Please use this identifier to cite or link to this item:
https://hdl.handle.net/20.500.11851/10779
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Luo, L. | - |
dc.contributor.author | Manda, S. | - |
dc.contributor.author | Park, Y. | - |
dc.contributor.author | Demir, B. | - |
dc.contributor.author | Sanchez, J. | - |
dc.contributor.author | Anantram, M.P. | - |
dc.contributor.author | Oren, E.E. | - |
dc.date.accessioned | 2023-10-24T07:03:36Z | - |
dc.date.available | 2023-10-24T07:03:36Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | https://doi.org/10.1038/s41467-023-40870-1 | - |
dc.identifier.uri | https://hdl.handle.net/20.500.11851/10779 | - |
dc.description.abstract | 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. © 2023, Springer Nature Limited. | en_US |
dc.description.sponsorship | National Science Foundation, NSF: 20-518; University of California, UC: 22-601; University of Washington, UW; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK: 2214-A | en_US |
dc.description.sponsorship | L.L., S.M., Y.P., B.D., J.S., M.P.A., E.E.O., A.G. and M.R. acknowledge the main financial support of the National Science Foundation (NSF 20-518). L.L. thanks to Dr. Tom Yuzvinsky in BSOE at University of California, Santa Cruz for his help about the fabrication of bioprotonic devices. B.D. acknowledges the support of the Hyak supercomputer system at the University of Washington and financial support from the TUBITAK International Doctoral Research Fellowship program (TUBITAK 2214-A). J.S. acknowledges the support of the University of California, Santa Cruz Research Experiences for Undergraduates (REU) in sustainable materials, which is supported by the National Science Foundation (NSF 22-601). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Nature Research | en_US |
dc.relation.ispartof | Nature Communications | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | brain natriuretic peptide | en_US |
dc.subject | DNA | en_US |
dc.subject | DNA | en_US |
dc.subject | biomarker | en_US |
dc.subject | DNA | en_US |
dc.subject | electrode | en_US |
dc.subject | electronic equipment | en_US |
dc.subject | lipid | en_US |
dc.subject | membrane | en_US |
dc.subject | molecular analysis | en_US |
dc.subject | peptide | en_US |
dc.subject | signal | en_US |
dc.subject | Article | en_US |
dc.subject | artificial membrane | en_US |
dc.subject | DNA structure | en_US |
dc.subject | genetic marker | en_US |
dc.subject | lipid bilayer | en_US |
dc.subject | membrane channel | en_US |
dc.subject | molecular recognition | en_US |
dc.subject | proton transport | en_US |
dc.subject | surface property | en_US |
dc.subject | artificial membrane | en_US |
dc.subject | cell membrane | en_US |
dc.subject | Cell Membrane | en_US |
dc.subject | DNA | en_US |
dc.subject | Lipid Bilayers | en_US |
dc.subject | Membranes, Artificial | en_US |
dc.subject | Nanopores | en_US |
dc.title | Dna Nanopores as Artificial Membrane Channels for Bioprotonics | en_US |
dc.type | Article | en_US |
dc.department | TOBB ETÜ | en_US |
dc.identifier.volume | 14 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.wos | WOS:001072382600015 | en_US |
dc.identifier.scopus | 2-s2.0-85169695721 | en_US |
dc.institutionauthor | … | - |
dc.identifier.pmid | 37666808 | en_US |
dc.identifier.doi | 10.1038/s41467-023-40870-1 | - |
dc.authorscopusid | 57283676900 | - |
dc.authorscopusid | 58251798400 | - |
dc.authorscopusid | 57201267069 | - |
dc.authorscopusid | 57204554850 | - |
dc.authorscopusid | 58561630000 | - |
dc.authorscopusid | 57203174991 | - |
dc.authorscopusid | 35846321000 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopusquality | Q1 | - |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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