Literature DB >> 10605437

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

F D Warner1, D R Mitchell.   

Abstract

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.

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Year:  1978        PMID: 10605437      PMCID: PMC2109981          DOI: 10.1083/jcb.76.2.261

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  17 in total

1.  Control of flagellar wave movement in Crithidia oncopelti.

Authors:  M E Holwill; J L McGregor
Journal:  Nature       Date:  1975-05-08       Impact factor: 49.962

2.  The structural basis of ciliary bend formation. Radial spoke positional changes accompanying microtubule sliding.

Authors:  F D Warner; P Satir
Journal:  J Cell Biol       Date:  1974-10       Impact factor: 10.539

3.  Aspects of the flagellar apparatus and associated microtubules in a marine alga.

Authors:  J Hyams; D Chasey
Journal:  Exp Cell Res       Date:  1974-03-15       Impact factor: 3.905

4.  Structural polarity and directional growth of microtubules of Chlamydomonas flagella.

Authors:  C Allen; G G Borisy
Journal:  J Mol Biol       Date:  1974-12-05       Impact factor: 5.469

5.  Flagellar movement and adenosine triphosphatase activity in sea urchin sperm extracted with triton X-100.

Authors:  B H Gibbons; I R Gibbons
Journal:  J Cell Biol       Date:  1972-07       Impact factor: 10.539

6.  Micromanipulation of the flagellum of Crithidia oncopelti. I. Mechanical effects.

Authors:  M E Holwill; J L McGregor
Journal:  J Exp Biol       Date:  1974-04       Impact factor: 3.312

7.  Arrangement of subunits in flagellar microtubules.

Authors:  L Amos; A Klug
Journal:  J Cell Sci       Date:  1974-05       Impact factor: 5.285

8.  A reinvestigation of cross-sections of cilia.

Authors:  R D Allen
Journal:  J Cell Biol       Date:  1968-06       Impact factor: 10.539

9.  Studies on cilia. 3. Further studies on the cilium tip and a "sliding filament" model of ciliary motility.

Authors:  P Satir
Journal:  J Cell Biol       Date:  1968-10       Impact factor: 10.539

10.  Properties of flagellar "rigor waves" formed by abrupt removal of adenosine triphosphate from actively swimming sea urchin sperm.

Authors:  B H Gibbons; I R Gibbons
Journal:  J Cell Biol       Date:  1974-12       Impact factor: 10.539

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  23 in total

1.  Changes in microtubule packing during the stretching of an extensible microtubule bundle in the ciliate Nassula.

Authors:  J V Wellings; J B Tucker
Journal:  Cell Tissue Res       Date:  1979-03-19       Impact factor: 5.249

2.  Structural-functional relationships of the dynein, spokes, and central-pair projections predicted from an analysis of the forces acting within a flagellum.

Authors:  Charles B Lindemann
Journal:  Biophys J       Date:  2003-06       Impact factor: 4.033

3.  Bend propagation in flagella. II. Incorporation of dynein cross-bridge kinetics into the equations of motion.

Authors:  M Hines; J J Blum
Journal:  Biophys J       Date:  1979-03       Impact factor: 4.033

Review 4.  Setting the dynein motor in motion: New insights from electron tomography.

Authors:  Danielle A Grotjahn; Gabriel C Lander
Journal:  J Biol Chem       Date:  2019-07-08       Impact factor: 5.157

5.  Disruption of respiratory cilia by proteases including those of Pseudomonas aeruginosa.

Authors:  S T Hingley; A T Hastie; F Kueppers; M L Higgins
Journal:  Infect Immun       Date:  1986-11       Impact factor: 3.441

6.  Polarity of some motility-related microtubules.

Authors:  U Euteneuer; J R McIntosh
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

7.  Self-interaction of dynein from Tetrahymena cilia.

Authors:  C Wells; A Molina-Garcia; S E Harding; A J Rowe
Journal:  J Muscle Res Cell Motil       Date:  1990-08       Impact factor: 2.698

8.  Inhibition and relaxation of sea urchin sperm flagella by vanadate.

Authors:  M Okuno
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

9.  Polarity of dynein-microtubule interactions in vitro: cross-bridging between parallel and antiparallel microtubules.

Authors:  F D Warner; D R Mitchell
Journal:  J Cell Biol       Date:  1981-04       Impact factor: 10.539

10.  ATP-dependent structural changes of the outer dynein arm in Tetrahymena cilia: a freeze-etch replica study.

Authors:  S Tsukita; S Tsukita; J Usukura; H Ishikawa
Journal:  J Cell Biol       Date:  1983-05       Impact factor: 10.539

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