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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.
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页数:12
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