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Selective volumetric excitation and imaging for single molecule localization microscopy in multicellular systems

Tommaso Galgani, Yasmina Fedala, Romeo Zapata, Laura Caccianini, Virgile Viasnoff, Jean-Baptiste Sibarita, Rémi Galland, Maxime Dahan, View ORCID ProfileBassam Hajj
doi: https://doi.org/10.1101/2022.12.02.518828
Tommaso Galgani
1Laboratoire Physico-Chimie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France
2Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France
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Yasmina Fedala
1Laboratoire Physico-Chimie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France
2Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France
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Romeo Zapata
1Laboratoire Physico-Chimie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France
2Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France
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Laura Caccianini
1Laboratoire Physico-Chimie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France
2Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France
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Virgile Viasnoff
3Mechanobiology Institute, National University of Singapore, Singapore, Singapore
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Jean-Baptiste Sibarita
4Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297, F-33000 Bordeaux, France
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Rémi Galland
4Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297, F-33000 Bordeaux, France
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Maxime Dahan
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Bassam Hajj
1Laboratoire Physico-Chimie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France
2Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France
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  • ORCID record for Bassam Hajj
  • For correspondence: bassam.hajj@curie.fr
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Abstract

Light sheet fluorescence microscopy (LSFM) has become a leading standard in high-resolution imaging of living samples in 2- and 3-dimensions. Biological samples are however not restricted to a single observation plane and several molecular processes evolve rapidly in 3D. The conventional mechanical scanning required in LSFM limits the range of observable dynamics and are usually restricted in resolution. Here we introduce a new strategy for instantaneous volumetric excitation and volumetric imaging of single-molecules in cell aggregates. The technique combines, for the first time, the use of light sheet microscopy and multifocus microscopy (MFM) and enables a volumetric 4D imaging of biological samples with single-molecule resolution. We engineered the excitation beam to yield a modular and uniform excitation matching the observable detection range of MFM. The strength of the method is highlighted with examples of single-molecule 3D tracking and 3D super-resolution imaging in multicellular samples.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted December 03, 2022.
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Selective volumetric excitation and imaging for single molecule localization microscopy in multicellular systems
Tommaso Galgani, Yasmina Fedala, Romeo Zapata, Laura Caccianini, Virgile Viasnoff, Jean-Baptiste Sibarita, Rémi Galland, Maxime Dahan, Bassam Hajj
bioRxiv 2022.12.02.518828; doi: https://doi.org/10.1101/2022.12.02.518828
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Selective volumetric excitation and imaging for single molecule localization microscopy in multicellular systems
Tommaso Galgani, Yasmina Fedala, Romeo Zapata, Laura Caccianini, Virgile Viasnoff, Jean-Baptiste Sibarita, Rémi Galland, Maxime Dahan, Bassam Hajj
bioRxiv 2022.12.02.518828; doi: https://doi.org/10.1101/2022.12.02.518828

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