Rawson S, Iadanza M G, Ranson N A, Muench S P
School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
Methods. 2016 May 1;100:35-41. doi: 10.1016/j.ymeth.2016.03.011. Epub 2016 Mar 24.
Recent advances in direct electron detectors and improved CMOS cameras have been accompanied by the development of a range of software to take advantage of the data they produce. In particular they allow for the correction of two types of motion in cryo electron microscopy samples: motion correction for movements of the sample particles in the ice, and differential masking to account for heterogeneity caused by flexibility within protein complexes. Here we provide several scripts that allow users to move between RELION and standalone motion correction and centring programs. We then compare the computational cost and improvements in data quality with each program. We also describe our masking procedures to account for conformational flexibility. For the different elements of this study we have used three samples; a high symmetry virus, flexible protein complex (∼1MDa) and a relatively small protein complex (∼550kDa), to benchmark four widely available motion correction packages. Using these as test cases we demonstrate how motion correction and differential masking, as well as an additional particle re-centring protocol can improve final reconstructions when used within the RELION image-processing package.
直接电子探测器和改进的互补金属氧化物半导体(CMOS)相机的最新进展,伴随着一系列利用它们所产生数据的软件的开发。特别是,它们允许校正冷冻电子显微镜样品中的两种运动:冰中样品颗粒运动的运动校正,以及用于解释蛋白质复合物内部灵活性所导致的异质性的差分掩蔽。在这里,我们提供了几个脚本,允许用户在RELION和独立的运动校正与居中程序之间切换。然后,我们比较了每个程序的计算成本和数据质量的改进。我们还描述了我们用于解释构象灵活性的掩蔽程序。对于本研究的不同部分,我们使用了三个样品;一种高对称性病毒、一种柔性蛋白质复合物(约1兆道尔顿)和一种相对较小的蛋白质复合物(约550千道尔顿),以对四个广泛使用的运动校正软件包进行基准测试。以这些作为测试案例,我们展示了运动校正和差分掩蔽,以及一种额外的粒子重新居中协议在RELION图像处理软件包中使用时如何能够改善最终重建结果。