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Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes

[Image: see text] Fluorescence lifetime multiplexing requires fluorescent probes with distinct fluorescence lifetimes but similar spectral properties. Even though synthetic probes for many cellular targets are available for multicolor live-cell fluorescence microscopy, few of them have been characte...

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Autores principales: Frei, Michelle S., Koch, Birgit, Hiblot, Julien, Johnsson, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207807/
https://www.ncbi.nlm.nih.gov/pubmed/35584304
http://dx.doi.org/10.1021/acschembio.2c00041
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author Frei, Michelle S.
Koch, Birgit
Hiblot, Julien
Johnsson, Kai
author_facet Frei, Michelle S.
Koch, Birgit
Hiblot, Julien
Johnsson, Kai
author_sort Frei, Michelle S.
collection PubMed
description [Image: see text] Fluorescence lifetime multiplexing requires fluorescent probes with distinct fluorescence lifetimes but similar spectral properties. Even though synthetic probes for many cellular targets are available for multicolor live-cell fluorescence microscopy, few of them have been characterized for their use in fluorescence lifetime multiplexing. Here, we demonstrate that, from a panel of 18 synthetic probes, eight pairwise combinations are suitable for fluorescence lifetime multiplexing in living mammalian cell lines. Moreover, combining multiple pairs in different spectral channels enables us to image four and with the help of self-labeling protein tags up to eight different biological targets, effectively doubling the number of observable targets. The combination of synthetic probes with fluorescence lifetime multiplexing is thus a powerful approach for live-cell imaging.
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spelling pubmed-92078072022-06-21 Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes Frei, Michelle S. Koch, Birgit Hiblot, Julien Johnsson, Kai ACS Chem Biol [Image: see text] Fluorescence lifetime multiplexing requires fluorescent probes with distinct fluorescence lifetimes but similar spectral properties. Even though synthetic probes for many cellular targets are available for multicolor live-cell fluorescence microscopy, few of them have been characterized for their use in fluorescence lifetime multiplexing. Here, we demonstrate that, from a panel of 18 synthetic probes, eight pairwise combinations are suitable for fluorescence lifetime multiplexing in living mammalian cell lines. Moreover, combining multiple pairs in different spectral channels enables us to image four and with the help of self-labeling protein tags up to eight different biological targets, effectively doubling the number of observable targets. The combination of synthetic probes with fluorescence lifetime multiplexing is thus a powerful approach for live-cell imaging. American Chemical Society 2022-05-18 2022-06-17 /pmc/articles/PMC9207807/ /pubmed/35584304 http://dx.doi.org/10.1021/acschembio.2c00041 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Frei, Michelle S.
Koch, Birgit
Hiblot, Julien
Johnsson, Kai
Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title_full Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title_fullStr Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title_full_unstemmed Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title_short Live-Cell Fluorescence Lifetime Multiplexing Using Synthetic Fluorescent Probes
title_sort live-cell fluorescence lifetime multiplexing using synthetic fluorescent probes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207807/
https://www.ncbi.nlm.nih.gov/pubmed/35584304
http://dx.doi.org/10.1021/acschembio.2c00041
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