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以牛乳头瘤病毒为载体的小鼠细胞组成型生产人干扰素。

Constitutive production of human interferons by mouse cells with bovine papillomavirus as a vector.

作者信息

Fukunaga R, Sokawa Y, Nagata S

出版信息

Proc Natl Acad Sci U S A. 1984 Aug;81(16):5086-90. doi: 10.1073/pnas.81.16.5086.

Abstract

Mouse C127I cells were transformed with a chimeric plasmid consisting of bovine papillomavirus and human interferon (HuIFN) gene (either IFN-gamma or IFN-alpha 5) placed under the control of simian virus 40 early promoter. The transformed cells retained 30-50 copies each of the hybrid plasmid extrachromosomally and secreted a high level of HuIFNs constitutively up to 3-4 X 10(5) international units/ml. The secreted HuIFN-gamma had no detectable activity on mouse cells, whereas HuIFN-alpha 5 was slightly active on mouse cells. Each IFN was neutralized either by anti-HuIFN-gamma or anti-HuIFN-alpha antiserum. The partially purified 35S-labeled HuIFN-gamma produced by the transformed cells showed heterogeneous bands with apparent Mrs of 22,000-25,000 on NaDodSO4/polyacrylamide gel electrophoresis. This value is similar to that of natural IFN-gamma and larger than the molecular weight calculated from the amino acid sequence, which suggests that HuIFN-gamma secreted by transformed mouse cells was glycosylated. The 35S-labeled IFN-alpha 5, immunoprecipitated with anti-HuIFN-alpha antiserum from the supernatant of the transformed cells, had a molecular weight of mature protein. These results suggest that the bovine papillomavirus vector can be used to produce a large quantity of foreign proteins in mammalian cells.

摘要

用一种嵌合质粒转化小鼠C127I细胞,该嵌合质粒由牛乳头瘤病毒和人干扰素(HuIFN)基因(IFN-γ或IFN-α5)组成,置于猴病毒40早期启动子的控制之下。转化细胞在染色体外各自保留30 - 50个拷贝的杂交质粒,并持续分泌高水平的HuIFN,最高可达3 - 4×10⁵国际单位/毫升。分泌的HuIFN-γ对小鼠细胞没有可检测到的活性,而HuIFN-α5对小鼠细胞有轻微活性。每种干扰素都可被抗HuIFN-γ或抗HuIFN-α抗血清中和。转化细胞产生的部分纯化的³⁵S标记的HuIFN-γ在十二烷基硫酸钠/聚丙烯酰胺凝胶电泳上显示出表观分子量为22,000 - 25,000的异质条带。这个值与天然IFN-γ的值相似,且大于根据氨基酸序列计算出的分子量,这表明转化的小鼠细胞分泌的HuIFN-γ是糖基化的。用抗HuIFN-α抗血清从转化细胞的上清液中免疫沉淀得到的³⁵S标记的IFN-α5具有成熟蛋白的分子量。这些结果表明,牛乳头瘤病毒载体可用于在哺乳动物细胞中大量生产外源蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/391642/4a2fff16302b/pnas00617-0088-a.jpg

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