IP Library Granted Patent US 10,584,376
Granted Patent B2
US 10,584,376 · App. 16/117,949 · Granted Mar 10, 2020

Compositions and methods for detecting a nucleic acid sequence in a sample comprising a primer oligonucleotide with a 3′-terminal region comprising a 2′-modified nucleotide

Inventors: Daniel Shaffer (Portland, ME); Stephen A. Judice (Portland, ME)
Assignee: ENVIROLOGIX INC.
C12Q1/6853C12Q1/6848C12Q1/68C12Q1/689C12Q1/6851
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Quick Facts
Patent No.
US 10,584,376
App. No.
16/117,949
Granted
Mar 10, 2020
Kind
B2
Abstract

The present invention features compositions and methods for quantifying detection of a target oligonucleotide in a sample in real time comprising one or more primer oligonucleotides comprising a 5′ nicking enzyme recognition site and a 3′-terminal region comprising a 2′-modified nucleotide. These methods are compatible with amplification of target oligonucleotides in a test sample, including biological samples, using a nicking amplification reaction.

Claims (19)

1. An isolated oligonucleotide comprising from 5′ to 3′,

i) a first region, and

ii) a second region,

wherein the first region comprises a nicking enzyme recognition sequence; wherein the second region comprises at least 9 nucleotides that specifically bind a complementary sequence on a target nucleic acid molecule; and wherein the second region comprises one or more 2′ modified nucleotides positioned at the 3′ terminus of the sequence complementary to the target nucleic acid molecule.

2. The isolated oligonucleotide of claim 1 , wherein the 2′ modification is selected from the group consisting of 2′-O-methyl, 2′-methoxyethoxy, 2′-fluoro, 2′-hydroxyl, 2′-allyl, 2′-O-[2-(methylamino)-2-oxoethyl], 4′-thio, 4′-CH 2 —O-2′-bridge, 4′-(CH 2 ) 2-O-2′-bridge, 2′-LNA, and 2′-O-(N-methylcarbamate) and base analogs.

3. The isolated oligonucleotide of claim 1 , wherein two or more 2′ modified nucleotides are contiguous.

4. The isolated oligonucleotide of claim 3 , wherein the number of contiguous 2′ modified nucleotides is 2, 3, 4, 5, or more.

5. The isolated oligonucleotide of claim 4 , wherein 5 contiguous 2′-O-methyl modified nucleotides are positioned at the 3′ end of the sequence complementary to the target nucleic acid molecule.

6. The isolated oligonucleotide of claim 1 , wherein the nicking enzyme recognition sequence is 5′-GAGT-3′.

7. An isolated oligonucleotide comprising from 5′ to 3′,

i) a first region, and

ii) a second region,

wherein the first region comprises a nicking enzyme recognition sequence; wherein the second region comprises at least 9 nucleotides that specifically bind a complementary sequence on a target nucleic acid molecule; and wherein the second region comprises one or more 2′ modified nucleotides positioned at the 5′ terminus of the sequence complementary to the target nucleic acid molecule.

8. The isolated oligonucleotide of claim 7 , wherein the 2′ modification is selected from the group consisting of 2′-O-methyl, 2′-methoxyethoxy, 2′-fluoro, 2′-hydroxyl, 2′-allyl, 2′-O-[2-(methylamino)-2-oxoethyl], 4′-thio, 4′-CH 2 —O-2′-bridge, 4′-(CH 2 ) 2 -0-2′-bridge, 2′-LNA, and 2′-O-(N-methylcarbamate) and base analogs.

9. The isolated oligonucleotide of claim 7 , wherein the one or more 2′ modified nucleotides positioned at the 5′ end of the sequence complementary to the target nucleic acid molecule are separated from the nick site by 1, 2, 3, 4, 5 or more unmodified nucleotides.

10. The isolated oligonucleotide of claim 7 , wherein two or more 2′ modified nucleotides are contiguous.

11. The isolated oligonucleotide of claim 10 , wherein the number of contiguous 2′ modified nucleotides is 2, 3, 4, 5, or more.

12. The isolated oligonucleotide of claim 11 , wherein 5 contiguous 2′-O-methyl modified nucleotides are positioned at the 5′ end of the sequence complementary to the target nucleic acid molecule.

13. The isolated oligonucleotide of claim 7 , wherein the nicking enzyme recognition sequence is 5′-GAGT-3′.

Assignments (4)
SECURITY INTEREST Recorded Sep 5, 2025
From: ENSIGN-BICKFORD INDUSTRIES, INC.; APPLIED FOOD BIOTECHNOLOGY, INC.; EB ANALYTICS, INC.; ENSIGN-BICKFORD AEROSPACE & DEFENSE COMPANY; ENVIROLOGIX INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 072815/0001 →
SECURITY INTEREST Recorded Feb 4, 2021
From: ENSIGN-BICKFORD INDUSTRIES, INC.; APPLIED FOOD BIOTECHNOLOGY, INC.; ENSIGN-BICKFORD AEROSPACE & DEFENSE COMPANY; EB ANALYTICS, INC.; ENVIROLOGIX INC.; HONEYBEE ROBOTICS, LTD.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 055223/0048 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME PREVIOUSLY RECORDED AT REEL: 046766 FRAME: 0237. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT . Recorded Sep 18, 2020
From: JUDICE, STEPHEN A.; SHAFFER, DANIEL
To: ENVIROLOGIX INC.
Reel/Frame 053812/0939 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2018
From: JUDICE, STEPHEN A.; SHAFFER, DANIEL
To: ENVIRLOGIX INC.
Reel/Frame 046776/0237 →
Continuity (7)
Continuation 15808442 · Nov 9, 2017
Continuation 15438330 · Feb 21, 2017
Continuation 14989687 · Jan 6, 2016
Continuation 14789545 · Jul 1, 2015
Continuation 14342766
Provisional Application 61621975 · Apr 9, 2012
Related Publication 20180363046A1 · Dec 20, 2018
Cited By (2)
US 12,258,637 US 12,392,001