Development of Antibody-Based PROTACs for the Degradation of the Cell-Surface Immune Checkpoint Protein PD-L1

被引:292
作者
Cotton, Adam D. [1 ]
Nguyen, Duy P. [1 ]
Gramespacher, Josef A. [1 ]
Seiple, Ian B. [1 ,2 ]
Wells, James A. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
关键词
RNF43; UBIQUITINATION; DISCOVERY; KNOCKDOWN; PLATFORM; LIGASE;
D O I
10.1021/jacs.0c10008
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:593 / 598
页数:6
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