Structural Investigation of the Anti-CRISPR Protein AcrIE7

被引:0
|
作者
Kang, Jeehee [1 ]
Park, Changkon [1 ]
Lee, Gyujin [1 ]
Koo, Jasung [1 ,2 ]
Oh, Hyejin [1 ]
Kim, Eun-Hee [3 ]
Bae, Euiyoung [1 ,2 ]
Suh, Jeong-Yong [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Agr Biotechnol, Seoul, South Korea
[2] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul, South Korea
[3] Korea Basic Sci Inst, Biopharmaceut Res Ctr, Ochang, South Korea
基金
新加坡国家研究基金会;
关键词
AcrIE7; AlphaFold; anti-CRISPR; CRISPR-Cas; protein structure; GUIDED SURVEILLANCE COMPLEX; CRYSTAL-STRUCTURE; EVOLUTIONARY CLASSIFICATION; RNA CLEAVAGE; SYSTEM; RECOGNITION; BACTERIA; ANGLES;
D O I
10.1002/prot.26832
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
The CRISPR-Cas system is an adaptive immune system in prokaryotes that provides protection against bacteriophages. As a countermeasure, bacteriophages have evolved various anti-CRISPR proteins that neutralize CRISPR-Cas immunity. Here, we report the structural and functional investigation of AcrIE7, which inhibits the type I-E CRISPR-Cas system in Pseudomonas aeruginosa. We determined both crystal and solution structures of AcrIE7, which revealed a novel helical fold. In binding assays using various biochemical methods, AcrIE7 did not tightly interact with a single Cas component in the type I-E Cascade complex or the CRISPR adaptation machinery. In contrast, AlphaFold modeling with our experimentally determined AcrIE7 structure predicted that AcrIE7 interacts with Cas3 in the type I-E CRISPR-Cas system in P. aeruginosa. Our findings are consistent with a model where AcrIE7 inhibits Cas3 and also highlight the effectiveness and limitations of AlphaFold modeling.
引用
收藏
页数:12
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