Literature DB >> 8873119

Role in fast inactivation of conserved amino acids in the IV/S4-S5 loop of the human muscle Na+ channel.

N Mitrovic1, H Lerche, R Heine, R Fleischhauer, U Pika-Hartlaub, U Hartlaub, A L George, F Lehmann-Horn.   

Abstract

Since it has been shown that point mutations in the S4-S5 loop of the Shaker K+ channel may disrupt fast inactivation, we investigated the role of three conserved amino acids in IV/S4-S5 of the adult human muscle Na+ channel (L1471, S1478, L1482). In contrast to the K+ channel mutations, the analogous substitutions in the Na+ channel (S1478A/C, L1482A) did not substantially affect fast inactivation. Nevertheless, the mutations S1478A/C/Q shifted the voltage dependence of steady-state inactivation; L1471Q and S1478C slowed recovery from inactivation. In contrast, a novel non-conserved IV/S4-S5 mutation causing paramyotonia congenita (F1473S) slowed fast inactivation 2-fold and accelerated recovery from inactivation 5-fold. The results indicate involvement of the IV/ S4-S5 loop of the human muscle Na+ channel in fast inactivation, but different roles for conserved amino acids among Na+ and K+ channels.

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Year:  1996        PMID: 8873119     DOI: 10.1016/0304-3940(96)12866-4

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  12 in total

1.  On mutations that uncouple sodium channel activation from inactivation.

Authors:  L Goldman
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

2.  Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis.

Authors:  H Lerche; W Peter; R Fleischhauer; U Pika-Hartlaub; T Malina; N Mitrovic; F Lehmann-Horn
Journal:  J Physiol       Date:  1997-12-01       Impact factor: 5.182

3.  A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation.

Authors:  Magali Bouhours; Sandrine Luce; Damien Sternberg; Jean Claude Willer; Bertrand Fontaine; Nacira Tabti
Journal:  J Physiol       Date:  2005-03-24       Impact factor: 5.182

4.  Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.

Authors:  S Bendahhou; T R Cummins; R Tawil; S G Waxman; L J Ptácek
Journal:  J Neurosci       Date:  1999-06-15       Impact factor: 6.167

5.  Cooperative effect of S4-S5 loops in domains D3 and D4 on fast inactivation of the Na+ channel.

Authors:  M Oana Popa; Alexi K Alekov; Sigrid Bail; Frank Lehmann-Horn; Holger Lerche
Journal:  J Physiol       Date:  2004-09-30       Impact factor: 5.182

6.  Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I.

Authors:  D S Green; A L George; S C Cannon
Journal:  J Physiol       Date:  1998-08-01       Impact factor: 5.182

7.  Fast- and slow-gating modes of the sodium channel are altered by a paramyotonia congenita-linked mutation.

Authors:  O Moran; R Melani; M Nizzari; F Conti
Journal:  J Bioenerg Biomembr       Date:  1998-12       Impact factor: 2.945

Review 8.  Sodium channelopathies of skeletal muscle and brain.

Authors:  Massimo Mantegazza; Sandrine Cestèle; William A Catterall
Journal:  Physiol Rev       Date:  2021-03-26       Impact factor: 46.500

9.  Movement of voltage sensor S4 in domain 4 is tightly coupled to sodium channel fast inactivation and gating charge immobilization.

Authors:  F J Kühn; N G Greeff
Journal:  J Gen Physiol       Date:  1999-08       Impact factor: 4.086

10.  Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable.

Authors:  Sulayman D Dib-Hajj; Mark Estacion; Brian W Jarecki; Lynda Tyrrell; Tanya Z Fischer; Mark Lawden; Theodore R Cummins; Stephen G Waxman
Journal:  Mol Pain       Date:  2008-09-19       Impact factor: 3.395

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