| Literature DB >> 20466138 |
Christopher Gell1, Volker Bormuth, Gary J Brouhard, Daniel N Cohen, Stefan Diez, Claire T Friel, Jonne Helenius, Bert Nitzsche, Heike Petzold, Jan Ribbe, Erik Schäffer, Jeffrey H Stear, Anastasiya Trushko, Vladimir Varga, Per O Widlund, Marija Zanic, Jonathon Howard.
Abstract
In vitro assays that reconstitute the dynamic behavior of microtubules provide insight into the roles of microtubule-associated proteins (MAPs) in regulating the growth, shrinkage, and catastrophe of microtubules. The use of total internal reflection fluorescence microscopy with fluorescently labeled tubulin and MAPs has allowed us to study microtubule dynamics at the resolution of single molecules. In this chapter we present a practical overview of how these assays are performed in our laboratory: fluorescent labeling methods, strategies to prolong the time to photo-bleaching, preparation of stabilized microtubules, flow-cells, microtubule immobilization, and finally an overview of the workflow that we follow when performing the experiments. At all stages, we focus on practical tips and highlight potential stumbling blocks. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20466138 DOI: 10.1016/S0091-679X(10)95013-9
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441