IP Library Granted Patent US 11,371,087
Granted Patent B2
US 11,371,087 · App. 16/091,066 · Granted Jun 28, 2022

Methods and compositions employing blocked primers

Inventors: Thomas D. Schaal (San Jose, CA); Jude Menlo Dunne (San Jose, CA); Maithreyan Srinivasan (San Jose, CA); Alain Mir (San Jose, CA)
Assignee: Takara Bio USA, Inc.
C12Q1/6853C12P19/34C12Q1/6844
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Quick Facts
Patent No.
US 11,371,087
App. No.
16/091,066
Granted
Jun 28, 2022
Kind
B2
Abstract

The present disclosure provides methods, compositions, and systems employing blocked primers. Aspects of the disclosure include providing a blocked primer reaction mixture that includes a blocked primer and a template nucleic acid component from a single cell; unblocking the blocked primer to produce an active primer reaction mixture and subjecting the activated primer reaction mixture to primer extension conditions, such as nucleic acid amplification conditions.

Claims (30)

1. A method comprising:

(a) combining a blocked primer comprising a light labile blocking moiety with a template nucleic acid component from a single cell to produce a blocked primer reaction mixture;

(b) unblocking the blocked primer of the blocked primer reaction mixture by exposing the blocked primer reaction mixture to light sufficient to remove the blocking moiety to produce an activated primer reaction mixture; and

(c) subjecting the activated primer reaction mixture to template dependent primer extension reaction conditions.

2. The method according to claim 1 , wherein the blocked primer is a member of a pair of blocked amplifications primers.

3. The method according to claim 2 , wherein the template dependent primer extension reaction conditions comprise nucleic acid amplification conditions.

4. The method according to claim 3 , wherein the nucleic acid amplification conditions comprise thermal cycling.

5. The method according to claim 1 , wherein the template nucleic acid component comprises a plurality of nucleic acids.

6. The method according to claim 5 , wherein the plurality of nucleic acids comprise ribonucleic acids or deoxyribonucleic acids.

7. The method according to claim 1 , wherein the method comprises producing the template nucleic acid component.

8. The method according to claim 7 , wherein the template nucleic acid component is produced by obtaining a single cell and lysing the obtained single cell.

9. The method according to claim 1 , wherein the method is performed in a well.

10. The method according to claim 9 , wherein the method comprises producing the blocked primer reaction mixture by introducing a single cell into a well comprising the blocked primer and lysing the introduced single cell.

11. The method according to claim 10 , wherein the blocked primer in the well is dried.

12. The method according to claim 1 , wherein the method further comprises performing a second template mediated primer extension reaction.

13. The method according to claim 12 , wherein the second template mediated primer extension reaction is performed with an activated primer produced by unblocking a second blocked primer that is differentially blocked from the first blocked primer.

14. The method according to claim 13 , wherein the second blocked primer is a member of a second pair of blocked amplification primers and the method comprises unblocking the second pair of blocked amplification primers and then using the unblocked second pair of amplification primers in a second nucleic acid amplification.

15. A method comprising:

(a) combining a blocked primer comprising a thermally labile blocking moiety with a template nucleic acid component from a single cell to produce a blocked primer reaction mixture;

(b) unblocking the blocked primer of the blocked primer reaction mixture by heating the blocked primer reaction mixture to a temperature sufficient to remove the thermally labile blocking moiety to produce an activated primer reaction mixture; and

(c) subjecting the activated primer reaction mixture to template dependent primer extension reaction conditions.

16. A method comprising:

(a) combining a blocked primer comprising an enzymatically labile blocking moiety with a template nucleic acid component from a single cell to produce a blocked primer reaction mixture;

(b) adding an enzyme to the blocked primer reaction mixture to enzymatically remove the enzymatically labile blocking moiety of the blocked primer, thereby unblocking the blocked primer of the blocked primer reaction mixture to produce an activated primer reaction mixture; and

(c) subjecting the activated primer reaction mixture to template dependent primer extension reaction conditions.

17. The method according to claim 1 , wherein the light labile blocking moiety is attached to the 3′ end of the blocked primer.

18. The method according to claim 17 , wherein the blocked primer further comprises a non-template sequence domain with a length of 10 to 40 nucleotides.

19. The method according to claim 16 , wherein the method further comprises producing the template nucleic acid component.

20. The method according to claim 19 , wherein the template nucleic acid component is produced by a polymerase mediated template dependent primer extension reaction.

21. The method according to claim 20 , wherein the polymerase mediated template dependent primer extension reaction comprises a reverse transcriptase mediated template dependent primer extension reaction.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2018
From: SCHAAL, THOMAS D.; DUNNE, JUDE; SRINIVASAN, MAITHREYAN; MIR, ALAIN
To: TAKARA BIO USA, INC.
Reel/Frame 047556/0293 →
Continuity (2)
Provisional Application 62348428 · Jun 10, 2016
Related Publication 20190112648A1 · Apr 18, 2019