Automated instrumentation for production of T-cell receptor peptide libraries

Patent metadata

Field	Value
Publication number	US-11396718-B2
Application number	US-202217690641-A
Country	US
Kind code	B2
Filing date	Mar 9, 2022
Priority date	Apr 24, 2018
Publication date	Jul 26, 2022
Grant date	Jul 26, 2022

Abstract

The present disclosure provides instrumentation and automated methods for creating cell surface display libraries, where the cells of the library display engineered peptides on their cell surfaces for identification of antigens that bind to T-cell receptors. The engineered peptides may be putative antigens or binding regions of the T-cell receptors.

First claim

We claim:

1. An automated method of creating a cell library co-expressing engineered proteins and MHC molecules, the method comprising:
processing a population of cells using an instrument for multiplexed nuclease-directed genome editing using introduced nucleic acids and a nuclease, wherein the introduced nucleic acids comprise nucleic acids that encode engineered proteins and MHC molecules configured to be displayed on surfaces of the cells, the engineered proteins comprising unique polypeptides linked to immobilization peptides for immobilization on the surfaces of the cells;
incubating the processed cells to facilitate nucleic acid editing in the cells, wherein the edited cells co-express the engineered proteins and MHC molecules in the cells; and
allowing the cells to display the engineered proteins and the MHC molecules on the surfaces of the cells.

2. The method of claim 1 , wherein the immobilization peptides comprise a first binding motif that selectively binds to a second binding motif present on the surfaces of the cells.

3. The method of claim 2 , wherein the first binding motif comprises avidin, streptavidin, or neutravidin.

4. The method of claim 2 , wherein the second binding motif comprises biotin.

5. The method of claim 1 , wherein the immobilization peptides comprise a transmembrane polypeptide, a polypeptide membrane anchor, a GPI-linked polypeptide, or a natural surface polypeptide.

6. The method of claim 1 , wherein the immobilization peptides are linked to a C-terminus or an N-terminus of the unique polypeptides.

7. The method of claim 1 , wherein the unique polypeptides comprise putative T-cell receptor (TCR) antigens.

8. The method of claim 1 , wherein the unique polypeptides comprise predicted T-cell receptor (TCR) binding regions.

9. An automated method of creating a cell library co-expressing engineered proteins and MHC molecules, the method comprising:
processing a population of cells using an instrument for multiplexed nuclease-directed genome editing using introduced nucleic acids and a nuclease, wherein the introduced nucleic acids comprise nucleic acids that encode engineered proteins and MHC molecules configured to be displayed on surfaces of the cells, the engineered proteins comprising unique polypeptides linked to immobilization peptides for immobilization on the surfaces of the cells, the unique polypeptides comprising putative T-cell receptor (TCR) antigens or predicted TCR binding regions;
incubating the processed cells to facilitate nucleic acid editing in the cells, wherein the edited cells co-express the engineered proteins and MHC molecules in the cells; and
allowing the cells to display the engineered proteins and the MHC molecules on the surfaces of the cells.

10. The method of claim 9 , wherein the immobilization peptides comprise a first binding motif that selectively binds to a second binding motif present on the surfaces of the cells.

11. The method of claim 10 , wherein the first binding motif comprises avidin, streptavidin, or neutravidin.

12. The method of claim 10 , wherein the second binding motif comprises biotin.

13. The method of claim 9 , wherein the immobilization peptides comprise a transmembrane polypeptide, a polypeptide membrane anchor, a GPI-linked polypeptide, or a natural surface polypeptide.

14. The method of claim 9 , wherein the immobilization peptides are linked to a C-terminus or an N-terminus of the unique polypeptides.

15. An automated method of creating a cell library expressing engineered proteins on surfaces of the cells, the method comprising:
processing a population of cells using an instrument for multiplexed nuclease-directed genome editing using introduced nucleic acids and a nuclease, wherein the introduced nucleic acids comprise nucleic acids that encode engineered proteins to be displayed on surfaces of the cells, the engineered proteins comprising unique polypeptides linked to immobilization peptides for immobilization on the surfaces of the cells;
incubating the processed cells to facilitate nucleic acid editing in the cells, wherein the edited cells express the engineered proteins in the cells; and
allowing the cells to display the engineered proteins on the surfaces of the cells.

16. The method of claim 15 , wherein the immobilization peptides comprise a first binding motif that selectively binds to a second binding motif present on the surfaces of the cells.

17. The method of claim 16 , wherein the first binding motif comprises avidin, streptavidin, or neutravidin.

18. The method of claim 16 , wherein the second binding motif comprises biotin.

19. The method of claim 15 , wherein the immobilization peptides comprise a transmembrane polypeptide, a polypeptide membrane anchor, a GPI-linked polypeptide, or a natural surface polypeptide.

20. The method of claim 15 , wherein the unique polypeptides comprise putative T-cell receptor (TCR) antigens or predicted TCR binding regions.

Assignees

• Inscripta Inc

Inventors

• Federowicz Stephen
• Church Deanna
• Graige Michael

Classifications

• C07K14/70539 Primary

  MHC-molecules, e.g. HLA-molecules · CPC title

• C12N9/22

  Ribonucleases {[RNase]; Deoxyribonucleases [DNase]} · CPC title

• C40B40/02

  Libraries contained in or displayed by microorganisms, e.g. bacteria or animal cells; Libraries contained in or displayed by vectors, e.g. plasmids; Libraries containing only microorganisms or vectors · CPC title

• C12N15/1037 Primary

  Screening libraries presented on the surface of microorganisms, e.g. phage display, E. coli display · CPC title

• C12N15/81

  for yeasts · CPC title