Simultaneous calibration heterogeneous immunoassay

• US 4,540,659 A
• Filed: 07/16/1982
• Issued: 09/10/1985
• Est. Priority Date: 04/17/1981
• 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): Kepplinger, Esther M.
• Application Number:
  US06/399,107
• Time in Patent Office: 1,152 Days
• Field of Search: 435/4, 435/7, 435/188, 435/810, 435/805, 436/524, 436/525, 436/527, 436/528, 436/529, 436/531, 436/546, 436/808, 436/810, 436/824, 422/55, 422/56, 422/61
• US Class Current: 435/7.91
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: Y10S 435/966 involving an enzyme system with high turnover rate or complement magnified assay, e.g. multi-enzyme systems
• CPC Class Codes: Y10S 435/967 Standards, controls, materials, e.g. validation studies, buffer systems
• CPC Class Codes: Y10S 436/824 Immunological separation techniques

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) comprising ligand and receptor. By providing a first measurement surface capable of specifically binding a labelled reagent in an amount depending upon the presence of analyte in the sample and a second calibration surface capable of binding a second labeled reagent in a manner unaffected by the presence of analyte in the sample, calibration of individual tests can be accomplished simultaneously with the performance of the test itself. A signal producing system includes an enzyme, a catalyst usually bonded to a mip which defines the first labeled reagent for binding to the measurement surface and the same catalyst conjugated to a ligand capable of binding to the calibration surface. Preferably, both labeled reagents have the same composition and the calibration surface includes anti-(first catalyst).

Claims

1. In a method for determining the presence in a sample of an analyte, which analyte is a member of a specific binding pair ("mip") consisting of ligand and receptor ("antiligand"),

said method employing a signal producing system having at least two enzymes, including one enzyme bound to a mip ("enzyme-bound-mip"), and a solute dye precursor which is catalytically transformed to an insoluble dye by one of said enzymes bound to a mip-containing measurement first surface, said insoluble dye producing a change in a detectable signal at said first surface in proportion to the amount of analyte, where said mip at said first surface provides for binding of enzyme-bound-mip through mip complex formation to said first surface, and contacting of said first surface with said sample and said enzyme-bound-mip results in binding of said enzyme-bound-mip to said first surface in proportion to the amount of analyte in said sample,

the improvement which comprises:

during said contacting, having adjacent to said first surface, a calibration second surface to which anti-enzyme receptor is bound in a predetermined amount and to which enzyme of said enzyme-bound-mip becomes bound through mip complex formation in an amount which provides substantially predetermined ratios to the amount of enzyme-bound-mip bound to said first surface, whereby the ratio of the change in signal at said second surface to the change in signal at said first surface defines the amount of analyte in said sample substantially independent of non-specific factors.

2. In a method for determining the presence in a sample of an analyte, which analyte is a member of a specific binding pair ("mip") consisting of ligand and receptor ("antiligand"),

said method employing a signal producing system having at least two enzymes, including one enzyme bound to a mip ("enzyme-bound-mip"), wherein a second ligand other than the ligand analyte is bonded to said enzyme, and a solute dye precursor which is catalytically transformed to an insoluble dye by one of said enzymes bound to a mip-containing measurement first surface, said insoluble dye producing a change in a detectable signal at said first surface in proportion to the amount of analyte, where said mip at said first surface provides for binding of enzyme-bound-mip through mip complex formation to said first surface, and contacting of said first surface with said sample and said enzyme-bound-mip results in binding of said enzyme-bound-mip to said first surface in proportion to the amount of analyte in said sample,

the improvement which comprises:

during said contacting, having adjacent to said first surface, a calibration second surface to which anti (second ligand) receptor is bound and to which enzyme of said enzyme-bound-mip becomes bound through mip complex formation in an amount which provides substantially predetermined ratios to the amount of enzyme-bound-mip bound to said first surface, whereby the ratio of the change in signal at said second surface to the change in signal at said first surface defines the amount of analyte in said sample substantially independent of non-specific factors.

3. A method according to claim 2, wherein said second ligand is conjugated to an enzyme molecule other than enzyme-bound-mip.

4. A method according to claim 2, wherein said second ligand is conjugated to the same enzyme molecule as said enzyme-bound-mip.