自噬
表皮生长因子受体
伴侣(临床)
泛素连接酶
肽
抗体
蛋白质降解
单克隆抗体
化学
细胞
细胞生物学
受体
泛素
生物化学
生物
医学
免疫学
细胞凋亡
病理
基因
作者
Jinning Shao,Xiangtao Lin,Haoting Wang,Chenchen Zhao,Shao Q. Yao,Jingyan Ge,Su Zeng,Linghui Qian
标识
DOI:10.1002/anie.202319232
摘要
Cell-surface proteins are important drug targets but historically have posed big challenges for the complete elimination of their functions. Herein, we report antibody-peptide conjugates (Ab-CMAs) in which a peptide targeting chaperone-mediated autophagy (CMA) was conjugated with commercially available monoclonal antibodies for specific cell-surface protein degradation by taking advantage of lysosomal degradation pathways. Unique features of Ab-CMAs, including cell-surface receptor- and E3 ligase-independent degradation, feasibility towards different cell-surface proteins (e.g., epidermal growth factor receptor (EGFR), programmed cell death ligand 1 (PD-L1), human epidermal growth factor receptor 2 (HER2)) by a simple change of the antibody, and successful tumor inhibition in vivo, make them attractive protein degraders for biomedical research and therapeutic applications. As the first example employing CMA to degrade proteins from the outside in, our findings may also shed new light on CMA, a degradation pathway typically targeting cytosolic proteins.
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