通过无标记纳米孔传感加速生物物理研究和应用。

Hirohito Yamazaki, Kan Shoji
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Accelerating biophysical studies and applications by label-free nanopore sensing.
Label-free single-molecule sensing technologies are attractive tools for investigating the properties of biological molecules via the understanding of molecular functionality. Among these technologies, nanopore sensing has become one of the growing technologies [1,2]. Nanopore sensing operates in the principle of resistive pulse sensing, where sensing molecules, such as DNA, RNA, and protein, pass through a pore under the electrical field, resulting in a blockade current due to the molecular occupation in a pore. The physical properties of sensing entities were obtained by analyzing blockade current, which can provide a fingerprint of sensing molecules (Figure 1) [3]. In this commentary article, we review the eight presentations at the symposium “Innovative label-free nanopore sensing toward biophysical studies and applications” of the 60th Annual Meeting of the Biophysical Society of Japan held in September 2022 and introduce how this sensing technology can be used as a tool to open new biophysical science or applications other than DNA sequencing. Kyle Briggs at Ottawa University/ Northern Nanopore Instruments talked about an automated method of electricalbased nanopore fabrication, which is one of the gold standard fabrication methods in the lab, and introduced how to accelerate solid-state nanopore research using this method [4,5]. He also presented the automated muti-pore fabrication tools having multi-channels fluidic flow cells with multi-membrane chips. Finally, he showed the nanopore trace analysis software, Nanolyzer, which has multiple functions such as multi-level blockade current fitting, overlay translocation events, kernel density estimation, etc. Kan Shoji at Nagaoka University of Technology presented a probe-type planer bilayer lipid membrane (pBLM) system [6,7] and its application for scanning ion conductance microscopy (SICM) [8]. In this system, pBLMs can be repeatedly formed at the tip of probes by inserting probes into a layered bath solution of an oil/lipid mixture and electrolyte. He mounted the probe into a SICM setup and demonstrated spatially-resolved chemical sensing by manipulating the probe. Additionally, he introduced an efficient current measurement system for synthetic DNA nanopores. Although DNA nanopore structures are expected to be applied for nanopore sensing, it is challenging to efficiently insert DNA nanopores into pBLMs. He prepared DNA nanopore-tethered gold electrodes and formed pBLMs on the surface of electrodes by inserting electrodes into the bath solution. Resultantly, efficient insertions of DNA nanopores were observed, and this method potentially accelerates applications of DNA nanopores for nanopore sensing. Figure 1 The fundamental working principle of nanopore sensing © 2023 THE BIOPHYSICAL SOCIETY OF JAPAN doi: 10.2142/biophysico.bppb-v20.0010
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