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颗粒溶素的表达纯化及生物学活性分析
钱琤,陈孙孝,周晔,王燕,谷明莉,陈波,陈燕,邓安梅,仲人前
0
(第二军医大学长征医院实验诊断科,全军临床免疫中心,上海,200003)
摘要:
目的:采用原核表达系统对颗粒溶素(granulysin,GNLY)进行体外表达,纯化及活性鉴定.方法:以体外培养的人外周血单个核细胞(PBMC)为模板,RT-PCR扩增编码GNLY的cDNA片段,插入pMD-18-T 载体,测序正确后再亚克隆到质粒pET28a(+) 中,构建重组表达质粒pET28a(+)-GNLY,转化大肠杆菌BL21(DE3) plysS,IPTG诱导表达融合蛋白,包涵体经变复性后用Ni亲和层析纯化,CFU法测定蛋白活性.结果:成功地将GNLY cDNA片段插入载体pET28a(+)中,构建了表达质粒pET28a(+)-GNLY.经诱导在原核表达系统中以包涵体形式高效表达了相对分子质量为9 000的融合蛋白,变复性纯化后的GNLY蛋白经CFU法检测,发现其具有细胞毒活性且细胞毒作用具有剂量依赖性.结论:本实验利用原核表达系统成功地表达了具有生物学活性的GNLY,为研究其功能、作用机制及临床应用奠定了基础.
关键词:  颗粒溶素、基因表达、生物学活性
DOI:10.3724/SP.J.1008.2006.00829
投稿时间:2005-12-12修订日期:2006-06-28
基金项目:国家自然科学基金(30471616)、上海市重大科技攻关基金(04DZ19116)、上海市重点科研支撑条件项目(051409012)和上海市青年科技启明星计划(QMX01423).
Expression, purification and bioactivity analysis of granulysin
QIAN Cheng,CHEN Sun-xiao,ZHOU Ye,WANG Yan,GU Ming-li,CHEN Bo,CHEN Yan,DENG An-mei,ZHONG Ren-qian
(第二军医大学长征医院实验诊断科,全军临床免疫中心,上海,200003)
Abstract:
Objective:To express the granulysin protein in E. coli and to detect its bioactivity after purification. Methods: Using cultured human peripheral blood mononuclear cells as the template, we selectively amplified the fragment coding granulysin by RT-PCR. The fragment was then inserted into the prokaryotic expression vector pET28a (+) for transforming E. coli BL21(DE3) plysS. Fusion protein expression was induced by isopropyl-Beta-D-thiogalactopyranoside (IPTG). After renaturation, the protein was purified by affinity chromatography and its bioactivity was examined by colony-forming unit. Results: We successfully inserted granulysin cDNA fragment into vector pET28a (+) and constructed the expression plasmid pET28a (+)GNLY. The fusion protein, with a molecular weight of 9 000, was obtained through IPTG induction. After renaturation and purification, the recombinant protein was proven to be bioactive by CFU and its cytotoxicity was in a dose-dependent manner. Conclusion: The fusion protein obtained in the present study is bioactive and can be used for further study on its function,mechanism of action and clinical application.
Key words:  granulysin  gene expression  bioactivity