FMN-Labeled specific binding assay
First Claim
1. A homogeneous specific binding assay method for determining a ligand in a liquid medium, comprising the steps of:
- forming a reaction mixture by contacting said liquid medium with(a) reagent means including a labeled conjugate comprising, as label component, flavin mononucleotide coupled to a binding component, such contact producing a binding reaction system in which a bound-species and a free-species of said labeled conjugate are formed, the proportion of the flavin mononucleotide label component in said two formed species being a function of the presence of said ligand in said liquid medium, and(b) an apoenzyme selected from the group consisting of apocytochrome reductase, apoNADPH;
oxidoreductase and apopyridoxine phosphate oxidase, the ability of the flavin mononucleotide label component to combine with the apoenzyme to produce a holoenzyme being different in activity in said two formed species, anddetermining the proportion of the flavin mononucleotide label component in said two formed species by measuring holoenzyme activity in said reaction mixture.
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Abstract
A specific binding assay for determining a ligand in a liquid medium employing an organic prosthetic group residue, such as a residue of flavin adenine dinucleotide, flavin mononucleotide, or heme, as a label component in the labeled conjugate. Preferably, the label component is the prosthetic group residue alone or is a holoenzyme residue comprising such prosthetic group residue combined with an apoenzyme in the form of a holoenzyme complex. In the former case, the label component preferably is monitored in the assay by adding an apoenzyme after the binding reaction has been initiated and measuring the resultant holoenzyme activity. In the latter case, the label component is monitored simply by measuring holoenzyme activity. The assay method may follow conventional homogeneous and heterogeneous schemes. Preferred apoenzymes for use in the assay are apoglucose oxidase and apoperoxidase. The assay offers the advantages of colorimetric read-out and of being readily adaptable to automated techniques. Also disclosed are prosthetic group-labeled and enzyme-labeled conjugates for use in the assay, as well as a method for preparing the latter conjugates.
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Citations
16 Claims
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1. A homogeneous specific binding assay method for determining a ligand in a liquid medium, comprising the steps of:
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forming a reaction mixture by contacting said liquid medium with (a) reagent means including a labeled conjugate comprising, as label component, flavin mononucleotide coupled to a binding component, such contact producing a binding reaction system in which a bound-species and a free-species of said labeled conjugate are formed, the proportion of the flavin mononucleotide label component in said two formed species being a function of the presence of said ligand in said liquid medium, and (b) an apoenzyme selected from the group consisting of apocytochrome reductase, apoNADPH;
oxidoreductase and apopyridoxine phosphate oxidase, the ability of the flavin mononucleotide label component to combine with the apoenzyme to produce a holoenzyme being different in activity in said two formed species, anddetermining the proportion of the flavin mononucleotide label component in said two formed species by measuring holoenzyme activity in said reaction mixture. - View Dependent Claims (2, 3, 4, 5)
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6. A homogeneous specific binding assay method for determining a ligand in a liquid medium, comprising the steps of:
forming a reaction mixture by combining said liquid medium with reagent means including (1) a labeled conjugate comprising, as label component, flavin mononucleotide coupled to said ligand or a binding analog thereof, (2) a specific binding partner of said ligand, and (3) an apoenzyme selected from the group consisting of apocytochrome reductase, apoNADPH;
oxidoreductase, and apopyridoxine phosphate oxidase, wherein the binding by said binding partner of said ligand or analog thereof in said labeled conjugate inhibits the ability of the flavin mononucleotide label component to combine with the apoenzyme to produce a holoenzyme; and
measuring the resulting holoenzyme activity in said reaction mixture.- View Dependent Claims (7, 8, 9, 10)
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11. In a reagent means for determining a ligand in a liquid medium,
which means comprises the reagents of a binding reaction system, including a conjugate having a label component and a binding component, in which reaction system upon contact with said liquid medium are formed a bound-species and a free-species of said labeled conjugate, the proportion of said label component in said two formed species being a function of the presence of said ligand in said liquid medium, the improvement wherein said label component comprises flavin mononucleotide and said means includes an apoenzyme selected from the group consisting of apocytochrome reductase, apoNADPH: - oxidoreductase, and apopyridoxine phosphate oxidase, which combines with the flavin mononucleotide label component to produce a holoenzyme.
- View Dependent Claims (12, 13)
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14. A test kit for determining a ligand in a liquid medium, comprising,
(1) a labeled conjugate comprising, as label component, flavin mononucleotide coupled to said ligand or a binding analog thereof, (2) a specific binding partner of said ligand, and (3) an apoenzyme selected from the group consisting of apocytochrome reductase, apoNADPH: - oxidoreductase, and apopyridoxine phosphate oxidase, which combines with the flavin mononucleotide label component to produce a holoenzyme wherein the binding partner, the conjugate, and the apoenzyme are present in amounts sufficient to detect the ligand.
- View Dependent Claims (15, 16)
Specification