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Hepatitis C virus E1 protein induces modification of membrane permeability in E. coli cells.

机译:丙型肝炎病毒E1蛋白诱导大肠杆菌细胞膜通透性的改变。

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摘要

The E1 gene of hepatitis C virus (HCV) has been cloned and expressed in BL21(DE3)pLys Escherichia coli strain by pET3a vector to analyze changes in membrane permeability produced by this protein. We showed that the expression of E1 (aa 192-383), as well as of two C-terminal fragments (aa 331-383 and aa 341-383) corresponding to the transmembrane (TM) region of this protein, induced a rapid lysis of cells. On the contrary, the expression of a mutant of E1 (aa 192-340), lacking the last 40 amino acids, did not cause cell lysis. The analysis of permeability changes revealed that modification of membrane permeability to several compounds were observed only in clones expressing E1 and C-terminal fragments, while the synthesis of the C-terminal-deleted mutant had little or no effect on permeability. These findings demonstrate that the TM domain of E1 protein has membrane-active properties that may be involved in some aspects of virus-cell interaction. Copyright 1998 Academic Press.
机译:已通过pET3a载体克隆了丙型肝炎病毒(HCV)的E1基因并在BL21(DE3)pLys大肠杆菌菌株中表达,以分析该蛋白产生的膜通透性变化。我们显示E1(aa 192-383)以及对应于该蛋白跨膜(TM)区的两个C端片段(aa 331-383和aa 341-383)的表达诱导了快速裂解细胞。相反,缺少最后40个氨基酸的E1突变体(aa 192-340)的表达不会引起细胞裂解。通透性变化的分析表明,仅在表达E1和C端片段的克隆中观察到膜对几种化合物通透性的修饰,而缺失C端突变体的合成对通透性几乎没有影响。这些发现表明,E1蛋白的TM结构域具有膜活性特性,可能与病毒-细胞相互作用的某些方面有关。版权所有1998学术出版社。

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