Morishita Ella Czarina
Basic Research Division, Veritas In Silico, Tokyo, Japan.
Expert Opin Drug Discov. 2023 Feb;18(2):207-226. doi: 10.1080/17460441.2022.2134852. Epub 2022 Nov 9.
The field of RNA-targeted small molecules is rapidly evolving, owing to the advances in experimental and computational technologies. With the identification of several bioactive small molecules that target RNA, including the FDA-approved risdiplam, the biopharmaceutical industry is gaining confidence in the field. This review, based on the literature obtained from PubMed, aims to disseminate information about the various technologies developed for targeting RNA with small molecules and propose areas for improvement to develop drugs more efficiently, particularly those linked to diseases with unmet medical needs.
The technologies for the identification of RNA targets, screening of chemical libraries against RNA, assessing the bioactivity and target engagement of the hit compounds, structure determination, and hit-to-lead optimization are reviewed. Along with the description of the technologies, their strengths, limitations, and examples of how they can impact drug discovery are provided.
Many existing technologies employed for protein targets have been repurposed for use in the discovery of RNA-targeted small molecules. In addition, technologies tailored for RNA targets have been developed. Nevertheless, more improvements are necessary, such as artificial intelligence to dissect important RNA structures and RNA-small-molecule interactions and more powerful chemical probing and structure prediction techniques.
由于实验技术和计算技术的进步,RNA靶向小分子领域正在迅速发展。随着包括美国食品药品监督管理局(FDA)批准的利司扑兰在内的几种靶向RNA的生物活性小分子的鉴定,生物制药行业对该领域的信心正在增强。本综述基于从PubMed获取的文献,旨在传播有关开发用于小分子靶向RNA的各种技术的信息,并提出改进领域,以更有效地开发药物,特别是那些与未满足医疗需求的疾病相关的药物。
综述了用于鉴定RNA靶点、针对RNA筛选化学文库、评估命中化合物的生物活性和靶点结合、结构测定以及从命中化合物到先导化合物优化的技术。除了对技术的描述外,还提供了它们的优势、局限性以及它们如何影响药物发现的实例。
许多用于蛋白质靶点的现有技术已被重新用于RNA靶向小分子的发现。此外,还开发了针对RNA靶点的技术。然而,仍需要更多改进,例如利用人工智能剖析重要的RNA结构和RNA-小分子相互作用,以及更强大的化学探测和结构预测技术。