2013/01/03 by David K. Jones, Colin H. Peters, Charlene R. Allard +2 · 29 citations
Biochemistry, Genetics and Molecular Biology · Chemistry · Medicine · Neuroscience · #Biochemistry #Biology #Biophysics #Cardiac electrophysiology and arrhythmias #Cardiac muscle #Chemistry #Endocrinology #Extracellular #Gene isoform #Ion channel regulation and function #Kinetics #Neuroscience and Neural Engineering #Physics #Proton #Sodium #Sodium channel #Xenopus
paper · pdf · doi:10.1074/jbc.m112.434266
published in Journal of Biological Chemistry 288(7), 4782-4791 (Elsevier BV)
openalex publication_date 2013/01/03 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28
Protons impart isoform-specific modulation of inactivation in neuronal, skeletal muscle, and cardiac voltage-gated sodium (Na V ) channels. Although the structural basis of proton block in Na V channels has been well described, the amino acid residues responsible for the changes in Na V kinetics during extracellular acidosis are as yet unknown. We expressed wild-type (WT) and two pore mutant constructs (H880Q and C373F) of the human cardiac Na V channel, Na V 1.5, in Xenopus oocytes. C373F and H880Q both attenuated proton block, abolished proton modulation of use-dependent inactivation, and altered pH modulation of the steady-state and kinetic parameters of slow inactivation. Additionally, C373F significantly reduced the maximum probability of use-dependent inactivation and slow inactivation, relative to WT. H880Q also significantly reduced the maximum probability of slow inactivation and shifted the voltage dependence of activation and fast inactivation to more positive potentials, relative to WT. These data suggest that Cys-373 and His-880 in Na V 1.5 are proton sensors for use-dependent and slow inactivation and have implications in isoform-specific modulation of Na V channels. Background: Protons modify cardiac sodium channel function, potentially contributing to cardiac arrhythmia during and following ischemia. Results: Protons binding amino acids at the pore alter cardiac sodium channel function. Conclusion: Sodium channel pore protonation mediates proton block and destabilization of sodium channel slow inactivation. Significance: Understanding sodium channel proton modulation is necessary to understand the pathophysiology of cardiac acidosis.