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An enhanced assay to characterize anti-CRISPR proteins using a cell-free transcription-translation system

机译:使用无细胞转录翻译系统表征抗克隆蛋白的增强的测定

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摘要

The characterization of CRISPR-Cas immune systems in bacteria was quickly followed by the discovery of anti-CRISPR proteins (Acrs) in bacteriophages. These proteins block different steps of CRISPR-based immunity and, as some inhibit Cas nucleases, can offer tight control over CRISPR technologies. While Acrs have been identified against a few CRISPR-Cas systems, likely many more await discovery and application. Here, we report a rapid and scalable method for characterizing putative Acrs against Cas nucleases using an E. cofi-derived cell-free transcription-translation system. Using known Acrs against type II Cas9 nucleases as models, we demonstrate how the method can be used to measure the inhibitory activity of individual Acrs in under two days. We also show how the method can overcome non-specific inhibition of gene expression observed for some Acrs. In total, the method should accelerate the interrogation and application of Acrs as CRISPR-Cas inhibitors.
机译:通过在噬菌体中发现抗克切者蛋白(ACRS)的抗克切者蛋白(ACRS)迅速地进行细菌的CRAP-CAS免疫系统的表征。 这些蛋白质阻断了基于CRISPR的抗扰度的不同步骤,并且作为一些抑制CAS核酸酶,可以对CRISPR技术进行密切控制。 虽然ACRS已经针对一些CRISPR-CAS系统识别,但可能更多地等待发现和应用。 在此,我们报告了一种快速和可扩展的方法,用于使用E.COFI衍生的细胞转录翻译系统对CAS核酸酶进行特征的快速和可扩展方法。 使用已知的来自II型CAS9核酸酶作为模型,我们证明了该方法如何用于测量两天内单个分量的抑制活性。 我们还展示了该方法如何克服对某些ACRS观察到的基因表达的非特异性抑制。 总的来说,该方法应加速ACRS作为CRISPR-CAS抑制剂的询问和应用。

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