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基于链置换扩增和金纳米粒子的 HPV16 光热生物传感器,使用温度计作为读出器。

Photothermal biosensor for HPV16 based on strand-displacement amplification and gold nanoparticles using a thermometer as readout.

机构信息

Department of Infectious Diseases, The Key Laboratory of Diagnosis and Controlment for The Development of Chronic Liver Disease of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325025, China.

Ministry of Education Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, College of Chemistry, Fuzhou University, 2 Xue Yuan Road, University Town Fuzhou, Fuzhou, 350116, Fujian, People's Republic of China.

出版信息

Mikrochim Acta. 2022 Nov 2;189(11):437. doi: 10.1007/s00604-022-05522-z.

Abstract

Gold nanoparticles (AuNPs) in aggregated state have a strong near infrared region (NIR) absorption and the causes a much stronger photothermal effect than that of the dispersed AuNPs. Strand-displacement amplification (SDA) can produce large amount of single-stranded DNA (ssDNA), which in turn effectively prevent AuNPs from aggregation. In this study, these characteristics had been applied to design a photothermal biosensor for human papilloma virus (HPV and HPV16 were chosen as model target) detection. In the absence of HPV16, AuNPs was in the aggregated state and large temperature rise can be detected after the irradiation by 808 nm laser. The presence of HPV16 triggers the SDA reaction with the help of Bst DNA polymerase and Nt.BstNBI nicking endonuclease resulting in the production of large amounts of ssDNA; this protects unmodified AuNPs from salt-induced aggregation. Therefore, AuNPs was in a dispersed state and the temperature change was not significant after the irradiation of 808 nm laser. The difference of the temperature changing can be applied for the quantitative detection of HPV16 using a thermometer as readout. The linear response range is 1.0 fM ~ 50 pM with a detection limit of 0.3 fM. The proposed method has been applied to detect HPV16 in clinical cervical sample and is competent for clinical analysis.

摘要

金纳米颗粒(AuNPs)在聚集状态下具有很强的近红外(NIR)吸收,比分散的 AuNPs 产生更强的光热效应。链置换扩增(SDA)可以产生大量的单链 DNA(ssDNA),这反过来又有效地防止 AuNPs 聚集。在这项研究中,这些特性被应用于设计用于检测人乳头瘤病毒(HPV)的光热生物传感器(HPV 和 HPV16 被选为模型靶标)。在不存在 HPV16 的情况下,AuNPs 处于聚集状态,在 808nm 激光照射后可以检测到较大的温升。在 Bst DNA 聚合酶和 Nt.BstNBI 切口内切酶的帮助下,HPV16 触发 SDA 反应,导致大量 ssDNA 的产生;这保护未经修饰的 AuNPs 免受盐诱导的聚集。因此,在 808nm 激光照射后,AuNPs 处于分散状态,温度变化不明显。温度变化的差异可用于使用温度计作为读出进行 HPV16 的定量检测。线性响应范围为 1.0 fM~50 pM,检测限为 0.3 fM。该方法已应用于临床宫颈样本中 HPV16 的检测,适用于临床分析。

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