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A simple label-free electrochemical DNA parity generator/checker for error detection during data transmission based on aptamer-nanoclaw-modulated protein steric hindrance

机译:一个简单的无标签的电化学DNA奇偶校验生成器/检查器用于基于适体-纳米齿调节的蛋白质空间位阻在数据传输过程中进行错误检测

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摘要

Versatile DNA logic devices have exhibited magical power in molecular-level computing and data processing. During any type of data transmission, the appearance of erroneous bits (which have severe impacts on normal computing) is unavoidable. Luckily, the erroneous bits can be detected via placing a parity generator (pG) at the sending module and a parity checker (pC) at the receiving module. However, all current DNA pG/pC systems use optical signals as outputs. In comparison, sensitive, facilely operated, electric-powered electrochemical outputs possess inherent advantages in terms of potential practicability and future integration with semiconductor transistors. Herein, taking an even pG/pC as a model device, we construct the first electrochemical DNA pG/pC system so far. Innovatively, a thrombin aptamer is integrated into the input-strand and it functions as a “nanoclaw” to selectively capture thrombin; the electrochemical impedance changes induced by the “nanoclaw/thrombin” complex are used as label-free outputs. Notably, this system is simple and can be operated within 2 h, which is comparable with previous fluorescent ones, but avoids the high-cost labeled-fluorophore and tedious nanoquencher. Moreover, taking non-interfering poly-T strands as additional inputs, a cascade logic circuit (OR-2 to 1 encoder) and a parity checker that could distinguish even/odd numbers from natural numbers (0 to 9) is also achieved based on the same system. This work not only opens up inspiring horizons for the design of novel electrochemical functional devices and complicated logic circuits, but also lays a solid foundation for potential logic-programmed target detection.
机译:多功能的DNA逻辑设备在分子水平的计算和数据处理中展现了神奇的力量。在任何类型的数据传输过程中,不可避免的会出现错误的位(对正常计算产生严重影响)。幸运的是,可以通过在发送模块上放置奇偶校验生成器(pG)在接收模块上放置奇偶校验器(pC)来检测错误位。但是,当前所有的DNA pG / pC系统都使用光信号作为输出。相比之下,灵敏,操作简便的电动电化学输出在潜在实用性和与半导体晶体管的未来集成方面具有固有优势。在此,以均匀的pG / pC为模型,构建了迄今为止第一个电化学DNA pG / pC系统。创新地将凝血酶适体整合到输入链中,并充当“纳米爪”来选择性捕获凝血酶。由“ nanoclaw /凝血酶”复合物引起的电化学阻抗变化被用作无标记的输出。值得注意的是,该系统很简单,可以在2小时内运行,这与以前的荧光灯系统相当,但是避免了昂贵的标记荧光团和乏味的纳米猝灭剂。此外,基于无干扰的poly-T链作为附加输入,还基于以下特性实现了级联逻辑电路(OR-2至1编码器)和可以将偶数/奇数与自然数(0至9)区分开的奇偶校验器相同的系统。这项工作不仅为新颖的电化学功能器件和复杂的逻辑电路的设计开辟了启发性的视野,而且为潜在的逻辑程序化目标检测奠定了坚实的基础。

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