Maximum-likelihood multi-reference refinement for electron microscopy images

被引:204
作者
Scheres, SHW
Valle, M
Nuñez, R
Sorzano, COS
Marabini, R
Herman, GT
Carazo, JM [1 ]
机构
[1] Univ Autonoma Madrid Canto Blanco, Ctr Nacl Biotecnol, Biocomp Unit, Madrid, Spain
[2] Univ San Pablo, CEU, Escuela Politecn Super, Madrid 28668, Spain
[3] Univ Autonoma Madrid, Escuela Politecn Super, E-28049 Madrid, Spain
[4] NYU, Grad Ctr, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
maximum-likelihood; multi-reference refinement; single-particles; 2D-alignment; classification;
D O I
10.1016/j.jmb.2005.02.031
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 maximum-likelihood approach to multi-reference image refinement is presented. In contrast to conventional cross-correlation refinement, the new approach includes a formal description of the noise, implying that it is especially suited to cases with low signal-to-noise ratios. Application of this approach to a cryo-electron microscopy dataset revealed two major classes for projections of simian virus 40 large T-antigen in complex with an asymmetric DNA-probe, containing the origin of simian virus 40 replication. Strongly bent projections of dodecamers showed density that may be attributed to the complexed double-stranded DNA, while almost straight projections revealed a twist in the relative orientation of the hexameric subunits. This new level of detail for large T-antigen projections was not detected using conventional techniques. For a negative stain dataset, maximum-likelihood refinement yielded results that were practically identical to those obtained using conventional multi-reference refinement. Results obtained using simulated data suggest that the efficiency of the maximum-likelihood approach may be further enhanced by explicitly incorporating the microscope contrast transfer function in the image formation model. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:139 / 149
页数:11
相关论文
共 38 条
[1]   Bacillus subtilis bacteriophage SPP1 hexameric DNA helciase, G40P, interacts with forked DNA [J].
Ayora, S ;
Weise, F ;
Mesa, P ;
Stasiak, A ;
Alonso, JC .
NUCLEIC ACIDS RESEARCH, 2002, 30 (11) :2280-2289
[2]   Polymorphic quaternary organization of the Bacillus subtilis bacteriophage SPP1 replicative helicase (G40P) [J].
Bárcena, M ;
San Martin, C ;
Weise, F ;
Ayora, S ;
Alonso, JC ;
Carazo, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 283 (04) :809-819
[3]   STRUCTURE OF MITOCHONDRIAL F1-ATPASE STUDIED BY ELECTRON-MICROSCOPY AND IMAGE-PROCESSING [J].
BOEKEMA, EJ ;
BERDEN, JA ;
VANHEEL, MG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 851 (03) :353-360
[4]   Some trends in microscope image processing [J].
Bonnet, N .
MICRON, 2004, 35 (08) :635-653
[5]   Artificial intelligence and pattern recognition techniques in microscope image processing and analysis [J].
Bonnet, N .
ADVANCES IN IMAGING AND ELECTRON PHYSICS, VOL 114, 2000, 114 :1-77
[6]   Experimental verification of conformational variation of human fatty acid synthase as predicted by normal mode analysis [J].
Brink, J ;
Ludtke, SJ ;
Kong, YF ;
Wakil, SJ ;
Ma, JP ;
Chiu, W .
STRUCTURE, 2004, 12 (02) :185-191
[7]   Recent developments for the efficient crystallographic refinement of macromolecular structures [J].
Brünger, AT ;
Adams, PD ;
Rice, LM .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1998, 8 (05) :606-611
[8]   HARMONIC ANALYSIS OF ELECTRON MICROSCOPE IMAGES WITH ROTATIONAL SYMMETRY [J].
CROWTHER, RA ;
AMOS, LA .
JOURNAL OF MOLECULAR BIOLOGY, 1971, 60 (01) :123-&
[9]   FUNCTIONAL INTERACTIONS OF THE SIMIAN VIRUS-40 CORE ORIGIN OF REPLICATION WITH FLANKING REGULATORY SEQUENCES [J].
DELUCIA, AL ;
DEB, S ;
PARTIN, K ;
TEGTMEYER, P .
JOURNAL OF VIROLOGY, 1986, 57 (01) :138-144
[10]   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