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利用纳米图案化DNA折纸纳米天线实现阿托摩尔检测的即时检测

Bringing Attomolar Detection to the Point-of-Care with Nanopatterned DNA Origami Nanoantennas.

作者信息

Yaadav Renukka, Trofymchuk Kateryna, Dass Mihir, Behrendt Vivien, Hauer Benedikt, Schütz Jan, Close Cindy, Scheckenbach Michael, Ferrari Giovanni, Mäurer Leoni, Sebina Sophia, Glembockyte Viktorija, Liedl Tim, Tinnefeld Philip

机构信息

Department of Chemistry and Center for NanoScience, Ludwig-Maximilians-University, Butenandtstraße 5-13, 81377, Munich, Germany.

Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-University, 80539, Munich, Germany.

出版信息

Adv Mater. 2025 Jul 26:e07407. doi: 10.1002/adma.202507407.

Abstract

Creating increasingly sensitive and cost-effective nucleic acid detection methods is critical for enhancing point-of-care (POC) applications. This requires highly specific capture of biomarkers and efficient transduction of capture events. However, the signal from biomarkers present at extremely low amounts often falls below the detection limit of typical fluorescence-based methods, necessitating molecular amplification. Here, we present single-molecule detection of a non-amplified, 151-nucleotide sequence specific to antibiotics-resistant Klebsiella pneumoniae down to attomolar concentrations, using Trident NanoAntennas with Cleared HOtSpots (NACHOS). This NACHOS-diagnostics assay leverages a compact microscope with a large field-of-view, including microfluidic flow to enhance capturing efficiency. Fluorescence enhancement is provided by NanoAntennas, arranged using a combination of nanosphere lithography and site-specific DNA origami placement. This method can detect 200 ± 50 out of 600 molecules in a 100 µL sample volume within an hour. This represents a typical number of pathogens in clinical samples commonly detected by Polymerase Chain Reaction. We achieve similar sensitivity in untreated human plasma, enhancing the practical applicability of the system. This platform can be adapted to detect shorter nucleic acid fragments that are not compatible with traditional amplification-based technologies. This provides a robust and scalable solution for sensitive nucleic acid detection in diverse clinical settings.

摘要

创建越来越灵敏且具有成本效益的核酸检测方法对于增强即时检测(POC)应用至关重要。这需要对生物标志物进行高度特异性捕获以及对捕获事件进行有效转导。然而,极低含量的生物标志物发出的信号通常低于典型荧光法的检测限,因此需要进行分子扩增。在此,我们展示了使用具有清除热点的三叉戟纳米天线(NACHOS)对耐抗生素肺炎克雷伯菌特有的151个核苷酸序列进行单分子检测,检测下限可达阿托摩尔浓度。这种NACHOS诊断检测方法利用了具有大视野的紧凑型显微镜,包括微流体流动以提高捕获效率。荧光增强由纳米天线提供,通过纳米球光刻和位点特异性DNA折纸放置相结合的方式进行排列。该方法能够在一小时内检测100微升样品体积中的600个分子中的200 ± 50个。这代表了临床样本中通常通过聚合酶链反应检测到的典型病原体数量。我们在未处理的人血浆中实现了类似的灵敏度,提高了该系统的实际适用性。该平台可适用于检测与传统基于扩增的技术不兼容的较短核酸片段。这为在各种临床环境中进行灵敏的核酸检测提供了一个强大且可扩展的解决方案。

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