Near-infrared fluorescent probes based on a quinoxaline skeleton for imaging nucleic acids in mitochondria.
Hai-Yan PengGang ZhangYu-Jie XuRu SunJian-Feng GePublished in: Organic & biomolecular chemistry (2022)
In this paper, two cationic probes 1a and 1b and a neutral dye 1c were successfully designed and synthesized according to the Knoevenagel condensation reaction, which combines the good optical properties of hemocyanine and the biocompatibility of nitrogen-containing heterocyclic rings based on a quinoxaline skeleton. Probes 1a and 1b showed an OFF-ON fluorescence response to nucleic acids with excellent selectivity. Specifically, the fluorescence intensity of probe 1a was enhanced by 18 and 133 times, respectively, along with the increase of DNA or RNA concentrations (0-600 μg mL -1 ). Furthermore, a good linear correlation between the fluorescence intensity of probes 1a and 1b and the concentrations of DNA or RNA (0-350 μg mL -1 ) was obtained. In particular, the maximum emission wavelengths of probes 1a and 1b reached the near-infrared region (660-664 nm) when DNA or RNA was detected, which might reduce the light damage to cells and facilitate cell experiments. Fluorescence imaging revealed that all three dyes could be localized in the mitochondria of HeLa cells. The difference was that probes 1a and 1b could stain the nucleic acid in the mitochondria, while dye 1c was only a neutral mitochondrial biomarker. The results indicated that probes 1a and 1b are promising in the development of low toxicity mitochondrial nucleic acid probes and are expected to be used in monitoring the normal state of mitochondrial nucleic acids for living cells, which will help improve the situation in that currently reported studies of fluorescent probes are mainly focused on the nucleic acids in the nucleus, but less so on DNA in the mitochondria.
Keyphrases
- nucleic acid
- living cells
- single molecule
- fluorescence imaging
- fluorescent probe
- oxidative stress
- small molecule
- cell death
- induced apoptosis
- photodynamic therapy
- cell cycle arrest
- quantum dots
- endoplasmic reticulum
- bone marrow
- reactive oxygen species
- circulating tumor
- highly efficient
- signaling pathway
- mesenchymal stem cells
- energy transfer
- oxide nanoparticles
- case control