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Confocal imaging capacity on a widefield microscope using a spatial light modulator
Confocal microscopes can reject out-of-focus and scattered light; however, widefield microscopes are far more common in biological laboratories due to their accessibility and lower cost. We report confocal imaging capacity on a widefield microscope by adding a spatial light modulator (SLM) and utili...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886194/ https://www.ncbi.nlm.nih.gov/pubmed/33591984 http://dx.doi.org/10.1371/journal.pone.0244034 |
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author | Wang, Yao L. Grooms, Noa W. F. Civale, Sabrina C. Chung, Samuel H. |
author_facet | Wang, Yao L. Grooms, Noa W. F. Civale, Sabrina C. Chung, Samuel H. |
author_sort | Wang, Yao L. |
collection | PubMed |
description | Confocal microscopes can reject out-of-focus and scattered light; however, widefield microscopes are far more common in biological laboratories due to their accessibility and lower cost. We report confocal imaging capacity on a widefield microscope by adding a spatial light modulator (SLM) and utilizing custom illumination and acquisition methods. We discuss our illumination strategy and compare several procedures for postprocessing the acquired image data. We assessed the performance of this system for rejecting out-of-focus light by comparing images taken at 1.4 NA using our widefield microscope, our SLM-enhanced setup, and a commercial confocal microscope. The optical sectioning capability, assessed on thin fluorescent film, was 0.85 ± 0.04 μm for our SLM-enhanced setup and 0.68 ± 0.04 μm for a confocal microscope, while a widefield microscope exhibited no sectioning capability. We demonstrate our setup by imaging the same set of neurons in C. elegans on widefield, SLM, and confocal microscopes. SLM enhancement greatly reduces background from the cell body, allowing visualization of dim fibers nearby. Our SLM-enhanced setup identified 96% of the dim neuronal fibers seen in confocal images while a widefield microscope only identified 50% of the same fibers. Our microscope add-on represents a very simple (2-component) and inexpensive (<$600) approach to enable widefield microscopes to optically section thick samples. |
format | Online Article Text |
id | pubmed-7886194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78861942021-02-23 Confocal imaging capacity on a widefield microscope using a spatial light modulator Wang, Yao L. Grooms, Noa W. F. Civale, Sabrina C. Chung, Samuel H. PLoS One Research Article Confocal microscopes can reject out-of-focus and scattered light; however, widefield microscopes are far more common in biological laboratories due to their accessibility and lower cost. We report confocal imaging capacity on a widefield microscope by adding a spatial light modulator (SLM) and utilizing custom illumination and acquisition methods. We discuss our illumination strategy and compare several procedures for postprocessing the acquired image data. We assessed the performance of this system for rejecting out-of-focus light by comparing images taken at 1.4 NA using our widefield microscope, our SLM-enhanced setup, and a commercial confocal microscope. The optical sectioning capability, assessed on thin fluorescent film, was 0.85 ± 0.04 μm for our SLM-enhanced setup and 0.68 ± 0.04 μm for a confocal microscope, while a widefield microscope exhibited no sectioning capability. We demonstrate our setup by imaging the same set of neurons in C. elegans on widefield, SLM, and confocal microscopes. SLM enhancement greatly reduces background from the cell body, allowing visualization of dim fibers nearby. Our SLM-enhanced setup identified 96% of the dim neuronal fibers seen in confocal images while a widefield microscope only identified 50% of the same fibers. Our microscope add-on represents a very simple (2-component) and inexpensive (<$600) approach to enable widefield microscopes to optically section thick samples. Public Library of Science 2021-02-16 /pmc/articles/PMC7886194/ /pubmed/33591984 http://dx.doi.org/10.1371/journal.pone.0244034 Text en © 2021 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Yao L. Grooms, Noa W. F. Civale, Sabrina C. Chung, Samuel H. Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title | Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title_full | Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title_fullStr | Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title_full_unstemmed | Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title_short | Confocal imaging capacity on a widefield microscope using a spatial light modulator |
title_sort | confocal imaging capacity on a widefield microscope using a spatial light modulator |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886194/ https://www.ncbi.nlm.nih.gov/pubmed/33591984 http://dx.doi.org/10.1371/journal.pone.0244034 |
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