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
重编程
作者
X. Xiao,Cheng Lu,Hao Chen,Jing Zhou,Yunyun Hu,Haonan Di,Guoqiang Su,X Y Yan
标识
DOI:10.1002/advs.202513341
摘要
ABSTRACT 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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