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Computational Photon Counting Using Multithreshold Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy
[Image: see text] Time-resolved photon counting methods have a finite bandwidth that restricts the acquisition speed of techniques like fluorescence lifetime imaging microscopy (FLIM). To enable faster imaging, computational methods can be employed to count photons when the output of a detector is d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389606/ https://www.ncbi.nlm.nih.gov/pubmed/35996369 http://dx.doi.org/10.1021/acsphotonics.2c00505 |
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author | Sorrells, Janet E. Iyer, Rishyashring R. Yang, Lingxiao Martin, Elisabeth M. Wang, Geng Tu, Haohua Marjanovic, Marina Boppart, Stephen A. |
author_facet | Sorrells, Janet E. Iyer, Rishyashring R. Yang, Lingxiao Martin, Elisabeth M. Wang, Geng Tu, Haohua Marjanovic, Marina Boppart, Stephen A. |
author_sort | Sorrells, Janet E. |
collection | PubMed |
description | [Image: see text] Time-resolved photon counting methods have a finite bandwidth that restricts the acquisition speed of techniques like fluorescence lifetime imaging microscopy (FLIM). To enable faster imaging, computational methods can be employed to count photons when the output of a detector is directly digitized at a high sampling rate. Here, we present computational photon counting using a hybrid photodetector in conjunction with multithreshold peak detection to count instances where one or more photons arrive at the detector within the detector response time. This method can be used to distinguish up to five photon counts per digitized point, whereas previous demonstrations of computational photon counting on data acquired with photomultiplier tubes have only counted one photon at a time. We demonstrate in both freely moving C. elegans and a human breast cancer cell line undergoing apoptosis that this novel multithreshold peak detection method can accurately characterize the intensity and fluorescence lifetime of samples producing photon rates up to 223%, higher than previously demonstrated photon counting FLIM systems. |
format | Online Article Text |
id | pubmed-9389606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93896062022-08-20 Computational Photon Counting Using Multithreshold Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy Sorrells, Janet E. Iyer, Rishyashring R. Yang, Lingxiao Martin, Elisabeth M. Wang, Geng Tu, Haohua Marjanovic, Marina Boppart, Stephen A. ACS Photonics [Image: see text] Time-resolved photon counting methods have a finite bandwidth that restricts the acquisition speed of techniques like fluorescence lifetime imaging microscopy (FLIM). To enable faster imaging, computational methods can be employed to count photons when the output of a detector is directly digitized at a high sampling rate. Here, we present computational photon counting using a hybrid photodetector in conjunction with multithreshold peak detection to count instances where one or more photons arrive at the detector within the detector response time. This method can be used to distinguish up to five photon counts per digitized point, whereas previous demonstrations of computational photon counting on data acquired with photomultiplier tubes have only counted one photon at a time. We demonstrate in both freely moving C. elegans and a human breast cancer cell line undergoing apoptosis that this novel multithreshold peak detection method can accurately characterize the intensity and fluorescence lifetime of samples producing photon rates up to 223%, higher than previously demonstrated photon counting FLIM systems. American Chemical Society 2022-07-12 2022-08-17 /pmc/articles/PMC9389606/ /pubmed/35996369 http://dx.doi.org/10.1021/acsphotonics.2c00505 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Sorrells, Janet E. Iyer, Rishyashring R. Yang, Lingxiao Martin, Elisabeth M. Wang, Geng Tu, Haohua Marjanovic, Marina Boppart, Stephen A. Computational Photon Counting Using Multithreshold Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title | Computational
Photon Counting Using Multithreshold
Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title_full | Computational
Photon Counting Using Multithreshold
Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title_fullStr | Computational
Photon Counting Using Multithreshold
Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title_full_unstemmed | Computational
Photon Counting Using Multithreshold
Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title_short | Computational
Photon Counting Using Multithreshold
Peak Detection for Fast Fluorescence Lifetime Imaging Microscopy |
title_sort | computational
photon counting using multithreshold
peak detection for fast fluorescence lifetime imaging microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389606/ https://www.ncbi.nlm.nih.gov/pubmed/35996369 http://dx.doi.org/10.1021/acsphotonics.2c00505 |
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