Photophysical, G-quadruplex DNA binding and cytotoxic properties of terpyridine complexes with a naphthalimide ligand
Update time:2016-04-14
Two novel metal complexes2–3(metal = PdII, PtII) have been synthesized by reacting the corresponding tolylterpyridine complexes and the 4-aminonaphthalimide derivative1. The interactions of the complexes with duplex DNA and telomeric G-quadruplex DNA have been investigated by UV-Vis spectroscopy and fluorescence spectroscopy. The studies reveal that the complexes2–3possess high affinity and reasonable selectivity for telomeric G-quadruplex DNA over duplex DNA. Spectroscopic and molecular docking studies suggest that the complexes2–3interact with telomeric G-quadruplex DNA mainly through groove binding. The compounds1–3are emissive (Φem> 0.22), making it possible to study the localization of1–3in A549 using fluorescence microscopy. The complexes2–3are mainly localized in nuclei, while1is localized in the nuclei and cytoplasmic region after 0.5 h incubation. The complex3inhibits A549 cells selectively over non-cancerous NIH3T3 cells, with higher antitumor activity than1and cisplatin.
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