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通过与中和抗体 Fab 复合物的低温电子显微镜观察鉴定出肠道病毒 71 的一个菌株特异性表位。

A strain-specific epitope of enterovirus 71 identified by cryo-electron microscopy of the complex with fab from neutralizing antibody.

机构信息

Department of Medicine, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.

出版信息

J Virol. 2013 Nov;87(21):11363-70. doi: 10.1128/JVI.01926-13. Epub 2013 Aug 14.

Abstract

Enterovirus 71 (EV71) is a picornavirus that causes outbreaks of hand, foot, and mouth disease (HFMD), primarily in the Asia-Pacific area. Unlike coxsackievirus A16, which also causes HFMD, EV71 induces severe neuropathology leading to high fatalities, especially among children under the age of 6 years. Currently, no established vaccines or treatments are available against EV71 infection. The monoclonal antibody MA28-7 neutralizes only specific strains of EV71 that have a conserved glycine at amino acid VP1-145, a surface-exposed residue that maps to the 5-fold vertex and that has been implicated in receptor binding. The cryo-electron microscopy structure of a complex between EV71 and the Fab fragment of MA28-7 shows that only one Fab fragment occupies each 5-fold vertex. A positively charged patch, which has also been implicated in receptor binding, lies within the Fab footprint. We identify the strain-specific epitope of EV71 and discuss the possible neutralization mechanisms of the antibody.

摘要

肠道病毒 71 型(EV71)是一种小 RNA 病毒,可引起手足口病(HFMD)爆发,主要发生在亚太地区。与同样引起 HFMD 的柯萨奇病毒 A16 不同,EV71 可导致严重的神经病理学,导致高死亡率,尤其是 6 岁以下儿童。目前,尚无针对 EV71 感染的既定疫苗或治疗方法。单克隆抗体 MA28-7 仅中和具有保守甘氨酸的特定 EV71 株,该氨基酸位于 VP1-145 处,这是一个位于表面的残基,与受体结合有关。EV71 与 MA28-7 的 Fab 片段之间的冷冻电镜结构表明,每个五重对称顶点仅占据一个 Fab 片段。一个带正电荷的斑块也与受体结合有关,位于 Fab 足迹内。我们确定了 EV71 的株特异性表位,并讨论了抗体的可能中和机制。

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