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大规模平行评估和计算预测 17 种小 Cas9 的活性和特异性。

Massively parallel evaluation and computational prediction of the activities and specificities of 17 small Cas9s.

机构信息

Department of Pharmacology, Yonsei University College of Medicine, Seoul, Republic of Korea.

Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.

出版信息

Nat Methods. 2023 Jul;20(7):999-1009. doi: 10.1038/s41592-023-01875-2. Epub 2023 May 15.

Abstract

Recently, various small Cas9 orthologs and variants have been reported for use in in vivo delivery applications. Although small Cas9s are particularly suited for this purpose, selecting the most optimal small Cas9 for use at a specific target sequence continues to be challenging. Here, to this end, we have systematically compared the activities of 17 small Cas9s for thousands of target sequences. For each small Cas9, we have characterized the protospacer adjacent motif and determined optimal single guide RNA expression formats and scaffold sequence. High-throughput comparative analyses revealed distinct high- and low-activity groups of small Cas9s. We also developed DeepSmallCas9, a set of computational models predicting the activities of the small Cas9s at matched and mismatched target sequences. Together, this analysis and these computational models provide a useful guide for researchers to select the most suitable small Cas9 for specific applications.

摘要

最近,已经有报道称,多种小型 Cas9 直系同源物和变体可用于体内递送应用。尽管小型 Cas9 特别适合此目的,但选择最适合特定靶序列的最佳小型 Cas9 仍然具有挑战性。为此,我们系统地比较了 17 种小型 Cas9 在数千个靶序列上的活性。对于每种小型 Cas9,我们都对其邻近基序进行了特征分析,并确定了最佳的单引导 RNA 表达格式和支架序列。高通量比较分析揭示了小型 Cas9 的高活性和低活性两个明显群组。我们还开发了 DeepSmallCas9,这是一组用于预测在匹配和错配靶序列中小 Cas9 活性的计算模型。总之,这项分析和这些计算模型为研究人员提供了有用的指导,以选择最适合特定应用的小型 Cas9。

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