Cargando…
Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II
[Image: see text] Nature employs a Tyr(Z)-His pair as a redox relay that couples proton transfer to the redox process between P680 and the water oxidizing catalyst in photosystem II. Artificial redox relays composed of different benzimidazole–phenol dyads (benzimidazole models His and phenol models...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445534/ https://www.ncbi.nlm.nih.gov/pubmed/28573198 http://dx.doi.org/10.1021/acscentsci.7b00125 |
_version_ | 1783238914067136512 |
---|---|
author | Huynh, Mioy T. Mora, S. Jimena Villalba, Matias Tejeda-Ferrari, Marely E. Liddell, Paul A. Cherry, Brian R. Teillout, Anne-Lucie Machan, Charles W. Kubiak, Clifford P. Gust, Devens Moore, Thomas A. Hammes-Schiffer, Sharon Moore, Ana L. |
author_facet | Huynh, Mioy T. Mora, S. Jimena Villalba, Matias Tejeda-Ferrari, Marely E. Liddell, Paul A. Cherry, Brian R. Teillout, Anne-Lucie Machan, Charles W. Kubiak, Clifford P. Gust, Devens Moore, Thomas A. Hammes-Schiffer, Sharon Moore, Ana L. |
author_sort | Huynh, Mioy T. |
collection | PubMed |
description | [Image: see text] Nature employs a Tyr(Z)-His pair as a redox relay that couples proton transfer to the redox process between P680 and the water oxidizing catalyst in photosystem II. Artificial redox relays composed of different benzimidazole–phenol dyads (benzimidazole models His and phenol models Tyr) with substituents designed to simulate the hydrogen bond network surrounding the Tyr(Z)-His pair have been prepared. When the benzimidazole substituents are strong proton acceptors such as primary or tertiary amines, theory predicts that a concerted two proton transfer process associated with the electrochemical oxidation of the phenol will take place. Also, theory predicts a decrease in the redox potential of the phenol by ∼300 mV and a small kinetic isotope effect (KIE). Indeed, electrochemical, spectroelectrochemical, and KIE experimental data are consistent with these predictions. Notably, these results were obtained by using theory to guide the rational design of artificial systems and have implications for managing proton activity to optimize efficiency at energy conversion sites involving water oxidation and reduction. |
format | Online Article Text |
id | pubmed-5445534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54455342017-06-01 Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II Huynh, Mioy T. Mora, S. Jimena Villalba, Matias Tejeda-Ferrari, Marely E. Liddell, Paul A. Cherry, Brian R. Teillout, Anne-Lucie Machan, Charles W. Kubiak, Clifford P. Gust, Devens Moore, Thomas A. Hammes-Schiffer, Sharon Moore, Ana L. ACS Cent Sci [Image: see text] Nature employs a Tyr(Z)-His pair as a redox relay that couples proton transfer to the redox process between P680 and the water oxidizing catalyst in photosystem II. Artificial redox relays composed of different benzimidazole–phenol dyads (benzimidazole models His and phenol models Tyr) with substituents designed to simulate the hydrogen bond network surrounding the Tyr(Z)-His pair have been prepared. When the benzimidazole substituents are strong proton acceptors such as primary or tertiary amines, theory predicts that a concerted two proton transfer process associated with the electrochemical oxidation of the phenol will take place. Also, theory predicts a decrease in the redox potential of the phenol by ∼300 mV and a small kinetic isotope effect (KIE). Indeed, electrochemical, spectroelectrochemical, and KIE experimental data are consistent with these predictions. Notably, these results were obtained by using theory to guide the rational design of artificial systems and have implications for managing proton activity to optimize efficiency at energy conversion sites involving water oxidation and reduction. American Chemical Society 2017-05-09 2017-05-24 /pmc/articles/PMC5445534/ /pubmed/28573198 http://dx.doi.org/10.1021/acscentsci.7b00125 Text en Copyright © 2017 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 | Huynh, Mioy T. Mora, S. Jimena Villalba, Matias Tejeda-Ferrari, Marely E. Liddell, Paul A. Cherry, Brian R. Teillout, Anne-Lucie Machan, Charles W. Kubiak, Clifford P. Gust, Devens Moore, Thomas A. Hammes-Schiffer, Sharon Moore, Ana L. Concerted One-Electron Two-Proton Transfer Processes in Models Inspired by the Tyr-His Couple of Photosystem II |
title | Concerted One-Electron Two-Proton Transfer Processes
in Models Inspired by the Tyr-His Couple of Photosystem II |
title_full | Concerted One-Electron Two-Proton Transfer Processes
in Models Inspired by the Tyr-His Couple of Photosystem II |
title_fullStr | Concerted One-Electron Two-Proton Transfer Processes
in Models Inspired by the Tyr-His Couple of Photosystem II |
title_full_unstemmed | Concerted One-Electron Two-Proton Transfer Processes
in Models Inspired by the Tyr-His Couple of Photosystem II |
title_short | Concerted One-Electron Two-Proton Transfer Processes
in Models Inspired by the Tyr-His Couple of Photosystem II |
title_sort | concerted one-electron two-proton transfer processes
in models inspired by the tyr-his couple of photosystem ii |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445534/ https://www.ncbi.nlm.nih.gov/pubmed/28573198 http://dx.doi.org/10.1021/acscentsci.7b00125 |
work_keys_str_mv | AT huynhmioyt concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT morasjimena concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT villalbamatias concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT tejedaferrarimarelye concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT liddellpaula concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT cherrybrianr concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT teilloutannelucie concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT machancharlesw concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT kubiakcliffordp concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT gustdevens concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT moorethomasa concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT hammesschiffersharon concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii AT mooreanal concertedoneelectrontwoprotontransferprocessesinmodelsinspiredbythetyrhiscoupleofphotosystemii |