Characterisation of a monoclonal antibody and its use to purify the cytotoxin of Helicobacter pylori

FEMS Microbiol Lett. 1998 Aug 1;165(1):79-84. doi: 10.1111/j.1574-6968.1998.tb13130.x.

Abstract

The vacuolating cytotoxin (VacA) is a major virulence factor of Helicobacter pylori which is not yet well characterised and is difficult to obtain in large quantities. Here we describe the production of a monoclonal antibody that recognises the native but not the denatured form of VacA. The antibody can be efficiently used in affinity chromatography for one-step purification of large quantities of VacA from culture supernatants. Elution at acidic pH dissociates the oligomeric molecule into monomers that reanneal in a time-dependent fashion. The purified cytotoxin is able to bind, and to intoxicate HeLa cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bacterial / biosynthesis
  • Antibodies, Bacterial / isolation & purification
  • Antibodies, Monoclonal* / biosynthesis
  • Antibodies, Monoclonal* / isolation & purification
  • Bacterial Proteins / immunology*
  • Bacterial Proteins / isolation & purification*
  • Chromatography, Affinity
  • Enzyme-Linked Immunosorbent Assay
  • HeLa Cells / metabolism
  • Helicobacter pylori / chemistry*
  • Helicobacter pylori / immunology
  • Humans
  • Immunoblotting
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Electron
  • Microscopy, Fluorescence

Substances

  • Antibodies, Bacterial
  • Antibodies, Monoclonal
  • Bacterial Proteins
  • VacA protein, Helicobacter pylori