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多频阻抗传感用于检测和大小分析 DNA 片段。

Multi-frequency impedance sensing for detection and sizing of DNA fragments.

机构信息

Department of Electrical and Computer Engineering, Rutgers University, New Brunswick, 94 Brett Rd, Piscataway, NJ, 08854, USA.

Department of Genetics, Yale University School of Medicine, 333 Cedar Street, PO Box 208005, New Haven, CT, 06520-8005, USA.

出版信息

Sci Rep. 2021 Mar 22;11(1):6490. doi: 10.1038/s41598-021-85755-9.

Abstract

Electronic biosensors for DNA detection typically utilize immobilized oligonucleotide probes on a signal transducer, which outputs an electronic signal when target molecules bind to probes. However, limitation in probe selectivity and variable levels of non-target material in complex biological samples can lead to nonspecific binding and reduced sensitivity. Here we introduce the integration of 2.8 μm paramagnetic beads with DNA fragments. We apply a custom-made microfluidic chip to detect DNA molecules bound to beads by measuring Impedance Peak Response (IPR) at multiple frequencies. Technical and analytical performance was evaluated using beads containing purified Polymerase Chain Reaction (PCR) products of different lengths (157, 300, 613 bp) with DNA concentration ranging from 0.039 amol to 7.8 fmol. Multi-frequency IPR correlated positively with DNA amounts and was used to calculate a DNA quantification score. The minimum DNA amount of a 300 bp fragment coupled on beads that could be robustly detected was 0.0039 fmol (1.54 fg or 4750 copies/bead). Additionally, our approach allowed distinguishing beads with similar molar concentration DNA fragments of different lengths. Using this impedance sensor, purified PCR products could be analyzed within ten minutes to determine DNA fragment length and quantity based on comparison to a known DNA standard.

摘要

用于 DNA 检测的电子生物传感器通常利用信号转换器上固定的寡核苷酸探针,当靶分子与探针结合时,会输出电子信号。然而,探针选择性的限制和复杂生物样品中非靶材料的变化水平可能导致非特异性结合和降低灵敏度。在这里,我们介绍了将 2.8μm 顺磁珠与 DNA 片段结合。我们应用定制的微流控芯片通过测量多个频率下的阻抗峰响应 (IPR) 来检测与珠结合的 DNA 分子。使用含有不同长度 (157、300、613bp) 的纯化聚合酶链反应 (PCR) 产物的珠以及 DNA 浓度范围为 0.039 amol 至 7.8 fmol 的珠来评估技术和分析性能。多频 IPR 与 DNA 量呈正相关,并用于计算 DNA 定量评分。能够可靠检测到的偶联在珠上的 300bp 片段的最小 DNA 量为 0.0039 fmol (1.54fg 或 4750 个拷贝/珠)。此外,我们的方法允许区分具有相似摩尔浓度但长度不同的 DNA 片段的珠。使用这种阻抗传感器,可以在十分钟内分析纯化的 PCR 产物,根据与已知 DNA 标准的比较来确定 DNA 片段长度和数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4f7/7985362/ed7965b6f97f/41598_2021_85755_Fig1_HTML.jpg

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