Homogenous affinity assay for quantitative drug and metabolite determination

• US 5,814,449 A
• Filed: 05/28/1996
• Issued: 09/29/1998
• Est. Priority Date: 05/28/1996
• Status: Expired due to Fees

• Current Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Original Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Inventors: Ballerstadt, Ralph, Schultz, Jerome S.
• Primary Examiner(s): Chin, Christopher L.
• Application Number:
  US08/653,844
• Time in Patent Office: 854 Days
• Field of Search: 422/55, 422/58, 422/82.07, 422/82.08, 422/82.09, 435/7.1, 435/7.8, 435/7.93, 435/7.94, 435/7.95, 435/288.5, 435/295.3, 435/968, 435/6, 435/287.1, 435/287.2, 435/288.7, 435/808, 204/415, 436/536, 436/537, 436/764, 436/765, 436/172, 436/800, 436/805, 436/518
• US Class Current: 435/6.11
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/66 involving blood sugars, e.g. galactose
• CPC Class Codes: Y10S 435/808 Optical sensing apparatus
• CPC Class Codes: Y10S 435/968 High energy substrates, e.g. fluorescent, chemiluminescent, radioactive
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

A homogenous affinity assay method, and sensor using such method, for the detection and measurement of analytes that uses an unmodified polyvalent receptor-bearing molecule and having a receptor with at least two binding sites that has an affinity for an analyte of interest, and two groups of molecules wherein one group of molecules is labeled with a molecule capable of generating a measurable response when in close proximity to a label molecule on the other group of molecules. In one embodiment, the groups of molecules also have grafted on them an analog to the analyte of interest. In the absence of the analyte of interest, members of the molecule groups are brought in close proximity to each other through affinity binding to receptor-bearing molecule. This affinity binding results in the formation of a binding complex consisting of members of the first and second groups of molecules and receptors and which results in a response between the labels on the molecules which is capable of measurement. In the presence of the analyte of interest, the binding complexes dissociate due to competitive replacement of the analog with the analyte of interest and affinity binding of the analyte of interest to at least one of the binding sites on the receptors and the labels on the molecules interact in inverse proportion the concentration of the analyte of interest. In another embodiment, the receptor is the analyte of interest and the formation of the binding complexes is a measure of the analyte of interest.

Claims

1. A homogenous affinity assay method for the detection and measurement of an analyte of interest comprising:

A. Providing;

i. an unmodified polyvalent receptor-bearing molecule having a receptor with at least two binding sites that have an affinity for the analyte of interest;

ii. a first group of molecules grafted with an analog to the analyte of interest labeled with a first label molecule which generates a measurable response when in close proximity to a second label molecule wherein said first label molecule is attached to at least one site on each member of said first group of molecules; and

iii. a second group of molecules grafted with said analog and labeled with said second label molecule, which said second label molecule is attached to at least one site on each member of said second group of molecules;

B. Exposing a sample suspected of containing the analyte of interest to said unmodified receptor and said first and second groups of molecules, wherein in the absence of the analyte of interest, members of said first group of molecules and members of said second group of molecules are brought in close proximity through affinity binding of said members of said first and second groups of molecules to said receptors which results in the formation of a binding complex, said binding complex consisting of said members of said first and second groups of molecules and said receptors, and which results in said response between said first label and said second label, said response being a change in the physicochemical properties of said first label molecule when it is in close proximity to said second label molecule;

wherein in the presence of the analyte of interest, said binding complexes dissociate or do not form due to competitive replacement or interaction of said analog with the analyte of interest and affinity binding of the analyte of interest to at least one said binding site on said receptors;

wherein said dissociation or said failure to form said binding complexes is in proportion to the concentration of the analyte of interest;

wherein said dissociation or said failure to form said binding complexes affects the magnitude of said response; and

wherein said response is conducted in the presence of a sensor which detects and measures said response, and which sensor detects and measures said response between said members of said first and second groups of molecules;

C. Detecting and measuring said response with a sensor to determine the presence and amount of the analyte of interest.

2. A method according to claim 1, wherein said first label is a fluorochrome with an emission spectrum and said second label is a fluorochrome with a fluorescence absorption spectrum that overlaps with said emission spectrum and said response is a transfer of energy that changes the intensity of light emitted by said first label.

3. A method according to claim 1, wherein said first label is a fluorochrome with an emission spectrum and said second label is a dye with a fluorescence absorption spectrum that overlaps with said emission spectrum and said response is a transfer of energy that changes the intensity of light emitted by said first label.

4. A method according to claim 1 wherein said receptor is a lectin, an antibody, a nucleic acid or a membrane receptor.

5. A method according to claim 1, wherein said sensor has a chamber which includes a semipermeable dialysis membrane and said receptor, said members of said first and second molecule groups are placed in said chamber, wherein said dialysis membrane is permeable to the analyte of interest but is not permeable to said receptor and said members of said first and second molecule groups, and wherein said sensor measures said response between members of said first and second molecule groups in said chamber.

6. A method according to claim 1, wherein said sensor is a device which consists of a sample holder and a detector, wherein said sample holder contains a mixture of said members of said first and second group of molecules.

7. A method according to claim 1, wherein said first and second label molecules exist on a multiplicity of sites on each member of the first and second molecule groups, respectively.

8. A method according to claim 1, wherein said first label is a radioactive beta emitter and said second label is a dye with a fluorescence absorption spectrum that interacts with said beta emitter and said response is the level of radioactivity emitted by said first label.

9. An affinity sensor comprising:

A. an unmodified polyvalent receptor-bearing molecule having at least two binding sites that have an affinity for an analyte of interest, wherein said binding sites are on either one receptor or a plurality of receptors, and wherein said binding sites are in close proximity to each other;

B. a first group of polymers grafted with an analog to the analyte of interest and labeled with a first label molecule which generates a measurable response when in close proximity to a second label molecule; and

C. a second group of polymers grafted with said analog and labeled with said second label molecule;

D. a chamber having a semipermeable dialysis membrane in which said receptors, said members of said first and second polymer groups are placed, wherein said dialysis membrane is permeable to the analyte of interest but is not permeable to said receptor and said members of said first and second polymer groups;

E. a detector; and

wherein in the absence of the analyte of interest, members of said first group of polymers and members of said second group of polymers are brought in close proximity through affinity binding of said members of said first and second groups of polymers to said receptors which results in the formation of a binding complex, said binding complex consisting of said members of said first and second groups of polymers and said receptors, which affinity binding results in said response between said first label and said second label, said response being a change in the physicochemical properties of said first label molecule when it is in close proximity to said second label molecule, which said reaction is measured;

wherein in the presence of the analyte of interest, said binding complexes dissociate from said receptors due to competitive replacement of said analog with the analyte of interest and affinity binding of the analyte of interest to at least one said binding site on said receptors;

wherein said dissociation is in proportion to the concentration of the analyte of interest;

wherein said dissociation causes a change in the magnitude of said response; and

wherein said detector measures said response between members of said first and second polymer groups in said chamber.

10. A sensor according to claim 9, wherein said first label is a fluorochrome with an emission spectrum and said second label is a fluorochrome or dye with an absorption spectrum that overlaps with said emission spectrum and said response is a transfer of energy that changes the intensity of light emitted by said first label which is measured.

11. A sensor according to claims 9 or 10, wherein said receptor is a lectin, an antibody, a nucleic acid or membrane receptor.

12. A homogenous affinity assay method for the detection and measurement of an analyte of interest comprising:

A. Providing;

i. an unmodified polyvalent receptor-bearing molecule having a receptor with at least two binding sites that have an affinity for the analyte of interest;

ii. a first group of molecules grafted with an analog to the analyte of interest labeled with a first label molecule which generates a measurable response when in close proximity to a second label molecule wherein said first label molecule is attached to at least one site on each member of said first group of molecules; and

iii. a second group of molecules grafted with said analog and labeled with said second label molecule, which said second label molecule is attached to at least one site on each member of said second group of molecules;

B. Exposing a sample suspected of containing the analyte of interest to said unmodified receptor and said first and second groups of molecules, wherein in the absence of the analyte of interest, members of said first group of molecules and members of said second group of molecules are brought in close proximity through affinity binding of said members of said first and second groups of molecules to said receptors which results in the formation of a binding complex, said binding complex consisting of said members of said first and second groups of molecules and said receptors, and which results in said response between said first label and said second label, said response being a change in the physicochemical properties of said first label molecule when it is in close proximity to said second label molecule;

wherein in the presence of the analyte of interest, said binding complexes dissociate or do not form due to competitive replacement or interaction of said analog with the analyte of interest and affinity binding of the analyte of interest to at least one said binding site on said receptors;

wherein said dissociation or said failure to form said binding complexes is in proportion to the concentration of the analyte of interest;

wherein said dissociation or said failure to form said binding complexes affects the magnitude of said response;

wherein said response is conducted in the presence of a sensor which detects and measures said response, and which sensor detects and measures said response between said members of said first and second groups of molecules; and

wherein said first label is a fluorochrome or dye with an emission spectrum and said second label is a fluorochrome or dye with a fluorescence absorption spectrum that overlaps with said emission spectrum and said response is a transfer of energy that changes the intensity of light emitted by said first label; and

C. Detecting and measuring said response with a sensor to determine the presence and amount of the analyte of interest.

13. A method according to claim 12, wherein said sensor is a device having a chamber with a semipermeable dialysis membrane and said receptor, said members of said first and second molecule groups are placed in said chamber, wherein said membrane is permeable to the analyte of interest but is not permeable to said receptor and said members of said first and second molecule groups, and wherein said sensor measures said interaction between members of said first and second molecule groups in said chamber.

14. A method according to claims 12 or 13 wherein the analyte of interest is glucose and said receptor is a mannose specific lectin concanavalin A, and said members of said first group of molecules labelled with said fluorochrome are mannosyldextran.

15. A method according to claims 12 or 13 wherein the analyte of interest is galactose and said receptor is a plant lectin and said members of said first group of molecules labelled with said fluorochrome are lactosyldextrans.

16. A method according to claim 15 wherein said receptor is plant lectin Ricinus communis agglutinin, RCAI.

17. A method according to claim 12 wherein said receptor is a lectin, an antibody, a nucleic acid or a membrane receptor.