Suppr超能文献

脊髓灰质炎病毒非结构蛋白在酿酒酵母中的克隆与诱导合成。

Cloning and inducible synthesis of poliovirus non-structural proteins in Saccharomyces cerevisiae.

作者信息

Barco A, Carrasco L

机构信息

Centro de Biología Molecular, Universidad Autónoma de Madrid, Spain.

出版信息

Gene. 1995 Apr 14;156(1):19-25. doi: 10.1016/0378-1119(94)00872-p.

Abstract

Several coding regions of the poliovirus (PV) genome were cloned in the yeast Saccharomyces cerevisiae, and placed under the control of the inducible hybrid promoter pGAL/CYC, such that expression was triggered by incubating the cells in galactose (Gal)-containing medium. A number of PV genes encoding non-structural proteins, including 2Apro, 2B, 2C, 3A, 3AB and 3Cpro, were cloned and expressed in this eukaryotic system. The presence of these proteins after induction was detected by immunoblot analysis using specific antisera against each protein. The levels and the kinetics of protein synthesis after induction varied according to the PV protein analyzed. Thus, 2C was detected soon after Gal addition (3-5 h) and was one of the major polypeptides synthesized by yeast cells after 16 h of induction. In contrast, only low levels of synthesis were observed for 3A or 3AB, and then only after several hours of growth in Gal. The induction of the PV protease, 2Apro, was highly toxic for the cells such that growth was arrested after 5 h of induction and cell survival sharply declined.

摘要

脊髓灰质炎病毒(PV)基因组的几个编码区被克隆到酿酒酵母中,并置于可诱导的杂交启动子pGAL/CYC的控制下,这样通过将细胞在含半乳糖(Gal)的培养基中培养来触发表达。一些编码非结构蛋白的PV基因,包括2A蛋白酶、2B、2C、3A、3AB和3C蛋白酶,在这个真核系统中被克隆并表达。诱导后这些蛋白的存在通过使用针对每种蛋白的特异性抗血清进行免疫印迹分析来检测。诱导后蛋白质合成的水平和动力学根据所分析的PV蛋白而有所不同。因此,在添加Gal后不久(3 - 5小时)就检测到了2C,并且它是诱导16小时后酵母细胞合成的主要多肽之一。相比之下,仅观察到3A或3AB的合成水平较低,且仅在Gal中生长数小时后才出现。PV蛋白酶2A蛋白酶的诱导对细胞具有高度毒性,以至于诱导5小时后生长停止且细胞存活率急剧下降。

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