An Off-On Two-Photon Carbazole-Based Fluorescent Probe: Highly Targeting and Super-Resolution Imaging of mtDNA

被引:33
|
作者
Gao, Fengli [1 ]
Li, Liuju [3 ]
Fan, Jiangli [1 ,5 ]
Cao, Jianfang [4 ]
Li, Yueqing [2 ]
Chen, Liangyi [3 ]
Peng, Xiaojun [1 ,5 ]
机构
[1] Dalian Univ Technol, Dept State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, Sch Pharmaceut Sci & Technol, 2 Linggong Rd, Dalian 116024, Peoples R China
[3] Peking Univ, Inst Mol Med, Beijing 100871, Peoples R China
[4] Liaoning Univ Technol, Sch Chem & Environm Engn, 169 Shiying Rd, Jinzhou 121001, Peoples R China
[5] Dalian Univ Technol Shenzhen, Res Inst, Gaoxin South Fourth Rd, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金;
关键词
MITOCHONDRIAL-DNA MUTATIONS; CIRCULAR-DICHROISM; BINDING MODE; SEQUENCE; DIFFERENTIATION; DISEASE; CELLS;
D O I
10.1021/acs.analchem.8b04418
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Many mitochondria-related diseases are associated with the mutation of mitochondrial DNA (mtDNA). Therefore, visualizing its dynamics in live cells is essential for the understanding of the function of mtDNA transcription and translation. By employing carbazole as the framework and designing a module for DNA minor-groove binding, here we have developed a novel fluorescent probe with a large Stokes shift (lambda(ab) = 480 nm and lambda(em) = 620 nm), CNQ, for mtDNA detection and visualization. It is almost nonfluorescent in PBS buffer and exhibits 182-fold enhancement in fluorescence within 20 s after the application of mtDNA in the solution, with a detection limit of 55.1 mu g/L. Using dual-color Hessian-structured illumination microscopy, we have demonstrated that CNQ-labeled mtDNA structures are distinct from those labeled by TFAM-EGFP. Finally, we have used two-photon confocal scanning microscopy (lambda(ex) = 850 nm) to monitor the nondestructive doxorubicin-induced mtDNA damage in live cells.
引用
收藏
页码:3336 / 3341
页数:6
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