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Spatiotemporal control of DNA-based chemical reaction network via electrochemical activation in microfluidics

机译:在微流体中通过电化学激活来控制基于DNA的化学反应网络的时空控制

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摘要

In recent years, DNA computing frameworks have been developed to create dynamical systems which can be used for information processing. These emerging synthetic biochemistry tools can be leveraged to gain a better understanding of fundamental biology but can also be implemented in biosensors and unconventional computing. Most of the efforts so far have focused on changing the topologies of DNA molecular networks or scaling them up. Several issues have thus received little attention and remain to be solved to turn them into real life technologies. In particular, the ability to easily interact in real-time with them is a key requirement. The previous attempts to achieve this aim have used microfluidic approaches, such as valves, which are cumbersome. We show that electrochemical triggering using DNA-grafted micro-fabricated gold electrodes can be used to give instructions to these molecular systems. We demonstrate how this approach can be used to release at specific times and locations DNA- based instructions. In particular, we trigger reaction-diffusion autocatalytic fronts in microfluidic channels. While limited by the stability of the Au-S bond, this easy to implement, versatile and scalable technique can be used in any biology laboratory to provide new ways to interact with any DNA-based computing framework.
机译:近年来,已经开发出DNA计算框架来创建可用于信息处理的动态系统。这些新兴的合成生物化学工具可以用来更好地了解基础生物学,但也可以在生物传感器和非常规计算中实现。迄今为止,大多数努力都集中在改变DNA分子网络的拓扑结构或扩大其规模上。因此,几个问题很少引起注意,仍然有待解决以将其转变为现实生活中的技术。特别是,与他们实时轻松交互的能力是关键要求。为实现该目的的先前尝试已经使用了麻烦的微流体方法,例如阀。我们表明,使用DNA嫁接的微型金电极的电化学触发可用于为这些分子系统提供指导。我们演示了如何使用该方法在特定时间和位置释放基于DNA的指令。特别是,我们在微流体通道中触发反应扩散自催化前沿。尽管受到Au-S键稳定性的限制,但这种易于实施,通用和可扩展的技术可以在任何生物学实验室中使用,以提供与任何基于DNA的计算框架进行交互的新方法。

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