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G-四链体结合配体:从天然存在到合理设计的分子。

G-quadruplex binding ligands: from naturally occurring to rationally designed molecules.

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon, Korea.

出版信息

Curr Pharm Des. 2012;18(14):1948-72. doi: 10.2174/138161212799958431.

Abstract

Guanine-rich nucleic acid sequences are known to form G-quadruplex - four-stranded DNA or RNA structures stabilized by an array of Hoogsteen hydrogen bonds. G-quadruplex structures are involved in the modulation of gene expression at the transcription and translation levels. Accordingly, G-quadruplexes are considered as novel therapeutic targets for anticancer drug development. In this review, the authors provide a brief, up-to-date summary of G-quadruplex binding ligands, including naturally occurring molecules, synthetic compounds, and molecules identified by computational database screening. The key structural motifs of G-quadruplex binding ligands, that is, an aromatic core and basic side chains, are addressed in the context of how these molecules interact with G-quadruplex. A better understanding of these interactions would facilitate the rational design of ligands selective for DNA or RNA G-quadruplex.

摘要

富含鸟嘌呤的核酸序列已知能形成 G-四链体——一种由一系列 Hoogsteen 氢键稳定的四链 DNA 或 RNA 结构。G-四链体结构参与转录和翻译水平的基因表达调控。因此,G-四链体被认为是抗癌药物开发的新型治疗靶点。在这篇综述中,作者简要、最新地总结了 G-四链体结合配体,包括天然存在的分子、合成化合物以及通过计算数据库筛选鉴定的分子。在讨论这些分子与 G-四链体相互作用时,提到了 G-四链体结合配体的关键结构基序,即芳香核心和碱性侧链。更好地理解这些相互作用将有助于设计选择性结合 DNA 或 RNA G-四链体的配体。

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