文章摘要
蒋青桃,冯旰珠,夏 梅,陈 霞,邱 文,赵 聃,王迎伟.结核杆菌ESAT-6抗原Th1优势表位与FL重组纳米疫苗的制备及其特性研究[J].南京医科大学学报,2011,(5):620~623
结核杆菌ESAT-6抗原Th1优势表位与FL重组纳米疫苗的制备及其特性研究
Preparation and characteristics of chitosan nanoparticles based on multiepitope DNA vaccine encoding ESAT-6 Th1 epitopes of Mycobacterium tuberculosis and FL
投稿时间:2010-12-03  
DOI:10.7655
中文关键词: 结核杆菌  疫苗  壳聚糖纳米粒
英文关键词: Mycobacterium tuberculosis  vaccine  chitosan-nanoparticles
基金项目:江苏省教育厅自然科学基金重大项目(09KJA310002);江苏省六大人才高峰资助项目(DG216D5016);江苏省现代病原生物学重点实验室开放课题(08bykf03)
作者单位
蒋青桃 南京医科大学微生物学与免疫学系,江苏 南京 210029 
冯旰珠 南京医科大学微生物学与免疫学系,江苏 南京 210029 
夏 梅 南京医科大学微生物学与免疫学系,江苏 南京 210029 
陈 霞 南京医科大学微生物学与免疫学系,江苏 南京 210029 
邱 文 南京医科大学微生物学与免疫学系,江苏 南京 210029 
赵 聃 南京医科大学微生物学与免疫学系,江苏 南京 210029 
王迎伟 南京医科大学微生物学与免疫学系,江苏 南京 210029 
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中文摘要:
      目的:制备适当粒径的壳聚糖纳米粒,并连接质粒,评价该壳聚糖纳米粒对该质粒的结合能力与保护作用,为进一步研究重组纳米疫苗的免疫效果提供基础?方法:采用离子交联法制备成pIRES-TH-FL-壳聚糖纳米粒复合物,用紫外分光光度计检测纳米颗粒对质粒的包埋率;经琼脂糖凝胶电泳分析纳米载体与质粒的结合能力及对该质粒的保护作用;通过喷金电镜观察其大小形态;另用zata电位仪测定粒径和zeta电位;最后用Western blot实验鉴定其在真核细胞中的表达情况?结果:紫外分光光度计检测到该壳聚糖纳米质粒的包埋率为99.28%,琼脂糖凝胶电泳结果显示壳聚糖纳米粒能保护该质粒免受DNaseⅠ的降解?制得的壳聚糖纳米质粒粒径为300 nm左右,zeta电位为32.4 mV?Western blot证实,该纳米质粒能转染293T细胞并表达目的融合蛋白?结论:本实验成功制备了粒径适当且分布均匀的壳聚糖纳米质粒,并能够在体外实现有效表达?
英文摘要:
      Objective:To prepare chitosan nanoparticles as gene carrier of multiepitope DNA vaccine,and explore the loading capability and its protection ability to plasmid. Methods:The chitosan nanoparticles were prepared with ionic cross-linking method. The encapsulation rate was determined by UV spectrophotometer. The binding ability and protective effect of plasmid pIRES-TH-FL were evaluated by agarose gel electrophoresis analysis. The size,morphology and distribution were observed by transmission electron microscope. The diameter and zeta potential were measured by zetasizer. The pIRES-TH-FL-chitosan nanoparticles were transfected into 293T cells in order to examine their expression. Results:The encapsulation efficiency of pIRES-TH-FL-chitosan nanoparticles was 99.28% by UV spectrophotometer. Agarose gel electrophoresis showed that chitosan nanoparticles can effectively combined with plasmid pIRES-TH-FL and protected it from nuclease degradation.The mean diameter of pIRES-TH-FL-chitosan nanoparticles was about 300 nm and the mean zeta potential was 32.4mV.Western blot assay result confirmed that the DNA-chitosan nanoparticles can be expressed in 293T cells. Conclusion:pIRES-TH-FL-chitosan nanoparticles of homogeneous diameter were prepared and successfully expressed in vitro.
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