Yan Bingjia, Ye Linzhi, Xu Weiliang, Liu Lei
Tsinghua-Peking Center for Life Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Tsinghua-Peking Center for Life Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Bioorg Med Chem. 2017 Sep 15;25(18):4953-4965. doi: 10.1016/j.bmc.2017.05.020. Epub 2017 May 10.
Solution of the three-dimensional structures of proteins is a critical step in deciphering the molecular mechanisms of their bioactivities. Among the many approaches for obtaining protein crystals, racemic protein crystallography has been developed as a unique method to solve the structures of an increasing number of proteins. Exploiting unnatural protein enantiomers in crystallization and resolution, racemic protein crystallography manifests two major advantages that are 1) to increase the success rate of protein crystallization, and 2) to obviate the phase problem in X-ray diffraction. The requirement of unnatural protein enantiomers in racemic protein crystallography necessitates chemical protein synthesis, which is hitherto accomplished through solid phase peptide synthesis and chemical ligation reactions. This review highlights the fundamental ideas of racemic protein crystallography and surveys the harvests in the field of racemic protein crystallography over the last five years from early 2012 to late 2016.
解析蛋白质的三维结构是解读其生物活性分子机制的关键步骤。在众多获取蛋白质晶体的方法中,外消旋蛋白质晶体学已发展成为一种独特的方法,用于解析越来越多蛋白质的结构。外消旋蛋白质晶体学利用非天然蛋白质对映体进行结晶和解析,具有两个主要优点:一是提高蛋白质结晶的成功率,二是消除X射线衍射中的相位问题。外消旋蛋白质晶体学对非天然蛋白质对映体的需求使得化学蛋白质合成成为必要,目前这是通过固相肽合成和化学连接反应来实现的。本综述重点介绍了外消旋蛋白质晶体学的基本概念,并概述了从2012年初到2016年末这五年在外消旋蛋白质晶体学领域所取得的成果。