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Live-cell fluorescence lifetime multiplexing using synthetic fluorescent probes

MPG-Autoren
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Frei,  Michelle S.
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Koch,  Birgit
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Hiblot,  Julien
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Johnsson,  Kai
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Zitation

Frei, M. S., Koch, B., Hiblot, J., & Johnsson, K. (2022). Live-cell fluorescence lifetime multiplexing using synthetic fluorescent probes. ACS Chemical Biology, 17(6), 1321-1327. doi:10.1021/acschembio.2c00041.


Zitierlink: https://hdl.handle.net/21.11116/0000-0009-D480-6
Zusammenfassung
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 up to six 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.