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DNA nanopores as artificial membrane channels for bioprotonics
Biological membrane channels mediate information exchange between cells and facilitate molecular recognition. While tuning the shape and function of membrane channels for precision molecular sensing via de-novo routes is complex, an even more significant challenge is interfacing membrane channels wi...
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/PMC10477224/ https://www.ncbi.nlm.nih.gov/pubmed/37666808 http://dx.doi.org/10.1038/s41467-023-40870-1 |
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author | Luo, Le Manda, Swathi Park, Yunjeong Demir, Busra Sanchez, Jesse Anantram, M. P. Oren, Ersin Emre Gopinath, Ashwin Rolandi, Marco |
author_facet | Luo, Le Manda, Swathi Park, Yunjeong Demir, Busra Sanchez, Jesse Anantram, M. P. Oren, Ersin Emre Gopinath, Ashwin Rolandi, Marco |
author_sort | Luo, Le |
collection | PubMed |
description | Biological membrane channels mediate information exchange between cells and facilitate molecular recognition. While tuning the shape and function of membrane channels for precision molecular sensing via de-novo routes is complex, an even more significant challenge is interfacing membrane channels with electronic devices for signal readout, which results in low efficiency of information transfer - one of the major barriers to the continued development of high-performance bioelectronic devices. To this end, we integrate membrane spanning DNA nanopores with bioprotonic contacts to create programmable, modular, and efficient artificial ion-channel interfaces. Here we show that cholesterol modified DNA nanopores spontaneously and with remarkable affinity span the lipid bilayer formed over the planar bio-protonic electrode surface and mediate proton transport across the bilayer. Using the ability to easily modify DNA nanostructures, we illustrate that this bioprotonic device can be programmed for electronic recognition of biomolecular signals such as presence of Streptavidin and the cardiac biomarker B-type natriuretic peptide, without modifying the biomolecules. We anticipate this robust interface will allow facile electronic measurement and quantification of biomolecules in a multiplexed manner. |
format | Online Article Text |
id | pubmed-10477224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104772242023-09-06 DNA nanopores as artificial membrane channels for bioprotonics Luo, Le Manda, Swathi Park, Yunjeong Demir, Busra Sanchez, Jesse Anantram, M. P. Oren, Ersin Emre Gopinath, Ashwin Rolandi, Marco Nat Commun Article Biological membrane channels mediate information exchange between cells and facilitate molecular recognition. While tuning the shape and function of membrane channels for precision molecular sensing via de-novo routes is complex, an even more significant challenge is interfacing membrane channels with electronic devices for signal readout, which results in low efficiency of information transfer - one of the major barriers to the continued development of high-performance bioelectronic devices. To this end, we integrate membrane spanning DNA nanopores with bioprotonic contacts to create programmable, modular, and efficient artificial ion-channel interfaces. Here we show that cholesterol modified DNA nanopores spontaneously and with remarkable affinity span the lipid bilayer formed over the planar bio-protonic electrode surface and mediate proton transport across the bilayer. Using the ability to easily modify DNA nanostructures, we illustrate that this bioprotonic device can be programmed for electronic recognition of biomolecular signals such as presence of Streptavidin and the cardiac biomarker B-type natriuretic peptide, without modifying the biomolecules. We anticipate this robust interface will allow facile electronic measurement and quantification of biomolecules in a multiplexed manner. Nature Publishing Group UK 2023-09-04 /pmc/articles/PMC10477224/ /pubmed/37666808 http://dx.doi.org/10.1038/s41467-023-40870-1 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 Luo, Le Manda, Swathi Park, Yunjeong Demir, Busra Sanchez, Jesse Anantram, M. P. Oren, Ersin Emre Gopinath, Ashwin Rolandi, Marco DNA nanopores as artificial membrane channels for bioprotonics |
title | DNA nanopores as artificial membrane channels for bioprotonics |
title_full | DNA nanopores as artificial membrane channels for bioprotonics |
title_fullStr | DNA nanopores as artificial membrane channels for bioprotonics |
title_full_unstemmed | DNA nanopores as artificial membrane channels for bioprotonics |
title_short | DNA nanopores as artificial membrane channels for bioprotonics |
title_sort | dna nanopores as artificial membrane channels for bioprotonics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477224/ https://www.ncbi.nlm.nih.gov/pubmed/37666808 http://dx.doi.org/10.1038/s41467-023-40870-1 |
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