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5株不同亚型HIV-1毒株gp120序列特征分析及其蛋白的表达
引用本文:王铮,李敬云,鲍作义,李韩平,庄道民,刘思杨,李林.5株不同亚型HIV-1毒株gp120序列特征分析及其蛋白的表达[J].中华微生物学和免疫学杂志,2009,29(5).
作者姓名:王铮  李敬云  鲍作义  李韩平  庄道民  刘思杨  李林
作者单位:军事医学科学院微生物流行病研究所全军艾滋病检测中心,病原微生物生物安全国家重点实验室,北京,100071
摘    要:目的 分析我国HIV-1主要亚型毒株的gp120区域的序列特征,并表达出gp120糖基化蛋白,为研究gp120的致病机制和设计疫苗奠定基础.方法 利用巢式PCR从来自于不同省份的5名HIV-1感染者外周血单个核细胞DNA中扩增全长gp120基因并测序,对序列特征进行分析,并将获得的gp120基因克隆入真核表达载体,体外表达获得gp120糖基化蛋白.结果 序列分析显示,此5条gp120序列分属HIV-1 Thai-B、BC重组和AE重组哑型,虽然亚型不同,但这些gp120序列在相同的位置都存在着一些保守的糖基化位点,且都具备相同的Furin蛋白酶第一切割位点,与参考序列比较发现,不同的HIV亚型序列中,除V3序列长度较为保守外,V1、V2、V4、V5各区域都有不同程度的缺失现象,与BC重组和AE重组亚型相比,Thai-B亚型V3的顶端环呈现出多种组合.最终将这5条gpl20序列都克隆人真核表达载体并表达出糖基化的gp120蛋白.结论 在设计疫苗和检测试剂时应考虑到膜区的高变性,gp120糖蛋白的体外表达有利于进一步开展针对我国主要HIV流行毒株膜蛋白致病机制和疫苗学的研究.

关 键 词:糖基化蛋白

The analysis of 5 HIV-1 gpl20 sequences from different clades and expression of their corresponding proteins in vitro
WANG Zheng,LI Jing-yun,BAO Zuo-yi,LI Han-ping,ZHUANG Dao-min,LIU Si-yang,LI Lin.The analysis of 5 HIV-1 gpl20 sequences from different clades and expression of their corresponding proteins in vitro[J].Chinese Journal of Microbiology and Immunology,2009,29(5).
Authors:WANG Zheng  LI Jing-yun  BAO Zuo-yi  LI Han-ping  ZHUANG Dao-min  LIU Si-yang  LI Lin
Abstract:Objective To characterize 5 gpl20 sequences from mainly circulating clades in China and expression of their gp120 glycoproteins. Methods gp120 genes were amplified from the PBMCs of 5 HIV-1 infected individuals in different provinces using nest PCR and their DNA sequences were determined. Sequence characteristics were analyzed and gp120 genes were sub-cloned into the mammalian expression vec-tor to produce gp120 glycoproteins. Results Sequence characteristics indicated these sequences belong to the clade Thai-B, CRF_BC and CRF_AE, respectively. There were some conservative N-linked glycosyla-tion sites and primary Furin protease cleavage motifs in the same positions within gp120 amino acid se-quences although these gp120 sequences were categorized into different clades. In comparison with referen-tial strains, amino acids deletions were found in the V1, V2, V4, V5 regions except for the V3 loop; above all, V3 tip motifs of Thai-B exhibited the more polymorphic forms than those of CRF_BC and CRF_AE. These 5 gp120 sequences were cloned into the eukaryotic expression vector and gpl20 glycoproteins were produced successfully. Conclusion Hyper-variable nature of Env should be considered while designing HIV-1 vaccine or test reagent, and gpl20 expression in vitro is helpful to further research on the Env patho-genesis and vaccine development against the mainly circulating HIV-1 isolates in China.
Keywords:HIV-1  gp120
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