蛋白质工程
高通量筛选
计算生物学
靶蛋白
定向进化
蛋白质配体
化学
受体酪氨酸激酶
吞吐量
蛋白质-蛋白质相互作用
生物化学
生物
受体
计算机科学
酶
基因
突变体
电信
无线
作者
Sung Won Lim,Bob Chen,Mihalis S. Kariolis,Ivan K. Dimov,T. M. Baer,Jennifer R. Cochran
标识
DOI:10.1021/acschembio.6b00794
摘要
Affinity maturation of protein-protein interactions requires iterative rounds of protein library generation and high-throughput screening to identify variants that bind with increased affinity to a target of interest. We recently developed a multipurpose protein engineering platform, termed μSCALE (Microcapillary Single Cell Analysis and Laser Extraction). This technology enables high-throughput screening of libraries of millions of cell-expressing protein variants based on their binding properties or functional activity. Here, we demonstrate the first use of the μSCALE platform for affinity maturation of a protein-protein binding interaction. In this proof-of-concept study, we engineered an extracellular domain of the Axl receptor tyrosine kinase to bind tighter to its ligand Gas6. Within 2 weeks, two iterative rounds of library generation and screening resulted in engineered Axl variants with a 50-fold decrease in kinetic dissociation rate, highlighting the use of μSCALE as a new tool for directed evolution.
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