Detection and separation of heterogeneity in molecular complexes by statistical analysis of their two-dimensional projections

被引:61
作者
Elad, Nadav
Clare, Daniel K.
Salbil, Helen R.
Orlova, Elena V.
机构
[1] Birkbeck Coll, Sch Crystallog, London WC1E 7HX, England
[2] Birkbeck Coll, Inst Struct Mol Biol, London WC1E 7HX, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
heterogeneity; electron microscopy; single particle analysis; multivariate statistical analysis; structural variations;
D O I
10.1016/j.jsb.2007.11.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Progress in molecular structure determination by cryo electron microscopy and single particle analysis has led to improvements in the resolution achievable. However, in many cases the limiting factor is structural heterogeneity of the sample. To address this problem, we have developed a method based on statistical analysis of the two-dimensional images to detect and sort localised structural variations caused, for example, by variable occupancy of a ligand. Images are sorted by two consecutive stages of multivariate statistical analysis (MSA) to dissect out the two main sources of variation, namely out of plane orientation and local structural changes. Heterogeneity caused by local changes is detected by MSA that reveals significant peaks in the higher order eigenimages. The eigenimages revealing local peaks are used for automated classification. Evaluation of differences between classes allows discrimination of molecular images with and without ligand. This method is very rapid, independent of any initial three-dimensional model, and can detect even minor subpopulations in an image ensemble. A strategy for using this technique was developed on model data sets. Here, we demonstrate the successful application of this method to both model and real EM data on chaperonin-substrate and ribosome-ligand complexes. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 120
页数:13
相关论文
共 36 条
[1]
CLASSIFICATION OF IMAGE DATA IN CONJUGATE REPRESENTATION SPACES [J].
BORLAND, L ;
VANHEEL, M .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1990, 7 (04) :601-610
[2]
THE CRYSTAL-STRUCTURE OF THE BACTERIAL CHAPERONIN GROEL AT 2.8-ANGSTROM [J].
BRAIG, K ;
OTWINOWSKI, Z ;
HEGDE, R ;
BOISVERT, DC ;
JOACHIMIAK, A ;
HORWICH, AL ;
SIGLER, PB .
NATURE, 1994, 371 (6498) :578-586
[3]
Classification and three-dimensional reconstruction of unevenly distributed or symmetry mismatched features of icosahedral particles [J].
Briggs, JAG ;
Huiskonen, JT ;
Fernando, KV ;
Gilbert, RJC ;
Scotti, P ;
Butcher, SJ ;
Fuller, SD .
JOURNAL OF STRUCTURAL BIOLOGY, 2005, 150 (03) :332-339
[4]
Single particle reconstructions of the transferrin-transferrin receptor complex obtained with different specimen preparation techniques [J].
Cheng, YF ;
Wolf, E ;
Larvie, M ;
Zak, O ;
Aisen, P ;
Grigorieff, N ;
Harrison, SC ;
Walz, T .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 355 (05) :1048-1065
[5]
THE PORTAL PROTEIN OF BACTERIOPHAGE-SPP1 - A DNA PUMP WITH 13-FOLD SYMMETRY [J].
DUBE, P ;
TAVARES, P ;
LURZ, R ;
VANHEEL, M .
EMBO JOURNAL, 1993, 12 (04) :1303-1309
[6]
Topologies of a substrate protein bound to the chaperonin GroEL [J].
Elad, Nadav ;
Farr, George W. ;
Clare, Daniel K. ;
Orlova, Elena V. ;
Horwich, Arthur L. ;
Saibil, Helen R. .
MOLECULAR CELL, 2007, 26 (03) :415-426
[7]
The 13Å structure of a chaperonin GroEL-protein substrate complex by cryo-electron microscopy [J].
Falke, S ;
Tama, F ;
Brooks, CL ;
Gogol, EP ;
Fisher, MT .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 348 (01) :219-230
[8]
CLASSIFICATION OF MACROMOLECULAR ASSEMBLIES STUDIED AS SINGLE PARTICLES [J].
FRANK, J .
QUARTERLY REVIEWS OF BIOPHYSICS, 1990, 23 (03) :281-329
[9]
SPIDER and WEB: Processing and visualization of images in 3D electron microscopy and related fields [J].
Frank, J ;
Radermacher, M ;
Penczek, P ;
Zhu, J ;
Li, YH ;
Ladjadj, M ;
Leith, A .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :190-199
[10]
Frank J., 2006, Three-Dimensional Electron Microscopy of Macromolecular Assemblies: Visualization of Biological Molecules in Their Native State