Targeting human telomeric and c-myc G-quadruplexes with alkynylplatinum(II) terpyridine complexes under molecular crowding conditions

被引:25
作者
Ou, Zhize [1 ]
Wang, Yunqing [1 ]
Gao, Yunyan [1 ]
Wang, Xiaobing [2 ]
Qian, Yimeng [1 ]
Li, Yi [3 ]
Wang, Xuesong [3 ]
机构
[1] Northwestem Polytech Univ, Dept Appl Chem, Key Lab Space Appl Phys & Chem, Sch Sci,Minist Educ, Xian 710072, Peoples R China
[2] Shaanxi Normal Univ, Coll Life Sci, Xian 710062, Peoples R China
[3] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkynylplatinum(II) terpyridine; G-quadruplex ligand; Molecular crowding; Anticancer drug design; Antiproliferative effect; METAL-COMPLEXES; CATIONIC PORPHYRIN; DNA QUADRUPLEXES; BINDING; INHIBITION; BINDERS; STABILIZATION; STABILITY; HYDRATION; PROMOTER;
D O I
10.1016/j.jinorgbio.2016.11.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interactions between alkynylplatinum(II) terpyridine complexes 1-3 and the G-quadruplex DNA, including c-myc and telomeric quadruplex DNA, are investigated both in dilute solution and under molecular crowding conditions. The UV-vis absorption spectroscopy, circular dichroism and molecular docicing studies suggest that 1-3 associate with telomeric and c-myc G-quadruplexes via groove binding, and electrostatic interactions. Experimental studies indicate that under molecular crowding conditions (in the presence of 40 wt% PEG 200),1-2 show weak affinity for c-myc, while 3 still displays high affinity and selectivity for c-myc. On the other hand, 1-3 act as efficient and selective ligand for telomeric quadruplex DNA under molecular crowding conditions. The complex 3 exhibits excellent cytotoxicity against A549, K562 and SGC-7901, with IC50 values that are 35.0-fold, 10.0-fold, and 12.1-fold lower than the values of cisplatin under the same conditions, respectively. (C) 2016 Elsevier Inc All rights reserved.
引用
收藏
页码:126 / 134
页数:9
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