Department of Bioactive Material Sciences, Chonbuk National University, Jeonju, Jeonbuk 561-567, South Korea.
Department of Chemistry, Chonbuk National University, Jeonju, Jeonbuk 561-567, South Korea.
Bioorg Med Chem. 2018 Sep 15;26(17):4881-4885. doi: 10.1016/j.bmc.2018.08.027. Epub 2018 Aug 25.
Large-Stokes-shift based simple folded DNA probing system (LSFP) had a simple folded DNA structure and exhibited a large Stokes-shifted (194 nm) fluorescence signal upon excitation at a single wavelength (386 nm). This Stokes shift was achieved through a simple combination of donor and acceptor fluorophores and employing multi-FRET systematically. This unique large Stokes-shifted fluorescence signal was used to detect target DNA with large increases in the fluorescence signal (9.7-14.2 fold). This LSFP exhibited enough selectivity, distinguishing a perfectly matched sequence from the probe itself and mismatched sequences. Surprisingly, when DSN was used for signal amplification with miR21P probing system whose target is miRNA 21, it showed high sensitivity (13.7 aM) and selectivity (one base mismatch discrimination). This system has several advantages over other molecular beacons (MBs): (i) it is easy to design and synthesize the probing system that does not require the construction of a finely designed stem and loop, as in most MBs (this can prevent the degradation of miR21P itself by DSN enzyme without special backbone modification); (ii) it can control unique fluorescence, such as large Stokes-shifted fluorescence through a simple combination of donor and acceptor fluorophores; and (iii) through signal amplification using DSN, it can efficiently detect extremely small amounts of target miRNA with high sensitivity (13.7 aM).
基于大斯托克斯位移的简单折叠 DNA 探测系统 (LSFP) 具有简单的折叠 DNA 结构,在单一波长 (386nm) 激发下表现出大斯托克斯位移 (194nm) 的荧光信号。这种斯托克斯位移是通过简单组合供体和受体荧光团并系统地采用多 FRET 实现的。这种独特的大斯托克斯位移荧光信号被用于检测靶 DNA,其荧光信号显著增加 (9.7-14.2 倍)。该 LSFP 表现出足够的选择性,能够区分与探针本身完全匹配的序列和不匹配的序列。令人惊讶的是,当 DSN 用于 miR21P 探测系统(其靶标是 miRNA 21)的信号放大时,它表现出高灵敏度 (13.7aM) 和选择性(一个碱基错配区分)。与其他分子信标 (MB) 相比,该系统具有几个优势:(i) 它易于设计和合成探测系统,不需要构建大多数 MB 中那样精细设计的茎环结构(这可以防止 DSN 酶对 miR21P 本身的降解,而无需特殊的骨架修饰);(ii) 它可以通过简单组合供体和受体荧光团来控制独特的荧光,如大斯托克斯位移荧光;(iii) 通过使用 DSN 进行信号放大,可以高效地检测到极少量的靶 miRNA,具有高灵敏度 (13.7aM)。