Interpreting the functional role of a novel interaction motif in prokaryotic sodium channels

J Gen Physiol. 2017 Jun 5;149(6):613-622. doi: 10.1085/jgp.201611740. Epub 2017 May 18.

Abstract

Voltage-gated sodium channels enable the translocation of sodium ions across cell membranes and play crucial roles in electrical signaling by initiating the action potential. In humans, mutations in sodium channels give rise to several neurological and cardiovascular diseases, and hence they are targets for pharmaceutical drug developments. Prokaryotic sodium channel crystal structures have provided detailed views of sodium channels, which by homology have suggested potentially important functionally related structural features in human sodium channels. A new crystal structure of a full-length prokaryotic channel, NavMs, in a conformation we proposed to represent the open, activated state, has revealed a novel interaction motif associated with channel opening. This motif is associated with disease when mutated in human sodium channels and plays an important and dynamic role in our new model for channel activation.

Publication types

  • Review

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism
  • Ion Channel Gating
  • Membrane Potentials
  • Protein Binding
  • Protein Domains
  • Voltage-Gated Sodium Channels / chemistry*
  • Voltage-Gated Sodium Channels / metabolism

Substances

  • Bacterial Proteins
  • Voltage-Gated Sodium Channels

Associated data

  • PDB/5HVX
  • PDB/5KLB