激子控制荧光:应用于杂交敏感的荧光DNA探针。

Akimitsu Okamoto, Shuji Ikeda, Takeshi Kubota, Mizue Yuki, Hiroyuki Yanagisawa
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引用次数: 1

摘要

利用荧光染料分子内激子相互作用引起的荧光猝灭的概念,设计了一种用于核酸检测的杂交敏感荧光探针。我们合成了一种双噻唑橙标记的核苷酸,该核苷酸具有高荧光强度,可以与目标核酸杂交,并且可以有效地猝灭单链状态。这种激子控制荧光探针应用于活的HeLa细胞,通过显微注射来观察细胞内mRNA的定位。将探针注入细胞后,立即观察到探针与目标RNA杂交的荧光。这种荧光在加入竞争对手DNA后迅速减弱。该探针的多色性使得同时检测多个靶核酸序列变得简单。该探针实现了荧光强度对靶核酸量的灵敏响应而发生大、快速、可逆的变化,便于对细胞内RNA的行为进行时空监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exciton-controlled fluorescence: application to hybridization-sensitive fluorescent DNA probe.

A hybridization-sensitive fluorescent probe has been designed for nucleic acid detection, using the concept of fluorescence quenching caused by the intramolecular excitonic interaction of fluorescence dyes. We synthesized a doubly thiazole orange-labeled nucleotide showing high fluorescence intensity for a hybrid with the target nucleic acid and effective quenching for the single-stranded state. This exciton-controlled fluorescent probe was applied to living HeLa cells using microinjection to visualize intracellular mRNA localization. Immediately after injection of the probe into the cell, fluorescence was observed from the probe hybridizing with the target RNA. This fluorescence rapidly decreased upon addition of a competitor DNA. Multicoloring of this probe resulted in the simple simultaneous detection of plural target nucleic acid sequences. This probe realized a large, rapid, reversible change in fluorescence intensity in sensitive response to the amount of target nucleic acid, and facilitated spatiotemporal monitoring of the behavior of intracellular RNA.

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