Optimized CRISPR-CAS double nickase systems, methods and compositions for sequence manipulation

Patent metadata

Field	Value
Publication number	US-12553065-B2
Application number	US-202318106039-A
Country	US
Kind code	B2
Filing date	Feb 6, 2023
Priority date	Jun 17, 2013
Publication date	Feb 17, 2026
Grant date	Feb 17, 2026

Abstract

The invention provides for delivery, engineering and optimization of systems, methods, and compositions for manipulation of sequences and/or activities of target sequences. Provided are vectors and vector systems, some of which encode one or more components of a CRISPR complex, as well as methods for the design and use of such vectors. Also provided are methods of directing CRISPR complex formation in prokaryotic and eukaryotic cells to ensure enhanced specificity for target recognition and avoidance of toxicity.

First claim

What is claimed is:

1 . An engineered CRISPR-Cas system for modifying a genomic locus of interest in a eukaryotic cell, comprising:
a Cas9 protein or a polynucleotide encoding the Cas9 protein, wherein the Cas9 protein comprises at least one mutation in a catalytic domain and is a nickase, wherein the Cas9 protein is fused to at least one nuclear localization signal (NLS); a first CRISPR-Cas system chimeric RNA engineered to hybridize to a first target sequence at the genomic locus of interest, wherein the first chimeric RNA is capable of forming a first CRISPR complex with the Cas9 protein and directing sequence-specific binding of the first CRISPR complex to the first target sequence in the nucleus of the eukaryotic cell, thereby allowing the Cas9 protein to cleave a first DNA strand of the genomic locus of interest to produce a first nick; and a second CRISPR-Cas system chimeric RNA engineered to hybridize to a second target sequence at the genomic locus of interest, wherein the second chimeric RNA is capable of forming a second CRISPR complex with the Cas9 protein and directing sequence-specific binding of the second CRISPR complex to the second target sequence in the nucleus of the eukaryotic cell, thereby allowing the Cas9 protein to cleave a second DNA strand of the genomic locus of interest to produce a second nick, wherein the first nick is located 26-200 nucleotides 5′ of the second nick.

2 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein is fused to at least two NLSs.

3 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein comprises at least one mutation in RuvC domain.

4 . The engineered CRISPR-Cas system of claim 3 , wherein the Cas9 protein comprises at least one mutation selected from the group consisting of D10A, E762A and D986A.

5 . The engineered CRISPR-Cas system of claim 3 , wherein the Cas9 protein comprises D10A mutation.

6 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein comprises at least one mutation in HNH domain.

7 . The engineered CRISPR-Cas system of claim 6 , wherein the Cas9 protein comprises at least one mutation selected from the group consisting of H840A, N854A and N863A.

8 . The engineered CRISPR-Cas system of claim 6 , wherein the Cas9 protein comprises H840A mutation.

9 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein is S. pyogenes Cas9.

10 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein is S. aureus Cas9.

11 . The engineered CRISPR-Cas system of claim 1 , wherein the Cas9 protein is fused to at least one heterologous protein domain.

12 . The engineered CRISPR-Cas system of claim 11 , wherein the heterologous protein domain is a methylase, a demethylase, a transcriptional activator, a transcriptional repressor, a recombinase, a transposase, a histone remodeler, a DNA methyltransferase, or a cryptochrome.

13 . The engineered CRISPR-Cas system of claim 1 , wherein the first nick is located 26-100 nucleotides 5′ of the second nick.

14 . The engineered CRISPR-Cas system of claim 1 , wherein the first nick is located 30-200 nucleotides 5′ of the second nick.

15 . The engineered CRISPR-Cas system of claim 1 , wherein the first nick is located 30-100 nucleotides 5′ of the second nick.

16 . The engineered CRISPR-Cas system of claim 1 , wherein the first nick is about 34-50 nucleotides 5′ of the second nick.

17 . The engineered CRISPR-Cas system of claim 1 , wherein the engineered CRISPR-Cas system comprises a viral vector encoding the Cas9.

18 . The engineered CRISPR-Cas system of claim 1 , wherein the engineered CRISPR-Cas system comprises an AAV vector encoding the Cas9.

19 . The engineered CRISPR-Cas system of claim 1 , wherein the engineered CRISPR-Cas system comprises an mRNA encoding the Cas9.

20 . The engineered CRISPR-Cas system of claim 1 , wherein the genomic locus of interest encodes a gene product.

21 . The engineered CRISPR-Cas system of claim 20 , wherein the gene product is a protein.

22 . The engineered CRISPR-Cas system of claim 1 , wherein the eukaryotic cell is a mammalian cell.

23 . The engineered CRISPR-Cas system of claim 1 , further comprising an exogenous recombination template for targeted integration into the genomic locus of interest.

24 . The engineered CRISPR-Cas system of claim 23 , wherein the exogenous recombination template is at least 1,000 nucleotides in length.

Assignees

• Broad Inst Inc
• Massachusetts Inst Technology
• Harvard College

Inventors

• Zhang Feng
• Hsu Patrick
• Lin Chie-Yu
• Ran Fei

Classifications

• C12N2800/80

  Vectors containing sites for inducing double-stranded breaks, e.g. meganuclease restriction sites · CPC title

• C12N15/102

  Mutagenizing nucleic acids · CPC title

• A61K48/005

  characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered · CPC title

• C12N15/63

  Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression · CPC title

• C12N15/1082

  Preparation or screening gene libraries by chromosomal integration of polynucleotide sequences, HR-, site-specific-recombination, transposons, viral vectors · CPC title