超氧化物
化学
斑马鱼
斯托克斯位移
活性氧
荧光
荧光团
单线态氧
自体荧光
生物物理学
体内
赫拉
光化学
氧气
生物化学
细胞
酶
生物
物理
生物技术
有机化学
量子力学
基因
作者
Xiongjie Zhao,Xinyi Chen,You Kure Wu,Jing Wang,Pengxu Lin,Liyi Zhou,Zongcheng Wang
标识
DOI:10.1016/j.saa.2023.123806
摘要
As one of the major reactive oxygen species (ROS), superoxide anion (O2•−) is engaged in maintaining redox homeostasis in the cell microenvironment. To identify the pathological roles in related disorders caused by abnormal expression of O2•−, it is of great significance to monitor and track the fluctuation of O2•− concentration in vivo. However, the low concentration of O2•− and the interference caused by tissue autofluorescence make the development of an ideal detection methodology full of challenges. Herein, a "Turn-On" chemical response near-infrared (NIR) fluorescence probe Dcm-Cu-OTf for O2•− detection in inflamed models, was constructed by conjugating the NIR fluorophore (dicyanisophorone derivative) with an O2•− sensing moiety (trifluoromethanesulfonate). Dcm-Cu-OTf exerted about 140-fold fluorescence enhancement after reacting 200 μM O2•− with an excellent limited of detection (LOD) as low as 149 nM. Additionally, Dcm-Cu-OTf exhibited a super large Stokes shift (260 nm) and high selectivity over other bio-analytes in stimulated conditions. Importantly, Dcm-Cu-OTf showed low toxicity and enabled imaging of the generation of O2•− in the Lipopolysaccharide (LPS)-stimulated HeLa cells, zebrafish, and LPS-induced inflamed mice. The present study provided a potential and reliable detection tool to inspect the physiological and pathological progress of O2•− in living biosystems.
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