Fast and Selective Two-Stage Ratiometric Fluorescent Probes for Imaging of Glutathione in Living Cells

2017 ◽  
Vol 89 (24) ◽  
pp. 13112-13119 ◽  
Author(s):  
Deyan Gong ◽  
Shi-Chong Han ◽  
Anam Iqbal ◽  
Jing Qian ◽  
Ting Cao ◽  
...  
RSC Advances ◽  
2021 ◽  
Vol 11 (34) ◽  
pp. 21116-21126
Author(s):  
Yu Li ◽  
Li Chen ◽  
Yan Zhu ◽  
Liming Chen ◽  
Xianglin Yu ◽  
...  

A reversible fluorescent probe for GSH was obtained through structure modulation, by which the intracellular GSH fluctuation was imaged.


1982 ◽  
Vol 16 (12) ◽  
pp. 871-876
Author(s):  
G. I. Morozova ◽  
G. M. Barenboim ◽  
G. E. Dobretsov

RSC Advances ◽  
2016 ◽  
Vol 6 (75) ◽  
pp. 70960-70971 ◽  
Author(s):  
Chun Zhang ◽  
Dan Wang ◽  
Li Zhang ◽  
Jing-Fu Guo ◽  
Ai-Min Ren

The two-photon fluorescent probes show dual signal for β-gal bio-imaging.


2018 ◽  
Vol 1033 ◽  
pp. 193-198 ◽  
Author(s):  
Xiangzhu Chen ◽  
Xiaodong Ma ◽  
Yuanyuan Zhang ◽  
Gui Gao ◽  
Jingjing Liu ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Qixin Chen ◽  
Hongbao Fang ◽  
Xintian Shao ◽  
Zhiqi Tian ◽  
Shanshan Geng ◽  
...  

AbstractMitochondria–lysosome interactions are essential for maintaining intracellular homeostasis. Although various fluorescent probes have been developed to visualize such interactions, they remain unable to label mitochondria and lysosomes simultaneously and dynamically track their interaction. Here, we introduce a cell-permeable, biocompatible, viscosity-responsive, small organic molecular probe, Coupa, to monitor the interaction of mitochondria and lysosomes in living cells. Through a functional fluorescence conversion, Coupa can simultaneously label mitochondria with blue fluorescence and lysosomes with red fluorescence, and the correlation between the red–blue fluorescence intensity indicates the progress of mitochondria–lysosome interplay during mitophagy. Moreover, because its fluorescence is sensitive to viscosity, Coupa allowed us to precisely localize sites of mitochondria–lysosome contact and reveal increases in local viscosity on mitochondria associated with mitochondria–lysosome contact. Thus, our probe represents an attractive tool for the localization and dynamic tracking of functional mitochondria–lysosome interactions in living cells.


Sign in / Sign up

Export Citation Format

Share Document