Yang Z H
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1989 Feb;11(1):41-5.
In order to differentiate a new EBV strain, H18, from other EBV strains, we prepared and screened by indirect immunofluorescence (IF) viable cells and fixed cells of a series hybridoma lines that produce monoclonal antibodies against H18 EBV membrane antigen (MA). T1-11 clone was used for further study: T14-11 antibody neutralizes EBV in vitro and recognizes polypeptides P220, P175 and P140 from purified H18 EBV particles, as shown by the Western Blot technique. The presence of the three polypeptides on the plasma membrane and in the cytoplasm may be detected by IF using T14-11 antibody. Treatment with puromycin completely abolished the expression of the antigen recognized by T14-11, and this Ab was shown to be specific for an early membrane antigen of EBV.
为了将一种新的EBV毒株H18与其他EBV毒株区分开来,我们制备了一系列产生抗H18 EBV膜抗原(MA)单克隆抗体的杂交瘤细胞系的活细胞和固定细胞,并通过间接免疫荧光(IF)进行筛选。T1-11克隆用于进一步研究:T14-11抗体在体外可中和EBV,并且如蛋白质印迹技术所示,可识别来自纯化的H18 EBV颗粒的多肽P220、P175和P140。使用T14-11抗体通过IF可检测到这三种多肽在质膜和细胞质中的存在。用嘌呤霉素处理可完全消除T14-11所识别抗原的表达,并且该抗体被证明对EBV的一种早期膜抗原有特异性。