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A large size-selective DNA nanopore with sensing applications
Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomole...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906287/ https://www.ncbi.nlm.nih.gov/pubmed/31827087 http://dx.doi.org/10.1038/s41467-019-13284-1 |
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author | Thomsen, Rasmus P. Malle, Mette Galsgaard Okholm, Anders Hauge Krishnan, Swati Bohr, Søren S.-R. Sørensen, Rasmus Schøler Ries, Oliver Vogel, Stefan Simmel, Friedrich C. Hatzakis, Nikos S. Kjems, Jørgen |
author_facet | Thomsen, Rasmus P. Malle, Mette Galsgaard Okholm, Anders Hauge Krishnan, Swati Bohr, Søren S.-R. Sørensen, Rasmus Schøler Ries, Oliver Vogel, Stefan Simmel, Friedrich C. Hatzakis, Nikos S. Kjems, Jørgen |
author_sort | Thomsen, Rasmus P. |
collection | PubMed |
description | Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomolecules and DNA sequencing have shown promise. Here, we use DNA origami to create a synthetic 9 nm wide DNA nanopore, controlled by programmable, lipidated flaps and equipped with a size-selective gating system for the translocation of macromolecules. Successful assembly and insertion of the nanopore into lipid bilayers are validated by transmission electron microscopy (TEM), while selective translocation of cargo and the pore mechanosensitivity are studied using optical methods, including single-molecule, total internal reflection fluorescence (TIRF) microscopy. Size-specific cargo translocation and oligonucleotide-triggered opening of the pore are demonstrated showing that the DNA nanopore can function as a real-time detection system for external signals, offering potential for a variety of highly parallelized sensing applications. |
format | Online Article Text |
id | pubmed-6906287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69062872019-12-13 A large size-selective DNA nanopore with sensing applications Thomsen, Rasmus P. Malle, Mette Galsgaard Okholm, Anders Hauge Krishnan, Swati Bohr, Søren S.-R. Sørensen, Rasmus Schøler Ries, Oliver Vogel, Stefan Simmel, Friedrich C. Hatzakis, Nikos S. Kjems, Jørgen Nat Commun Article Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomolecules and DNA sequencing have shown promise. Here, we use DNA origami to create a synthetic 9 nm wide DNA nanopore, controlled by programmable, lipidated flaps and equipped with a size-selective gating system for the translocation of macromolecules. Successful assembly and insertion of the nanopore into lipid bilayers are validated by transmission electron microscopy (TEM), while selective translocation of cargo and the pore mechanosensitivity are studied using optical methods, including single-molecule, total internal reflection fluorescence (TIRF) microscopy. Size-specific cargo translocation and oligonucleotide-triggered opening of the pore are demonstrated showing that the DNA nanopore can function as a real-time detection system for external signals, offering potential for a variety of highly parallelized sensing applications. Nature Publishing Group UK 2019-12-11 /pmc/articles/PMC6906287/ /pubmed/31827087 http://dx.doi.org/10.1038/s41467-019-13284-1 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Thomsen, Rasmus P. Malle, Mette Galsgaard Okholm, Anders Hauge Krishnan, Swati Bohr, Søren S.-R. Sørensen, Rasmus Schøler Ries, Oliver Vogel, Stefan Simmel, Friedrich C. Hatzakis, Nikos S. Kjems, Jørgen A large size-selective DNA nanopore with sensing applications |
title | A large size-selective DNA nanopore with sensing applications |
title_full | A large size-selective DNA nanopore with sensing applications |
title_fullStr | A large size-selective DNA nanopore with sensing applications |
title_full_unstemmed | A large size-selective DNA nanopore with sensing applications |
title_short | A large size-selective DNA nanopore with sensing applications |
title_sort | large size-selective dna nanopore with sensing applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906287/ https://www.ncbi.nlm.nih.gov/pubmed/31827087 http://dx.doi.org/10.1038/s41467-019-13284-1 |
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