Department of Electrical Engineering , Pennsylvania State University , University Park , Pennsylvania 16802 , United States.
Department of Biomedical Engineering , Pennsylvania State University , University Park , Pennsylvania 16802 , United States.
Anal Chem. 2019 Sep 3;91(17):11178-11184. doi: 10.1021/acs.analchem.9b01924. Epub 2019 Jul 19.
Nanopore sensor conceptually represents an ideal single molecule counting device due to its unique partitioning-free, label-free electronic sensing. Existing theories and experiments have shown that sample concentration is proportional to the molecule translocation rate. However, a detailed nanopore geometry and size characterization or a calibration curve of concentration standards are often required for quantifying the unknown sample. In this work, we proposed and validated a calibration-free nanopore single molecule digital counting method for isolated molecule quantification. With the background ions as the in situ references, the molecule translocation rates can be normalized to the ion translocation rates (i.e., baseline current). This in situ reference alleviates the requirement for knowing the nanopore geometry and size or generating a calibration curve. In recognition of this effect, we developed a quantitative model for nanopore quantification without the need for prior knowledge of experimental conditions such as nanopore geometry, size, and applied voltage. This model was experimentally validated for different nanopores and DNA molecules with different sizes. We anticipate this calibration-free digital counting approach would provide a new avenue for nanopore-based molecule sensing.
纳米孔传感器由于其独特的无分区、无标记的电子传感,从概念上代表了一种理想的单分子计数设备。现有理论和实验表明,样品浓度与分子迁移率成正比。然而,对于定量未知样品,通常需要对纳米孔的几何形状和尺寸进行详细的特征描述,或者生成浓度标准的校准曲线。在这项工作中,我们提出并验证了一种无需校准的纳米孔单分子数字计数方法,用于对分离分子进行定量。利用背景离子作为原位参照,可以将分子迁移率归一化为离子迁移率(即基线电流)。这种原位参考减轻了对纳米孔几何形状和尺寸的了解或生成校准曲线的要求。我们认识到这种影响,开发了一种无需事先了解实验条件(如纳米孔几何形状、尺寸和施加电压)的纳米孔定量的定量模型。该模型已在不同的纳米孔和不同大小的 DNA 分子上进行了实验验证。我们预计这种无校准的数字计数方法将为基于纳米孔的分子传感提供新途径。