Variant libraries of the immunological synapse and synthesis thereof

Patent metadata

Field	Value
Publication number	US-10894959-B2
Application number	US-201815921537-A
Country	US
Kind code	B2
Filing date	Mar 14, 2018
Priority date	Mar 15, 2017
Publication date	Jan 19, 2021
Grant date	Jan 19, 2021

Abstract

Disclosed herein are methods for the generation of highly accurate nucleic acid libraries encoding for predetermined variants of a nucleic acid sequence. The nucleic acid sequence may encode for all or part of a reference domain of a CAR. The degree of variation may be complete, resulting in a saturated variant library, or less than complete, resulting in a non-saturating library of variants. The variant nucleic acid libraries described herein may be designed for further processing by transcription or translation. The variant nucleic acid libraries described herein may be designed to generate variant RNA, DNA and/or protein populations. Further provided herein are method for identifying variant species with increased or decreased activities, with applications in regulating biological functions and the design of therapeutics for treatment or reduction of a disease, such as cancer.

First claim

What is claimed is:

1. A method of synthesizing an oligonucleotide library, comprising:
a. providing a first set of preselected oligonucleotide sequences encoding for at least 400 sequences of a chimeric antigen receptor gene or gene fragment, wherein each sequence comprises at least one variation of at least two preselected codons for an amino acid residue in an antigen recognition domain;
b. synthesizing the first set of preselected oligonucleotide sequences; and
c. screening a first activity for proteins encoded by the first set of oligonucleotide sequences, wherein the first activity is specificity, avidity, affinity, stability, or expression, wherein the first set of preselected oligonucleotides comprises all variations of the at least two preselected codons.

2. The method of claim 1 , wherein each oligonucleotide is at least 50 bases or at least 100 bases in length.

3. The method of claim 1 , wherein each sequence comprises at least one variation of at least three preselected codons.

4. The method of claim 1 , wherein each sequence comprises at least one variation of four or more preselected codons.

5. The method of claim 1 , wherein the at least two preselected codons are consecutive codons.

6. The method of claim 1 , further comprising amplification of the first set of oligonucleotide sequences to generate a first library of expression constructs.

7. The method of claim 6 , further comprising transferring the expression constructs into mammalian cells to generate a first library of cell populations expressing variant chimeric expression antigens.

8. The method of claim 1 , wherein the chimeric antigen receptor gene or gene fragment is from a tumor antigen.

9. The method of claim 7 , further comprising:
a. screening the variant chimeric expression antigens for binding specificity;
b. generating a second library of expression constructs from the variant chimeric expression antigens showing increased specificity; and
c. transferring the second library of expression constructs to mammalian cells to generate a second library of cell populations expressing variant chimeric expression antigens.

10. The method of claim 1 , further comprising:
a. contacting the oligonucleotide sequences with DNA polymerase reagents to generate a polymerase cycling assembly (PCA) reaction;
b. annealing the oligonucleotide sequences;
c. filling gaps with an extension reaction; and
d. ligating the oligonucleotide sequences into expression vectors.

11. A method of synthesizing an oligonucleotide library, comprising:
a. providing a first set of preselected oligonucleotide sequences encoding for at least 400 sequences of a chimeric antigen receptor gene or gene fragment, wherein each sequence comprises at least one variation of at least two preselected codons for an amino acid residue in an antigen recognition domain; and
b. synthesizing the first set of preselected oligonucleotide sequences, wherein the first set of preselected oligonucleotides comprises all variations of the at least two preselected codons.

12. The method of claim 11 , wherein each oligonucleotide is at least 50 bases or at least 100 bases in length.

13. The method of claim 11 , wherein the at least two preselected codons are consecutive codons.

Assignees

• Twist Bioscience Corp

Inventors

• Cox Anthony
• Chen Siyuan

Classifications

• C12N15/1093 Primary

  General methods of preparing gene libraries, not provided for in other subgroups · CPC title

• C12N15/1027 Primary

  by DNA shuffling, e.g. RSR, STEP, RPR · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title