An Off-On Two-Photon Carbazole-Based Fluorescent Probe: Highly Targeting and Super-Resolution Imaging of mtDNA.
Fengli GaoLiuju LiJiangli FanJianfang CaoYueqing LiLiangyi ChenXiaojun PengPublished in: Analytical chemistry (2019)
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 (λab = 480 nm and λem = 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 μg/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 (λex = 850 nm) to monitor the nondestructive doxorubicin-induced mtDNA damage in live cells.
Keyphrases
- mitochondrial dna
- fluorescent probe
- living cells
- copy number
- single molecule
- high resolution
- induced apoptosis
- cell cycle arrest
- label free
- photodynamic therapy
- cell death
- optical coherence tomography
- genome wide
- dna methylation
- oxidative stress
- drug delivery
- high throughput
- pet imaging
- endoplasmic reticulum stress
- high glucose
- mass spectrometry
- electron microscopy
- endothelial cells
- cell proliferation
- dna binding
- single cell
- raman spectroscopy
- nucleic acid
- binding protein
- light emitting