Khalid Muhammad Asad Ullah, Ahamed Md Ahasan, Politza Anthony J, Guan Weihua
Department of Intelligent Systems Engineering, Indiana University, Bloomington, Indiana 47408, United States.
Department of Electrical Engineering, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
ACS Sens. 2025 Jun 26. doi: 10.1021/acssensors.5c00803.
DNA sequencing is a powerful tool for diagnosing conditions such as infectious diseases and cancers. Even though current workflows demand rigorous quality control (QC) of DNA samples, this QC is typically limited to lab settings despite recent advances in portable nanopore sequencers. For personalized health care to truly benefit from the portable sequencer, QC must be performed right where the samples are processed. Here, we present a solid-state nanopore device that provides label-free, controlled quantification and qualification of cell-free DNA (cfDNA). We demonstrated the use of a 1 kbp double-stranded DNA internal marker at a known concentration to measure the concentration of a representative cfDNA target in the presence of genomic DNA. We also found that nanopores with diameters ranging from 6 to 19 nm yield consistent measurements with a maximum coefficient of variation (CV) of less than 15%. Moreover, analyzing data from multiple nanopores over longer acquisition times can reduce the uncertainty to below 10% CV. Finally, we applied our nanopore QC assay to a plasma cfDNA sample and compared the results to those from a capillary electrophoresis (CE) assay. Both methods produced highly correlated measurements, demonstrating the potential of our nanopore QC assay for effective cfDNA assessment at the point of need.
DNA测序是诊断传染病和癌症等疾病的强大工具。尽管当前的工作流程要求对DNA样本进行严格的质量控制(QC),但尽管便携式纳米孔测序仪最近取得了进展,这种质量控制通常仅限于实验室环境。为了使个性化医疗真正受益于便携式测序仪,必须在样本处理的地方进行质量控制。在这里,我们展示了一种固态纳米孔装置,它可以对游离DNA(cfDNA)进行无标记、可控的定量和定性分析。我们展示了使用已知浓度的1 kbp双链DNA内部标记物,在基因组DNA存在的情况下测量代表性cfDNA靶标的浓度。我们还发现,直径在6到19纳米之间的纳米孔产生的测量结果一致,最大变异系数(CV)小于15%。此外,在更长的采集时间内分析来自多个纳米孔的数据可以将不确定性降低到CV低于10%。最后,我们将纳米孔质量控制分析应用于血浆cfDNA样本,并将结果与毛细管电泳(CE)分析的结果进行比较。两种方法产生的测量结果高度相关,证明了我们的纳米孔质量控制分析在需要时有效评估cfDNA的潜力。