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Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction Center Biophotocathode
[Image: see text] The high quantum efficiency of photosynthetic reaction centers (RCs) makes them attractive for bioelectronic and biophotovoltaic applications. However, much of the native RC efficiency is lost in communication between surface-bound RCs and electrode materials. The state-of-the-art...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520101/ https://www.ncbi.nlm.nih.gov/pubmed/28635267 http://dx.doi.org/10.1021/acsami.7b03278 |
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author | Friebe, Vincent M. Millo, Diego Swainsbury, David J. K. Jones, Michael R. Frese, Raoul N. |
author_facet | Friebe, Vincent M. Millo, Diego Swainsbury, David J. K. Jones, Michael R. Frese, Raoul N. |
author_sort | Friebe, Vincent M. |
collection | PubMed |
description | [Image: see text] The high quantum efficiency of photosynthetic reaction centers (RCs) makes them attractive for bioelectronic and biophotovoltaic applications. However, much of the native RC efficiency is lost in communication between surface-bound RCs and electrode materials. The state-of-the-art biophotoelectrodes utilizing cytochrome c (cyt c) as a biological wiring agent have at best approached 32% retained RC quantum efficiency. However, bottlenecks in cyt c-mediated electron transfer have not yet been fully elucidated. In this work, protein film voltammetry in conjunction with photoelectrochemistry is used to show that cyt c acts as an electron-funneling antennae that shuttle electrons from a functionalized rough silver electrode to surface-immobilized RCs. The arrangement of the two proteins on the electrode surface is characterized, revealing that RCs attached directly to the electrode via hydrophobic interactions and that a film of six cyt c per RC electrostatically bound to the electrode. We show that the additional electrical connectivity within a film of cyt c improves the high turnover demands of surface-bound RCs. This results in larger photocurrent onset potentials, positively shifted half-wave reduction potentials, and higher photocurrent densities reaching 100 μA cm(–2). These findings are fundamental for the optimization of bioelectronics that utilize the ubiquitous cyt c redox proteins as biological wires to exploit electrode-bound enzymes. |
format | Online Article Text |
id | pubmed-5520101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-55201012017-07-24 Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction Center Biophotocathode Friebe, Vincent M. Millo, Diego Swainsbury, David J. K. Jones, Michael R. Frese, Raoul N. ACS Appl Mater Interfaces [Image: see text] The high quantum efficiency of photosynthetic reaction centers (RCs) makes them attractive for bioelectronic and biophotovoltaic applications. However, much of the native RC efficiency is lost in communication between surface-bound RCs and electrode materials. The state-of-the-art biophotoelectrodes utilizing cytochrome c (cyt c) as a biological wiring agent have at best approached 32% retained RC quantum efficiency. However, bottlenecks in cyt c-mediated electron transfer have not yet been fully elucidated. In this work, protein film voltammetry in conjunction with photoelectrochemistry is used to show that cyt c acts as an electron-funneling antennae that shuttle electrons from a functionalized rough silver electrode to surface-immobilized RCs. The arrangement of the two proteins on the electrode surface is characterized, revealing that RCs attached directly to the electrode via hydrophobic interactions and that a film of six cyt c per RC electrostatically bound to the electrode. We show that the additional electrical connectivity within a film of cyt c improves the high turnover demands of surface-bound RCs. This results in larger photocurrent onset potentials, positively shifted half-wave reduction potentials, and higher photocurrent densities reaching 100 μA cm(–2). These findings are fundamental for the optimization of bioelectronics that utilize the ubiquitous cyt c redox proteins as biological wires to exploit electrode-bound enzymes. American Chemical Society 2017-06-21 2017-07-19 /pmc/articles/PMC5520101/ /pubmed/28635267 http://dx.doi.org/10.1021/acsami.7b03278 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Friebe, Vincent M. Millo, Diego Swainsbury, David J. K. Jones, Michael R. Frese, Raoul N. Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction Center Biophotocathode |
title | Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction
Center Biophotocathode |
title_full | Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction
Center Biophotocathode |
title_fullStr | Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction
Center Biophotocathode |
title_full_unstemmed | Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction
Center Biophotocathode |
title_short | Cytochrome c Provides an Electron-Funneling Antenna for Efficient Photocurrent Generation in a Reaction
Center Biophotocathode |
title_sort | cytochrome c provides an electron-funneling antenna for efficient photocurrent generation in a reaction
center biophotocathode |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520101/ https://www.ncbi.nlm.nih.gov/pubmed/28635267 http://dx.doi.org/10.1021/acsami.7b03278 |
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