Structural basis of cytoplasmic NaV1.5 and NaV1.4 regulation

• Published in: The Journal of general physiology Vol. 153; no. 1; p. 1
• Main Authors: Nathan, Sara, Gabelli, Sandra B, Yoder, Jesse B, Srinivasan, Lakshmi, Aldrich, Richard W, Tomaselli, Gordon F, Ben-Johny, Manu, Amzel, L Mario
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 04.01.2021
• Subjects: Action potential; Biophysics; Calcium-binding protein; Calmodulin; Cardiac muscle; Dimerization; Electron microscopy; Isoforms; Membrane proteins; Review; Skeletal muscle; Sodium channels (voltage-gated)
• ISSN: 0022-1295; 1540-7748
• DOI: 10.1085/jgp.202012722

Voltage-gated sodium channels (NaVs) are membrane proteins responsible for the rapid upstroke of the action potential in excitable cells. There are nine human voltage-sensitive NaV1 isoforms that, in addition to their sequence differences, differ in tissue distribution and specific function. This review focuses on isoforms NaV1.4 and NaV1.5, which are primarily expressed in skeletal and cardiac muscle cells, respectively. The determination of the structures of several eukaryotic NaVs by single-particle cryo-electron microscopy (cryo-EM) has brought new perspective to the study of the channels. Alignment of the cryo-EM structure of the transmembrane channel pore with x-ray crystallographic structures of the cytoplasmic domains illustrates the complementary nature of the techniques and highlights the intricate cellular mechanisms that modulate these channels. Here, we review structural insights into the cytoplasmic C-terminal regulation of NaV1.4 and NaV1.5 with special attention to Ca2+ sensing by calmodulin, implications for disease, and putative channel dimerization.