Methods and compositions for manipulating nucleic acids

Patent metadata

Field	Value
Publication number	US-2026022417-A1
Application number	US-202519339877-A
Country	US
Kind code	A1
Filing date	Sep 25, 2025
Priority date	Nov 7, 2017
Publication date	Jan 22, 2026
Grant date	—

Abstract

The present disclosure provides methods, compositions and kits as well as systems for manipulating nucleic acids, including implementing isothermal amplification, such as recombinase-polymerase amplification (RPA), of a nucleic acid template using a pre-seeded solid support. Provided are rapid and efficient methods for generating template nucleic acid molecules comprising specific nucleotide sequence bound to solid support. Such methods can be used, for example, in manipulating nucleic acids in preparation for analysis methods that utilize monoclonal populations of nucleic acids.

First claim

What is claimed is:

1 . A method for generating one or more templated solid supports, comprising:
a) performing a pre-seeding reaction by incubating a pre-seeding reaction mixture comprising a population of template nucleic acid molecules and a population of solid supports comprising a population of attached identical first primers under pre-seeding reaction conditions to generate a population of pre-seeded solid supports, wherein the pre-seeding reaction conditions comprise incubating the pre-seeding reaction mixture under isothermal conditions and wherein the pre-seeded solid supports each have substantially monoclonal nucleic acid molecules attached thereto and/or the pre-seeding reaction conditions comprise incubating the preseeding reaction mixture under isothermal conditions, wherein the pre-seeded solid supports comprise:
i. a substantially monoclonal population of template nucleic acid molecules attached to the solid support by the first primer, and
ii. attached first primers that are attached to the pre-seeded solid supports and are not bound to template nucleic acid molecules;
b) forming a templating reaction mixture by including the one or more pre-seeded solid supports in a recombinase-polymerase amplification (RPA) reaction mixture, wherein template nucleic acid molecules not associated with the pre-seeded solid supports are not included in the templating reaction mixture, wherein the templating reaction mixture further comprises a population of identical second primers in solution not attached to any substrate, and wherein the template nucleic acid molecules comprise a primer binding site for the second primer at or near a terminal end that is opposite a proximal segment comprising the first primer; c) initiating a templating reaction by adding a cation to the templating reaction mixture; d) incubating the initiated templating reaction mixture under isothermal conditions to amplify the template nucleic acid molecules in a templating reaction to generate one or more templated solid supports.

2 . A method according to claim 1 , further comprising sequencing the template nucleic acid molecules on the one or more templated solid supports.

3 . A method according to claim 1 , wherein the template nucleic acid molecules comprise two or more template nucleic acid molecules with different sequences.

4 . A method according to claim 1 , wherein the substantially monoclonal template nucleic acid molecules comprise the proximal segment having 20 to 50 identical nucleotides attaching a template nucleic acid molecule to a solid support.

5 . A method according to claim 1 , wherein the substantially monoclonal template nucleic acid molecules comprise fewer than 100 identical nucleotides at the proximal segment attaching a template nucleic acid molecule to a solid support.

6 . A method according to claim 1 , wherein the templated solid supports are templated beads and wherein the sequencing comprises distributing the templated beads in wells of a second solid support before a sequencing reaction is performed.

7 . A method according to claim 6 , wherein at least 40% of the wells in the second solid support comprise one templated bead comprising a substantially monoclonal population of template nucleic acid molecules.

8 . A method according to claim 6 , wherein at least 60% of the templated beads comprise substantially monoclonal template nucleic acid molecules.

9 . A method according to claim 1 , wherein each pre-seeded solid support of the population of pre-seeded solid supports has between 10 and 100,000 substantially monoclonal template nucleic acid molecules attached thereto and the population of pre-seeded solid supports is beads.

10 . A method according to claim 1 , wherein the substantially monoclonal template nucleic acid molecules attached to each pre-seeded solid support comprise at least 60% of the template nucleic acid molecules attached to that pre-seeded solid support.

11 . A method according to claim 1 , wherein the pre-seeding reaction mixture and/or the templating reaction mixture further comprise a recombinase-accessory protein.

12 . A method according to claim 11 , wherein the recombinase-accessory protein is a single stranded binding protein and/or a recombinase-loading protein.

13 . A method according to claim 1 , wherein the templating reaction mixture is incubated for between 10 and 60 minutes at a temperature between 35° C. and 45° C.

14 . A method according to claim 13 , wherein the pre-seeded solid supports are generated using a first recombinase-polymerase amplification (RPA) reaction and the templating reaction is a second RPA reaction.

15 . A method according to claim 14 , wherein the first RPA reaction is performed by incubating an RPA reaction mixture for 2 to 5 minutes at a temperature between 35° C. and 45° C.

16 . A method according to claim 1 , wherein the pre-seeding reaction mixture further comprises a population of identical second primers in solution, and wherein the template nucleic acid molecules comprise a primer binding site for the first primer at or near a first terminus.

17 . A method of generating one or more template nucleic acid populations on a solid support, comprising:
(a) obtaining a population of nucleic acid molecules in which each molecule comprises a first adapter sequence of contiguous nucleotides at the 5′ end of the molecule, a second adapter sequence of contiguous nucleotides at the 3′ end of the molecule and a third nucleotide sequence positioned between the first and second nucleotide sequences, wherein the first adapter nucleotide sequence and the second adapter nucleotide sequence are different and the first adapter nucleotide sequences of the nucleic acid molecules are substantially identical and the second adapter nucleotide sequences of the nucleic acid molecules are substantially identical and wherein the first adapter nucleotide sequence is modified to comprise a first linker moiety attached thereto; (b) generating single strands of the population of nucleic acid molecules and contacting the single-stranded nucleic acids with solid supports under annealing conditions to generate solid supports having single-stranded nucleic acids attached thereto through hybridization with the second adapter sequence of the nucleic acids, wherein the solid supports comprise a plurality of primer oligonucleotides having a nucleotide sequence complementary to the second adapter sequence of the nucleic acids immobilized thereto and the number of solid supports exceeds the number of nucleic acid molecules; (c) transferring the solid supports having nucleic acids attached thereto to a surface comprising microwells whereby the solid supports having nucleic acids attached thereto are individually loaded into separate microwells; (d) extending the immobilized primers of the solid support that are hybridized to a nucleic acid strand to generate double-stranded nucleic acids bound to the solid supports; (e) subjecting the nucleic acid molecules bound to the solid supports to a cycle of nucleic acid amplification in the presence of a first primer in solution, wherein (1) the first primer comprises an oligonucleotide sequence substantially identical to the first adapter nucleotide sequence and is modified to comprise a linker moiety attached thereto, (2) the amplification generates a limited number of additional single-stranded nucleic acids attached to the solid supports through hybridization between the primer oligonucleotides having a nucleotide sequence complementary to the second adapter sequence immobilized o

Assignees

• Life Technologies Corp

Inventors

• Rosenbaum Abraham
• Gray Jeremy
• Seeger Collyn
• Yu Hua

Classifications

• C12Q2600/16

  Primer sets for multiplex assays · CPC title

• C12Q1/6876

  Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes · CPC title

• C12Q1/6853

  using modified primers or templates · CPC title

• C12Q1/6834

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

• C12Q1/6874

  involving nucleic acid arrays, e.g. sequencing by hybridisation · CPC title