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Homogeneous Entropy-Driven Amplified Detection of Biomolecular Interactions

机译:均质熵驱动的生物分子相互作用的放大检测

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While a range of artificial biochemical circuits is likely to play a significant role in biological engineering, one of the challenges in the field is the design of circuits that can transduce between biomolecule classes (e.g., moving beyond nucleic acid only circuits). Herein, we design a transduction mechanism whereby a protein signal is transduced into an amplified nucleic acid output using DNA nanotechnology. In this system, a protein is recognized by nucleic acid bound recognition elements to form a catalytic complex that drives a hybridization/displacement reaction on a multicomponent nucleic acid substrate, releasing multiple target single-stranded oligonucleotides in an amplified fashion. Amplification power and simple one-pot reaction conditions lead us to apply the scheme in an assay format, achieving homogeneous and rapid (similar to 10 min) analyte detection that is also robust (operable in whole blood and plasma). In addition, we demonstrate the assay in a microfluidic digital assay format leading to improved quantification and sensitivity approaching single-molecule levels. The present scheme we believe will have a significant impact on a range of applications from fundamental molecular interaction studies to design of artificial circuits in vivo to high-throughput, multiplexed assays for screening or point-of-care diagnostics.
机译:尽管一系列的人工生化回路可能在生物工程中发挥重要作用,但该领域的挑战之一是设计可以在生物分子类别之间转换的回路(例如,超越仅核酸回路)。在本文中,我们设计了一种转导机制,其中使用DNA纳米技术将蛋白质信号转导为扩增的核酸输出。在该系统中,蛋白质被核酸结合的识别元件识别以形成催化复合物,该催化复合物在多组分核酸底物上驱动杂交/置换反应,以扩增的方式释放多个靶标单链寡核苷酸。强大的扩增能力和简单的一锅式反应条件使我们能够以检测形式应用该方案,从而实现均一且快速(类似于10分钟)的分析物检测,而且检测能力也很强健(可在全血和血浆中使用)。此外,我们以微流体数字化分析形式展示了该分析方法,从而提高了定量和灵敏度,使其接近单分子水平。我们相信,该方案将对从基础分子相互作用研究到体内人工电路设计,再到用于筛选或即时诊断的高通量,多重测定的一系列应用产生重大影响。

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