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信号肽序列对禽流感病毒H5N1HA蛋白GFP融合分子在真核细胞中表达的影响 被引量:4

Effects of signal peptide sequence of hemagglutinin on the expression of green fluorescent protein and hemagglutinin fusion gene
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摘要 【目的】构建绿色荧光蛋白(GFP)与禽流感病毒(AIV)HA基因的融合表达载体,观察信号肽序列的有无及位置对HA-GFP在293T细胞中的表达影响。【方法】应用PCR方法从H5N1亚型AIV质粒DNA中扩增出完整的或除去信号肽序列的HA基因片段,PCR产物经XhoⅠ和SmaⅠ双酶切后定向插入绿色荧光蛋白真核表达载体pEGFP-C1的不同位点,将得到的重组体M1,M2和M3分别转化宿主菌DH5α,经双酶切及DNA测序鉴定分析后,采用脂质体转染法将pEGFP-C1,M1,M2和M3转染人胚肾细胞系293T细胞,荧光显微镜下观察HA-GFP的表达,流式细胞仪检测表达HA蛋白的细胞百分数。【结果】经酶切及测序鉴定成功构建了HA-GFP重组表达载体M1,M2和M3,荧光显微镜及流式细胞仪检测到重组质粒转染的293T细胞表达强的荧光蛋白,信号肽的有无对HA-GFP融合蛋白在293T细胞中的表达有显著影响,信号肽序列使HA-GFP融合蛋白在293T细胞中的表达减少,而信号肽的位置对融合蛋白表达量的影响不显著。【结论】信号肽的有无对HA-GFP融合蛋白在细胞中的表达有显著影响。 [Objective] Purified avian influenza virus (AIV) hemagglutinin (HA) gene fragment was inserted into green fluorescent protein (GFP) expression vector, pEGFP-C1. The role of signal peptide in the HA-GFP expression in 293T cells was investigated by cutting the signal peptide or placing it in different locations of HA-GFP fusion gene.[Methods] The expression of GFP in 293T cells was examined directly with fluorescence microscope and flow cytometry analysis.[Results] After transfected with pEGFP-C1, M1, M2 and M3 plasmid, under fluorescent microscope the HA-GFP fusion protein was successfully expressed. Fluorescence was seen homogeneously distributed in the entire cell body of the cells transfected by the empty vector pEGFP-C1, whereas signal peptide could obviously reduced the expression of GFP-HA compared with recombinant plasmid without signal peptide. In addition, we found that there was no significant effect of the location of signal peptide on the expression of HA-GFP fusion protein.
出处 《微生物学报》 CAS CSCD 北大核心 2009年第3期351-356,共6页 Acta Microbiologica Sinica
基金 国家“973项目”(2005CB523001)~~
关键词 禽流感病毒HA蛋白 绿色荧光蛋白 融合分子 真核表达 信号肽序列 avain influenza virus HA protein green fluorescent protein recombinant expression signal peptide
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