Pearson G R, Qualtiere L F
J Virol. 1978 Oct;28(1):344-51. doi: 10.1128/JVI.28.1.344-351.1978.
The Epstein-Barr virus (EBV)-induced membrane antigen (MA) was successfully solubilized from the membranes of viable EBV-infected Raji cells by treatment with papain (5 to 6 U per 1 X 10(7) to 2 X 10(7) cells). The loss of MA from viable cells was monitored by membrane immunofluorescence and antibody-dependent cellular cytotoxicity. Soluble MA was demonstrated in papain digests through inhibition of antibody-dependent cellular cytotoxicity and by inhibition of the binding of anti-MA antibodies to cells as detected by use of 125I-labeled staphylococcal protein A. Approximately 75% of the MA activity in the extracts was not sedimentable at 100,000 X g,, indicating that the majority of EBV MA activity that was released by this procedure was associated with small-molecular-weight material. Antiserum prepared from an owl monkey immunized with these papain extracts contained antibody to MA and neutralizing antibodies, but lacked detectable antibodies against viral capsid antigens and EBV-induced early antigens.
通过用木瓜蛋白酶(每1×10⁷至2×10⁷个细胞5至6单位)处理,成功地从存活的爱泼斯坦 - 巴尔病毒(EBV)感染的拉吉细胞的膜中溶解出EBV诱导的膜抗原(MA)。通过膜免疫荧光和抗体依赖性细胞毒性监测存活细胞中MA的损失。通过抑制抗体依赖性细胞毒性以及通过使用¹²⁵I标记的葡萄球菌蛋白A检测抑制抗MA抗体与细胞的结合,在木瓜蛋白酶消化物中证实了可溶性MA。提取物中约75%的MA活性在100,000×g下不可沉淀,表明通过该程序释放的大多数EBV MA活性与小分子物质相关。用这些木瓜蛋白酶提取物免疫的夜猴制备的抗血清含有抗MA抗体和中和抗体,但缺乏针对病毒衣壳抗原和EBV诱导的早期抗原的可检测抗体。