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工程化的基因组编辑蛋白 Cas9 沿 DNA 滑动。

Engineering of the genome editing protein Cas9 to slide along DNA.

机构信息

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai, 980-8577, Japan.

Department of Chemistry, Graduate School of Science, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai, 980-8577, Japan.

出版信息

Sci Rep. 2021 Jul 8;11(1):14165. doi: 10.1038/s41598-021-93685-9.

Abstract

The genome editing protein Cas9 faces engineering challenges in improving off-target DNA cleavage and low editing efficiency. In this study, we aimed to engineer Cas9 to be able to slide along DNA, which might facilitate genome editing and reduce off-target cleavage. We used two approaches to achieve this: reducing the sliding friction along DNA by removing the interactions of Cas9 residues with DNA and facilitating sliding by introducing the sliding-promoting tail of Nhp6A. Seven engineered mutants of Cas9 were prepared, and their performance was tested using single-molecule fluorescence microscopy. Comparison of the mutations enabled the identification of key residues of Cas9 to enhance the sliding along DNA in the presence and absence of single guide RNA (sgRNA). The attachment of the tail to Cas9 mutants enhanced sliding along DNA, particularly in the presence of sgRNA. Together, using the proposed approaches, the sliding ability of Cas9 was improved up to eightfold in the presence of sgRNA. A sliding model of Cas9 and its engineering action are discussed herein.

摘要

基因组编辑蛋白 Cas9 在提高脱靶 DNA 切割和低编辑效率方面面临工程挑战。在这项研究中,我们旨在设计 Cas9 以能够沿着 DNA 滑动,这可能有助于基因组编辑并减少脱靶切割。我们使用两种方法来实现这一目标:通过去除 Cas9 残基与 DNA 的相互作用来减少沿着 DNA 的滑动摩擦,并通过引入 Nhp6A 的滑动促进尾巴来促进滑动。制备了 Cas9 的七个工程突变体,并使用单分子荧光显微镜测试了它们的性能。对突变体的比较使我们能够确定 Cas9 的关键残基,以增强在有和没有单指导 RNA(sgRNA)的情况下沿着 DNA 的滑动。尾巴与 Cas9 突变体的连接增强了 DNA 的滑动,尤其是在有 sgRNA 的情况下。总之,使用提出的方法,Cas9 在有 sgRNA 的情况下的滑动能力提高了多达八倍。本文讨论了 Cas9 的滑动模型及其工程作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dfd/8266852/376c655ce5e3/41598_2021_93685_Fig1_HTML.jpg

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