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拓展靶向蛋白质降解的视野:非小分子视角

Expanding the horizons of targeted protein degradation: A non-small molecule perspective.

作者信息

Huang Xiaowei, Wu Fengbo, Ye Jing, Wang Lian, Wang Xiaoyun, Li Xiang, He Gu

机构信息

Department of Pharmacy and Department of Dermatology & Venerology, West China Hospital, Sichuan University, Chengdu 610041, China.

Laboratory of Dermatology, Clinical Institute of Inflammation and Immunology, Frontiers Science Center for Disease-Related Molecular Network and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Acta Pharm Sin B. 2024 Jun;14(6):2402-2427. doi: 10.1016/j.apsb.2024.01.010. Epub 2024 Jan 20.

Abstract

Targeted protein degradation (TPD) represented by proteolysis targeting chimeras (PROTACs) marks a significant stride in drug discovery. A plethora of innovative technologies inspired by PROTAC have not only revolutionized the landscape of TPD but have the potential to unlock functionalities beyond degradation. Non-small-molecule-based approaches play an irreplaceable role in this field. A wide variety of agents spanning a broad chemical spectrum, including peptides, nucleic acids, antibodies, and even vaccines, which not only prove instrumental in overcoming the constraints of conventional small molecule entities but also provided rapidly renewing paradigms. Herein we summarize the burgeoning non-small molecule technological platforms inspired by PROTACs, including three major trajectories, to provide insights for the design strategies based on novel paradigms.

摘要

以靶向蛋白质降解嵌合体(PROTAC)为代表的靶向蛋白质降解(TPD)是药物研发领域的一项重大进展。受PROTAC启发的大量创新技术不仅彻底改变了TPD的格局,而且有可能解锁降解以外的功能。基于非小分子的方法在该领域发挥着不可替代的作用。各种各样化学性质广泛的试剂,包括肽、核酸、抗体,甚至疫苗,不仅有助于克服传统小分子实体的局限性,还提供了快速更新的模式。在此,我们总结了受PROTAC启发而蓬勃发展的非小分子技术平台,包括三条主要发展轨迹,为基于新范式的设计策略提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ef/11143490/b9fb89e5f373/ga1.jpg

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