适体
糖酵解
氧化磷酸化
精氨酸
癌细胞
生物化学
化学
癌症治疗
一氧化氮
氧化应激
细胞生物学
酶
生物物理学
癌症
生物
氨基酸
分子生物学
有机化学
遗传学
作者
Xiao Fang,Meng Yuan,Junduan Dai,Qianying Lin,Yu-Hong Lin,Wenli Wang,Yi-Fan Jiang,Haihui Wang,Fang Zhao,Junye Wu,Shumeng Bai,Chunhua Lu,Huanghao Yang
出处
期刊:Nano Research
[Springer Nature]
日期:2022-04-20
卷期号:15 (7): 6278-6287
被引量:1
标识
DOI:10.1007/s12274-022-4237-2
摘要
Dual inhibition of glycolysis and oxidative phosphorylation (OXPHOS) can break the metabolic plasticity of cancer cells to inhibit most energy supply and lead to effective cancer therapy. However, the pharmacokinetic difference among drugs hinders these two inhibitions to realize a uniform temporal and spatial distribution. Herein, we report an aptamer-based artificial enzyme for simultaneous dual inhibition of glycolysis and OXPHOS, which is constructed by arginine aptamer modified carbon-dots-doped graphitic carbon nitride (AptCCN). AptCCN can circularly capture intracellular arginine attribute to the specific binding ability of arginine aptamers to arginine, and further catalyze the oxidation of enriched arginine to nitric oxide (NO) under red light irradiation. In vitro and in vivo experiments showed that arginine depletion and NO stress could inhibit glycolysis and OXPHOS, leading to energy blockage and apoptosis of cancer cells. The presented aptamer-based artificial enzyme strategy provides a new path for cell pathway regulation and synergistic cancer therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI