US 4,299,916 AGranted

Preferential signal production on a surface in immunoassays

AssigneeSyva Company

InventorsDavid J. Litman, Edwin F. Ullman

Life of this patent

Estimating the term…

Loading patent…

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.

Claims43

Dependent claims

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.

7 more elements

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.

8 more elements

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.

9 more elements

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.

9 more elements

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.

10 more elements

Dependencies are inferred from the claim text.

Facts

Application: 06/106,620Filed 26 Dec 1979
Granted: 10 Nov 1981
Term ends: Not estimatedThe source records don’t support an estimate.

Classification21 codes

G01N 33/543
Immunoassay; Biospecific binding assay; Materials therefor: with an insoluble carrier for immobilising immunochemicals
G01N 33/52
Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing: use of…
G01N 33/542
With immune complex formed in liquid phase: with steric inhibition or signal modification, e.g. fluorescent quenching
G01N 33/54306
With an insoluble carrier for immobilising immunochemicals: solid-phase reaction mechanisms