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作 者:李越希[1] 周宗安[1] 陶开华[1] 乔仁良[1] 邓小昭[1] 郑纪山[1] 仲晓萍[1]
出 处:《药物生物技术》1999年第4期198-202,共5页Pharmaceutical Biotechnology
基 金:全军青年基金!课题:编号96Q12
摘 要:通过分析丙肝病毒(HCV) 的非结构4 区(NS4) 和5 区(NS5)蛋白的氨基酸序列,推测确定抗原决定簇位点。用RT- PCR 技术从中国丙肝病人血清中扩增克隆含抗原决定簇基因的NS4 及NS5 基因,将该两段基因分别克隆至质粒表达载体pET28a( + ) 内,转化大肠杆菌BL21(DE3) ,构建成功了高效表达NS4 和NS5 蛋白的工程菌,IPTG 诱导后两蛋白在工程菌内的表达量分别约占菌体蛋白的33 % 和28 % 。经Sepharcryl S- 200 分子筛及Ni- NTASepharose 螯合层析纯化,获得了较纯的重组NS4 和NS5 蛋白。用纯化的NS4 和NS5 蛋白作抗原ELISA 法检测HCV抗体阴、阳性血清,证实它们有较好的抗原性和特异性。The NS 4 and NS 5 gene fragments of hepatitis C virus were cloned from anti HCV positive sera by RT PCR, the recombinant plasmids expressing NS 4 or NS 5protein were constructed by inserting the cloned NS 4 or NS 5 gene fragments into plasmid vector pET28a(+), the expressed NS 4 protein is about 33% of total host ( E.coli BL21) proteins, and the NS 5 is about 28%. After purification, the expressed NS 4 and NS 5 protein were used to detect 87 anti HCV (anti HCV core and or NS 3 antigen) positive sera and 160 anti HCV(anti core and NS 3 antigens) negative sera, of the 87 positive sera, 28 (31%) sera are anti NS 4 positive and 62(70%) sera are anti NS 5positive; of the 160 negative sera, 2 sera are anti NS 4 weak positive and 1 serum is anti NS 5 weak positive. The results suggest that the NS 4 and NS 5 proteins have excellent antigenicity and specificity, and may increase the detection rate of anti HCV when being added in ELISA kit for detection of anti HCV.
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