人CD63真核表达质粒的构建及在TCA8113细胞中的表达与定位

Construction of eukaryotic expressing plasmid of human CD63 gene and its expression and location in TCA8113 cells

  • 摘要: 目的 构建人CD63真核表达质粒,观察其在人舌鳞癌细胞TCA8113中的表达与定位。 方法 提取TCA8113细胞总RNA,RT-PCR方法扩增CD63全长基因序列,亚克隆至pcDNA3.1真核表达质粒中,构建pcDNA3.1-CD63表达质粒,转化E.coli DH5α,筛选阳性克隆,酶切及测序鉴定正确后,将重组质粒转染TCA8113细胞,Western blot检测蛋白表达,间接免疫荧光方法观察CD63蛋白在TCA8113细胞中的表达与定位。 结果 成功构建了pcDNA3.1-CD63真核表达质粒,Western bolt结果检测到外源CD63高表达,间接免疫荧光结果表明CD63融合蛋白与内源CD63蛋白定位相似,均表达于细胞膜。 结论 外源CD63融合蛋白能在TCA8113中高表达并定位于细胞膜。

     

    Abstract: Objective Toconstruct an eukaryotic expressing plasmidof human CD63 gene and observe its expression and location in TCA8113 tongue squamous cell carcinoma cell line. Methods Total RNA was extractedfromTCA8113 cells. The CD63 gene was amplifiedby PCR methodand subclonedtopcDNA3.1 (+) plasmid. The recombinant plasmids were transformedintoE.coli DH5α and screenedby restriction enzyme digestion and DNA sequencing. Then, pcDNA3.1-CD63 plasmids were transfectedintoTCA8113 cells. Western blot was usedtodetect the expression of protein, the subcellular location between endogenous CD63 and pcDNA3.1-CD63 in TCA8113 cells was detectedand comparedby indirect immunofluorescence staining. Results The recombinant eukaryotic expressing plasmid, pcDNA3.1-CD63, was successfully constructed. The expression of recombinant plasmidin TCA8113 cells was provedby Western blot. Andthe indirect immunofluorescence staining showedthat the location of pcDNA3.1-CD63 protein was similar with endogenous CD63 protein, and they both locatedin the outer membrane of TCA8113 cells. Conclusion The fusion protein pcDNA3.1-CD63 can be successfully expressedin TCA8113 cells and locatedin the outer membrane.

     

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