Direct electron detection yields cryo-EM reconstructions at resolutions beyond 3/4 Nyquist frequency

被引:111
作者
Bammes, Benjamin E. [1 ,2 ]
Rochat, Ryan H. [1 ,2 ]
Jakana, Joanita [1 ]
Chen, Dong-Hua [1 ]
Chiu, Wah [1 ,2 ]
机构
[1] Baylor Coll Med, Verna & Marrs Mclean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
[2] Baylor Coll Med, Grad Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Cryo-EM; Electron cryo-microscopy; Direct detection device; Active pixel sensor; CMOS detector; Nyquist frequency; DIRECT-DETECTION DEVICE; PIXEL SENSOR ARRAY; CCD CAMERA; IMAGES; CRYOMICROSCOPY; ACQUISITION; PERFORMANCE; PROTEIN; OPTIMIZATION; MICROSCOPY;
D O I
10.1016/j.jsb.2012.01.008
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
One limitation in electron cryo-microscopy (cryo-EM) is the inability to recover high-resolution signal from the image-recording media at the full-resolution limit of the transmission electron microscope. Direct electron detection using CMOS-based sensors for digitally recording images has the potential to alleviate this shortcoming. Here, we report a practical performance evaluation of a Direct Detection Device (DDD (R)) for biological cryo-EM at two different microscope voltages: 200 and 300 kV. Our DDD images of amorphous and graphitized carbon show strong per-pixel contrast with image resolution near the theoretical sampling limit of the data. Single-particle reconstructions of two frozen-hydrated bacteriophages, P22 and epsilon 15, establish that the DDD is capable of recording usable signal for 3D reconstructions at about 4/5 of the Nyquist frequency, which is a vast improvement over the performance of conventional imaging media. We anticipate the unparalleled performance of this digital recording device will dramatically benefit cryo-EM for routine tomographic and single-particle structural determination of biological specimens. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:589 / 601
页数:13
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