IP Library Granted Patent US 10,407,721
Granted Patent B2
US 10,407,721 · App. 15/444,826 · Granted Sep 10, 2019

Modified nucleosides or nucleotides

Inventors: Xiaohai Liu (Nr Saffron Walden, GB); Xiaolin Wu (Nr Saffron Walden, GB); Geoffrey Paul Smith (Nr Saffron Walden, GB)
Assignee: Illumina Cambridge Limited
C12Q1/6869C07H19/073C07H19/10C07H19/14C07H19/173C07H19/20C12Q1/6876Y02P20/55
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Quick Facts
Patent No.
US 10,407,721
App. No.
15/444,826
Granted
Sep 10, 2019
Kind
B2
Abstract

Some embodiments described herein relate to modified nucleotide and nucleoside molecules with novel 3′-hydroxy protecting groups. Also provided herein are methods to prepare such modified nucleotide and nucleoside molecules and sequencing by synthesis processes using such modified nucleotide and nucleoside molecules.

Claims (33)

1. A modified nucleotide or nucleoside molecule comprising a ribose or deoxyribose sugar moiety having a removable 3′-hydroxy protecting group forming a structure —O—CH(R)N 3 covalently attached to the 3′-carbon atom, wherein

R is selected from the group consisting of —C(R 1 ) m (R 2 ) n , —C(═O)OR 3 , —C(═O)NR 4 R 5 , —C(R 6 ) 2 O(CH 2 ) p NR 7 R 8 and —C(R 9 ) 2 O-Ph-C(═O)NR 10 R 11 ;

R 1 is hydrogen, or optionally substituted alkyl;

R 2 is halogen;

R 3 is hydrogen or optionally substituted alkyl;

each of R 4 and R 5 is independently selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted aralkyl;

each of R 6 and R 9 is selected from the group consisting of hydrogen, optionally substituted alkyl and halogen;

each of R 7 , R 8 , R 10 and R 11 is independently selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted aralkyl;

m is an integer of 1 or 2;

n is an integer of 1 or 2; provided that m+n is equal to 3; and

p is an integer of 0 to 6.

2. The modified nucleotide or nucleoside molecule of claim 1 , wherein R is —C(R 1 ) m (R 2 ) n and wherein R 1 is hydrogen.

3. The modified nucleotide or nucleoside molecule of claim 2 , wherein R is —CHF 2 , —CH 2 F, —CHCl 2 or —CH 2 Cl.

4. The modified nucleotide or nucleoside molecule of claim 3 , wherein R is —CHF 2 .

5. The modified nucleotide or nucleoside molecule of claim 3 , wherein R is —CH 2 F.

6. The modified nucleotide or nucleoside molecule of claim 1 , wherein R is —C(═O)NR 4 R 5 .

7. The modified nucleotide or nucleoside molecule of claim 1 , wherein R 4 is hydrogen and R 5 is C 1-6 alkyl.

8. The modified nucleotide or nucleoside molecule of claim 1 , wherein said modified nucleoside or nucleotide is linked to a detectable label via a cleavable linker or a non-cleavable linker.

9. The modified nucleotide or nucleoside molecule of claim 8 , wherein the linker is cleavable.

10. The modified nucleotide or nucleoside molecule of claim 8 , wherein the linker is acid labile, photo labile or comprises a disulfide linkage.

11. The modified nucleotide or nucleoside molecule of claim 8 , wherein the detectable label is a fluorophore.

12. The modified nucleotide or nucleoside molecule of claim 1 , wherein said 3′-hydroxy protecting group is linked to a detectable label via a cleavable linker or a non-cleavable linker.

13. The modified nucleotide or nucleoside molecule of claim 12 , wherein the linker is cleavable.

14. The modified nucleotide or nucleoside molecule of claim 12 , wherein the linker is acid labile, photo labile or comprises a disulfide linkage.

15. The modified nucleotide or nucleoside molecule of claim 12 , wherein the detectable label is a fluorophore.

16. A method of preparing a growing polynucleotide complementary to a target single-stranded polynucleotide in a sequencing reaction, comprising incorporating a modified nucleotide molecule of claim 1 into a growing complementary polynucleotide, wherein the incorporation of the modified nucleotide prevents the introduction of any subsequent nucleotide into the growing complementary polynucleotide.

17. The method of claim 15 , wherein the incorporation of the modified nucleotide molecule is accomplished by a terminal transferase, a terminal polymerase or a reverse transcriptase.

18. A method of determining the sequence of a target single-stranded polynucleotide, comprising

monitoring the sequential incorporation of complementary nucleotides, wherein at least one complementary nucleotide incorporated is a modified nucleotide molecule of claim 8 ; and

detecting the identity of the modified nucleotide molecule.

19. The method of claim 18 , wherein the identity of the modified nucleotide is determined by detecting the detectable label.

20. The method of claim 18 , wherein the 3′-hydroxy protecting group and the detectable label are removed prior to introducing the next complementary nucleotide.

21. A kit comprising one or more modified nucleotide or nucleoside molecule of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2017
From: LIU, XIAOHAI; WU, XIAOLIN; SMITH, GEOFFREY PAUL
To: ILLUMINA CAMBRIDGE LIMITED
Reel/Frame 042326/0071 →
Continuity (2)
Continuation 14771481
Related Publication 20170166961A1 · Jun 15, 2017
Cited By (1)
US 12,565,641