Literature DB >> 6241263

Structural comparison of purified dynein proteins with in situ dynein arms.

U Goodenough, J Heuser.   

Abstract

Using the quick-freeze deep-etch technique, we describe the structure of outerarm dynein proteins from Chlamydomonas and Tetrahymena after adsorption to a mica surface, after high-salt dissociation, and after glutaraldehyde fixation, and compare these images to the configuration of outer arms bound to microtubules. After adsorption to mica, the extracted dyneins from both organisms look like three-headed "bouquets", as reported for Tetrahymena by Johnson & Wall (1983b). High magnification images demonstrate that each head carries a slender "stalk" and a long "stem", and that small subunits decorate the stems and create a "flowerpot" domain at the base of the bouquet. Exposure to high salt induces this trimer to dissociate into a two-headed species and a single-headed species; it also stimulates the decorative elements to dissociate from the stems. Dynein is thus constructed on the same general plan as myosin, with large globular heads, narrow stems and additional small subunits that associate with the stems. The splayed-out image of the bouquet appears to be a distortion arising during adsorption to mica since, after brief glutaraldehyde fixation, the three heads remain closely associated as vertices of a triangular unit. In situ, the three heads also adopt this trigonal configuration. Two of the three are visible from the exterior of the axoneme and constitute the bilobed rigor head we described previously (Goodenough & Heuser, 1982). The third head faces the interior of the axoneme where, we propose, it forms the "hook" of the outer arm as seen in thin section. We further propose that the decorative elements associated with the stem coalesce to form the two outer-arm "feet" seen in situ, and that at least one of the in vitro stalks is equivalent to the in situ stalk, which extends from the head to the B microtubule. Deep-etch images of stretched axonemes, partially extracted axonemes, and dynein-decorated brain microtubules indicate that each outer arm, as traditionally viewed, is a hybrid of two dynein molecules: its two feet derive from one molecule, whereas its trigonal head derives from the molecule located distally. The resultant overlapping configuration creates the diagonal "linkers" seen in situ, which correspond to the in vitro stems. Thus, a row of dynein arms is essentially a dynein polymer that extends from the tip to the base of a doublet microtubule, each head riding on its neighbor's feet like a row of circus elephants.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6241263     DOI: 10.1016/0022-2836(84)90272-9

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  66 in total

1.  Processive movement of single 22S dynein molecules occurs only at low ATP concentrations.

Authors:  E Hirakawa; H Higuchi; Y Y Toyoshima
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-14       Impact factor: 11.205

2.  Functional elements within the dynein microtubule-binding domain.

Authors:  M P Koonce; I Tikhonenko
Journal:  Mol Biol Cell       Date:  2000-02       Impact factor: 4.138

3.  Dynein and kinesin share an overlapping microtubule-binding site.

Authors:  Naoko Mizuno; Shiori Toba; Masaki Edamatsu; Junko Watai-Nishii; Nobutaka Hirokawa; Yoko Y Toyoshima; Masahide Kikkawa
Journal:  EMBO J       Date:  2004-06-03       Impact factor: 11.598

4.  The affinity of the dynein microtubule-binding domain is modulated by the conformation of its coiled-coil stalk.

Authors:  I R Gibbons; Joan E Garbarino; Carol E Tan; Samara L Reck-Peterson; Ronald D Vale; Andrew P Carter
Journal:  J Biol Chem       Date:  2005-04-11       Impact factor: 5.157

5.  Two modes of microtubule sliding driven by cytoplasmic dynein.

Authors:  Tomohiro Shima; Takahide Kon; Kenji Imamula; Reiko Ohkura; Kazuo Sutoh
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-03       Impact factor: 11.205

6.  The coordination of cyclic microtubule association/dissociation and tail swing of cytoplasmic dynein.

Authors:  Kenji Imamula; Takahide Kon; Reiko Ohkura; Kazuo Sutoh
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-02       Impact factor: 11.205

7.  Partially functional outer-arm dynein in a novel Chlamydomonas mutant expressing a truncated gamma heavy chain.

Authors:  Zhongmei Liu; Hiroko Takazaki; Yuki Nakazawa; Miho Sakato; Toshiki Yagi; Takuo Yasunaga; Stephen M King; Ritsu Kamiya
Journal:  Eukaryot Cell       Date:  2008-05-16

8.  The Mr 140,000 intermediate chain of Chlamydomonas flagellar inner arm dynein is a WD-repeat protein implicated in dynein arm anchoring.

Authors:  P Yang; W S Sale
Journal:  Mol Biol Cell       Date:  1998-12       Impact factor: 4.138

Review 9.  The origins and evolution of freeze-etch electron microscopy.

Authors:  John E Heuser
Journal:  J Electron Microsc (Tokyo)       Date:  2011

10.  Helix sliding in the stalk coiled coil of dynein couples ATPase and microtubule binding.

Authors:  Takahide Kon; Kenji Imamula; Anthony J Roberts; Reiko Ohkura; Peter J Knight; I R Gibbons; Stan A Burgess; Kazuo Sutoh
Journal:  Nat Struct Mol Biol       Date:  2009-02-08       Impact factor: 15.369

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