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Voltage-gated Sodium Channels: Structure, Function and Channelopathies

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Cover of 'Voltage-gated Sodium Channels: Structure, Function and Channelopathies'

Table of Contents

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    Book Overview
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    Chapter 43 Cardiac Arrhythmias Related to Sodium Channel Dysfunction
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    Chapter 44 Structural Models of Ligand-Bound Sodium Channels
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    Chapter 45 The Cardiac Sodium Channel and Its Protein Partners
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    Chapter 46 Effects of Benzothiazolamines on Voltage-Gated Sodium Channels
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    Chapter 47 Sodium Channel Trafficking
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    Chapter 48 Voltage-Gated Sodium Channel β Subunits and Their Related Diseases
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    Chapter 52 Sodium Channelopathies of Skeletal Muscle
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    Chapter 53 Regulation of Cardiac Voltage-Gated Sodium Channel by Kinases: Roles of Protein Kinases A and C
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    Chapter 54 Gating Pore Currents in Sodium Channels
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    Chapter 61 Structural and Functional Analysis of Sodium Channels Viewed from an Evolutionary Perspective
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    Chapter 63 Calculating the Consequences of Left-Shifted Nav Channel Activity in Sick Excitable Cells
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    Chapter 66 Toxins That Affect Voltage-Gated Sodium Channels
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    Chapter 69 Posttranslational Modification of Sodium Channels
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    Chapter 70 Evolutionary History of Voltage-Gated Sodium Channels
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    Chapter 73 Mechanisms of Drug Binding to Voltage-Gated Sodium Channels
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    Chapter 75 Mining Protein Evolution for Insights into Mechanisms of Voltage-Dependent Sodium Channel Auxiliary Subunits
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    Chapter 91 Translational Model Systems for Complex Sodium Channel Pathophysiology in Pain
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    Chapter 97 Selective Ligands and Drug Discovery Targeting the Voltage-Gated Sodium Channel Nav1.7
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    Chapter 99 pH Modulation of Voltage-Gated Sodium Channels
Attention for Chapter 44: Structural Models of Ligand-Bound Sodium Channels
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Chapter title
Structural Models of Ligand-Bound Sodium Channels
Chapter number 44
Book title
Voltage-gated Sodium Channels: Structure, Function and Channelopathies
Published in
Handbook of experimental pharmacology, January 2017
DOI 10.1007/164_2017_44
Pubmed ID
Book ISBNs
978-3-31-990283-8, 978-3-31-990284-5
Authors

Boris S. Zhorov, Zhorov, Boris S.

Abstract

X-ray and cryo-EM structures of tetrameric and pseudo-tetrameric P-loop channels are used to elaborate homology models of mammalian voltage-gated sodium channels with drugs and neurotoxins. Such models integrate experimental data, assist in planning new experiments, and may facilitate drug design. This chapter outlines sodium channel models with local anesthetics, anticonvulsants, and antiarrhythmics, which are used to manage pain and treat sodium channelopathies. Further summarized are sodium channel models with tetrodotoxin, mu-conotoxins, batrachotoxin, scorpion toxins, and insecticides. Possible involvement of sodium ions in the action of some ligands is discussed.

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Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 13%
Researcher 2 13%
Student > Ph. D. Student 2 13%
Student > Doctoral Student 1 7%
Student > Bachelor 1 7%
Other 5 33%
Unknown 2 13%
Readers by discipline Count As %
Medicine and Dentistry 4 27%
Biochemistry, Genetics and Molecular Biology 3 20%
Unspecified 1 7%
Business, Management and Accounting 1 7%
Pharmacology, Toxicology and Pharmaceutical Science 1 7%
Other 2 13%
Unknown 3 20%