Proceedings of the National Academy of Sciences of the United States of America · 2000
Crystal structure of an anti-carbohydrate antibody directed against Vibrio cholerae O1 in complex with antigen: molecular basis for serotype specificity.
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Villeneuve S, Souchon H, Riottot M M, Mazie J C, Lei P, Glaudemans C P, Kovác P, Fournier J M, Alzari P M
Аннотация
The crystal structure of the murine Fab S-20-4 from a protective anti-cholera Ab specific for the lipopolysaccharide Ag of the Ogawa serotype has been determined in its unliganded form and in complex with synthetic fragments of the Ogawa O-specific polysaccharide (O-SP). The upstream terminal O-SP monosaccharide is shown to be the primary antigenic determinant. Additional perosamine residues protrude outwards from the Ab surface and contribute only marginally to the binding affinity and specificity. A complementary water-excluding hydrophobic interface and five Ab-Ag hydrogen bonds are crucial for carbohydrate recognition. The structure reported here explains the serotype specificity of anti-Ogawa Abs and provides a rational basis toward the development of a synthetic carbohydrate-based anti-cholera vaccine.
Предметные рубрики MeSH
AnimalsAntibodies, BacterialAntibodies, MonoclonalAntibody SpecificityAntigen-Antibody ReactionsAntigens, BacterialCarbohydrate SequenceCrystallography, X-RayImmunoglobulin Fab FragmentsLipopolysaccharidesMiceModels, MolecularMolecular Sequence DataProtein ConformationSerotypingStructure-Activity RelationshipVibrio cholerae