化学
三磷酸腺苷
荧光
活体细胞成像
ATP合酶
荧光寿命成像显微镜
ATP-ADP转位酶
离解(化学)
线粒体
生物物理学
细胞
生物化学
酶
线粒体内膜
光学
生物
物理
物理化学
作者
Tian‐Bing Ren,Siyu Wen,Lu Wang,Lu Peng,Bin Xiong,Lin Yuan,Xiaobing Zhang
标识
DOI:10.1021/acs.analchem.0c00506
摘要
Real-time imaging and quantification of adenosine triphosphate (ATP) fluctuation in cells are significant for understanding the relationship between energy metabolism and cell functions. However, few synthetic fluorescent probes have been reported to tackle this challenge due to lack of accurate fluorescence readout and suitable response concentration. Herein we designed and synthesized a ratiometric fluorescent probe (Rh6G–ACFPN) for quantitatively detecting the fluctuation of mitochondrial ATP in living cells. Rh6G–ACFPN selectively and reversibly responds to ATP with an ideal dissociation constant (Kd) of 4.65 mM (3–10 mM: the range of mitochondrial ATP concentrations). Live-cell imaging allows us to directly monitor the dynamic changes of mitochondrial ATP in high temporal resolution. Moreover, for the first time, mitochondrial ATP in normal and cancer cells lines was successfully quantified and discriminated. These results demonstrate the versatility of Rh6G–ACFPN as a useful imaging tool to elucidate the function of mitochondrial ATP in living cells.
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