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通过使用上转换和金纳米颗粒的发光共振能量转移对病毒cDNA进行量子增强检测。

Quantum-Enhanced Detection of Viral cDNA via Luminescence Resonance Energy Transfer Using Upconversion and Gold Nanoparticles.

作者信息

Esmaeili Shahriar, Rajil Navid, Hazrathosseini Ayla, Neuman Benjamin W, Alkahtani Masfer H, Sen Dipankar, Hu Qiang, Wu Hung-Jen, Yi Zhenhuan, Brick Robert W, Sokolov Alexei V, Hemmer Philip R, Scully Marlan O

机构信息

Institute for Quantum Science and Engineering, Texas A&M University, College Station, TX 77843, USA.

Department of Physics and Astronomy, Texas A&M University, College Station, TX 77843, USA.

出版信息

ArXiv. 2024 Oct 14:arXiv:2410.10911v1.

Abstract

The COVID-19 pandemic has profoundly impacted global economies and healthcare systems, revealing critical vulnerabilities in both. In response, our study introduces a groundbreaking method for the detection of SARS-CoV-2 cDNA, leveraging Luminescence resonance energy transfer (LRET) between upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) to achieve an unprecedented detection limit of 242 femtomolar (fM). This innovative sensing platform utilizes UCNPs conjugated with one primer and AuNPs with another, targeting the 5' and 3' ends of the SARS-CoV-2 cDNA, respectively, enabling precise differentiation of mismatched DNA sequences and significantly enhancing detection specificity. Through rigorous experimental analysis, we established a quenching efficiency range from 10.4% to 73.6%, with an optimal midpoint of 42%, thereby demonstrating the superior sensitivity of our method. By comparing the quenching efficiency of mismatched DNAs to the target DNA, we identified an optimal DNA:UCNP:AuNP ratio that ensures accurate detection. Our comparative analysis with existing SARS-CoV-2 detection methods revealed that our approach not only provides a lower detection limit but also offers higher specificity and potential for rapid, on-site testing. This study demonstrates the superior sensitivity and specificity of using UCNPs and AuNPs for SARS-CoV-2 cDNA detection, offering a significant advancement in rapid, accessible diagnostic technologies. Our method, characterized by its low detection limit and high precision, represents a critical step forward in managing current and future viral outbreaks, contributing to the enhancement of global healthcare responsiveness and infectious disease control.

摘要

新冠疫情对全球经济和医疗系统产生了深远影响,暴露出两者的关键脆弱性。作为回应,我们的研究引入了一种突破性的检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)互补脱氧核糖核酸(cDNA)的方法,利用上转换纳米颗粒(UCNPs)和金纳米颗粒(AuNPs)之间的发光共振能量转移(LRET),实现了前所未有的242飞摩尔(fM)检测限。这个创新的传感平台使用分别与一种引物共轭的UCNPs和与另一种引物共轭的AuNPs,分别靶向SARS-CoV-2 cDNA的5'和3'端,能够精确区分错配的DNA序列,并显著提高检测特异性。通过严格的实验分析,我们确定了淬灭效率范围为10.4%至73.6%,最佳中点为42%,从而证明了我们方法的卓越灵敏度。通过比较错配DNA与目标DNA的淬灭效率,我们确定了确保准确检测的最佳DNA:UCNP:AuNP比例。我们与现有SARS-CoV-2检测方法的比较分析表明,我们的方法不仅提供了更低的检测限,还具有更高的特异性以及快速现场检测的潜力。这项研究证明了使用UCNPs和AuNPs检测SARS-CoV-2 cDNA具有卓越的灵敏度和特异性,在快速、便捷的诊断技术方面取得了重大进展。我们的方法具有低检测限和高精度的特点,是应对当前和未来病毒爆发的关键一步,有助于提高全球医疗响应能力和传染病防控水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ba/11527101/02ef85cc3110/nihpp-2410.10911v1-f0001.jpg

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