Development and Application of Cationic Nile Blue Probes in Live-Cell Super-Resolution Imaging and Specific Targeting to Mitochondria

被引:3
|
作者
Li, Yunsheng [1 ,2 ]
Bai, Xiaoyu [2 ]
Yang, Dan [1 ,3 ]
机构
[1] Westlake Univ, Sch Life Sci, Hangzhou 310024, Peoples R China
[2] Univ Hong Kong, Dept Chem, Morningside Lab Chem Biol, Hong Kong 999077, Peoples R China
[3] Westlake Lab Life Sci & Biomed, Hangzhou 310024, Peoples R China
关键词
FLUORESCENCE; DYES; LOCALIZATION; MECHANISMS; PACLITAXEL; TAXOL; RED;
D O I
10.1021/acscentsci.4c00073
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mitochondria are essential organelles involved in various metabolic processes in eukaryotes. The imaging, targeting, and investigation of cell death mechanisms related to mitochondria have garnered significant interest. Small-molecule fluorescent probes have proven to be robust tools for utilizing light to advance the study of mitochondrial biology. In this study, we present the rational design of cationic Nile blue probes carrying a permanent positive charge for these purposes. The cationic Nile blue probes exhibit excellent mitochondrial permeability, unique solvatochromism, and resistance to oxidation. We observed weaker fluorescence in aqueous solutions compared to lipophilic solvents, thereby minimizing background fluorescence in the cytoplasm. Additionally, we achieved photoredox switching of the cationic Nile blue probes under mild conditions. This enabled us to demonstrate their application for the first time in single-molecule localization microscopy of mitochondria, allowing us to observe mitochondrial fission and fusion behaviors. Compared to conventional cyanine fluorophores, this class of dyes demonstrated prolonged resistance to photobleaching, likely due to their antioxidation properties. Furthermore, we extended the application of cationic Nile blue probes to the mitochondria-specific delivery of taxanes, facilitating the study of direct interactions between the drug and organelles. Our approach to triggering cell death without reliance on microtubule binding provides valuable insights into anticancer drug research and drug-resistance mechanisms.
引用
收藏
页码:1221 / 1230
页数:10
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