Xiong Yong
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA.
Acta Crystallogr D Biol Crystallogr. 2008 Jan;64(Pt 1):76-82. doi: 10.1107/S090744490705398X. Epub 2007 Dec 5.
Multi-component molecular complexes are increasingly being tackled by structural biology, bringing X-ray crystallography into the purview of electron-microscopy (EM) studies. X-ray crystallography can utilize a low-resolution EM map for structure determination followed by phase extension to high resolution. Test studies have been conducted on five crystal structures of large molecular assemblies, in which EM maps are used as models for structure solution by molecular replacement (MR) using various standard MR packages such as AMoRe, MOLREP and Phaser. The results demonstrate that EM maps are viable models for molecular replacement. Possible difficulties in data analysis, such as the effects of the EM magnification error, and the effect of MR positional/rotational errors on phase extension are discussed.
多组分分子复合物越来越多地由结构生物学来处理,将X射线晶体学纳入电子显微镜(EM)研究的范围。X射线晶体学可以利用低分辨率的EM图谱进行结构测定,随后进行相位扩展至高分辨率。已对大分子组装体的五个晶体结构进行了测试研究,其中EM图谱被用作通过使用各种标准分子置换(MR)程序包(如AMoRe、MOLREP和Phaser)进行分子置换(MR)来解析结构的模型。结果表明,EM图谱是可行的分子置换模型。讨论了数据分析中可能遇到的困难,如EM放大误差的影响,以及MR位置/旋转误差对相位扩展的影响。