| HCV E2区基因在原核系统中的表达 |
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| 引用本文： | 张东伟,祁自柏,等.HCV E2区基因在原核系统中的表达[J].Virologica Sinica,2003,18(1):1-4. |
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| 作者姓名： | 张东伟 祁自柏 等 |
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| 作者单位： | [1]中国科学院武汉病理研究所,湖北武汉430071 [2]中国药品生物制品检定所,北京100050 |
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| 摘 要： | 用提取的重组表达载体pET-E2转化BL21（DE3）感受态细胞，经IPTG诱导，再进行SDS－PAGE，可得到有一条约34kDa的表达带，与理论推测的蛋白分子量一致，通过Western-blot鉴定，证明此带即为目的蛋白带。该产物有一个六聚组氨酸尾，主要以包涵体形式存在；计算机扫描分析考马斯亮兰染色后的蛋白胶显示：目的蛋白占整个菌体蛋白的36％以上，经Ni-柱纯化的E2蛋白纯度可达95％以上；以纯化的E2蛋白为抗原，用ELISA方法检测了20份抗HCV阳性血清，结果表明15份抗HCV阳必血清中检出5份E2抗体阳性血清，而5份抗HCV阴性血清中没有检测到E2抗体。
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| 关 键 词： | HCV E2 原核系统 基因表达 纯化 |
Expression of HCV E2 Gene in Prokaryotic Expression System |
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| ZHANG Dong-wei,LIANG Bu-feng,LI Wei-dong,QI Zi-bai,LING Shi-gan.Expression of HCV E2 Gene in Prokaryotic Expression System[J].中国病毒学(英文版),2003,18(1):1-4. |
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| Authors: | ZHANG Dong-wei LIANG Bu-feng LI Wei-dong QI Zi-bai LING Shi-gan |
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| Abstract: | Rceomdinant plasmid pET-E2 was transformed into BL21 (DE3) competent cell, then induced the amplified culture with IPTG. There was a 34 kDa band in SDS-PAGE gel. The molecular weight of the expressed protein was comsistent to that of deduced E2 protein. Tested by western-blot, It showed that the product was HCV E2 protein. It contained a six-Histidine tag and aggregated into the inclusion body. Computer scan analysis showed the protein interested took the percentage more than 36 of the total bacterial proteins and the rate of purification was higher than 95% after purified by Ni-column. The activity of pruified E2 protein was tested by ELISA. The result showed that the 5/15 HCVpositive sera had anti-E2 antibody, and the other 5 negative HCV sera hadn't anti-E2 antibody. |
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| Keywords: | HCV E2 Prodaryotic system Gene expression Purification |
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