Literature DB >> 20409799

Protein engineering approaches to study the dynein mechanism using a Dictyostelium expression system.

Takahide Kon1, Tomohiro Shima, Kazuo Sutoh.   

Abstract

Dyneins are microtubule-based motor complexes that power a wide variety of motile processes within eukaryotic cells, including the beating of cilia and flagella and intracellular trafficking along microtubules. Mechanistic studies on dynein have been hampered by their enormous size (molecular masses of 0.5-3MDa) and molecular complexity. However, the recent establishment of recombinant expression systems for cytoplasmic dynein, together with structural and functional analyses, has advanced our understanding of the molecular mechanisms of dynein motility. Here, we describe several protocols for protein engineering approaches to the dynein mechanism using a Dictyostelium discoideum expression system. We first describe the design and preparation of recombinant dynein suitable for mechanistic studies. We then discuss two distinct functional assays that take advantage of the recombinant dynein. One is for detection of dynein's conformational changes during the ATPase cycle. Another is an in vitro motility assay at multiple- and single-molecule levels for examination of the dynamic behavior of dynein moving on a microtubule. 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 20409799     DOI: 10.1016/S0091-679X(08)92005-7

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  4 in total

1.  The 2.8 Å crystal structure of the dynein motor domain.

Authors:  Takahide Kon; Takuji Oyama; Rieko Shimo-Kon; Kenji Imamula; Tomohiro Shima; Kazuo Sutoh; Genji Kurisu
Journal:  Nature       Date:  2012-03-07       Impact factor: 49.962

2.  X-ray structure of a functional full-length dynein motor domain.

Authors:  Takahide Kon; Kazuo Sutoh; Genji Kurisu
Journal:  Nat Struct Mol Biol       Date:  2011-05-22       Impact factor: 15.369

3.  Tug-of-war of microtubule filaments at the boundary of a kinesin- and dynein-patterned surface.

Authors:  Junya Ikuta; Nagendra K Kamisetty; Hirofumi Shintaku; Hidetoshi Kotera; Takahide Kon; Ryuji Yokokawa
Journal:  Sci Rep       Date:  2014-06-13       Impact factor: 4.379

4.  A flipped ion pair at the dynein-microtubule interface is critical for dynein motility and ATPase activation.

Authors:  Seiichi Uchimura; Takashi Fujii; Hiroko Takazaki; Rie Ayukawa; Yosuke Nishikawa; Itsushi Minoura; You Hachikubo; Genji Kurisu; Kazuo Sutoh; Takahide Kon; Keiichi Namba; Etsuko Muto
Journal:  J Cell Biol       Date:  2015-01-12       Impact factor: 10.539

  4 in total

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