共 50 条
In vitro binding interaction of atorvastatin with calf thymus DNA: multispectroscopic, gel electrophoresis and molecular docking studies
被引:48
作者:
Mirzaei-Kalar, Zeinab
[1
,2
]
机构:
[1] SUAT, Dept Mat Engn & Nanotechnol, Namin, Iran
[2] Univ Mohaghegh Ardabili, Dept Adv Technol, Namin, Ardabil, Iran
关键词:
Atorvastatin;
DNA interaction;
Fluorescence study;
Groove binding;
Molecular docking;
DNA cleavage;
HUMAN SERUM-ALBUMIN;
DEOXYRIBONUCLEIC-ACID;
DRUG;
COMPLEXES;
CLEAVAGE;
CARCINOGENESIS;
INTERCALATION;
ANTIOXIDANT;
COPPER(II);
STABILITY;
D O I:
10.1016/j.jpba.2018.08.033
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
The interaction of atorvastatin with calf thymus DNA (CT-DNA) was investigated in vitro under simulated physiological conditions by using absorption and emission spectroscopy, viscosity measurements, gel electrophoresis and molecular docking studies. Analysis of UV-vis absorbance spectra indicates the formation of complex between atorvastatin and CT-DNA, and obtained binding constant (K-b = 8.2 x 10(4) L.mol(-1)) is comparable to groove binder drugs. Slight increase of viscosity of CT-DNA demonstrated the groove binding mode. Hoechst 33,258 and methylene blue (MB) displacement studies further confirmed such mode of atorvastatin interaction. Thermodynamic parameters Delta G, Delta H, and Delta S measurements were taken at different temperatures indicated that hydrophobic forces played main role in the binding process. Molecular docking provided detailed computational interaction of atorvastatin with CT-DNA which proved that atorvastatin binds to the groove of CT-DNA. Cleavage experiments showed that atorvastatin does not induce any cleavage under the experimental setup. Finally, all results indicated that atorvastatin interacts with CT-DNA via groove binding mode. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 109
页数:9
相关论文
共 50 条