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Monoclonal antibodies to P24 and P61 immunodominant antigens from Nocardia brasiliensis.

机译:来自巴西诺卡氏菌的针对P24和P61免疫显性抗原的单克隆抗体。

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摘要

We prepared a Nocardia brasiliensis cell extract and purified two immunodominant antigens with molecular weights of 61,000 and 24,000. The isolated proteins were shown to be reasonably pure when analyzed with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (8 to 18% polyacrylamide gradient) and stained with Coomassie blue and silver nitrate. By using an immunoelectrotransfer blot method (Western blotting), we demonstrated that these two purified proteins reacted strongly with serum from N. brasiliensis-infected mycetoma patients. To obtain anti-P61 and anti-P24 monoclonal antibodies (MAbs), we used an N. brasiliensis cell extract as the antigen for the first immunization; 2 weeks later female mice were reimmunized with a semipurified antigen containing the P24 or P61 fraction. A booster injection was given 3 days before the fusion was carried out. Two hybrids that reacted strongly with P24 were cloned by limiting dilution, the generated MAbs were analyzed for isotyping, and their specificity was tested in a Western blot assay with cell extracts from Nocardia asteroides and Mycobacterium tuberculosis cultures. Anti-P24 MAbs were shown to be specific for N. brasiliensis HUJEG-1 and did not cross-react with either the N. asteroides or M. tuberculosis strains used. However, additional studies with several N. asteroides and N. brasiliensis strains are needed to investigate whether there are cross-reactions between strains or species when these MAbs are used. The anti-P61 and anti-24 MAbs were used to locate the antigen in N. brasiliensis cells by immunofluorescence. The lack of reaction with intact cells suggests that the P24 and P61 antigens are not exposed in the complete bacterial cell surface or that the recognized epitopes are different. Only one anti-P61 MAb that reacted specifically with the N. brasiliensis cell extract was obtained.
机译:我们制备了巴西诺卡氏菌细胞提取物,并纯化了两种免疫显性抗原,分子量分别为61,000和24,000。用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(8%至18%聚丙烯酰胺梯度)进行分析,并用考马斯亮蓝和硝酸银染色时,分离出的蛋白质显示出合理的纯度。通过使用免疫电转移印迹方法(Western印迹),我们证明了这两种纯化的蛋白质与来自巴西猪传染性支原体感染的菌丝瘤患者的血清强烈反应。为了获得抗P61和抗P24单克隆抗体(MAbs),我们使用巴西猪笼草细胞提取物作为抗原进行首次免疫; 2周后,雌性小鼠用含有P24或P61级分的半纯化抗原再免疫。在进行融合前3天进行加强注射。通过有限稀释克隆了两个与P24强烈反应的杂种,分析了产生的单克隆抗体的同种型,并用来自小野诺卡氏菌和结核分枝杆菌培养物的细胞提取物在Western blot分析中测试了它们的特异性。已显示抗P24 MAb对巴西猪笼草HUJEG-1具有特异性,并且与所用的小行星猪笼草或结核分枝杆菌菌株均无交叉反应。但是,还需要对几种小行星猪笼草和巴西猪笼草菌株进行额外的研究,以调查使用这些单克隆抗体时菌株或物种之间是否存在交叉反应。抗P61和抗24 MAb用于通过免疫荧光在巴西猪笼草细胞中定位抗原。与完整细胞的反应缺乏表明P24和P61抗原没有暴露在完整的细菌细胞表面中,或者所识别的表位是不同的。仅获得了一种与巴西猪笼草细胞提取物特异性反应的抗P61 MAb。

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