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Focus image scanning microscopy for sharp and gentle super-resolved microscopy
To date, the feasibility of super-resolution microscopy for imaging live and thick samples is still limited. Stimulated emission depletion (STED) microscopy requires high-intensity illumination to achieve sub-diffraction resolution, potentially introducing photodamage to live specimens. Moreover, th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747786/ https://www.ncbi.nlm.nih.gov/pubmed/36513680 http://dx.doi.org/10.1038/s41467-022-35333-y |
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author | Tortarolo, Giorgio Zunino, Alessandro Fersini, Francesco Castello, Marco Piazza, Simonluca Sheppard, Colin J. R. Bianchini, Paolo Diaspro, Alberto Koho, Sami Vicidomini, Giuseppe |
author_facet | Tortarolo, Giorgio Zunino, Alessandro Fersini, Francesco Castello, Marco Piazza, Simonluca Sheppard, Colin J. R. Bianchini, Paolo Diaspro, Alberto Koho, Sami Vicidomini, Giuseppe |
author_sort | Tortarolo, Giorgio |
collection | PubMed |
description | To date, the feasibility of super-resolution microscopy for imaging live and thick samples is still limited. Stimulated emission depletion (STED) microscopy requires high-intensity illumination to achieve sub-diffraction resolution, potentially introducing photodamage to live specimens. Moreover, the out-of-focus background may degrade the signal stemming from the focal plane. Here, we propose a new method to mitigate these limitations without drawbacks. First, we enhance a STED microscope with a detector array, enabling image scanning microscopy (ISM). Therefore, we implement STED-ISM, a method that exploits the working principle of ISM to reduce the depletion intensity and achieve a target resolution. Later, we develop Focus-ISM, a strategy to improve the optical sectioning and remove the background of any ISM-based imaging technique, with or without a STED beam. The proposed approach requires minimal architectural changes to a conventional microscope but provides substantial advantages for live and thick sample imaging. |
format | Online Article Text |
id | pubmed-9747786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97477862022-12-15 Focus image scanning microscopy for sharp and gentle super-resolved microscopy Tortarolo, Giorgio Zunino, Alessandro Fersini, Francesco Castello, Marco Piazza, Simonluca Sheppard, Colin J. R. Bianchini, Paolo Diaspro, Alberto Koho, Sami Vicidomini, Giuseppe Nat Commun Article To date, the feasibility of super-resolution microscopy for imaging live and thick samples is still limited. Stimulated emission depletion (STED) microscopy requires high-intensity illumination to achieve sub-diffraction resolution, potentially introducing photodamage to live specimens. Moreover, the out-of-focus background may degrade the signal stemming from the focal plane. Here, we propose a new method to mitigate these limitations without drawbacks. First, we enhance a STED microscope with a detector array, enabling image scanning microscopy (ISM). Therefore, we implement STED-ISM, a method that exploits the working principle of ISM to reduce the depletion intensity and achieve a target resolution. Later, we develop Focus-ISM, a strategy to improve the optical sectioning and remove the background of any ISM-based imaging technique, with or without a STED beam. The proposed approach requires minimal architectural changes to a conventional microscope but provides substantial advantages for live and thick sample imaging. Nature Publishing Group UK 2022-12-13 /pmc/articles/PMC9747786/ /pubmed/36513680 http://dx.doi.org/10.1038/s41467-022-35333-y Text en © The Author(s) 2022 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 Tortarolo, Giorgio Zunino, Alessandro Fersini, Francesco Castello, Marco Piazza, Simonluca Sheppard, Colin J. R. Bianchini, Paolo Diaspro, Alberto Koho, Sami Vicidomini, Giuseppe Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title | Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title_full | Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title_fullStr | Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title_full_unstemmed | Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title_short | Focus image scanning microscopy for sharp and gentle super-resolved microscopy |
title_sort | focus image scanning microscopy for sharp and gentle super-resolved microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747786/ https://www.ncbi.nlm.nih.gov/pubmed/36513680 http://dx.doi.org/10.1038/s41467-022-35333-y |
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