文章摘要
张李钰 何威 杨颖 孙宏利 宋佳凝 冯帆 武海滨.新型核酸适配体荧光纳米微粒用于人干扰素-γ的测定[J].,2016,16(27):5241-5245
新型核酸适配体荧光纳米微粒用于人干扰素-γ的测定
Establishment of a Novel Fluorescent Nanomagnetic Beads for the Detectionof Human IFN-γ based on Aptamer
  
DOI:
中文关键词: 核酸适配体  IFN-γ  磁性纳米颗粒  三明治夹心结构  荧光
英文关键词: Aptamer  IFN-γ  Nanomagnetic Beads  Sandwich structure  Fluorescence
基金项目:西安市科技计划项目(SF1510(4))
作者单位
张李钰 何威 杨颖 孙宏利 宋佳凝 冯帆 武海滨 西安市儿童医院陕西省儿科疾病研究所西安市儿童医院口腔科沈阳军区总医院药剂科西安市儿童医院儿科重症监护病房 
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中文摘要:
      目的:利用由两条核酸适配体与人干扰素-γ(Interferon-γ, IFN-γ)的高亲和力构建的三明治结构和磁性纳米颗粒的磁性分离 技术,设计并制作了一种新型荧光纳米微粒,建立基于核酸适配体的新型荧光纳米微粒用于人IFN-γ的检测。方法:流式细胞术检 测IFN-γ核酸适配体B1-4 和T2 对IFN-γ的结合特异性;将生物素修饰的B1-4 固定于链霉亲和素包被的纳米磁珠上,连接B1-4 的纳米磁珠可通过B1-4 与IFN-γ的亲和性捕获IFN-γ,再利用另一条FAM修饰的IFN-γ核酸适配体T2 形成(B1-4)-(IFN-γ)-(T2) 三明治夹心结构,构建新型核酸适配体荧光纳米微粒;IFN-γ分别与核酸适配体荧光纳米微粒孵育不同时间以探索该检测系统中 IFN-酌与磁珠的最佳孵育时间;流式细胞术检测磁珠12 h内荧光变化,探索时间对检测体系的影响;流式细胞术检测与不同浓度 IFN-酌孵育的磁珠表面荧光强度,绘制IFN-酌检测标准曲线;检测血清对检测特异性的影响。结果:B1-4 和T2 对IFN-酌的结合特 异性高;三明治夹心结构对IFN-酌检测特异性好,任意改变其中一因素则磁珠表面荧光信号显著下降,三明治夹心结构构建失败; 此法对IFN-酌的响应线性浓度为0~50 ng/L,其线性方程为y=3.512x+1.060,敏感度为1 ng/L;12 h内测得的荧光信号稳定,并无 明显衰减;血清对体系检测特异性无明显影响。结论:成功构建核酸适配体荧光纳米微粒用于人IFN-γ的测定。
英文摘要:
      Objective:To establish and produce a novel nanoparticle which was based on fluorescent nanomagnetic beads mediated by aptamers for the detection of human IFN-γ, we constructed a sandwich structure utilized two aptamers' binding abilities to IFN-γand magnetic separation technology of magnetic nanoparticles.Methods:Flow cytometry was employed to monitor the binding specificities of aptamer B1-4 and T2 to IFN-酌; Aptamer B1-4 modified with biotin was linked to the magnetic beads which were coated by streptavidin, then these beads could capture IFN-酌because of the B1-4's binding affinity to IFN-酌. Next, another IFN-酌aptamer T2 modified with FAM was added to form sandwich structure (B1-4)-(IFN-γ)-(T2), then the aptamer mediated fluorescent nanomagnetic beads were constructed successfully; Fluorescence intensities of nanomagnetic beads incubated with IFN-γfor different time were detected to study the optimum IFN-γ incubation time; Flow cytometry was employed to detect the fluorescence change of beads within 12 h to study the influence of time to IFN-γdetection system; Flow cytometry was utilized to assess the fluorescence intensities under different IFN-γconcentration to make the linear equation of the IFN-γdetection; The influence caused by serum to detection specificity of nanoparticle systemwas investigated.Results:B1-4 and T2 showed high binding specificity to IFN-γ; The sandwich structure showed high binding specificity to IFN-γ, and the fluorescence intensities decreased significantly when changed anyone of the three elements in sandwich structure, which mean the construction failure of sandwich structure; The response linear range of IFN-γdetection is 0~50 ng/L, and the linear equation is y=3.512x+1.060, the sensitivity is 1 ng/L; The fluorescence intensities showed no obvious decline within 12 h which meanthe fluorescence of nanoparticlewasstable; Serumhad noobvious effect onthe detectionspecificityof sandwichstructure.Conclusion:Successfully established a novel nano-particle which is based on fluorescent nanomagnetic beads mediated by aptamer for the detection of human IFN-γ.
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