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Light Science & ApplicationsBiophysicsPeer-reviewed journal article

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

Nathan RoncerayiD, Salim Bennani, Marianna Fanouria MitsioniiD, Nicole SiegeliD, María J. MarcaidaiD, Claudio E. BruschiniiD, Edoardo Charbon AiD, Rahul RoyiD, Matteo Dal PeraroiD, Guillermo P. AcunaiD, Aleksandra RađenovićiD

PDFDOIPreprint
Citations
15
FWCI
5.08
Field percentile
top 3%

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 (512x512) 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 Forster 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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