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冠状病毒、涎泪腺炎病毒和帕克大鼠冠状病毒结构蛋白的初步特征分析

Preliminary characterization of the structural proteins of the coronaviruses, sialodacryoadenitis virus and Parker's rat coronavirus.

作者信息

Barker M G, Percy D H, Hovland D J, MacInnes J I

机构信息

Department of Pathology, University of Guelph, Ontario.

出版信息

Can J Vet Res. 1994 Apr;58(2):99-103.

Abstract

A procedure was developed for the partial purification of the rat coronaviruses, sialodacryoadenitis virus (SDAV) and Parker's rat coronavirus (PRC). The SDAV and PRC were replicated in L-2 cell monolayer cultures, precipitated with ammonium sulphate, and further concentrated using sucrose density gradient centrifugation. The major SDAV and PRC proteins were identified by immunoblotting and compared with those of the JHM strain of mouse hepatitis virus (MHV-JHM). Monoclonal antibodies (MAb) against the M protein of JHM recognized proteins interpreted to be slightly smaller in immunoblots of SDAV and PRC (22.8 vs 23K for JHM). Similarly, a monoclonal antibody against the JHM N protein reacted with proteins of 53K in SDAV and PRC (vs 56 K for JHM). Polyclonal antisera to all three viruses also cross-reacted with the M and N proteins. Some cross-reactivity amongst the S proteins was observed. Based on these data, the structural proteins of the rat coronaviruses, SDAV and PRC are closely related to those of MHV-JHM.

摘要

已开发出一种用于大鼠冠状病毒——涎泪腺炎病毒(SDAV)和帕克大鼠冠状病毒(PRC)部分纯化的方法。SDAV和PRC在L - 2细胞单层培养物中进行复制,用硫酸铵沉淀,然后通过蔗糖密度梯度离心进一步浓缩。通过免疫印迹鉴定了SDAV和PRC的主要蛋白质,并与小鼠肝炎病毒JHM株(MHV - JHM)的蛋白质进行了比较。针对JHM的M蛋白的单克隆抗体(MAb)在SDAV和PRC的免疫印迹中识别出被认为略小的蛋白质(JHM为23K,SDAV和PRC为22.8K)。同样,一种针对JHM N蛋白的单克隆抗体与SDAV和PRC中53K的蛋白质发生反应(JHM为56K)。针对这三种病毒的多克隆抗血清也与M和N蛋白发生交叉反应。在S蛋白之间观察到了一些交叉反应性。基于这些数据,大鼠冠状病毒SDAV和PRC的结构蛋白与MHV - JHM的结构蛋白密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24f9/1263673/478ac4d55d53/cjvetres00030-0027-a.jpg

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