Mechanical fractionation reveals structural requirements for enteropathogenic Escherichia coli Tir insertion into host membranes

Infect Immun. 2000 Jul;68(7):4344-8. doi: 10.1128/IAI.68.7.4344-4348.2000.

Abstract

Enteropathogenic Escherichia coli (EPEC) inserts its receptor for intimate adherence (Tir) into host cell membranes by using a type III secretion system. Detergents are frequently used to fractionate infected host cells to investigate bacterial protein delivery into mammalian cells. In this study, we found that the Triton X-100-soluble membrane fraction from EPEC-infected HeLa cells was contaminated with bacterial proteins. We therefore applied a mechanical method of cell lysis and ultracentrifugation to fractionate infected HeLa cells to investigate the biology and biochemistry of Tir delivery and translocation. This method demonstrates that the translocation of Tir into the host cell membrane requires its transmembrane domains, but not tyrosine phosphorylation or binding to Tir's ligand, intimin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism*
  • Biological Transport, Active
  • Cell Fractionation / methods
  • Cell Membrane / metabolism
  • Cell Membrane / microbiology
  • Detergents
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Escherichia coli / pathogenicity*
  • Escherichia coli Proteins*
  • Genes, Bacterial
  • HeLa Cells
  • Humans
  • Mutation
  • Octoxynol
  • Peptide Fragments / genetics
  • Peptide Fragments / isolation & purification
  • Peptide Fragments / metabolism
  • Protein Structure, Tertiary
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / isolation & purification
  • Receptors, Cell Surface / metabolism*

Substances

  • Bacterial Proteins
  • Detergents
  • Escherichia coli Proteins
  • Peptide Fragments
  • Receptors, Cell Surface
  • Tir protein, E coli
  • Octoxynol