IP Library Granted Patent US 10,196,680
Granted Patent B2
US 10,196,680 · App. 15/614,606 · Granted Feb 5, 2019

Methods of detecting target nucleic acids

Inventors: Muhammad A. Sharaf (Oakland, CA); Timothy Woudenberg (San Francisco, CA); Khairuzzaman Bashar Mullah (Union City, CA)
Assignee: APPLIED BIOSYSTEMS, LLC
C12Q1/6825C12Q1/6816C12Q1/6823C12Q1/6827C12Q1/6832C12Q1/6876G01N27/44726G01N27/44791
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Quick Facts
Patent No.
US 10,196,680
App. No.
15/614,606
Granted
Feb 5, 2019
Kind
B2
Abstract

The present disclosure relates to methods of identifying target nucleic acids by using coded molecules and its analysis by translocation through a nanopore. Generally, coded molecules are subject to a target polynucleotide dependent modification. The modified coded molecule is detected by isolating the modified coded molecules from the unmodified coded molecules prior to analysis through the nanopore or by detecting a change in the signal pattern of the coded molecule when analyzed through the nanopore.

Claims (12)

1. A method of detecting a target polynucleotide, comprising:

a) contacting a coded molecule with a target polynucleotide, wherein the coded molecule comprises

(i) one or more block polymer regions, and

(ii) a target probe capable of hybridizing to the target polynucleotide;

b) modifying the target probe with a modifying agent, wherein the modification is dependent on the target polynucleotide hybridized to the target probe; and

c) translocating the coded molecule through a nanopore and detecting a signal pattern associated with the coded molecule;

wherein the target polynucleotide comprises adjacent first and second regions, and the target probe comprises a 5-prime region and a 3-prime region, and wherein the method further comprises hybridizing a FLAP probe to the target polynucleotide, wherein the FLAP probe comprises a 3-prime segment that hybridizes to the first region, and the 3-prime region of the target probe hybridizes to the second region such that the 3-prime segment of the FLAP probe and the 3-prime region of the target probe are adjacently hybridized to the target polynucleotide to form a FLAP substrate, and wherein the modifying agent is a FLAP endonuclease and the modification is cleavage of the target probe.

2. The method of claim 1 , further comprising the step of rendering the coded molecule single-stranded prior to translocation through the nanopore.

3. The method of claim 1 , further comprising comparing the detected signal pattern to a signal pattern of an unmodified coded molecule, wherein a difference in the detected signal pattern of the modified coded molecule compared to the signal pattern of the unmodified coded molecule indicates the presence of the target polynucleotide.

4. The method of claim 1 , further comprising associating the detected signal pattern to the target probe.

5. The method of claim 1 in which the 5-prime region of the target probe is non-complementary to the target polynucleotide.

6. The method of claim 1 in which the FLAP probe further comprises a 3-prime unpaired segment that overlaps with the 5-prime region of the target probe in the FLAP substrate, thereby forming a double FLAP substrate.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2018
From: SHARAF, MUHAMMAD A.; WOUDENBERG, TIMOTHY M.; MULLAH, K. BASHAR
To: APPLERA CORPORATION
Reel/Frame 044995/0240 →
MERGER Recorded Feb 22, 2018
From: APPLERA CORPORATION
To: APPLIED BIOSYSTEMS INC.
Reel/Frame 044995/0247 →
MERGER Recorded Feb 22, 2018
From: ATOM ACQUISITION CORPORATION
To: APPLIED BIOSYSTEMS INC.
Reel/Frame 044995/0254 →
MERGER Recorded Feb 22, 2018
From: ATOM ACQUISITION, LLC & APPLIED BIOSYSTEMS INC.
To: APPLIED BIOSYSTEMS, LLC
Reel/Frame 044995/0261 →
Continuity (7)
Continuation 15241711 · Aug 19, 2016
Continuation 14790369 · Jul 2, 2015
Continuation 14137376 · Dec 20, 2013
Continuation 13590794 · Aug 21, 2012
Continuation 11685189 · Mar 12, 2007
Provisional Application 60781780 · Mar 12, 2006
Related Publication 20170275678A1 · Sep 28, 2017
Cited By (1)
US 12,338,470