MRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Department of Biochemistry and Biophysics, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.
Elife. 2018 Jun 1;7:e36861. doi: 10.7554/eLife.36861.
Macromolecular complexes that exhibit continuous forms of structural flexibility pose a challenge for many existing tools in cryo-EM single-particle analysis. We describe a new tool, called multi-body refinement, which models flexible complexes as a user-defined number of rigid bodies that move independently from each other. Using separate focused refinements with iteratively improved partial signal subtraction, the new tool generates improved reconstructions for each of the defined bodies in a fully automated manner. Moreover, using principal component analysis on the relative orientations of the bodies over all particle images in the data set, we generate movies that describe the most important motions in the data. Our results on two test cases, a cytoplasmic ribosome from , and the spliceosomal B-complex from yeast, illustrate how multi-body refinement can be useful to gain unique insights into the structure and dynamics of large and flexible macromolecular complexes.
表现出连续形式结构灵活性的大分子复合物对冷冻电镜单颗粒分析中的许多现有工具构成了挑战。我们描述了一种新工具,称为多体精修,它将柔性复合物建模为用户定义数量的刚体,这些刚体彼此独立移动。使用带有迭代改进的部分信号减法的单独聚焦精修,该新工具以全自动方式为每个定义的刚体生成改进的重建。此外,通过对数据集所有粒子图像中刚体相对取向的主成分分析,我们生成描述数据中最重要运动的电影。我们在两个测试案例(来自 的细胞质核糖体和酵母中的剪接体 B 复合物)上的结果说明了多体精修如何有助于深入了解大型和柔性大分子复合物的结构和动态。