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刚地弓形虫:用单克隆抗体对四种免疫显性抗原进行免疫细胞化学研究

Toxoplasma gondii: immunocytochemistry of four immunodominant antigens with monoclonal antibodies.

作者信息

Bonhomme A, Boulanger F, Bharadwaj L M, Puygauthier-Toubas D, Bonhomme P, Pluot M, Pinon J M

机构信息

Unité INSERM U.314, Hôpital Maison Blanche, Reims, France.

出版信息

Exp Parasitol. 1990 Nov;71(4):439-51. doi: 10.1016/0014-4894(90)90070-s.

Abstract

Four monoclonal antibodies in which diagnostic usefulness has been observed, concerning congenital, acquired, and reactivated toxoplasmosis, were raised against Toxoplasma gondii tachyzoïtes in order to localize immunodominant antigens. On immunoblots, it appears that McAb IV47, McAB GII9, McAb II38, and McAb IE10 identify families of proteins with estimated molecular weights of 28-30 kDa, 30 kDa, 45-50 kDa, and 66-70 kDa, respectively. By immunogold preembedding techniques one can observe an homogeneous labeling of the outer pellicle of the tachyzoïtes with the McAb GII9 and IV47 and a light labeling with the McAb II38 and IE10. The three-dimensional observation of cell surface antigens is performed by applying a modified metal extraction replica method, i.e., A plasma polymerization method of glow discharge by Tanaka (1979). By immunogold preembedding techniques [with saponin permeabilization (0.1%)], and by immunogold postembedding techniques, a labeling of the rhoptries is observed with McAb GII9 and McAb IV47 but essentially all label is found with McAb II38 and IE10. With McAb GII9 a uniform labeling is observed on the cell surface. By immunoenzymatic techniques (peroxidase) a cell surface labeling is observed with the four McAb. Intracellular Toxoplasma, the outer pellicle, and the vesicles of the network (elaborated by Toxoplasma in parasitophorous vacuole) are also labeled with McAb IE10. These results indicate that McAb GII9 recognizes antigens of the antigen family (P 30) located on the cell surface and in the rhoptries. The antigen recognized by McAb IV47 is essentially located on and beneath the Toxoplasma cell surface membrane, and McAb II38 and IE10 identify preferentially rhoptry proteins.

摘要

为了定位免疫显性抗原,针对刚地弓形虫速殖子制备了四种单克隆抗体,已观察到它们在先天性、获得性和再激活型弓形虫病诊断中的应用价值。在免疫印迹上,似乎单克隆抗体IV47、单克隆抗体GII9、单克隆抗体II38和单克隆抗体IE10分别识别估计分子量为28 - 30 kDa、30 kDa、45 - 50 kDa和66 - 70 kDa的蛋白质家族。通过免疫金预包埋技术,可以观察到单克隆抗体GII9和IV47对速殖子外膜的均匀标记,以及单克隆抗体II38和IE10的轻度标记。通过应用改良的金属提取复型方法,即田中(1979年)的辉光放电等离子体聚合方法,对细胞表面抗原进行三维观察。通过免疫金预包埋技术[用皂苷通透(0.1%)]和免疫金包埋后技术,观察到单克隆抗体GII9和单克隆抗体IV47对棒状体有标记,但基本上所有标记都见于单克隆抗体II38和IE10。用单克隆抗体GII9在细胞表面观察到均匀标记。通过免疫酶技术(过氧化物酶),用这四种单克隆抗体观察到细胞表面标记。细胞内的弓形虫、外膜以及网络小泡(由弓形虫在寄生泡中形成)也被单克隆抗体IE10标记。这些结果表明,单克隆抗体GII9识别位于细胞表面和棒状体中的抗原家族(P 30)的抗原。单克隆抗体IV47识别的抗原主要位于弓形虫细胞表面膜上和膜下,而单克隆抗体II38和IE10优先识别棒状体蛋白。

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