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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2020
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.
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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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