Assay procedure using fluorogenic tracers

• US 7,153,654 B2
• Filed: 10/31/2002
• Issued: 12/26/2006
• Est. Priority Date: 07/23/1993
• Status: Expired due to Fees

• Current Assignee: University of Utah Research Foundation (State of Utah)
• Original Assignee: University of Utah Research Foundation (State of Utah)
• Inventors: Wei, Ai-Ping, Herron, James N.
• Primary Examiner(s): FREDMAN, JEFFREY NORMAN
• Application Number:
  US10/286,600
• Publication Number:
  US 20030099999A1
• Time in Patent Office: 1,517 Days
• Field of Search: None
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: G01N 33/582 with fluorescent label

Abstract

Fluorescent energy transfer dyes capable of moving between a more stacked configuration to exhibit fluorescent quenching and a more spaced configuration to exhibit fluorescence can be conjugated to a peptide epitope or nucleic acid for use in the detection of an unknown antibody in bulk solution. The resulting labeled peptide reagent can be used in an immunoassay procedure by placing it in bulk solution along with the unknown antibody to be detected. When the antibody binds to the peptide epitope, the pair of dyes carried by the peptide epitope will have their configuration altered from a stacked to an unstacked configuration and will exhibit a fluorescent increase in response thereto.

Claims

1. An assay procedure for detecting a target strand of DNA, said assay procedure comprising:

providing a detector probe comprising a DNA sequence labeled with two chromophores, one of the two chromophores attached to the 3′

end and the second of the two chromophores attached to the 5′

end of the DNA sequence, wherein the detector probe is capable of moving between a stacked configuration that exhibits fluorescence quenching and a spaced configuration that exhibits fluorescence;

adding the detector probe to a sample potentially containing a target strand of DNA, the configuration of the detector probe moving between the stacked configuration and the spaced configuration upon hybridization of the detector probe to the target strand of DNA; and

detecting the presence or absence of the target strand of DNA by measuring a change in fluorescence in the sample.

2. The assay procedure of claim 1, wherein the fluorescence quenching occurs as a result of physical interaction between the two chromophores.

3. The assay procedure of claim 1, wherein the fluorescence occurs by increasing the distance between the two chromophores upon hybridization of the detector probe to the target strand of DNA.

4. The assay procedure of claim 1, wherein providing a detector probe comprising a DNA sequence comprises providing a detector probe comprising at least one DNA analogue.

5. The assay procedure of claim 1, wherein the stacked configuration occurs by dimerization of the two chromophores.

6. The assay procedure of claim 1, wherein the spaced configuration occurs when the target strand of DNA hybridizes to the DNA sequence of the detector probe.

7. The assay procedure of claim 1, wherein at least one of the chromophores is a fluorophore.

8. The assay procedure of claim 1, wherein the two chromophores are two planar, aromatic fluorophores capable of forming homodimers or heterodimers.

9. The assay procedure of claim 8, wherein the planar, aromatic fluorophores are selected from the group consisting of fluoresceins, rhodamines, cyanines, Texas Red, rhodamine B, and tetramethylrhodamine.

10. The assay procedure of claim 1, wherein providing a detector probe comprising a DNA sequence labeled with two chromophores comprises providing the detector probe immobilized on a solid support.

11. An assay procedure for detecting and quantifying a target strand of DNA, comprising:

providing a detector probe comprising a DNA sequence labeled with a pair of chromophores attached to the 3′ and

5′

ends of the DNA sequence, at least one of the pair of chromophores comprising a fluorophore, wherein the detector probe is capable of moving between a first configuration in which the chromophores physically interact to exhibit fluorescence quenching and a second configuration in which the distance between the chromophores is increased to exhibit fluorescence;

adding the detector probe to a sample potentially containing a target strand of DNA, the configuration of the detector probe shifting between the first configuration and the second configuration upon hybridization of the detector probe to the target strand of DNA;

detecting the presence or absence of the target strand of DNA by measuring changes in fluorescence in the sample; and

quantifying the presence of the target strand of DNA by measuring the changed fluorescence in the sample.

12. An assay procedure for detecting a target strand of DNA, said assay procedure comprising:

providing a detector probe comprising a DNA sequence labeled with two chromophores, one of the two chromophores attached to the 3′

end and the second of the two chromophores attached to the 5′

end of the DNA sequence, wherein the detector probe is capable of moving between a first configuration that exhibits fluorescence quenching and a second configuration that exhibits fluorescence;

adding the detector probe to a sample potentially containing a target strand of DNA, the configuration of the detector probe moving between the first configuration and the second configuration upon hybridization of the detector probe to the target strand of DNA; and

detecting the presence or absence of the target strand of DNA by measuring a change in fluorescence in the sample.