Literature DB >> 8757791

Structure and function of voltage-dependent sodium channels: comparison of brain II and cardiac isoforms.

H A Fozzard1, D A Hanck.   

Abstract

Cardiac and nerve Na channels have broadly similar functional properties and amino acid sequences, but they demonstrate specific differences in gating, permeation, ionic block, modulation, and pharmacology. Resolution of three-dimensional structures of Na channels is unlikely in the near future, but a number of amino acid sequences from a variety of species and isoforms are known so that channel differences can be exploited to gain insight into the relationship of structure to function. The combination of molecular biology to create chimeras and channels with point mutations and high-resolution electrophysiological techniques to study function encourage the idea that predictions of structure from function are possible. With the goal of understanding the special properties of the cardiac Na channel, this review examines the structural (sequence) similarities between the cardiac and nerve channels and considers what is known about the relationship of structure to function for voltage-dependent Na channels in general and for the cardiac Na channels in particular.

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Year:  1996        PMID: 8757791     DOI: 10.1152/physrev.1996.76.3.887

Source DB:  PubMed          Journal:  Physiol Rev        ISSN: 0031-9333            Impact factor:   37.312


  65 in total

1.  Novel mechanism of blocking axonal Na(+) channels by three macrocyclic polyamine analogues and two spider toxins.

Authors:  M Yakehiro; Y Furukawa; T Koike; E Kimura; T Nakajima; K Yamaoka; I Seyama
Journal:  Br J Pharmacol       Date:  2001-01       Impact factor: 8.739

2.  A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation.

Authors:  Y Y Vilin; E Fujimoto; P C Ruben
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

3.  Structural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.

Authors:  Y Y Vilin; N Makita; A L George; P C Ruben
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

4.  A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state.

Authors:  J P O'Reilly; S Y Wang; G K Wang
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

5.  Cardiac sodium channel Markov model with temperature dependence and recovery from inactivation.

Authors:  L A Irvine; M S Jafri; R L Winslow
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

6.  Role of the C-terminal domain in inactivation of brain and cardiac sodium channels.

Authors:  M Mantegazza; F H Yu; W A Catterall; T Scheuer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-11       Impact factor: 11.205

7.  Residues in Na(+) channel D3-S6 segment modulate both batrachotoxin and local anesthetic affinities.

Authors:  S Y Wang; C Nau; G K Wang
Journal:  Biophys J       Date:  2000-09       Impact factor: 4.033

Review 8.  Using the deadly mu-conotoxins as probes of voltage-gated sodium channels.

Authors:  Ronald A Li; Gordon F Tomaselli
Journal:  Toxicon       Date:  2004-08       Impact factor: 3.033

Review 9.  Pain disorders and erythromelalgia caused by voltage-gated sodium channel mutations.

Authors:  Ron Dabby
Journal:  Curr Neurol Neurosci Rep       Date:  2012-02       Impact factor: 5.081

10.  Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na+ channel to methanethiosulfonate reagents.

Authors:  Akihiko Sunami; Arlene Tracey; Ian W Glaaser; Gregory M Lipkind; Dorothy A Hanck; Harry A Fozzard
Journal:  J Physiol       Date:  2004-10-07       Impact factor: 5.182

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