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Converting lateral scanning into axial focusing to speed up three-dimensional microscopy
In optical microscopy, the slow axial scanning rate of the objective or the sample has traditionally limited the speed of volumetric imaging. Recently, by conjugating either a movable mirror to the image plane in a remote-focusing geometry or an electrically tuneable lens (ETL) to the back focal pla...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501866/ https://www.ncbi.nlm.nih.gov/pubmed/33024553 http://dx.doi.org/10.1038/s41377-020-00401-9 |
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author | Chakraborty, Tonmoy Chen, Bingying Daetwyler, Stephan Chang, Bo-Jui Vanderpoorten, Oliver Sapoznik, Etai Kaminski, Clemens F. Knowles, Tuomas P. J. Dean, Kevin M. Fiolka, Reto |
author_facet | Chakraborty, Tonmoy Chen, Bingying Daetwyler, Stephan Chang, Bo-Jui Vanderpoorten, Oliver Sapoznik, Etai Kaminski, Clemens F. Knowles, Tuomas P. J. Dean, Kevin M. Fiolka, Reto |
author_sort | Chakraborty, Tonmoy |
collection | PubMed |
description | In optical microscopy, the slow axial scanning rate of the objective or the sample has traditionally limited the speed of volumetric imaging. Recently, by conjugating either a movable mirror to the image plane in a remote-focusing geometry or an electrically tuneable lens (ETL) to the back focal plane, rapid axial scanning has been achieved. However, mechanical actuation of a mirror limits the axial scanning rate (usually only 10–100 Hz for piezoelectric or voice coil-based actuators), while ETLs introduce spherical and higher-order aberrations that prevent high-resolution imaging. In an effort to overcome these limitations, we introduce a novel optical design that transforms a lateral-scan motion into a spherical aberration-free axial scan that can be used for high-resolution imaging. Using a galvanometric mirror, we scan a laser beam laterally in a remote-focusing arm, which is then back-reflected from different heights of a mirror in the image space. We characterize the optical performance of this remote-focusing technique and use it to accelerate axially swept light-sheet microscopy by an order of magnitude, allowing the quantification of rapid vesicular dynamics in three dimensions. We also demonstrate resonant remote focusing at 12 kHz with a two-photon raster-scanning microscope, which allows rapid imaging of brain tissues and zebrafish cardiac dynamics with diffraction-limited resolution. |
format | Online Article Text |
id | pubmed-7501866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75018662020-10-05 Converting lateral scanning into axial focusing to speed up three-dimensional microscopy Chakraborty, Tonmoy Chen, Bingying Daetwyler, Stephan Chang, Bo-Jui Vanderpoorten, Oliver Sapoznik, Etai Kaminski, Clemens F. Knowles, Tuomas P. J. Dean, Kevin M. Fiolka, Reto Light Sci Appl Article In optical microscopy, the slow axial scanning rate of the objective or the sample has traditionally limited the speed of volumetric imaging. Recently, by conjugating either a movable mirror to the image plane in a remote-focusing geometry or an electrically tuneable lens (ETL) to the back focal plane, rapid axial scanning has been achieved. However, mechanical actuation of a mirror limits the axial scanning rate (usually only 10–100 Hz for piezoelectric or voice coil-based actuators), while ETLs introduce spherical and higher-order aberrations that prevent high-resolution imaging. In an effort to overcome these limitations, we introduce a novel optical design that transforms a lateral-scan motion into a spherical aberration-free axial scan that can be used for high-resolution imaging. Using a galvanometric mirror, we scan a laser beam laterally in a remote-focusing arm, which is then back-reflected from different heights of a mirror in the image space. We characterize the optical performance of this remote-focusing technique and use it to accelerate axially swept light-sheet microscopy by an order of magnitude, allowing the quantification of rapid vesicular dynamics in three dimensions. We also demonstrate resonant remote focusing at 12 kHz with a two-photon raster-scanning microscope, which allows rapid imaging of brain tissues and zebrafish cardiac dynamics with diffraction-limited resolution. Nature Publishing Group UK 2020-09-18 /pmc/articles/PMC7501866/ /pubmed/33024553 http://dx.doi.org/10.1038/s41377-020-00401-9 Text en © The Author(s) 2020 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 Chakraborty, Tonmoy Chen, Bingying Daetwyler, Stephan Chang, Bo-Jui Vanderpoorten, Oliver Sapoznik, Etai Kaminski, Clemens F. Knowles, Tuomas P. J. Dean, Kevin M. Fiolka, Reto Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title | Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title_full | Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title_fullStr | Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title_full_unstemmed | Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title_short | Converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
title_sort | converting lateral scanning into axial focusing to speed up three-dimensional microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501866/ https://www.ncbi.nlm.nih.gov/pubmed/33024553 http://dx.doi.org/10.1038/s41377-020-00401-9 |
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