1. Academic Validation
  2. Carbazole-based fluorescent probes for G-quadruplex DNA targeting with superior selectivity and low cytotoxicity

Carbazole-based fluorescent probes for G-quadruplex DNA targeting with superior selectivity and low cytotoxicity

  • Bioorg Med Chem. 2020 Sep 1;28(17):115641. doi: 10.1016/j.bmc.2020.115641.
Quan-Qi Yu 1 Ming-Qi Wang 2
Affiliations

Affiliations

  • 1 School of Pharmacy, Jiangsu University, Zhenjiang 212013, PR China.
  • 2 School of Pharmacy, Jiangsu University, Zhenjiang 212013, PR China. Electronic address: [email protected].
Abstract

G-quadruplex DNA plays a very important role in clinical diagnosis and fluorescence analysis has attracted extensive attention. A class of carbazole-based fluorescent probes for the detection of G-quadruplex DNA was established in this work. In this system, the installation of an oligo(ethylene glycol) chain on the scaffold will improve the water-solubility and biocompatibility. The presence of styrene-like different side groups could tune the selectivity toward G-quadruplex DNA binding. Results revealed that the substitution pattern and position gave a great influence on the ability for the discrimination of the G-quadruplex from other DNA structures. Especially, probe E1 bound to G-quadruplex DNA with superior selectivity, which exhibiting almost no fluorescence response in the presence of non-G-quadruplex DNA structures. Comprehensive analyses revealed that E1 could bind both ends of the G-quadruplex, resulting in a significant increase of fluorescence emission intensity. Cellular uptake assay suggested that E1 could pass through membrane and enter living cells with low cytotoxicity.

Keywords

Carbazole; Cell imaging; Cytotoxicity; Fluorescent probe; G-quadruplex DNA.

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