化学
计算生物学
药物发现
蛋白质降解
合理设计
蛋白质工程
降级(电信)
翻译(生物学)
纳米技术
蛋白质-蛋白质相互作用
细胞生物学
靶蛋白
合成生物学
化学生物学
生物化学
药品
靶向给药
转化式学习
机制(生物学)
药物开发
底物特异性
生化工程
药物设计
蛋白质设计
作者
Yixuan Wang,Jingyuan Zhao,Hong Yuan,Shuai Li
标识
DOI:10.1021/acs.jmedchem.5c02379
摘要
Peptide-based targeted protein degradation (TPD) has emerged as a transformative approach in drug discovery, enabling selective elimination of disease-associated proteins. This review summarizes advances in peptide-driven degradation technologies, covering ubiquitin-proteasome system-based strategies such as Peptide-based PROTACs (P-PROTACs) and hydrophobic tagging (HyT). It also highlights lysosome-targeting strategies-exemplified by lysosome-targeting chimeras (LYTACs)-that utilize the endocytosis-lysosome pathway for degrading extracellular and membrane proteins. Emerging autophagy-based approaches, including autophagosome-tethering compounds (ATTECs), further expand the degradable protein landscape. Additionally, peptide-based nanoself-assembly strategies are discussed as promising means to enhance targeting precision. The review covers fundamental principles, molecular design strategies, mechanisms, recent progress, and limitations of each platform. These innovations advance our understanding of cellular degradation pathways and offer promising therapeutic avenues for complex diseases, guiding the rational design and clinical translation of peptide-based degraders in next-generation precision medicine.
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