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抗同种异型抗体诱导产生的小鼠单克隆抗体展现出兔VHa1同种异型的内影像:免疫电子显微镜直接观察

Mouse monoclonal antibodies induced by anti-allotype antibody display internal images of the rabbit VHa1 allotype: direct visualization by immunoelectron microscopy.

作者信息

Van Cleave V H, Murti K G, Metzger D W

出版信息

Eur J Immunol. 1986 Jun;16(6):701-7. doi: 10.1002/eji.1830160619.

Abstract

We have previously shown that injection of adult rabbits with anti-immunoglobulin (Ig) antibody (Ab) induces the expression of genetically unexpected Ig markers, i.e., a1 allotypic determinants. We now show that these rabbit Ig markers can also be induced in mice by a similar treatment; in the latter case the a1 determinants are located in the antigen-combining site and thus represent "internal images". Two monoclonal antibodies (mAb) were developed from mice treated with anti-allotype Ab. These mAb were reactive with all homologous and heterologous anti-a1 Ab but not normal Ig; efficiently inhibited the binding of rabbit a1 Ig to anti-a1 Ab; and elicited the production of anti-allotype Ab when injected into normal mice. To determine whether the a1-like determinants on these mAb were located in the antigen-combining site, immunoelectron microscopy was utilized to directly visualize Ab complexes. Complexes composed of intact Ab and anti-a1 Fab fragments yielded uniform binding patterns which were identical to those produced by anti-idiotypic reactions. In each case, an identical tip-to-tip binding configuration was observed with a single Fab fragment attached at an approximate 180 degree angle to the V region terminus of each Ab arm. In contrast, rabbit a1 Ig bound as many as two anti-a1 fragments per Ig arm; these fragments were attached laterally and at right angles to the intact molecule. These mAb thus provide the first direct evidence that Ab2 beta determinants are located in, or near, the antigen-combining site.

摘要

我们之前已经表明,给成年兔子注射抗免疫球蛋白(Ig)抗体(Ab)可诱导出基因上意外的Ig标记物,即a1同种异型决定簇。我们现在表明,通过类似的处理也可在小鼠中诱导出这些兔子Ig标记物;在后一种情况下,a1决定簇位于抗原结合位点,因此代表“内影像”。从用抗同种异型Ab处理的小鼠中制备了两种单克隆抗体(mAb)。这些mAb与所有同源和异源抗a1 Ab反应,但不与正常Ig反应;有效抑制兔a1 Ig与抗a1 Ab的结合;当注入正常小鼠时可引发抗同种异型Ab的产生。为了确定这些mAb上的a1样决定簇是否位于抗原结合位点,利用免疫电子显微镜直接观察Ab复合物。由完整Ab和抗a1 Fab片段组成的复合物产生均匀的结合模式,这与抗独特型反应产生的模式相同。在每种情况下,观察到相同的尖端对尖端结合构型,单个Fab片段以大约180度角连接到每个Ab臂的V区末端。相比之下,兔a1 Ig每个Ig臂可结合多达两个抗a1片段;这些片段横向且与完整分子成直角连接。因此,这些mAb提供了首个直接证据,表明Ab2β决定簇位于抗原结合位点或其附近。

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