Literature DB >> 28840247

Biophysics of Microtubule End Coupling at the Kinetochore.

Ekaterina L Grishchuk1.   

Abstract

The main physiological function of mitotic kinetochores is to provide durable attachment to spindle microtubules, which segregate chromosomes in order to partition them equally between the two daughter cells. Numerous kinetochore components that can bind directly to microtubules have been identified, including ATP-dependent motors and various microtubule-associated proteins with no motor activity. A major challenge facing the field is to explain chromosome motions based on the biochemical and structural properties of these individual kinetochore components and their assemblies. This chapter reviews the molecular mechanisms responsible for the motions associated with dynamic microtubule tips at the single-molecule level, as well as the activities of multimolecular ensembles called couplers. These couplers enable persistent kinetochore motion even under load, but their exact composition and structure remain unknown. Because no natural or artificial macro-machines function in an analogous manner to these molecular nano-devices, understanding their underlying biophysical mechanisms will require conceptual advances.

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Year:  2017        PMID: 28840247     DOI: 10.1007/978-3-319-58592-5_17

Source DB:  PubMed          Journal:  Prog Mol Subcell Biol        ISSN: 0079-6484


  8 in total

Review 1.  The mammalian kinetochore-microtubule interface: robust mechanics and computation with many microtubules.

Authors:  Alexandra F Long; Jonathan Kuhn; Sophie Dumont
Journal:  Curr Opin Cell Biol       Date:  2019-05-25       Impact factor: 8.382

2.  In vitro reconstitution of lateral to end-on conversion of kinetochore-microtubule attachments.

Authors:  Manas Chakraborty; Ekaterina V Tarasovetc; Ekaterina L Grishchuk
Journal:  Methods Cell Biol       Date:  2018-05-11       Impact factor: 1.441

Review 3.  Structural view of the yeast Dam1 complex, a ring-shaped molecular coupler for the dynamic microtubule end.

Authors:  Shaowen Wu; Ekaterina L Grishchuk
Journal:  Essays Biochem       Date:  2020-09-04       Impact factor: 8.000

4.  Microtubule Tip Tracking by the Spindle and Kinetochore Protein Ska1 Requires Diverse Tubulin-Interacting Surfaces.

Authors:  Julie K Monda; Ian P Whitney; Ekaterina V Tarasovetc; Elizabeth Wilson-Kubalek; Ronald A Milligan; Ekaterina L Grishchuk; Iain M Cheeseman
Journal:  Curr Biol       Date:  2017-11-16       Impact factor: 10.834

5.  Multivalency of NDC80 in the outer kinetochore is essential to track shortening microtubules and generate forces.

Authors:  Vladimir A Volkov; Pim J Huis In 't Veld; Marileen Dogterom; Andrea Musacchio
Journal:  Elife       Date:  2018-04-09       Impact factor: 8.140

6.  Microtubule end conversion mediated by motors and diffusing proteins with no intrinsic microtubule end-binding activity.

Authors:  Manas Chakraborty; Ekaterina V Tarasovetc; Anatoly V Zaytsev; Maxim Godzi; Ana C Figueiredo; Fazly I Ataullakhanov; Ekaterina L Grishchuk
Journal:  Nat Commun       Date:  2019-04-11       Impact factor: 14.919

7.  Individual kinetochore-fibers locally dissipate force to maintain robust mammalian spindle structure.

Authors:  Alexandra F Long; Pooja Suresh; Sophie Dumont
Journal:  J Cell Biol       Date:  2020-08-03       Impact factor: 10.539

8.  Microneedle manipulation of the mammalian spindle reveals specialized, short-lived reinforcement near chromosomes.

Authors:  Pooja Suresh; Alexandra F Long; Sophie Dumont
Journal:  Elife       Date:  2020-03-19       Impact factor: 8.140

  8 in total

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