Liu Zheng, Guo Fei, Wang Feng, Li Tian-Cheng, Jiang Wen
Department of Biological Sciences, Markey Center for Structural Biology, Purdue University, West Lafayette, IN 47907, USA.
Department of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-murayama, Tokyo 208-0011, Japan.
Structure. 2016 Feb 2;24(2):319-28. doi: 10.1016/j.str.2015.12.006. Epub 2016 Jan 14.
Single-particle cryoelectron microscopy typically discards close-packed particle images as unusable data. Here, we report an image processing strategy and case study of obtaining near-atomic resolution 3D reconstructions from close-packed particles. Multiple independent de novo initial models were constructed to determine and cross-validate the particle parameters. The particles with consistent views were further refined including not only Euler angles and center positions but also defocus, astigmatism, beam tilt, and overall and anisotropic magnification. We demonstrated this strategy with a 2.9 Å resolution reconstruction of a 1.67 MDa virus-like particle of a circovirus, PCV2, recorded on 86 photographic films. The map resolution was further validated with a phase-randomization test and local resolution assessment, and the atomic model was validated with MolProbity and EMRinger. Close-packed virus particles were thus shown not only to be useful for high-resolution 3D reconstructions but also to allow data collection at significantly improved throughput for near-atomic resolution reconstructions.
单颗粒冷冻电子显微镜通常会将紧密堆积的颗粒图像作为不可用数据丢弃。在此,我们报告一种图像处理策略及案例研究,即从紧密堆积的颗粒中获得近原子分辨率的三维重建。构建了多个独立的从头初始模型以确定并交叉验证颗粒参数。对具有一致视角的颗粒进行进一步优化,不仅包括欧拉角和中心位置,还包括散焦、像散、束倾斜以及整体和各向异性放大率。我们用在86张照相底片上记录的圆环病毒PCV2的1.67 MDa病毒样颗粒以2.9 Å分辨率重建展示了这一策略。通过相位随机化测试和局部分辨率评估进一步验证了图谱分辨率,并用MolProbity和EMRinger验证了原子模型。因此,紧密堆积的病毒颗粒不仅被证明可用于高分辨率三维重建,还能在显著提高近原子分辨率重建通量的情况下进行数据收集。