| Literature DB >> 32503371 |
Tanner Wiegand1, Shweta Karambelkar2, Joseph Bondy-Denomy2,3, Blake Wiedenheft1.
Abstract
More than 50 protein families have been identified that inhibit CRISPR (clustered regularly interspaced short palindromic repeats)-Cas-mediated adaptive immune systems. Here, we analyze the available anti-CRISPR (Acr) structures and describe common themes and unique mechanisms of stoichiometric and enzymatic suppressors of CRISPR-Cas. Stoichiometric inhibitors often function as molecular decoys of protein-binding partners or nucleic acid targets, while enzymatic suppressors covalently modify Cas ribonucleoprotein complexes or degrade immune signaling molecules. We review mechanistic insights that have been revealed by structures of Acrs, discuss some of the trade-offs associated with each of these strategies, and highlight how Acrs are regulated and deployed in the race to overcome adaptive immunity.Entities:
Keywords: CRISPR-Cas; Cas9; anti-CRISPR; bacteriophage; immunity
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Year: 2020 PMID: 32503371 PMCID: PMC7712631 DOI: 10.1146/annurev-micro-020518-120107
Source DB: PubMed Journal: Annu Rev Microbiol ISSN: 0066-4227 Impact factor: 15.500