IP Library Granted Patent US 8,034,598
Granted Patent B2
US 8,034,598 · App. 12/456,857 · Granted Oct 11, 2011

Engineered cleavage half-domains

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Quick Facts
Patent No.
US 8,034,598
App. No.
12/456,857
Granted
Oct 11, 2011
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 (18)

1. A polypeptide comprising an engineered FokI cleavage half-domain, wherein

(i) the engineered cleavage half-domain comprises a mutation in one or more wild-type amino acid residue 483, 486, 487, 490, 499, 538 or combinations thereof, wherein the amino acid residues are numbered relative to full length wild-type FokI;

(ii) the engineered cleavage half-domain forms an obligate heterodimer with a wild-type cleavage half-domain or a second engineered cleavage half-domain; and

(iii) if the engineered cleavage half-domain comprises a mutation at amino acid residue 490, it further comprises at least one additional amino acid mutation.

2. The polypeptide of claim 1 , wherein the amino acid residues at positions 490 and 538 are mutated.

3. The polypeptide of the claim 2 , wherein the engineered cleavage half-domain comprises the polypeptide designated E490K:1538K.

4. The polypeptide of claim 1 , wherein the wild-type amino acid at position 486 is mutated.

5. The polypeptide of claim 4 , wherein the engineered cleavage half-domain comprises the polypeptide designated Q486E.

6. The polypeptide of claim 1 , wherein the wild-type amino acid residue at position 499 is mutated.

7. The polypeptide of claim 6 , wherein the engineered cleavage half-domain comprises the polypeptide designated 1499L.

8. The polypeptide of claim 7 , wherein the engineered cleavage half-domain comprises the polypeptide designated Q486E:1499L.

9. A heterodimer comprising an engineered cleavage half-domain of claim 1 and a wild-type Fokl cleavage half-domain.

10. The heterodimer of claim 9 , wherein the engineered cleavage half-domain comprises the polypeptide designated E490K:1538K.

11. A heterodimer comprising a first engineered cleavage half-domain of claim 1 and a second engineered cleavage half-domain.

12. The heterodimer of claim 11 , wherein the first engineered cleavage half-domain comprises mutation in amino acid residue 490 and/or amino acid residue 538.

13. The heterodimer of claim 11 , wherein the second engineered cleavage half-domain comprises a mutation in amino acid residue 486 and/or amino acid residue 499.

14. The polypeptide of claim 1 , further comprising a zinc finger protein DNA-binding domain.

15. An isolated cell comprising the polypeptide of claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Jul 9, 2019
From: SANGAMO BIOSCIENCES, INC.
To: SANGAMO THERAPEUTICS, INC.
Reel/Frame 049706/0242 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2009
From: MILLER, JEFFREY C.
To: SANGAMO BIOSCIENCES, INC.
Reel/Frame 023081/0943 →