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Trends Pharmacol Sci. 2011 Sep;32(9):521-33. doi: 10.1016/j.tips.2011.05.002. Epub 2011 Jun 15.

β-Arrestin-mediated receptor trafficking and signal transduction.

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1
Department of Medicine, Duke University Medical Center, Box 3821, Durham, NC 27710, USA. sudha@receptor-biol.duke.edu

Abstract

β-Arrestins function as endocytic adaptors and mediate trafficking of a variety of cell-surface receptors, including seven-transmembrane receptors (7TMRs). In the case of 7TMRs, β-arrestins carry out these tasks while simultaneously inhibiting upstream G-protein-dependent signaling and promoting alternate downstream signaling pathways. The mechanisms by which β-arrestins interact with a continuously expanding ensemble of protein partners and perform their multiple functions including trafficking and signaling are currently being uncovered. Molecular changes at the level of protein conformation as well as post-translational modifications of β-arrestins probably form the basis for their dynamic interactions during receptor trafficking and signaling. It is becoming increasingly evident that β-arrestins, originally discovered as 7TMR adaptor proteins, indeed have much broader and more versatile roles in maintaining cellular homeostasis. In this review paper, we assess the traditional and novel functions of β-arrestins and discuss the molecular attributes that might facilitate multiple interactions in regulating cell signaling and receptor trafficking.

PMID:
21680031
PMCID:
PMC3159699
DOI:
10.1016/j.tips.2011.05.002
[Indexed for MEDLINE]
Free PMC Article
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