Simultaneous immunoassay of two analytes using dual enzyme labelled antibodies

• US 5,108,896 A
• Filed: 03/02/1987
• Issued: 04/28/1992
• Est. Priority Date: 03/21/1986
• Status: Expired due to Fees

• Current Assignee: Biocem Immunosystems, LLC
• Original Assignee: Applied Research Systems ARS Holding NV (Merck & Co., Inc.)
• Inventors: Allen, Gerald J., Philo, Roger D.
• Primary Examiner(s): Kepplinger, Esther M.
• Application Number:
  US07/020,462
• Time in Patent Office: 1,884 Days
• Field of Search: 435/7, 435/14, 435/18, 435/19, 435/21, 435/810, 435/7.5, 435/7.92, 436/518, 436/536, 436/538, 436/540, 436/543, 436/544, 436/808, 436/500
• US Class Current: 435/7.5
• CPC Class Codes: G01N 33/548 Carbohydrates, e.g. dextran
• CPC Class Codes: G01N 33/581 with enzyme label (including co-enzymes, co-factors, enzyme inhibitors or substrates)
• CPC Class Codes: G01N 33/76 Human chorionic gonadotropin including luteinising hormone, follicle stimulating hormone, thyroid stimulating hormone or their receptors
• CPC Class Codes: G01N 33/78 Thyroid gland hormones , e.g. T3, T4, TBH, TBG or their receptors
• CPC Class Codes: Y10S 435/973 Simultaneous determination of more than one analyte
• CPC Class Codes: Y10S 435/975 Kit

Abstract

The present invention relates to dual analyte enzyme immunoassays for assaying two antigens in a single liquid sample wherein the two immunoreactions are carried out simultaneously and wherein subsequently the two enzyme reactions occur simultaneously. Suitable enzyme/substrate pairs are beta-galactosidase/nitrophenyl-beta-D-galactoside (p- an/or o-) and alkaline phosphatase/phenolphthalein monophosphate.

Claims

1. A dual analyte immunoassay process for simultaneously determining first and second analyte ligands present in a liquid sample which comprises:

(a) incubating the liquid sample simultaneously with at least one alkaline phosphatase labelled antibody specifically bindable to an epitope of the first analyte ligand and at least one β

-galactosidase labelled antibody specifically bindable to an epitope of the second analyte ligand so as to form corresponding distinctly labelled antibody-ligand complexes in a liquid phase,

(b) separating the distinctly labelled antibody-ligand complexes as a solid phase from the liquid phase,

(c) incubating either the solid phase or the liquid phase simultaneously with both o- or p-nitrophenyl-β

-D-galactoside and phenolphthalein monophosphate, and

(d) simultaneously monitoring the production of o- or p-nitrophenol and phenolphthalein and determining the first and second analyte ligands therefrom.

2. The method of claim 1 wherein step (c) is conducted at a pH between 7 and 10 in the presence of diethanolamine at a concentration of 0.25M to 1M.

3. The method of claim 2 wherein step (c) is conducted at a pH between 8.5 and 8.7.

4. The method of claim 3 wherein step (c) is conducted with 3-10 mM phenolphthalein and about 50 mM p-nitrophenyl-β

-D-galactoside.

5. The method of claim 3 wherein the concentration of o- or p-nitrophenyl-β

-D-galactoside is sufficient to substantially offset inhibition of β

-galactosidase by the diethanolamine.

6. The method of claim 5 wherein the monitoring of step (d) comprises simultaneously measuring absorbance at about 404 nm and about 554 nm.

7. The method of claim 1 wherein the incubation step (a) additionally comprises unlabelled antibodies specifically bindable to a different epitope of the first analyte ligand and unlabelled antibodies specifically bindable to a different epitope of the second analyte ligand, each of said unlabelled antibodies being conjugated to a reagent X which is a hapten, avidin, or biotin, and wherein the solid phase of separating step (b) comprises a specific binding partner for reagent X.

8. The method of claim 7 wherein step (c) is conducted at a pH between 8.5 and 8.7 in the presence of diethanolamine at a concentration of 0.25M to 1M.

9. The method of claim 8 wherein reagent X is FITC and the specific binding partner for reagent X is an anti-FITC antibody.

10. A dual analyte immunoassay process for simultaneously determining first and second analyte ligands present in a liquid sample which comprises:

(a) incubating the liquid sample simultaneously with a ligand analogue of the first analyte ligand, a ligand analogue of the second analyte ligand, at least one alkaline phosphatase labelled antibody specifically bindable to an epitope of the first analyte ligand and ligand analogue, and at least one β

-galactosidase labelled antibody specifically bindable to an epitope of the second analyte ligand and ligand analogue so as to form corresponding distinctly labelled antibody-ligand and antibody-ligand analogue complexes in a liquid phase,

(b) separating the distinctly labelled antibody-ligand analogue complexes as a solid phase from the liquid phase,

(c) incubating either the solid phase or the liquid phase simultaneously with both o- or p-nitrophenyl-β

-d-galactoside and phenolphthalein monophosphate, and

(d) simultaneously monitoring the production of o- or p-nitrophenol and phenolphthalein and determining the first and second analyte ligands therefrom.

11. The method of claim 10 wherein step (c) is conducted at a pH between 7 and 10 in the presence of diethanolamine at a concentration of 0.25M to 1M.

12. The method of claim 11 wherein step (c) is conducted at a pH between 8.5 and 8.7.

13. The method of claim 12 wherein step (c) is conducted with 3-10 mM phenolphthalein and about 50 mM p-nitrophenyl-β

-D-galactoside.

14. The method of claim 12 wherein the concentration of o- or p-nitrophenyl-β

-D-galactoside is sufficient to substantially offset inhibition of β

-galactosidase by the diethanolamine.

15. The method of claim 14 wherein the monitoring of step (d) comprises simultaneously measuring absorbance at about 404 nm and about 554 nm.

16. The method of claim 15 wherein each of the ligand analogues is conjugated to a reagent X which is a hapten, avidin, or biotin, and wherein the solid phase of separating step (b) comprises a specific binding partner for reagent X.

17. The method of claim 16 wherein reagent X is FITC and the specific binding partner for reagent X is an anti-FITC antibody.

18. A dual analyte immunoassay process for simultaneously determining first and second analyte ligands present in a liquid sample which comprises:

(a) incubating the liquid sample simultaneously with a ligand analogue of the first analyte ligand, unlabelled antibody specifically bindable to an epitope of the second analyte ligand, at least one first enzyme labelled antibody specifically bindable to an epitope of the first analyte ligand and ligand analogue, and at least one second enzyme labelled antibody specifically bindable to a different epitope of the second analyte ligand, wherein one of said first and second enzyme labels is alkaline phosphatase and the other is β

-galactosidase, so as to form corresponding distinctly labelled antibody-ligand, antibody-ligand analogue, and antibody-ligand-unlabelled antibody complexes in a liquid phase,

(b) separating the distinctly labelled antibody-ligand analogue and antibody-ligand-unlabelled antibody complexes as a solid phase from the liquid phase,

(c) incubating either the solid phase or the liquid phase simultaneously with both o- or p-nitrophenyl-β

-D-galactoside and phenolphthalein monophosphate, and

(d) simultaneously monitoring the production of o- or p-nitrophenol and phenolphthalein and determining the first and second analyte ligands therefrom.

19. The method of claim 18 wherein step (c) is conducted at a pH between 7 and 10 in the presence of diethanolamine at a concentration of 0.25M to 1M.

20. The method of claim 19 wherein step (c) is conducted at a pH between 8.5 and 8.7.

21. The method of claim 20 wherein step (c) is conducted with 3-10 mM phenolphthalein and about 50 mM p-nitrophenyl-β

-D-galactoside.

22. The method of claim 20 wherein the concentration of o- or p-nitrophenyl-β

-D-galactoside is sufficient to substantially offset inhibition of β

-galactosidase by the diethanolamine.

23. The method of claim 22 wherein the monitoring of step (d) comprises simultaneously measuring absorbance at about 404 nm and about 554 nm.

24. The method of claim 23 wherein each of the ligand analogue and the unlabelled antibody is conjugated to a reagent X which is a hapten, avidin, or biotin, and wherein the solid phase of separating step (b) comprises a specific binding partner for reagent X.

25. The method of claim 24 wherein reagent X is FITC and the specific binding partner for reagent X is anti-FITC antibody.

26. A dual analyte immunoassay reagent kit for the simultaneous assay of first and second analytes present in a liquid sample comprising, as separate kit components:

(a) a reagent solution comprising a mixture of (i) at least one alkaline phosphatase labelled antibody specifically bindable to an epitope of the first analyte ligand, (ii) at least one β

-galactosidase labelled antibody specifically bindable to an epitope of the second analyte ligand, (iii) either unlabelled antibody specifically bindable to a different epitope of the first analyte ligand or a ligand analogue to the first analyte ligand, and (iv) either unlabelled antibody specifically bindable to a different epitope of the second analyte ligand or a ligand analogue to the second analyte ligand, each of said unlabelled antibodies or ligand analogues being conjugated to a reagent X wherein X is which is a hapten, avidin, or biotin;

(b) a solid phase support bound to a specific binding partner for reagent X; and

(c) a buffered reagent solution comprising a mixture of o- or p-nitrophenyl-β

-D-galactoside and phenolphthalein monophosphate.

27. The reagent kit of claim 26 wherein component (c) is at a pH between 8.5 and 8.7.

28. The reagent kit of claim 27 wherein component (c) additionally comprises diethanolamine at a concentration of 0.25M to 1M.