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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2009, Vol. 29 Issue (03): 30-35    
研究报告     
人NANOGP8蛋白的原核表达及多克隆抗体的制备
张经余1,王爱娥2,李美香3,戴建武3
1. 北京大学临床肿瘤学院;北京市肿瘤防治研究所
2. 中国人民解放军第二炮兵总医院呼吸内科
3. 中国科学院遗传与发育生物学研究所
Prokaryotic expression and Preparation of Polyclonal Antibody of Human NANOGP8
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摘要:

为获得抗人 NANOGP8基因的多克隆抗体,采用PCR法扩增了NANOGP8基因,经序列测定正确后,连接到pET-28a质粒上,将获得的重组质粒pET-28a-NANOGP8转化到大肠杆菌BL21(DE3)中,在16℃和37℃下分别进行诱导表达,经SDS-PAGE检测发现融合蛋白以包涵体形式存在于37℃诱导表达的沉淀中,大小约为45kDa。对包涵体进行洗涤、溶解处理,经Chelating Sepharose Fast Flow亲和层析柱进行纯化。对纯化得到的蛋白进行SDS-PAGE及Western blot免疫印记杂交检测,得到了单一条带。用获得的高纯度融合蛋白免疫新西兰兔,得到兔来源的抗人NANOGP8血清。对抗血清进行蛋白免疫印记杂交反应和酶联免疫吸附反应检测,结果显示成功制备了高滴度和特异性的兔抗人NANOGP8多克隆抗体,与市售抗人Nanog多克隆抗体相比,杂交更迅速,效果更明显。为进一步研究NANOGP8基因在肿瘤发生、发展中的作用奠定了基础。

Abstract:

To obtain polyclonal antibody against human NANOGP8, the NANOGP8 gene was amplified by PCR from the template obtained in our previous work and identified by DNA sequence analysis. Then it was digested by EcoRⅠand SalⅠ, and ligated with pET-28a vector which was by the same treatment. Sequenced and blasted with the NCBI GenBank, the recombinant plasmid was named as pET-28a-NANOGP8. The recombinant plasmid was transformed into E.coli BL21 (DE3) and induced by 1mM IPTG at 16℃ and 37℃. SDS-PAGE showed that the fusion protein was expressed in the form of inclusion body in the sediment when induced at 37℃. After dissolution and affinity purification with Chelating Sepharose Fast Flow, a single protein band about 45 KD was identified in the SDS-PAGE and Western-blot analysis. One new zealand rabbit was immunized with purified NANOGP8 protein to prepare for the polyclonal antibody against NANOGP8. The NANOGP8 antiserum was obtained and characterized by Western-blot, ELISA, and compared with commercial goat anti-human Nanog antibody. Results showed that the antibody had high affinity and specificity, and higher titer compared with commercial anti-human Nanog antibody. The studies provide a favorable tool for further study on relation of tumorigenesis, development and NANOGP8 in the future.

收稿日期: 2008-10-24 出版日期: 2009-03-31
基金资助:

国家自然科学基金

通讯作者: 张经余   
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张经余 王爱娥 李美香 戴建武

引用本文:

张经余,王爱娥,李美香,戴建武. 人NANOGP8蛋白的原核表达及多克隆抗体的制备[J]. 中国生物工程杂志, 2009, 29(03): 30-35.

ZHANG Jing-Tu- Wang-Ai-E- Li-Mei-Xiang- Dai-Jian-Wu. Prokaryotic expression and Preparation of Polyclonal Antibody of Human NANOGP8. China Biotechnology, 2009, 29(03): 30-35.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2009/V29/I03/30

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