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G Protein-Coupled Receptors in the Sweet Spot: Glycosylation and other Post-translational Modifications

Christoffer K. Goth, Ulla E. Petäjä‐Repo, Mette M. Rosenkilde

2020ACS Pharmacology & Translational Science75 citationsDOIOpen Access PDF

Abstract

Post-translational modifications (PTMs) are a fundamental phenomenon across all classes of life and several hundred different types have been identified. PTMs contribute widely to the biological functions of proteins and greatly increase their diversity. One important class of proteins regulated by PTMs, is the cell surface expressed G protein-coupled receptors (GPCRs). While most PTMs have been shown to exert distinct biological functions, we are only beginning to approach the complexity that the potential interplay between different PTMs may have on biological functions and their regulation. Importantly, PTMs and their potential interplay represent an appealing mechanism for cell and tissue specific regulation of GPCR function and may partially contribute to functional selectivity of some GPCRs. In this review we highlight examples of PTMs located in GPCR extracellular domains, with special focus on glycosylation and the potential interplay with other close-by PTMs such as tyrosine sulfation, proteolytic cleavage, and phosphorylation.

Topics & Concepts

G protein-coupled receptorGlycosylationPhosphorylationPosttranslational modificationReceptorFunction (biology)BiologyComputational biologyCell biologyCrosstalkChemistryBiochemistryPhysicsOpticsEnzymeReceptor Mechanisms and SignalingNeuropeptides and Animal PhysiologyChemokine receptors and signaling
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