Cryo-EM of macromolecular assemblies at near-atomic resolution

被引:64
|
作者
Baker, Matthew L. [1 ]
Zhang, Junjie [1 ]
Ludtke, Steven J. [1 ]
Chiu, Wah [1 ]
机构
[1] Baylor Coll Med, Natl Ctr Macromol Imaging, Verna & Marrs Mclean Dept Biochem & Mol Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SECONDARY STRUCTURE ELEMENTS; PROTEIN-STRUCTURE; ELECTRON CRYOMICROSCOPY; SINGLE PARTICLES; PREDICTION; RECONSTRUCTION; MECHANISM; CHAPERONIN; CLOSURE; IMAGES;
D O I
10.1038/nprot.2010.126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With single-particle electron cryomicroscopy (cryo-EM), it is possible to visualize large, macromolecular assemblies in near-native states. Although subnanometer resolutions have been routinely achieved for many specimens, state of the art cryo-EM has pushed to near-atomic (3.3-4.6 angstrom) resolutions. At these resolutions, it is now possible to construct reliable atomic models directly from the cryo-EM density map. In this study, we describe our recently developed protocols for performing the three-dimensional reconstruction and modeling of Mm-cpn, a group II chaperonin, determined to 4.3 angstrom resolution. This protocol, utilizing the software tools EMAN, Gorgon and Coot, can be adapted for use with nearly all specimens imaged with cryo-EM that target beyond 5 angstrom resolution. Additionally, the feature recognition and computational modeling tools can be applied to any near-atomic resolution density maps, including those from X-ray crystallography.
引用
收藏
页码:1697 / 1708
页数:12
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