泛素连接酶
化学
细胞生物学
泛素
蛋白质降解
蛋白质稳态
蛋白质水解
重组DNA
生物化学
生物
酶
基因
作者
Adam D. Cotton,Duy Nguyen,Josef A. Gramespacher,Ian B. Seiple,James A. Wells
摘要
Targeted protein degradation has emerged as a new paradigm to manipulate cellular proteostasis. Proteolysis-targeting chimeras (PROTACs) are bifunctional small molecules that recruit an E3 ligase to a target protein of interest, promoting its ubiquitination and subsequent degradation. Here, we report the development of antibody-based PROTACs (AbTACs), fully recombinant bispecific antibodies that recruit membrane-bound E3 ligases for the degradation of cell-surface proteins. We show that an AbTAC can induce the lysosomal degradation of programmed death-ligand 1 by recruitment of the membrane-bound E3 ligase RNF43. AbTACs represent a new archetype within the PROTAC field to target cell-surface proteins with fully recombinant biological molecules.
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