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微量热法和光谱法研究倍他洛尔与 DNA 的相互作用。

Microcalorimetric and spectrographic studies on the interaction of DNA with betaxolol.

机构信息

College of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, Shandong Province, PR China.

出版信息

Int J Pharm. 2010 Feb 15;386(1-2):165-71. doi: 10.1016/j.ijpharm.2009.11.015. Epub 2009 Dec 1.

Abstract

The interaction of calf thymus deoxyribonucleic acid (ct-DNA) with betaxolol (BET) in aqueous buffer solution (pH 7.40) has been investigated using isothermal titration calorimetry (ITC), ultraviolet absorption (UV), fluorescence spectroscopy (FS) and circular dichroism (CD). Thermodynamic parameters, i.e., equilibrium constants, standard changes of enthalpy (DeltaH degrees ), Gibbs free energy (DeltaG degrees) and entropy (DeltaS degrees ), for the binding process of the drug to the bio-macromolecules have been derived from the calorimetric data. Analysis of the thermodynamic data indicates that there are two classes of binding sites on the DNA molecules being able to coordinate with BET molecules. One class of binding takes place at the sites formed by base pairs, which is synergistically driven by enthalpy and entropy, while the other one takes place on phosphate groups and shown as an entropy driven process. The thermodynamic behavior of the DNA-drug supramolecular system has been discussed in the light of the important weak interactions, hydrophobic force, hydrogen bond and electrostatic force, according to the UV, FS and CD spectra.

摘要

采用等温滴定量热法(ITC)、紫外吸收光谱(UV)、荧光光谱(FS)和圆二色光谱(CD)研究了小牛胸腺 DNA(ct-DNA)与倍他洛尔(BET)在水缓冲溶液(pH 7.40)中的相互作用。从量热数据推导出了药物与生物大分子结合过程的热力学参数,即平衡常数、标准焓变(DeltaH 度)、吉布斯自由能(DeltaG 度)和熵变(DeltaS 度)。热力学数据分析表明,DNA 分子上有两类结合位点能够与 BET 分子配位。一类结合发生在碱基对形成的部位,由焓和熵协同驱动,而另一类结合发生在磷酸基团上,表现为熵驱动的过程。根据 UV、FS 和 CD 光谱,根据氢键、疏水作用力、静电相互作用等重要的弱相互作用,讨论了 DNA-药物超分子体系的热力学行为。

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