Institute of Parasitology, McGill University, Ste. Anne de Bellevue, Quebec H9X 3 V9, Canada.
Molecular Recognition Section, Laboratory of Bioorganic Chemistry, NIDDK, National Institutes of Health, 9000, Rockville Pike, Bethesda, Maryland 20892, United States.
ACS Infect Dis. 2024 Sep 13;10(9):3289-3303. doi: 10.1021/acsinfecdis.4c00394. Epub 2024 Aug 9.
RNA editing pathway is a validated target in kinetoplastid parasites (, , and spp.) that cause severe diseases in humans and livestock. An essential large protein complex, the editosome, mediates uridine insertion and deletion in RNA editing through a stepwise process. This study details the discovery of editosome inhibitors by screening a library of widely used human drugs using our previously developed biochemical Ribozyme Insertion Deletion Editing (RIDE) assay. Subsequent studies on the mode of action of the identified hits and hit expansion efforts unveiled compounds that interfere with RNA-editosome interactions and novel ligase inhibitors with IC values in the low micromolar range. Docking studies on the ligase demonstrated similar binding characteristics for ATP and our novel epigallocatechin gallate inhibitor. The inhibitors demonstrated potent trypanocidal activity and are promising candidates for drug repurposing due to their lack of cytotoxic effects. Further studies are necessary to validate these targets using more definitive gene-editing techniques and to enhance the safety profile.
RNA 编辑途径是一种已被验证的靶标,存在于引起人类和家畜严重疾病的动基体原生动物(克鲁斯锥虫、利什曼原虫和锥虫属 spp.)中。一种必需的大型蛋白复合物——编辑体,通过逐步的过程介导 RNA 编辑中的尿嘧啶插入和缺失。本研究通过使用我们之前开发的生化核酶插入缺失编辑(RIDE)测定法筛选广泛使用的人类药物文库,详细描述了编辑体抑制剂的发现。对鉴定出的命中靶点的作用模式和命中靶点扩展工作的后续研究揭示了干扰 RNA-编辑体相互作用的化合物和具有低微摩尔范围 IC 值的新型连接酶抑制剂。对连接酶的对接研究表明,ATP 和我们的新型表没食子儿茶素没食子酸酯抑制剂具有相似的结合特征。这些抑制剂表现出很强的杀变形虫活性,由于它们没有细胞毒性作用,因此是药物再利用的有前途的候选物。需要进一步的研究来使用更明确的基因编辑技术验证这些靶点,并增强其安全性。