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免疫球蛋白分子上独特型和同种异型的免疫电子显微镜定位

Immunoelectron microscopic localization of idiotypes and allotypes on immunoglobulin molecules.

作者信息

Roux K H, Metzger D W

出版信息

J Immunol. 1982 Dec;129(6):2548-53.

PMID:6183337
Abstract

We have developed a novel approach to the analysis of antigenic (allotypic and idiotypic) determinants on intact immunoglobulin molecules. Immune complexes composed of IgG in combination with anti-idiotype or anti-allotype antibody were "visualized" by transmission electron microscopy. Individual Fab fragments of anti-idiotype or anti-allotype antibody, when bound to the IgG, altered the "Y" configuration in a reproducible and interpretable manner. Anti-idiotype antibody (either as Fab or IgG) bound to the terminus of the presumed V region of the IgG molecule, thus extending the apparent length of the Fab arms. Analysis of a rabbit VH framework allotype (a1) revealed that the determinant(s) is (are) located on the lateral portion of the V region of IgG. Binding of the anti-a1 Fab fragments was always at approximately right angles to the axis of the Fab arms of IgG. Fab antibody to the rabbit kappa light chain (b4) allotype bound to the lateral portion of the terminal half of the IgG Fab arms. This technique should be of value in localizing less well defined immunoglobulin determinants.

摘要

我们开发了一种新方法,用于分析完整免疫球蛋白分子上的抗原(同种异型和独特型)决定簇。由IgG与抗独特型或抗同种异型抗体组成的免疫复合物通过透射电子显微镜进行“可视化”。抗独特型或抗同种异型抗体的单个Fab片段与IgG结合时,会以可重复且可解释的方式改变“Y”构型。抗独特型抗体(无论是Fab还是IgG)与IgG分子假定V区的末端结合,从而延长了Fab臂的表观长度。对兔VH框架同种异型(a1)的分析表明,决定簇位于IgG V区的外侧部分。抗a1 Fab片段的结合总是与IgG Fab臂的轴大约成直角。针对兔κ轻链(b4)同种异型的Fab抗体与IgG Fab臂末端一半的外侧部分结合。这项技术在定位不太明确的免疫球蛋白决定簇方面应该具有价值。

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