Literature DB >> 11472092

Dealing with particles in different conformational states by electron microscopy and image processing.

C Mellwig1, B Böttcher.   

Abstract

Electron microscopy and image processing are powerful tools for investigating different conformational states of enzymes. It is not always possible to isolate these often unstable intermediates as single species. As a result electron micrographs show a snapshot of enzymes in various conformational states. We describe here how to recognize that the imaged particles have different conformations and how to obtain for each species a three-dimensional model using single-particle image processing. We investigated the ATP synthase from chloroplasts, which has a molecular mass of about 550 kDa. It is a membrane-bound enzyme and consists of two segments, a membrane-embedded hydrophobic F(0) part and a hydrophilic F(1) part. Analysis of the particle images indicated that the molecules were in two different conformations. For both conformations three-dimensional models were calculated, which showed that the structures differed mainly in the tilt of the F(0) part with respect to the F(1) part. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11472092     DOI: 10.1006/jsbi.2001.4340

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


  2 in total

1.  Structure of the mitochondrial ATP synthase by electron cryomicroscopy.

Authors:  John L Rubinstein; John E Walker; Richard Henderson
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

Review 2.  Exploring conformational modes of macromolecular assemblies by multiparticle cryo-EM.

Authors:  Christian M T Spahn; Pawel A Penczek
Journal:  Curr Opin Struct Biol       Date:  2009-09-18       Impact factor: 6.809

  2 in total

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