Citation: OU Zhi-Ze, JU Bao-Long, GAO Yun-Yan, WANG Zi-Chao, HUANG Gan, QIAN Yi-Meng. Alkynylplatinum(Ⅱ) 2,6-Bis(N-ethylbenzimidazol-2'-yl)pyridine Complexes: Effect of Alkynyl Ligand on G-quadruplex Binding Properties and Anticancer Activity[J]. Acta Physico-Chimica Sinica, ;2015, 31(12): 2386-2394. doi: 10.3866/PKU.WHXB201510137
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Three alkynylplatinum(Ⅱ)-2,6-bis(N-ethylbenzimidazol-2'-yl)pyridine complexes 2-4 were synthesized and characterized. The alkynyl ligand in complex 2 is the anticancer drug erlotinib. The interactions between the Pt(Ⅱ) complexes and G-quadruplexes, including human telomeric (Hetelo) and cmyc oncogene (c-myc) quadruplexes, were investigated using UV-Vis spectroscopy, circular dichroism (CD), and fluorescence resonance energy transfer (FRET) melting assays. These studies show that the Pt(Ⅱ) complexes 2-4 have high affinities for G-quadruplexes (Ka > 106 L·mol-1), and can promote the formation of G-quadruplexes even in the absence of alkali cations. The Pt(Ⅱ) complexes 2 and 3, containing a phenylacetylene moiety, induce a high degree of stabilization of the c-myc G-quadruplex, with a melting temperature increase (ΔTm) of more than 24 ℃, but complex 4, containing a propyne moiety, only induces ΔTm of 9.0 ℃. These results indicate that the structure of the alkynyl ligand is important in the interactions between Pt(Ⅱ) complexes and G-quadruplexes. The cytotoxicity of complex 2 to the human adenocarcinoma A549 cell line is higher than those of complexes 3, 4, and erlotinib.
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