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Biochemistry. 2023 Feb 7;62(3):601-623. doi: 10.1021/acs.biochem.2c00245. Epub 2022 Jul 20.
Targeted protein degradation is a rapidly exploding drug discovery strategy that uses small molecules to recruit disease-causing proteins for rapid destruction mainly via the ubiquitin-proteasome pathway. It shows great potential for treating diseases such as cancer and infectious, inflammatory, and neurodegenerative diseases, especially for those with "undruggable" pathogenic protein targets. With the recent rise of the "molecular glue" type of protein degraders, which tighten and simplify the connection of an E3 ligase with a disease-causing protein for ubiquitination and subsequent degradation, new therapies for unmet medical needs are being designed and developed. Here we use data from the CAS Content Collection and the publication landscape of recent research on targeted protein degraders to provide insights into these molecules, with a special focus on molecular glues. We also outline the advantages of the molecular glues and summarize the advances in drug discovery practices for molecular glue degraders. We further provide a thorough review of drug candidates in targeted protein degradation through E3 ligase recruitment. Finally, we highlight the progression of molecular glues in drug discovery pipelines and their targeted diseases. Overall, our paper provides a comprehensive reference to support the future development of molecular glues in medicine.
靶向蛋白降解是一种快速发展的药物发现策略,它使用小分子招募致病蛋白进行快速破坏,主要通过泛素-蛋白酶体途径。它在治疗癌症和传染病、炎症和神经退行性疾病等疾病方面具有巨大的潜力,特别是对于那些具有“不可成药”的致病蛋白靶标的疾病。随着最近“分子胶水”型蛋白降解剂的兴起,它简化并加强了 E3 连接酶与致病蛋白的连接,用于泛素化和随后的降解,新的治疗方法正在为未满足的医疗需求而设计和开发。在这里,我们使用来自 CAS 内容集和最近靶向蛋白降解研究的出版物景观的数据,提供对这些分子的深入了解,特别关注分子胶水。我们还概述了分子胶水的优势,并总结了分子胶水降解剂药物发现实践的进展。我们进一步通过 E3 连接酶招募全面审查了靶向蛋白降解的候选药物。最后,我们强调了分子胶水在药物发现管道及其靶向疾病中的进展。总的来说,我们的论文提供了一个全面的参考,以支持未来在医学领域中分子胶水的发展。