用于体内高效降解目标蛋白质的多功能拆分混合脂质体 PROTAC 平台

JACS Au Pub Date : 2024-07-11 DOI:10.1021/jacsau.4c00278
Chunli Song, Zijun Jiao, Zhanfeng Hou, Yun Xing, Xinrui Sha, Yuechen Wang, Jiaxin Chen, Susheng Liu, Zigang Li, Feng Yin
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引用次数: 0

摘要

PROTAC(Proteolysis TArgeting Chimeras)是一种很有前景的靶向蛋白质降解治疗方法,它能将E3泛素连接酶招募到特定的相关蛋白质(POI)上,从而使其被蛋白酶体降解。最近,我们开发了一种基于脂质体自组装的新型分离混合 PROTAC 系统(LipoSM-PROTAC),它能以与小分子相当的浓度实现目标蛋白降解。在本研究中,我们基于 LipoSM-PROTAC 平台扩展了蛋白质靶点,并进一步研究了其在体内的治疗效果。值得注意的是,该平台可高效降解 A375 细胞中的 MEK1/2 蛋白水平或 NCI-H2228 细胞中的 Alk 蛋白水平,并显示出明显的肿瘤抑制作用(抑制率达 60-70%),且毒性可忽略不计。这项研究进一步证明了 LipoSM-PROTAC 的应用潜力。
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Versatile Split-and-Mix Liposome PROTAC Platform for Efficient Degradation of Target Protein In Vivo
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.
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