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阿托伐他汀与小牛胸腺 DNA 的体外结合相互作用:多谱学、凝胶电泳和分子对接研究。

In vitro binding interaction of atorvastatin with calf thymus DNA: multispectroscopic, gel electrophoresis and molecular docking studies.

机构信息

Department of Materials Engineering and Nanotechnology, Sabalan University of Advanced Technologies (SUAT), Namin, Iran; Department of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Ardabil, Iran.

出版信息

J Pharm Biomed Anal. 2018 Nov 30;161:101-109. doi: 10.1016/j.jpba.2018.08.033. Epub 2018 Aug 18.

Abstract

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 = 8.2×10 L. mol) 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 ΔG, ΔH, and ΔS 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.

摘要

在模拟生理条件下,通过吸收和发射光谱、粘度测量、凝胶电泳和分子对接研究,研究了阿托伐他汀与小牛胸腺 DNA(CT-DNA)的相互作用。紫外可见吸收光谱分析表明,阿托伐他汀与 CT-DNA 形成复合物,所得结合常数(K=8.2×10 L·mol)可与沟结合药物相媲美。CT-DNA 粘度的轻微增加表明存在沟结合模式。Hoechst 33258 和亚甲基蓝(MB)置换研究进一步证实了阿托伐他汀的这种相互作用模式。在不同温度下测量热力学参数ΔG、ΔH 和ΔS 表明,疏水作用力在结合过程中起主要作用。分子对接提供了阿托伐他汀与 CT-DNA 的详细计算相互作用,证明阿托伐他汀与 CT-DNA 的沟结合。切割实验表明,在实验设置下,阿托伐他汀不会诱导任何切割。最后,所有结果表明,阿托伐他汀通过沟结合模式与 CT-DNA 相互作用。

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