Preferential signal production on a surface in immunoassays

• US 4,299,916 A
• Filed: 12/26/1979
• Issued: 11/10/1981
• Est. Priority Date: 12/26/1979
• Status: Expired due to Term

• Current Assignee: DADE Behring Beteiligungs GmbH (Siemens AG)
• Original Assignee: Syva Co.
• Inventors: Ullman, Edwin F., Litman, David J.
• Primary Examiner(s): Wiseman, Thomas G.
• Application Number:
  US06/106,620
• Time in Patent Office: 685 Days
• Field of Search: 435/6, 435/7, 435/178, 435/179, 435/810, 435/805, 23/230 B, 424/8, 424/12, 252/408 R, 422/56
• US Class Current: 435/6.11
• CPC Class Codes: G01N 33/52 Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements immunological elements G01N33/54386; involving labelled immunochemicals G01N33/58; for haemoglobin or occult blood G01N33/72
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: G01N 33/543 with an insoluble carrier for immobilising immunochemicals
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/581 with enzyme label (including co-enzymes, co-factors, enzyme inhibitors or substrates)
• CPC Class Codes: Y10S 435/805 Test papers
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 435/967 Standards, controls, materials, e.g. validation studies, buffer systems
• CPC Class Codes: Y10S 435/97 Test strip or test slide
• CPC Class Codes: Y10S 435/973 Simultaneous determination of more than one analyte
• CPC Class Codes: Y10S 435/975 Kit
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property
• CPC Class Codes: Y10S 436/808 Automated or kit
• CPC Class Codes: Y10S 436/811 Test for named disease, body condition or organ function
• CPC Class Codes: Y10S 436/815 Test for named compound or class of compounds
• CPC Class Codes: Y10S 436/82 Hepatitis associated antigens and antibodies
• CPC Class Codes: Y10S 436/826 Additives, e.g. buffers, diluents, preservatives

Abstract

An assay method and compositions are provided for determining the presence of an analyte in a sample. The analyte is a member of an immunological pair (mip) of immunogens--ligand and receptor. The method has two basic elements: a solid surface to which one of the members of the immunological pair is bonded and a signal producing system, which includes a catalytic member bonded to a mip, which signal producing system results in a measurable signal on said solid surface related to the amount of analyte in the medium. The signal generating compound is produced without separation of the catalyst labeled mip bound to the solid surface from the catalyst labeled mip free in solution.

In a preferred embodiment, an enzyme is bonded to a mip which acts in conjunction with a solute to produce a signal generating product which binds preferentially to the solid surface when the enzyme is bound to the surface, resulting in a signal which is readily differentiated from signal generating compound produced by the catalyst and solute in the bulk solution.

Claims

1. A method for detecting the presence of an analyte in a sample suspected of containing said analyte, where said analyte is a member of an immunological pair (mip) consisting of ligand and homologous antiligand;

said method involving (1) the partitioning of an enzyme bound to a mip--enzyme-bound-mip--between a surface and a liquid phase, where said partitioning is through the intermediacy of ligand-antiligand binding to a mip-bound-surface in relation to the amount of analyte in said sample;

, said surface being porous and permitting approach and binding of enzyme-bound-mip to mip of said mip-bound-surface, either directly or in combination with said ligand and (2) the change in intensity of a detectible signal from a surface resulting from the change in concentration of a signal generating compound associated with said surface, said change in intensity being related to the amount of reaction product produced by said enzyme bound to said surface;

said method comprising;

(a) combining in an aqueous assay medium;

(1) said sample;

(2) mip-bound-surface, substantially immersed in said medium wherein substantially all of said mip-bound-surface is uniformly contacted with said sample in said medium;

(3) enzyme-bound-mip; and

(4) the remaining members of the signal producing system, which system includes at least a second enzyme other than said enzyme-bound-mip, wherein the product of one enzyme is the substrate of the other enzyme, and a solute which is capable of undergoing a catalyzed reaction to produce a product which results in a change in amount of a signal generating compound associated with said surface and capable of producing a detectible signal,

(b) waiting a sufficient time for enzyme-bound-mip to diffuse to said surface and at least a portion of said enzyme-bound-mip to bind to said surface through the intermediacy of ligand-antiligand binding and for a change in the amount of signal generating compound associated with said surface in relation to the amount of analyte in said sample;

(c) determining the intensity of said detectible signal at said surface as a function of the amount of analyte in said sample.

2. A method according to claim 1, wherein the product of said second enzyme is the substrate of said enzyme-bound-mip.

3. A method according to any one of claims 1 or 2, where said signal generating compound is an insoluble dye produced by desolubilization of a soluble precursor.

4. A method according to any one of claims 1 or 2, where said second enzyme is bound to said surface.

5. A method according to any one of claims 1 or 2, where a scavenger is included in the signal producing system which reacts with a component of said signal producing system to inhibit operation of said signal producing system in said liquid phase.

6. A method according to claim 1, wherein the concentration ratio in the void volume of said surface, at the maximum concentration of analyte, of enzyme-bound-mip unbound to said surface to enzyme-bound-mip bound to said surface is not greater than about 10:

1.

7. A method according to claim 1, wherein said sample and mip-bound-surface are combined and said mip-bound-surface to which analyte has bound separated from said sample prior to combining with said signal producing system.

8. A method for detecting an haptenic ligand analyte in a sample suspected of containing said analyte, where said analyte is a member of an immunological pair (mip) consisting of haptenic ligand and homologous antiligand;

said method involving (1) the partitioning of an enzyme catalyst bound to a haptenic ligand--enzyme-bound-haptenic ligand--between a surface and a liquid phase, where said partitioning is through the intermediacy of ligand-antiligand binding to an antiligand-bound-surface, said surface being porous and permitting approach and binding of enzyme-bound-haptenic ligand to antiligand of said antiligand-bound-surface, where said partitioning is in relation to the amount of haptenic ligand analyte in said sample; and

(2) the change in concentration of a signal generating compound associated with said surface, where said signal generating compound is an insoluble dye produced as a product of said enzyme of said enzyme-bound-haptenic ligand, said change in concentration being in relation to the amount of insoluble dye produced by said enzyme bound to said surface;

said method comprising, combining in an aqueous assay medium

(1) said sample;

(2) antiligand-bound-surface substantially immersed in said medium and wherein substantially all of said antiligand-bound-surface is uniformly contacted with said sample in said medium;

(3) enzyme-bound-haptenic ligand; and

(4) the remaining members of the signal producing system, which system includes at least a second enzyme other than said enzyme-bound-haptenic ligand, wherein the product of one enzyme is the substrate of the other enzyme, and one or more enzyme substrates which include a leuco dye or source of leuco dye which is capable of undergoing an enzyme catalyzed reaction to produce an insoluble dye which precipitates on said surface,

(b) waiting a sufficient time for enzyme-bound-haptenic ligand to diffuse to said surface and said enzyme-bound-haptenic ligand to bind to said surface through the intermediacy of ligand-antiligand binding and for a change to occur in the amount of said insoluble dye associated with said surface in relation to the amount of haptenic ligand in said sample; and

(c) determining the amount of detectible signal at said surface from said insoluble dye as a function of the amount of haptenic ligand in said sample.

9. A method according to claim 8, wherein said second enzyme reacts with a solute to produce a product which is said leuco dye and which is a substrate for said enzyme of said enzyme-bound-haptenic ligand.

10. A method according to any of claims 8 or 9, wherein said haptenic ligand is a hormone.

11. A method according to any of claims 8 or 9, wherein said haptenic ligand is an analgesic.

12. A method according to any of claims 8 or 9, wherein said haptenic ligand is an aralkyl amine.

13. A method according to any of claims 8 to 9, wherein said haptenic ligand is a steroid.

14. A method according to any of claims 8 or 9, wherein said haptenic ligand is a heterocyclic drug.

15. A method according to any of claims 8 or 9, wherein said haptenic ligand is a thyroid hormone.

16. A method according to any of claims 8 or 9, wherein said haptenic ligand is an antibiotic.

17. A method according to any of claims 8 or 9, wherein said haptenic ligand is tetrahydrocannabinol or derivative thereof.

18. A method for detecting the presence of a polyepitopic antigenic analyte in a sample suspected of containing said analyte, where said antigenic analyte is a member of an immunological pair (mip) consisting of ligand and homologous antiligand;

said method involving (1) the partitioning of an enzyme catalyst bound to a mip--enzyme-bound-mip--between a surface and a liquid phase, said surface being porous and permitting approach and binding of enzyme-bound-mip to mip of said mip-bound-surface, either directly or in combination with said ligand, where said partitioning is through the intermediacy of ligand-antiligand binding to a mip-bound-surface in relation to the amount of analyte in said sample; and

(2) measuring the change in concentration of a signal generating compound associated with said surface, where said signal generating compound is an insoluble dye, said change in concentration being in proportion to the amount of insolable dye produced by said enzyme bound to said surface;

said method comprising;

(a) combining in an aqueous assay medium,

(1) said sample;

(2) mip-bound-surface substantially immersed in said medium, wherein substantially all of said mip-bound-surface is uniformly contacted with said sample;

(3) enzyme-bound-mip, wherein one of the mips of said mip-bound-surface and enzyme-bound mip is antiligand; and

(4) remaining members of said signal producing system, which system includes at least a second enzyme other than said enzyme-bound-mip, wherein the product of one enzyme is the substrate of the other enzyme, and wherein the enzyme catalyzed reaction of said enzyme-bound-mip results in the production of an insoluble dye as the signal generating compound, which precipitates onto said surface through the intermediacy of ligand-antiligand binding,

(b) waiting a sufficient time for enzyme-bound-mip to diffuse to said surface and said enzyme-bound-mip to bind to said surface through the intermediacy of ligand-antiligand binding and for a change in the amount of signal generating compound associated with said surface in relation to the amount of analyte in said sample; and

(c) determining the amount of detectible signal at said surface as a function of the amount of analyte in said sample.

19. A method according to claim 18, wherein said mip of said enzyme-bound-mip and said mip-bound-surface are both antiligand.

20. A method according to claim 18, wherein said second enzyme reacts with a solute to produce a product which is a substrate of said enzyme of said enzyme-bound-mip.

21. A method according to any of claims 18 or 19, wherein said antigenic ligand is an immunoglobulin.

22. A method according to any of claims 18 or 19, wherein said antigenic ligand is a surface antigen.

23. A method according to claim 22, wherein said surface antigen is a bacterial surface antigen.

24. A method according to claim 22, wherein said surface antigen is a viral antigen.

25. A method according to any of claims 18 or 19, wherein said antigenic ligand is a complement factor.

26. A method according to any of claims 18 or 19, wherein said antigenic ligand is a hormone.

27. A method according to claim 20, wherein at least one of said enzymes is an oxidoreductase.

28. A method according to claim 20, wherein at least one of said enzymes is a hydrolase.

29. A method according to claim 18, wherein said sample and mip-bound-surface are combined and said mip-bound-surface to which said analyte has bound separated from said sample prior to combining with said signal producing system.

30. A method for detecting the presence of a ligand analyte in a sample suspected of containing said analyte, where said ligand analyte is a member of an immunological pair (mip) consisting of ligand and homologous antiligand;

said method involving (1) the partitioning of an enzyme bound to a mip--enzyme-bound-mip--between a surface and a liquid phase, said surface being porous and permitting approach and binding of enzyme-bound-mip to mip of said mip-bound-surface, either directly or in combination with said ligand, where said partitioning is through the intermediacy of ligand-antiligand binding to a mip-bound-surface in relation to the amount of analyte in said sample; and

(2) the change in concentration of a signal generating compound associated with such surface, said change in concentration being in relation to the amount of reaction product produced by said enzyme bound to said surface;

said method comprising

(a) combining in an aqueous assay medium,

(1) said sample;

(2) mip-bound-surface substantially completely immersed in said sample, wherein substantially all of said mip-bound-surface is uniformly contacted with said sample; and

(3) enzyme-bound-mip;

(b) incubating said mixture for a time sufficient to allow enzyme-bound-mip to bind to said surface through the intermediacy of ligand-antiligand binding in an amount proportional to the amount of analyte in said sample;

(c) after said sufficient time, and without separation of said surface from said aqueous assay medium, adding remaining components of said signal producing system, where components of said signal producing system include the enzyme of said enzyme-bound-mip and a second enzyme and a solute which is capable of undergoing a catalyzed reaction to produce a product which results in the formation of an insoluble dye associated with said surface, the amount of dye associated with said surface being related to the amount of enzyme-bound-mip bound to said surface; and

(d) determining the amount of detectible signal from said insoluble dye at said surface as a function of the amount of analyte in said sample.

31. A method according to claim 30, wherein said second enzyme is bonded to said surface and catalyzes a reaction of said solute to produce a product which is the substrate of said enzyme of said enzyme-bound-mip.

32. A method according to claim 31, wherein said second enzyme is glucose oxidase, said solute is glucose and said enzyme of said enzyme-bound-mip is horse radish peroxidase.

33. A method according to any of claims 30, 31 or 32, wherein said analyte is a hapten, said mip of said enzyme bound mip is a ligand, and said mip of said mip-bound-surface is antiligand.

34. A method according to any of claims 30, 31, or 32, wherein said analyte is a polyepitopic antigen, said mip of said enzyme-bound-mip is antiligand and said mip of said mip-bound-surface is antiligand.

35. A method for detecting the presence of a ligand analyte in a sample suspected of containing said ligand where said ligand is a member of an immunological pair (mip) consisting of ligand and homologous antiligand;

said method involving (1) the partitioning of an enzyme bound to a mip--enzyme-bound-mip--between a surface and a liquid phase, said surface being porous and permitting approach and binding of enzyme-bound-mip to mip of said mip-bound-surface, either directly or in combination with said ligand, where said partitioning is through the intermediacy of ligand-antiligand binding to a mip-bound-surface in relation to the amount of analyte in said sample; and

(2) the change in concentration of a signal generating compound associated with said surface, where said signal generating compound is an insoluble dye, said change in concentration being in relation to the amount of insoluble dye produced by said enzyme bound to said surface

said method comprising;

(a) combining in an aqueous assay medium,

(1) said sample;

(2) mip-bound-surface, wherein said mip-bound-surface is immersed in said medium and is substantially uniformly contacted with said sample;

(b) incubating for sufficient time for ligand analyte to bind to said mip-bound-surface;

(c) after sufficient time for said incubation, adding substantially concurrently enzyme-bound-mip; and

(d) remaining members of said signal producing system, which system includes at least said enzyme of said enzyme-bound-mip, a second enzyme and a solute which is capable of undergoing a catalyzed reaction to produce a product which results in the formation of a signal generating compound, which is an insoluble dye capable of producing a detectible signal, wherein the product of one enzyme is the substrate of the other enzyme

(e) incubating for sufficient time for enzyme-bound-mip to diffuse to said surface and for said insoluble dye to precipitate on said surface in proportion to the amount of analyte in said sample; and

(f) determining the amount of said detectible signal on said surface as a function of the amount of analyte in said sample.

36. A method according to claim 35, wherein said mip-bound-surface to which said ligand analyte has bound is separated from said sample prior to adding said signal producing system.

37. A method according to claim 35, wherein said solute is the substrate of said second enzyme which results in the formation of a product which is the substrate of said enzyme of said enzyme-bound-mip.

38. A method according to claim 36, wherein said second enzyme is glucose oxidase and said enzyme-bound-mip is horse radish peroxidase.

39. A method according to claim 36, wherein said signal producing system includes a scavenger in the liquid medium which reacts with a component of said signal producing system to inhibit operation of said signal producing system in said liquid phase.

40. A method according to claim 39, wherein said scavenger is an enzyme which reacts with an intermediate product of said signal producing system.

41. A method according to claim 35, wherein said analyte is a hapten.

42. A method according to claim 35, wherein said analyte is a polyepitopic antigen.

43. A kit for use in an immunoassay comprising in combination a member of an immunological pair, an enzyme bound to an insoluble surface, an enzyme bound to a member of an immunological pair, and a leuco dye which undergoes an enzymatically catalyzed reaction to produce an insoluble dye capable of binding to said surface, wherein the amount of enzyme bound to said member of an immunological pair is related to the amount of said member of an immunological pair bound to an insoluble surface in an amount to substantially optimize the sensitivity of said immunoassay.