Malins Lara R, Payne Richard J
School of Chemistry, The University of Sydney, Camperdown, NSW, 2006, Australia,
Top Curr Chem. 2015;362:27-87. doi: 10.1007/128_2014_584.
Over the past 20 years, native chemical ligation has facilitated the synthesis of numerous complex peptide and protein targets, with and without post-translational modifications, as well as the design and construction of a variety of engineered protein variants. This powerful methodology has also served as a platform for the development of related chemoselective ligation technologies which have greatly expanded the scope and flexibility of ligation chemistry. This chapter details a number of important extensions of the original native chemical ligation manifold, with particular focus on the application of new methods in the total chemical synthesis of proteins. Topics covered include the development of auxiliary-based ligation methods, the post-ligation manipulation of Cys residues, and the synthesis and utility of unnatural amino acid building blocks (bearing reactive thiol or selenol functionalities) in chemoselective ligation chemistry. Contemporary applications of these techniques to the total chemical synthesis of peptides and proteins are described.
在过去20年里,天然化学连接法推动了众多复杂肽和蛋白质靶标的合成,无论有无翻译后修饰,还推动了各种工程化蛋白质变体的设计与构建。这种强大的方法还为相关化学选择性连接技术的发展提供了一个平台,极大地扩展了连接化学的范围和灵活性。本章详细介绍了原始天然化学连接体系的一些重要扩展,特别关注新方法在蛋白质全化学合成中的应用。涵盖的主题包括基于辅助基团的连接方法的发展、半胱氨酸残基连接后的操作,以及在化学选择性连接化学中(带有反应性硫醇或硒醇官能团的)非天然氨基酸构建模块的合成与应用。描述了这些技术在肽和蛋白质全化学合成中的当代应用。