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日本血吸虫信号蛋白14-3-3的制备与特性

[Preparation and characteristics of Schistosoma japonicum signaling protein 14-3-3].

作者信息

Yin Xu-Ren, Yu Chuan-Xin, Xie Shu-Ying, Qian Chun-Yan, Song Li-Jun, Wang Jie, Zhang Wei, Xu Yong-liang

机构信息

Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Wuxi 214064, China.

出版信息

Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2011 Apr;23(2):168-72.

Abstract

OBJECTIVE

To prepare soluble recombinant signal transduction protein 14-3-3 of Schistosoma japonicum (rSj14-3-3) and investigate its immunologic features.

METHODS

The cDNA fragment of signal transduction protein 14-3-3 gene was prepared from Schistosoma japonicum adult worm mRNA, and was subcloned to the downstream of glutathione S transferase gene of expression vector pGEX-4T-3 to construct a recombinant expression plasmid 14-3-3/pGEX-4T-3. The recombinant plasmids were transferred into E. coli BL21, the transforments containing recombinant plasmid were induced by IPTG, and the expression situation of fusion protein GST-14-3-3 was observed by SDS-PAGE. The pure recombinant 14-3-3 protein was prepared by digesting the fusion protein GST-rSj14-3-3 with thrombin and affinity chromatography. The specific antibody against rSj14-3-3 protein was prepared by an immunized rabbit with rSj14-3-3 protein. The immunogenicity and immune reactivity of rSj14-3-3 protein were analyzed by Western blotting.

RESULTS

The gene encoding signal transduction protein 14-3-3 of Schistosoma japonicum Jiangsu strain was cloned successfully, the homology of open read frame sequence to the registrated sequence of Sj14-3-3 protein in genbank was 99.08%. A 55 kilo Dalton fusion protein GST-rSj14-3-3 was expressed by transferring the recombinant plasmid 14-3-3/pGEX-4T-3 into E. coli BL21 and induced with IPTG. The high titer antibody against rSj14-3-3 was produced by the immunized rabbit with rSj14-3-3 ,and could recognize the nature and recombinant rSj14-3-3 proteins.

CONCLUSIONS

The soluble rSj14-3-3 protein has been prepared successfully in this study, and it has good immunogenicity and reactivity.

摘要

目的

制备日本血吸虫可溶性重组信号转导蛋白14-3-3(rSj14-3-3)并研究其免疫学特性。

方法

从日本血吸虫成虫mRNA中制备信号转导蛋白14-3-3基因的cDNA片段,并亚克隆至表达载体pGEX-4T-3的谷胱甘肽S转移酶基因下游,构建重组表达质粒14-3-3/pGEX-4T-3。将重组质粒转入大肠杆菌BL21,用异丙基-β-D-硫代半乳糖苷(IPTG)诱导含重组质粒的转化子,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)观察融合蛋白GST-14-3-3的表达情况。用凝血酶消化融合蛋白GST-rSj14-3-3并经亲和层析制备纯重组14-3-3蛋白。用rSj14-3-3蛋白免疫家兔制备抗rSj14-3-3蛋白的特异性抗体。通过蛋白质印迹法分析rSj14-3-3蛋白的免疫原性和免疫反应性。

结果

成功克隆了日本血吸虫江苏株信号转导蛋白14-3-3的编码基因,其开放阅读框序列与基因库中已注册的Sj14-3-3蛋白序列的同源性为99.08%。将重组质粒14-3-3/pGEX-4T-3转入大肠杆菌BL21并用IPTG诱导后,表达出了55千道尔顿的融合蛋白GST-rSj14-3-3。用rSj14-3-3免疫家兔产生了高滴度的抗rSj14-3-3抗体,该抗体可识别天然和重组的rSj14-3-3蛋白。

结论

本研究成功制备了可溶性rSj14-3-3蛋白,其具有良好的免疫原性和反应性。

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