Department of Physics, University of Ottawa, Ottawa, Ontario, Canada.
PLoS One. 2023 Aug 23;18(8):e0290559. doi: 10.1371/journal.pone.0290559. eCollection 2023.
Molecular carriers represent an increasingly common strategy in the field of nanopore sensing to use secondary molecules to selectively report on the presence of target analytes in solution, allowing for sensitive assays of otherwise hard-to-detect molecules such as small, weakly-charged proteins. However, existing carrier designs can often introduce drawbacks to nanopore experiments including higher levels of cost/complexity and carrier-pore interactions that lead to ambiguous signals and elevated clogging rates. In this work, we present a simple method of carrier production based on sticky-ended DNA molecules that emphasizes ease-of-synthesis and compatibility with nanopore sensing and analysis. In particular, our method incorporates the ability to flexibly control the length of the DNA carriers produced, enhancing the multiplexing potential of this carrier system through the separable nanopore signals they could generate for distinct targets. A proof-of-concept nanopore experiment is also presented, involving carriers produced by our method with multiple lengths and attached to DNA nanostructure targets, in order to validate the capabilities of the system. As the breadth of applications for nanopore sensors continues to expand, the availability of tools such as those presented here to help translate the outcomes of these applications into robust nanopore signals will be of major importance.
分子载体在纳米孔传感领域是一种越来越常见的策略,它使用次级分子来选择性地报告溶液中目标分析物的存在,从而能够对其他难以检测的分子(如小而带弱电荷的蛋白质)进行灵敏的检测。然而,现有的载体设计通常会给纳米孔实验带来一些缺点,包括更高的成本/复杂性和载体-孔相互作用,导致信号模糊和堵塞率升高。在这项工作中,我们提出了一种基于粘性末端 DNA 分子的简单载体生产方法,强调了易于合成以及与纳米孔传感和分析的兼容性。特别是,我们的方法能够灵活地控制所产生的 DNA 载体的长度,通过它们能够为不同的目标生成可分离的纳米孔信号,增强了该载体系统的多路复用潜力。还提出了一个基于我们的方法的带有多个长度的载体的纳米孔实验,以验证该系统的性能。随着纳米孔传感器的应用范围不断扩大,像这里提出的工具的可用性将变得非常重要,这些工具将有助于将这些应用的结果转化为稳健的纳米孔信号。