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北京地区两株人偏肺病毒M蛋白基因的原核表达及抗原活性分析
引用本文:曹守春,钱渊,李国华,朱汝南,赵林清,丁雅馨. 北京地区两株人偏肺病毒M蛋白基因的原核表达及抗原活性分析[J]. 病毒学报, 2007, 23(1): 60-62
作者姓名:曹守春  钱渊  李国华  朱汝南  赵林清  丁雅馨
作者单位:首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020;首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020;首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020;首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020;首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020;首都儿科研究所,病毒研究室,北京市感染与免疫中心实验室,北京,100020
基金项目:国家自然科学基金(30570080)和北京市自然科学基金(7052020)
摘    要:人偏肺病毒(Human metapneumovirus,hMPV)是最近发现的可引起人类呼吸道感染的一种副粘病毒,现被归类于偏肺病毒属(Metapneumovirus),是至今发现的第一个与人类疾病相关的偏肺病毒属成员[1]。目前已经受到世界范围的重视,已有十多个国家报道了不同年龄组人群中hMPV的感染情况。

关 键 词:人偏肺病毒  基质蛋白M  原核表达  抗原活性分析
文章编号:1000-8721(2007)01-0060-03
修稿时间:2006-10-162006-11-07

Prokaryotic Expression and Antigenic Activity Analysis on the Matrix Protein Genes of Two Strains of Human Metapneumovirus Recently Identified in Beijing
CAO Shou-chun,QIAN Yuan,LI Guo-hua,ZHU Ru-nan,ZHAO Lin-qing,DING Ya-xin. Prokaryotic Expression and Antigenic Activity Analysis on the Matrix Protein Genes of Two Strains of Human Metapneumovirus Recently Identified in Beijing[J]. Chinese journal of virology, 2007, 23(1): 60-62
Authors:CAO Shou-chun  QIAN Yuan  LI Guo-hua  ZHU Ru-nan  ZHAO Lin-qing  DING Ya-xin
Affiliation:Laboratory of Virology, Beijing Municipal Laboratory of Infection and Immunity, Capital Institute of Pediatrics, Beijing 100020, China
Abstract:Human metapneumovirus (hMPV) is a recently identified respiratory virus more like human respiratory syncytial virus in clinical symptoms. Matrix protein (M) is one of the most important structural proteins. For further studying of hMPV, the full length of M genes from the recombinant plasmid pUCm-M1816 and pUCmM1817 were cloned by PCR and sub-cloned into the pET30a(+) vector, which is a prokaryotic expression vector, after dual-enzyme digestion with Bam HI and Xho I. The positive recombinated plasmids were transformed into E. coli BL21 (DE3) and expressed under the inducing of IPTG. Target proteins were characterized by SDS-PAGE and Western blotting. In this article, we' ve successfully constructed the recombinated plasmids pET30a-M1816 and pET30a-M1817 which have correct open reading frames confirmed by dual-enzyme digestion analysis and sequencing. The fusion proteins with 6 x His-N were highly produced after inducing by 1mmol/ L IPTG at 37 degrees C. A unique protein band with approximate 27.6 kD was characterized by SDS-PAGE. Most of the target protein existed in inclusion body. Western blot analysis showed that the target protein has specific binding reaction to rabbit antiserum against polypeptides of the matrix protein of hMPV. So the M genes were highly expressed in the prokaryotic system and the expressed M proteins have specific antigenic activities. It can be used for further studying of hMPV infections in Beijing.
Keywords:human metapneumovirus  matrix protein  prokaryotic expression  antigenic activity analysis
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