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用于电致化学发光检测甲基转移酶活性的线框轨道加速双足 DNA walker。

Wireframe Orbit-Accelerated Bipedal DNA Walker for Electrochemiluminescence Detection of Methyltransferase Activity.

机构信息

Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

ACS Sens. 2022 Aug 26;7(8):2475-2482. doi: 10.1021/acssensors.2c01262. Epub 2022 Aug 17.

Abstract

In spite of the DNA walkers executing the signal accumulation task in the process of moving along the predetermined paths, the enhancement of walking dynamics and walking path controllability are still challenging due to the unprogrammed arrangements of DNA orbits. Taking these dilemmas into account, a bipedal DNA walker was designed skillfully by the virtue of wireframe orbits assembled by DNA cubes in order, which improved the efficiency and the continuity of walking. It could be attributed to the fact that both the contact chance and the dynamic interaction between walking strands and designated orbits were beneficial to minimize the possibility of derailment and improve the accumulation of signal. In addition, the hollow titanium dioxide nanospheres coated with rubrene (Rub@TiO NSs) were prepared by the etching of inner silicon dioxide nanoparticles (SiO NPs) to regulate the distribution pattern of rubrene (Rub) molecules and expose more electrochemically active sites for high-efficient electrochemiluminescence (ECL). Benefiting by the pore confinement-enhanced ECL, the electron and mass transfer was significantly accelerated because of the hollow structure of Rub@TiO NSs. Subsequently, endogenous dissolved oxygen as the coreactant and palladium nanoparticles (Pd NPs) as the coreaction accelerator were employed to constitute a ternary ECL system with explosive signal response. Combining with this ECL platform, the bipedal walker activated by the target can autonomously and directionally move on the DNA wireframe orbits to release the quenching probes continuously. In this way, the biosensor displayed a low detection limit (2.30 × 10 U·mL) and a wide linear range (1.0 × 10 to 1.0 × 10 U·mL) for the sensitive detection of Dam methyltransferase (Dam MTase) activity. Therefore, a novel strategy for the accurate quantification of epigenetic targets was developed by virtue of improving the walking dynamics of DNA walker and amplifying the ECL of Rub molecules.

摘要

尽管 DNA 步行者在沿着预定路径移动的过程中执行信号累积任务,但由于 DNA 轨道的未编程排列,仍然难以增强步行动力学和步行路径可控性。考虑到这些困境,巧妙地设计了一种双足 DNA 步行者,通过 DNA 立方体按顺序组装的线框轨道来提高步行的效率和连续性。这可以归因于这样一个事实,即行走链与指定轨道之间的接触机会和动态相互作用都有利于最大限度地减少脱轨的可能性,并提高信号的累积。此外,通过蚀刻内部二氧化硅纳米颗粒(SiO NPs)制备了涂覆有苝(Rub)的二氧化钛纳米球(Rub@TiO NSs),以调节 Rub 分子的分布模式并暴露更多的电化学活性位点以实现高效电化学发光(ECL)。得益于孔限制增强的 ECL,由于 Rub@TiO NSs 的空心结构,电子和质量转移明显加速。随后,将内源性溶解氧作为共反应物和钯纳米颗粒(Pd NPs)作为共反应加速剂用于构成具有爆炸信号响应的三元 ECL 系统。结合此 ECL 平台,由靶标激活的双足步行者可以在 DNA 线框轨道上自主和定向移动,以连续释放猝灭探针。这样,该生物传感器对 Dam 甲基转移酶(Dam MTase)活性的灵敏检测显示出低检测限(2.30×10 U·mL)和宽线性范围(1.0×10 至 1.0×10 U·mL)。因此,通过提高 DNA 步行者的步行动力学和放大 Rub 分子的 ECL,开发了一种用于精确量化表观遗传靶标的新策略。

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