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Super-resolution imaging has become an essential tool used by the bioimaging community. In this study, we present a novel technique to resolve emitters located closer than the diffraction limit, by using the differences in their fluorescence lifetime. By calculating the centre of mass of the point spread function of the emitter on the timescale of the fluorescence decay, protein-protein interactions via FRET can be identified. This technique will also be able to distinguish the number of proximal neighbouring donors without the need to fit the time-resolved fluorescence decays.
Ani A. Jose
"Functional localization microscopy by FLIM-FRET imaging (Conference Presentation)", Proc. SPIE PC12386, Single Molecule Spectroscopy and Superresolution Imaging XVI, PC1238606 (15 March 2023); https://doi.org/10.1117/12.2650757
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Ani A. Jose, "Functional localization microscopy by FLIM-FRET imaging (Conference Presentation)," Proc. SPIE PC12386, Single Molecule Spectroscopy and Superresolution Imaging XVI, PC1238606 (15 March 2023); https://doi.org/10.1117/12.2650757