Abstract Heating enhanced sensitive and selective electrochemical detection of Hg <ce:sup loc='post'>2+</ce:sup> based on T-Hg <ce:sup loc='post'>2+</ce:sup>-T structure and exonuclease III-assisted target recycling amplification strategy at heated gold disk electrode
首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Heating enhanced sensitive and selective electrochemical detection of Hg 2+ based on T-Hg 2+-T structure and exonuclease III-assisted target recycling amplification strategy at heated gold disk electrode
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Heating enhanced sensitive and selective electrochemical detection of Hg 2+ based on T-Hg 2+-T structure and exonuclease III-assisted target recycling amplification strategy at heated gold disk electrode

机译:加热增强的敏感和选择性电化学检测HG 2 + 基于T-HG 2 + -T结构和外切核酸酶III辅助目标回收加热金盘电极的循环扩增策略

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AbstractA sensitive and selective electrochemical Hg2+sensor was developed based on T-Hg2+-T structure and exonuclease (Exo) III -assisted target recycling amplification at heated gold disk electrode (HAuDE). First, a DNA signal probe P1 was for the first time designed and labeled with ferrocene (Fc) near the attached SH-5′-end, so as to shorten the distance between Fc and the electrode and enhance the initial current of Fc compared with that labeled at the 3′-end far from the electrode. Then the signal amplification was achieved by Exo III-assisted Hg2+recycling. Briefly, the P1 was complementary to the assistant DNA P2 except the T-T mismatches. In the presence of Hg2+, the P1 self-assembled on the HAuDE could hybridize with P2 and form DNA duplex with blunt end at the 3′- terminus, triggering Exo III to stepwise digest mononucleotides from the 3′-terminus of P1, ultimately liberating Hg2+and P2, which could be “recycled”, resulting in the digestion of a large amount of P1 and significantly decrease the amount of Fc. The electrochemical signal difference before and after digestion was proportional to the Hg2+concentration. Furthermore, during the digestion period, the Exo III activity could be significantly increased by elevating the electrode temperature, great improving the sensitivity and efficiency for Hg2+detection. A detection limit of 6.2 pM (S/N = 3) could be obtained with an electrode temperature of 40°C during 60min digestion period, which was lower ca. two magnitudes than tha
机译:<![cdata [ 抽象 一个敏感和选择性电化学HG 2 + 传感器是基于T开发的-hg 2 + -t结构和外切核酸酶(Exo)III - 加热金盘电极(Haude)的目标回收放大。首先,DNA信号探针P1是第一次使用连接的SH-5'-END附近设计和标记的第一次设计和标记,以缩短FC和电极之间的距离,并增强FC的初始电流在远离电极的3'端标记。然后通过EXO III辅助Hg 2 + 回收来实现信号扩增。简而言之,除了T-T不匹配之外,P1与辅助DNA P2互补。在HG 2 + 中,在Haude上自组装的P1可以用P2杂交,并在3'末端与钝端形成DNA双链体,从P1的3'-末端触发EXO III,最终释放HG 2 + 和P2,这可能是“回收”的,导致消化大量p1并显着降低Fc的量。消化前后的电化学信号差与Hg 2 + 浓度。此外,在消化期间,通过升高电极温度,可以显着提高EXO III活性,从而提高HG 2 + 检测。在60min消化期间,可以在60℃的电极温度下获得6.2μm(s / n = 3)的检出限,该电极温度为较低的Ca.两个大于tha

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