Super-resolved FRET imaging by confocal fluorescence-lifetime single-molecule localization microscopy

Cecilia Zaza; Germán Chiarelli; Ludovit P. Zweifel; Mauricio Pilo-Pais; Evangelos Sisamakis; Fabio Barachati; Fernando D. Stefani; Guillermo P. Acuna

arXiv · 2211.15332

Super-resolved FRET imaging by confocal fluorescence-lifetime single-molecule localization microscopy

Cecilia Zaza·Germán Chiarelli·Ludovit P. Zweifel·Mauricio Pilo-Pais·Evangelos Sisamakis·Fabio Barachati·Fernando D. Stefani·Guillermo P. Acuna

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Abstract

FRET-based approaches are a unique tool for sensing the immediate surroundings and interactions of (bio)molecules. FRET imaging and FLIM (Fluorescence Lifetime Imaging Microscopy) enable the visualization of the spatial distribution of molecular interactions and functional states. However, conventional FLIM and FRET imaging provide average information over an ensemble of molecules within a diffraction-limited volume, which limits the spatial information, accuracy, and dynamic range of the observed signals. Here, we demonstrate an approach to obtain super-resolved FRET imaging based on single-molecule localization microscopy using an early prototype of a commercial time-resolved confocal microscope. DNA Points Accumulation for Imaging in Nanoscale Topography (DNA-PAINT) with fluorogenic probes provides a suitable combination of background reduction and blinking kinetics compatible with the scanning speed of usual confocal microscopes. A single laser is used to excite the donor, a broad detection band is employed to retrieve both donor and acceptor emission, and FRET events are detected from lifetime information.

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Cecilia Zaza, Germán Chiarelli, Ludovit P. Zweifel, Mauricio Pilo-Pais, Evangelos Sisamakis, Fabio Barachati, Fernando D. Stefani, Guillermo P. Acuna. 2022-11-28. Super-resolved FRET imaging by confocal fluorescence-lifetime single-molecule localization microscopy. https://arxiv.org/abs/2211.15332

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