携带神经营养因子-3基因的重组腺病毒的构建和鉴定
Construction and identification of recombinant adenovirus with NT-3 gene
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摘要: 目的:构建含人神经营养因子-3(neurotrophin-3,NT-3)的重组腺病毒载体,为初步研究NT-3的在体功能做准备。方法:酶切法从已构建好的真核表达载体NT-3-pIRES2-DsRed2质粒中切下含有NT-3和DsRed2(包括连接区域pIRES2)的目的片段,将其插入到腺病毒骨架质粒pAdShuttle-CMV的多克隆位点中,电穿孔法将腺病毒骨架载体pAdShuttle-CMV-NT-3-DsRed2和预转入人肠杆菌BJ5183的穿梭载体pAdEasy-1进行细菌内同源重组。PacⅠ酶切线性化鉴定正确的同源重组载体,脂质体法转染293T细胞,包装形成表达NT-3目的蛋白和红色荧光的腺病毒。通过293T细胞3轮扩增病毒,氯化铯密度梯度离心,获得高滴度的纯化腺病毒。Western blot方法检测蛋白表达情况。结果:同源重组质粒载体的DNA测序证实腺病毒载体中含有NT-3的目的片段,Western blot证实感染重组腺病毒的293T细胞中有相应的NT-3蛋白表达;病毒滴度为109PFU/ml。结论:利用细菌内同源重组的方法可以成功构建同时表达NT-3蛋白和红色荧光的重组腺病毒。Abstract: Objective:To construct the recombinant adenovirus vector carrying neurotrophin-3 (NT-3) gene.Methods:NT-3 and DsRed2 (including the ligation region pIRES2) fragment which had been digested by proper enzyme from NT-3-pIRES2-DsRed2 plasmid were cloned into adenovirus pAdShuttle-CMV plasmid.Adenovirus vector pAdShuttle-CMV-NT-3-DsRed2 were electroporated into BJ5183 which had been transformed into pAdEasy-1 previously to have the recombination with pAdEasy-1.Recombinant AdEasy plasmid DNA was analyzed and linearized by PacⅠ,then transfected into 293A cells with liposome method.The adenovirus that expressed NT-3 ptotein and red fluorescence was successfully constructed.The adenovirus was amplified in 293A cells three times,and high quality adenovirus was obtained by cesium chloride density gradient centrifugation.Western blot confirmed the expresseion of the NT-3 protein in 293T cells.Results:With the system of Adshuttle,a recombinant adenovirus expressing NT-3 protein and red fluorescence was successfully constructed.Conclusions:The recombinant adenovirus carrying NT-3 gene can be constructed with the system of Adeasy.