Targeted Degradation of Cell‐Surface Proteins via Chaperone‐Mediated Autophagy by Using Peptide‐Conjugated Antibodies

Author:

Shao Jinning1,Lin Xuefen1,Wang Haoting1,Zhao Chuhan1,Yao Shao Q.2,Ge Jingyan3,Zeng Su1,Qian Linghui1ORCID

Affiliation:

1. Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, National Key Laboratory of Advanced Drug Delivery and Release Systems, College of Pharmaceutical Sciences, Cancer Center, & Hangzhou Institute of Innovative Medicine Zhejiang University Hangzhou China 310058

2. Department of Chemistry National University of Singapore 4 Science Drive 2 Singapore 117544 Singapore

3. Key Laboratory of Bioorganic Synthesis of Zhejiang Province, College of Biotechnology Zhejiang University of Technology Hangzhou China 310014

Abstract

AbstractCell‐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.

Funder

National Natural Science Foundation of China

Ministry of Higher Education and Scientific Research

Publisher

Wiley

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