Literature DB >> 24630104

Assaying microtubule nucleation by the γ-tubulin ring complex.

Yuk-Kwan Choi1, Robert Z Qi2.   

Abstract

Microtubule organization by microtubule-organizing centers such as the centrosome requires γ-tubulin, which exists in the γ-tubulin ring complex (γTuRC) that nucleates microtubules. The γTuRC is a ring-shaped, macromolecular complex whose core components are γ-tubulin and the γ-tubulin complex proteins. Despite the recent identification of additional γTuRC components, the molecular composition and regulatory properties of the complex remain poorly understood. The ability to purify the γTuRC at a large scale for characterization may hold a key to understanding the mechanism by which the γTuRC nucleates microtubules. In this chapter, we describe methods to isolate the γTuRC from human cell cultures and to perform assays on the purified γTuRC.
© 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CDK5RAP2; Electron microscopy; Microtubules; Nucleation; γ-Tubulin ring complex

Mesh:

Substances:

Year:  2014        PMID: 24630104     DOI: 10.1016/B978-0-12-397924-7.00007-8

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  2 in total

1.  The catalytic subunit of DNA polymerase δ inhibits γTuRC activity and regulates Golgi-derived microtubules.

Authors:  Yuehong Shen; Pengfei Liu; Taolue Jiang; Yu Hu; Franco K C Au; Robert Z Qi
Journal:  Nat Commun       Date:  2017-09-15       Impact factor: 14.919

2.  XMAP215 is a microtubule nucleation factor that functions synergistically with the γ-tubulin ring complex.

Authors:  Akanksha Thawani; Rachel S Kadzik; Sabine Petry
Journal:  Nat Cell Biol       Date:  2018-04-25       Impact factor: 28.824

  2 in total

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