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Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes
The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objective lens, eyepiece and image sensor are all designed to capture light emitted from a 2D ‘object plane’. Existing technologies, such as confocal or light sheet fluorescence microscopy have to utilize mec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985622/ https://www.ncbi.nlm.nih.gov/pubmed/27527813 http://dx.doi.org/10.1038/srep31445 |
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author | Ma, Qian Khademhosseinieh, Bahar Huang, Eric Qian, Haoliang Bakowski, Malina A. Troemel, Emily R. Liu, Zhaowei |
author_facet | Ma, Qian Khademhosseinieh, Bahar Huang, Eric Qian, Haoliang Bakowski, Malina A. Troemel, Emily R. Liu, Zhaowei |
author_sort | Ma, Qian |
collection | PubMed |
description | The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objective lens, eyepiece and image sensor are all designed to capture light emitted from a 2D ‘object plane’. Existing technologies, such as confocal or light sheet fluorescence microscopy have to utilize mechanical scanning, a time-multiplexing process, to capture a 3D image. In this paper, we present a 3D optical microscopy method based upon simultaneously illuminating and detecting multiple focal planes. This is implemented by adding two diffractive optical elements to modify the illumination and detection optics. We demonstrate that the image quality of this technique is comparable to conventional light sheet fluorescent microscopy with the advantage of the simultaneous imaging of multiple axial planes and reduced number of scans required to image the whole sample volume. |
format | Online Article Text |
id | pubmed-4985622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49856222016-08-22 Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes Ma, Qian Khademhosseinieh, Bahar Huang, Eric Qian, Haoliang Bakowski, Malina A. Troemel, Emily R. Liu, Zhaowei Sci Rep Article The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objective lens, eyepiece and image sensor are all designed to capture light emitted from a 2D ‘object plane’. Existing technologies, such as confocal or light sheet fluorescence microscopy have to utilize mechanical scanning, a time-multiplexing process, to capture a 3D image. In this paper, we present a 3D optical microscopy method based upon simultaneously illuminating and detecting multiple focal planes. This is implemented by adding two diffractive optical elements to modify the illumination and detection optics. We demonstrate that the image quality of this technique is comparable to conventional light sheet fluorescent microscopy with the advantage of the simultaneous imaging of multiple axial planes and reduced number of scans required to image the whole sample volume. Nature Publishing Group 2016-08-16 /pmc/articles/PMC4985622/ /pubmed/27527813 http://dx.doi.org/10.1038/srep31445 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ma, Qian Khademhosseinieh, Bahar Huang, Eric Qian, Haoliang Bakowski, Malina A. Troemel, Emily R. Liu, Zhaowei Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title_full | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title_fullStr | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title_full_unstemmed | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title_short | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
title_sort | three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985622/ https://www.ncbi.nlm.nih.gov/pubmed/27527813 http://dx.doi.org/10.1038/srep31445 |
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