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PMID: 18379987 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Mechanism of light-induced translocation of arrestin and transducin in photoreceptors: interaction-restricted diffusion.

IUBMB life ·Vol. 60 ·No. 1 ·2008-01-00 ·Pages 2-9

Slepak VZ, Hurley JB

Abstract

Many signaling proteins change their location within cells in response to external stimuli. In photoreceptors, this phenomenon is remarkably robust. The G protein of rod photoreceptors and rod transducin concentrates in the outer segments (OS) of these neurons in darkness. Within approximately 30 minutes after illumination, rod transducin redistributes throughout all of the outer and inner compartments of the cell. Visual arrestin concurrently relocalises from the inner compartments to become sequestered primarily within the OS. In the past several years, the question of whether these proteins are actively moved by molecular motors or whether they are redistributed by simple diffusion has been extensively debated. This review focuses on the most essential works in the area and concludes that the basic principle driving this protein movement is diffusion. The directionality and light dependence of this movement is achieved by the interactions of arrestin and transducin with their spatially restricted binding partners.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Arrestin/metabolism Diffusion Light Molecular Motor Proteins/physiology Photoreceptor Cells/physiology,radiation effects Protein Transport Rhodopsin/physiology Signal Transduction Transducin/metabolism
Chemicals
Arrestin Molecular Motor Proteins Adenosine Triphosphate Rhodopsin Transducin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Slepak Vladlen Z
Department of Molecular and Cellular Pharmacology and Neuroscience Program, University of Miami Miller School of Medicine, Miami, FL, USA. V.Slepak@miami.edu
Hurley James B
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Article Info
Journal
IUBMB life
Abbr.
IUBMB Life
ISSN
1521-6543
Published
2008-01-00
Pages
2-9
Language
English
Region
England
NLM ID
100888706
PMCID
PMC2717607
Subset
IM
Grants
NEI NIH HHS · R01 EY006641 · United States
NEI NIH HHS · F32 EY006641 · United States
NIGMS NIH HHS · GM 060019 · United States
NEI NIH HHS · R01 EY018666 · United States
NIGMS NIH HHS · R01 GM060019-09 · United States
NIGMS NIH HHS · R01 GM060019 · United States
NEI NIH HHS · EY 06641 · United States
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