Wang Jimin, Li Yue, Modis Yorgo
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.
Acta Crystallogr D Biol Crystallogr. 2014 Jul;70(Pt 7):1873-83. doi: 10.1107/S1399004714008943. Epub 2014 Jun 29.
Structure determination using the single isomorphous replacement (SIR) or single-wavelength anomalous diffraction (SAD) methods with weak derivatives remains very challenging. In a recent structure determination of glycoprotein E2 from bovine viral diarrhea virus, three isomorphous uranium-derivative data sets were merged to obtain partially interpretable initial experimental maps. Small differences between them were then exploited by treating them as three independent SAD data sets plus three circular pairwise SIR data sets to improve the experimental maps. Here, how such subtle structural differences were exploited for experimental phasing is described in detail. The basis for why this approach works is also provided: the effective resolution of isomorphous signals between highly isomorphous derivatives is often much higher than the effective resolution of the anomalous signals of individual derivative data sets. Hence, the new phasing approaches outlined here will be generally applicable to structure determinations involving weak derivatives.
使用单同晶置换(SIR)或单波长反常衍射(SAD)方法结合弱衍生物进行结构测定仍然极具挑战性。在最近对牛病毒性腹泻病毒糖蛋白E2的结构测定中,三个同晶铀衍生物数据集被合并以获得部分可解释的初始实验图谱。然后将它们之间的微小差异视为三个独立的SAD数据集加上三个圆形成对SIR数据集来处理,以改进实验图谱。在此详细描述了如何利用这种细微的结构差异进行实验定相。还提供了这种方法奏效的依据:高度同晶衍生物之间同晶信号的有效分辨率通常远高于单个衍生物数据集反常信号的有效分辨率。因此,这里概述的新定相方法将普遍适用于涉及弱衍生物的结构测定。