线粒体分裂
线粒体DNA
扫描电镜
类核
程序性细胞死亡
细胞生物学
生物物理学
线粒体
生物
分子生物学
物理
细胞凋亡
遗传学
受激发射
光学
基因
激光器
大肠杆菌
作者
Hongzhi Cao,Shaoqi Zhong,Yu Shen,Mengqi Lv,Yuhan Zhu,Yupeng Tian,Kui Luo,Wei Huang,Giuseppe Battaglia,Qiyong Gong,Xiaohe Tian
标识
DOI:10.1016/j.cej.2022.137763
摘要
• We show that the BDP: • specifically and selectivity mark mtDNA. • excellent optical properties and low working concentration. • excellent photostability under continuous irradiation with STED laser. • real-time super-resolution fluorescence imaging to understand mtDNA adaptations. Mitochondrial nucleoids or mitochondrial DNA (mtDNA) encodes for a variety of enzymes and proteins that are essential for oxidative phosphorylation, mitochondrial fussion/fission and apoptotic processes. However, visulization of mtDNA dynamics in response to external stumili has not yet been achieved. Herein, we developed a fluorescent probe, named BDP, that is capable of specifically bind to mtDNA in vitro and in living cells, without interfering mitochondrial functions. Its large Stokes-Shift and red-emission tail render its suitability for stimulated emission depletion (STED) visulization of mtDNA dynamics in living cells. We sucessfully demonstrated for the first time how apoptotic induced anti-cancer drug could impact on mitochondrial nucleoids, and the morphology evolution of mtDNA from segmentation to dispersion was recorded, in a single mitochondria at nanoscale.
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