Monomer-monomer interactions drive the prepore to pore conversion of a beta-barrel-forming cholesterol-dependent cytolysin

J Biol Chem. 2002 Mar 29;277(13):11597-605. doi: 10.1074/jbc.M111039200. Epub 2002 Jan 17.

Abstract

Perfringolysin O (PFO), a cholesterol-dependent cytolysin, forms large oligomeric pore complexes comprised of up to 50 PFO molecules. In the present studies a mutant of PFO (PFO(Y181A)) has been identified that traps PFO in a multimeric prepore complex that cannot insert its transmembrane beta-hairpins and therefore cannot form a pore. Remarkably, PFO(Y181A) can be induced to insert its transmembrane beta-hairpins if functional PFO is incorporated into the PFO(Y181A) oligomeric prepore complex. Furthermore, the transition from prepore to pore appears to be an "all or none" process; partial insertion of the transmembrane beta-barrel does not occur. Therefore, cooperative interactions between the monomers of the prepore drive the prepore to pore conversion that results in the formation of the transmembrane beta-barrel.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacterial Toxins / metabolism*
  • Cholesterol / metabolism*
  • Energy Transfer
  • Glutathione / metabolism
  • Hemolysin Proteins
  • Spectrometry, Fluorescence
  • beta-Amylase / metabolism

Substances

  • Bacterial Toxins
  • Hemolysin Proteins
  • Clostridium perfringens theta-toxin
  • Cholesterol
  • beta-Amylase
  • Glutathione