Per-pixel unmixing of spectrally overlapping ...
Document type :
Article dans une revue scientifique: Article original
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Title :
Per-pixel unmixing of spectrally overlapping fluorophores using intra-exposure excitation modulation.
Author(s) :
Valenta, H. [Auteur]
Bierbuesse, F. [Auteur]
Vitale, Raffaele [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Ruckebusch, Cyril [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Vandenberg, W. [Auteur]
Dedecker, P. [Auteur]
Bierbuesse, F. [Auteur]
Vitale, Raffaele [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Ruckebusch, Cyril [Auteur]

Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Vandenberg, W. [Auteur]
Dedecker, P. [Auteur]
Journal title :
Talanta
Abbreviated title :
Talanta
Volume number :
269
Pages :
125397
Publication date :
2023-12-05
ISSN :
1873-3573
English keyword(s) :
Multiplexed imaging
Per-pixel unmixing
Reversibly photoswitchable fluorescent
proteins
Per-pixel unmixing
Reversibly photoswitchable fluorescent
proteins
HAL domain(s) :
Chimie/Chimie théorique et/ou physique
English abstract : [en]
Multilabel fluorescence imaging is essential for the visualization of complex systems, though a major challenge is the limited width of the useable spectral window. Here, we present a new method, exNEEMO, that enables ...
Show more >Multilabel fluorescence imaging is essential for the visualization of complex systems, though a major challenge is the limited width of the useable spectral window. Here, we present a new method, exNEEMO, that enables per-pixel quantification of spectrally-overlapping fluorophores based on their light-induced dynamics, in a way that is compatible with a very broad range of timescales over which these dynamics may occur. Our approach makes use of intra-exposure modulation of the excitation light to distinguish the different emitters given their reference responses to this modulation. We use the approach to simultaneously image four green photochromic fluorescent proteins at the full spatial resolution of the imaging.Show less >
Show more >Multilabel fluorescence imaging is essential for the visualization of complex systems, though a major challenge is the limited width of the useable spectral window. Here, we present a new method, exNEEMO, that enables per-pixel quantification of spectrally-overlapping fluorophores based on their light-induced dynamics, in a way that is compatible with a very broad range of timescales over which these dynamics may occur. Our approach makes use of intra-exposure modulation of the excitation light to distinguish the different emitters given their reference responses to this modulation. We use the approach to simultaneously image four green photochromic fluorescent proteins at the full spatial resolution of the imaging.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
CNRS
Collections :
Submission date :
2024-02-28T22:05:04Z
2024-03-11T15:50:38Z
2024-03-11T15:50:38Z
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