A novel near-infrared fluorescent probe with hemicyanine scaffold for sensitive mitochondrial pH detection and mitophagy study

被引:8
|
作者
Fang, Mingxi [1 ,3 ]
Zhou, Xiaoyu [1 ]
Wang, Shaocai [1 ]
Yang, Yinshuang [1 ]
Cheng, Yueting [2 ]
Wang, Boling [2 ]
Rong, Xiaoqian [2 ]
Zhang, Xiuli [1 ]
Xu, Kai [1 ]
Zhang, Yibin [2 ]
Zheng, Shaohui [1 ]
机构
[1] Xuzhou Med Univ, Sch Med Imaging, Xuzhou 221006, Jiangsu, Peoples R China
[2] Yangtze Normal Univ, Coll Chem & Chem Engn, Chongqing 408100, Peoples R China
[3] Xuzhou Med Univ, Canc Inst, Jiangsu Ctr Collaborat & Innovat Canc Biotherapy, Xuzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Near -infrared emission; Mitochondrial pH sensing; Mitophagy monitoring; Deep tissue penetration; In vivo tumor imaging; RATIONAL DESIGN; VISUALIZATION; CELLS; DYE; RED;
D O I
10.1016/j.saa.2023.122791
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Mitochondria, as an energy-producing powerhouse in live cells, is considered to be directly linked to cellular health. However, dysfunctional mitochondria and abnormal mitochondria pH would possibly activate mitophagy, cell apoptosis and intercellular acidification process. In this work, we synthesized a novel near infrared fluorescent probe (FNIR-pH) for measurement of mitochondrial pH based on the hemicyanine skeleton as a fluorophore. The FNIR-pH probe functioned as a mitochondrial pH substrate and exhibited quick and sensitive turn-on fluorescence responses to mitochondrial pH in basic solution due to the deprotonation of hydroxy group in the structure. From pH 3.0 to 10.0, the FNIR-pH exhibited almost 100-fold increase in fluorescence intensity at 766 nm wavelength. The FNIR-pH also displayed superior selectivity to various metal ions, excellent photostability, and low cytotoxicity, which facilitated further biological application. Owing to the proper pKa value of 7.2, the FNIR-pH paved the way for real-time monitoring of mitochondria pH changes in live cells and sensitive sensing of mitophagy. Moreover, the FNIR-pH probe was also implemented for fluorescent imaging of tumorbearing mice to validate its potential application for in vivo imaging of bioanalytes and biomarkers.
引用
收藏
页数:10
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