[Construction of recombinant CHO cell strain for high expression of HBsAg].

中华实验和临床病毒学杂志 Pub Date : 2013-08-01
Yao Yi, Min-Zhuo Guo, Rui-Guang Tian, Qiu-Dong Su, Xue-Xin Lu, Feng Qiu, Wen-Ting Zhou, Zhi-Yuan Jia, Sheng-Li Bi
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引用次数: 0

Abstract

Objective: To overexpress hepatitis B virus S gene in CHO cells cultured in serum-free media.

Method: Plasmid was constructed by cloning of HBV S gene and then it was transfected into CHO cells. After cell screen, the positive clones were identified and isolated into a serum-free media followed by the serological and morphological characterization of the expression product.

Result: CHO cell strains which can express HBsAg efficiently and stably were obtained. Spherical and filamentous HBsAg could be detected under electronic microscope. The titer of the expression product was up to 1:5000.

Conclusion: Serum-free media cultured CHO cell strain for overexpression of HBsAg was successfully constructed and the expression product was high antigenic.

高表达HBsAg重组CHO细胞株的构建
目的:在无血清培养基培养的CHO细胞中过表达乙型肝炎病毒S基因。方法:克隆HBV S基因构建质粒,转染CHO细胞。细胞筛选后,鉴定阳性克隆并分离到无血清培养基中,随后对表达产物进行血清学和形态学表征。结果:获得了高效、稳定表达HBsAg的CHO细胞株。电镜下可见球状和丝状HBsAg。表达产物效价高达1:50 000。结论:成功构建了无血清培养基培养HBsAg过表达CHO细胞株,表达产物具有较高的抗原性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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