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Spinning disk-remote focusing microscopy

Fast confocal imaging was achieved by combining remote focusing with differential spinning disk optical sectioning to rapidly acquire images of live samples at cellular resolution. Axial and lateral full width half maxima less than 5 µm and 490 nm respectively are demonstrated over 130 µm axial rang...

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Detalles Bibliográficos
Autores principales: Gintoli, Michele, Mohanan, Sharika, Salter, Patrick, Williams, Elizabeth, Beard, James D., Jekely, Gaspar, Corbett, Alexander D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316025/
https://www.ncbi.nlm.nih.gov/pubmed/32637230
http://dx.doi.org/10.1364/BOE.389904
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author Gintoli, Michele
Mohanan, Sharika
Salter, Patrick
Williams, Elizabeth
Beard, James D.
Jekely, Gaspar
Corbett, Alexander D.
author_facet Gintoli, Michele
Mohanan, Sharika
Salter, Patrick
Williams, Elizabeth
Beard, James D.
Jekely, Gaspar
Corbett, Alexander D.
author_sort Gintoli, Michele
collection PubMed
description Fast confocal imaging was achieved by combining remote focusing with differential spinning disk optical sectioning to rapidly acquire images of live samples at cellular resolution. Axial and lateral full width half maxima less than 5 µm and 490 nm respectively are demonstrated over 130 µm axial range with a 256 × 128 µm field of view. A water-index calibration slide was used to achieve an alignment that minimises image volume distortion. Application to live biological samples was demonstrated by acquiring image volumes over a 24 µm axial range at 1 volume/s, allowing for the detection of calcium-based neuronal activity in Platynereis dumerilii larvae.
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spelling pubmed-73160252020-07-06 Spinning disk-remote focusing microscopy Gintoli, Michele Mohanan, Sharika Salter, Patrick Williams, Elizabeth Beard, James D. Jekely, Gaspar Corbett, Alexander D. Biomed Opt Express Article Fast confocal imaging was achieved by combining remote focusing with differential spinning disk optical sectioning to rapidly acquire images of live samples at cellular resolution. Axial and lateral full width half maxima less than 5 µm and 490 nm respectively are demonstrated over 130 µm axial range with a 256 × 128 µm field of view. A water-index calibration slide was used to achieve an alignment that minimises image volume distortion. Application to live biological samples was demonstrated by acquiring image volumes over a 24 µm axial range at 1 volume/s, allowing for the detection of calcium-based neuronal activity in Platynereis dumerilii larvae. Optical Society of America 2020-05-04 /pmc/articles/PMC7316025/ /pubmed/32637230 http://dx.doi.org/10.1364/BOE.389904 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. Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License (http://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.
spellingShingle Article
Gintoli, Michele
Mohanan, Sharika
Salter, Patrick
Williams, Elizabeth
Beard, James D.
Jekely, Gaspar
Corbett, Alexander D.
Spinning disk-remote focusing microscopy
title Spinning disk-remote focusing microscopy
title_full Spinning disk-remote focusing microscopy
title_fullStr Spinning disk-remote focusing microscopy
title_full_unstemmed Spinning disk-remote focusing microscopy
title_short Spinning disk-remote focusing microscopy
title_sort spinning disk-remote focusing microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316025/
https://www.ncbi.nlm.nih.gov/pubmed/32637230
http://dx.doi.org/10.1364/BOE.389904
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