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Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species

Lipid peroxidation by reactive oxygen species (ROS) during oxidative stress is non-enzymatic damage that affects the integrity of biological membrane, and alters the fluidity and permeability. We conducted molecular dynamic simulation studies to evaluate the structural properties of the bilayer afte...

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Autores principales: Yadav, Dharmendra Kumar, Kumar, Surendra, Choi, Eun-Ha, Chaudhary, Sandeep, Kim, Mi-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418262/
https://www.ncbi.nlm.nih.gov/pubmed/30872693
http://dx.doi.org/10.1038/s41598-019-40913-y
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author Yadav, Dharmendra Kumar
Kumar, Surendra
Choi, Eun-Ha
Chaudhary, Sandeep
Kim, Mi-Hyun
author_facet Yadav, Dharmendra Kumar
Kumar, Surendra
Choi, Eun-Ha
Chaudhary, Sandeep
Kim, Mi-Hyun
author_sort Yadav, Dharmendra Kumar
collection PubMed
description Lipid peroxidation by reactive oxygen species (ROS) during oxidative stress is non-enzymatic damage that affects the integrity of biological membrane, and alters the fluidity and permeability. We conducted molecular dynamic simulation studies to evaluate the structural properties of the bilayer after lipid peroxidation and to measure the permeability of distinct ROS. The oxidized membrane contains free fatty acid, ceramide, cholesterol, and 5α-hydroperoxycholesterol (5α-CH). The result of unconstrained molecular dynamic simulations revealed that lipid peroxidation causes area-per-lipid of the bilayer to increase and bilayer thickness to decrease. The simulations also revealed that the oxidized group of 5α-CH (-OOH) moves towards the aqueous layer and its backbone tilts causing lateral expansion of the bilayer membrane. These changes are detrimental to structural and functional properties of the membrane. The measured free energy profile for different ROS (H(2)O(2), HO(2), HO, and O(2)) across the peroxidized lipid bilayer showed that the increase in lipid peroxidation resulted in breaching barrier decrease for all species, allowing easy traversal of the membrane. Thus, lipid peroxidation perturbs the membrane barrier and imposes oxidative stress resulting into apoptosis. The collective insights increase the understanding of oxidation stress at the atomic level.
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spelling pubmed-64182622019-03-18 Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species Yadav, Dharmendra Kumar Kumar, Surendra Choi, Eun-Ha Chaudhary, Sandeep Kim, Mi-Hyun Sci Rep Article Lipid peroxidation by reactive oxygen species (ROS) during oxidative stress is non-enzymatic damage that affects the integrity of biological membrane, and alters the fluidity and permeability. We conducted molecular dynamic simulation studies to evaluate the structural properties of the bilayer after lipid peroxidation and to measure the permeability of distinct ROS. The oxidized membrane contains free fatty acid, ceramide, cholesterol, and 5α-hydroperoxycholesterol (5α-CH). The result of unconstrained molecular dynamic simulations revealed that lipid peroxidation causes area-per-lipid of the bilayer to increase and bilayer thickness to decrease. The simulations also revealed that the oxidized group of 5α-CH (-OOH) moves towards the aqueous layer and its backbone tilts causing lateral expansion of the bilayer membrane. These changes are detrimental to structural and functional properties of the membrane. The measured free energy profile for different ROS (H(2)O(2), HO(2), HO, and O(2)) across the peroxidized lipid bilayer showed that the increase in lipid peroxidation resulted in breaching barrier decrease for all species, allowing easy traversal of the membrane. Thus, lipid peroxidation perturbs the membrane barrier and imposes oxidative stress resulting into apoptosis. The collective insights increase the understanding of oxidation stress at the atomic level. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418262/ /pubmed/30872693 http://dx.doi.org/10.1038/s41598-019-40913-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yadav, Dharmendra Kumar
Kumar, Surendra
Choi, Eun-Ha
Chaudhary, Sandeep
Kim, Mi-Hyun
Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title_full Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title_fullStr Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title_full_unstemmed Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title_short Molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
title_sort molecular dynamic simulations of oxidized skin lipid bilayer and permeability of reactive oxygen species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418262/
https://www.ncbi.nlm.nih.gov/pubmed/30872693
http://dx.doi.org/10.1038/s41598-019-40913-y
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