RELION: Implementation of a Bayesian approach to cryo-EM structure determination

被引:3883
作者
Scheres, Sjors H. W. [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Electron microscopy; Single-particle analysis; Maximum likelihood; Image processing; Software development; ELECTRON-MICROSCOPY; MAXIMUM-LIKELIHOOD; CRYSTAL-STRUCTURE; ATOMIC-STRUCTURE; CLASSIFICATION; ARCHITECTURE; INFORMATION; ROTAVIRUS; PROTEIN; FILE;
D O I
10.1016/j.jsb.2012.09.006
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
RELION, for REgularized Likelihood OptimizatioN, is an open-source computer program for the refinement of macromolecular structures by single-particle analysis of electron cryo-microscopy (cryo-EM) data. Whereas alternative approaches often rely on user expertise for the tuning of parameters, RELION uses a Bayesian approach to infer parameters of a statistical model from the data. This paper describes developments that reduce the computational costs of the underlying maximum a posteriori (MAP) algorithm, as well as statistical considerations that yield new insights into the accuracy with which the relative orientations of individual particles may be determined. A so-called gold-standard Fourier shell correlation (FSC) procedure to prevent overfitting is also described. The resulting implementation yields high-quality reconstructions and reliable resolution estimates with minimal user intervention and at acceptable computational costs. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:519 / 530
页数:12
相关论文
共 47 条
[1]  
[Anonymous], J STRUCTURA IN PRESS
[2]   Direct electron detection yields cryo-EM reconstructions at resolutions beyond 3/4 Nyquist frequency [J].
Bammes, Benjamin E. ;
Rochat, Ryan H. ;
Jakana, Joanita ;
Chen, Dong-Hua ;
Chiu, Wah .
JOURNAL OF STRUCTURAL BIOLOGY, 2012, 177 (03) :589-601
[3]   Crystal structure of wild-type chaperonin GroEL [J].
Bartolucci, C ;
Lamba, D ;
Grazulis, S ;
Manakova, E ;
Heumann, H .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 354 (04) :940-951
[4]   In-focus electron microscopy of frozen-hydrated biological samples with a Boersch phase plate [J].
Barton, B. ;
Rhinow, D. ;
Walter, A. ;
Schroeder, R. ;
Benner, G. ;
Majorovits, E. ;
Matijevic, M. ;
Niebel, H. ;
Mueller, H. ;
Haider, M. ;
Lacher, M. ;
Schmitz, S. ;
Holik, P. ;
Kuehlbrandt, W. .
ULTRAMICROSCOPY, 2011, 111 (12) :1696-1705
[5]   Determination of the fold of the core protein of hepatitis B virus ky electron cryomicroscopy [J].
Bottcher, B ;
Wynne, SA ;
Crowther, RA .
NATURE, 1997, 386 (6620) :88-91
[6]   Beam-induced motion of vitrified specimen on holey carbon film [J].
Brilot, Axel F. ;
Chen, James Z. ;
Cheng, Anchi ;
Pan, Junhua ;
Harrison, Stephen C. ;
Potter, Clinton S. ;
Carragher, Bridget ;
Henderson, Richard ;
Grigorieff, Nikolaus .
JOURNAL OF STRUCTURAL BIOLOGY, 2012, 177 (03) :630-637
[7]   Molecular interactions in rotavirus assembly and uncoating seen by high-resolution cryo-EM [J].
Chen, James Z. ;
Settembre, Ethan C. ;
Aoki, Scott T. ;
Zhang, Xing ;
Bellamy, A. Richard ;
Dormitzer, Philip R. ;
Harrison, Stephen C. ;
Grigorieff, Nikolaus .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (26) :10644-10648
[8]   MAXIMUM LIKELIHOOD FROM INCOMPLETE DATA VIA EM ALGORITHM [J].
DEMPSTER, AP ;
LAIRD, NM ;
RUBIN, DB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-METHODOLOGICAL, 1977, 39 (01) :1-38
[9]   Role of Met-542 as a guide for the conformational changes of Phe-601 that occur during the reaction of β-galactosidase (Escherichia coli) [J].
Dugdale, Megan L. ;
Dymianiw, Dayna L. ;
Minhas, Bhawanjot K. ;
D'Angelo, Igor ;
Huber, Reuben E. .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 2010, 88 (05) :861-869
[10]   Ribosome dynamics and tRNA movement by time-resolved electron cryomicroscopy [J].
Fischer, Niels ;
Konevega, Andrey L. ;
Wintermeyer, Wolfgang ;
Rodnina, Marina V. ;
Stark, Holger .
NATURE, 2010, 466 (7304) :329-333