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作 者:沈惠 李昌麟[1,2] 林明群 张宗梁[1,2] 申庆祥[1,2]
机构地区:[1]中国科学院上海细胞生物学研究所 [2]上海市计划生育科学研究所
出 处:《生物工程学报》1998年第4期359-365,共7页Chinese Journal of Biotechnology
摘 要:人白细胞介素12(hIL12)是一种异源二聚体细胞因子,由p40和p35两个亚基通过二硫键连接而成。首先构建了两个表达载体pVL1392hp40和pVL1393hp35,并分别与线性化多角体病毒基因组DNA共转染昆虫细胞株Sf9,用目视法筛选出重组病毒AcNPVhp40和AcNPVhp35。利用PHA激活的人淋巴细胞增殖试验,在条件培液中检测到重组hIL12的生物活性,表达量约为15~2μg/106细胞。经实时BIA和Northernblot分析,hp35和hp40两亚基在昆虫细胞中获得表达。非还原条件下的Westernblot结果显示,重组hIL12的表观分子量为76kDa,hp40同源二聚体的表观分子量为92kDa。重组ph40具有明显抑制hIL12生物活性的作用。Human interleukin 12(hIL 12) is a heterodimer cytokine,which consists of two disulfide linked subunits,p40 and p35.This paper reports the expression of hIL 12 using Baculovirus Expression System in insect cells.We firstly constructed two expression vectors pVL1392 hp40 and pVL1393 hp35,and then they were used to co transfect the insect cells(Sf9) separately with linearized polyhedrosis virus genomic DNA.Two kinds of recombinant viruses Ac NPV hp40 and AcNPV hp35 were visually screened out.Biological activity of the recombinant hIL 12(rhIL 12) was detected in the conditioned medium using proliferation assay of PHA activated human lymphocytes and the expression level was about 1 5~2μg/10 6cells.The results of real time Biomolecular Interaction Analysis (BIA) and Northern blot demonstrated that the subunits of rhIL 12,hp35 and hp40 were expressed successfully in the insect cells.The apparent molecular weights of rhIL 12 and hp40 homodimer were 76kDa and 92kDa under non reducing conditions of Western blot,respectively.The recombinant hp40 can significantly inhibit the biological activity of hIL 12.
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