Biocompatible TADF Probes for Highly Multiplexed Fluorescence Lifetime Imaging

Fluorescence lifetime imaging microscopy (FLIM) is an optical imaging modality that can provide multiplexed readouts with remarkable sensitivity to cellular microenvironments. Even though fluorescence lifetimes can distinguish fluorophores having overlapping spectral profiles, conventional fluorophores possess a narrow range of emission lifetimes (typically shorter than 5 ns) that limits their potential for multiplexed imaging. In this work, we have systematically designed and evaluated a combination of thermally activated delayed fluorescence (TADF) nanoprobes for multiplexed FLIM. We have synthesized a collection of 36 TADF biocompatible nanoprobes with long and diverse fluorescence lifetimes in aqueous media (up to 15 ns) and employed selected probes for live-cell imaging of bacterial cells under physiological conditions. By leveraging the exceptionally broad range of fluorescence lifetimes of these TADF emitters, we have achieved unprecedented simultaneous imaging of five nanoprobes within a single spectral window using a FLIM-phasor strategy. These findings demonstrate that TADF emitters are excellent scaffolds to unlock the capabilities of fluorescence lifetime imaging for multi-color biological studies.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-01-15
DOI
https://doi.org/10.1002/anie.202521482
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

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Biocompatible TADF Probes for Highly Multiplexed Fluorescence Lifetime Imaging

A. Jung, Yanzi Zhou, Tomas Matulaitis, Pilar Suárez de Cepeda et al.
Angewandte Chemie International Edition
Advanced Fluorescence Microscopy Techniques
article

Biocompatible TADF Probes for Highly Multiplexed Fluorescence Lifetime Imaging

A. Jung, Yanzi Zhou, Tomas Matulaitis, Pilar Suárez de Cepeda, Charles Lochenie, Ferran Nadal‐Bufí, Prof. Dr. Stefan Bräse, Marc Vendrell, Janine Haug, Quan Qi, Dongyang Chen, Eli Zysman‐Colman, Concepción González‐Bello
article en

Abstract

Fluorescence lifetime imaging microscopy (FLIM) is an optical imaging modality that can provide multiplexed readouts with remarkable sensitivity to cellular microenvironments. Even though fluorescence lifetimes can distinguish fluorophores having overlapping spectral profiles, conventional fluorophores possess a narrow range of emission lifetimes (typically shorter than 5 ns) that limits their potential for multiplexed imaging. In this work, we have systematically designed and evaluated a combination of thermally activated delayed fluorescence (TADF) nanoprobes for multiplexed FLIM. We have synthesized a collection of 36 TADF biocompatible nanoprobes with long and diverse fluorescence lifetimes in aqueous media (up to 15 ns) and employed selected probes for live-cell imaging of bacterial cells under physiological conditions. By leveraging the exceptionally broad range of fluorescence lifetimes of these TADF emitters, we have achieved unprecedented simultaneous imaging of five nanoprobes within a single spectral window using a FLIM-phasor strategy. These findings demonstrate that TADF emitters are excellent scaffolds to unlock the capabilities of fluorescence lifetime imaging for multi-color biological studies.

Angewandte Chemie International EditionVol. 65(8)
Karlsruhe Institute of Technology (DE), University of St Andrews (GB), MRC Centre for Regenerative Medicine (GB), Center for Research in Molecular Medicine and Chronic Diseases (ES), Centre for Inflammation Research (GB)
Studienstiftung des Deutschen Volkes, Axencia Galega de Innovación, Xunta de Galicia, Centro Singular de Investigación de Galicia, Engineering and Physical Sciences Research Council, European Regional Development Fund
Openalex Percentile: Top 87%
Advanced Fluorescence Microscopy Techniques
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