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Vi 荚膜多糖的结构与免疫学特性之间的关系。

Relation between structure and immunologic properties of the Vi capsular polysaccharide.

作者信息

Szu S C, Li X R, Stone A L, Robbins J B

机构信息

Laboratory of Developmental and Molecular Immunity, National Institute of Child Health and Human Development, Bethesda, Maryland 20892.

出版信息

Infect Immun. 1991 Dec;59(12):4555-61. doi: 10.1128/iai.59.12.4555-4561.1991.

Abstract

The Vi capsular polysaccharide of Salmonella typhi is a linear homopolymer of poly-alpha(1----4)GalNAcp variably O acetylated at the C-3 position. Serum antibodies elicited by this antigen confer protective immunity against typhoid fever. The relation between the immunologic properties and structure of Vi was investigated by carboxyl reduction, O deacetylation, and acid hydrolysis. The immunogenicity of Vi was closely related to its degree of O acetylation. Partial O deacetylation slightly increased immunogenicity; complete O deacetylation eliminated the immunogenicity of Vi. O-deacetylated Vi, however, still reacted with antisera prepared by injection of whole bacteria. Carboxyl reduction, in contrast, had a comparatively slight effect upon both the immunogenicity and antigenicity of Vi. Retention levels of antigenicity after acid treatment were greater for both the native and carboxyl-reduced Vi than for the O-deacetylated product. The Courtauld-Koltun space-filling model of a pentamer of Vi demonstrated that the bulky nonpolar O-acetyls, which protrude in rows on both sides, make up most of the surface. The carboxyls are less exposed and are partially shielded by the O-acetyls. The molecular model thus provides an explantation for the dominant role of the O-acetyls, as well as the lesser effect of carboxyl reduction, upon the immunologic properties of Vi.

摘要

伤寒沙门氏菌的Vi荚膜多糖是一种聚-α(1----4)GalNAcp的线性同聚物,在C-3位可变地进行O-乙酰化。由该抗原引发的血清抗体赋予针对伤寒热的保护性免疫。通过羧基还原、O-脱乙酰化和酸水解研究了Vi的免疫学性质与结构之间的关系。Vi的免疫原性与其O-乙酰化程度密切相关。部分O-脱乙酰化略微增加了免疫原性;完全O-脱乙酰化消除了Vi的免疫原性。然而,O-脱乙酰化的Vi仍与通过注射全菌制备的抗血清发生反应。相比之下,羧基还原对Vi的免疫原性和抗原性的影响相对较小。酸处理后,天然Vi和羧基还原Vi的抗原性保留水平均高于O-脱乙酰化产物。Vi五聚体的库尔陶德-科尔通空间填充模型表明,在两侧成排突出的庞大非极性O-乙酰基构成了大部分表面。羧基较少暴露,部分被O-乙酰基屏蔽。因此,分子模型为O-乙酰基在Vi免疫学性质上的主导作用以及羧基还原的较小影响提供了解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68c6/259077/03f3bc2d837f/iai00048-0276-a.jpg

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