Literature DB >> 28600951

Structural mechanism of arrestin activation.

Patrick Scheerer1, Martha E Sommer2.   

Abstract

The large and multifunctional family of G protein-coupled receptors (GPCRs) are regulated by a small family of structurally conserved arrestin proteins. In order to bind an active GPCR, arrestin must first be activated by interaction with the phosphorylated receptor C-terminus. Recent years have witnessed major developments in high-resolution crystal structures of pre-active arrestins and arrestin or arrestin-derived peptides in complex with an active GPCR. Although each structure individually offers only a limited snapshot, taken together and interpreted in light of recent complementary functional data, they offer valuable insight into how arrestin is activated by and couples to a phosphorylated active GPCR.
Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Year:  2017        PMID: 28600951     DOI: 10.1016/j.sbi.2017.05.001

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  23 in total

Review 1.  Many faces of the GPCR-arrestin interaction.

Authors:  Kiae Kim; Ka Young Chung
Journal:  Arch Pharm Res       Date:  2020-08-14       Impact factor: 4.946

Review 2.  Structure and dynamics of GPCR signaling complexes.

Authors:  Daniel Hilger; Matthieu Masureel; Brian K Kobilka
Journal:  Nat Struct Mol Biol       Date:  2018-01-08       Impact factor: 15.369

3.  The arrestin-1 finger loop interacts with two distinct conformations of active rhodopsin.

Authors:  Matthias Elgeti; Roman Kazmin; Alexander S Rose; Michal Szczepek; Peter W Hildebrand; Franz J Bartl; Patrick Scheerer; Klaus Peter Hofmann
Journal:  J Biol Chem       Date:  2018-01-23       Impact factor: 5.157

Review 4.  GPCR drug discovery: integrating solution NMR data with crystal and cryo-EM structures.

Authors:  Ichio Shimada; Takumi Ueda; Yutaka Kofuku; Matthew T Eddy; Kurt Wüthrich
Journal:  Nat Rev Drug Discov       Date:  2018-11-09       Impact factor: 84.694

5.  Structure-function analysis of β-arrestin Kurtz reveals a critical role of receptor interactions in downregulation of GPCR signaling in vivo.

Authors:  Fei Chai; Wenjian Xu; Timothy Musoke; George Tarabelsi; Steven Assaad; Jason Freedman; Rachel Peterson; Katarzyna Piotrowska; Jarrett Byrnes; Stephen Rogers; Alexey Veraksa
Journal:  Dev Biol       Date:  2019-07-17       Impact factor: 3.582

Review 6.  Endo-lysosomal sorting of G-protein-coupled receptors by ubiquitin: Diverse pathways for G-protein-coupled receptor destruction and beyond.

Authors:  Michael R Dores; JoAnn Trejo
Journal:  Traffic       Date:  2018-11-18       Impact factor: 6.215

Review 7.  The structural basis of the arrestin binding to GPCRs.

Authors:  Vsevolod V Gurevich; Eugenia V Gurevich
Journal:  Mol Cell Endocrinol       Date:  2019-01-28       Impact factor: 4.102

8.  A non-GPCR-binding partner interacts with a novel surface on β-arrestin1 to mediate GPCR signaling.

Authors:  Ya Zhuo; Vsevolod V Gurevich; Sergey A Vishnivetskiy; Candice S Klug; Adriano Marchese
Journal:  J Biol Chem       Date:  2020-08-04       Impact factor: 5.157

Review 9.  Structural Basis of Arrestin-Dependent Signal Transduction.

Authors:  Qiuyan Chen; Tina M Iverson; Vsevolod V Gurevich
Journal:  Trends Biochem Sci       Date:  2018-04-07       Impact factor: 13.807

10.  Crystal Structure of β-Arrestin 2 in Complex with CXCR7 Phosphopeptide.

Authors:  Kyungjin Min; Hye-Jin Yoon; Ji Young Park; Mithu Baidya; Hemlata Dwivedi-Agnihotri; Jagannath Maharana; Madhu Chaturvedi; Ka Young Chung; Arun K Shukla; Hyung Ho Lee
Journal:  Structure       Date:  2020-06-23       Impact factor: 5.006

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