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Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement
In single-molecule measurements, metal nanogap electrodes directly measure the current of a single molecule. This technique has been actively investigated as a new detection method for a variety of samples. Machine learning has been applied to analyze signals derived from single molecules to improve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241884/ https://www.ncbi.nlm.nih.gov/pubmed/37277540 http://dx.doi.org/10.1038/s41598-023-35724-1 |
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author | Ryu, Jiho Komoto, Yuki Ohshiro, Takahito Taniguchi, Masateru |
author_facet | Ryu, Jiho Komoto, Yuki Ohshiro, Takahito Taniguchi, Masateru |
author_sort | Ryu, Jiho |
collection | PubMed |
description | In single-molecule measurements, metal nanogap electrodes directly measure the current of a single molecule. This technique has been actively investigated as a new detection method for a variety of samples. Machine learning has been applied to analyze signals derived from single molecules to improve the identification accuracy. However, conventional identification methods have drawbacks, such as the requirement of data to be measured for each target molecule and the electronic structure variation of the nanogap electrode. In this study, we report a technique for identifying molecules based on single-molecule measurement data measured only in mixed sample solutions. Compared with conventional methods that require training classifiers on measurement data from individual samples, our proposed method successfully predicts the mixing ratio from the measurement data in mixed solutions. This demonstrates the possibility of identifying single molecules using only data from mixed solutions, without prior training. This method is anticipated to be particularly useful for the analysis of biological samples in which chemical separation methods are not applicable, thereby increasing the potential for single-molecule measurements to be widely adopted as an analytical technique. |
format | Online Article Text |
id | pubmed-10241884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102418842023-06-07 Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement Ryu, Jiho Komoto, Yuki Ohshiro, Takahito Taniguchi, Masateru Sci Rep Article In single-molecule measurements, metal nanogap electrodes directly measure the current of a single molecule. This technique has been actively investigated as a new detection method for a variety of samples. Machine learning has been applied to analyze signals derived from single molecules to improve the identification accuracy. However, conventional identification methods have drawbacks, such as the requirement of data to be measured for each target molecule and the electronic structure variation of the nanogap electrode. In this study, we report a technique for identifying molecules based on single-molecule measurement data measured only in mixed sample solutions. Compared with conventional methods that require training classifiers on measurement data from individual samples, our proposed method successfully predicts the mixing ratio from the measurement data in mixed solutions. This demonstrates the possibility of identifying single molecules using only data from mixed solutions, without prior training. This method is anticipated to be particularly useful for the analysis of biological samples in which chemical separation methods are not applicable, thereby increasing the potential for single-molecule measurements to be widely adopted as an analytical technique. Nature Publishing Group UK 2023-06-05 /pmc/articles/PMC10241884/ /pubmed/37277540 http://dx.doi.org/10.1038/s41598-023-35724-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ryu, Jiho Komoto, Yuki Ohshiro, Takahito Taniguchi, Masateru Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title | Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title_full | Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title_fullStr | Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title_full_unstemmed | Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title_short | Direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
title_sort | direct biomolecule discrimination in mixed samples using nanogap-based single-molecule electrical measurement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241884/ https://www.ncbi.nlm.nih.gov/pubmed/37277540 http://dx.doi.org/10.1038/s41598-023-35724-1 |
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