Antibody-Proteolysis Targeting Chimera Conjugate Enables Selective Degradation of Receptor-Interacting Serine/Threonine-Protein Kinase 2 in HER2+ Cell Lines
Author:
Affiliation:
1. GSK, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom
2. Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow G1 1XL, United Kingdom
Funder
Engineering and Physical Sciences Research Council
University of Strathclyde
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.3c00366
Reference31 articles.
1. PROTAC targeted protein degraders: the past is prologue
2. Discovery of small molecule ligands for the von Hippel-Lindau (VHL) E3 ligase and their use as inhibitors and PROTAC degraders
3. Protacs: Chimeric molecules that target proteins to the Skp1-Cullin-F box complex for ubiquitination and degradation
4. Catalytic in vivo protein knockdown by small-molecule PROTACs
5. Homobivalent, Trivalent, and Covalent PROTACs: Emerging Strategies for Protein Degradation
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