Structural Investigation of the Anti‐ <scp>CRISPR</scp> Protein <scp>AcrIE7</scp>

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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Publication Details

Journal
Proteins Structure Function and Bioinformatics
Published
2025-05-03
DOI
https://doi.org/10.1002/prot.26832
Citations
3
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
2.42

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article

Structural Investigation of the Anti‐ CRISPR Protein AcrIE7

Gyujin Lee, Jeong‐Yong Suh, Euiyoung Bae, Changkon Park et al.
3 citations
Proteins Structure Function and Bioinformatics
CRISPR and Genetic Engineering
2.42
article

Structural Investigation of the Anti‐ CRISPR Protein AcrIE7

Gyujin Lee, Jeong‐Yong Suh, Euiyoung Bae, Changkon Park, Jong‐Soo Kang, Eun‐Hee Kim, Hyejin Oh, Jasung Koo
article en
3 citations

Abstract

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.

Proteins Structure Function and BioinformaticsVol. 93(9)
Seoul National University (KR), Korea Basic Science Institute (KR)
Korea Basic Science Institute, National Research Foundation of Korea
Openalex Percentile: Top 12%
CRISPR and Genetic Engineering
2.42
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Structural Investigation of the Anti‐ <scp>CRISPR</scp> Protein <scp>AcrIE7</scp> — Gyujin Lee, Jeong‐Yong Suh, et al. · Proteins Structure Function and Bioinformatics (2025) | TGRS Research Map | TGRS