Quantification of Cytoskeletal Dynamics in Time-Lapse Recordings.

catastrophe growth speed live-cell imaging microtubule dynamics microtubule-end labeling quantitative fluorescence microscopy rescue shrink speed

Journal

Current protocols in plant biology
ISSN: 2379-8068
Titre abrégé: Curr Protoc Plant Biol
Pays: United States
ID NLM: 101685882

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 16 5 2019
medline: 27 11 2019
entrez: 16 5 2019
Statut: ppublish

Résumé

The cytoskeleton is key to many essential processes in a plant cell, e.g., growth, division, and defense. Contrary to what "skeleton" implies, the cytoskeleton is highly dynamic, and is able to re-organize itself continuously. The advent of live-cell microscopy and the development of genetically encoded fluorophores enabled detailed observation of the organization and dynamics of the cytoskeleton. Despite the biological importance of the cytoskeletal dynamics, quantitative analyses remain laborious endeavors that only a handful of research teams regularly conduct. With this protocol, we provide a standardized step-by-step guide to analyze the dynamics of microtubules. We provide example data and code for post-processing in Fiji that enables researchers to modify and adapt the routine to their needs. More such tools are needed to quantitatively assess the cytoskeleton and thus to better understand cell biology. © 2019 by John Wiley & Sons, Inc.

Identifiants

pubmed: 31091014
doi: 10.1002/cppb.20091
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e20091

Informations de copyright

© 2019 John Wiley & Sons, Inc.

Auteurs

René Schneider (R)

Max Planck Institute of Molecular Plant Physiology, Potsdam, Germany.

Arun Sampathkumar (A)

Max Planck Institute of Molecular Plant Physiology, Potsdam, Germany.

Staffan Persson (S)

School of Biosciences, University of Melbourne, Parkville, Victoria, Australia.

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Classifications MeSH