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基于 PCR 扩增子的固态纳米孔检测筛查 A 组链球菌病。

Screening for Group A Streptococcal Disease via Solid-State Nanopore Detection of PCR Amplicons.

机构信息

Department of Physics, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.

Division of Microbiology and Infectious Disease, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.

出版信息

ACS Sens. 2022 Jan 28;7(1):207-214. doi: 10.1021/acssensors.1c01972. Epub 2022 Jan 7.

Abstract

Single-molecule detection methods are becoming increasingly important for diagnostic applications. Practical early detection of disease requires sensitivity down to the level of single copies of the targeted biomarkers. Of the candidate technologies that can address this need, solid-state nanopores show great promise as digital sensors for single-molecule detection. Here, we present work detailing the use of solid-state nanopores as downstream sensors for a polymerase chain reaction (PCR)-based assay targeting group A streptococcus (strep A), which can be readily extended to detect any pathogen that can be identified with a short nucleic acid sequence. We demonstrate that with some simple modifications to the standard PCR reaction mixture, nanopores can be used to reliably identify strep A in clinical samples. We also discuss methodological best practices for both adapting PCR-based assays to solid-state nanopore readout and analytical approaches by which to decide on sample status.

摘要

单分子检测方法在诊断应用中变得越来越重要。实际的疾病早期检测需要达到靶向生物标志物单拷贝的灵敏度。在能够满足这一需求的候选技术中,固态纳米孔作为用于单分子检测的数字传感器具有很大的前景。在这里,我们介绍了使用固态纳米孔作为基于聚合酶链反应(PCR)的针对 A 组链球菌(链球菌 A)的检测的下游传感器的工作,该检测可以很容易地扩展到检测任何可以通过短核酸序列识别的病原体。我们证明,通过对标准 PCR 反应混合物进行一些简单的修改,纳米孔可以可靠地识别临床样本中的链球菌 A。我们还讨论了将基于 PCR 的检测方法适应固态纳米孔读出以及通过分析方法来确定样品状态的最佳方法。

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