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Studies on synthesis, characterization, and G-quadruplex binding of Ru(II) complexes containing two dppz ligands
Authors:Sun Jing  An Yan  Zhang Li  Chen Huo-Yan  Han Yan  Wang Yu-Jia  Mao Zong-Wan  Ji Liang-Nian
Institution:
  • a MOE Key laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou, 510275, China
  • b School of Pharmacy, Guangdong Medical College, Dongguan, 523808, China
  • c Institute of Marine Materials Science and Engineering, Shanghai Maritime University, Shanghai 201306, China
  • Abstract:In this work, the interaction between the guanine-rich single-strand oligomer AG3(T2AG3)3 quadruplex and two Ru(II) complexes, Ru(L1)(dppz)2](PF6)4 (1) and Ru(L2)(dppz)2](PF6)4 (2) (L1 = 5,5′-di(1-(trimethylammonio)methyl)-2,2′-dipyridyl cation, L2 = 5,5′-di(1-(triethylammonio)methyl)-2,2′-dipyridyl cation, dppz = dipyrido3,2-a:2′,3′-c] phenazine), has been studied by UV-Visible, fluorescence, DNA melting, and circular dichroism in K+ buffer. The two complexes after binding to G-quadruplex have shown different DNA stability and fluorescence enhancement. The results show that both complexes can induce the stabilization of quadruplex DNA. ΔTm values of complexes 1 and 2 at Ru]/DNA] ratio of 1:1 were 9.4 and 7.0, respectively. Binding stoichiometry along with the quadruplex was investigated through a luminescence-based Job plot. The major inflection points for complexes 1 and 2 were 0.49 and 0.46, respectively. The data were consistent with the binding mode at a quadruplex]/complex] ratio of 1:1. In addition, the conformation of G-quadruplex was not changed by the complexes at the high ionic strength of K+ buffer.
    Keywords:Synthesis  Ru(II) complex  dppz  G-quadruplex
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