IP Library Granted Patent US 9,868,985
Granted Patent B2
US 9,868,985 · App. 15/647,657 · Granted Jan 16, 2018

Massive parallel method for decoding DNA and RNA

Inventors: Jingyue Ju (Englewood Cliffs, NJ); Zengmin Li (Flushing, NY); John Robert Edwards (St. Louis, MO); Yasuhiro Itagaki (New York, NY)
Assignee: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
C12Q1/6869C07H19/14C07H21/00C12Q1/68C12Q1/686C12Q1/6872C12Q1/6874C07B2200/11C12Q2525/117C12Q2535/101C12Q2535/122C12Q2563/107C40B40/00
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Quick Facts
Patent No.
US 9,868,985
App. No.
15/647,657
Granted
Jan 16, 2018
Kind
B2
Abstract

This invention provides methods for attaching a nucleic acid to a solid surface and for sequencing nucleic acid by detecting the identity of each nucleotide analog after the nucleotide analog is incorporated into a growing strand of DNA in a polymerase reaction. The invention also provides nucleotide analogs which comprise unique labels attached to the nucleotide analog through a cleavable linker, and a cleavable chemical group to cap the —OH group at the 3′-position of the deoxyribose.

Claims (13)

1. A method for sequencing a nucleic acid which comprises detecting the identity of a nucleotide analogue incorporated into the end of a growing strand of DNA in a polymerase reaction, wherein the nucleotide analogue is any of the following:

wherein R (a) represents a small, chemically cleavable, chemical group capping the oxygen at the 3′ position of the deoxyribose of tl deoxyribonucleotide analogue, (b) does not interfere with recognition of the analogue as a substrate by a DNA polymerase, (c) is stable during a DNA polymerase reaction, and (d) does not contain a ketone group;

wherein OR is not a methoxy group or an ester group;

wherein the covalent bond between the 3′-oxygen and R is stable during a DNA polymerase reaction;

wherein tag represents a detectable fluorescent moiety;

wherein Y represents a chemically cleavable, chemical linker which (a) does not interfere with recognition of the analogue as a substrate by a DNA polymerase and (b) is stable during a DNA polymerase reaction;

wherein the nucleotide analogue:

i) is recognized as a substrate by a DNA polymerase,

ii) is incorporated at the end of a growing strand of DNA during a DNA polymerase reaction,

iii) produces a 3′-OH group on the deoxyribose upon cleavage of R, and

iv) no longer includes a tag on the base upon cleavage of Y;

and wherein if the nucleotide analogue is: (A), it is capable of forming hydrogen bonds with cytosine or a cytosine nucleotide analogue; (B), it is capable of forming hydrogen bonds with thymine or a thymine nucleotide analogue; (C), it is capable of forming hydrogen bonds with guanine or a guanine nucleotide analogue; or (D), it is capable of forming hydrogen bonds with adenine or an adenine nucleotide analogue.

2. A method for simultaneously sequencing a plurality of different nucleic acids which comprises simultaneously applying the method of claim 1 to the plurality of different nucleic acids.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2017
From: JU, JINGYUE; LI, ZENGMIN; EDWARDS, JOHN ROBERT; ITAGAKI, YASUHIRO
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 043177/0865 →
Continuity (12)
Continuation 15167917 · May 27, 2016
Continuation 14670748 · Mar 27, 2015
Continuation 13959660 · Aug 5, 2013
Continuation 13672437 · Nov 8, 2012
Continuation 13339089 · Dec 28, 2011
Continuation 12804284 · Jul 19, 2010
Continuation 11810509 · Jun 5, 2007
Continuation In Part 10702203 · Nov 4, 2003
Division 09972364 · Oct 5, 2001
Continuation In Part 09684670 · Oct 6, 2000
Provisional Application 60300894 · Jun 26, 2001
Related Publication 20170313737A1 · Nov 2, 2017