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CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging
Rapid cryopreservation of biological specimens is the gold standard for visualizing cellular structures in their true structural context. However, current commercial cryo-fluorescence microscopes are limited to low resolutions. To fill this gap, we have developed cryoSIM, a microscope for 3D super-r...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262592/ https://www.ncbi.nlm.nih.gov/pubmed/34277893 http://dx.doi.org/10.1364/OPTICA.393203 |
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author | Phillips, Michael A. Harkiolaki, Maria Susano Pinto, David Miguel Parton, Richard M. Palanca, Ana Garcia-Moreno, Manuel Kounatidis, Ilias Sedat, John W. Stuart, David I. Castello, Alfredo Booth, Martin J. Davis, Ilan Dobbie, Ian M. |
author_facet | Phillips, Michael A. Harkiolaki, Maria Susano Pinto, David Miguel Parton, Richard M. Palanca, Ana Garcia-Moreno, Manuel Kounatidis, Ilias Sedat, John W. Stuart, David I. Castello, Alfredo Booth, Martin J. Davis, Ilan Dobbie, Ian M. |
author_sort | Phillips, Michael A. |
collection | PubMed |
description | Rapid cryopreservation of biological specimens is the gold standard for visualizing cellular structures in their true structural context. However, current commercial cryo-fluorescence microscopes are limited to low resolutions. To fill this gap, we have developed cryoSIM, a microscope for 3D super-resolution fluorescence cryo-imaging for correlation with cryo-electron microscopy or cryo-soft X-ray tomography. We provide the full instructions for replicating the instrument mostly from off-the-shelf components and accessible, user-friendly, open-source Python control software. Therefore, cryoSIM democratizes the ability to detect molecules using super-resolution fluorescence imaging of cryopreserved specimens for correlation with their cellular ultrastructure. |
format | Online Article Text |
id | pubmed-8262592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-82625922021-07-16 CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging Phillips, Michael A. Harkiolaki, Maria Susano Pinto, David Miguel Parton, Richard M. Palanca, Ana Garcia-Moreno, Manuel Kounatidis, Ilias Sedat, John W. Stuart, David I. Castello, Alfredo Booth, Martin J. Davis, Ilan Dobbie, Ian M. Optica Article Rapid cryopreservation of biological specimens is the gold standard for visualizing cellular structures in their true structural context. However, current commercial cryo-fluorescence microscopes are limited to low resolutions. To fill this gap, we have developed cryoSIM, a microscope for 3D super-resolution fluorescence cryo-imaging for correlation with cryo-electron microscopy or cryo-soft X-ray tomography. We provide the full instructions for replicating the instrument mostly from off-the-shelf components and accessible, user-friendly, open-source Python control software. Therefore, cryoSIM democratizes the ability to detect molecules using super-resolution fluorescence imaging of cryopreserved specimens for correlation with their cellular ultrastructure. Optical Society of America 2020-07-13 /pmc/articles/PMC8262592/ /pubmed/34277893 http://dx.doi.org/10.1364/OPTICA.393203 Text en Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. https://creativecommons.org/licenses/by/4.0/Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) . Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. 2334-2536/20/070802-11 |
spellingShingle | Article Phillips, Michael A. Harkiolaki, Maria Susano Pinto, David Miguel Parton, Richard M. Palanca, Ana Garcia-Moreno, Manuel Kounatidis, Ilias Sedat, John W. Stuart, David I. Castello, Alfredo Booth, Martin J. Davis, Ilan Dobbie, Ian M. CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title | CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title_full | CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title_fullStr | CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title_full_unstemmed | CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title_short | CryoSIM: super-resolution 3D structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
title_sort | cryosim: super-resolution 3d structured illumination cryogenic fluorescence microscopy for correlated ultrastructural imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262592/ https://www.ncbi.nlm.nih.gov/pubmed/34277893 http://dx.doi.org/10.1364/OPTICA.393203 |
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