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亚微米尺度自主重构的元 DNA 链置换

Meta-DNA Strand Displacement for Sub-Micron-Scale Autonomous Reconfiguration.

机构信息

School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, China.

State Key Laboratory of Oncogenes and Related Genes, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China.

出版信息

J Am Chem Soc. 2023 Aug 2;145(30):16812-16820. doi: 10.1021/jacs.3c04884. Epub 2023 Jul 25.

Abstract

Dynamic molecular interactions in chemical reaction networks lead to complex behaviors in living systems. Whereas recent advances in programming DNA molecular reactions have reached a high level of complexity at molecular and nanometer scales, achieving programmable autonomous behavior at submicron or even larger scales remains challenging. Here, we present a mechanism of meta-DNA strand displacement reactions (M-SDRs) that is mediated solely by meta-toehold (M-toehold) using versatile submicron building blocks of meta-DNA (M-DNA). M-SDR emulates the toehold binding and branch migration processes of conventional strand displacement. Importantly, the kinetics of M-SDR can be modulated over a range of five orders of magnitude reaching a maximum rate of about 1.62 × 10 M s. Further, we demonstrate the use of M-SDR to program autonomous reconfiguration in information transmission and logical computation systems. We envision that M-SDR serves as a versatile mechanism for emulating autonomous behavior approaching the cellular level.

摘要

化学反应网络中的动态分子相互作用导致生命系统中出现复杂的行为。尽管最近在编程 DNA 分子反应方面取得了进展,在分子和纳米尺度上达到了很高的复杂程度,但在亚微米甚至更大的尺度上实现可编程的自主行为仍然具有挑战性。在这里,我们提出了一种仅由亚稳态(M-toehold)介导的元 DNA 链置换反应(M-SDR)机制,该机制使用元 DNA(M-DNA)的多功能亚微米构建块实现。M-SDR 模拟了传统链置换的结合和分支迁移过程。重要的是,M-SDR 的动力学可以在五个数量级的范围内进行调节,达到约 1.62×10 M s 的最大速率。此外,我们证明了使用 M-SDR 来编程信息传输和逻辑计算系统中的自主重构。我们设想 M-SDR 作为一种通用的机制,可以模拟接近细胞水平的自主行为。

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