Department of Life Sciences, Imperial College London, London, UK.
Department of Chemistry, Imperial College London, London, UK.
Mol Syst Biol. 2020 Jun;16(6):e9475. doi: 10.15252/msb.20209475.
Rational molecular engineering of proteins with CRISPR-based approaches is challenged by the gene-centric nature of gRNA design tools. To address this, we have developed CRISPR-TAPE, a protein-centric gRNA design algorithm that allows users to target specific residues, or amino acid types within proteins. gRNA outputs can be customized to support maximal efficacy of homology-directed repair for engineering purposes, removing time-consuming post hoc curation, simplifying gRNA outputs and reducing CPU times.
基于 CRISPR 的蛋白质理性分子工程受到 gRNA 设计工具以基因为中心性质的挑战。为了解决这个问题,我们开发了 CRISPR-TAPE,这是一种以蛋白质为中心的 gRNA 设计算法,允许用户针对蛋白质中的特定残基或氨基酸类型。gRNA 输出可以定制,以支持同源定向修复的最大功效,从而消除耗时的事后策管,简化 gRNA 输出并减少 CPU 时间。