Interferometric excitation fluorescence lifetime imaging microscopy
Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
101030656
EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020)
22-03875S
Grantová Agentura České Republiky (Grant Agency of the Czech Republic)
22-03875S
Grantová Agentura České Republiky (Grant Agency of the Czech Republic)
PubMed
39271727
PubMed Central
PMC11399241
DOI
10.1038/s41467-024-52333-2
PII: 10.1038/s41467-024-52333-2
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Fluorescence lifetime imaging microscopy (FLIM) is a well-established technique with numerous imaging applications. Yet, one of the limitations of FLIM is that it only provides information about the emitting state. Here, we present an extension of FLIM by interferometric measurement of fluorescence excitation spectra. Interferometric Excitation Fluorescence Lifetime Imaging Microscopy (ixFLIM) reports on the correlation of the excitation spectra and emission lifetime, providing the correlation between the ground-state absorption and excited-state emission. As such, it extends the applicability of FLIM and removes some of its limitations. We introduce ixFLIM on progressively more complex systems, directly compare it to standard FLIM, and apply it to quantitative resonance energy transfer imaging from a single measurement.
Department of Proteomics Institute of Hematology and Blood Transfusion Prague Czech Republic
Faculty of Mathematics and Physics Institute of Physics Charles University Prague Czech Republic
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