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Coherent Electron Transport across a 3 nm Bioelectronic Junction Made of Multi-Heme Proteins
[Image: see text] Multi-heme cytochromes (MHCs) are fascinating proteins used by bacterial organisms to shuttle electrons within, between, and out of their cells. When placed in solid-state electronic junctions, MHCs support temperature-independent currents over several nanometers that are 3 orders...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681787/ https://www.ncbi.nlm.nih.gov/pubmed/33142062 http://dx.doi.org/10.1021/acs.jpclett.0c02686 |
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author | Futera, Zdenek Ide, Ichiro Kayser, Ben Garg, Kavita Jiang, Xiuyun van Wonderen, Jessica H. Butt, Julea N. Ishii, Hisao Pecht, Israel Sheves, Mordechai Cahen, David Blumberger, Jochen |
author_facet | Futera, Zdenek Ide, Ichiro Kayser, Ben Garg, Kavita Jiang, Xiuyun van Wonderen, Jessica H. Butt, Julea N. Ishii, Hisao Pecht, Israel Sheves, Mordechai Cahen, David Blumberger, Jochen |
author_sort | Futera, Zdenek |
collection | PubMed |
description | [Image: see text] Multi-heme cytochromes (MHCs) are fascinating proteins used by bacterial organisms to shuttle electrons within, between, and out of their cells. When placed in solid-state electronic junctions, MHCs support temperature-independent currents over several nanometers that are 3 orders of magnitude higher compared to other redox proteins of similar size. To gain molecular-level insight into their astonishingly high conductivities, we combine experimental photoemission spectroscopy with DFT+Σ current–voltage calculations on a representative Gold-MHC-Gold junction. We find that conduction across the dry, 3 nm long protein occurs via off-resonant coherent tunneling, mediated by a large number of protein valence-band orbitals that are strongly delocalized over heme and protein residues. This picture is profoundly different from the electron hopping mechanism induced electrochemically or photochemically under aqueous conditions. Our results imply that the current output in solid-state junctions can be even further increased in resonance, for example, by applying a gate voltage, thus allowing a quantum jump for next-generation bionanoelectronic devices. |
format | Online Article Text |
id | pubmed-7681787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-76817872020-11-24 Coherent Electron Transport across a 3 nm Bioelectronic Junction Made of Multi-Heme Proteins Futera, Zdenek Ide, Ichiro Kayser, Ben Garg, Kavita Jiang, Xiuyun van Wonderen, Jessica H. Butt, Julea N. Ishii, Hisao Pecht, Israel Sheves, Mordechai Cahen, David Blumberger, Jochen J Phys Chem Lett [Image: see text] Multi-heme cytochromes (MHCs) are fascinating proteins used by bacterial organisms to shuttle electrons within, between, and out of their cells. When placed in solid-state electronic junctions, MHCs support temperature-independent currents over several nanometers that are 3 orders of magnitude higher compared to other redox proteins of similar size. To gain molecular-level insight into their astonishingly high conductivities, we combine experimental photoemission spectroscopy with DFT+Σ current–voltage calculations on a representative Gold-MHC-Gold junction. We find that conduction across the dry, 3 nm long protein occurs via off-resonant coherent tunneling, mediated by a large number of protein valence-band orbitals that are strongly delocalized over heme and protein residues. This picture is profoundly different from the electron hopping mechanism induced electrochemically or photochemically under aqueous conditions. Our results imply that the current output in solid-state junctions can be even further increased in resonance, for example, by applying a gate voltage, thus allowing a quantum jump for next-generation bionanoelectronic devices. American Chemical Society 2020-11-03 2020-11-19 /pmc/articles/PMC7681787/ /pubmed/33142062 http://dx.doi.org/10.1021/acs.jpclett.0c02686 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Futera, Zdenek Ide, Ichiro Kayser, Ben Garg, Kavita Jiang, Xiuyun van Wonderen, Jessica H. Butt, Julea N. Ishii, Hisao Pecht, Israel Sheves, Mordechai Cahen, David Blumberger, Jochen Coherent Electron Transport across a 3 nm Bioelectronic Junction Made of Multi-Heme Proteins |
title | Coherent Electron Transport across a 3 nm Bioelectronic
Junction Made of Multi-Heme Proteins |
title_full | Coherent Electron Transport across a 3 nm Bioelectronic
Junction Made of Multi-Heme Proteins |
title_fullStr | Coherent Electron Transport across a 3 nm Bioelectronic
Junction Made of Multi-Heme Proteins |
title_full_unstemmed | Coherent Electron Transport across a 3 nm Bioelectronic
Junction Made of Multi-Heme Proteins |
title_short | Coherent Electron Transport across a 3 nm Bioelectronic
Junction Made of Multi-Heme Proteins |
title_sort | coherent electron transport across a 3 nm bioelectronic
junction made of multi-heme proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681787/ https://www.ncbi.nlm.nih.gov/pubmed/33142062 http://dx.doi.org/10.1021/acs.jpclett.0c02686 |
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