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Molecular tension microscopy of the LINC complex in live cells

We present a protocol to measure the effect of pharmacological treatments on the mechanical tension experienced by nesprins at the cytoplasmic surface of the nuclear envelope of mammalian cells in culture. We apply this protocol to MDCK epithelial cells exposed to the actin depolymerization agent cy...

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Detalles Bibliográficos
Autores principales: Sipieter, François, Laurent, Louis, Girard, Philippe P., Borghi, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294191/
https://www.ncbi.nlm.nih.gov/pubmed/35841591
http://dx.doi.org/10.1016/j.xpro.2022.101538
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author Sipieter, François
Laurent, Louis
Girard, Philippe P.
Borghi, Nicolas
author_facet Sipieter, François
Laurent, Louis
Girard, Philippe P.
Borghi, Nicolas
author_sort Sipieter, François
collection PubMed
description We present a protocol to measure the effect of pharmacological treatments on the mechanical tension experienced by nesprins at the cytoplasmic surface of the nuclear envelope of mammalian cells in culture. We apply this protocol to MDCK epithelial cells exposed to the actin depolymerization agent cytochalasin D. To do so, we perform confocal spectral imaging of transiently expressed molecular tension sensors of mini-nesprin 2G and analyze the FRET signal from the sensors with a custom-made Fiji script. For complete details on the use and execution of this protocol, please refer to Déjardin et al. (2020).
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spelling pubmed-92941912022-07-20 Molecular tension microscopy of the LINC complex in live cells Sipieter, François Laurent, Louis Girard, Philippe P. Borghi, Nicolas STAR Protoc Protocol We present a protocol to measure the effect of pharmacological treatments on the mechanical tension experienced by nesprins at the cytoplasmic surface of the nuclear envelope of mammalian cells in culture. We apply this protocol to MDCK epithelial cells exposed to the actin depolymerization agent cytochalasin D. To do so, we perform confocal spectral imaging of transiently expressed molecular tension sensors of mini-nesprin 2G and analyze the FRET signal from the sensors with a custom-made Fiji script. For complete details on the use and execution of this protocol, please refer to Déjardin et al. (2020). Elsevier 2022-07-16 /pmc/articles/PMC9294191/ /pubmed/35841591 http://dx.doi.org/10.1016/j.xpro.2022.101538 Text en © 2022 The Author(s) https://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
Sipieter, François
Laurent, Louis
Girard, Philippe P.
Borghi, Nicolas
Molecular tension microscopy of the LINC complex in live cells
title Molecular tension microscopy of the LINC complex in live cells
title_full Molecular tension microscopy of the LINC complex in live cells
title_fullStr Molecular tension microscopy of the LINC complex in live cells
title_full_unstemmed Molecular tension microscopy of the LINC complex in live cells
title_short Molecular tension microscopy of the LINC complex in live cells
title_sort molecular tension microscopy of the linc complex in live cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294191/
https://www.ncbi.nlm.nih.gov/pubmed/35841591
http://dx.doi.org/10.1016/j.xpro.2022.101538
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