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1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity

Superoxide (O(2)(·−)) is the primary reactive oxygen species in mammal cells. Detecting superoxide is crucial for understanding redox signaling but remains challenging. Herein, we introduce a class of activity-based sensing probes. The probes utilize 1,2,4,5-tetrazine as a superoxide-responsive trig...

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Autores principales: Jiang, Xuefeng, Li, Min, Wang, Yule, Wang, Chao, Wang, Yingchao, Shen, Tianruo, Shen, Lili, Liu, Xiaogang, Wang, Yi, Li, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014963/
https://www.ncbi.nlm.nih.gov/pubmed/36918556
http://dx.doi.org/10.1038/s41467-023-37121-8
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author Jiang, Xuefeng
Li, Min
Wang, Yule
Wang, Chao
Wang, Yingchao
Shen, Tianruo
Shen, Lili
Liu, Xiaogang
Wang, Yi
Li, Xin
author_facet Jiang, Xuefeng
Li, Min
Wang, Yule
Wang, Chao
Wang, Yingchao
Shen, Tianruo
Shen, Lili
Liu, Xiaogang
Wang, Yi
Li, Xin
author_sort Jiang, Xuefeng
collection PubMed
description Superoxide (O(2)(·−)) is the primary reactive oxygen species in mammal cells. Detecting superoxide is crucial for understanding redox signaling but remains challenging. Herein, we introduce a class of activity-based sensing probes. The probes utilize 1,2,4,5-tetrazine as a superoxide-responsive trigger, which can be modularly tethered to various fluorophores to tune probe sensitivity and emission color. These probes afford ultra-specific and ultra-fluorogenic responses towards superoxide, and enable multiplexed imaging of various cellular superoxide levels in an organelle-resolved way. Notably, the probes reveal the aberrant superoxide generation in the pathology of myocardial ischemia/reperfusion injury, and facilitate the establishment of a high-content screening pipeline for mediators of superoxide homeostasis. One such identified mediator, coprostanone, is shown to effectively ameliorating oxidative stress-induced injury in mice with myocardial ischemia/reperfusion injury. Collectively, these results showcase the potential of 1,2,4,5-tetrazine-tethered probes as versatile tools to monitor superoxide in a range of pathophysiological settings.
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spelling pubmed-100149632023-03-16 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity Jiang, Xuefeng Li, Min Wang, Yule Wang, Chao Wang, Yingchao Shen, Tianruo Shen, Lili Liu, Xiaogang Wang, Yi Li, Xin Nat Commun Article Superoxide (O(2)(·−)) is the primary reactive oxygen species in mammal cells. Detecting superoxide is crucial for understanding redox signaling but remains challenging. Herein, we introduce a class of activity-based sensing probes. The probes utilize 1,2,4,5-tetrazine as a superoxide-responsive trigger, which can be modularly tethered to various fluorophores to tune probe sensitivity and emission color. These probes afford ultra-specific and ultra-fluorogenic responses towards superoxide, and enable multiplexed imaging of various cellular superoxide levels in an organelle-resolved way. Notably, the probes reveal the aberrant superoxide generation in the pathology of myocardial ischemia/reperfusion injury, and facilitate the establishment of a high-content screening pipeline for mediators of superoxide homeostasis. One such identified mediator, coprostanone, is shown to effectively ameliorating oxidative stress-induced injury in mice with myocardial ischemia/reperfusion injury. Collectively, these results showcase the potential of 1,2,4,5-tetrazine-tethered probes as versatile tools to monitor superoxide in a range of pathophysiological settings. Nature Publishing Group UK 2023-03-14 /pmc/articles/PMC10014963/ /pubmed/36918556 http://dx.doi.org/10.1038/s41467-023-37121-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jiang, Xuefeng
Li, Min
Wang, Yule
Wang, Chao
Wang, Yingchao
Shen, Tianruo
Shen, Lili
Liu, Xiaogang
Wang, Yi
Li, Xin
1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title_full 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title_fullStr 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title_full_unstemmed 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title_short 1,2,4,5-Tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
title_sort 1,2,4,5-tetrazine-tethered probes for fluorogenically imaging superoxide in live cells with ultrahigh specificity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014963/
https://www.ncbi.nlm.nih.gov/pubmed/36918556
http://dx.doi.org/10.1038/s41467-023-37121-8
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