IP Library Granted Patent US 10,240,195
Granted Patent B2
US 10,240,195 · App. 14/666,124 · Granted Mar 26, 2019

Chemical methods for producing tagged nucleotides

Inventors: Carl W. Fuller (Berkeley Heights, NJ); Shiv Kumar (Belle Mead, NJ); Jingyue Ju (Englewood Cliffs, NJ); Randall Davis (Pleasanton, CA); Roger Chen (Saratoga, CA)
Assignees: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK; GENIA TECHNOLOGIES, INC.
C12Q1/6874C07H17/02C07H19/10C07H19/20C12Q1/6806
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Quick Facts
Patent No.
US 10,240,195
App. No.
14/666,124
Granted
Mar 26, 2019
Kind
B2
Abstract

This disclosure provides systems and methods for attaching nanopore-detectable tags to nucleotides. The disclosure also provides methods for sequencing nucleic acids using the disclosed tagged nucleotides.

Claims (35)

1. A tagged nucleotide, comprising a poly-phosphate moiety having a terminal phosphate at the 5′ position of the nucleotide, and a tag covalently coupled to the terminal phosphate of the nucleotide by a triazole, a 1,2-diazine, a disulfide, a secondary amine, a hydrazone, a thio-acetamide, or a maleimide-thioadduct,

wherein the tag comprises an oligonucleotide, wherein:

(i) the oligonucleotide comprises a non-naturally occurring internucleotide linkage;

(ii) the 5′-end of the oligonucleotide is covalently coupled to the terminal phosphate and the 3′ terminus of the oligonucleotide has a chemical modification which protects it from exonuclease degradation, or the 3′-end of the oligonucleotide is covalently coupled to the terminal phosphate and the 5′ terminus of the oligonucleotide has a chemical modification which protects it from exonuclease degradation; or

(iii) the oligonucleotide comprises at least one abasic spacer (dSp).

2. The tagged nucleotide of claim 1 , wherein the tag is covalently coupled to the terminal phosphate at the 5′ position of the nucleotide by a 1,2-diazine or a triazole having the structure:

wherein R 1 comprises the tag, and R 2 comprises the nucleotide; or

wherein R 1 comprises the nucleotide, and R 2 comprises the tag; or

a triazole having the structure:

wherein R 1 and R 3 combine to form a cyclic moiety; and

wherein R 1 and R 3 combined comprise a tag, and R 2 comprises a nucleotide; or

wherein R 1 and R 3 combined comprise a nucleotide, and R 2 comprises a tag.

3. The tagged nucleotide of claim 1 , wherein the poly-phosphate moiety comprises at least 3phosphates, or from 4 to 6 phosphates; wherein the tag further comprises nucleotides, peptides, polyethylene glycol (PEG), or any combination thereof; wherein the oligonucleotide of the tag comprises at least 7 monomer units, or at least 30 monomer units; wherein the 5′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate; or wherein the 3′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate.

4. The tagged nucleotide of claim 3 ,

wherein the 5′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate and the oligonucleotide comprises a chemical modification of its 3′ terminus that protects it from exonuclease degradation; wherein the 5′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate and the oligonucleotide comprises a chemical modification of its 3′ terminus that protects it from exonuclease degradation, and the chemical modification of its 3′ terminus is selected from phosphorylation, and covalent coupling with C 3 -alkyl to C 12 -alkyl spacers having terminal hydroxyl groups; wherein the 3′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate and the oligonucleotide comprises a chemical modification of its 5′ terminus that protects it from exonuclease degradation; or wherein the 3′-end of the oligonucleotide of the tag is covalently coupled to the terminal and the oligonucleotide comprises a chemical modification of its 5′ terminus that protects it from exonuclease degradation, and the chemical modification of its 5′ terminus is selected from phosphorylation, and covalent coupling with C 3 -alkyl to C 12 -alkyl spacers having terminal hydroxyl groups.

5. The tagged nucleotide of claim 3 , wherein the oligonucleotide of the tag comprises a cyanine dye moiety, or a cyanine dye moiety which is a Cy3 moiety; wherein the oligonucleotide of the tag comprises a spacer moiety comprising an alkyl group of at least 2 carbons to about 12 carbons; wherein the oligonucleotide of the tag comprises a spacer comprising an abasic unit; wherein the oligonucleotide of the tag comprises a spacer selected from the group consisting of idSp, iSp9, iSp18, iSpC3, iSpC6, and iSpC12; or wherein the oligonucleotide of the tag comprises a spacer selected from the group consisting of pyrolidine, spermine, nitropyrrole, nitroindole, nebularine, benimidazole, benzene, 7-deazapurines, 5-substituted pyrimidine, fluorescein-dT, fluorescein, rhodamine, and ROX.

6. The tagged nucleotide of claim 1 , wherein the tag further comprises oligo-saccharides, carbohydrates, peptide nucleic acids (PNA), vinyl polymers, other water-soluble polymers or any combination thereof; wherein the oligonucleotide of the tag comprises an unnatural nucleotide; wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a group selected from the group consisting of an L-nucleotide, a 2′, 5′-linkage, an α-D-nucleotide, a non-naturally occurring internucleotide linkage, a non-naturally-occurring base, a non-naturally occurring sugar moiety, and any combination thereof; wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a non-naturally occurring base selected from the group consisting of nitropyrrole, nitroindole, nebularine, zebularine, benzene, and benzene derivatives; or wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a non-naturally occurring internucleotide linkage selected from the group consisting of a phosphotriester, phosphorothioate, methylphosphonate, boronophosphate, phosphoramidate, and a morpholino moiety.

7. The tagged nucleotide of claim 1 , wherein the tag is represented by SEQ ID NOS. 109-114, or the tag is represented by SEQ ID NOS. 17, 18, 22-33, 42-72, 74-82, 86-88, 90, or 94-102; wherein the tag is represented by SEQ ID NOS. 6, 8-16, 19-21, or 34-41; wherein the tag is represented by SEQ ID NOS. 89, 91-93, or 103-105; wherein the tag is represented by SEQ ID NOS. 73, 83-85, or 106; wherein the tagged nucleotide is selected from the group consisting of dG6P-(T 4 -Npy2) 6 -C3, dG6P-(T 4 -Neb2) 6 -C3, dT6P-dT 6 -C7-NH 6 -dT 18 -C3, dT6P-dT 6 -Pyrd 6 -dT 18 -C3, dA6P-dT 6 -dTNH 6 -dT 18 -C3, dG6P-dT 4 -sperm-dT 22 -C3, dT6P-dT 4 -sperm-dSp 3 -dT 19 -C3, dC6P-dT 4 -sperm-iFlrT-dT 21 -C3, dG6P-sperm-dT 30 -C3, dT6P-Cy3.5-dT 30 -C3, dT6P-Cy3-Cy3-dT 30 -C3, dT6P -dT 6 -Cy3-dT 23 -C3, dT6P-dT 10 -Cy3-dT 19 -C3, dT6P -Hairpin Block, dA6P-Cy3-T2-Sp18-T 22 -C3, dT6P-Cy3-dT4-dSp 8 -T 18 -C3, dT6P-Hex-dT 6 -dTC2NH 6 -dT 18 -C3, dA6P-Cy3-dT 4 -Sp9-T 23 -C3, dC6P-Cy3-T-dSp 3 -T 26- C3, dC6P-Cy3-T 4 -dSp 3 -T 23- C3, dC6P-Cy3-T 7 -dSp 3 -T 20- C3, dC6P-Cy3-T 10 -dSp 3 -T 17- C3, dC6P-Cy3-T 4 -iFluorT 3 -T23-C3, dC6P-Cy3 T 4 -iFluorT-T-iFluorT-T 23 -C3, Bio-Spermine-dT 30 -C3, dT6P-dT 30 -Cy3-C3, dG6P-dT 8 -Spermine-dT 20 -C3, dA6P-Cy3-T 4 -iFluorT-T-iFluorT-T 23 -C3, dT6P-CY3-dT4-Aptamer-dT25-C3, dT6P-Cy3-dT4-12Hairpin-dT25-C3, dT6P-Cy3-dT 5 -dSp 3 -dT 22 -C3, dT6P-Cy3-dT 6 -dSp 3 -dT 21 -C3, dT6P-Cy3-dT 4 -dSp 4 -dT 22 -C3, dT6P-Cy3-dT 4 -dSp 5 -dT 21 -C3, dC6P-Cy3-dT 5 -SpC12-dT 23 -C3, dC6P-Cy3-dT 4 -SpC6-SpC6-dT 24 -C 3 , dC6P-Cy3-dT 4 -(SpC3) 3 -dT 23 -C3, dG6P-Cy3-dT 30 -C3, dT6P-Cy3-dT 2 -dSp 8 -dT 20 -C3, dC6P-Cy3-T 30 -(C 3 ) 4 -PO 4 , dC6P-Cy3-T 30 -PO 4 , dC6P-Cy3-T 30 -C 3 -NH 2 , dG6PαS-Cy3-dT 2 -dSp 8 -dT 20 -C3, Rev-P-T 30 -Cy3-dG6P, Rev-P-T 24 -dSp 3 -T 3 -Cy3-dC6P, dT6P-Cy3-dT 4 -HP6-dT 25 -C 3 , dA6P-Cy3-dT4-dI6-dT20-C3, dA6P-Cy3-dT4-Nitrindole6-dT20-C3, dA6P-Cy3-dT4-dC6-dT20-C3, dA6P-Cy3-dT4-5IU6-dT20-C3, dA6P-Cy3-dT4-PyrndU6-dT20-C3, dT6P-Cy3-dT 4 -(idSP-T) 4 -dT 18 -C 3 , dT6P-Cy3-dT 5 -(idSP-T) 4 -dT 17 -C3, dT6P-Cy3-dT 4 -Propyl 6 -dT 20 -C3, dT6P-Cy3-LdT 30 -C3, dT6P-Cy3-dT 4 -L111-dT 26 -C3, dT6P-Cy3-dT 4 -L121-dT 26 -C3, dT6P-Cy3-dT 4 -SpC12-SpC12-dT 24 -C3, dT6P-Cy3-dT 4 -(SpC6) 4 -dT 25 -C3, dT6P-Cy3-dT 4 -Spermine-dT 25 -C3, dT6P-Cy3-dT2-Spermine-dT 27 -C3, dT6P-Cy3-dT2-Spermine-Spermine-dT 26 -C3, dT6P-Cy3-dT 4 -Pyrn-dU-TT-Pyrn-dU-dT 22 -C3, dT6P-Cy3-dT 4 -Tmp 6 -dT 20 -C3, dT6P-Cy3-dT 4 -Pyrrolidine 6 -dT 20 -C3, dT6P-Pyrrolidine-dT 30 -C3, dT6P-Pyrrolidine-Pyrrolidine-dT 30 -C3, and dT6P-Pyrrolidine 3 -dT 30 -C3; wherein the tagged nucleotide is selected from the group consisting of dA6P-T* 30— ODD, dT6P-T 6 -dSp 8 -T 16 , dC6P-T 6 -T* 10 -T 14 , dC6P-T 4 -dSp 3 -T 23 , dC6P-T 7 -dSp 3 -T 20 , dC6P-T 10 -dSp 3 -T 17 , dC6P-T 13 -dSp 3 -T 14 , dG6P-T 30 -C6, dG6P-Cy3-T 30 -C6, dT6P-T 4 -dSp 10 -T 16 -C6, dA6P-T 4 -Sp18-T 22 -C3, dA6P-T 4 -Sp18 2 -T 19- C 3 , dA6P-T 4 -Sp9 2 -T 22- C3, dT6P-T 6 -dSp 8 -T 16 -C3, dA6P-Cy3-T 30 -C6, dT6P-Cy3-T 30 -C6, dC6P-Cy3-T 30 -C6, dA6P-Cy3-dT* 30— ODD, dA6P-T* 30 , dA6P-Cy3-T* 30 , dG6P-Cy3-T 30 -C3, dG6P-Cy3-T 15 -C3, dG6P-Cy3-T 20 -C3, and dG6P-Cy3-T 25 -C3; wherein the tagged nucleotide is selected from the group consisting of dT6P-Cy3-dT 3 -(SpC12) 3 -dT 24 -C3, dT6P-Cy3-dT 4 -(SpC6) 5 -dT 23 -C3, dT6P-Cy3-dT5-(SpC6) 4 -dT 24 -C3, dT6P-Cy3-dT 2 -(SpC6) 5 -dT 25 -C3, dT6P-SpC3-Cy3-dT 30 -C3, dT6P-SpC3-SpC3-Cy3-dT 30 -C3, and dT6P-SpC6-Cy3-dT 30 -C3; wherein the tagged nucleotide is selected from the group consisting of dT6P-Cy3-dC 30 -C3, dT6P-Cy3-LdT 4 -dSp 3 -LdT 23 -C3, dT6P-Cy3-LdT 4 -dSp 8 -LdT 18-C 3, dT6P-Cy3-LdT 4 -dI 6 -LdT 20 -C3, and dT6P-Cy3-dT 4 (alpha-dT) 3 -dT 23 -C3; wherein the tag comprises a chemical modification selected from the group consisting of the chemical modifications listed in Table 6; or wherein the tagged nucleotide comprises a linker comprising a cyanine dye moiety, or a cyanine dye moiety which is a Cy3 moiety has an improved rate of capture by a polymerase.

8. The tagged nucleotide of claim 1 , wherein the tag is covalently coupled to the terminal phosphate at the 5′ position of the nucleotide by a 1,2-diazine or a triazole having the structure:

wherein R 1 comprises the tag, and R 2 comprises the nucleotide; or

wherein R 1 comprises the nucleotide, and R 2 comprises the tag.

9. The tagged nucleotide of claim 8 , wherein:

(i) the poly-phosphate moiety comprises 6 phosphates; and

(ii) the 5′-end of the oligonucleotide of the tag is covalently coupled to the terminal phosphate of a poly-phosphate moiety.

10. The tagged nucleotide of claim 9 , wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a group selected from the groups consisting of an L-nucleotide, a 2′,5′-linkage, an α-D-nucleotide, a non-naturally occurring internucleotide linkage, a non-naturally occurring base, a non-naturally occurring sugar moiety, an abasic unit, a chemical modification selected from the group consisting of the chemical modifications listed in table 6, and any combination thereof.

11. The tagged nucleotide of claim 9 , wherein the oligonucleotide of the tag comprises at least 30 monomer units.

12. The tagged nucleotide of claim 9 , wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a group selected from the groups consisting of a non-naturally occurring base, a non-naturally occurring sugar moiety, an abasic unit, a chemical modification selected from the group consisting of the chemical modifications listed in table 6, and any combination thereof.

13. The tagged nucleotide of claim 12 , wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a non-naturally occurring internucleotide linkage.

14. The tagged nucleotide of claim 13 wherein the non-naturally occurring internucleotide linkage is a phosphotriester or thiophosphate diester.

15. The tagged nucleotide of claim 14 wherein the tag is represented by SEQ ID NOS. 6, 9, and 36, or wherein the tagged nucleotide is selected from the group consisting of dA6P-T* 30— ODD, dC6P-T 6 -T* 10 -T 14 , and dA6P-T* 30 .

16. The tagged nucleotide of claim 13 , wherein the oligonucleotide of the tag comprises an unnatural nucleotide comprising a spacer moiety comprising an alkyl group of at least 2 carbons to about 12 carbons.

17. The tagged nucleotide of claim 16 , wherein the oligonucleotide of the tag comprises a chemical modification at its 3′-terminus that protects it from exonuclease degradation.

18. The tagged nucleotide of claim 17 , wherein the chemical modification is selected from the group consisting of phosphorylation and covalent coupling with C3-alkyl to C12-alkyl spacers having terminal hydroxyl groups.

19. The tagged nucleotide of claim 18 , wherein the tag is represented by SEQ ID NOS. 16, 19-21, 24, or 34, or wherein the tagged nucleotide is selected from the group consisting of dT6P-T 4 -dSp 10 -T 16 -C6, dA6P-T 4 -Sp18-T 22 -C3, dA6P-T 4 -Sp18 2 -T 19- C 3 , dA6P-T 4 -Sp9 2 -T 22- C3, dA6P-dT 6 -dTNH 6 -dT 18 .-C3, and dT6P-T 6 -dSp B -T 16 -C3.

20. A kit for sequencing nucleic acid comprising a tagged nucleotide of claim 1 .

Assignments (4)
MERGER Recorded Apr 1, 2020
From: GENIA TECHNOLOGIES, INC.
To: ROCHE SEQUENCING SOLUTIONS, INC.
Reel/Frame 052289/0425 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2019
From: FULLER, CARL W.; KUMAR, SHIV; JU, JINGYUE
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 048850/0053 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2019
From: DAVIS, RANDALL; CHEN, ROGER
To: GENIA TECHNOLOGIES, INC.
Reel/Frame 048850/0071 →
CONFIRMATORY LICENSE Recorded Aug 3, 2015
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036252/0433 →
Continuity (2)
Provisional Application 61969628 · Mar 24, 2014
Related Publication 20150368710A1 · Dec 24, 2015
Cited By (7)
US 12,188,086 US 12,215,122 US 12,215,124 US 12,337,009 US 12,378,600 US 12,503,730 US 12,595,508