Experimental and computational studies on the effects of valganciclovir as an antiviral drug on calf thymus DNA

N. Shahabadi, Mehdi Pourfoulad, Neda Hosseinpour Moghadam
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引用次数: 10

Abstract

ABSTRACT DNA-binding properties of an antiviral drug, valganciclovir (valcyte) was studied by using emission, absorption, circular dichroism, viscosity, differential pulse voltammetry, fluorescence techniques, and computational studies. The drug bound to calf thymus DNA (ct-DNA) in a groove-binding mode. The calculated binding constant of UV-vis, Ka, is comparable to groove-binding drugs. Competitive fluorimetric studies with Hoechst 33258 showed that valcyte could displace the DNA-bound Hoechst 33258. The drug could not displace intercalated methylene blue from DNA double helix. Furthermore, the induced detectable changes in the CD spectrum of ct-DNA as well as changes in its viscosity confirm the groove-binding mode. In addition, an integrated molecular docking was employed to further investigate the binding interactions between valcyte and calf thymus DNA.
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缬更昔洛韦抗病毒药物对小牛胸腺DNA影响的实验和计算研究
利用发射、吸收、圆二色性、粘度、差分脉冲伏安法、荧光技术和计算研究了抗病毒药物缬更昔洛韦(valganciclovir, valcyte)的dna结合特性。该药物以凹槽结合方式与小牛胸腺DNA (ct-DNA)结合。计算得到的UV-vis结合常数Ka与凹槽结合药物相当。与Hoechst 33258的竞争荧光研究表明,膜片细胞可以取代dna结合的Hoechst 33258。该药物不能取代DNA双螺旋上插入的亚甲基蓝。此外,ct-DNA CD谱的可检测变化及其粘度的变化证实了凹槽结合模式。此外,我们还利用整合的分子对接进一步研究了瓣膜细胞与小牛胸腺DNA的结合相互作用。
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