核糖核酸
计算生物学
核糖开关
小分子
配体(生物化学)
药物发现
片段(逻辑)
化学空间
生物
化学
生物化学
非编码RNA
受体
计算机科学
基因
程序设计语言
作者
Jordan T. Koehn,Simon Felder,Kevin M. Weeks
标识
DOI:10.1016/j.sbi.2023.102550
摘要
A subset of functional regions within large RNAs fold into complex structures able to bind small-molecule ligands with high affinity and specificity. Fragment-based ligand discovery (FBLD) offers notable opportunities for discovery and design of potent small molecules that bind pockets in RNA. Here we share an integrated analysis of recent innovations in FBLD, emphasizing opportunities resulting from fragment elaboration via both linking and growing. Analysis of elaborated fragments emphasizes that high–quality interactions form with complex tertiary structures in RNA. FBLD-inspired small molecules have been shown to modulate RNA functions by competitively inhibiting protein binding and by selectively stabilizing dynamic RNA states. FBLD is creating a foundation to interrogate the relatively unknown structural space for RNA ligands and for discovery of RNA-targeted therapeutics.
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