2-Aminoperimidine, a specific inhibitor of bacterial NhaA Na(+)/H(+) antiporters

FEBS Lett. 2005 Jan 17;579(2):373-8. doi: 10.1016/j.febslet.2004.11.098.

Abstract

The diuretic drug amiloride and its numerous derivatives are competitive inhibitors of mammalian Na(+)/H(+) antiporters and other eukaryotic antiporters. Most prokaryotic antiporters, including the major NhaA family of enterobacteria, are resistant to these compounds. We show that 2-aminoperimidine (AP), a guanidine-containing naphthalene derivative with some similarity to amiloride, acts as a specific inhibitor of NhaA from Escherichia coli. Similar concentrations (IC(50) of 0.9 muM) inhibit the proton motive force dependent Na(+)(Li(+))/H(+) exchange reaction in inside-out sub-bacterial vesicles (at 10 mM NaCl, pH 8) as well as the initial rate of (22)Na(+)/Na(+) exchange mediated by pure NhaA in proteoliposomes. The inhibitor is specific to NhaA type antiporters, so AP is a new tool to study the mechanism and roles of NhaA antiporters of enterobacteria as well as the molecular basis of inhibition by an amiloride-like compound.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amiloride / analogs & derivatives
  • Cell Membrane / physiology
  • Escherichia coli Proteins / antagonists & inhibitors*
  • Proteolipids / drug effects
  • Proteolipids / physiology
  • Quinazolines / chemistry
  • Quinazolines / pharmacology*
  • Sodium / metabolism
  • Sodium-Hydrogen Exchangers / antagonists & inhibitors*

Substances

  • 2-aminoperimidine
  • Escherichia coli Proteins
  • NhaA protein, E coli
  • Proteolipids
  • Quinazolines
  • Sodium-Hydrogen Exchangers
  • proteoliposomes
  • Amiloride
  • Sodium