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In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy

Dynamic microtubules are essential for many processes in the lives of eukaryotic cells. To study and understand the mechanisms of microtubule dynamics and regulation, in vitro reconstitution with purified components has proven a vital approach. Imaging microtubule dynamics can be instructive for a g...

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Detalles Bibliográficos
Autores principales: Hirst, William Graham, Kiefer, Christine, Abdosamadi, Mohammad Kazem, Schäffer, Erik, Reber, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757405/
https://www.ncbi.nlm.nih.gov/pubmed/33377071
http://dx.doi.org/10.1016/j.xpro.2020.100177
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author Hirst, William Graham
Kiefer, Christine
Abdosamadi, Mohammad Kazem
Schäffer, Erik
Reber, Simone
author_facet Hirst, William Graham
Kiefer, Christine
Abdosamadi, Mohammad Kazem
Schäffer, Erik
Reber, Simone
author_sort Hirst, William Graham
collection PubMed
description Dynamic microtubules are essential for many processes in the lives of eukaryotic cells. To study and understand the mechanisms of microtubule dynamics and regulation, in vitro reconstitution with purified components has proven a vital approach. Imaging microtubule dynamics can be instructive for a given species, isoform composition, or biochemical modification. Here, we describe two methods that visualize microtubule dynamics at high speed and high contrast: (1) total internal reflection fluorescence microscopy and (2) label-free interference reflection microscopy. For complete details on the use and execution of this protocol, please refer to Hirst et al. (2020).
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spelling pubmed-77574052020-12-28 In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy Hirst, William Graham Kiefer, Christine Abdosamadi, Mohammad Kazem Schäffer, Erik Reber, Simone STAR Protoc Protocol Dynamic microtubules are essential for many processes in the lives of eukaryotic cells. To study and understand the mechanisms of microtubule dynamics and regulation, in vitro reconstitution with purified components has proven a vital approach. Imaging microtubule dynamics can be instructive for a given species, isoform composition, or biochemical modification. Here, we describe two methods that visualize microtubule dynamics at high speed and high contrast: (1) total internal reflection fluorescence microscopy and (2) label-free interference reflection microscopy. For complete details on the use and execution of this protocol, please refer to Hirst et al. (2020). Elsevier 2020-11-24 /pmc/articles/PMC7757405/ /pubmed/33377071 http://dx.doi.org/10.1016/j.xpro.2020.100177 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Hirst, William Graham
Kiefer, Christine
Abdosamadi, Mohammad Kazem
Schäffer, Erik
Reber, Simone
In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title_full In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title_fullStr In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title_full_unstemmed In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title_short In Vitro Reconstitution and Imaging of Microtubule Dynamics by Fluorescence and Label-free Microscopy
title_sort in vitro reconstitution and imaging of microtubule dynamics by fluorescence and label-free microscopy
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757405/
https://www.ncbi.nlm.nih.gov/pubmed/33377071
http://dx.doi.org/10.1016/j.xpro.2020.100177
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