8HJ4

CryoEM structure of an anti-CRISPR protein AcrIIC5 bound to Nme1Cas9-sgRNA complex

8HJ4 の概要

• エントリーDOI: 10.2210/pdb8hj4/pdb
• EMDBエントリー: 34832
• 分子名称: CRISPR-associated endonuclease Cas9, sgRNA, Phage protein (3 entities in total)
• 機能のキーワード: cas9, anti-crispr proteins, cleavage inhibition, antimicrobial protein, hydrolase-rna-antimicrobial protein complex, hydrolase/rna/antimicrobial protein
• 由来する生物種: Neisseria meningitidis serogroup C (strain 8013); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 183160.15

構造登録者

Wang, Y.,Sun, W. (登録日: 2022-11-22, 公開日: 2023-01-25, 最終更新日: 2024-07-03)

主引用文献

Sun, W.,Zhao, X.,Wang, J.,Yang, X.,Cheng, Z.,Liu, S.,Wang, J.,Sheng, G.,Wang, Y.
Anti-CRISPR AcrIIC5 is a dsDNA mimic that inhibits type II-C Cas9 effectors by blocking PAM recognition.
Nucleic Acids Res., 51:1984-1995, 2023

PubMed Abstract: Anti-CRISPR proteins are encoded by phages to inhibit the CRISPR-Cas systems of the hosts. AcrIIC5 inhibits several naturally high-fidelity type II-C Cas9 enzymes, including orthologs from Neisseria meningitidis (Nme1Cas9) and Simonsiella muelleri (SmuCas9). Here, we solve the structure of AcrIIC5 in complex with Nme1Cas9 and sgRNA. We show that AcrIIC5 adopts a novel fold to mimic the size and charge distribution of double-stranded DNA, and uses its negatively charged grooves to bind and occlude the protospacer adjacent motif (PAM) binding site in the target DNA cleft of Cas9. AcrIIC5 is positioned into the crevice between the WED and PI domains of Cas9, and one end of the anti-CRISPR interacts with the phosphate lock loop and a linker between the RuvC and BH domains. We employ biochemical and mutational analyses to build a model for AcrIIC5's mechanism of action, and identify residues on both the anti-CRISPR and Cas9 that are important for their interaction and inhibition. Together, the structure and mechanism of AcrIIC5 reveal convergent evolution among disparate anti-CRISPR proteins that use a DNA-mimic strategy to inhibit diverse CRISPR-Cas surveillance complexes, and provide new insights into a tool for potent inhibition of type II-C Cas9 orthologs.

PubMed: 36744495
DOI: 10.1093/nar/gkad052

実験手法

ELECTRON MICROSCOPY (3.1 Å)