ISOTHERMAL DETECTION METHODS AND USES THEREOF

• US 20110020819A1
• Filed: 01/08/2009
• Published: 01/27/2011
• Est. Priority Date: 01/08/2008
• Status: Abandoned Application

• Current Assignee: Zygem Corporation Ltd.
• Original Assignee: Zygem Corporation Ltd.
• Inventors: Saul, David James, Payne, Leo Samuel
• Application Number:
  US12/812,202
• Publication Number:
  US 20110020819A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6865 Promoter-based amplification, e.g. nucleic acid sequence amplification [NASBA], self-sustained sequence replication [3SR] or transcription-based amplification system [TAS]
• CPC Class Codes: C12Q 2525/131 incorporating a restriction site
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites

Abstract

The present disclosure relates to methods and probes for rapid, single temperature (isothermal) detection of specific nucleic acid sequences. The methods and probes provide a simple method for detecting bioagents including bacteria and viruses, and the detection of specific genetic markers on any nucleic sequence.

Claims

1. A method for detecting a target nucleic acid in a sample, the method comprising the steps of:

a) providing a sample comprising a single-stranded target nucleic acid, wherein the single-stranded target nucleic acid has a free 3′

terminus;

b) providing a monomeric polynucleotide probe comprising

i) at least two target binding domains, wherein the domains are separated by a nuclease cleavage element or a domain susceptible to nuclease degradation, or

ii) a target binding domain and a copy of at least a portion of the target nucleic acid, wherein the target binding domain and the target nucleic acid are separated by a nuclease cleavage element or a domain susceptible to nuclease degradation;

c) contacting the sample with more than one copy of the monomeric polynucleotide probe;

d) contacting the sample with a polymerase that synthesizes the reverse complement of the monomeric probe;

e) contacting the sample with at least one nuclease to cleave the nuclease cleavage element or degrade the domain susceptible to nuclease degradation, and

f) detecting the cleavage or degradation of the probe.

2. The method of claim 1, wherein the reverse complement of the monomeric probe comprises at least one copy of target nucleic acid and at least one copy of target binding domain.

3. The method of claim 1, wherein the geometry of the cut sites is such that the number of paired nucleotides in the cleavage products is reduced.

4. The method of claim 1, wherein the cleavage or degradation of the probe is detected by fluorescence.

5. The method of claim 1, wherein the cleavage or degradation of the probe is detected by colorimetric methods.

6. The method of claim 1, wherein the cleavage or degradation of the probe is detected by immunological methods.

7. The method of claim 1, wherein the cleavage or degradation of the probe is detected by electrophoretic methods.

8. The method of claim 1, wherein the cleavage or degradation of the probe is detected by hybridization methods.

9. The method of claim 1, wherein the cleavage or degradation of the probe is detected using nanopore technology.