Protein Inhibitors of CRISPR-Cas9

被引:41
|
作者
Bondy-Denomy, Joseph [1 ]
机构
[1] Univ Calif San Francisco, Quantitat Biosci Inst, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
ANTI-CRISPR; DNA; MECHANISMS; NUCLEASES; VIRUSES; CLASSIFICATION; ENDONUCLEASE; COMPLEX;
D O I
10.1021/acschembio.7b00831
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacteria are under constant predation from viruses, called bacteriophages (phages). This threat has driven the evolution of multiple defense systems, including the CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR associated genes) immune pathway. Phages are not passive bystanders in their CRISPR-mediated demise, however, as many have developed potent protein inhibitors of the bacterial adaptive immune system. Here, I review the work that led to the discovery of many distinct "anti-CRISPR" proteins. Furthermore, I outline how understanding their mechanisms of action has provided a suite of specific and high-affinity reagents to modulate and study CRISPR-Cas applications.
引用
收藏
页码:417 / 423
页数:7
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