氨基酸
计算生物学
蛋白质表达
生物化学
体外
转移RNA
蛋白质工程
突变体
克隆(编程)
蛋白质生物合成
荧光蛋白
生物
合成生物学
化学
基因
核糖核酸
酶
计算机科学
绿色荧光蛋白
程序设计语言
作者
Song‐Min Schinn,William T. Bradley,Ashtyn Groesbeck,Jeffrey C. Wu,Andrew Broadbent,Bradley C. Bundy
摘要
ABSTRACT The incorporation of unnatural amino acids (uAA) can introduce novel functional groups into proteins site‐specifically, with important applications in basic sciences and protein engineering. However, uAA incorporation can impact protein expression and functional activity depending on its location within the protein—a process that is not yet completely understood and difficult to predict. Therefore, practical applications often necessitate a time‐consuming optimization of uAA location by individual gene cloning, expressions, purification, and evaluations for each location tested. To address this limitation, we introduce a streamlined and versatile in vitro system to rapidly express and screen uAA‐containing proteins without cumbersome cell culturing or purification procedures. We utilized this technology to simultaneously screen 24 different t4‐lysozyme mutants with different uAA incorporation sites in a matter of hours, compared to weeks‐long workflow of conventional methods. Screening data offered a mechanistic explanation to some effects of uAA incorporation on expression and activity. Despite these insights, rational prediction of such effects remained challenging, further confirming the value of a rapid screening approach. Biotechnol. Bioeng. 2017;114: 2412–2417. © 2017 Wiley Periodicals, Inc.
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