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粒细胞—巨噬细胞集落刺激因子与HBsAg融合蛋白基因的 …
引用本文:薛净,程云.粒细胞—巨噬细胞集落刺激因子与HBsAg融合蛋白基因的 …[J].中华实验和临床病毒学杂志,1998,12(4):310-312.
作者姓名:薛净  程云
作者单位:解放军302医院,第四军医大学,首都医科大学传染病教研组
摘    要:目的 研究粒细胞-巨噬细胞集落刺激因子(GM-CSF)的免疫活性。方法 用聚合酶链反应(PCR)技术扩增出粒细胞-巨噬细胞集落刺激因子(GM-CSF)384bp的基因片段及HBsAg846bp基因片段,扩增产物经柱纯化后,由T4DNA酶连结因子1230bp的片段,将此片段命名为LGH,克隆到pUC19质粒中,利用菌落PCR法快速筛选阳性克隆及限制酶切鉴定片段的大小。结果 该基因全长1230bp,经

关 键 词:HBV  HBsAg  GM-CSF  聚合酶链反应

Cloning and sequencing of fusion protein gene of recombinant GM-HBsAg
Xue Jing,Cheng Yun,Luo Qinghua et al. Hospital of PLA,Beijing.Cloning and sequencing of fusion protein gene of recombinant GM-HBsAg[J].Chinese Journal of Experimental and Clinical Virology,1998,12(4):310-312.
Authors:Xue Jing  Cheng Yun  Luo Qinghua Hospital of PLA  Beijing
Institution:302 Hospital of PLA, Beijing 100039.
Abstract:GM-CSF is an effective adjuvant for immunology, it was used to improve the immunological function of antigen and to increase the anti-HBs responses. Through using polymerase chain reaction (PCR) technique, we amplified 384bp and 846bp gene fragments from GM-CSF and HBsAg. The products were extracted and purified; a 1230bp gene fragment was obtained by T4 DNA linkage. This amplified product was cloned into pUC19 vector. The positive clones were scereened and the inserted fragment was determined by restriction enzymes. The gene fragment length determined is 1230bp, the sequence analysis showed that the gene fragment is GM-CSF-HBsAg gene. The successful construction of GM-HBsAg fusion protein gene provides basis for research of its biologieal activity and expression.
Keywords:Granulocyte-macrophage-colony stimulating factor    HBsAg    Polymerase chain reaction
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