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Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy
Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imag...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783475/ https://www.ncbi.nlm.nih.gov/pubmed/31594938 http://dx.doi.org/10.1038/s41467-019-12535-5 |
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author | Bowman, Adam J. Klopfer, Brannon B. Juffmann, Thomas Kasevich, Mark A. |
author_facet | Bowman, Adam J. Klopfer, Brannon B. Juffmann, Thomas Kasevich, Mark A. |
author_sort | Bowman, Adam J. |
collection | PubMed |
description | Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imaging. We demonstrate the use of Pockels cells for wide-field image gating with nanosecond temporal resolution and high photon collection efficiency. Two temporal frames are obtained by combining a Pockels cell with a pair of polarizing beam-splitters. We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-molecule lifetime spectroscopy, and fast single-frame FLIM at the camera frame rate with 10(3)–10(5) times higher throughput than single photon counting. Finally, we demonstrate a space-to-time image multiplexer using a re-imaging optical cavity with a tilted mirror to extend the Pockels cell technique to multiple temporal frames. These methods enable nanosecond imaging with standard optical systems and sensors, opening a new temporal dimension for wide-field low-light microscopy. |
format | Online Article Text |
id | pubmed-6783475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67834752019-10-10 Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy Bowman, Adam J. Klopfer, Brannon B. Juffmann, Thomas Kasevich, Mark A. Nat Commun Article Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imaging. We demonstrate the use of Pockels cells for wide-field image gating with nanosecond temporal resolution and high photon collection efficiency. Two temporal frames are obtained by combining a Pockels cell with a pair of polarizing beam-splitters. We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-molecule lifetime spectroscopy, and fast single-frame FLIM at the camera frame rate with 10(3)–10(5) times higher throughput than single photon counting. Finally, we demonstrate a space-to-time image multiplexer using a re-imaging optical cavity with a tilted mirror to extend the Pockels cell technique to multiple temporal frames. These methods enable nanosecond imaging with standard optical systems and sensors, opening a new temporal dimension for wide-field low-light microscopy. Nature Publishing Group UK 2019-10-08 /pmc/articles/PMC6783475/ /pubmed/31594938 http://dx.doi.org/10.1038/s41467-019-12535-5 Text en © The Author(s) 2019 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 Bowman, Adam J. Klopfer, Brannon B. Juffmann, Thomas Kasevich, Mark A. Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title | Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title_full | Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title_fullStr | Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title_full_unstemmed | Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title_short | Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
title_sort | electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783475/ https://www.ncbi.nlm.nih.gov/pubmed/31594938 http://dx.doi.org/10.1038/s41467-019-12535-5 |
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