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冠状病毒MHV的RNA结合蛋白:用RNA覆盖-蛋白质印迹法检测单体和多聚体N蛋白

RNA-binding proteins of coronavirus MHV: detection of monomeric and multimeric N protein with an RNA overlay-protein blot assay.

作者信息

Robbins S G, Frana M F, McGowan J J, Boyle J F, Holmes K V

出版信息

Virology. 1986 Apr 30;150(2):402-10. doi: 10.1016/0042-6822(86)90305-3.

Abstract

RNA-binding proteins of coronavirus MHV-A59 were identified using an RNA overlay-protein blot assay (ROPBA). The major viral RNA-binding protein in virions and infected cells was the phosphorylated nucleocapsid protein N (50K). A new 140K virus structural protein was identified as a minor RNA-binding protein both in virions and in infected cells. The 140K protein was antigenically related to N, and upon reduction, yielded only 50K N. Thus, the 140K protein is probably a trimer of N subunits linked by intermolecular disulfide bonds. Several cellular RNA-binding proteins were also detected. RNA-binding of N was not nucleotide sequence specific. Single-stranded RNA of MHV, VSV, or cellular origin, a DNA probe of the MHV leader sequence, and double-stranded bovine rotavirus RNA could all bind to N. Binding of MHV RNA was optimal between pH 7 and 8, and the RNA could be eluted in 0.1 M NaCl. The ROPBA is a useful method for the initial identification of RNA-binding proteins, such as N and the 140K protein of murine coronavirus.

摘要

利用RNA覆盖蛋白印迹分析(ROPBA)鉴定了冠状病毒MHV - A59的RNA结合蛋白。病毒粒子和感染细胞中的主要病毒RNA结合蛋白是磷酸化核衣壳蛋白N(50K)。一种新的140K病毒结构蛋白在病毒粒子和感染细胞中均被鉴定为次要RNA结合蛋白。140K蛋白与N在抗原性上相关,还原后仅产生50K的N。因此,140K蛋白可能是通过分子间二硫键连接的N亚基三聚体。还检测到了几种细胞RNA结合蛋白。N的RNA结合不具有核苷酸序列特异性。MHV、VSV或细胞来源的单链RNA、MHV前导序列的DNA探针以及双链牛轮状病毒RNA都能与N结合。MHV RNA在pH 7至8之间结合最佳,且RNA可在0.1 M NaCl中洗脱。ROPBA是初步鉴定RNA结合蛋白(如鼠冠状病毒的N和140K蛋白)的一种有用方法。

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