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Electrochemical nucleic acid detection based on parallel structural dsDNA/recombinant azurin hybrid

机译:基于平行结构dsDNA /重组天青蛋白杂交体的电化学核酸检测

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摘要

Several challenges remained to fabricate a molecular-level nucleic acid biosensor such as surface immobilization control, single mismatch detection and low current response. To overcome those issues, for the first time, authors presented a novel parallel structural dsDNA/recombinant azurin (PSD/rAzu) hybrid structure for the general nucleic acid detection. The PSD was designed and introduced by the optimized 8 Ag ions to have greater conductivity than the canonical dsDNA, and conjugated with rAzu to develop a general platform for electrochemical detection of miRNAs and viral DNAs with high reproducibility and ultra-sensitivity towards single base pair mutation. Thanks to the bifunctional rAzu as the selective spacer and electrochemical signal mediator, in the presence of the target strand, the imperfect PSD switched rapidly to the upright position where the Ag ions intercalated between C-C mismatches of dsDNAs at the top of each structure brought further from the electrode surface resulting in a significant electrochemical signal drop of the Ag ions. The charge transfer (CT) mechanism across the hybrid structure was simply clarified on the basis of the redox potential location of the species. The electrical conductivity of DNAs were measured using scanning tunneling spectroscopy (STS) at the molecular scale and cyclic voltammetry (CV) technique based on the reduction of Ag ion. The proposed PSD/rAzu hybrid structure with a great capability of single mutation recognition and miRNA expression level profiling in cancer cells holds a very promising platform to be studied for further development of various kinds of nanoscale biosensors, bioelectronic devices.
机译:制造分子水平的核酸生物传感器仍面临一些挑战,例如表面固定控制,单个错配检测和低电流响应。为了克服这些问题,作者首次提出了一种新颖的平行结构dsDNA /重组天青蛋白(PSD / rAzu)杂合结构,用于常规核酸检测。通过优化的8 Ag离子设计和引入PSD,以使其具有比经典dsDNA更大的电导率,并与rAzu偶联以开发用于电化学检测miRNA和病毒DNA的通用平台,该平台具有高重复性和对单碱基对突变的超灵敏性。由于双功能rAzu作为选择性间隔子和电化学信号介体,在存在目标链的情况下,不完善的PSD迅速切换到直立位置,在此位置,Ag离子插在每个结构顶部的dsDNA的CC不匹配之间,从而进一步偏离了电极表面会导致Ag离子明显的电化学信号下降。根据物种的氧化还原电位位置,可以简单阐明跨杂化结构的电荷转移(CT)机制。 DNA的电导率使用扫描隧道光谱(STS)在分子尺度上进行测量,并基于Ag离子的还原使用循环伏安法(CV)技术进行测量。拟议的PSD / rAzu杂合结构在癌细胞中具有强大的单突变识别和miRNA表达水平特征分析能力,为研究各种纳米级生物传感器,生物电子设备的发展提供了非常有希望的平台。

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