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Electron Transport Lipids Fold Within Membrane-Like Interfaces

Lipoquinones, such as ubiquinones (UQ) and menaquinones (MK), function as essential lipid components of the electron transport system (ETS) by shuttling electrons and protons to facilitate the production of ATP in eukaryotes and prokaryotes. Lipoquinone function in membrane systems has been widely s...

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Autores principales: Braasch-Turi, Margaret M., Koehn, Jordan T., Kostenkova, Kateryna, Van Cleave, Cameron, Ives, Jacob W., Murakami, Heide A., Crick, Dean C., Crans, Debbie C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957872/
https://www.ncbi.nlm.nih.gov/pubmed/35350775
http://dx.doi.org/10.3389/fchem.2022.827530
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author Braasch-Turi, Margaret M.
Koehn, Jordan T.
Kostenkova, Kateryna
Van Cleave, Cameron
Ives, Jacob W.
Murakami, Heide A.
Crick, Dean C.
Crans, Debbie C.
author_facet Braasch-Turi, Margaret M.
Koehn, Jordan T.
Kostenkova, Kateryna
Van Cleave, Cameron
Ives, Jacob W.
Murakami, Heide A.
Crick, Dean C.
Crans, Debbie C.
author_sort Braasch-Turi, Margaret M.
collection PubMed
description Lipoquinones, such as ubiquinones (UQ) and menaquinones (MK), function as essential lipid components of the electron transport system (ETS) by shuttling electrons and protons to facilitate the production of ATP in eukaryotes and prokaryotes. Lipoquinone function in membrane systems has been widely studied, but the exact location and conformation within membranes remains controversial. Lipoquinones, such as Coenzyme Q (UQ-10), are generally depicted simply as “Q” in life science diagrams or in extended conformations in primary literature even though specific conformations are important for function in the ETS. In this study, our goal was to determine the location, orientation, and conformation of UQ-2, a truncated analog of UQ-10, in model membrane systems and to compare our results to previously studied MK-2. Herein, we first carried out a six-step synthesis to yield UQ-2 and then demonstrated that UQ-2 adopts a folded conformation in organic solvents using (1)H-(1)H 2D NOESY and ROESY NMR spectroscopic studies. Similarly, using (1)H-(1)H 2D NOESY NMR spectroscopic studies, UQ-2 was found to adopt a folded, U-shaped conformation within the interface of an AOT reverse micelle model membrane system. UQ-2 was located slightly closer to the surfactant-water interface compared to the more hydrophobic MK-2. In addition, Langmuir monolayer studies determined UQ-2 resided within the monolayer water-phospholipid interface causing expansion, whereas MK-2 was more likely to be compressed out and reside within the phospholipid tails. All together these results support the model that lipoquinones fold regardless of the headgroup structure but that the polarity of the headgroup influences lipoquinone location within the membrane interface. These results have implications regarding the redox activity near the interface as quinone vs. quinol forms may facilitate locomotion of lipoquinones within the membrane. The location, orientation, and conformation of lipoquinones are critical for their function in generating cellular energy within membrane ETS, and the studies described herein shed light on the behavior of lipoquinones within membrane-like environments.
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spelling pubmed-89578722022-03-28 Electron Transport Lipids Fold Within Membrane-Like Interfaces Braasch-Turi, Margaret M. Koehn, Jordan T. Kostenkova, Kateryna Van Cleave, Cameron Ives, Jacob W. Murakami, Heide A. Crick, Dean C. Crans, Debbie C. Front Chem Chemistry Lipoquinones, such as ubiquinones (UQ) and menaquinones (MK), function as essential lipid components of the electron transport system (ETS) by shuttling electrons and protons to facilitate the production of ATP in eukaryotes and prokaryotes. Lipoquinone function in membrane systems has been widely studied, but the exact location and conformation within membranes remains controversial. Lipoquinones, such as Coenzyme Q (UQ-10), are generally depicted simply as “Q” in life science diagrams or in extended conformations in primary literature even though specific conformations are important for function in the ETS. In this study, our goal was to determine the location, orientation, and conformation of UQ-2, a truncated analog of UQ-10, in model membrane systems and to compare our results to previously studied MK-2. Herein, we first carried out a six-step synthesis to yield UQ-2 and then demonstrated that UQ-2 adopts a folded conformation in organic solvents using (1)H-(1)H 2D NOESY and ROESY NMR spectroscopic studies. Similarly, using (1)H-(1)H 2D NOESY NMR spectroscopic studies, UQ-2 was found to adopt a folded, U-shaped conformation within the interface of an AOT reverse micelle model membrane system. UQ-2 was located slightly closer to the surfactant-water interface compared to the more hydrophobic MK-2. In addition, Langmuir monolayer studies determined UQ-2 resided within the monolayer water-phospholipid interface causing expansion, whereas MK-2 was more likely to be compressed out and reside within the phospholipid tails. All together these results support the model that lipoquinones fold regardless of the headgroup structure but that the polarity of the headgroup influences lipoquinone location within the membrane interface. These results have implications regarding the redox activity near the interface as quinone vs. quinol forms may facilitate locomotion of lipoquinones within the membrane. The location, orientation, and conformation of lipoquinones are critical for their function in generating cellular energy within membrane ETS, and the studies described herein shed light on the behavior of lipoquinones within membrane-like environments. Frontiers Media S.A. 2022-03-08 /pmc/articles/PMC8957872/ /pubmed/35350775 http://dx.doi.org/10.3389/fchem.2022.827530 Text en Copyright © 2022 Braasch-Turi, Koehn, Kostenkova, Van Cleave, Ives, Murakami, Crick and Crans. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Braasch-Turi, Margaret M.
Koehn, Jordan T.
Kostenkova, Kateryna
Van Cleave, Cameron
Ives, Jacob W.
Murakami, Heide A.
Crick, Dean C.
Crans, Debbie C.
Electron Transport Lipids Fold Within Membrane-Like Interfaces
title Electron Transport Lipids Fold Within Membrane-Like Interfaces
title_full Electron Transport Lipids Fold Within Membrane-Like Interfaces
title_fullStr Electron Transport Lipids Fold Within Membrane-Like Interfaces
title_full_unstemmed Electron Transport Lipids Fold Within Membrane-Like Interfaces
title_short Electron Transport Lipids Fold Within Membrane-Like Interfaces
title_sort electron transport lipids fold within membrane-like interfaces
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957872/
https://www.ncbi.nlm.nih.gov/pubmed/35350775
http://dx.doi.org/10.3389/fchem.2022.827530
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