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Depolarization of the Conductance-voltage Relationship in the NaV1.5 Mutant, E1784K, is Due to Altered Fast Inactivation

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Journal PLoS One
Date 2017 Sep 13
PMID 28898267
Citations 11
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Abstract

E1784K is the most common mixed long QT syndrome/Brugada syndrome mutant in the cardiac voltage-gated sodium channel NaV1.5. E1784K shifts the midpoint of the channel conductance-voltage relationship to more depolarized membrane potentials and accelerates the rate of channel fast inactivation. The depolarizing shift in the midpoint of the conductance curve in E1784K is exacerbated by low extracellular pH. We tested whether the E1784K mutant shifts the channel conductance curve to more depolarized membrane potentials by affecting the channel voltage-sensors. We measured ionic currents and gating currents at pH 7.4 and pH 6.0 in Xenopus laevis oocytes. Contrary to our expectation, the movement of gating charges is shifted to more hyperpolarized membrane potentials by E1784K. Voltage-clamp fluorimetry experiments show that this gating charge shift is due to the movement of the DIVS4 voltage-sensor being shifted to more hyperpolarized membrane potentials. Using a model and experiments on fast inactivation-deficient channels, we show that changes to the rate and voltage-dependence of fast inactivation are sufficient to shift the conductance curve in E1784K. Our results localize the effects of E1784K to DIVS4, and provide novel insight into the role of the DIV-VSD in regulating the voltage-dependencies of activation and fast inactivation.

Citing Articles

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PMID: 36496974 PMC: 9735811. DOI: 10.3390/cells11233714.


The L1624Q Variant in Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function.

Jones L, Peters C, Rosch R, Owers M, Hughes E, Pal D Front Pharmacol. 2021; 12:788192.

PMID: 34925043 PMC: 8675213. DOI: 10.3389/fphar.2021.788192.


E1784K, the most common Brugada syndrome and long-QT syndrome type 3 mutant, disrupts sodium channel inactivation through two separate mechanisms.

Peters C, Watkins A, Poirier O, Ruben P J Gen Physiol. 2020; 152(9).

PMID: 32569350 PMC: 7478868. DOI: 10.1085/jgp.202012595.


An interaction between the III-IV linker and CTD in NaV1.5 confers regulation of inactivation by CaM and FHF.

Gade A, Marx S, Pitt G J Gen Physiol. 2019; 152(2).

PMID: 31865383 PMC: 7062510. DOI: 10.1085/jgp.201912434.


Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient with Overlap Syndrome due to the E1784K SCN5A Mutation.

Hasebe H, Yokoya T, Murakoshi N, Kurebayashi N Intern Med. 2019; 59(1):83-87.

PMID: 31484910 PMC: 6995720. DOI: 10.2169/internalmedicine.3430-19.


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