Scaffolded nucleic acid polymer particles and methods of making and using

Patent metadata

Field	Value
Publication number	US-9249461-B2
Application number	US-201314044712-A
Country	US
Kind code	B2
Filing date	Oct 2, 2013
Priority date	May 29, 2009
Publication date	Feb 2, 2016
Grant date	Feb 2, 2016

Abstract

The invention provides particle compositions having applications in nucleic acid analysis. Nucleic acid polymer particles of the invention allow polynucleotides to be attached throughout their volumes for higher loading capacities than those achievable solely with surface attachment. In one aspect, nucleic acid polymer particles of the invention comprise polyacrylamide particles with uniform size distributions having low coefficients of variations, which result in reduced particle-to-particle variation in analytical assays. Such particle compositions are used in various amplification reactions to make amplicon libraries from nucleic acid fragment libraries.

First claim

What is claimed is:

1. A method of sequencing a template nucleic acid comprising:
(a) disposing a particle in a reaction chamber comprising or capacitively coupled to a field effect transistor, wherein the particle includes a non-nucleosidic polymer network and a plurality of template nucleic acids attached to the non-nucleosidic polymer network through its volume at an average density of at least 6.9×10 4 per μm 3 , the particle having a coefficient of variance of volume of not greater than 15%, the non-nucleosidic polymer network includes a polyacrylamide gel having a total monomer percentage in a range of 3% to 20% and being permeable to proteins having a size in the range of 50 kilodaltons to 200 kilodaltons;
(b) performing a polymerase extension reaction on a primer annealed to one or more of the plurality of template nucleic acids to incorporate a nucleotide into the primer; and
(c) detecting a signal output in the field effect transistor indicative of the incorporation of the nucleotide into the primer.

2. The method of claim 1 , further including disposing a plurality of particles into a plurality of reaction chambers in an array of reaction chambers, wherein at least one of the reaction chambers of the plurality of reaction chambers includes or is operatively coupled to a field effect transistor.

3. The method of claim 2 , wherein the array of reaction chambers includes at least 10 5 microwells.

4. The method of claim 2 , wherein at least one particle in the plurality of particles includes a template nucleic acid having a sequence that differs from the sequence of a template nucleic acid of at least one other particle in the plurality of particles.

5. The method of claim 2 , wherein the plurality of particles have an average diameter of from about 0.5 μm to about 10 μm.

6. The method of claim 1 , wherein the reaction chamber has a volume that is no greater than 10 μm 3 .

7. The method of claim 1 , wherein the particle includes a substantially clonal population of nucleic acids.

8. The method of claim 1 , wherein the reaction chamber includes no more than one particle.

9. The method of claim 1 , wherein the particle is substantially spherical or spheroidal in shape.

10. The method of claim 1 , wherein the field effect transistor is an ion-sensitive field effect transistor.

11. A method of analyzing an amplicon library, comprising:
(a) combining a library of polynucleotides and a population of particles in an amplification reaction mixture, wherein at least one polynucleotide includes a primer binding site and at least one particle includes a hydrophilic non-nucleosidic polymer network and a plurality of primers that are attached to the non-nucleosidic polymer network throughout the volume of the at least one particle at an average density of at least 1×10 5 per μm 3 , the population of particles having a coefficient of variance of volume of not greater than 15%, the non-nucleosidic polymer network includes a polyacrylamide gel having a total monomer percentage in a range of 3% to 20% and being permeable to proteins having a size in the range of 50 kilodaltons to 200 kilodaltons, the primer binding site being complementary to the plurality of primers;
(b) performing an amplification reaction in the amplification reaction mixture, thereby forming an amplicon library including a plurality of particles having a clonal population of polynucleotides from the population of particles; and
(c) introducing at least one particle having a clonal population of polynucleotides into a reaction chamber coupled to a field effect transistor.

12. The method of claim 11 , further including forming an emulsion of micelles prior to performing the amplification reaction, wherein the emulsion includes a plurality of micelles containing a single polynucleotide of the library of polynucleotides and a particle of the population of particles.

13. The method of claim 12 , further comprising breaking the emulsion.

14. The method of claim 11 , further including enriching to separate the plurality of particles including amplicons from other particles of the population of particles that do not include amplicons.

15. The method of claim 14 , wherein the enriching includes separating the plurality of particles including amplicons from the other particles using affinity-based separation.

16. The method of claim 11 , wherein the amplification reaction is a polymerase chain reaction.

17. The method of claim 11 , wherein the amplification reaction is an isothermal reaction.

18. The method of claim 11 , further comprising detecting a signal indicative of nucleotide incorporation with the field effect transistor.

19. The method of claim 18 , wherein the nucleotide incorporation includes incorporation of a nucleotide into a polynucleotide covalently attached, or hybridized, to a particle having a clonal population of polynucleotides.

20. The method of claim 18 , wherein the signal indicates presence of a sequencing reaction byproduct.

Assignees

• Life Technologies Corp

Inventors

• Hinz Wolfgang
• Leamon John
• Light David
• Rothberg Jonathan M

Classifications

• B01J2219/00722

  Nucleotides · CPC title

• Y10T428/2982

  Particulate matter [e.g., sphere, flake, etc.] · CPC title

• B01J19/0046

  Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays (synthesis methods per se C40B50/00) · CPC title

• B01J2219/00596

  Solid-phase processes · CPC title

• B01J2219/005

  Beads · CPC title