Gomez-Gutierrez Patricia, Perez Juan J
Departament d'Enginyeria Química, Universitat Politècnica de Catalunya-Barcelona Tech, Edifici ETSEIB, Av. Diagonal 647, 08028 Barcelona, Catalonia, Spain.
Pharmaceuticals (Basel). 2025 Sep 15;18(9):1377. doi: 10.3390/ph18091377.
Proteases constitute one of the largest sub-classes of enzymes, accounting for ca. 2% of the proteins encoded in the human genome. They play a key role in protein degradation and signaling, regulating a variety of physiological processes. Dysregulation of their activity is associated with various pathological conditions like cancer, neurodegenerative disorders, inflammatory or cardiovascular diseases. Protease activity can be controlled by regulating enzyme concentrations, but also by inhibitors, molecules that modulate enzyme function, inspiring the development of small molecule protease inhibitors for therapeutic purposes. Protease inhibitors can be designed from the corresponding substrates by isostere replacement at the scissile bond. This process yields a first-generation of inhibitors that usually exhibit poor drug-like profiles that need subsequently be improved to generate a second-generation, by smoothing their peptide-like features. This process is reviewed in the present report and exemplified in the successful discovery stories of different inhibitors that correspond to four types of proteases, including the angiotensin converting enzyme (metalloprotease); HIV protease (aspartate protease); thrombin (serine protease) and the proteasome (threonine protease). A detailed description of the stories behind their design from their initial discovery to the final product is described in this report. Moreover, despite successful discovery stories, the challenges associated with designing novel protease inhibitors are examined. Finally, the relevance of these drugs in the present drug market is also reported.
蛋白酶是酶类中最大的亚类之一,约占人类基因组编码蛋白质的2%。它们在蛋白质降解和信号传导中起关键作用,调节多种生理过程。其活性失调与多种病理状况相关,如癌症、神经退行性疾病、炎症或心血管疾病。蛋白酶活性可通过调节酶浓度来控制,但也可通过抑制剂来控制,抑制剂是调节酶功能的分子,这激发了用于治疗目的的小分子蛋白酶抑制剂的开发。蛋白酶抑制剂可通过在可裂解键处进行等排体置换,从相应底物设计而来。这一过程产生第一代抑制剂,其通常表现出较差的类药特性,随后需要通过改善其类肽特征来改进,以产生第二代抑制剂。本报告对这一过程进行了综述,并以对应四种蛋白酶的不同抑制剂的成功发现案例进行了举例说明,这四种蛋白酶包括血管紧张素转换酶(金属蛋白酶);HIV蛋白酶(天冬氨酸蛋白酶);凝血酶(丝氨酸蛋白酶)和蛋白酶体(苏氨酸蛋白酶)。本报告详细描述了从最初发现到最终产品的设计背后的故事。此外,尽管有成功的发现案例,但也探讨了设计新型蛋白酶抑制剂所面临的挑战。最后,还报告了这些药物在当前药物市场中的相关性。