Journal article

Lipid-Dependent Activation of the Orphan G Protein-Coupled Receptor, GPR3

Isabella C Russell, Xin Zhang, Fabian Bumbak, Samantha M McNeill, Tracy M Josephs, Michael G Leeming, George Christopoulos, Hariprasad Venugopal, Maria M Flocco, Patrick M Sexton, Denise Wootten, Matthew J Belousoff

Biochemistry | American Chemical Society | Published : 2024

Abstract

The class A orphan G protein-coupled receptor (GPCR), GPR3, has been implicated in a variety of conditions, including Alzheimer’s and premature ovarian failure. GPR3 constitutively couples with Gαs, resulting in the production of cAMP in cells. While tool compounds and several putative endogenous ligands have emerged for the receptor, its endogenous ligand, if it exists, remains a mystery. As novel potential drug targets, the structures of orphan GPCRs have been of increasing interest, revealing distinct modes of activation, including autoactivation, presence of constitutively activating mutations, or via cryptic ligands. Here, we present a cryo-electron microscopy (cryo-EM) structure of the..

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University of Melbourne Researchers

Grants

Funding Acknowledgements

This work was supported by resources from the Bio21 Institute Ian Holmes Imaging Centre, the Monash Massive M3 computational infrastructure, and the Monash Ramaciotti Centre for Cryo-Electron Microscopy. We acknowledge the use and assistance of the Bio21 Mass Spectrometry and Proteomics Facility at the University of Melbourne.