IP Library Granted Patent US 10,640,790
Granted Patent B2
US 10,640,790 · App. 16/055,525 · Granted May 5, 2020

Artificial nucleases including engineered FokI cleavage half-domains

Inventors: Yannick Doyon (Quebec, CA); Jeffrey C. Miller (Richmond, CA)
Assignee: Sangamo Therapeutics, Inc.
C12N15/907C07K7/06C07K14/47C12N9/22C12N15/85C07K2319/50C07K2319/80C07K2319/81C12Y301/21004
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Quick Facts
Patent No.
US 10,640,790
App. No.
16/055,525
Granted
May 5, 2020
Kind
B2
Abstract

Disclosed herein are engineered cleavage half-domains; fusion polypeptides comprising these engineered cleavage half-domains; polynucleotides encoding the engineered cleavage half-domains and fusion proteins; and cells comprising said polynucleotides and/or fusion proteins. Also described are methods of using these polypeptides and polynucleotides, for example for targeted cleavage of a genomic sequence.

Claims (14)

1. An artificial nuclease comprising:

(i) a DNA-binding domain that binds to a target site in the genome of the cell; and

(ii) a polypeptide comprising an engineered FokI cleavage half-domain consisting of substitution mutations at least two of the following positions: 483, 486, 487, 490, 496, 499, 537 or 538, numbered relative to a wild-type FokI sequence as shown in SEQ ID NO:57, wherein if the FokI cleavage half-domain includes a mutation at position 486, position 490 is not mutated.

2. An artificial nuclease comprising:

(i) a DNA-binding domain that binds to a target site in the genome of the cell; and

(ii) a polypeptide comprising an engineered FokI cleavage half-domain consisting of substitution mutations at least two of the following positions: 483, 486, 487, 490, 496, 499, 537 or 538, wherein if the FokI cleavage half-domain includes a mutation at position 486, position 490 is not mutated and an additional amino acid substitution at one or more of positions 418, 432, 441, 481, 486, 523, 527 and 559, numbered relative to a wild-type FokI sequence as shown in SEQ ID NO:57.

3. A method of making a genomic modification in a cell, the method comprising administering at least one nuclease according to claim 1 to a cell, wherein the nuclease genetically modifies a gene locus in the cell.

4. The method of claim 3 , wherein the gene locus is inactivated.

5. The method of claim 3 , wherein the genomic modification wherein the genomic modification comprises an insertion.

6. The method of claim 5 , wherein a transgene is inserted into the gene locus.

7. The method of claim 3 , wherein the genomic modification comprises a deletion.

8. The method of claim 7 , wherein the genomic modification further comprises an insertion.

9. The method of claim 8 , wherein a transgene is inserted into the gene locus.

10. The method of claim 3 , wherein the cell is a T-cell, a hematopoietic stem cell or a liver cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2022
From: DOYON, YANNICK; MILLER, JEFFREY C.
To: SANGAMO BIOSCIENCES, INC.
Reel/Frame 061816/0800 →
CHANGE OF NAME Recorded Nov 17, 2022
From: SANGAMO BIOSCIENCES, INC.
To: SANGAMO THERAPEUTICS, INC.
Reel/Frame 061963/0933 →
Continuity (7)
Continuation 15660072 · Jul 26, 2017
Continuation 15160571 · May 20, 2016
Continuation 14627812 · Feb 20, 2015
Continuation 12931660 · Feb 7, 2011
Provisional Application 61337769 · Feb 8, 2010
Provisional Application 61403916 · Sep 23, 2010
Related Publication 20180334689A1 · Nov 22, 2018