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[严重急性呼吸综合征冠状病毒核衣壳蛋白的表达及其DNA疫苗的构建]

[Expression of SARS coronavirus nucleocapsid protein and construction of its DNA vaccine].

作者信息

Xiang Kai-jun, Zeng Qi-yi, Ding Yong-qiang, Zhu Bing, Zhou Rong

机构信息

Guangzhou Huayin Genetic Science and Technology Co., Ltd., Guangzhou 510150, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2005 Nov;21(6):731-3, 737.

Abstract

AIM

To express the nucleocapsid (N) protein of SARS coronavirus (SARS-CoV) in E. coli and construct its DNA vaccine.

METHODS

The prokaryotic expression vector pQEN containing N gene was constructed and transformed into the E. coli. The recombinant N protein was then expressed and purified by Ni(2+)-NTA affinity resin. In addition, the N gene was cloned into the eukaryotic expression plasmid pSecTagB and the eukaryotic recombinant expression vector pSecN was obtained. The DNA vaccine pSecN was injected to immunize the BALB/c mice to produce the antiserum against N protein of SARS-CoV. Subsequently, the reactivity of the antiserum with recombinant N protein and SARS-CoV particles was assayed by ELISA.

RESULTS

Recombinant N protein reacted strongly and specifically with the sera from immunized mice and SARS patients. Similarly, the sera of immunized mice could also react specifically with SARS-CoV particles.

CONCLUSION

The recombinant N protein could be used as a good antigen to detect SARS. The DNA vaccine pSecN could also efficiently induce the production of IgG against N protein of SARS-CoV, which offered clues to the development of a potential DNA vaccine.

摘要

目的

在大肠杆菌中表达严重急性呼吸综合征冠状病毒(SARS-CoV)的核衣壳(N)蛋白并构建其DNA疫苗。

方法

构建含N基因的原核表达载体pQEN并转化至大肠杆菌。随后通过镍离子螯合亲和树脂表达并纯化重组N蛋白。此外,将N基因克隆至真核表达质粒pSecTagB,获得真核重组表达载体pSecN。注射DNA疫苗pSecN免疫BALB/c小鼠以产生抗SARS-CoV N蛋白的抗血清。随后,通过酶联免疫吸附测定法检测抗血清与重组N蛋白及SARS-CoV颗粒的反应性。

结果

重组N蛋白与免疫小鼠及SARS患者的血清发生强烈且特异性反应。同样,免疫小鼠的血清也能与SARS-CoV颗粒发生特异性反应。

结论

重组N蛋白可作为检测SARS的良好抗原。DNA疫苗pSecN也能有效诱导产生抗SARS-CoV N蛋白的IgG,为潜在DNA疫苗的研发提供了线索。

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