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[巢蛋白的克隆、表达、抗体制备及免疫组织化学分析]

[Cloning, expression, and antibody preparation of nestin with immunohistochemical analysis].

作者信息

Chen Xin-lin, Liu Yong, Xiao Xin-li, Zhang Jin, Lü Hai-xia, Zhang Peng-bo, Liu Jian-xin, Zhao Jian-jun

机构信息

Research Center for Neuroscience, Medical School of Xi'an Jiaotong University, Xi'an 710061, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2006 Feb;26(2):196-200.

PMID:16503528
Abstract

OBJECTIVE

To obtain recombinant nestin and prepare anti-nestin polyclonal antibody (mAb) to explore the biological roles of nestin in the central nervous system development.

METHODS

The nestin cDNA was cloned from human neural stem cells by RT-PCR and ligated to prokaryotic expression plasmid pQE30 for construction of the recombinant vector pQE30-nestin. After sequencing, the recombinant vector was transformed into E.coli M15 and His-tagged nestin was induced by IPTG. The nestin was purified by Ni-NTA affinity chromatography column and characterized by SDS-PAGE and Western blotting. BALB/c mice were immunized with the purified recombinant protein to prepare the antiserum, which was analyzed by Western blotting, enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry.

RESULTS

The nestin gene was successfully cloned from human neural stem cells, which was identical to that reported in GenBank. After IPTG induction, the E.coli transformed with pQE30-nestin plasmid expressed a 25,000 His-tagged protein, which was successfully purified and identified as nestin by Western blotting. Western blotting, ELISA and immunohistochemistry demonstrated that the antiserum could specifically bind to the recombinant nestin as well as to nestin in fetal human and rat brains.

CONCLUSION

We successfully cloned the nestin gene and expressed the nestin, and nestin mAb prepared can specifically recognize not only the recombinant nestin, but also nestin from human and rats brain tissues.

摘要

目的

获取重组巢蛋白并制备抗巢蛋白多克隆抗体,以探讨巢蛋白在中枢神经系统发育中的生物学作用。

方法

通过逆转录聚合酶链反应(RT-PCR)从人神经干细胞中克隆巢蛋白cDNA,并将其连接到原核表达质粒pQE30上,构建重组载体pQE30-巢蛋白。测序后,将重组载体转化到大肠杆菌M15中,用异丙基-β-D-硫代半乳糖苷(IPTG)诱导表达带有His标签的巢蛋白。通过镍-亚氨基二乙酸(Ni-NTA)亲和层析柱纯化巢蛋白,并用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹法(Western blotting)进行鉴定。用纯化的重组蛋白免疫BALB/c小鼠制备抗血清,通过蛋白质免疫印迹法、酶联免疫吸附测定(ELISA)和免疫组织化学法对其进行分析。

结果

成功从人神经干细胞中克隆出巢蛋白基因,与GenBank中报道的序列一致。用IPTG诱导后,转染pQE30-巢蛋白质粒的大肠杆菌表达出一种25000的带有His标签的蛋白,该蛋白经成功纯化,且通过蛋白质免疫印迹法鉴定为巢蛋白。蛋白质免疫印迹法、ELISA和免疫组织化学法表明,抗血清能特异性结合重组巢蛋白以及人胎儿和大鼠脑组织中的巢蛋白。

结论

成功克隆了巢蛋白基因并表达了巢蛋白,所制备的巢蛋白单克隆抗体不仅能特异性识别重组巢蛋白,还能识别来自人和大鼠脑组织的巢蛋白。

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