Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1783436819212271616 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6641635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zottilindaa electrontransportthroughhomopeptidesaretheyreallygoodconductors AT cuevasjuancarlos electrontransportthroughhomopeptidesaretheyreallygoodconductors |