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The First Human Epitope Map of the Alphaviral E1 and E2 Proteins Reveals a New E2 Epitope with Significant Virus Neutralizing Activity

机译:甲病毒E1和E2蛋白的第一个人类抗原决定簇图揭示了具有重要病毒中和活​​性的新E2表位

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摘要

Although the murine immune response to Venezuelan equine encephalitis virus (VEEV) is well-characterized, little is known about the human antibody response to VEEV. In this study we used phage display technology to isolate a panel of 11 VEEV-specfic Fabs from two human donors. Seven E2-specific and four E1-specific Fabs were identified and mapped to five E2 epitopes and three E1 epitopes. Two neutralizing Fabs were isolated, E2-specific F5 and E1-specific L1A7, although the neutralizing capacity of L1A7 was 300-fold lower than F5. F5 Fab was expressed as a complete IgG1 molecule, F5 native (n) IgG. Neutralization-escape VEEV variants for F5 nIgG were isolated and their structural genes were sequenced to determine the theoretical binding site of F5. Based on this sequence analysis as well as the ability of F5 to neutralize four neutralization-escape variants of anti-VEEV murine monoclonal antibodies (mapped to E2 amino acids 182–207), a unique neutralization domain on E2 was identified and mapped to E2 amino acids 115–119.
机译:尽管鼠类对委内瑞拉马脑炎病毒(VEEV)的免疫反应具有很好的特征,但对人对VEEV的抗体反应知之甚少。在这项研究中,我们使用噬菌体展示技术从两个人类供体中分离出11种VEEV特异性Fab。确定了七个E2特异性和四个E1特异性Fab,并将其定位到五个E2表位和三个E1表位。分离了两个中和Fab,E2特异性F5和E1特异性L1A7,尽管L1A7的中和能力比F5低300倍。 F5 Fab被表达为完整的IgG1分子,即F5天然(n)IgG。分离了用于F5 nIgG的中和逃逸VEEV变体,并对它们的结构基因进行测序以确定F5的理论结合位点。基于此序列分析以及F5中和抗VEEV鼠单克隆抗体的四种中和逃逸变体(映射至E2氨基酸182-207)的能力,鉴定了E2上的独特中和结构域并将其定位到E2氨基酸115–119。

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