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Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors

F(1)F(o)‐ATP synthase is one of the best studied macromolecular machines in nature. It can be inhibited by a range of small molecules, which include the polyphenols, resveratrol and piceatannol. Here, we introduce Photoswitchable Inhibitors of ATP Synthase, termed PIAS, which were synthetically deri...

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Detalles Bibliográficos
Autores principales: Eisel, Bianca, Hartrampf, Felix W.W., Meier, Thomas, Trauner, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175411/
https://www.ncbi.nlm.nih.gov/pubmed/29292505
http://dx.doi.org/10.1002/1873-3468.12958
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author Eisel, Bianca
Hartrampf, Felix W.W.
Meier, Thomas
Trauner, Dirk
author_facet Eisel, Bianca
Hartrampf, Felix W.W.
Meier, Thomas
Trauner, Dirk
author_sort Eisel, Bianca
collection PubMed
description F(1)F(o)‐ATP synthase is one of the best studied macromolecular machines in nature. It can be inhibited by a range of small molecules, which include the polyphenols, resveratrol and piceatannol. Here, we introduce Photoswitchable Inhibitors of ATP Synthase, termed PIAS, which were synthetically derived from these polyphenols. They can be used to reversibly control the enzymatic activity of purified yeast Yarrowia lipolytica ATP synthase by light. Our experiments indicate that the PIAS bind to the same site in the ATP synthase F(1) complex as the polyphenols in their trans form, but they do not bind in their cis form. The PIAS could be useful tools for the optical precision control of ATP synthase in a variety of biochemical and biotechnological applications.
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spelling pubmed-61754112018-10-19 Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors Eisel, Bianca Hartrampf, Felix W.W. Meier, Thomas Trauner, Dirk FEBS Lett Research Letters F(1)F(o)‐ATP synthase is one of the best studied macromolecular machines in nature. It can be inhibited by a range of small molecules, which include the polyphenols, resveratrol and piceatannol. Here, we introduce Photoswitchable Inhibitors of ATP Synthase, termed PIAS, which were synthetically derived from these polyphenols. They can be used to reversibly control the enzymatic activity of purified yeast Yarrowia lipolytica ATP synthase by light. Our experiments indicate that the PIAS bind to the same site in the ATP synthase F(1) complex as the polyphenols in their trans form, but they do not bind in their cis form. The PIAS could be useful tools for the optical precision control of ATP synthase in a variety of biochemical and biotechnological applications. John Wiley and Sons Inc. 2018-02-01 2018-02 /pmc/articles/PMC6175411/ /pubmed/29292505 http://dx.doi.org/10.1002/1873-3468.12958 Text en © 2018 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Letters
Eisel, Bianca
Hartrampf, Felix W.W.
Meier, Thomas
Trauner, Dirk
Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title_full Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title_fullStr Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title_full_unstemmed Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title_short Reversible optical control of F(1)F(o)‐ATP synthase using photoswitchable inhibitors
title_sort reversible optical control of f(1)f(o)‐atp synthase using photoswitchable inhibitors
topic Research Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175411/
https://www.ncbi.nlm.nih.gov/pubmed/29292505
http://dx.doi.org/10.1002/1873-3468.12958
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