Versatile Split-and-Mix Liposome PROTAC Platform for Efficient Degradation of Target Protein In Vivo

被引:1
|
作者
Song, Chunli [1 ]
Jiao, Zijun [2 ,3 ]
Hou, Zhanfeng [1 ]
Xing, Yun [1 ]
Sha, Xinrui [2 ]
Wang, Yuechen [1 ]
Chen, Jiaxin [2 ]
Liu, Susheng [2 ]
Li, Zigang [1 ,2 ]
Yin, Feng [1 ,2 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, State Key Lab Chem Oncogen, Shenzhen 518055, Peoples R China
[2] Pingshan Translat Med Ctr, Shenzhen Bay Lab, Shenzhen 518118, Peoples R China
[3] Frontiers Med Ctr, Tianfu Jincheng Lab, Chengdu 610212, Sichuan, Peoples R China
来源
JACS AU | 2024年 / 4卷 / 08期
基金
国家重点研发计划;
关键词
split-and-mix; LipoSM-PROTAC; protein degradation; in vivo therapeutic; tumor inhibition; MEK INHIBITOR PD0325901; GROWTH;
D O I
10.1021/jacsau.4c00278
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
PROTAC (Proteolysis TArgeting Chimeras) is a promising therapeutic approach for targeted protein degradation that recruits an E3 ubiquitin ligase to a specific protein of interest (POI), leading to its degradation by the proteasome. Recently, we developed a novel split-and-mix PROTAC system based on liposome self-assembly (LipoSM-PROTAC) which could achieve target protein degradation at comparable concentrations comparable to small molecules. In this study, we expanded protein targets based on the LipoSM-PROTAC platform and further examined its therapeutic effects in vivo. Notably, this platform could efficiently degrade the protein level of MEK1/2 in A375 cells or Alk in NCI-H2228 cells and display obvious tumor inhibition (60-70% inhibition rate) with negligible toxicity. This study further proved the LipoSM-PROTAC's application potentials.
引用
收藏
页码:2915 / 2924
页数:10
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