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Proc Natl Acad Sci U S A. 2015 Mar 10;112(10):2984-9. doi: 10.1073/pnas.1501698112. Epub 2015 Feb 23.

Rational design of a split-Cas9 enzyme complex.

Author information

1
Department of Molecular and Cell Biology.
2
Department of Chemistry.
3
Howard Hughes Medical Institute, and.
4
Biophysics Graduate Group, University of California, Berkeley, CA 94720; and.
5
Department of Molecular and Cell Biology, Department of Chemistry, Howard Hughes Medical Institute, and Biophysics Graduate Group, University of California, Berkeley, CA 94720; and Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 doudna@berkeley.edu.

Abstract

Cas9, an RNA-guided DNA endonuclease found in clustered regularly interspaced short palindromic repeats (CRISPR) bacterial immune systems, is a versatile tool for genome editing, transcriptional regulation, and cellular imaging applications. Structures of Streptococcus pyogenes Cas9 alone or bound to single-guide RNA (sgRNA) and target DNA revealed a bilobed protein architecture that undergoes major conformational changes upon guide RNA and DNA binding. To investigate the molecular determinants and relevance of the interlobe rearrangement for target recognition and cleavage, we designed a split-Cas9 enzyme in which the nuclease lobe and α-helical lobe are expressed as separate polypeptides. Although the lobes do not interact on their own, the sgRNA recruits them into a ternary complex that recapitulates the activity of full-length Cas9 and catalyzes site-specific DNA cleavage. The use of a modified sgRNA abrogates split-Cas9 activity by preventing dimerization, allowing for the development of an inducible dimerization system. We propose that split-Cas9 can act as a highly regulatable platform for genome-engineering applications.

KEYWORDS:

CRISPR-Cas9; genome engineering; split enzyme

PMID:
25713377
PMCID:
PMC4364227
DOI:
10.1073/pnas.1501698112
[Indexed for MEDLINE]
Free PMC Article

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