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用杆状病毒表达系统表达的HIV-2 gp105和gp36的反应原性与抗原特异性分析
引用本文:张应玖,金宁一,王宏伟,黄薇,张东威,沈家骢.用杆状病毒表达系统表达的HIV-2 gp105和gp36的反应原性与抗原特异性分析[J].吉林大学学报(理学版),2002,40(1):105-107.
作者姓名:张应玖  金宁一  王宏伟  黄薇  张东威  沈家骢
作者单位:1. 吉林大学生命科学学院, 长春 130023; 2. 中国人民解放军军需大学基因工程实验室, 长春 130062;3. 吉林省中医中药研究院, 长春 130021
基金项目:国家杰出青年基金 (批准号 :3 9770 661)
摘    要:用ELISA方法分析由杆状病毒/昆虫细胞表达系统表达的HIV-2外膜蛋白gp105和跨膜蛋白gp36的反应原性和特异性. 结果表明, 二者均具有很好的反应原性和抗原特异性, 可作为免疫抗原和检测抗原加以应用.

关 键 词:人体免疫缺陷病毒Ⅱ型(HIV-2)  外膜蛋白gp105  跨膜蛋白gp36  反应原性  抗原特异性  
文章编号:1671-5489(2002)01-0105-03
收稿时间:2001-11-02
修稿时间:2001年11月2日

Reactiongenicity and Antigenic Specificity of Human Immunodeficiency Virus Type 2 External Glycoprotein gp105 and Transmembrane Glycoprotein gp36 Expressed in Baculovirus Expression System
ZHANG Ying Jiu ,JIN Ning Yi ,WANG Hong wei ,HUANG Wei ,ZHANG Dong wei ,SHEN Jia Cong.Reactiongenicity and Antigenic Specificity of Human Immunodeficiency Virus Type 2 External Glycoprotein gp105 and Transmembrane Glycoprotein gp36 Expressed in Baculovirus Expression System[J].Journal of Jilin University: Sci Ed,2002,40(1):105-107.
Authors:ZHANG Ying Jiu  JIN Ning Yi  WANG Hong wei  HUANG Wei  ZHANG Dong wei  SHEN Jia Cong
Institution:1. College of Life Science, Jilin University, Changchun 130023, P.R.China; 2. Gene Engineering Laboratory,the Ququartermaster University of PLA, Changchun 130062, P.R.China; 3. Academy of TraditionalChinese Medicine and Material Medical of Jilin Province, Changchun 130012, P.R.China
Abstract:To develop effective vaccines and diagnostic agents of AIDS, reactiongenicity and antigenic specificity of the external glycoprotein gp105 and transmembrane glycoprotein gp36 of human immunodeficiency virus type 2, expressed in insect cells spodoptera frugiperda (SF9) using baculovirus expression system were determined by ELISA. The results showed that as an antigen, the expressed gp105 and gp36 showed the ability to react with HIV 2 antisera, and their reactive capacity was similar to that of the positive control (standard HIV 2 external glycoprotein or transmembrane glycoprotein), which demonstrated that the expressed gp105 and gp36 might be used as a diagnostic agent or their components and the material for immunological studies. Furthermore, the results showed that the expressed gp105 and gp36 exhibited a stronger reactiongenicity with HIV 2 antisera than with HIV 1 antisera, i.e ., they exhibited a high specificity. The HIV 2 gp105 or gp36 shares approximately 40% amino acid sequence homology with that of HIV 1, and the weaker cross reactivity is often observed. Because HIV external glycoprotein and transmembrane glycoprotein mediate the attachment and fusion of the virion to the host cell, many vaccine strategies have focused on them. Similar to native gp105 and gp36, the expressed gp105 and gp36 in this study exhibitied a good reactiongenicity and antigenic specificity, thus they can be used for the studies on its ability to induce immune responses in primate models.
Keywords:human immunodeficiency virus type Ⅱ (HIV-2)  external  glycoprotein gp105  transmembrane glycoprotein gp36  reactiongenicity  antigenic specificity  
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