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Infect. Immun., Sep 1997, 3961-3965, Vol 65, No. 9
L Brade, R Engel, WJ Christ and ET Rietschel
Lipid A monoclonal antibodies, which require for binding the presence of
the bisphosphorylated D-glucosamine disaccharide lipid A backbone, were
tested against synthetic lipid A precursor Ia and compound B 1047 by enzyme
immunoassay. The last-named compound is a precursor Ia analog with a
methoxy instead of a hydroxy group at C6' and was chosen to determine why
these antibodies failed to recognize the bound lipid A present in
lipopolysaccharide (LPS). Whereas all antibodies tested bound to precursor
Ia, none of them bound to compound B 1047 or Escherichia coli Re LPS to a
significant extent. Compared to the natural substituent at C6', i.e.,
3-deoxy-D-manno-octulosonic acid (Kdo), the methoxy group is neither bulky
nor charged. Thus, the data suggest that it is not hindrance by Kdo but
rather the generation of a neoantigen that endows lipid A with
immunoreactivity upon liberation from LPS by acid hydrolysis.
Copyright © 1997, American Society for Microbiology
A nonsubstituted primary hydroxyl group in position 6' of free lipid A is required for binding of lipid A monoclonal antibodies
Department of Immunochemistry and Biochemical Microbiology, Center for Medicine and Biosciences, Research Center Borstel, Germany.
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