Xiang J, Liu E, Moyana T, Qi Y
Saskatoon Cancer Center, Department of Microbiology, University of Saskatchewan, Canada.
Immunol Cell Biol. 1994 Aug;72(4):275-85. doi: 10.1038/icb.1994.42.
Recombinant DNA techniques were used to clone, construct and express the bifunctional molecule FV/IL-2. The FV/IL-2 is a single-chain 37 kDa fusion protein expressed in Escherichia coli under control of the strong T7 bacteriophage promoter in the expression vector pT7-7-FV-IL-2. The fused gene fragment FV-IL-2 contains a single-chain anti-TAG72 FV gene fragment and the human recombinant cDNA fragment of the IL-2 molecule. The renatured soluble form of FV/IL-2 was purified from E. coli inclusion bodies using hydroxylapatite chromatography. The yield of this fusion protein was estimated at 2.0 mg/L. Our data showed that the FV/IL-2 molecule retained the TAG72 antigen-binding specificity and the IL-2 activity as measured in the standard T cell proliferation as well as cytotoxicity assays. Therefore, it may prove to be useful in targeting the biological effect of IL-2 to tumour cells and stimulating its immune destruction.
采用重组DNA技术克隆、构建并表达双功能分子FV/IL-2。FV/IL-2是一种单链37 kDa融合蛋白,在表达载体pT7-7-FV-IL-2中,在强T7噬菌体启动子的控制下于大肠杆菌中表达。融合基因片段FV-IL-2包含一个单链抗TAG72 FV基因片段和IL-2分子的人重组cDNA片段。采用羟基磷灰石色谱法从大肠杆菌包涵体中纯化复性后的可溶性FV/IL-2。该融合蛋白的产量估计为2.0 mg/L。我们的数据表明,在标准T细胞增殖及细胞毒性试验中,FV/IL-2分子保留了TAG72抗原结合特异性和IL-2活性。因此,它可能被证明在将IL-2的生物学效应靶向肿瘤细胞并刺激其免疫破坏方面是有用的。