The hinge portion of the S. aureus alpha-toxin crosses the lipid bilayer and is part of the trans-mouth of the channel

Biochim Biophys Acta. 1997 Oct 2;1329(1):51-60. doi: 10.1016/s0005-2736(97)00087-4.

Abstract

This paper compares the functional properties of ion channels formed in planar lipid membranes by the wild and mutant Staphylococcus aureus alpha-toxin. It was shown that replacement of the amino acid Gly at position 130 by Cys in the primary structure of the toxin decreases the single-channel conductance with a concomitant decrease in the pH at which the channel becomes unable to discriminate between Cl- and K+ ions. The mutation also induced an increase in the asymmetry in the current-voltage relationship of the channel. The results of our experiments suggest that the trans-mouth of the channel is responsible for all the observed changes in channel properties. It was assumed that this entrance is built by the glycine-rich hinge portion of the toxin and is situated close to the surface of monolayer facing the trans-compartment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins / chemistry*
  • Bacterial Toxins / genetics
  • Bacterial Toxins / metabolism
  • Electric Conductivity
  • Electrophysiology
  • Glucose / metabolism
  • Hemolysin Proteins / chemistry*
  • Hemolysin Proteins / genetics
  • Hemolysin Proteins / metabolism
  • Hydrogen-Ion Concentration
  • Ion Channels / metabolism*
  • Lipid Bilayers / metabolism*
  • Membrane Potentials
  • Mutation
  • Particle Size
  • Phosphatidylcholines / metabolism
  • Phospholipids / metabolism
  • Polyethylene Glycols / metabolism
  • Staphylococcus aureus / chemistry*
  • Sucrose / metabolism

Substances

  • Bacterial Toxins
  • Hemolysin Proteins
  • Ion Channels
  • Lipid Bilayers
  • Phosphatidylcholines
  • Phospholipids
  • staphylococcal alpha-toxin
  • Polyethylene Glycols
  • Sucrose
  • asolectin
  • Glucose