Single-Particle Refinement and Variability Analysis in EMAN2.1

被引:65
作者
Ludtke, S. J. [1 ]
机构
[1] Baylor Coll Med, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
来源
RESOLUTION REVOLUTION: RECENT ADVANCES IN CRYOEM | 2016年 / 579卷
关键词
CRYO-EM STRUCTURE; FATTY-ACID SYNTHASE; ELECTRON-MICROSCOPY; CHAPERONIN TRIC/CCT; ESCHERICHIA-COLI; GROEL; VALIDATION; IMAGES; RECONSTRUCTIONS; CRYOMICROSCOPY;
D O I
10.1016/bs.mie.2016.05.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
CryoEM single-particle reconstruction has been growing rapidly over the last 3 years largely due to the development of direct electron detectors, which have provided data with dramatic improvements in image quality. It is now possible in many cases to produce near-atomic resolution structures, and yet 2/3 of published structures remain at substantially lower resolutions. One important cause for this is compositional and conformational heterogeneity, which is both a resolution-limiting factor and presenting a unique opportunity to better relate structure to function. This manuscript discusses the canonical methods for high-resolution refinement in EMAN2.12, and then considers the wide range of available methods within this package for resolving structural variability, targeting both improved resolution and additional knowledge about particle dynamics.
引用
收藏
页码:159 / 189
页数:31
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