核糖核酸
单线态氧
荧光团
生物物理学
化学
线粒体
荧光
细胞凋亡
RNA干扰
生物化学
生物
氧气
物理
有机化学
量子力学
基因
作者
Yali Feng,Jing Fang,Yan Zhao,Shuyue Ye,Anna Wang,Yuqi Zhang,Jinfeng Zhu,Jiachen Li,Zhengzhong Lv,Zhongsheng Zhao,Haibin Shi
标识
DOI:10.1002/anie.202218969
摘要
Mitochondrial RNA (mtRNA) plays a critical role in synthesis of mitochondrial proteins. Interfering mtRNA is a highly effective way to induce cell apoptosis. Herein, we report a near-infrared (NIR) light-mediated mitochondrial RNA modification approach for long-term imaging and effective suppression of tumors. A tumor-targetable NIR fluorescent probe f-CRI consisting of a cyclic RGD peptide, a NIR fluorophore IR780, and a singlet oxygen (1 O2 )-labile furan group for RNA modification was rationally designed and synthesized. This probe was demonstrated to dominantly accumulate in cellular mitochondria and could be covalently conjugated onto mtRNA upon 808 nm irradiation resulting in prolonged retention in tumors. More notably, this covalent modification of mtRNA by f-CRI could perturb the function of mitochondria leading to remarkable tumor suppression. We thus envision that our current approach would offer a potential approach for cancer RNA interference therapeutics.
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