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Two-photon lifetime-based photoconversion of EGFP for 3D-photostimulation in FLIM

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Author
Strachotová, DitaORCiD Profile - 0000-0003-1645-5635WoS Profile - T-4457-2019Scopus Profile - 36999557300
Holoubek, Aleš
Brodska, Barbora
Heřman, PetrORCiD Profile - 0000-0001-6918-2576WoS Profile - A-2626-2008Scopus Profile - 7201563438

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Publication date
2023
Published in
Methods and Applications in Fluorescence
Volume / Issue
11 (3)
ISBN / ISSN
ISSN: 2050-6120
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  • Faculty of Mathematics and Physics

This publication has a published version with DOI 10.1088/2050-6120/acdb31

Abstract
Enhanced green fluorescence protein (EGFP) is a fluorescent tag commonly used in cellular and biomedical applications. Surprisingly, some interesting photochemical properties of EGFP have remained unexplored. Here we report on two-photon-induced photoconversion of EGFP, which can be permanently converted by intense IR irradiation to a form with a short fluorescence lifetime and spectrally conserved emission. Photoconverted EGFP thus can be distinguished from the unconverted tag by the time-resolved detection. Nonlinear dependence of the two-photon photoconversion efficiency on the light intensity allows for an accurate 3D localization of the photoconverted volume within cellular structures, which is especially useful for kinetic FLIM applications. For illustration, we used the two photon photoconversion of EGFP for measurements of redistribution kinetics of nucleophosmin and histone H2B in nuclei of live cells. Measurements revealed high mobility of fluorescently tagged histone H2B in the nucleoplasm and their redistribution between spatially separated nucleoli.
Keywords
fluorescence lifetime imaging, photoconversion, two-photon imaging, cellular tracking, protein dynamics, nucleophosmin, histone H2B
Permanent link
https://hdl.handle.net/20.500.14178/2292
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WOS:001003431600001
SCOPUS:2-s2.0-85162096822
PUBMED:37267995
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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