杜氏利什曼原虫LACK基因真核表达重组质粒及其在真核细胞中的表达

利什曼原虫的 L ACK抗原是利什曼原虫活性蛋白激酶 C受体同源物 ,是一种新发现的抗原蛋白。我们以本实验室的重组质粒 T- L ACK为模板 ,PCR扩增获得 L ACK基因 ,与真核表达载体 pc DNA3.1( )定向重组 ,重组质粒经酶切和 PCR分析 ,含有约 95 0 bp的 L ACK基因 ,成功构建含有 L ACK基因的真核表达重组质粒 pc D-NA3- L ACK。将此重组质粒转染 COS- 7细胞 ,通过 RT- PCR及免疫荧光检测 L ACK基因在真核细胞中的表达。实验结果显示转染了重组质粒的 COS- 7细胞 ,其 RT- PCR及免疫荧光检测均呈阳性反应 ,证实重组质粒 pc DNA3-L ACK能在 COS- 7细胞中有效表达 L ACK蛋白。

Construction of LACK Gene Recombinant Plasmid and Detection of Its Expression in Eukaryotic Cell

The LACK gene from Leishmania, an analogue of the receptor of activated protein kinase C, was discovered recently. In this study, the LACK gene of Leishmania donovani was obtained from the recombinant plasmid T LACK by PCR. The gene was cloned into eukaryotic expressed plasmid pcDNA3.1( ) to construct recombinant plasmid. This recombinant plasmid then was transfected into the eukaryotic cell COS 7, and the expression of LACK gene in eukaryotic cell was detected by RT PCR and immunofluorescent staining. Both RT PCR and immunofluorescent staining of recombinant plasmid transfected COS 7 showed positive reaction, thus indicating that the recombinant plasmid pcDNA3 LACK can express LACK protein in euka ryotic cell COS 7.