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在下游开放阅读框中编码的鼠冠状病毒非结构蛋白的检测。

Detection of a murine coronavirus nonstructural protein encoded in a downstream open reading frame.

作者信息

Leibowitz J L, Perlman S, Weinstock G, DeVries J R, Budzilowicz C, Weissemann J M, Weiss S R

机构信息

Department of Pathology and Laboratory Medicine, University of Texas Health Science Center, Houston 77225.

出版信息

Virology. 1988 May;164(1):156-64. doi: 10.1016/0042-6822(88)90631-9.

Abstract

Mouse hepatitis virus (MHV) gene 5 contains two open reading frames. We have expressed the second open reading frame of this gene (gene 5 ORF 2) in an Escherichia coli expression system. This system utilized a plasmid which contained the promoter and the first 36 codons of the recA gene fused in frame with the MHV gene 5 ORF 2, which is fused in turn to the beta-galactosidase gene. The protein product of this gene fusion was used to raise antibody to gene 5 ORF 2. The specificity of the antibody was verified by immunoprecipitation of the in vitro transcribed and translated protein product of gene 5 ORF 2. The second reading frame of MHV gene 5 was shown to be expressed during the course of infection by immunocytochemistry and radioimmunoprecipitation using the antibody raised against the E. coli fusion protein and by two-dimensional gel electrophoresis.

摘要

小鼠肝炎病毒(MHV)基因5含有两个开放阅读框。我们已在大肠杆菌表达系统中表达了该基因的第二个开放阅读框(基因5开放阅读框2)。该系统使用了一种质粒,该质粒包含recA基因的启动子和前36个密码子,它们与MHV基因5开放阅读框2框内融合,而MHV基因5开放阅读框2又与β-半乳糖苷酶基因融合。该基因融合的蛋白质产物用于制备针对基因5开放阅读框2的抗体。通过对基因5开放阅读框2的体外转录和翻译的蛋白质产物进行免疫沉淀,验证了抗体的特异性。利用针对大肠杆菌融合蛋白产生的抗体,通过免疫细胞化学、放射免疫沉淀以及二维凝胶电泳表明,MHV基因5的第二个阅读框在感染过程中得以表达。

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