Method for detection of nucleic acid using total internal reflectance

• US 5,585,242 A
• Filed: 08/31/1995
• Issued: 12/17/1996
• Est. Priority Date: 04/06/1992
• Status: Expired due to Term

• Current Assignee: Abbott Laboratories Incorporated
• Original Assignee: Abbott Laboratories Incorporated
• Inventors: Khalil, Omar S., Pabich, Edward K., Bouma, Stanley R.
• Primary Examiner(s): ARTHUR, LISA BENNETT
• Application Number:
  US08/522,623
• Time in Patent Office: 474 Days
• Field of Search: 435/6, 435/91.2, 435/288, 435/7.1, 435/7.2, 435/7.21, 435/7.32, 935/77, 935/78
• US Class Current: 435/6.12
• CPC Class Codes: B01L 7/52 with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples amplification or hybridisation processes per se C12Q1/68; controlling sequential reactions for synthesis B01J19/0046
• CPC Class Codes: C12Q 1/6813 Hybridisation assays
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/6862 Ligase chain reaction [LCR]
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2565/537 characterised by the capture oligonucleotide acting as a primer
• CPC Class Codes: C12Q 2565/549 characterised by the capture oligonucleotide being a reporter labelled capture oligonucleotide
• CPC Class Codes: G01N 2021/6484 Optical fibres
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence

Abstract

An apparatus and method for detecting amplified target nucleic acid is provided wherein the presence and concentration of amplified target is determined by total internal reflection over the course of the amplification reaction. A method and apparatus for detecting target nucleic acid is also provided wherein the presence and concentration of target is determined by total internal reflection and coupling of the target to the TIR element by scissile linkage. An improved immunoassay using total internal reflection and differential temperature cycling is further provided.

Claims

1. A method of detecting amplified target nucleic acid using total internal reflection, comprising the steps

providing a closed static-volumetric reaction vessel having disposed therein (a) reaction sample, containing the target nucleic acid, (b) a total internal reflection (TIR) element, (c) a plurality of members of at least one initiator sequence set and reagents for producing amplification of target nucleic acid present in the reaction sample, (d) label means which is coupled to a fluorophore, and (e) capture means for bringing said fluorophore within the penetration depth of said element, wherein said label means or said capture means is specific for said target nucleic acid;

producing an evanescent electromagnetic wave in the TIR element which penetrates into the reaction sample adjacent the element and has an associated penetration depth;

reacting the reaction sample, the members of said initiator sequence set and amplification reagents under conditions sufficient to amplify target nucleic acid present in the reaction sample to produce amplification products wherein said amplification products are labeled with said label means during amplification or said amplification products are labeled with said labels means by contacting said amplification products with a specific binding member attached to a label;

capturing said label amplification products within the penetration depth as a function of the presence or amount of target nucleic acid; and

detecting within the TIR element a change in fluorescence as a measure of target nucleic acid to thereby amplify and detect said target sequence in said closed static-volumetric reaction vessel.

2. The method of claim 1 wherein at least one member of the initiator sequence set is coupled to a specific binding member which serves also as the capture means or label means.

3. The method of claim 2 wherein said specific binding member comprises a hapten and either the capture means further comprises antihapten antibody immobilized on the element, or the label means further comprises antihapten conjugated to a fluorophore.

4. The method of claim 2 wherein said specific binding member comprises a polynucleotide tail and either the capture means further comprises a complementary polynucleotide tail immobilized on the element, or the label means further comprises a complementary polynucleotide tail conjugated to a fluorophore.

5. The method of claim 1 wherein at least one member of the initiator sequence set is coupled to the TIR element by covalent bonding.

6. The method of claim 5 wherein said at least one member of an initiator sequence set is coupled to the TIR element via a spacer molecule.

7. The method of claim 1 wherein a capture probe complementary to a portion of the amplified target is immobilized on said TIR element.

8. The method of claim 1 wherein the reaction sample, initiator sequence sets and amplification reagents are reacted under thermal cycling conditions.

9. The method of claim 8 wherein the amplification reagents include an enzymatic agent that induces amplification, said enzymatic agent selected from thermostable DNA polymerase, thermostable DNA ligase or a combination thereof.

10. The method of claim 9 wherein the target nucleic acid present in the reaction sample is amplified by polymerase chain reaction or ligase chain reaction.

11. The method of claim 1 wherein the reaction sample, initiator sequence sets and amplification reagents are reacted under isothermal conditions.

12. The method of claim 1 wherein the step of producing an evanescent wave adjacent to the TIR element comprises directing a beam emitted by an excitation source onto the TIR element and totally internally reflecting the beam in the TIR element.

13. A method of detecting target nucleic acid in a reaction vessel using total internal reflection, comprising the steps of:

providing a closed static-volumetric reaction vessel having disposed therein (a) a reaction sample, (b) a total internal reflection (TIR) element, (c) a plurality of members of an initiator sequence, each sequence comprising a capture segment linked to a label segment by a scissile linkage, wherein said initiator includes a portion of nucleotide sequences which are capable of hybridizing with the target nucleic acid, and wherein said label segment is coupled to a fluorophore, and (d) means for cleaving the scissile linkage when target is hybridized to the initiator;

producing an evanescent electromagnetic wave in the TIR element which penetrates into the reaction sample adjacent the element and has an associated penetration depth, and detecting in the TIR element the fluorescence resulting from the linked fluorophore present within the penetration depth;

reacting the reaction sample, initiator sequences and means for cleaving under conditions sufficient to (a) hybridize target nucleic acid present in the reaction sample to the initiator sequences, and (b), in the presence of target, cleave the scissile linkage, thereby freeing the fluorophore from the penetration depth; and

detecting in the TIR element a change in fluorescence as a measure of target nucleic acid to thereby react and detect said target nucleic acid in said closed static-volumetric reaction vessel.