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A novel approach to the structural analysis of partially decorated actin based filaments

We describe a novel set of single particle based procedures for the structural analysis of electron microscope images of muscle thin filaments and other partially decorated actin based filaments. The thin filament comprises actin and the regulatory proteins tropomyosin and troponin in a 7:1:1 M rati...

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Detalles Bibliográficos
Autores principales: Paul, Danielle M., Squire, John M., Morris, Edward P.
Formato: Texto
Lenguaje:English
Publicado: Academic Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862299/
https://www.ncbi.nlm.nih.gov/pubmed/20025974
http://dx.doi.org/10.1016/j.jsb.2009.12.010
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author Paul, Danielle M.
Squire, John M.
Morris, Edward P.
author_facet Paul, Danielle M.
Squire, John M.
Morris, Edward P.
author_sort Paul, Danielle M.
collection PubMed
description We describe a novel set of single particle based procedures for the structural analysis of electron microscope images of muscle thin filaments and other partially decorated actin based filaments. The thin filament comprises actin and the regulatory proteins tropomyosin and troponin in a 7:1:1 M ratio. Prior to our work, structure analysis from electron microscope images of the thin filament has largely involved either helical averaging defined by the underlying actin helix or the use of single particle analysis but using a starting model as a reference structure. Our single particle based approach yields an accurate structure for the complete thin filament by avoiding the loss of information from troponin and tropomyosin associated with helical averaging and also removing the potential reference bias associated with the use of a starting model. The approach is more widely applicable to sub-stoichiometric complexes of F-actin and actin-binding proteins.
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spelling pubmed-28622992010-05-25 A novel approach to the structural analysis of partially decorated actin based filaments Paul, Danielle M. Squire, John M. Morris, Edward P. J Struct Biol Article We describe a novel set of single particle based procedures for the structural analysis of electron microscope images of muscle thin filaments and other partially decorated actin based filaments. The thin filament comprises actin and the regulatory proteins tropomyosin and troponin in a 7:1:1 M ratio. Prior to our work, structure analysis from electron microscope images of the thin filament has largely involved either helical averaging defined by the underlying actin helix or the use of single particle analysis but using a starting model as a reference structure. Our single particle based approach yields an accurate structure for the complete thin filament by avoiding the loss of information from troponin and tropomyosin associated with helical averaging and also removing the potential reference bias associated with the use of a starting model. The approach is more widely applicable to sub-stoichiometric complexes of F-actin and actin-binding proteins. Academic Press 2010-05 /pmc/articles/PMC2862299/ /pubmed/20025974 http://dx.doi.org/10.1016/j.jsb.2009.12.010 Text en © 2010 Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Paul, Danielle M.
Squire, John M.
Morris, Edward P.
A novel approach to the structural analysis of partially decorated actin based filaments
title A novel approach to the structural analysis of partially decorated actin based filaments
title_full A novel approach to the structural analysis of partially decorated actin based filaments
title_fullStr A novel approach to the structural analysis of partially decorated actin based filaments
title_full_unstemmed A novel approach to the structural analysis of partially decorated actin based filaments
title_short A novel approach to the structural analysis of partially decorated actin based filaments
title_sort novel approach to the structural analysis of partially decorated actin based filaments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862299/
https://www.ncbi.nlm.nih.gov/pubmed/20025974
http://dx.doi.org/10.1016/j.jsb.2009.12.010
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