Literature DB >> 20932926

Mass spectrometry-based phosphoproteomics reveals multisite phosphorylation on mammalian brain voltage-gated sodium and potassium channels.

Je-Hyun Baek1, Oscar Cerda, James S Trimmer.   

Abstract

Voltage-gated sodium and potassium channels underlie electrical activity of neurons, and are dynamically regulated by diverse cell signaling pathways that ultimately exert their effects by altering the phosphorylation state of channel subunits. Recent mass spectrometric-based studies have led to a new appreciation of the extent and nature of phosphorylation of these ion channels in mammalian brain. This has allowed for new insights into how neurons dynamically regulate the localization, activity and expression through multisite ion channel phosphorylation.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20932926      PMCID: PMC3043121          DOI: 10.1016/j.semcdb.2010.09.009

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  61 in total

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8.  Brain phosphoproteome obtained by a FASP-based method reveals plasma membrane protein topology.

Authors:  Jacek R Wiśniewski; Nagarjuna Nagaraj; Alexandre Zougman; Florian Gnad; Matthias Mann
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Journal:  Nat Neurosci       Date:  2004-06-13       Impact factor: 24.884

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  22 in total

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3.  CaMKII Phosphorylation of Na(V)1.5: Novel in Vitro Sites Identified by Mass Spectrometry and Reduced S516 Phosphorylation in Human Heart Failure.

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Review 5.  The axon initial segment in nervous system disease and injury.

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Review 6.  Diverse roles for auxiliary subunits in phosphorylation-dependent regulation of mammalian brain voltage-gated potassium channels.

Authors:  Helene Vacher; James S Trimmer
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7.  Properties of Calmodulin Binding to NaV1.2 IQ Motif and Its Autism-Associated Mutation R1902C.

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8.  The Nav1.2 channel is regulated by GSK3.

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9.  Cell type-specific spatial and functional coupling between mammalian brain Kv2.1 K+ channels and ryanodine receptors.

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10.  Reciprocal changes in phosphorylation and methylation of mammalian brain sodium channels in response to seizures.

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