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Macroscale fluorescence imaging against autofluorescence under ambient light
Macroscale fluorescence imaging is increasingly used to observe biological samples. However, it may suffer from spectral interferences that originate from ambient light or autofluorescence of the sample or its support. In this manuscript, we built a simple and inexpensive fluorescence macroscope, wh...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261969/ https://www.ncbi.nlm.nih.gov/pubmed/30510693 http://dx.doi.org/10.1038/s41377-018-0098-6 |
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author | Zhang, Ruikang Chouket, Raja Plamont, Marie-Aude Kelemen, Zsolt Espagne, Agathe Tebo, Alison G. Gautier, Arnaud Gissot, Lionel Faure, Jean-Denis Jullien, Ludovic Croquette, Vincent Le Saux, Thomas |
author_facet | Zhang, Ruikang Chouket, Raja Plamont, Marie-Aude Kelemen, Zsolt Espagne, Agathe Tebo, Alison G. Gautier, Arnaud Gissot, Lionel Faure, Jean-Denis Jullien, Ludovic Croquette, Vincent Le Saux, Thomas |
author_sort | Zhang, Ruikang |
collection | PubMed |
description | Macroscale fluorescence imaging is increasingly used to observe biological samples. However, it may suffer from spectral interferences that originate from ambient light or autofluorescence of the sample or its support. In this manuscript, we built a simple and inexpensive fluorescence macroscope, which has been used to evaluate the performance of Speed OPIOM (Out of Phase Imaging after Optical Modulation), which is a reference-free dynamic contrast protocol, to selectively image reversibly photoswitchable fluorophores as labels against detrimental autofluorescence and ambient light. By tuning the intensity and radial frequency of the modulated illumination to the Speed OPIOM resonance and adopting a phase-sensitive detection scheme that ensures noise rejection, we enhanced the sensitivity and the signal-to-noise ratio for fluorescence detection in blot assays by factors of 50 and 10, respectively, over direct fluorescence observation under constant illumination. Then, we overcame the strong autofluorescence of growth media that are currently used in microbiology and realized multiplexed fluorescence observation of colonies of spectrally similar fluorescent bacteria with a unique configuration of excitation and emission wavelengths. Finally, we easily discriminated fluorescent labels from the autofluorescent and reflective background in labeled leaves, even under the interference of incident light at intensities that are comparable to sunlight. The proposed approach is expected to find multiple applications, from biological assays to outdoor observations, in fluorescence macroimaging. |
format | Online Article Text |
id | pubmed-6261969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62619692018-12-03 Macroscale fluorescence imaging against autofluorescence under ambient light Zhang, Ruikang Chouket, Raja Plamont, Marie-Aude Kelemen, Zsolt Espagne, Agathe Tebo, Alison G. Gautier, Arnaud Gissot, Lionel Faure, Jean-Denis Jullien, Ludovic Croquette, Vincent Le Saux, Thomas Light Sci Appl Article Macroscale fluorescence imaging is increasingly used to observe biological samples. However, it may suffer from spectral interferences that originate from ambient light or autofluorescence of the sample or its support. In this manuscript, we built a simple and inexpensive fluorescence macroscope, which has been used to evaluate the performance of Speed OPIOM (Out of Phase Imaging after Optical Modulation), which is a reference-free dynamic contrast protocol, to selectively image reversibly photoswitchable fluorophores as labels against detrimental autofluorescence and ambient light. By tuning the intensity and radial frequency of the modulated illumination to the Speed OPIOM resonance and adopting a phase-sensitive detection scheme that ensures noise rejection, we enhanced the sensitivity and the signal-to-noise ratio for fluorescence detection in blot assays by factors of 50 and 10, respectively, over direct fluorescence observation under constant illumination. Then, we overcame the strong autofluorescence of growth media that are currently used in microbiology and realized multiplexed fluorescence observation of colonies of spectrally similar fluorescent bacteria with a unique configuration of excitation and emission wavelengths. Finally, we easily discriminated fluorescent labels from the autofluorescent and reflective background in labeled leaves, even under the interference of incident light at intensities that are comparable to sunlight. The proposed approach is expected to find multiple applications, from biological assays to outdoor observations, in fluorescence macroimaging. Nature Publishing Group UK 2018-11-28 /pmc/articles/PMC6261969/ /pubmed/30510693 http://dx.doi.org/10.1038/s41377-018-0098-6 Text en © The Author(s) 2018 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 Zhang, Ruikang Chouket, Raja Plamont, Marie-Aude Kelemen, Zsolt Espagne, Agathe Tebo, Alison G. Gautier, Arnaud Gissot, Lionel Faure, Jean-Denis Jullien, Ludovic Croquette, Vincent Le Saux, Thomas Macroscale fluorescence imaging against autofluorescence under ambient light |
title | Macroscale fluorescence imaging against autofluorescence under ambient light |
title_full | Macroscale fluorescence imaging against autofluorescence under ambient light |
title_fullStr | Macroscale fluorescence imaging against autofluorescence under ambient light |
title_full_unstemmed | Macroscale fluorescence imaging against autofluorescence under ambient light |
title_short | Macroscale fluorescence imaging against autofluorescence under ambient light |
title_sort | macroscale fluorescence imaging against autofluorescence under ambient light |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261969/ https://www.ncbi.nlm.nih.gov/pubmed/30510693 http://dx.doi.org/10.1038/s41377-018-0098-6 |
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