β-Arrestin condensates regulate G-protein-coupled receptor function.
β-Arrestins 1 and 2 are multifunctional adaptor proteins1 that regulate the signalling of G-protein-coupled receptors (GPCRs), the largest class of receptors, which impact nearly all aspects of physiology and are one of the most common drug targets2. Although β-arrestins interact with a wide array of signalling effectors at many GPCRs, it is unclear how β-arrestins promote such varied functions. Here we show that β-arrestins undergo liquid-liquid phase separation, forming condensates that regulate GPCR function. We show that condensation is specific to visual arrestins and β-arrestins, and demonstrate that β-arrestin oligomerization occurs in proximity to the GPCR to regulate GPCR functions such as internalization and signalling. Our work provides a paradigm for β-arrestin condensates as regulators of GPCR function, with liquid-liquid phase separation serving as an important promoter of signalling compartmentalization at GPCRs.
Duke Scholars
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- beta-Arrestins
- Signal Transduction
- Receptors, G-Protein-Coupled
- Protein Multimerization
- Phase Separation
- Humans
- HEK293 Cells
- General Science & Technology
- Endocytosis
- Biomolecular Condensates
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- beta-Arrestins
- Signal Transduction
- Receptors, G-Protein-Coupled
- Protein Multimerization
- Phase Separation
- Humans
- HEK293 Cells
- General Science & Technology
- Endocytosis
- Biomolecular Condensates