开发有效的lc3靶向AUTAC工具,用于选择性自噬蛋白降解†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Junping Pei, Xiaoli Pan, Aoxue Wang, Wen Shuai, Faqian Bu, Pan Tang, Shuai Zhang, Yiwen Zhang, Guan Wang and Liang Ouyang
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引用次数: 13

摘要

基于自噬的蛋白质降解正在成为一种有前途的抗疾病和创新药物发现技术。在这里,我们展示了一种新型的自噬靶向嵌合体(AUTAC)通过靶向自噬关键蛋白LC3来降解蛋白质。最佳化合物10f通过自噬途径有效降解BRD4蛋白,并在多种肿瘤细胞中表现出良好的抗增殖活性,为药物化学家研究基于自噬的疾病相关靶点提供了强大的工具箱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Developing potent LC3-targeting AUTAC tools for protein degradation with selective autophagy†

Developing potent LC3-targeting AUTAC tools for protein degradation with selective autophagy†

Autophagy-based protein degradation is emerging as a promising technology for anti-diseases and innovative drug discovery. Here, we demonstrate a novel type of autophagy-targeting chimera (AUTAC) to degrade protein by targeting autophagy key protein LC3. The best compound 10f powerfully degraded BRD4 protein through the autophagy pathway and exhibited good anti-proliferative activity in multiple tumor cells, providing a powerful toolbox for medicinal chemists to study disease-related targets with autophagy-based degradation.

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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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