The application of targeted protein degradation technologies to G protein‐coupled receptors

Author:

Keen Alastair C.1ORCID,Jörg Manuela23ORCID,Halls Michelle L.1ORCID

Affiliation:

1. Drug Discovery Biology Theme, Monash Institute of Pharmaceutical Sciences Monash University 399 Royal Parade Parkville 3052 Victoria Australia

2. Medicinal Chemistry Theme, Monash Institute of Pharmaceutical Sciences Monash University 399 Royal Parade Parkville 3052 Victoria Australia

3. Newcastle University Centre for Cancer, Chemistry – School of Natural and Environmental Sciences Newcastle University Bedson Building Newcastle Upon Tyne NE1 7RU UK

Abstract

The ubiquitin‐proteasome system is one of the major pathways for the degradation of cellular proteins. In recent years, methods have been developed to exploit the ubiquitin‐proteasome system to artificially degrade target proteins. Targeted protein degraders are extremely useful as biological tools for discovery research. They have also been developed as novel therapeutics with several targeted protein degraders currently in clinical trials. However, almost all targeted protein degrader technologies have been developed for cytosolic proteins. The G protein‐coupled receptor (GPCR) superfamily is one of the most important classes of drug targets, yet only limited examples of GPCR degradation exist. Here, we review these examples and provide a perspective on the different strategies that have been used to apply targeted protein degradation to GPCRs. We also discuss whether alternative approaches that have been used to degrade other integral membrane proteins could be applied to the degradation of GPCRs.

Funder

Sylvia and Charles Viertel Charitable Foundation

Research England

Publisher

Wiley

Subject

Pharmacology

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