. The method of claim 1 wherein said light emissions are filtered by different light filtering means, said means filtering light over different wavelength ranges, and the filtered light is detected.

17. The method of claim 4 wherein a first of said different labels is an acridinium ester substituted with electron withdrawing groups and a second of said different labels is an acridinium ester substituted with electron donating groups, and wherein, upon simultaneous induction of light emission from said labels, light emission from the first label occurs over a period of time in excess of light emission from said second label, wherein said groups are selected such that emission of light occurs over said distinguishable times.

18. The method of claim 4 wherein, upon induction of light emission from said labels, a first of said different labels is an acridinium ester which emits light at a first wavelength and a second of said different labels is an acridinium ester having a greater degree of electronic conjugation than said first label, which emits light at a second wavelength longer than the first wavelength.

19. The method of claim 18 wherein said first label emits maximum light in a wavelength range of from 400 to 500 nm and said second label emits maximum light in a wavelength range of from 500 to 700 nm.

20. The method of claim 1 or 4 wherein each said label is covalently or non-covalently joined to said specific binding partner.

21. The method of claim 4 wherein two or more of said different labels are each an aryl acridinium ester.

22. The method of claim 4 wherein each said specifically labeled specific binding pairs comprise analyte bound to a specific binding partner by an interaction selected from the group consisting of an immunoassay binding reaction, a receptor binding reaction and a nucleic acid hybridization reaction.

23. The method of claim 1 wherein at least two of said specific labeled reagents individually comprise a chemiluminescent label.

24. A kit for the detection of more than one analyte in a test sample comprising two or more specifically labeled reagents, each said reagent comprising

(i) a member of a specific binding pair to which an individual analyte is a member, and

(ii) a different, specific label covalently or non-covalently joined to said binding pair member, said label being detectable by the emission of light from said label,

wherein each of the labels emit light at separate and distinct emission maxima, or emit peak energy at separate and distinct times after the generation of said emission, from at least one other of said labels, and wherein upon contacting said reagents with a test sample containing said analytes, the presence or amount of each said analyte is determined after the initiation of light emission.

25. The kit of claim 24 wherein each of said labels is independently selected from the group consisting of acridinium compounds, phenanthridium-compounds, phthalhydrazides, oxalate esters, dioxetanes and dioxtaetanones.

26. The kit of claim 25 wherein two or more of said different labels are each an aryl acridinium ester.

27. The kit of claim 24 wherein said binding pair member is selected from the group consisting of a nucleic acid and a protein.

28. The kit of claim 26 wherein a first of said different labels is an acridinium ester substituted with electron withdrawing groups and a second of said different labels is an acridinium ester substituted with electron donating groups, and wherein, upon simultaneous induction of light emission from said labels, light emission from the first label occurs over a period of time in excess of light emission from said second label, wherein said groups are selected such that emission of light occurs over said distinguishable times.

29. The kit of claim 24 wherein, upon induction of light emission from said labels, a first of said different labels is an acridinium ester which emits light at a first wavelength and a second of said different labels is an acridinium ester having a greater degree of electronic conjugation than said first label, which emits light at a second wavelength longer than the first wavelength.