Summary information and primary citation

PDB-id
6i1k; DSSR-derived features in text and JSON formats
Class
hydrolase
Method
X-ray (2.65 Å)
Summary
Crystal structure of catalytically inactive fncas12a in complex with a crrna guide and a dsDNA target
Reference
Swarts DC, Jinek M (2019): "Mechanistic Insights into the cis- and trans-Acting DNase Activities of Cas12a." Mol. Cell, 73, 589-600.e4. doi: 10.1016/j.molcel.2018.11.021.
Abstract
CRISPR-Cas12a (Cpf1) is an RNA-guided DNA-cutting nuclease that has been repurposed for genome editing. Upon target DNA binding, Cas12a cleaves both the target DNA in cis and non-target single-stranded DNAs (ssDNAs) in trans. To elucidate the molecular basis for both DNase cleavage modes, we performed structural and biochemical studies on Francisella novicida Cas12a. We show that guide RNA-target strand DNA hybridization conformationally activates Cas12a, triggering its trans-acting, non-specific, single-stranded DNase activity. In turn, cis cleavage of double-stranded DNA targets is a result of protospacer adjacent motif (PAM)-dependent DNA duplex unwinding, electrostatic stabilization of the displaced non-target DNA strand, and ordered sequential cleavage of the non-target and target DNA strands. Cas12a releases the PAM-distal DNA cleavage product and remains bound to the PAM-proximal DNA cleavage product in a catalytically competent, trans-active state. Together, these results provide a revised model for the molecular mechanisms of both the cis- and the trans-acting DNase activities of Cas12a enzymes, enabling their further exploitation as genome editing tools.

Cartoon-block schematics in six views (download the tarball)

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