9G9H

CryoEM structure of Enterococcus italicus Csm-crRNA-CTR1 complex bound to pNppA3 and AMPNPP

これはPDB形式変換不可エントリーです。

9G9H の概要

• エントリーDOI: 10.2210/pdb9g9h/pdb
• EMDBエントリー: 51152
• 分子名称: CRISPR system single-strand-specific deoxyribonuclease Cas10/Csm1 (subtype III-A), MAGNESIUM ION, CRISPR system Cms protein Csm5, ... (10 entities in total)
• 機能のキーワード: type iii-a crispr-cas rna-guided nuclease endoribonuclease cyclic oligoadenylate synthetase hd nuclease, rna binding protein
• 由来する生物種: Enterococcus italicus DSM 15952; 詳細
• タンパク質・核酸の鎖数: 10
• 化学式量合計: 300916.32

構造登録者

Jungfer, K.,Jinek, M. (登録日: 2024-07-25, 公開日: 2025-01-29)

主引用文献

Jungfer, K.,Moravcik, S.,Garcia-Doval, C.,Knorlein, A.,Hall, J.,Jinek, M.
Mechanistic determinants and dynamics of cA6 synthesis in type III CRISPR-Cas effector complexes.
Nucleic Acids Res., 53:-, 2025

PubMed Abstract: Type III clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) systems (type III CRISPR-Cas systems) use guide RNAs to recognize RNA transcripts of foreign genetic elements, which triggers the generation of cyclic oligoadenylate (cOA) second messengers by the Cas10 subunit of the type III effector complex. In turn, cOAs bind and activate ancillary effector proteins to reinforce the host immune response. Type III systems utilize distinct cOAs, including cyclic tri- (cA3), tetra- (cA4) and hexa-adenylates (cA6). However, the molecular mechanisms dictating cOA product identity are poorly understood. Here we used cryoelectron microscopy to visualize the mechanism of cA6 biosynthesis by the Csm effector complex from Enterococcus italicus (EiCsm). We show that EiCsm synthesizes oligoadenylate nucleotides in 3'-5' direction using a set of conserved binding sites in the Cas10 Palm domains to determine the size of the nascent oligoadenylate chain. Our data also reveal that conformational dynamics induced by target RNA binding results in allosteric activation of Cas10 to trigger oligoadenylate synthesis. Mutations of a key structural element in Cas10 perturb cOA synthesis to favor cA3 and cA4 formation. Together, these results provide comprehensive insights into the dynamics of cOA synthesis in type III CRISPR-Cas systems and reveal key determinants of second messenger product selectivity, thereby illuminating potential avenues for their engineering.

PubMed: 39817514
DOI: 10.1093/nar/gkae1277

実験手法

ELECTRON MICROSCOPY (2.99 Å)