Binding interaction between sorafenib and calf thymus DNA: Spectroscopic methodology, viscosity measurement and molecular docking

被引:147
作者
Shi, Jie-Hua [1 ,2 ]
Chen, Jun [1 ]
Wang, Jing [1 ]
Zhu, Ying-Yao [1 ]
机构
[1] Zhejiang Univ Technol, Coll Pharmaceut Sci, Hangzhou 310032, Zhejiang, Peoples R China
[2] Zhejiang Univ Technol, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310032, Zhejiang, Peoples R China
关键词
Sorafenib; Calf thymus-DNA; UV-vis spectroscopy; Circular dichroism; Fluorescence spectroscopy; Molecular docking; CIRCULAR-DICHROISM; DRUG; CARCINOMA; COMBINATION; CELLS; MODE; RAF;
D O I
10.1016/j.saa.2014.09.056
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The binding interaction of sorafenib with calf thymus DNA (ct-DNA) was studied using UV-vis absorption spectroscopy, fluorescence emission spectroscopy, circular dichroism (CD), viscosity measurement and molecular docking methods. The experimental results revealed that there was obvious binding interaction between sorafenib and ct-DNA. The binding constant (K-b) of sorafenib with ct-DNA was 5.6 x 10(3) M-1 at 298 K. The enthalpy and entropy changes (Delta H-0 and Delta S-0) in the binding process of sorafenib with ct-DNA were -27.66 KJ mol(-1) and -21.02 J mol(-1) K-1, respectively, indicating that the main binding interaction forces were van der Waals force and hydrogen bonding. The docking results suggested that sorafenib preferred to bind on the minor groove of A-T rich DNA and the binding site of sorafenib was 4 base pairs long. The conformation change of sorafenib in the sorafenib-DNA complex was obviously observed and the change was close relation with the structure of DNA, implying that the flexibility of sorafenib molecule played an important role in the formation of the stable sorafenib-ct-DNA complex. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:443 / 450
页数:8
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