Review of the impact of fragment-based drug design on PROTAC degrader discovery

被引:4
作者
Chen, Peiqi [1 ]
Li, Qiang [1 ]
Lei, Xiaoguang [1 ,2 ,3 ]
机构
[1] Shenzhen Bay Lab, Inst Canc Res, Shenzhen 518132, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Dept Chem Biol, Key Lab Bioorgan Chem & Mol Engn,Beijing Natl Lab, Beijing 100871, Peoples R China
[3] Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
Proteolysis targeting chimera (PROTAC); Ubiquitin; Fragment-based drug design (FBDD); Degrader discovery; BCL-2; FAMILY; HIT IDENTIFICATION; PRACTICAL ASPECTS; LEAD DISCOVERY; PROTEINS; TARGET; CANCER; OPPORTUNITIES; OPTIMIZATION; DEGRADATION;
D O I
10.1016/j.trac.2024.117539
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Proteolysis targeting chimera (PROTAC) is an emerging therapeutic strategy using small molecules to induce ubiquitin-dependent degradation of proteins. Fragment-based drug design (FBDD) has achieved great success in the discovery of highly active PROTAC molecules. Here, we highlight the progress of FBDD in screening PROTAC molecules. Key features of the FBDD method and the procedure of designing PROTAC molecules by FBDD are summarized and analyzed. PROTAC molecules that is entered clinical studies has introduced as case studies to help understand the fragment-to-PROTAC optimization process. We also present the future trends of applying the FBDD method to screen PROTAC molecules. Thus, this review will provide helpful guidance for new PROTAC discoveries.
引用
收藏
页数:10
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