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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...

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Autores principales: Cabriel, Clément, Bourg, Nicolas, Jouchet, Pierre, Dupuis, Guillaume, Leterrier, Christophe, Baron, Aurélie, Badet-Denisot, Marie-Ange, Vauzeilles, Boris, Fort, Emmanuel, Lévêque-Fort, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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