Near-atomic resolution reconstructions using a mid-range electron microscope operated at 200 kV

被引:13
作者
Campbell, Melody G. [1 ,2 ]
Kearney, Bradley M. [1 ]
Cheng, Anchi [1 ,2 ]
Potter, Clinton S. [1 ,2 ]
Johnson, John E. [1 ]
Carragher, Bridget [1 ,2 ]
Veesler, David [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Natl Resource Automated Mol Microscopy, La Jolla, CA 92037 USA
关键词
Single-particle electron microscopy; Direct detectors; Near-atomic resolution; CRYO-EM STRUCTURE; BEAM-INDUCED MOTION; CRYOMICROSCOPY; SUBUNIT; VIRUS; TRANSLOCATION; DETECTORS; REVEALS; CAMERA;
D O I
10.1016/j.jsb.2014.09.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new era has begun for single particle cryo-electron microscopy (cryoEM) which can now compete with X-ray crystallography for determination of protein structures. The development of direct detectors constitutes a revolution that has led to a wave of near-atomic resolution cryoEM reconstructions. However, regardless of the sample studied, virtually all high-resolution reconstructions reported to date have been achieved using high-end microscopes. We demonstrate that the new generation of direct detectors coupled to a widely used mid-range electron microscope also enables obtaining cryoEM maps of sufficient quality for de novo modeling of protein structures of different sizes and symmetries. We provide an outline of the strategy used to achieve a 3.7 angstrom resolution reconstruction of Nudaurelia capensis omega virus and a 4.2 angstrom resolution reconstruction of the Thermoplasma acidophilum T20S proteasome. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:183 / 187
页数:5
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