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硕大利什曼原虫:阶段特异性抗原以及前鞭毛体和无鞭毛体共有的抗原的鉴定

Leishmania major: identification of stage-specific antigens and antigens shared by promastigotes and amastigotes.

作者信息

Handman E, Jarvis H M, Mitchell G F

出版信息

Parasite Immunol. 1984 May;6(3):223-33. doi: 10.1111/j.1365-3024.1984.tb00795.x.

Abstract

A battery of antisera to Leishmania major was used to identify stage-specific antigens, or antigens expressed predominantly in amastigotes or promastigotes. At least 30 protein antigens common to amastigotes and promastigotes could be detected in 35S-methionine labelled preparations. They ranged in molecular weight from 25 000 to 165 000. Two amastigote specific antigens and five antigens expressed predominantly in the amastigote were detected in biosynthetically-labelled preparations. Five promastigote specific antigens were also identified. Antibodies from hyperimmunized mice that were resistant to reinfection with L. major recognized mainly antigens shared by the two life-cycle stages of the parasite. Analysis of parasite antigens on 'western blots' provided a different picture from that obtained by immunoprecipitation and gel electrophoresis of 35S-methionine labelled polypeptides. Only 19 antigens were detected and they were all shared by the two parasite forms. However, the abundance and immunogenicity of some of these antigens may be different in the two life-cycle stages of the parasite. Using the various sera, seven shared membrane antigens were identified in radio-iodinated preparations. Antibodies from hyperimmunized resistant mice that recognized shared antigens in 35S-methionine labelled preparations, detected four amastigote membrane antigens not detected by other sera. The function of the stage-specific antigens remains to be established. It is expected that individual antigens produced by recombinant DNA technology will allow these studies to proceed.

摘要

使用一组针对硕大利什曼原虫的抗血清来鉴定阶段特异性抗原,即主要在无鞭毛体或前鞭毛体中表达的抗原。在35S-甲硫氨酸标记的制剂中可检测到至少30种无鞭毛体和前鞭毛体共有的蛋白质抗原。它们的分子量范围从25000到165000。在生物合成标记的制剂中检测到两种无鞭毛体特异性抗原和五种主要在无鞭毛体中表达的抗原。还鉴定出五种前鞭毛体特异性抗原。来自对硕大利什曼原虫再感染具有抗性的超免疫小鼠的抗体主要识别该寄生虫两个生命周期阶段共有的抗原。对“蛋白质免疫印迹”上的寄生虫抗原分析提供了与通过对35S-甲硫氨酸标记的多肽进行免疫沉淀和凝胶电泳所获得的不同结果。仅检测到19种抗原,并且它们均为两种寄生虫形式所共有。然而,其中一些抗原在寄生虫的两个生命周期阶段中的丰度和免疫原性可能不同。使用各种血清,在放射性碘化制剂中鉴定出七种共有的膜抗原。来自超免疫抗性小鼠的抗体在35S-甲硫氨酸标记的制剂中识别共有抗原,检测到其他血清未检测到的四种无鞭毛体膜抗原。阶段特异性抗原的功能仍有待确定。预计通过重组DNA技术产生的单个抗原将使这些研究得以进行。

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