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| 重组人白细胞介素21在毕赤酵母中的分泌表达及活性分析 | |
| 引用本文： | 李栋,俞慧清,火蓉芬,陈建泉,成国祥.重组人白细胞介素21在毕赤酵母中的分泌表达及活性分析[J].生物工程学报,2009,25(11):1711-1717. |
| 作者姓名： | 李栋 俞慧清 火蓉芬 陈建泉 成国祥 |
| 作者单位： | 1. 同济大学生命科学与技术学院,上海,200092 2. 上海交通大学医学院附属瑞金医院,上海,200025;上海转基因研究中心,上海,201210 3. 上海转基因研究中心,上海,201210 4. 同济大学生命科学与技术学院,上海,200092;上海交通大学医学院附属瑞金医院,上海,200025;上海转基因研究中心,上海,201210 |
| 基金项目： | 国家高技术研究发展计划(863计划)(No.2007AA100502)资助~~ |
| 摘 要： | 为了获得有活性的重组人白细胞介素21(rhIL-21),本研究建立了在毕赤酵母(Pichia pastoris)中分泌表达rhIL-21的技术。首先,通过RT-PCR从人外周血淋巴细胞中扩增IL-21cDNA,克隆到酵母表达载体pPIC9K中,构建了重组酵母表达载体pPIC9K-hIL21 cDNA;然后,线性化的载体转化毕赤酵母表达菌株GS115,经抗性梯度筛选获得了多拷贝重组酵母菌;加入甲醇诱导培养后,SDS-PAGE和Western blotting检测到培养液中有rhIL-21的分泌表达,相对分子量约为16kD,ELISA结果显示摇瓶表达量可达229.28mg/L;表达上清经阳离子交换介质SPSepharose Fast Flow纯化后,目的蛋白纯度达到95%。细胞增殖试验结果显示该rhIL-21联合刀豆蛋白A(ConA)对人淋巴细胞的增殖具有显著的促进作用。本研究首次成功在毕赤酵母表达系统中分泌表达了有生物活性的rhIL-21,为相关疾病免疫治疗的研究奠定了基础。 |
| 关 键 词： | 白细胞介素21 毕赤酵母 分泌表达 |
| 收稿时间： | 2009/7/27 0:00:00 |
Expression and analysis of the recombinant human interleukin-21 (rhIL-21) in Pichia pastoris |
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| Dong Li,Huiqing Yu,Rongfen Huo,Jianquan Chen and Guoxiang Cheng.Expression and analysis of the recombinant human interleukin-21 (rhIL-21) in Pichia pastoris[J].Chinese Journal of Biotechnology,2009,25(11):1711-1717. | |
| Authors: | Dong Li Huiqing Yu Rongfen Huo Jianquan Chen and Guoxiang Cheng |
| Institution: | School of Life Science and Technology, Tongji University, Shanghai 200092, China;Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China; Shanghai Transgenic Research Center, Shanghai 201210, China;Shanghai Transgenic Research Center, Shanghai 201210, China;Shanghai Transgenic Research Center, Shanghai 201210, China;School of Life Science and Technology, Tongji University, Shanghai 200092, China; 2 Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China; Shanghai Transgenic Research Center, Shanghai 201210, China |
| Abstract: | Interleukin-21 is a type I cytokine mainly produced by activated CD4+ T cells that acts as a regulator of immune system.In this work,hIL-21cDNA was amplified from human peripheral blood lymphocytes by RT-PCR,and then inserted into pPIC9K.The recombinant vector pPIC9K-hIL21cDNA was linearized by Sac I,and transformed into Pichia pastoris strain GS115 by electroporation.Transformants were selected by G418 and confirmed by PCR.The recombinant protein was expressed and secreted into the supernatant after induci... |
| Keywords: | Interleukin-21 Pichia pastoris secreted expression |
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