Ionic selectivity and thermal adaptations within the voltage-gated sodium channel family of alkaliphilic Bacillus

Elife. 2014 Nov 11:3:e04387. doi: 10.7554/eLife.04387.

Abstract

Entry and extrusion of cations are essential processes in living cells. In alkaliphilic prokaryotes, high external pH activates voltage-gated sodium channels (Nav), which allows Na(+) to enter and be used as substrate for cation/proton antiporters responsible for cytoplasmic pH homeostasis. Here, we describe a new member of the prokaryotic voltage-gated Na(+) channel family (NsvBa; <underline>N</underline>on-<underline>s</underline>elective <underline>v</underline>oltage-gated, <underline>B</underline>acillus <underline>a</underline>lcalophilus) that is nonselective among Na(+), Ca(2+) and K(+) ions. Mutations in NsvBa can convert the nonselective filter into one that discriminates for Na(+) or divalent cations. Gain-of-function experiments demonstrate the portability of ion selectivity with filter mutations to other Bacillus Nav channels. Increasing pH and temperature shifts their activation threshold towards their native resting membrane potential. Furthermore, we find drugs that target Bacillus Nav channels also block the growth of the bacteria. This work identifies some of the adaptations to achieve ion discrimination and gating in Bacillus Nav channels.

Keywords: antibiotics; bacteria physiology; biochemical adaptations; biophysics; evolution; infectious disease; ion selectivity; microbiology; none; pharmacology; structural biology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Biological / drug effects*
  • Alkalies / pharmacology
  • Amino Acid Sequence
  • Bacillus / drug effects
  • Bacillus / growth & development
  • Bacillus / physiology*
  • Cations
  • Cell Membrane Permeability
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Movement / drug effects
  • Multigene Family*
  • Mutation / genetics
  • Sodium Channel Blockers / pharmacology
  • Temperature*
  • Voltage-Gated Sodium Channels / chemistry
  • Voltage-Gated Sodium Channels / metabolism*

Substances

  • Alkalies
  • Cations
  • Sodium Channel Blockers
  • Voltage-Gated Sodium Channels