Cargando…

Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia

The sliding tubule model of ciliary motion requires that active sliding of microtubules occur by cyclic cross-bridging of the dynein arms. When isolated, demembranated Tetrahymena cilia are allowed to spontaneously disintegrate in the presence of ATP, the structural conformation of the dynein arms c...

Descripción completa

Detalles Bibliográficos
Autores principales: Warner, F. D., Mitchell, D. R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109981/
https://www.ncbi.nlm.nih.gov/pubmed/10605437
_version_ 1782139453408542720
author Warner, F. D.
Mitchell, D. R.
author_facet Warner, F. D.
Mitchell, D. R.
author_sort Warner, F. D.
collection PubMed
description The sliding tubule model of ciliary motion requires that active sliding of microtubules occur by cyclic cross-bridging of the dynein arms. When isolated, demembranated Tetrahymena cilia are allowed to spontaneously disintegrate in the presence of ATP, the structural conformation of the dynein arms can be clearly resolved by negative contrast electron microscopy. The arms consist of three structural subunits that occur in two basic conformations with respect to the adjacent B subfiber. The inactive conformation occurs in the absence of ATP and is characterized by a uniform, 32 degrees base-directed polarity of the arms. Inactive arms are not attached to the B subfiber of adjacent doublets. The bridged conformation occurs strictly in the presence of ATP and is characterized by arms having the same polarity as inactive arms, but the terminal subunit of the arms has become attached to the B subfiber. In most instances the bridged conformation is accompanied by substantial tip-directed sliding displacement of the bridged doublets. Because the base-directed polarity of the bridged arms is opposite to the direction required for force generation in these cilia and because the bridges occur in the presence of ATP, it is suggested that the bridged conformation may represent the initial attachment phase of the dynein cross-bridge cycle. The force-generating phase of the cycle would then require a tip-directed deflection of the arm subunit attached to the B subfiber.
format Text
id pubmed-2109981
institution National Center for Biotechnology Information
language English
publishDate 1978
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21099812008-05-01 Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia Warner, F. D. Mitchell, D. R. J Cell Biol Journal Article The sliding tubule model of ciliary motion requires that active sliding of microtubules occur by cyclic cross-bridging of the dynein arms. When isolated, demembranated Tetrahymena cilia are allowed to spontaneously disintegrate in the presence of ATP, the structural conformation of the dynein arms can be clearly resolved by negative contrast electron microscopy. The arms consist of three structural subunits that occur in two basic conformations with respect to the adjacent B subfiber. The inactive conformation occurs in the absence of ATP and is characterized by a uniform, 32 degrees base-directed polarity of the arms. Inactive arms are not attached to the B subfiber of adjacent doublets. The bridged conformation occurs strictly in the presence of ATP and is characterized by arms having the same polarity as inactive arms, but the terminal subunit of the arms has become attached to the B subfiber. In most instances the bridged conformation is accompanied by substantial tip-directed sliding displacement of the bridged doublets. Because the base-directed polarity of the bridged arms is opposite to the direction required for force generation in these cilia and because the bridges occur in the presence of ATP, it is suggested that the bridged conformation may represent the initial attachment phase of the dynein cross-bridge cycle. The force-generating phase of the cycle would then require a tip-directed deflection of the arm subunit attached to the B subfiber. The Rockefeller University Press 1978-02-01 /pmc/articles/PMC2109981/ /pubmed/10605437 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Journal Article
Warner, F. D.
Mitchell, D. R.
Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title_full Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title_fullStr Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title_full_unstemmed Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title_short Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia
title_sort structural conformation of ciliary dynein arms and the generation of sliding forces in tetrahymena cilia
topic Journal Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109981/
https://www.ncbi.nlm.nih.gov/pubmed/10605437
work_keys_str_mv AT warnerfd structuralconformationofciliarydyneinarmsandthegenerationofslidingforcesintetrahymenacilia
AT mitchelldr structuralconformationofciliarydyneinarmsandthegenerationofslidingforcesintetrahymenacilia