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在昆虫细胞中表达的普马拉病毒核衣壳蛋白的抗原特性及诊断潜力

Antigenic properties and diagnostic potential of puumala virus nucleocapsid protein expressed in insect cells.

作者信息

Vapalahti O, Lundkvist A, Kallio-Kokko H, Paukku K, Julkunen I, Lankinen H, Vaheri A

机构信息

Haartman Institute, Department of Virology, Helsinki University, Finland.

出版信息

J Clin Microbiol. 1996 Jan;34(1):119-25. doi: 10.1128/jcm.34.1.119-125.1996.

Abstract

Puumala virus (PUU) is a member of the genus Hantavirus in the family Bunyaviridae and the causative agent of nephropathia epidemica, a European form of hemorrhagic fever with renal syndrome. Sera of nephropathia epidemica patients react specifically with PUU nucleocapsid (N) protein. In order to safely provide large quantities of antigen for diagnostic purposes, PUU Sotkamo strain N protein was expressed by using the baculovirus system in Sf9 insect cells to up to 30 to 50% of the total cellular protein. The recombinant N protein (bac-PUU-N) was solubilized with 6 M urea, dialyzed, and purified by anion-exchange liquid chromatography. In an immunoglobulin M mu-capture assay purified and unpurified bac-PUU-N antigen showed identical results compared with the results of a similar assay based on native PUU antigen grown in Vero E6 cells. An immunoglobulin G monoclonal antibody-capture assay based on unpurified bac-PUU-N also showed results identical to those of an assay with native PUU-N antigen. Moreover, a panel of monoclonal antibodies reactive with eight different epitopes showed identical reactivity patterns with both natural and bac-PUU-N antigen, while two epitopes in PUU-N expressed as a fusion protein in Escherichia coli were not recognized. Puumala hantavirus N protein expressed by the baculovirus system offers a safe and inexpensive source of specific antigen for large-scale diagnostic and seroepidemiological purposes.

摘要

普马拉病毒(PUU)是布尼亚病毒科汉坦病毒属的成员,是流行性肾病的病原体,流行性肾病是欧洲的一种肾综合征出血热形式。流行性肾病患者的血清与普马拉病毒核衣壳(N)蛋白发生特异性反应。为了安全地提供大量用于诊断目的的抗原,利用杆状病毒系统在Sf9昆虫细胞中表达普马拉病毒索特卡莫株N蛋白,其表达量高达细胞总蛋白的30%至50%。重组N蛋白(bac-PUU-N)用6 M尿素溶解、透析,并通过阴离子交换液相色谱法纯化。在免疫球蛋白Mμ捕获试验中,纯化和未纯化的bac-PUU-N抗原与基于在Vero E6细胞中培养的天然普马拉病毒抗原的类似试验结果相比,显示出相同的结果。基于未纯化的bac-PUU-N的免疫球蛋白G单克隆抗体捕获试验也显示出与天然普马拉病毒N抗原试验相同的结果。此外,一组与八个不同表位反应的单克隆抗体对天然和bac-PUU-N抗原显示出相同的反应模式,而在大肠杆菌中作为融合蛋白表达的普马拉病毒N中的两个表位未被识别。通过杆状病毒系统表达的普马拉汉坦病毒N蛋白为大规模诊断和血清流行病学目的提供了一种安全且廉价的特异性抗原来源。

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