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A synergistic strategy to develop photostable and bright dyes with long Stokes shift for nanoscopy
by
D’Este, Elisa
, Johnsson, Kai
, Xiong, Bin
, Ren, Tian-Bing
, Yuan, Lin
, Xiong, Mengyi
, Zhang, Xiao-Bing
, Wang, Lu
, Jiang, Gangwei
in
14
/ 14/19
/ 14/34
/ 14/69
/ 639/624/1107/510
/ 639/638/11/874
/ 639/638/11/942
/ Biosensors
/ Brightness
/ Charge transfer
/ Chemical compounds
/ Depletion
/ Dyes
/ Electron density
/ Fluorescent Dyes - chemistry
/ Fluorescent indicators
/ Fluorophores
/ Humanities and Social Sciences
/ Image resolution
/ Ionophores
/ Medical imaging
/ Microscopy
/ Microscopy, Fluorescence - methods
/ multidisciplinary
/ Optical Imaging
/ Probes
/ Quinoxaline
/ Quinoxalines
/ Rhodamine
/ Science
/ Science (multidisciplinary)
/ Stimulated emission
2022
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A synergistic strategy to develop photostable and bright dyes with long Stokes shift for nanoscopy
by
D’Este, Elisa
, Johnsson, Kai
, Xiong, Bin
, Ren, Tian-Bing
, Yuan, Lin
, Xiong, Mengyi
, Zhang, Xiao-Bing
, Wang, Lu
, Jiang, Gangwei
in
14
/ 14/19
/ 14/34
/ 14/69
/ 639/624/1107/510
/ 639/638/11/874
/ 639/638/11/942
/ Biosensors
/ Brightness
/ Charge transfer
/ Chemical compounds
/ Depletion
/ Dyes
/ Electron density
/ Fluorescent Dyes - chemistry
/ Fluorescent indicators
/ Fluorophores
/ Humanities and Social Sciences
/ Image resolution
/ Ionophores
/ Medical imaging
/ Microscopy
/ Microscopy, Fluorescence - methods
/ multidisciplinary
/ Optical Imaging
/ Probes
/ Quinoxaline
/ Quinoxalines
/ Rhodamine
/ Science
/ Science (multidisciplinary)
/ Stimulated emission
2022
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A synergistic strategy to develop photostable and bright dyes with long Stokes shift for nanoscopy
by
D’Este, Elisa
, Johnsson, Kai
, Xiong, Bin
, Ren, Tian-Bing
, Yuan, Lin
, Xiong, Mengyi
, Zhang, Xiao-Bing
, Wang, Lu
, Jiang, Gangwei
in
14
/ 14/19
/ 14/34
/ 14/69
/ 639/624/1107/510
/ 639/638/11/874
/ 639/638/11/942
/ Biosensors
/ Brightness
/ Charge transfer
/ Chemical compounds
/ Depletion
/ Dyes
/ Electron density
/ Fluorescent Dyes - chemistry
/ Fluorescent indicators
/ Fluorophores
/ Humanities and Social Sciences
/ Image resolution
/ Ionophores
/ Medical imaging
/ Microscopy
/ Microscopy, Fluorescence - methods
/ multidisciplinary
/ Optical Imaging
/ Probes
/ Quinoxaline
/ Quinoxalines
/ Rhodamine
/ Science
/ Science (multidisciplinary)
/ Stimulated emission
2022
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A synergistic strategy to develop photostable and bright dyes with long Stokes shift for nanoscopy
Journal Article
A synergistic strategy to develop photostable and bright dyes with long Stokes shift for nanoscopy
2022
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Overview
The quality and application of super-resolution fluorescence imaging greatly lie in the dyes’ properties, including photostability, brightness, and Stokes shift. Here we report a synergistic strategy to simultaneously improve such properties of regular fluorophores. Introduction of quinoxaline motif with fine-tuned electron density to conventional rhodamines generates new dyes with vibration structure and inhibited twisted-intramolecular-charge-transfer (TICT) formation synchronously, thus increasing the brightness and photostability while enlarging Stokes shift. The new fluorophore
YL578
exhibits around twofold greater brightness and Stokes shift than its parental fluorophore, Rhodamine B. Importantly, in Stimulated Emission Depletion (STED) microscopy,
YL578
derived probe possesses a superior photostability and thus renders threefold more frames than carbopyronine based probes (CPY-Halo and 580CP-Halo), known as photostable fluorophores for STED imaging. Furthermore, the strategy is well generalized to offer a new class of bright and photostable fluorescent probes with long Stokes shift (up to 136 nm) for bioimaging and biosensing.
Super-resolution microscopy is a powerful tool for cellular studies but requires bright and stable fluorescent probes. Here, the authors report on a strategy to introduce quinoxaline motifs to conventional probes to make them brighter, more photostable, larger Stokes shift, and demonstrate the probes for biosensing applications.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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