首页> 外文期刊>Journal of Fluorescence >A novel single fluorophore-labeled double-stranded oligonucleotide probe for fluorescence-enhanced nucleic acid detection based on the inherent quenching ability of deoxyguanosine bases and competitive strand-displacement reaction
【24h】

A novel single fluorophore-labeled double-stranded oligonucleotide probe for fluorescence-enhanced nucleic acid detection based on the inherent quenching ability of deoxyguanosine bases and competitive strand-displacement reaction

机译:基于脱氧鸟苷碱基固有的猝灭能力和竞争性链置换反应的新型单荧光团标记双链寡核苷酸探针,用于荧光增强的核酸检测

获取原文
获取原文并翻译 | 示例
       

摘要

We develop a novel single fluorophore-labeled double-stranded oligonucleotide (OND) probe for rapid, nanostructure-free, fluorescence-enhanced nucleic acid detection for the first time. We further demonstrate such probe is able to well discriminate single-base mutation in nucleic acid. The design takes advantage of an inherent quenching ability of guanine bases. The short strand of the probe is designed with an end-labeled fluorophore that is placed adjacent to two guanines as the quencher located on the long opposite strand, resulting in great quenching of dye fluorescence. In the presence of a target complementary to the long strand of the probe, a competitive stranddisplacement reaction occurs and the long strand forms a more stable duplex with the target, resulting in the two strands of the probe being separated from each other. As a consequence of this displacement, the fluorophore and the quencher are no longer in close proximity and dye fluorescence increases, signaling the presence of target.
机译:我们首次开发了一种新型的单荧光团标记的双链寡核苷酸(OND)探针,用于快速,无纳米结构,荧光增强的核酸检测。我们进一步证明了这种探针能够很好地区分核酸中的单碱基突变。该设计利用了鸟嘌呤碱基固有的淬灭能力。探针的短链设计有末端标记的荧光团,该荧光团与两个鸟嘌呤相邻放置,作为位于相对的长链上的淬灭剂,可导致染料荧光的极大淬灭。在存在与探针的长链互补的靶标时,发生竞争性链置换反应,并且长链与靶标形成更稳定的双链体,导致探针的两条链彼此分离。这种置换的结果是,荧光团和猝灭剂不再紧密靠近,并且染料荧光增加,表明存在靶标。

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