Zhu Jinhua, Chen Lanlan, Dong Yingying, Li Jiazhong, Liu Xiuhua
Institute of Environmental and Analytical Sciences, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004, China.
Institute of Environmental and Analytical Sciences, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Apr 24;124:78-83. doi: 10.1016/j.saa.2013.12.091. Epub 2014 Jan 6.
In this work, the interaction of 5-Hydroxymethyl-2-furfural (5-HMF) with calf thymus DNA (ctDNA) under simulated physiological conditions (Tris-HCl buffer of pH 7.40), was explored by UV absorption spectroscopy, fluorescence spectroscopy and molecular modeling method, using ethidium bromide (EB) as a fluorescence probe of DNA. The fluorescence quenching mechanism of EB-ctDNA by 5-HMF was confirmed to be a static quenching, which derived from the formation of a new complex. The binding constants of 5-HMF with DNA in the presence of EB were calculated to be 2.17×10(3), 4.24×10(3) and 6.95×10(3) L mol(-1) at 300, 305 and 310 K, respectively. The calculated thermodynamic parameters, enthalpy change ΔH and entropy change ΔS, suggested that both hydrophobic interactions and hydrogen bonds played a predominant role in the binding of 5-HMF to DNA. According to the UV absorption spectroscopy and melting temperature (Tm) curve results, the binding mode of 5-HMF with DNA was indicative of a non-intercalative binding, which was supposed to be a groove binding. The molecular modeling results showed that 5-HMF could bind into the hydrophobic region of ctDNA and supported the conclusions obtained from the above experiments.
在本研究中,以溴化乙锭(EB)作为DNA的荧光探针,采用紫外吸收光谱、荧光光谱和分子模拟方法,探究了5-羟甲基糠醛(5-HMF)在模拟生理条件(pH 7.40的Tris-HCl缓冲液)下与小牛胸腺DNA(ctDNA)的相互作用。证实5-HMF对EB-ctDNA的荧光猝灭机制为静态猝灭,源于新复合物的形成。在300、305和310 K时,5-HMF与存在EB时DNA的结合常数分别计算为2.17×10³、4.24×10³和6.95×10³ L mol⁻¹。计算得到的热力学参数,焓变ΔH和熵变ΔS,表明疏水相互作用和氢键在5-HMF与DNA的结合中均起主要作用。根据紫外吸收光谱和熔解温度(Tm)曲线结果,5-HMF与DNA的结合模式表明为非嵌入结合,推测为沟槽结合。分子模拟结果表明,5-HMF可结合到ctDNA的疏水区域,支持了上述实验所得结论。