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
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies, Bacterial / biosynthesis
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Antibodies, Bacterial / isolation & purification
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Antibodies, Monoclonal* / biosynthesis
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Antibodies, Monoclonal* / isolation & purification
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Bacterial Proteins / immunology*
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Bacterial Proteins / isolation & purification*
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Chromatography, Affinity
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Enzyme-Linked Immunosorbent Assay
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HeLa Cells / metabolism
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Helicobacter pylori / chemistry*
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Helicobacter pylori / immunology
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Humans
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Immunoblotting
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Mice
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Mice, Inbred BALB C
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Microscopy, Electron
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Microscopy, Fluorescence
Substances
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Antibodies, Bacterial
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Antibodies, Monoclonal
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Bacterial Proteins
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VacA protein, Helicobacter pylori