Suppr超能文献

干扰素、双链RNA与RNA降解。从艾氏腹水瘤细胞中分离出均一的pppA(2'p5'A)n-1合成酶。

Interferon, double-stranded RNA, and RNA degradation. Isolation of homogeneous pppA(2'p5'A)n-1 synthetase from Ehrlich ascites tumor cells.

作者信息

Dougherty J P, Samanta H, Farrell P J, Lengyel P

出版信息

J Biol Chem. 1980 May 10;255(9):3813-6.

PMID:6154703
Abstract

pppA(2'p5'A)n-1 ((2'-5')(A)n) synthetase is one of the mediators of interferon action. On activation by double-stranded RNA, it converts ATP into (2'-5')(A)n; in turn, (2'-5')(A)n activates an endonuclease (RNase L) which cleaves single-stranded RNA. We report a simple procedure for the isolation of pure (2'-5')(A)n synthetase from interferon-treated Ehrlich ascites tumor cells. The procedure involves differential precipitation of the ribosomal salt wash fraction with ammonium sulfate and chromatography on DEAE-cellulose and CM-cellulose. The apparent molecular weight of the enzyme is 105,000 as determined by gel electrophoresis in sodium dodecyl sulfate and about 85,000 when determined by centrifugation through a glycerol gradient. The size range of the (2'-5')(A)n produced by the enzyme extends from the dimer to at least the pentadecamer.

摘要

pppA(2'p5'A)n-1((2'-5')(A)n)合成酶是干扰素作用的介质之一。在双链RNA激活后,它将ATP转化为(2'-5')(A)n;反过来,(2'-5')(A)n激活一种核酸内切酶(RNase L),该酶可切割单链RNA。我们报道了一种从经干扰素处理的艾氏腹水瘤细胞中分离纯化(2'-5')(A)n合成酶的简单方法。该方法包括用硫酸铵对核糖体盐洗部分进行分级沉淀,以及在DEAE-纤维素和CM-纤维素上进行色谱分离。通过十二烷基硫酸钠凝胶电泳测定,该酶的表观分子量为105,000,而通过甘油梯度离心测定时约为85,000。该酶产生的(2'-5')(A)n的大小范围从二聚体到至少十五聚体。

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