化学
激酶
蛋白质水解
泛素
蛋白酶体
癌症研究
小分子
蛋白质降解
泛素连接酶
氨基酸
细胞生物学
生物化学
生物
酶
基因
作者
Jianchao Zhang,Xiao Chen,Congli Chen,Fengming Li,Xiaoxiao Song,Chaowei Liu,Kai Liao,Ming-Yuan Su,Chris Soon Heng Tan,Lijing Fang,Hai Rao
标识
DOI:10.1021/acs.jmedchem.4c00208
摘要
Proteolysis-targeting chimeras (PROTACs) selectively eliminate detrimental proteins by exploiting the ubiquitin-proteasome system (UPS), representing a promising therapeutic strategy against various diseases. Effective adaptations of degradation signal sequences and E3 ligases for PROTACs remain limited. Here, we employed three amino acids─Gly, Pro, and Lys─as the ligand to recruit the corresponding E3 ligases: CRL2
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