Department of Biopharmacy, Medical University of Lublin, Ul.W.Chodzki 4a, 20-093 Lublin, Poland.
Eur J Med Chem. 2024 Dec 5;279:116837. doi: 10.1016/j.ejmech.2024.116837. Epub 2024 Sep 10.
Proteolysis-Targeting Chimeras (PROTACs) are a novel class of bifunctional small molecules that alter protein levels by targeted degradation. This innovative approach uses the ubiquitin-proteasome system to selectively eradicate disease-associated proteins, providing a novel therapeutic strategy for a wide spectrum of diseases. This review delineates detailed synthetic approaches involved in PROTAC building blocks, including the ligand and protein binding parts, linker attached structural components of PROTACs and the actual PROTAC molecules. Furthermore, the recent advancements in PROTAC-mediated degradation of specific oncogenic and other disease-associated proteins, such as those involved in neurodegenerative, antiviral, and autoimmune diseases, were also discussed. Additionally, we described the current landscape of PROTAC clinical trials and highlighted key studies that underscore the translational potential of this emerging therapeutic modality. These findings demonstrate the versatility of PROTACs in modulating the levels of key proteins involved in various severe diseases.
蛋白水解靶向嵌合体(PROTACs)是一类新型的双功能小分子,通过靶向降解来改变蛋白质水平。这种创新方法利用泛素-蛋白酶体系统选择性地清除与疾病相关的蛋白质,为广泛的疾病提供了一种新的治疗策略。本综述详细描述了 PROTAC 构建块中涉及的合成方法,包括配体和蛋白质结合部分、PROTAC 连接子附着的结构组件以及实际的 PROTAC 分子。此外,还讨论了 PROTAC 介导的特定致癌和其他与疾病相关的蛋白质(如神经退行性疾病、抗病毒和自身免疫性疾病相关的蛋白质)降解的最新进展。此外,我们还描述了 PROTAC 临床试验的现状,并强调了突显这种新兴治疗模式转化潜力的关键研究。这些发现表明 PROTACs 在调节各种严重疾病中关键蛋白水平方面的多功能性。