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Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields
Non-uniform illumination limits quantitative analyses of fluorescence imaging techniques. In particular, single molecule localization microscopy (SMLM) relies on high irradiances, but conventional Gaussian-shaped laser illumination restricts the usable field of view to around 40 µm × 40 µm. We prese...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144377/ https://www.ncbi.nlm.nih.gov/pubmed/34031402 http://dx.doi.org/10.1038/s41467-021-23405-4 |
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author | Mau, Adrien Friedl, Karoline Leterrier, Christophe Bourg, Nicolas Lévêque-Fort, Sandrine |
author_facet | Mau, Adrien Friedl, Karoline Leterrier, Christophe Bourg, Nicolas Lévêque-Fort, Sandrine |
author_sort | Mau, Adrien |
collection | PubMed |
description | Non-uniform illumination limits quantitative analyses of fluorescence imaging techniques. In particular, single molecule localization microscopy (SMLM) relies on high irradiances, but conventional Gaussian-shaped laser illumination restricts the usable field of view to around 40 µm × 40 µm. We present Adaptable Scanning for Tunable Excitation Regions (ASTER), a versatile illumination technique that generates uniform and adaptable illumination. ASTER is also highly compatible with optical sectioning techniques such as total internal reflection fluorescence (TIRF). For SMLM, ASTER delivers homogeneous blinking kinetics at reasonable laser power over fields-of-view up to 200 µm × 200 µm. We demonstrate that ASTER improves clustering analysis and nanoscopic size measurements by imaging nanorulers, microtubules and clathrin-coated pits in COS-7 cells, and β2-spectrin in neurons. ASTER’s sharp and quantitative illumination paves the way for high-throughput quantification of biological structures and processes in classical and super-resolution fluorescence microscopies. |
format | Online Article Text |
id | pubmed-8144377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81443772021-06-07 Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields Mau, Adrien Friedl, Karoline Leterrier, Christophe Bourg, Nicolas Lévêque-Fort, Sandrine Nat Commun Article Non-uniform illumination limits quantitative analyses of fluorescence imaging techniques. In particular, single molecule localization microscopy (SMLM) relies on high irradiances, but conventional Gaussian-shaped laser illumination restricts the usable field of view to around 40 µm × 40 µm. We present Adaptable Scanning for Tunable Excitation Regions (ASTER), a versatile illumination technique that generates uniform and adaptable illumination. ASTER is also highly compatible with optical sectioning techniques such as total internal reflection fluorescence (TIRF). For SMLM, ASTER delivers homogeneous blinking kinetics at reasonable laser power over fields-of-view up to 200 µm × 200 µm. We demonstrate that ASTER improves clustering analysis and nanoscopic size measurements by imaging nanorulers, microtubules and clathrin-coated pits in COS-7 cells, and β2-spectrin in neurons. ASTER’s sharp and quantitative illumination paves the way for high-throughput quantification of biological structures and processes in classical and super-resolution fluorescence microscopies. Nature Publishing Group UK 2021-05-24 /pmc/articles/PMC8144377/ /pubmed/34031402 http://dx.doi.org/10.1038/s41467-021-23405-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mau, Adrien Friedl, Karoline Leterrier, Christophe Bourg, Nicolas Lévêque-Fort, Sandrine Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title | Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title_full | Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title_fullStr | Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title_full_unstemmed | Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title_short | Fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
title_sort | fast widefield scan provides tunable and uniform illumination optimizing super-resolution microscopy on large fields |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144377/ https://www.ncbi.nlm.nih.gov/pubmed/34031402 http://dx.doi.org/10.1038/s41467-021-23405-4 |
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