Evidence map›Paper›PMID 40754532›Full record

ArticleLight, science & applications2025

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

Nathan Ronceray, Salim Bennani, Marianna Fanouria Mitsioni, Nicole Siegel, Maria J Marcaida, Claudio Bruschini, Edoardo Charbon, Rahul Roy, Matteo Dal Peraro, Guillermo P Acuna and 1 more

Abstract read
In one paragraph

Article in Light, science & applications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Fluorescence-lifetime optical electrophysiology in contracting cardiomyocytes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Single-Photon Single-Particle Tracking.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Nathan RoncerayInstitute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland. nathan.ronceray@epfl.ch.ORCID http://orcid.org/0000-0001-8069-2411
Salim BennaniInstitute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland.
Marianna Fanouria MitsioniInstitute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland.
Nicole SiegelDepartment of Physics, University of Fribourg, Fribourg, Switzerland.
Maria J MarcaidaNCCR Bio-Inspired Materials, EPFL, Lausanne, Switzerland.
Claudio BruschiniAQUA, EPFL, Neuchâtel, Switzerland.ORCID http://orcid.org/0000-0002-6636-6596
Edoardo CharbonAQUA, EPFL, Neuchâtel, Switzerland.ORCID http://orcid.org/0000-0002-0620-3365
Rahul RoyDepartment of Chemical Engineering and Department of Bioengineering, Indian Institute of Science Bangalore, Bangalore, India.
Matteo Dal PeraroInstitute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland.
Guillermo P AcunaDepartment of Physics, University of Fribourg, Fribourg, Switzerland.ORCID http://orcid.org/0000-0001-8066-2677
Aleksandra RadenovicInstitute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland. aleksandra.radenovic@epfl.ch.ORCID http://orcid.org/0000-0001-8194-2785

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC Advanced Grant 2D Liquid
6 · The paper itself

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.

Identifiers

PMID40754532
PMCPMC12319105

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.