Loop probe hybridization assay for polynucleotide analysis

• US 7,129,048 B2
• Filed: 11/17/2003
• Issued: 10/31/2006
• Est. Priority Date: 03/22/2000
• Status: Expired due to Fees

• Current Assignee: Invitrogen Corp. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Invitrogen Corp. (Thermo Fisher Scientific Incorporated)
• Inventors: Lai, Jennifer, Bruchez, Marcel P., Wong, Edith, Phillips, Vince, Watson, Andrew R.
• Primary Examiner(s): Horlick, Kenneth R.
• Application Number:
  US10/716,063
• Publication Number:
  US 20040171039A1
• Time in Patent Office: 1,079 Days
• Field of Search: 435/6, 435/91.2, 536/24.3
• US Class Current: 435/6.14
• CPC Class Codes: B82Y 10/00 Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
• CPC Class Codes: B82Y 5/00 Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2561/119 Fluorescence polarisation

Abstract

Methods, compositions and articles of manufacture for assaying a sample for a target polynucleotide and/or an amplification product therefrom are provided. The methods comprise contacting a sample suspected of containing the target polynucleotide with a polynucleotide that can bind specifically thereto; this polynucleotide is conjugated to a substrate, preferably an encoded bead conjugate. An amplification reaction can first be used to produce the amplification product from the target polynucleotide so that it can be used to indirectly assay for the target polynucleotide. An amplification product detection complex and method of forming the same are also provided. The methods are particularly useful in multiplex settings where a plurality of targets are present. Amplification product assay complexes and amplification product assay arrays are also provided, along with methods of forming the same. Kits comprising reagents for performing such methods are also provided.

Claims

1. A kit comprising:

a substrate attached to an unlabeled probe polynucleotide comprising first and second complementary regions and a third region located between the first and second complementary regions, wherein the probe polynucleotide can form a stem-loop structure in which the first and second complementary regions hybridize to each other to form a stem and the third region forms a loop, wherein at least a part of the third region is complementary to at least a part of a capture sequence of an amplification product from a target polynucleotide, wherein the unlabeled probe polynucleotide can preferentially hybridize to the amplification product and thereby disrupt formation of the stem-loop structure under at least one set of hybridization conditions;

a reagent for incorporating a label into the amplification product;

a housing for retaining the substrate and the reagent; and

instructions provided with said housing that describe how to use the components of the kit to assay a sample for the amplification product.

2. The kit of claim 1, wherein the reagent is a labeled nucleotide.

3. The kit of claim 1, wherein the reagent is a labeled primer.

4. The kit of claim 1 wherein the substrate is attached to a plurality of different unlabelled probe polynucleotides, wherein each of said different unlabelled probe polynucleotides is attached at an identifiable location on the substrate, wherein each of said different probe polynucleotides can preferentially hybridize to a corresponding different amplification product, each of said corresponding different amplification products comprising a label that can be the same or different as the label on the other corresponding different amplification products, wherein each of said different probe polynucleotides comprises first and second complementary regions and a third region located between the first and second complementary regions, and further wherein each of said different probe polynucleotides can form a stem-loop structure in which, the first and second complementary regions hybridize to each other to form a stem and the third region forms a loop, wherein at least a part of the third region of each of said different probe polynucleotides is complementary to at least a part of its corresponding different amplification product, and wherein each of said different probe polynucleotides can preferentially hybridize to its corresponding different amplification product and thereby disrupt formation of its stem-loop structure under at least one set of hybridization conditions, and wherein said instructions further describe how to use the components of the kit to assay the sample for each of said corresponding different amplification products.