Dong Yalun, Wang Liyue, Liang Wenfang, Zhu Jiqin, Sun Lu, Yi Long
State Key Laboratory of Organic-Inorganic Composites and Beijing Key Lab of Bioprocess, Beijing University of Chemical Technology, Beijing 100029, China.
Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics, School of Pharmacy, Tianjin Medical University, Tianjin 300070, China.
Sensors (Basel). 2024 Dec 24;25(1):34. doi: 10.3390/s25010034.
Glutathione (GSH) plays a crucial role in various physiological processes and its imbalances are closely related to various pathological conditions. Probes for detection and imaging of GSH are not only useful for understanding GSH chemical biology but are also important for exploring potential theranostic agents. Herein, we report a fast intramolecular thiol-activated arylselenoamides ()-based fluorescent probe using 2,4-dinitrophenyl alkylthioether as a sulfydryl-selective receptor for the first time. The fluorescence of the probe was low due to the double effects of PET, while the probe exhibits an 86-fold fluorescence enhancement at 460 nm after GSH activation and a detection limit of 0.95 μM. Furthermore, the probe is low-toxic and capable of imaging cellular GSH. This work further expands the design and applicability of the -based platform, offering a new thiol-deprotection strategy for development of fluorescent probes.
谷胱甘肽(GSH)在各种生理过程中起着至关重要的作用,其失衡与各种病理状况密切相关。用于检测和成像GSH的探针不仅有助于理解GSH化学生物学,对于探索潜在的治疗诊断剂也很重要。在此,我们首次报道了一种基于2,4-二硝基苯基烷基硫醚作为巯基选择性受体的快速分子内硫醇激活的芳基硒酰胺()荧光探针。由于PET的双重作用,探针的荧光较低,而在GSH激活后,该探针在460 nm处表现出86倍的荧光增强,检测限为0.95 μM。此外,该探针毒性低,能够对细胞内的GSH进行成像。这项工作进一步扩展了基于该平台的设计和适用性,为荧光探针的开发提供了一种新的硫醇脱保护策略。