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锥虫可变表面抗原:使用二维凝胶电泳和单克隆抗体的研究

Trypanosome variable surface antigens: studies using two-dimensional gel electrophoresis and monoclonal antibodies.

作者信息

Pearson T W, Kar S K, McGuire T C, Lundin L B

出版信息

J Immunol. 1981 Mar;126(3):823-8.

PMID:7007502
Abstract

Variable surface antigens of cloned populations of African trypanosomes were studied using 2-dimensional gel electrophoresis and monoclonal antibodies. Two-dimensional gel maps showed that the only major differences in protein profiles of the non-nuclear materials from different clones of solubilized trypanosomes were attributable to the variable surface antigens and that purification doesn't alter these molecules, at least with respect to charge and apparent m.w. Purified variable surface antigens were used as immunogens and a number of monoclonal antibodies were derived using cell-fusion technology. In radioimmunoassay, each of the monoclonal reagents was shown to be specific for the immunizing antigen, and in immunofluorescence tests using acetone-fixed trypanosomes, each bound specifically to the clone from which the antigens were purified. Only 20% of the monoclonal reagents bound to living trypanosomes, however, providing evidence for both exposed and nonexposed antigenic sites on the variable surface antigens. Those reagents derived to a single antigen bound to different nonoverlapping antigenic sites, which were on the protein portion of the molecules and not the carbohydrate moieties. The data show that monoclonal antibodies are ideal probes for studying localization of antigenic sites on the antigen molecules and for studying antigen synthesis, glycosylation, and architecture in relation to the cell surface. In addition, the finding of exposed and nonexposed antigenic sites on trypanosome variable antigens allows a possible explanation for the role of the antigens in pathogenesis of African trypanosomiasis.

摘要

利用二维凝胶电泳和单克隆抗体对克隆的非洲锥虫群体的可变表面抗原进行了研究。二维凝胶图谱显示,来自不同克隆的溶解锥虫的非核物质的蛋白质谱中唯一的主要差异归因于可变表面抗原,并且纯化不会改变这些分子,至少在电荷和表观分子量方面不会改变。纯化的可变表面抗原被用作免疫原,并使用细胞融合技术获得了许多单克隆抗体。在放射免疫测定中,每种单克隆试剂都显示对免疫抗原具有特异性,并且在使用丙酮固定的锥虫的免疫荧光试验中,每种试剂都特异性结合从中纯化抗原的克隆。然而,只有20%的单克隆试剂与活锥虫结合,这为可变表面抗原上暴露和未暴露的抗原位点提供了证据。那些针对单一抗原产生的试剂结合到不同的非重叠抗原位点,这些位点位于分子的蛋白质部分而非碳水化合物部分。数据表明,单克隆抗体是研究抗原分子上抗原位点定位以及研究与细胞表面相关的抗原合成、糖基化和结构的理想探针。此外,在锥虫可变抗原上发现暴露和未暴露的抗原位点,为这些抗原在非洲锥虫病发病机制中的作用提供了一种可能的解释。

相似文献

1
Trypanosome variable surface antigens: studies using two-dimensional gel electrophoresis and monoclonal antibodies.锥虫可变表面抗原:使用二维凝胶电泳和单克隆抗体的研究
J Immunol. 1981 Mar;126(3):823-8.
2
Monoclonal xenogeneic antibodies to murine cell surface antigens: identification of novel leukocyte differentiation antigens.针对鼠细胞表面抗原的单克隆异种抗体:新型白细胞分化抗原的鉴定。
Eur J Immunol. 1978 Aug;8(8):539-51. doi: 10.1002/eji.1830080802.
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Analysis of the variable antigen composition of Trypanosoma brucei brucei metacyclic trypanosomes using monoclonal antibodies.利用单克隆抗体分析布氏布氏锥虫循环后期锥虫的可变抗原组成。
Acta Trop. 1983 Mar;40(1):19-24.
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Evidence for reappearance of Trypanosoma brucei variable antigen types in relapse populations.布氏锥虫可变抗原类型在复发群体中重现的证据。
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Identification of a tryptophan-like epitope borne by the variable surface glycoprotein (VSG) of African trypanosomes.非洲锥虫可变表面糖蛋白(VSG)携带的色氨酸样表位的鉴定。
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引用本文的文献

1
Monoclonal antibodies against microorganisms.抗微生物单克隆抗体。
Eur J Clin Microbiol. 1984 Oct;3(5):387-98. doi: 10.1007/BF02017358.
2
Hybridomas: a new dimension in biological analyses.杂交瘤:生物学分析的新维度。
In Vitro. 1981 Dec;17(12):1036-50. doi: 10.1007/BF02618601.
3
Antibody responses in resistant and susceptible inbred mice infected with Trypanosoma congolense.感染刚果锥虫的抗性和易感近交系小鼠的抗体反应。
Immunology. 1986 Feb;57(2):297-303.
4
A flagellar pocket membrane fraction from Trypanosoma brucei rhodesiense: immunogold localization and nonvariant immunoprotection.来自布氏罗得西亚锥虫的鞭毛袋膜组分:免疫金定位和非可变免疫保护
Infect Immun. 1988 Jan;56(1):92-8. doi: 10.1128/iai.56.1.92-98.1988.
5
T-cell-independent and T-cell-dependent B-cell responses to exposed variant surface glycoprotein epitopes in trypanosome-infected mice.锥虫感染小鼠中针对暴露的变异表面糖蛋白表位的非T细胞依赖性和T细胞依赖性B细胞应答。
Infect Immun. 1990 Jul;58(7):2337-42. doi: 10.1128/iai.58.7.2337-2342.1990.