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解析敌百辛与小牛胸腺 DNA 相互作用的机制。

Deciphering the mechanism of interaction of edifenphos with calf thymus DNA.

机构信息

Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India.

Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2018 Jan 5;188:244-251. doi: 10.1016/j.saa.2017.07.014. Epub 2017 Jul 13.

Abstract

Edifenphos is an important organophosphate pesticide with many antifungal and anti-insecticidal properties but it may cause potential hazards to human health. In this work, we have tried to explore the binding mode of action and mechanism of edifenphos to calf thymus DNA (CT-DNA). Several experiments such as ultraviolet-visible absorption spectra and emission spectroscopy showed complex formation between edifenphos and CT-DNA and low binding constant values supporting groove binding mode. These results were further confirmed by circular dichroism (CD), CT-DNA melting studies, viscosity measurements, density functional theory and molecular docking. CD study suggests that edifenphos does not alter native structure of CT-DNA. Isothermal calorimetry reveals that binding of edifenphos with CT-DNA is enthalpy driven process. Competitive binding assay and effect of ionic strength showed that edifenphos binds to CT-DNA via groove binding manner. Hence, edifenphos is a minor groove binder preferably interacting with A-T regions with docking score -6.84kJ/mol.

摘要

敌敌畏是一种重要的有机磷农药,具有许多抗真菌和杀虫特性,但它可能对人类健康造成潜在危害。在这项工作中,我们试图探索敌敌畏与小牛胸腺 DNA(CT-DNA)的作用模式和机制。紫外可见吸收光谱和荧光光谱等实验表明,敌敌畏与 CT-DNA 形成复合物,并且结合常数值较低,支持沟结合模式。这些结果通过圆二色性(CD)、CT-DNA 熔融研究、粘度测量、密度泛函理论和分子对接进一步得到证实。CD 研究表明,敌敌畏不会改变 CT-DNA 的天然结构。等温量热法表明,敌敌畏与 CT-DNA 的结合是焓驱动过程。竞争结合实验和离子强度的影响表明,敌敌畏通过沟结合方式与 CT-DNA 结合。因此,敌敌畏是一种小沟结合物,优选与 A-T 区域相互作用,对接得分为-6.84kJ/mol。

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