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Structure and Orientation of Troponin in the Thin Filament

The troponin complex on the thin filament plays a crucial role in the regulation of muscle contraction. However, the precise location of troponin relative to actin and tropomyosin remains uncertain. We have developed a method of reconstructing thin filaments using single particle analysis that does...

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Detalles Bibliográficos
Autores principales: Paul, Danielle M., Morris, Edward P., Kensler, Robert W., Squire, John M.
Formato: Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685683/
https://www.ncbi.nlm.nih.gov/pubmed/19321455
http://dx.doi.org/10.1074/jbc.M808615200
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author Paul, Danielle M.
Morris, Edward P.
Kensler, Robert W.
Squire, John M.
author_facet Paul, Danielle M.
Morris, Edward P.
Kensler, Robert W.
Squire, John M.
author_sort Paul, Danielle M.
collection PubMed
description The troponin complex on the thin filament plays a crucial role in the regulation of muscle contraction. However, the precise location of troponin relative to actin and tropomyosin remains uncertain. We have developed a method of reconstructing thin filaments using single particle analysis that does not impose the helical symmetry of actin and is independent of a starting model. We present a single particle three-dimensional reconstruction of the thin filament. Atomic models of the F-actin filament were fitted into the electron density maps and troponin and tropomyosin located. The structure provides evidence that the globular head region of troponin labels the two strands of actin with a 27.5-Å axial stagger. The density attributed to troponin appears tapered with the widest point toward the barbed end. This leads us to interpret the polarity of the troponin complex in the thin filament as reversed with respect to the widely accepted model.
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spelling pubmed-26856832009-05-29 Structure and Orientation of Troponin in the Thin Filament Paul, Danielle M. Morris, Edward P. Kensler, Robert W. Squire, John M. J Biol Chem Protein Structure and Folding The troponin complex on the thin filament plays a crucial role in the regulation of muscle contraction. However, the precise location of troponin relative to actin and tropomyosin remains uncertain. We have developed a method of reconstructing thin filaments using single particle analysis that does not impose the helical symmetry of actin and is independent of a starting model. We present a single particle three-dimensional reconstruction of the thin filament. Atomic models of the F-actin filament were fitted into the electron density maps and troponin and tropomyosin located. The structure provides evidence that the globular head region of troponin labels the two strands of actin with a 27.5-Å axial stagger. The density attributed to troponin appears tapered with the widest point toward the barbed end. This leads us to interpret the polarity of the troponin complex in the thin filament as reversed with respect to the widely accepted model. American Society for Biochemistry and Molecular Biology 2009-05-29 /pmc/articles/PMC2685683/ /pubmed/19321455 http://dx.doi.org/10.1074/jbc.M808615200 Text en Copyright © 2009, The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle Protein Structure and Folding
Paul, Danielle M.
Morris, Edward P.
Kensler, Robert W.
Squire, John M.
Structure and Orientation of Troponin in the Thin Filament
title Structure and Orientation of Troponin in the Thin Filament
title_full Structure and Orientation of Troponin in the Thin Filament
title_fullStr Structure and Orientation of Troponin in the Thin Filament
title_full_unstemmed Structure and Orientation of Troponin in the Thin Filament
title_short Structure and Orientation of Troponin in the Thin Filament
title_sort structure and orientation of troponin in the thin filament
topic Protein Structure and Folding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685683/
https://www.ncbi.nlm.nih.gov/pubmed/19321455
http://dx.doi.org/10.1074/jbc.M808615200
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