Universal template strands for enzymatic polynucleotide synthesis

Patent metadata

Field	Value
Publication number	US-11739359-B2
Application number	US-202016865262-A
Country	US
Kind code	B2
Filing date	May 1, 2020
Priority date	May 1, 2020
Publication date	Aug 29, 2023
Grant date	Aug 29, 2023

Abstract

A universal template strand built with universal base analogs is used as a template for polynucleotide synthesis. The universal template strand can hybridize to any sequence of nucleotides. A new polynucleotide is synthesized by using a polymerase to extend a primer hybridized to the universal template strand. Unlike primer extension in polymerase chain reactions, base pairing with nucleotides in the template strand does not specify the sequence of the new polynucleotide. Instead, the sequence of the new polynucleotide is specified by the order of addition of protected nucleotides. After addition of a single species of protected nucleotide, the blocking group is removed and another protected nucleotide is added. The order of nucleotide addition can be varied to create any sequence. After synthesis, the polynucleotide can be dehybridized from the universal template strand. The universal template strand may then be reused to synthesize a different polynucleotide.

First claim

The invention claimed is:

1. A method of enzymatic synthesis of a polynucleotide, the method comprising:
a. contacting a first primer region of a universal template strand comprising universal base analogs with a complementary primer, wherein the universal template strand comprises a universal region consisting of a mixture of natural bases and the universal base analogs;
b. removing a blocking group;
c. contacting the universal template strand with a protected nucleotide selected according to a predetermined polynucleotide sequence and a polymerase so that the protected nucleotide is incorporated into the complementary primer or extended version thereof hybridized to the universal template strand; and
d. repeating steps b-c to synthesize the polynucleotide.

2. The method of claim 1 , wherein the natural bases are present at regular intervals among the universal base analogs.

3. The method of claim 1 , wherein the universal base analogs comprise hydrogen bonding bases that form hydrogen bonds with any natural nucleobases.

4. The method of claim 1 , wherein the universal base analogs consist of inosine and derivative thereof.

5. The method of claim 1 , wherein the complementary primer includes the blocking group.

6. The method of claim 1 , wherein the blocking group is a 3′ blocking group.

7. The method of claim 1 , wherein the complementary primer has a T m that is greater than 60° C.

8. The method of claim 1 , wherein the blocking group is thermolabile, acid-labile, redox-labile, or photolabile.

9. The method of claim 1 , wherein the polymerase is a DNA-dependent DNA polymerase.

10. The method of claim 1 , wherein the polymerase is terminal deoxynucleotidyl transferase (TdT).

11. The method of claim 1 , wherein a backbone of the universal template strand comprises peptide nucleic acids, bridged nucleic acids, locked nucleic acids, or ribose phosphate with a 2′-deoxy substitution.

12. The method of claim 1 , further comprising:
determining that synthesis of the predetermined polynucleotide sequence of the polynucleotide is complete; and
dehybrizing the polynucleotide from the universal template strand.

13. The method of claim 1 , wherein the universal template strand further comprises a second primer region and the method further comprises contacting the universal template strand with a mixture of nucleotides without blocking groups.

14. A method of synthesizing a plurality of polynucleotides having different, predetermined sequences, the method comprising:
a. contacting primer regions of a plurality of universal template strands with complementary primers, wherein the universal template strands comprise universal regions consisting of a mixture of natural bases and universal base analogs and the universal template strands are bound to a solid substrate;
b. removing blocking groups from nucleotides hybridized to a subset of the universal template strands;
c. contacting the plurality of universal template strands with a protected nucleotide selected according to a predetermined polynucleotide sequence and a polymerase so that the protected nucleotide is incorporated into one or more complementary primers or extended versions thereof hybridized to the subset of the universal template strands; and
d. repeating steps b-c with variations in the subset of the universal template strands and in a base of the protected nucleotide to synthesize the plurality of polynucleotides having different, predetermined sequences.

15. The method of claim 14 , wherein the solid substrate comprises a microelectrode array and removing the blocking groups comprises activating a subset of electrodes in the microelectrode array.

16. The method of claim 15 , wherein the blocking groups are removed by a redox reaction.

17. A system for synthesizing a plurality of polynucleotides having different, predetermined sequences, the system comprising:
a solid substrate coated with a plurality of universal template strands comprising primer regions and universal regions, wherein the universal regions comprise a mixture of natural bases and universal base analogs;
a reaction chamber containing the solid substrate;
a plurality of fluid delivery pathways each configured to introduce a single species of protected nucleotide into the reaction chamber; and
control circuitry configured to selectively change local conditions on a portion of the surface of the solid substrate resulting in cleavage of blocking groups attached to the protected nucleotides and to selectively open the plurality of fluid delivery pathways to introduce protected nucleotides into the reaction chamber according to a predetermined polynucleotide sequence.

18. The system of claim 17 , wherein the solid substrate comprises a microelectrode array and the control circuitry is configured to selectively activate electrodes in the microelectrode array.

19. The system of claim 17 , further comprises a fluid delivery pathway configured to introduce complementary primers each having a blocking group into the reaction chamber.

20. The system of claim 17 , wherein the natural bases are present at regular intervals among the universal base analogs.

Assignees

• Microsoft Technology Licensing Llc

Inventors

• Nguyen Bichlien
• Smith Jake
• Carlson Robert
• Strauss Karin

Classifications

• C12P19/34 Primary

  Polynucleotides, e.g. nucleic acids, oligoribonucleotides · CPC title

• C12N15/10

  Processes for the isolation, preparation or purification of DNA or RNA (chemical preparation of DNA or RNA C07H21/00; preparation of non-structural polynucleotides from microorganisms or with enzymes C12P19/34) · CPC title

• C12Q1/68

  involving nucleic acids · CPC title

• C12Q1/6834

  Enzymatic or biochemical coupling of nucleic acids to a solid phase · CPC title

• C12Q2521/101

  DNA polymerase · CPC title