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In vivo biosynthesis of an Ala-scan library based on the cyclic peptide SFTI-1

机译:基于环肽SFTI-1的Ala扫描文库的体内生物合成

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摘要

We present the in vivo biosynthesis of wild-type sunflower trypsin inhibitor 1 (SFTI-1) inside E. coli cells using an intramolecular native chemical ligation in combination with a modified protein splicing unit. SFTI-1 is a small backbone cyclized polypeptide with a single disulfide bridge. A small library containing multiple Ala mutants was also biosynthesized and its activity was assayed using a trypsin-binding assay. This study clearly demonstrates the exciting possibility of generating large cyclic peptide libraries in live E. coli cells, and is a critical first step for developing in vivo screening and directed evolution technologies using the cyclic peptide SFTI-1 as a molecular scaffold.
机译:我们目前使用分子内天然化学连接结合修饰的蛋白剪接单元在大肠杆菌细胞内的野生型向日葵胰蛋白酶抑制剂1(SFTI-1)的体内生物合成。 SFTI-1是具有单个二硫键的小骨架环化多肽。还生物合成了包含多个Ala突变体的小型文库,并使用胰蛋白酶结合测定法对其活性进行了测定。这项研究清楚地证明了在活的大肠杆菌细胞中产生大型环状肽文库的令人兴奋的可能性,并且是使用环状肽SFTI-1作为分子支架开发体内筛选和定向进化技术的关键的第一步。

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