Regulation of G protein-coupled receptor signaling by scaffold proteins.

dc.contributor.author

Hall, Randy A

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Lefkowitz, Robert J

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United States

dc.date.accessioned

2012-10-23T22:04:16Z

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2002-10-18

dc.description.abstract

The actions of many hormones and neurotransmitters are mediated through stimulation of G protein-coupled receptors. A primary mechanism by which these receptors exert effects inside the cell is by association with heterotrimeric G proteins, which can activate a wide variety of cellular enzymes and ion channels. G protein-coupled receptors can also interact with a number of cytoplasmic scaffold proteins, which can link the receptors to various signaling intermediates and intracellular effectors. The multicomponent nature of G protein-coupled receptor signaling pathways makes them ideally suited for regulation by scaffold proteins. This review focuses on several specific examples of G protein-coupled receptor-associated scaffolds and the roles they may play in organizing receptor-initiated signaling pathways in the cardiovascular system and other tissues.

dc.identifier

https://www.ncbi.nlm.nih.gov/pubmed/12386143

dc.identifier.eissn

1524-4571

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https://hdl.handle.net/10161/5917

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eng

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Ovid Technologies (Wolters Kluwer Health)

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Circ Res

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Circulation Research

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Animals

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Arrestins

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Heterotrimeric GTP-Binding Proteins

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Macromolecular Substances

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Models, Biological

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Myocardium

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Proteins

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Receptors, Adrenergic

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Receptors, Cell Surface

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Signal Transduction

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beta-Arrestins

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Regulation of G protein-coupled receptor signaling by scaffold proteins.

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Journal article

duke.description.issue

8

duke.description.volume

91

pubs.author-url

https://www.ncbi.nlm.nih.gov/pubmed/12386143

pubs.begin-page

672

pubs.end-page

680

pubs.issue

8

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Basic Science Departments

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Biochemistry

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Chemistry

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Clinical Science Departments

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Duke

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Duke Cancer Institute

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Institutes and Centers

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Medicine

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Medicine, Cardiology

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Pathology

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School of Medicine

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Trinity College of Arts & Sciences

pubs.publication-status

Published

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91

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