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用单克隆抗体检测爱泼斯坦-巴尔病毒诱导的早期膜蛋白

Detection by monoclonal antibodies of an early membrane protein induced by Epstein-Barr virus.

作者信息

Balachandran N, Pittari J, Hutt-Fletcher L M

出版信息

J Virol. 1986 Nov;60(2):369-75. doi: 10.1128/JVI.60.2.369-375.1986.

Abstract

Two monoclonal antibodies, E8B3 and E8D2, were raised against Epstein-Barr virus (EBV)-producing cells and were shown to immunoprecipitate a protein with an approximate molecular weight of 105,000 (p105). The protein was detectable only in EBV-containing cells which were supporting the virus lytic cycle, and its synthesis increased after cells were induced with phorbol esters. The molecule was radiolabeled and immunoprecipitated from virus-producing cells that had been extrinsically labeled with 125I, and the antibodies E8B3 and E8D2 reacted in immunofluorescence assays with infected cells; the molecule was also associated with virion particles. Synthesis of p105 was not blocked by phosphonoacetic acid and could be induced in Raji cells by superinfection with virus derived from P3HR1 cells. These data support the conclusion that p105 is an EBV-specific early membrane protein.

摘要

两种单克隆抗体E8B3和E8D2是针对产生爱泼斯坦-巴尔病毒(EBV)的细胞制备的,它们能免疫沉淀一种分子量约为105,000的蛋白质(p105)。该蛋白质仅在支持病毒裂解周期的含EBV细胞中可检测到,在用佛波酯诱导细胞后其合成增加。该分子经放射性标记后,从用125I进行外部标记的病毒产生细胞中进行免疫沉淀,并且抗体E8B3和E8D2在免疫荧光试验中与感染细胞发生反应;该分子也与病毒粒子相关。p105的合成不受膦甲酸的阻断,并且通过用源自P3HR1细胞的病毒超感染Raji细胞可诱导其合成。这些数据支持p105是一种EBV特异性早期膜蛋白的结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/848f/288902/c389d9f373bf/jvirol00168-0044-a.jpg

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