药品
DNA
化学
计算生物学
组合化学
纳米技术
生化工程
材料科学
药理学
生物
生物化学
工程类
作者
Adriana Corina Hangan,L. Oprean,Lucia Dican,Lucia Maria Procopciuc,Bogdan Sevastre,Roxana Liana Lucaciu
出处
期刊:Molecules
[MDPI AG]
日期:2024-09-13
卷期号:29 (18): 4361-4361
标识
DOI:10.3390/molecules29184361
摘要
DNA structure has many potential places where endogenous compounds and xenobiotics can bind. Therefore, xenobiotics bind along the sites of the nucleic acid with the aim of changing its structure, its genetic message, and, implicitly, its functions. Currently, there are several mechanisms known to be involved in DNA binding. These mechanisms are covalent and non-covalent interactions. The covalent interaction or metal base coordination is an irreversible binding and it is represented by an intra-/interstrand cross-link. The non-covalent interaction is generally a reversible binding and it is represented by intercalation between DNA base pairs, insertion, major and/or minor groove binding, and electrostatic interactions with the sugar phosphate DNA backbone. In the present review, we focus on the types of DNA-metal complex interactions (including some representative examples) and on presenting the methods currently used to study them.
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