| Literature DB >> 20719263 |
Sarah Gierke1, Praveen Kumar, Torsten Wittmann.
Abstract
The spatiotemporal regulation of intracellular microtubule polymerization dynamics, by numerous microtubule-associated proteins and other mechanisms, is central to many cell processes. Here, we give an overview and practical guide on how to acquire and analyze time-lapse sequences of dynamic microtubules in live cells by either fluorescently labeling entire microtubules or by utilizing proteins that specifically associate only with growing microtubule ends and summarize the strengths and weaknesses of different approaches. We give practical recommendations for imaging conditions, and discuss important limitations of such analysis that are dictated by the maximum achievable spatial and temporal sampling frequencies. 2010 Elsevier Inc. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20719263 PMCID: PMC3495240 DOI: 10.1016/S0091-679X(10)97002-7
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441