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Ten-fold Robust Expansion Microscopy
Expansion microscopy (ExM) is a powerful technique to overcome the diffraction limit of light microscopy that can be applied in both tissues and cells. In ExM, samples are embedded in a swellable polymer gel to physically expand the sample and isotropically increase resolution in x, y, and z. By sys...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bio-Protocol
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308184/ https://www.ncbi.nlm.nih.gov/pubmed/37397797 http://dx.doi.org/10.21769/BioProtoc.4698 |
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author | Damstra, Hugo G. J. Mohar, Boaz Eddison, Mark Akhmanova, Anna Kapitein, Lukas C. Tillberg, Paul W. |
author_facet | Damstra, Hugo G. J. Mohar, Boaz Eddison, Mark Akhmanova, Anna Kapitein, Lukas C. Tillberg, Paul W. |
author_sort | Damstra, Hugo G. J. |
collection | PubMed |
description | Expansion microscopy (ExM) is a powerful technique to overcome the diffraction limit of light microscopy that can be applied in both tissues and cells. In ExM, samples are embedded in a swellable polymer gel to physically expand the sample and isotropically increase resolution in x, y, and z. By systematic exploration of the ExM recipe space, we developed a novel ExM method termed Ten-fold Robust Expansion Microscopy (TREx) that, as the original ExM method, requires no specialized equipment or procedures. TREx enables ten-fold expansion of both thick mouse brain tissue sections and cultured human cells, can be handled easily, and enables high-resolution subcellular imaging with a single expansion step. Furthermore, TREx can provide ultrastructural context to subcellular protein localization by combining antibody-stained samples with off-the-shelf small molecule stains for both total protein and membranes. |
format | Online Article Text |
id | pubmed-10308184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bio-Protocol |
record_format | MEDLINE/PubMed |
spelling | pubmed-103081842023-06-30 Ten-fold Robust Expansion Microscopy Damstra, Hugo G. J. Mohar, Boaz Eddison, Mark Akhmanova, Anna Kapitein, Lukas C. Tillberg, Paul W. Bio Protoc Methods Article Expansion microscopy (ExM) is a powerful technique to overcome the diffraction limit of light microscopy that can be applied in both tissues and cells. In ExM, samples are embedded in a swellable polymer gel to physically expand the sample and isotropically increase resolution in x, y, and z. By systematic exploration of the ExM recipe space, we developed a novel ExM method termed Ten-fold Robust Expansion Microscopy (TREx) that, as the original ExM method, requires no specialized equipment or procedures. TREx enables ten-fold expansion of both thick mouse brain tissue sections and cultured human cells, can be handled easily, and enables high-resolution subcellular imaging with a single expansion step. Furthermore, TREx can provide ultrastructural context to subcellular protein localization by combining antibody-stained samples with off-the-shelf small molecule stains for both total protein and membranes. Bio-Protocol 2023-06-20 /pmc/articles/PMC10308184/ /pubmed/37397797 http://dx.doi.org/10.21769/BioProtoc.4698 Text en ©Copyright : © 2023 The Authors; This is an open access article under the CC BY license https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Methods Article Damstra, Hugo G. J. Mohar, Boaz Eddison, Mark Akhmanova, Anna Kapitein, Lukas C. Tillberg, Paul W. Ten-fold Robust Expansion Microscopy |
title | Ten-fold Robust Expansion Microscopy |
title_full | Ten-fold Robust Expansion Microscopy |
title_fullStr | Ten-fold Robust Expansion Microscopy |
title_full_unstemmed | Ten-fold Robust Expansion Microscopy |
title_short | Ten-fold Robust Expansion Microscopy |
title_sort | ten-fold robust expansion microscopy |
topic | Methods Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308184/ https://www.ncbi.nlm.nih.gov/pubmed/37397797 http://dx.doi.org/10.21769/BioProtoc.4698 |
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