Literature DB >> 29071507

Posttranslational Modification of Sodium Channels.

Zifan Pei1,2, Yanling Pan3, Theodore R Cummins4,5,6.   

Abstract

Voltage-gated sodium channels (VGSCs) are critical determinants of excitability. The properties of VGSCs are thought to be tightly controlled. However, VGSCs are also subjected to extensive modifications. Multiple posttranslational modifications that covalently modify VGSCs in neurons and muscle have been identified. These include, but are not limited to, phosphorylation, ubiquitination, palmitoylation, nitrosylation, glycosylation, and SUMOylation. Posttranslational modifications of VGSCs can have profound impact on cellular excitability, contributing to normal and abnormal physiology. Despite four decades of research, the complexity of VGSC modulation is still being determined. While some modifications have similar effects on the various VGSC isoforms, others have isoform-specific interactions. In addition, while much has been learned about how individual modifications can impact VGSC function, there is still more to be learned about how different modifications can interact. Here we review what is known about VGSC posttranslational modifications with a focus on the breadth and complexity of the regulatory mechanisms that impact VGSC properties.

Keywords:  Nav; Nitrosylation; Palmitoylation; Phosphorylation

Mesh:

Substances:

Year:  2018        PMID: 29071507     DOI: 10.1007/164_2017_69

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  5 in total

1.  S-Palmitoylation of the sodium channel Nav1.6 regulates its activity and neuronal excitability.

Authors:  Yanling Pan; Yucheng Xiao; Zifan Pei; Theodore R Cummins
Journal:  J Biol Chem       Date:  2020-03-11       Impact factor: 5.157

2.  CaMKII Inhibition Attenuates Distinct Gain-of-Function Effects Produced by Mutant Nav1.6 Channels and Reduces Neuronal Excitability.

Authors:  Agnes S Zybura; Firoj K Sahoo; Andy Hudmon; Theodore R Cummins
Journal:  Cells       Date:  2022-07-04       Impact factor: 7.666

3.  Nonmuscle myosin II isoforms interact with sodium channel alpha subunits.

Authors:  Bhagirathi Dash; Chongyang Han; Stephen G Waxman; Sulayman D Dib-Hajj
Journal:  Mol Pain       Date:  2018-06-29       Impact factor: 3.395

Review 4.  Fenestropathy of Voltage-Gated Sodium Channels.

Authors:  Tamer M Gamal El-Din; Michael J Lenaeus
Journal:  Front Pharmacol       Date:  2022-02-11       Impact factor: 5.810

Review 5.  Druggability of Voltage-Gated Sodium Channels-Exploring Old and New Drug Receptor Sites.

Authors:  Goragot Wisedchaisri; Tamer M Gamal El-Din
Journal:  Front Pharmacol       Date:  2022-03-17       Impact factor: 5.810

  5 in total

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