Literature DB >> 15467096

The VGL-chanome: a protein superfamily specialized for electrical signaling and ionic homeostasis.

Frank H Yu1, William A Catterall.   

Abstract

Complex multicellular organisms require rapid and accurate transmission of information among cells and tissues and tight coordination of distant functions. Electrical signals and resulting intracellular calcium transients, in vertebrates, control contraction of muscle, secretion of hormones, sensation of the environment, processing of information in the brain, and output from the brain to peripheral tissues. In nonexcitable cells, calcium transients signal many key cellular events, including secretion, gene expression, and cell division. In epithelial cells, huge ion fluxes are conducted across tissue boundaries. All of these physiological processes are mediated in part by members of the voltage-gated ion channel protein superfamily. This protein superfamily of 143 members is one of the largest groups of signal transduction proteins, ranking third after the G protein-coupled receptors and the protein kinases in number. Each member of this superfamily contains a similar pore structure, usually covalently attached to regulatory domains that respond to changes in membrane voltage, intracellular signaling molecules, or both. Eight families are included in this protein superfamily-voltage-gated sodium, calcium, and potassium channels; calcium-activated potassium channels; cyclic nucleotide-modulated ion channels; transient receptor potential (TRP) channels; inwardly rectifying potassium channels; and two-pore potassium channels. This article identifies all of the members of this protein superfamily in the human genome, reviews the molecular and evolutionary relations among these ion channels, and describes their functional roles in cell physiology.

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Year:  2004        PMID: 15467096     DOI: 10.1126/stke.2532004re15

Source DB:  PubMed          Journal:  Sci STKE        ISSN: 1525-8882


  188 in total

1.  Structural basis for gating charge movement in the voltage sensor of a sodium channel.

Authors:  Vladimir Yarov-Yarovoy; Paul G DeCaen; Ruth E Westenbroek; Chien-Yuan Pan; Todd Scheuer; David Baker; William A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-12       Impact factor: 11.205

Review 2.  Voltage-gated sodium channels at 60: structure, function and pathophysiology.

Authors:  William A Catterall
Journal:  J Physiol       Date:  2012-04-02       Impact factor: 5.182

Review 3.  Rise of the sensors: nociception and pruritus.

Authors:  James N Baraniuk
Journal:  Curr Allergy Asthma Rep       Date:  2012-04       Impact factor: 4.806

4.  Principles of conduction and hydrophobic gating in K+ channels.

Authors:  Morten Ø Jensen; David W Borhani; Kresten Lindorff-Larsen; Paul Maragakis; Vishwanath Jogini; Michael P Eastwood; Ron O Dror; David E Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-15       Impact factor: 11.205

5.  Genetic loss of HCN1 channels is exciting, but is it epileptic?

Authors:  Nicholas P Poolos
Journal:  Epilepsy Curr       Date:  2010-03       Impact factor: 7.500

Review 6.  Structural correlates of selectivity and inactivation in potassium channels.

Authors:  Jason G McCoy; Crina M Nimigean
Journal:  Biochim Biophys Acta       Date:  2011-09-16

7.  Finding Channels.

Authors:  William A Catterall
Journal:  J Biol Chem       Date:  2015-10-02       Impact factor: 5.157

Review 8.  Electrical resonance with voltage-gated ion channels: perspectives from biophysical mechanisms and neural electrophysiology.

Authors:  Lin Ge; Xiao-dong Liu
Journal:  Acta Pharmacol Sin       Date:  2016-01       Impact factor: 6.150

Review 9.  Functional diversity of potassium channel voltage-sensing domains.

Authors:  León D Islas
Journal:  Channels (Austin)       Date:  2016-01-21       Impact factor: 2.581

Review 10.  Structure and function of voltage-gated sodium channels at atomic resolution.

Authors:  William A Catterall
Journal:  Exp Physiol       Date:  2013-10-04       Impact factor: 2.969

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