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Combining 3D single molecule localization strategies for reproducible bioimaging
Here, we present a 3D localization-based super-resolution technique providing a slowly varying localization precision over a 1 μm range with precisions down to 15 nm. The axial localization is performed through a combination of point spread function (PSF) shaping and supercritical angle fluorescence...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491430/ https://www.ncbi.nlm.nih.gov/pubmed/31040275 http://dx.doi.org/10.1038/s41467-019-09901-8 |
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author | Cabriel, Clément Bourg, Nicolas Jouchet, Pierre Dupuis, Guillaume Leterrier, Christophe Baron, Aurélie Badet-Denisot, Marie-Ange Vauzeilles, Boris Fort, Emmanuel Lévêque-Fort, Sandrine |
author_facet | Cabriel, Clément Bourg, Nicolas Jouchet, Pierre Dupuis, Guillaume Leterrier, Christophe Baron, Aurélie Badet-Denisot, Marie-Ange Vauzeilles, Boris Fort, Emmanuel Lévêque-Fort, Sandrine |
author_sort | Cabriel, Clément |
collection | PubMed |
description | Here, we present a 3D localization-based super-resolution technique providing a slowly varying localization precision over a 1 μm range with precisions down to 15 nm. The axial localization is performed through a combination of point spread function (PSF) shaping and supercritical angle fluorescence (SAF), which yields absolute axial information. Using a dual-view scheme, the axial detection is decoupled from the lateral detection and optimized independently to provide a weakly anisotropic 3D resolution over the imaging range. This method can be readily implemented on most homemade PSF shaping setups and provides drift-free, tilt-insensitive and achromatic results. Its insensitivity to these unavoidable experimental biases is especially adapted for multicolor 3D super-resolution microscopy, as we demonstrate by imaging cell cytoskeleton, living bacteria membranes and axon periodic submembrane scaffolds. We further illustrate the interest of the technique for biological multicolor imaging over a several-μm range by direct merging of multiple acquisitions at different depths. |
format | Online Article Text |
id | pubmed-6491430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64914302019-05-02 Combining 3D single molecule localization strategies for reproducible bioimaging Cabriel, Clément Bourg, Nicolas Jouchet, Pierre Dupuis, Guillaume Leterrier, Christophe Baron, Aurélie Badet-Denisot, Marie-Ange Vauzeilles, Boris Fort, Emmanuel Lévêque-Fort, Sandrine Nat Commun Article Here, we present a 3D localization-based super-resolution technique providing a slowly varying localization precision over a 1 μm range with precisions down to 15 nm. The axial localization is performed through a combination of point spread function (PSF) shaping and supercritical angle fluorescence (SAF), which yields absolute axial information. Using a dual-view scheme, the axial detection is decoupled from the lateral detection and optimized independently to provide a weakly anisotropic 3D resolution over the imaging range. This method can be readily implemented on most homemade PSF shaping setups and provides drift-free, tilt-insensitive and achromatic results. Its insensitivity to these unavoidable experimental biases is especially adapted for multicolor 3D super-resolution microscopy, as we demonstrate by imaging cell cytoskeleton, living bacteria membranes and axon periodic submembrane scaffolds. We further illustrate the interest of the technique for biological multicolor imaging over a several-μm range by direct merging of multiple acquisitions at different depths. Nature Publishing Group UK 2019-04-30 /pmc/articles/PMC6491430/ /pubmed/31040275 http://dx.doi.org/10.1038/s41467-019-09901-8 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Cabriel, Clément Bourg, Nicolas Jouchet, Pierre Dupuis, Guillaume Leterrier, Christophe Baron, Aurélie Badet-Denisot, Marie-Ange Vauzeilles, Boris Fort, Emmanuel Lévêque-Fort, Sandrine Combining 3D single molecule localization strategies for reproducible bioimaging |
title | Combining 3D single molecule localization strategies for reproducible bioimaging |
title_full | Combining 3D single molecule localization strategies for reproducible bioimaging |
title_fullStr | Combining 3D single molecule localization strategies for reproducible bioimaging |
title_full_unstemmed | Combining 3D single molecule localization strategies for reproducible bioimaging |
title_short | Combining 3D single molecule localization strategies for reproducible bioimaging |
title_sort | combining 3d single molecule localization strategies for reproducible bioimaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491430/ https://www.ncbi.nlm.nih.gov/pubmed/31040275 http://dx.doi.org/10.1038/s41467-019-09901-8 |
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