Classification and reconstruction of a heterogeneous set of electron microscopic images: A case study of GroEL-substrate complexes

被引:7
作者
Falke, S
Fisher, MT
Gogol, EP [1 ]
机构
[1] Univ Missouri, Sch Biol Sci, Kansas City, MO 64110 USA
[2] Univ Kansas, Med Ctr, Dept Biochem & Mol Biol, Kansas City, KS 66160 USA
关键词
chaperonin; electron microscopy; GroEL; image reconstruction;
D O I
10.1006/jsbi.2001.4354
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
Image analysis methods were used to separate images of a large macromolecular complex, the chaperonin GroEL, in a preparation in which it is partially liganded to a nonnative protein substrate, glutamine synthetase. The relatively small difference (similar to6%) in size between the chaperonin in its free and complexed forms, and the absence of gross changes in overall conformation, made separation of the two types of particles challenging. Different approaches were evaluated and used for alignment and classification of images, both in two common projections and in three dimensions, yielding 2D averages and a 3D reconstruction. The results of 3D analysis describe the conformational changes effected by binding of this particular protein substrate and demonstrate the utility of 2D analysis as an indicator of structural change in this system. (C) 2001 Academic Press.
引用
收藏
页码:203 / 213
页数:11
相关论文
共 20 条
[1]   A model-based approach for determining orientations of biological macromolecules imaged by cryoelectron microscopy [J].
Baker, TS ;
Cheng, RH .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :120-130
[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]   The crystal structure of a GroEL/peptide complex: Plasticity as a basis for substrate diversity [J].
Chen, LL ;
Sigler, PB .
CELL, 1999, 99 (07) :757-768
[4]   LOCATION OF A FOLDING PROTEIN AND SHAPE CHANGES IN GROEL-GROES COMPLEXES IMAGED BY CRYOELECTRON MICROSCOPY [J].
CHEN, S ;
ROSEMAN, AM ;
HUNTER, AS ;
WOOD, SP ;
BURSTON, SG ;
RANSON, NA ;
CLARKE, AR ;
SAIBIL, HR .
NATURE, 1994, 371 (6494) :261-264
[5]  
FALKE S, 2001, IN PRESS J MOL BIOL
[6]  
FISHER MT, 1994, J BIOL CHEM, V269, P13629
[7]   PROMOTION OF THE INVITRO RENATURATION OF DODECAMERIC GLUTAMINE-SYNTHETASE FROM ESCHERICHIA-COLI IN THE PRESENCE OF GROEL (CHAPERONIN-60) AND ATP [J].
FISHER, MT .
BIOCHEMISTRY, 1992, 31 (16) :3955-3963
[8]   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
[9]   DIRECT 3-DIMENSIONAL RECONSTRUCTION FOR MACROMOLECULAR COMPLEXES FROM ELECTRON-MICROGRAPHS [J].
HARAUZ, G ;
OTTENSMEYER, FP .
ULTRAMICROSCOPY, 1984, 12 (04) :309-320
[10]   CHAPERONIN-MEDIATED PROTEIN FOLDING - GROES BINDS TO ONE END OF THE GROEL CYLINDER, WHICH ACCOMMODATES THE PROTEIN SUBSTRATE WITHIN ITS CENTRAL CAVITY [J].
LANGER, T ;
PFEIFER, G ;
MARTIN, J ;
BAUMEISTER, W ;
HARTL, FU .
EMBO JOURNAL, 1992, 11 (13) :4757-4765