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Real-space and real-time dynamics of CRISPR-Cas9 visualized by high-speed atomic force microscopy

机译:高速原子力显微镜观察CRISPR-Cas9的实时和实时动力学

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摘要

The CRISPR-associated endonuclease Cas9 binds to a guide RNA and cleaves double-stranded DNA with a sequence complementary to the RNA guide. The Cas9–RNA system has been harnessed for numerous applications, such as genome editing. Here we use high-speed atomic force microscopy (HS-AFM) to visualize the real-space and real-time dynamics of CRISPR-Cas9 in action. HS-AFM movies indicate that, whereas apo-Cas9 adopts unexpected flexible conformations, Cas9–RNA forms a stable bilobed structure and interrogates target sites on the DNA by three-dimensional diffusion. These movies also provide real-time visualization of the Cas9-mediated DNA cleavage process. Notably, the Cas9 HNH nuclease domain fluctuates upon DNA binding, and subsequently adopts an active conformation, where the HNH active site is docked at the cleavage site in the target DNA. Collectively, our HS-AFM data extend our understanding of the action mechanism of CRISPR-Cas9.
机译:CRISPR相关的核酸内切酶Cas9与向导RNA结合,并以与RNA向导互补的序列切割双链DNA。 Cas9–RNA系统已被用于许多应用,例如基因组编辑。在这里,我们使用高速原子力显微镜(HS-AFM)可视化CRISPR-Cas9的实际空间和实时动态。 HS-AFM电影表明,尽管apo-Cas9具有出乎意料的灵活构象,但是Cas9-RNA形成了稳定的双叶结构,并通过三维扩散询问DNA上的靶位。这些电影还提供了Cas9介导的DNA切割过程的实时可视化。值得注意的是,Cas9 HNH核酸酶结构域在DNA结合后发生波动,并随后采用活性构象,其中HNH活性位点停靠在目标DNA的切割位点。总而言之,我们的HS-AFM数据扩展了我们对CRISPR-Cas9作用机制的理解。

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