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Electron Transport Through Homopeptides: Are They Really Good Conductors?

[Image: see text] Motivated by recent experiments, we performed a theoretical study of electron transport through single-molecule junctions incorporating four kinds of homopeptides (based on alanine, glutamic acid, lysine, and tryptophan). Our results suggest that these molecules are rather insulati...

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Detalles Bibliográficos
Autores principales: Zotti, Linda A., Cuevas, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641635/
https://www.ncbi.nlm.nih.gov/pubmed/31458620
http://dx.doi.org/10.1021/acsomega.7b01917
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author Zotti, Linda A.
Cuevas, Juan Carlos
author_facet Zotti, Linda A.
Cuevas, Juan Carlos
author_sort Zotti, Linda A.
collection PubMed
description [Image: see text] Motivated by recent experiments, we performed a theoretical study of electron transport through single-molecule junctions incorporating four kinds of homopeptides (based on alanine, glutamic acid, lysine, and tryptophan). Our results suggest that these molecules are rather insulating and operate in off-resonance tunneling as their main transport mechanism. We ascribe their poor performance as conductors to the high localization of their frontier orbitals. We found that binding scenarios in which side chains lie on the side of gold protuberances could give rise to an increase in conductance with respect to end-to-end binding configurations. These findings provide an insight into the conductance mechanism of the building blocks of proteins and identify key issues that need to be further investigated.
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spelling pubmed-66416352019-08-27 Electron Transport Through Homopeptides: Are They Really Good Conductors? Zotti, Linda A. Cuevas, Juan Carlos ACS Omega [Image: see text] Motivated by recent experiments, we performed a theoretical study of electron transport through single-molecule junctions incorporating four kinds of homopeptides (based on alanine, glutamic acid, lysine, and tryptophan). Our results suggest that these molecules are rather insulating and operate in off-resonance tunneling as their main transport mechanism. We ascribe their poor performance as conductors to the high localization of their frontier orbitals. We found that binding scenarios in which side chains lie on the side of gold protuberances could give rise to an increase in conductance with respect to end-to-end binding configurations. These findings provide an insight into the conductance mechanism of the building blocks of proteins and identify key issues that need to be further investigated. American Chemical Society 2018-04-03 /pmc/articles/PMC6641635/ /pubmed/31458620 http://dx.doi.org/10.1021/acsomega.7b01917 Text en Copyright © 2018 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 Zotti, Linda A.
Cuevas, Juan Carlos
Electron Transport Through Homopeptides: Are They Really Good Conductors?
title Electron Transport Through Homopeptides: Are They Really Good Conductors?
title_full Electron Transport Through Homopeptides: Are They Really Good Conductors?
title_fullStr Electron Transport Through Homopeptides: Are They Really Good Conductors?
title_full_unstemmed Electron Transport Through Homopeptides: Are They Really Good Conductors?
title_short Electron Transport Through Homopeptides: Are They Really Good Conductors?
title_sort electron transport through homopeptides: are they really good conductors?
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641635/
https://www.ncbi.nlm.nih.gov/pubmed/31458620
http://dx.doi.org/10.1021/acsomega.7b01917
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