硒代半胱氨酸
计算生物学
折叠(DSP实现)
化学
翻译(生物学)
生物化学
转移RNA
蛋白质工程
氨基酸
纳米技术
组合化学
基因
酶
生物
工程类
信使核糖核酸
材料科学
核糖核酸
电气工程
半胱氨酸
作者
Christina Z. Chung,Dieter Söll,Natalie Krahn
标识
DOI:10.1007/978-1-0716-3251-2_5
摘要
The selenium moiety in selenocysteine (Sec) imparts enhanced chemical properties to this amino acid and ultimately the protein in which it is inserted. These characteristics are attractive for designing highly active enzymes or extremely stable proteins and studying protein folding or electron transfer, to name a few. There are also 25 human selenoproteins, of which many are essential for our survival. The ability to create or study these selenoproteins is significantly hindered by the inability to easily produce them. Engineering translation has yielded simpler systems to facilitate site-specific insertion of Sec; however, Ser misincorporation remains problematic. Therefore, we have designed two Sec-specific reporters which promote high-throughput screening of Sec translation systems to overcome this barrier. This protocol outlines the workflow to engineer these Sec-specific reporters, with the application to any gene of interest and the ability to transfer this strategy to any organism.
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