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作 者:李红[1] 周佳敏[1] 王国华[1] 高杰英[1] 陈德蕙[1]
机构地区:[1]军事医学科学院微生物流行病研究所,军事医学科学院基础医学研究所
出 处:《单克隆抗体通讯》1994年第1期36-39,74,共5页
摘 要:本文报告应用抗福氏2a痢疾杆菌膜成份McAb及胶体金探针对细菌膜抗原进行了定位。结果显示4种抗脂多糖McAb(3A6、2E6、4F1.2A3)可不均一的识别位于细菌表面的抗原,而另外一种抗LPSMCAb(1G8)和一抗膜蛋白McAb(1A1)识别的抗原未暴露于细菌表面。应用细菌膜碎片包埋前染色成功地定位了抗胰蛋白McAb1A1位于细菌内膜的抗原。与McAb的生物学活性比较表明。阳性标记细菌表面抗原的McAb的抗原与其阻断志贺氏菌接触性溶血试验和对小鼠的被动保护力密切相关。提示免疫电镜标记技术确定抗原表位在细菌表面的可及性和拷贝数对构建和筛选痢疾工程菌苗具有重要意义。The localizations of Shigella flexneri 2a membrane antigens were determined by electron mieroscpy by using six McAbs against Shigella flexneri 2a membrane components and immunogold labbing.Binding of the McAbs on whole bacterial cells indicated that the antigens recognized by McAbs 3A6,2E6,4F1 and 2A3 were exposed on the cell surface,and those by McAbs 1A1 and 1G8 were not. Labeling for McAb 1A1was successfully performed by using sonicated bacterial sediment and pre-embeded immunogold staining. Gold particles on the inner membrane of the bacteria were observed.Comparing with the biological activities of these McAbs,the results showed that exposure of the antigenic determinents on the bacteria surface had a direct bearing on their bloking activities of the contact haemolysis and the passive protecting capacities in mice.All these suggested that understanding of the accessibility and numbers of copies to the bacterial protecting antigenic determinents had a great significance in the construction and s election of Shigella vaccine.
分 类 号:R378.25[医药卫生—病原生物学]
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