氧化磷酸化
生物能学
ATP合酶
寡霉素
三磷酸腺苷
线粒体
生物化学
己糖激酶
化学
生物
癌细胞
柠檬酸循环
细胞生物学
糖酵解
胞浆
代谢组学
磷酸化
二磷酸腺苷
质子泵
粒线体疾病
代谢组
丙酮酸激酶
酶
基诺美
谷氨酰胺酶
呼吸链
作者
Xu Xiao,Cheng Lu,Hao Chen,Jing Zhou,Yunyun Hu,Haonan Di,Guoqiang Su,Xiaomei Yan
标识
DOI:10.1002/advs.202513341
摘要
Mitochondrial adenosine triphosphate (mitoATP) serves as the primary bioenergetic currency for oxidative phosphorylation (OXPHOS)-driven malignancies, yet its precise organelle-level quantification remains challenging due to mitochondrial heterogeneity and cytosolic interference. Herein, we report MitoATP-nFCM, a nano-flow cytometry platform enabling single-mitochondrion ATP measurement via simultaneous fluorescence and side scatter detection. We uncover 1.7-1.9-fold higher ATP levels in isolated mitochondria from breast (MCF-7, MDA-MB-231) and colon (HCT-15, HCT-116) cancer cells than in their normal counterparts. Single-organelle analysis further reveals coordinated metabolic reprogramming in cancer mitochondria, featuring elevated membrane potential, increased ATP synthase expression, and reduced hexokinase 2 levels, demonstrating their OXPHOS-dominant bioenergetic phenotype that contrasts with classical Warburg-effect expectations. Furthermore, we establish a screening strategy to identify highly potent cancer-selective inhibitors targeting mitochondrial metabolism. We find that bedaquiline (ATP synthase inhibitor) outperforms oligomycin A in specificity, VLX600 (electron transport chain inhibitor) shows superior selectivity to rotenone/metformin, and CPI-613 (tricarboxylic acid cycle blocker) surpasses other glutaminase inhibitors. MitoATP-nFCM establishes a quantitative single-organelle platform that profiles elevated mitoATP levels in cancer cells and enables precision screening of OXPHOS-targeting inhibitors.
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