IP Library Granted Patent US 12,060,559
Granted Patent B2
US 12,060,559 · App. 15/734,522 · Granted Aug 13, 2024

Compositions and methods involving non-natural aptamer libraries

Inventors: Jia Niu (Stanford, CA); Chelsea Lyons Gordon (Stanford, CA); Hyongsok Tom Soh (San Francisco, CA)
Assignees: CZ Biohub SF, LLC; The Board of Trustees of the Leland Stanford Junior University
C12N15/115C12Q1/6811C12Q1/686C12N2310/16C12N2320/13
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Quick Facts
Patent No.
US 12,060,559
App. No.
15/734,522
Granted
Aug 13, 2024
Kind
B2
Abstract

The disclosure is directed to methods and compositions for screening a library of aptamers for aptamers having a binding affinity to a target molecule. Specifically, non-natural nucleotides can be introduced onto aptamers immobilized on the surface of beads. The non-natural nucleotides can then be subsequently chemically modified to include additional binding agents. For example, copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions can be used to introduce a wide range of binding agents onto non-natural nucleotides on beads.

Claims (26)

1. A plurality of beads linked to aptamers comprising at least one non-natural nucleotide, wherein the sequences of aptamers linked to different beads are different, wherein each bead in the plurality are linked to multiple copies of only one aptamer, and wherein the base of the non-natural nucleotide is covalently bonded to a binding agent.

2. The plurality of beads of claim 1 , wherein the non-natural nucleotide is covalently bonded to the binding agent via a triazole moiety.

3. The plurality of beads of claim 1 , wherein the non-natural nucleotide is C8-alkyne-dUTP.

4. The plurality of beads of claim 1 , wherein aptamers linked to the beads comprise at least first and a second non-natural nucleotides that are structurally-different.

5. The plurality of beads of claim 4 , wherein the first non-natural nucleotide is linked to the binding agent and the second non-natural nucleotide is not linked to a binding agent.

6. The plurality of beads of claim 5 , wherein the second non-natural nucleotide comprises an aldehyde.

7. The plurality of beads of claim 4 , wherein the first non-natural nucleotide is linked to the binding agent and the second non-natural nucleotide is linked to a second binding agent.

8. The plurality of beads of claim 1 , wherein the binding agent is an amino acid, a sugar, a peptide, or a protein.

9. The plurality of beads of claim 8 , wherein the binding agent is an azide-modified tyrosine.

10. The plurality of beads of claim 8 , wherein the binding agent is an azide-modified tryptophan.

11. The plurality of beads of claim 8 , wherein the binding agent is an azide-modified boronic acid.

12. The plurality of beads of claim 1 , wherein the plurality of beads comprises at least 100 beads each linked to a different aptamer having a different sequence.

13. A method of making the plurality of beads linked to aptamers of claim 1 , the method comprising,

providing a plurality of aqueous droplets wherein a majority of the droplets comprise only one bead linked to a forward primer and only one aptamer template polynucleotide, wherein the droplets in the majority each comprise an aptamer template polynucleotide having a different sequence;

performing amplification within the droplets, wherein the droplets contain nucleotide triphosphates (NTPs) and a non-natural nucleotide triphosphate having a nucleotide base linked to a functional group, wherein the forward primer hybridizes to the aptamer template polynucleotide and is extended by a polymerase using the aptamer template polynucleotide as a template to generate an extension product linked to the bead and comprising an aptamer sequence and wherein the non-natural nucleotide is incorporated into the aptamer sequence, thereby forming a plurality of beads linked to aptamers comprising at least one non-natural nucleotide; and

reacting the functional group with a reactive species comprising a binding agent such that the non-natural nucleotide is covalently bonded to the binding agent.

14. The methods of claim 13 , wherein the functional group is an alkyne or an azide.

15. The method of claim 13 , wherein the droplets contain at least a first and a second non-natural nucleotide triphosphate that are structurally-different and wherein the first and the second non-natural nucleotide are incorporated into the aptamer sequence.

16. The method of claim 15 , wherein the first non-natural nucleotide comprises an alkyne or an azide functional group and the second non-natural nucleotide comprises an aldehyde.

17. The method of claim 13 , further comprising combining contents of the droplets after the performing of the amplification and before the reacting.

18. The method of claim 13 , wherein the non-natural nucleotide is C8-alkyne-dUTP.

19. The method of claim 13 , wherein a first non-natural nucleotide comprises an alkyne and the reactive species comprises an azide and during the reacting the azide undergoes Cu-catalyzed azide-alkyne cycloaddition (CuAAC) with the alkyne in the non-natural nucleotide to form a covalent bond.

20. A method of identifying an aptamer that binds a target molecule, the method comprising

contacting the plurality of beads of claim 1 to the target molecule;

enriching the plurality of beads for beads that bind the target molecule; and

determining the sequence of aptamers that bind the target molecule.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2021
From: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
To: CHAN ZUCKERBERG BIOHUB, INC.; THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 056257/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2020
From: NIU, JIA; GORDON, CHELSEA LYONS; SOH, HYONGSOK TOM
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 054521/0628 →
Continuity (2)
Provisional Application 62680441 · Jun 4, 2018
Related Publication 20210332360A1 · Oct 28, 2021