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The Application of Cell-Free Protein Synthesis in Genetic Code Expansion for Post-translational Modifications

机译:无细胞蛋白质合成在遗传密码扩展中的翻译后修饰应用

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摘要

The translation system is a sophisticated machinery that synthesizes proteins from 20 canonical amino acids. Recently, the repertoire of such composition has been expanded by the introduction of non-canonical amino acids (ncAAs) with the genetic code expansion strategy, which provides proteins with designed properties and structures for protein studies and engineering. Although the genetic code expansion strategy has been mostly implemented by using living cells as the host, a number of limits such as poor cellular uptake or solubility of specific ncAA substrates and the toxicity of target proteins have hindered the production of certain ncAA-modified proteins. To overcome those challenges, cell-free protein synthesis (CFPS) has been applied as it allows the precise control of reaction components. Several approaches have been recently developed to increase the purity and efficiency of ncAA incorporation in CFPS. Here, we summarized recent development of CFPS with an emphasis on its applications in generating site-specific protein post-translational modifications by the genetic code expansion strategy.
机译:翻译系统是一种复杂的机制,可以从20种规范氨基酸合成蛋白质。最近,通过引入具有遗传密码扩展策略的非规范氨基酸(ncAAs),扩展了此类组成的组成范围,该策略为蛋白质研究和工程设计提供了具有设计特性和结构的蛋白质。尽管遗传密码扩展策略主要是通过使用活细胞作为宿主来实施的,但许多局限性,例如不良的细胞摄取或特定ncAA底物的溶解性以及靶蛋白的毒性,都阻碍了某些ncAA修饰蛋白的生产。为了克服这些挑战,已经应用了无细胞蛋白质合成(CFPS),因为它可以精确控制反应成分。最近已经开发了几种方法来提高ncAA掺入CFPS的纯度和效率。在这里,我们总结了CFPS的最新发展,重点介绍了CFPS在通过遗传密码扩展策略生成位点特异性蛋白质翻译后修饰中的应用。

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