Wide-field fluorescence lifetime imaging of single molecules with a gated single-photon camera

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool to discriminate fluorescent molecules or probe their nanoscale environment. Traditionally, FLIM uses time-correlated single-photon counting (TCSPC), which is precise but intrinsically low-throughput due to its dependence on point detectors. Although time-gated cameras have demonstrated the potential for high-throughput FLIM in bright samples with dense labeling, their use in single-molecule microscopy has not been explored extensively. Here, we report fast and accurate single-molecule FLIM with a commercial time-gated single-photon camera. Our optimized acquisition scheme achieves single-molecule lifetime measurements with a precision only about three times less than TCSPC, while imaging with a large number of pixels (512 × 512) allowing for the spatial multiplexing of over 3000 molecules. With this approach, we demonstrate parallelized lifetime measurements of large numbers of labeled pore-forming proteins on supported lipid bilayers, and temporal single-molecule Förster resonance energy transfer measurements at 5-25 Hz. This method holds considerable promise for the advancement of multi-target single-molecule localization microscopy and biopolymer sequencing.

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Publication Details

Journal
Light Science & Applications
Published
2025-08-04
DOI
https://doi.org/10.1038/s41377-025-01901-2
Citations
6
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
9.80

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article

Wide-field fluorescence lifetime imaging of single molecules with a gated single-photon camera

Edoardo Charbon, Guillermo P. Acuna, María J. Marcaida, Aleksandra Rađenović et al.
6 citations
Light Science & Applications
Advanced Fluorescence Microscopy Techniques
9.80
article

Wide-field fluorescence lifetime imaging of single molecules with a gated single-photon camera

Edoardo Charbon, Guillermo P. Acuna, María J. Marcaida, Aleksandra Rađenović, Claudio Bruschini, Matteo Dal Peraro, Nathan Ronceray, Rahul Roy, Nicole Siegel, Marianna Fanouria Mitsioni, Salim Bennani
article en
6 citations

Abstract

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool to discriminate fluorescent molecules or probe their nanoscale environment. Traditionally, FLIM uses time-correlated single-photon counting (TCSPC), which is precise but intrinsically low-throughput due to its dependence on point detectors. Although time-gated cameras have demonstrated the potential for high-throughput FLIM in bright samples with dense labeling, their use in single-molecule microscopy has not been explored extensively. Here, we report fast and accurate single-molecule FLIM with a commercial time-gated single-photon camera. Our optimized acquisition scheme achieves single-molecule lifetime measurements with a precision only about three times less than TCSPC, while imaging with a large number of pixels (512 × 512) allowing for the spatial multiplexing of over 3000 molecules. With this approach, we demonstrate parallelized lifetime measurements of large numbers of labeled pore-forming proteins on supported lipid bilayers, and temporal single-molecule Förster resonance energy transfer measurements at 5-25 Hz. This method holds considerable promise for the advancement of multi-target single-molecule localization microscopy and biopolymer sequencing.

Light Science & ApplicationsVol. 14(1)
University of Fribourg (CH), Inspire (CH), Indian Institute of Management Bangalore (IN), École Polytechnique Fédérale de Lausanne (CH), Indian Institute of Science Bangalore (IN)
National Science Foundation, European Commission, École Polytechnique Fédérale de Lausanne, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Horizon 2020 Framework Programme, National Center of Competence in Research Bio-Inspired Materials, University of Fribourg
Reduced inequalities
Openalex Percentile: Top 2%
Advanced Fluorescence Microscopy Techniques
9.80
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