Literature DB >> 11472091

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

S Falke1, M T Fisher, E P Gogol.   

Abstract

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 ( approximately 6%) 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. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11472091     DOI: 10.1006/jsbi.2001.4354

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  2 in total

1.  Strategies for folding of affinity tagged proteins using GroEL and osmolytes.

Authors:  Hiroo Katayama; Mitchell McGill; Andrew Kearns; Marek Brzozowski; Nicholas Degner; Bliss Harnett; Boris Kornilayev; Dubravka Matković-Calogović; Todd Holyoak; James P Calvet; Edward P Gogol; John Seed; Mark T Fisher
Journal:  J Struct Funct Genomics       Date:  2008-12-12

2.  Probing the kinetic stabilities of Friedreich's ataxia clinical variants using a solid phase GroEL chaperonin capture platform.

Authors:  Ana R Correia; Subhashchandra Naik; Mark T Fisher; Cláudio M Gomes
Journal:  Biomolecules       Date:  2014-10-20
  2 in total

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