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Expansion microscopy-based imaging of nuclear structures in cultured cells

Expansion microscopy is a sample preparation technique in which fixed and immunostained cells or tissues are embedded in a cross-linked network of swellable polyelectrolyte hydrogel that expands isotropically upon addition of deionized water. We utilize the X10 method for tenfold expansion of U2OS c...

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Autores principales: Gaudreau-Lapierre, Antoine, Mulatz, Kirk, Béïque, Jean-Claude, Trinkle-Mulcahy, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8243706/
https://www.ncbi.nlm.nih.gov/pubmed/34223201
http://dx.doi.org/10.1016/j.xpro.2021.100630
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author Gaudreau-Lapierre, Antoine
Mulatz, Kirk
Béïque, Jean-Claude
Trinkle-Mulcahy, Laura
author_facet Gaudreau-Lapierre, Antoine
Mulatz, Kirk
Béïque, Jean-Claude
Trinkle-Mulcahy, Laura
author_sort Gaudreau-Lapierre, Antoine
collection PubMed
description Expansion microscopy is a sample preparation technique in which fixed and immunostained cells or tissues are embedded in a cross-linked network of swellable polyelectrolyte hydrogel that expands isotropically upon addition of deionized water. We utilize the X10 method for tenfold expansion of U2OS cells with concurrent DNA staining. A custom 3D-printed gel cutter and chambered slides minimize gel drift, facilitating analysis of the components of nuclear structures at nanoscale resolution by conventional microscopy or Airyscan confocal imaging. For complete information on the generation and use of this protocol, please refer to Do et al. (2020).
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spelling pubmed-82437062021-07-02 Expansion microscopy-based imaging of nuclear structures in cultured cells Gaudreau-Lapierre, Antoine Mulatz, Kirk Béïque, Jean-Claude Trinkle-Mulcahy, Laura STAR Protoc Protocol Expansion microscopy is a sample preparation technique in which fixed and immunostained cells or tissues are embedded in a cross-linked network of swellable polyelectrolyte hydrogel that expands isotropically upon addition of deionized water. We utilize the X10 method for tenfold expansion of U2OS cells with concurrent DNA staining. A custom 3D-printed gel cutter and chambered slides minimize gel drift, facilitating analysis of the components of nuclear structures at nanoscale resolution by conventional microscopy or Airyscan confocal imaging. For complete information on the generation and use of this protocol, please refer to Do et al. (2020). Elsevier 2021-06-26 /pmc/articles/PMC8243706/ /pubmed/34223201 http://dx.doi.org/10.1016/j.xpro.2021.100630 Text en © 2021 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
Gaudreau-Lapierre, Antoine
Mulatz, Kirk
Béïque, Jean-Claude
Trinkle-Mulcahy, Laura
Expansion microscopy-based imaging of nuclear structures in cultured cells
title Expansion microscopy-based imaging of nuclear structures in cultured cells
title_full Expansion microscopy-based imaging of nuclear structures in cultured cells
title_fullStr Expansion microscopy-based imaging of nuclear structures in cultured cells
title_full_unstemmed Expansion microscopy-based imaging of nuclear structures in cultured cells
title_short Expansion microscopy-based imaging of nuclear structures in cultured cells
title_sort expansion microscopy-based imaging of nuclear structures in cultured cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8243706/
https://www.ncbi.nlm.nih.gov/pubmed/34223201
http://dx.doi.org/10.1016/j.xpro.2021.100630
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