Determination of the ribosome structure to a resolution of 2.5 Å by single-particle cryo-EM

被引:24
作者
Liu, Zheng [1 ]
Gutierrez-Vargas, Cristina [2 ]
Wei, Jia [2 ]
Grassucci, Robert A. [1 ]
Sun, Ming [2 ]
Espina, Noel [3 ]
Madison-Antenucci, Susan [3 ]
Tong, Liang [2 ]
Frank, Joachim [1 ,2 ,4 ]
机构
[1] Columbia Univ, Dept Biochem & Mol Biophys, 630 W 168th St, New York, NY 10032 USA
[2] Columbia Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[3] Wadsworth Ctr, New York State Dept Hlth, Div Infect Dis, Albany, NY 12201 USA
[4] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
关键词
high resolution cryo-EM; single particle analysis; ribosome structure; 2.5 angstrom resolution; Trypanosoma cruzi; NEAR-ATOMIC-RESOLUTION; ELECTRON-MICROSCOPY; DATA-ACQUISITION; NEW-GENERATION; IMAGE; MODEL; RECONSTRUCTION; VISUALIZATION; MICROGRAPHS; VALIDATION;
D O I
10.1002/pro.3068
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
With the advance of new instruments and algorithms, and the accumulation of experience over decades, single-particle cryo-EM has become a pivotal part of structural biology. Recently, we determined the structure of a eukaryotic ribosome at 2.5 angstrom for the large subunit. The ribosome was derived from Trypanosoma cruzi, the protozoan pathogen of Chagas disease. The high-resolution density map allowed us to discern a large number of unprecedented details including rRNA modifications, water molecules, and ions such as Mg2+ and Zn2+. In this paper, we focus on the procedures for data collection, image processing, and modeling, with particular emphasis on factors that contributed to the attainment of high resolution. The methods described here are readily applicable to other macromolecules for high-resolution reconstruction by single-particle cryo-EM.
引用
收藏
页码:82 / 92
页数:11
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