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Tetracyanoquinodimethane nanoparticles as an effective sensing platform for fluorescent nucleic acid detection

机译:Tetracyanoquinodimethanemethane纳米颗粒作为荧光核酸检测的有效传感平台

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In this communication, we report on the use of tetracyanoquinodimethane nanoparticles (TNs) as an effective fluorescent sensing platform for nucleic acid detection for the first time. The general concept used in this approach is based on adsorption of fluorescently labeled single-stranded DNA (ssDNA) probe by TN, due to the strong π–π stacking between unpaired DNA bases and TN. As a result, the fluorophor is brought into close proximity of TN, leading to substantial fluorescence quenching via photoinduced electron transfer between fluorescent dye and TN. Upon presence of the target ssDNA, specific hybridization with the target takes place to form a double-stranded DNA (dsDNA). The helix cannot be adsorbed by TN due to its rigid conformation and the absence of unpaired DNA bases. Thus, the fluorophor is seperated from TN accompanied by fluorescence recovery. This fluorescence enhancement signals completion of the assay. It also suggests that this sensing platform can well differentiate perfect complementary and mismatched sequences. A detection limit as low as 1.5 nM was obtained...
机译:在本次交流中,我们首次报道了将四氰基喹二甲烷纳米颗粒(TNs)用作核酸检测的有效荧光传感平台。由于未配对的DNA碱基和TN之间有很强的π-π堆积,因此该方法使用的一般概念是基于TN吸附荧光标记的单链DNA(ssDNA)探针。结果,荧光团被带到TN的附近,通过荧光染料和TN之间的光感应电子转移,导致大量的荧光猝灭。在存在靶标ssDNA时,与靶标发生特异性杂交以形成双链DNA(dsDNA)。螺旋由于其刚性构象和不成对的DNA碱基而不能被TN吸附。因此,荧光团与TN分离,伴随着荧光的恢复。这种荧光增强表明测定已完成。这也表明该传感平台可以很好地区分完美的互补序列和错配序列。检出限低至1.5 nM ...

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