9L12

Crystal structure of Cas12h ternary complex

9L12 の概要

• エントリーDOI: 10.2210/pdb9l12/pdb
• 分子名称: Cas12h, DNA (28-MER), DNA (5'-D(P*AP*GP*TP*CP*GP*AP*TP*GP*TP*TP*CP*T)-3'), ... (5 entities in total)
• 機能のキーワード: rna, dna, complex, dna binding protein
• 由来する生物種: unidentified; 詳細
• タンパク質・核酸の鎖数: 12
• 化学式量合計: 394033.29

構造登録者

Xiang, W.,Chen, J.,Liu, L. (登録日: 2024-12-13, 公開日: 2025-06-11)

主引用文献

Xiang, W.,Lin, X.,Yang, Y.,Huang, L.,Chen, Y.,Chen, J.,Liu, L.
Cas12h is a crRNA-guided DNA nickase that can be utilized for precise gene editing.
Cell Rep, 44:115718-115718, 2025

PubMed Abstract: Type V-H CRISPR-Cas system, an important subtype of type V CRISPR-Cas systems, has remained enigmatic in terms of its structure and function despite being discovered several years ago. Here, we comprehensively characterize the type V-H CRISPR-Cas system and elucidate its role as a DNA nicking system. The unique CRISPR RNA (crRNA) employed by Cas12h effector protein enables specific targeting of double-stranded DNA (dsDNA), while its RuvC domain is responsible for cleaving the non-target strand (NTS) of dsDNA. We present the structure of Cas12h bound to crRNA and target DNA. Our structural analysis reveals that the RuvC domain possesses a narrow active pocket that facilitates recognition of NTS but potentially hinders access to the target strand. Furthermore, we demonstrate that Cas12h confers adaptive immunity against invading mobile genetic elements through transcriptional gene inhibition. We have engineered an adenine base editor by fusing Cas12h with an adenine deaminase, achieving effective A-to-G substitution.

PubMed: 40372912
DOI: 10.1016/j.celrep.2025.115718

実験手法

X-RAY DIFFRACTION (3.81 Å)