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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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). |
format | Online Article Text |
id | pubmed-8243706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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