Suppr超能文献

烟草蚀纹病毒多聚蛋白加工的突变分析:含49千道尔顿蛋白酶的多聚蛋白的顺式和反式蛋白水解活性

Mutational analysis of tobacco etch virus polyprotein processing: cis and trans proteolytic activities of polyproteins containing the 49-kilodalton proteinase.

作者信息

Carrington J C, Cary S M, Dougherty W G

机构信息

Department of Microbiology, Oregon State University, Corvallis 97331-3804.

出版信息

J Virol. 1988 Jul;62(7):2313-20. doi: 10.1128/JVI.62.7.2313-2320.1988.

Abstract

The genome of tobacco etch virus contains a single open reading frame with the potential to encode a 346-kilodalton (kDa) polyprotein. The large polyprotein is cleaved at several positions by a tobacco etch virus genome-encoded, 49-kDa proteinase. The locations of the 49-kDa proteinase-mediated cleavage sites flanking the 71-kDa cytoplasmic pinwheel inclusion protein, 6-kDa protein, 49-kDa proteinase, and 58-kDa putative polymerase have been determined by using cell-free expression, proteolytic processing, and site-directed mutagenesis systems. Each of these sites is characterized by the conserved sequence motif Glu-Xaa-Xaa-Tyr-Xaa-Gln-Ser or Gly (in which cleavage occurs after the Gln residue). The amino acid residue (Gln) predicted to occupy the -1 position relative to the scissile bond has been substituted, by mutagenesis of cloned cDNA, at each of four cleavage sites. The altered sites were not cleaved by the 49-kDa proteinase. A series of synthetic polyproteins that contained the 49-kDa proteinase linked to adjoining proteins via defective cleavage sites were expressed, and their proteolytic activities were analyzed. As part of a polyprotein, the proteinase was found to exhibit cis (intramolecular) and trans (intermolecular) activity.

摘要

烟草蚀纹病毒的基因组包含一个单一的开放阅读框,有可能编码一种346千道尔顿(kDa)的多聚蛋白。这种大的多聚蛋白在几个位置被烟草蚀纹病毒基因组编码的49-kDa蛋白酶切割。通过使用无细胞表达、蛋白水解加工和定点诱变系统,已经确定了位于71-kDa细胞质风车状内含体蛋白、6-kDa蛋白、49-kDa蛋白酶和58-kDa推定聚合酶两侧的49-kDa蛋白酶介导的切割位点的位置。这些位点中的每一个都以保守的序列基序Glu-Xaa-Xaa-Tyr-Xaa-Gln-Ser或Gly为特征(其中切割发生在Gln残基之后)。通过对克隆的cDNA进行诱变,在四个切割位点中的每一个位点上,预测相对于切割键占据-1位置的氨基酸残基(Gln)都被取代。改变后的位点不能被49-kDa蛋白酶切割。表达了一系列通过有缺陷的切割位点将49-kDa蛋白酶与相邻蛋白连接的合成多聚蛋白,并分析了它们的蛋白水解活性。作为多聚蛋白的一部分,发现该蛋白酶表现出顺式(分子内)和反式(分子间)活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad8/253386/fe4bb431d3b5/jvirol00086-0114-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验