粒体自噬
化学
氧化还原
生物物理学
线粒体
氧化应激
荧光
溶酶体
原位
细胞生物学
生物化学
自噬
酶
生物
细胞凋亡
物理
有机化学
量子力学
作者
Junbin Li,Lifei Song,Weiguo Hu,Qin Zuo,R. Li,Min Dai,Yibo Zhou,Zhihe Qing
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-08-29
卷期号:95 (36): 13668-13673
被引量:10
标识
DOI:10.1021/acs.analchem.3c02717
摘要
Mitophagy is the lysosome-dependent degradation of damaged and dysfunctional mitochondria, which is closely associated with H2O2-related redox imbalance and pathological processes. However, development of fast-responding and highly sensitive reversible fluorescent probes for monitoring of mitochondrial H2O2 dynamics is still lacking. Herein, we report a reversible fluorescent probe (M-HP) that enables real-time imaging of H2O2-related redox imbalance. In vitro studies demonstrated that M-HP had a rapid response and high sensitivity to the H2O2/GSH redox cycle, with a detection limit of 17 nM for H2O2. M-HP was applied to imaging of H2O2 fluctuation in living cells with excellent reversibility and mitochondrial targeting. M-HP reveals an increase in mitochondrial H2O2 under lipopolysaccharide stimulation and a decrease in H2O2 following the combined treatment with rapamycin. This suggests that the level of oxidative stress is significantly suppressed after the enhancement of mitophagy. The rationally designed M-HP offers a powerful tool for understanding redox imbalance during mitophagy.
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