清脆的
Cas9
DNA
劈理(地质)
基因组编辑
核酸酶
化学
分子动力学
生物物理学
生物
基因
计算化学
生物化学
断裂(地质)
古生物学
作者
Łukasz Nierzwicki,Kyle W. East,Jonas M. Binz,Rohaine V. Hsu,Mohd Ahsan,Pablo Ricardo Arantes,Erin Skeens,Martin Pačesa,Martin Jínek,George P. Lisi,Giulia Palermo
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2022-10-06
卷期号:5 (10): 912-922
被引量:21
标识
DOI:10.1038/s41929-022-00848-6
摘要
At the core of the CRISPR–Cas9 genome-editing technology, the endonuclease Cas9 introduces site-specific breaks in DNA. However, precise mechanistic information to ameliorate Cas9 function is still missing. Here, multimicrosecond molecular dynamics, free energy and multiscale simulations are combined with solution NMR and DNA cleavage experiments to resolve the catalytic mechanism of target DNA cleavage. We show that the conformation of an active HNH nuclease is tightly dependent on the catalytic Mg2+, unveiling its cardinal structural role. This activated Mg2+-bound HNH is consistently described through molecular simulations, nuclear magnetic resonance (NMR) and DNA cleavage assays, revealing also that the protonation state of the catalytic H840 is strongly affected by active site mutations. Finally, ab initio quantum mechanics (density functional theory)/molecular mechanics simulations and metadynamics establish the catalytic mechanism, showing that the catalysis is activated by H840 and completed by K866, thus rationalizing DNA cleavage experiments. This information is critical to enhancing the enzymatic function of CRISPR–Cas9 towards improved genome editing. A detailed understanding of the catalytic target DNA cleavage mechanism by CRISPR–Cas9 has been lacking. Now the key modulating role of Mg2+ in the conformational activation of Cas9 and the influence of active site residues on the protonation state of catalytic H840 are demonstrated, ultimately unravelling the catalytic mechanism.
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