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PMID: 21680031 Published · ppublish English Journal Article Review

β-Arrestin-mediated receptor trafficking and signal transduction.

Trends in pharmacological sciences ·Vol. 32 ·No. 9 ·2011-09-00 ·Pages 521-33

Shenoy SK, Lefkowitz RJ

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.

MeSH Terms
Animals Arrestins/metabolism Humans Protein Conformation Protein Processing, Post-Translational Protein Transport Receptors, G-Protein-Coupled/metabolism Signal Transduction beta-Arrestins
Chemicals
Arrestins Receptors, G-Protein-Coupled beta-Arrestins seven-transmembrane G-protein-coupled receptor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Shenoy Sudha K
Department of Medicine, Duke University Medical Center, Box 3821, Durham, NC 27710, USA. sudha@receptor-biol.duke.edu
Lefkowitz Robert J
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Article Info
Journal
Trends in pharmacological sciences
Abbr.
Trends Pharmacol Sci
ISSN
1873-3735
Published
2011-09-00
Epub
2011-00-15
Pages
521-33
Language
English
Region
England
NLM ID
7906158
PMCID
PMC3159699
Subset
IM
Grants
NHLBI NIH HHS · R01 HL016037-40 · United States
NHLBI NIH HHS · R01 HL016037 · United States
NHLBI NIH HHS · R01 HL080525-06 · United States
NHLBI NIH HHS · R01 HL080525 · United States
NHLBI NIH HHS · R01 HL070631 · United States
NHLBI NIH HHS · R01 HL070631-09 · United States
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