期刊文献+

疏水蛋白HFBI融合标签能显著提高外源基因在植物中的表达水平 被引量:3

Effect of the hydrophobin HFBI-fusion tag on exogenous protein accumulation in tobacco plant
下载PDF
导出
摘要 目的针对植物生物反应器中外源基因表达水平普遍较低的问题,探索和评价丝状真菌瑞氏木霉(Trichode rma re e s e i)编码的小分子疏水蛋白(Hydrophobin,HFBI)作为融合标签在植物生物反应器中提高系统表达量的应用潜力;分析其提高外源基因表达水平的可能机制。方法以绿色荧光蛋白(GFP)为报道基因,采用基因体外合成技术和亚克隆技术构建GFP和GFPHFBI融合植物表达载体。利用农杆菌渗滤技术接种植物本明烟(Nicotiana be nthamiana)。通过GFP荧光观察,荧光显微镜镜检,Western blot,ELISA和RT-PCR等实验手段测定报告基因GFP在植物中的表达情况,探明HFBI融合标签在植物中表达外源基因的作用效果和特点并分析其可能的作用机制。结果 HFBI融合标签对植物细胞无明显的细胞毒性;GFP-HFBI融合蛋白在植物中的积累水平显著高于对照;GFP-HFBI融合蛋白在细胞内形成致密的蛋白质颗粒。结论 HFBI融合标签能够显著提高外源基因在植物中的积累水平。推测形成的蛋白质颗粒隔绝了细胞内源性蛋白酶对目的表达产物的降解,进而提高了外源基因产物在细胞中的积累。 Objective To explore the mechanisms by which HFBI fusions increase recombinant fusion protein accumulation in plants. Methods The HFBI sequence from Trichoderma reesei was synthesized and two plant expression vectors for expression of green fluorescence protein(GFP) and GFP- HFBI were constructed. The vectors were inoculated in Nicotiana benthamiana plants through agroinfiltration, and the expression levels and m RNA accumulation levels of GFP in Nicotiana leaves were examined by Western blotting, ELISA and RT- PCR. Results The HFBI fusion tag significantly enhanced the accumulation of GFP in the leaves of N. benthamiana without causing toxic effects. Endoplasmic reticulum- targeted GFP- HFBI fusion induced the formation of spherical protein particles in the plant cells. Conclusion HFBI fusions can increase the accumulation of its fusion partner in plants by forming stable protein particles, which probably shields the target protein from endogenous protease-induced degadation. HFBI fusion technology provides an alternative to improving recombinant protein expression in plants from agroinfection-compatible expression vectors.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2015年第12期1665-1671,共7页 Journal of Southern Medical University
基金 国家自然科学基金(31160032)~~
关键词 真菌疏水蛋白 融合标签 绿色荧光蛋白 瑞氏木霉 本明烟 hydrophobin fusion tags green fluorescent protein Trichoderma reesei Nicotiana benthamiana
  • 相关文献

参考文献30

  • 1Redkiewicz P, Sirko A, Kamel KA, et al. Plant expression systems for production of hemagglutinin as a vaccine against influenza virus[J]. Acta Biochim Pol, 2014, 61(3): 551-60.
  • 2Virdi V, Depicker A. Role of plant expression systems in antibody production for passive immunization[J]. Int J Dev Biol, 2013, 57(6/8): 587-93.
  • 3Mortimer CL, Dugdale B, Dale JL. Updates in inducible transgene expression using viral vectors: from transient to stable expression[J]. Curr Opin Biotechnol, 2015, 32(8): 85-92.
  • 4Bell MR, Engleka MJ, Malik A, et al. To fuse or not to fuse:what is your purpose[J]. Protein Sci, 2013, 22(11): 1466-77.
  • 5Waugh DS. Making the most of affinity tags[J]. Trends Biotechnol,2005, 23(6): 316-20.
  • 6Mishra S, Yadav DK, Tuli R. Ubiquitin fusion enhances cholera toxin B subunit expression in transgenic plants and the plantexpressed protein binds GM1 receptors more efficiently[J]. J Biotechnol, 2006, 127(1): 95-108.
  • 7Dus Santos MJ, Wigdorovitz A, Trono K, et al. A novel methodology to develop a foot and mouth disease virus (FMDV) peptide-based vaccine in transgenic plants[J].Vaccine, 2002, 20(7/8): 1141-7.
  • 8Kim TG, Ruprecht R, Langridge WH. Synthesis and assembly of a cholera toxin B subunit SHIV 89.6p Tat fusion protein in transgenic potato[J]. Protein Expr Purif, 2004, 35(2): 313-9.
  • 9Ca?izares MC, Nicholson L, Lomonossoff GP. Use of viral vectors for vaccine production in plants[J]. Immunol Cell Biol, 2005, 83(3): 263-70.
  • 10Obregon P, Chargelegue D, Drake PM, et al. HIV-1 p24-immunoglobulin fusion molecule: a new strategy for plant-based protein production[J]. Plant Biotechnol J, 2006, 4(2): 195-207.

同被引文献47

引证文献3

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部