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由人多肽链延伸因子1α启动子驱动的双顺反子载体的开发,用于创建稳定表达高水平重组蛋白的哺乳动物细胞系。

Development of a bicistronic vector driven by the human polypeptide chain elongation factor 1alpha promoter for creation of stable mammalian cell lines that express very high levels of recombinant proteins.

作者信息

Hobbs S, Jitrapakdee S, Wallace J C

机构信息

Institute of Cancer Research, London, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1998 Nov 18;252(2):368-72. doi: 10.1006/bbrc.1998.9646.

Abstract

We have developed a new vector for the stable expression of recombinant protein in mammalian cells. In this vector, designated pEFIRES-P, both the recombinant cDNA and the puromycin resistant gene (pac) are transcribed as a single message driven by the strong human polypeptide chain elongation factor 1alpha promoter. The presence of an internal ribosome entry site ensures any clones that are resistant to puromycin also express high levels of recombinant protein encoded by cDNA cloned upstream from the pac gene. We report the use of this vector to generate stable cell lines expressing human pyruvate carboxylase and show that following transfection and clonal selection, all twenty colonies that conferred high dose resistance to puromycin also expressed very high levels of functional pyruvate carboxylase. Use of pEFIRES-P should permit the rapid and efficient generation of stable cell lines for the characterisation of recombinant proteins.

摘要

我们开发了一种用于在哺乳动物细胞中稳定表达重组蛋白的新型载体。在这个命名为pEFIRES-P的载体中,重组cDNA和嘌呤霉素抗性基因(pac)均由强大的人类多肽链延长因子1α启动子驱动转录为单一信使。内部核糖体进入位点的存在确保了任何对嘌呤霉素具有抗性的克隆也能高水平表达由克隆在pac基因上游的cDNA编码的重组蛋白。我们报道了使用该载体产生表达人丙酮酸羧化酶的稳定细胞系,并表明转染和克隆选择后,所有对高剂量嘌呤霉素具有抗性的20个菌落也都表达了非常高水平的功能性丙酮酸羧化酶。使用pEFIRES-P应该能够快速有效地产生用于重组蛋白表征的稳定细胞系。

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