...
首页> 外文期刊>Nanomaterials >A Paper-Based Sandwich Format Hybridization Assay for Unlabeled Nucleic Acid Detection Using Upconversion Nanoparticles as Energy Donors in Luminescence Resonance Energy Transfer
【24h】

A Paper-Based Sandwich Format Hybridization Assay for Unlabeled Nucleic Acid Detection Using Upconversion Nanoparticles as Energy Donors in Luminescence Resonance Energy Transfer

机译:基于纸上的三明治格式杂交检测未标记的核酸,该检测使用上转换纳米粒子作为发光共振能量转移中的能量供体

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Bioassays based on cellulose paper substrates are gaining increasing popularity for the development of field portable and low-cost diagnostic applications. Herein, we report a paper-based nucleic acid hybridization assay using immobilized upconversion nanoparticles (UCNPs) as donors in luminescence resonance energy transfer (LRET). UCNPs with intense green emission served as donors with Cy3 dye as the acceptor. The avidin functionalized UCNPs were immobilized on cellulose paper and subsequently bioconjugated to biotinylated oligonucleotide probes. Introduction of unlabeled oligonucleotide targets resulted in a formation of probe-target duplexes. A subsequent hybridization of Cy3 labeled reporter with the remaining single stranded portion of target brought the Cy3 dye in close proximity to the UCNPs to trigger a LRET-sensitized emission from the acceptor dye. The hybridization assays provided a limit of detection (LOD) of 146.0 fmol and exhibited selectivity for one base pair mismatch discrimination. The assay was functional even in undiluted serum samples. This work embodies important progress in developing DNA hybridization assays on paper. Detection of unlabeled targets is achieved using UCNPs as LRET donors, with minimization of background signal from paper substrates owing to the implementation of low energy near-infrared (NIR) excitation.
机译:基于纤维素纸基材的生物测定法在现场便携式和低成本诊断应用的开发中越来越受欢迎。在本文中,我们报告了一种基于纸张的核酸杂交测定方法,该方法使用固定化的上转换纳米颗粒(UCNP)作为发光共振能量转移(LRET)中的供体。具有强烈绿色发射的UCNPs以Cy3染料为受体充当供体。将抗生物素蛋白功能化的UCNPs固定在纤维素纸上,然后与生物素化的寡核苷酸探针进行生物偶联。未标记的寡核苷酸靶标的引入导致探针-靶标双链体的形成。随后将Cy3标记的报告分子与靶标的其余单链部分杂交,使Cy3染料紧贴UCNP,从而触发了受体染料的LRET敏化发射。杂交测定提供了146.0 fmol的检测限(LOD),并显示出对一个碱基对错配判别的选择性。该测定甚至在未稀释的血清样品中也能起作用。这项工作体现了在纸上开发DNA杂交测定的重要进展。使用UCNP作为LRET供体,可以检测未标记的靶标,并且由于实施了低能量近红外(NIR)激发,可将来自纸张基材的背景信号降至最低。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号