首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >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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Crystal structure of an anti-carbohydrate antibody directed against Vibrio cholerae O1 in complex with antigen: Molecular basis for serotype specificity

机译:抗霍乱弧菌O1与碳水化合物复合的抗碳水化合物抗体的晶体结构:血清型特异性的分子基础

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摘要

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.
机译:来自Ogawa血清型脂多糖Ag的保护性抗霍乱抗体Ab的鼠Fab S-20-4的晶体结构已确定为非配体形式,并与Ogawa O特异性多糖(O -SP)。上游末端O-SP单糖被证明是主要的抗原决定簇。其他的过胺残基从Ab表面向外突出,仅对结合亲和力和特异性贡献很小。互补的不包括水的疏水界面和五个Ab-Ag氢键对于碳水化合物的识别至关重要。此处报道的结构解释了抗小川抗体的血清型特异性,并为开发合成的基于碳水化合物的抗霍乱疫苗提供了合理的基础。

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