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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2009, Vol. 29 Issue (06): 36-40    
研究报告     
DC-SIGN蛋白在家蚕系统中的表达及生物活性研究
唐晖1|汤绍辉1|杨冬华1|吕正兵2|余威2|张耀洲2|周天鸿3|陈炫1|刘芳1|肖昕4
1. 暨南大学附属第一医院
2. 浙江理工大学生命科学学院生物化学研究所
3. 暨南大学生命科学技术学院
4. 中山大学附属第六医院
Study on DC-SIGN protein expression and its biological activity measurement
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摘要: 目的:构建人DC-SIGN基因片段的家蚕表达系统,进行目的产物表达、鉴定及生物活性分析。方法:从体外刺激分化的DC细胞中克隆出DC-SIGN cDNA,在家蚕表达载体pBacPAK8的BamHⅠ和EcoRⅠ位点构建成重组质粒pBacPAK8-DC-SIGN,与线性化的Bm-BacPAK6病毒基因组DNA共转染家蚕细胞,空斑筛选得到重组病毒Bm-BacPAK-DC-SIGN,重组病毒感染家蚕细胞BmN,Western blot检测表达产物;HIV-1包膜糖蛋白gp120与表达产物孵育检测其生物活性。结果:构建了稳定表达人DC-SIGN蛋白片段的家蚕杆状病毒表达系统;成功表达了DC-SIGN蛋白片段,且能特异性地与HIV-1包膜糖蛋白gp120结合。结论:成功地在家蚕杆状病毒表达系统中表达了人DC-SIGN蛋白片段,具有天然DC-SIGN蛋白样的生物活性,为其抗体制备及AIDS防治药物的研发奠定了基础。
关键词: HIV;DC-SIGN;蛋白表达;生物活性分析    
Abstract:

Study on DC-SIGN protein expression and its biological activity measurement TANG Hui1 TANG Shao-hui1 YANG Dong-hua1 LV Zheng-bing2 YU Wei2 ZHANG Yao-zhou2 ZHOU Tian-hong3 XIAO Xin4 (1The First Affiliated Hospital,Jinan University,Guangzhou 510632,China);(2(Institute of Biochemistry,Zhejiang Sci-Tech University,Hangzhou310018 ,China);(3College of Life Science and Technology,Jinan University,Guangzhou 510632 ,China);(4the Sixth Affiliated Hospital,Sun Yat-sen University,Guangzhou 510655,China ) [Abastract] Objective:To construct expression system of Bombyx mori baculovirus expressing DC-SIGN protein fragmen, and to measure the biological activity of it. Methods:Human DC-SIGN cDNA was amplied by RT-PCR from the differentiated DCs.The DC-SIGN gene was inserted into the bacubvirus transfer vector pBacPAK8,and the recombiant plasmid pBacPAK8-DC-SIGN were cotransfected into Bombyx mori cell lines with the linearized Bm-BacPAK6 virus genome DNA.After recombination in the cells and screening by the plaque assay, the recombinated virus Bm-BacPAK-DC-SIGN were obtained and again infected into Bombyx mori cell lines to express DC-SIGN protein fragmen which were detected by Western blot. The biological activity of the expressed DC-SIGN protein fragmen was measured by its combination with HIV-1 gp120.Results:Expression system of Bombyx mori baculovirus expressing human DC-SIGN protein fragment was constructed, Human DC-SIGN protein fragment was expressed and it can bind specifically with HIV-1 gp120.Conclusion: Human DC-SIGN protein fragment was successfully expressed in expression system of Bombyx mori baculovirus, which showed the natural DC-SIGN protein-like biological activity. It became the work basis of the antibody preparation against it and drug study on prevention and treatment of AIDS. [Key words]: Human immunodeficiency virus;DC-SIGN;Protein expression;biological activity measurement

Key words: Human immunodeficiency virus;DC-SIGN;Protein expression;biological activity measurement
收稿日期: 2009-03-19 出版日期: 2009-07-02
ZTFLH:  Q786  
通讯作者: 肖昕     E-mail: txiaoxin1049@163.com
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唐晖1
汤绍辉1
杨冬华1
吕正兵2
余威2
张耀洲2
周天鸿3
陈炫1
刘芳1
肖昕4

引用本文:

唐晖1,汤绍辉1,杨冬华1,吕正兵2,余威2,张耀洲2,周天鸿3,陈炫1,刘芳1,肖昕4. DC-SIGN蛋白在家蚕系统中的表达及生物活性研究[J]. 中国生物工程杂志, 2009, 29(06): 36-40.

TANG Hui-1, SHANG Chao-Hui-1, YANG Dong-Hua-1, LV Zheng-Bing-2, TU Wei-2, ZHANG Yao-Zhou-2, ZHOU Tian-Hong-3, CHEN Xuan-1, LIU Fang-1, XIAO Cuan-4. Study on DC-SIGN protein expression and its biological activity measurement. China Biotechnology, 2009, 29(06): 36-40.

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https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2009/V29/I06/36

[1] 曾毅主编. 艾滋病毒及其有关病毒.天津:南开大学出版社,1999.1~3 Zeng Y .HIV Virus and Associated Virus.Tianjin:NanKai University Press,1999.1~3 [2] Zhu T F, Feng T J,Xiao X,et al.Global human genetics of HIV-1 infection and China. Cell Research, 2005, 15(11-12):833~842 [3] Burleigh L,Lozach P Y,Schiffer C,et al.Infection of dendritic cells (DCs), not DC-SIGN-mediated internalization of human immunodeficiency virus, is required for long-term transfer of virus to T cells. J Virol,2006,80(6):2949~2957 [4] Hong P W, Nguyen S, Young S, et al.Identification of the optimal DC-SIGN binding site on human immunodeficiency virus type 1 gp120.J Virol,2007,81(15):8325~8336 [5] Poelmann S,Baribaud F,Doms R W.DC-SIGN and DC-SIGNR: helping hands for HIV.Trend in Immunology, 2001, 22(12):643~645 [6] Wang J H, Janas A M, Olson W J,et al.CD4 coexpression regulates DC-SIGN-mediated transmission of human immunodeficiency virus type 1.J Virol,2007, 81(5):2497~2507 [7] Soilleux E J, Barten R, Trowsdale J.DC-SIGN; a related gene, and CD23 form a cluster on 19p13. J Immunol, 2000,165(6):2937~2942 [8] Hong P, Ninonuevo M R,Lee B,et al.Oligomerisation of the macrophage mannose receptor enhances GP120 mediated binding of HIV-1.Br J Nutr, 2009,101(4):482~486 [9] Borggren M,Repits J,Kuylenstierna C, et al.Evolution of DC-SIGN use revealed by fitness studies of R5 HIV-1 variants emerging during AIDS progression.Retrovirology, 2008,27;5:28 [10] Lee B,Leslie G,Soilleux E,et al.cis expression of DC-SIGN allows for more efficient entry of human and simian immunodeficiency viruses via CD4 and a coreceptor.J Virol,2001,75(24): 12028~12038 [11] Doranz B J, Filion L G, Diaz-Mitoma F,et al.Safe use of the CXCR4 inhibitor ALX40-4C in humans. AIDS Res Hum Retroviruses, 2001, 17(6):475~486 [12] Nair M P, Reynolds J L, Mahajan S D,et al.RNAi-directed inhibition of DC-SIGN by dendritic cells: prospects for HIV-1 therapy. AAPS J, 2005, 7(3):E572~E578 [13] Ikonmou L,Schneider Y J,Agathos S N.Insect cell culture for industrial production of recombinant proteins.Appl Microbiol Biotechnol,2003,62(1):1~20
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