Puncturing lipid membranes: onset of pore formation and the role of hydrogen bonding in the presence of flavonoids

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Publikace nespadá pod Lékařskou fakultu, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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SADZAK Anja BRKLJACA Zlatko ERAKOVIC Mihael KRIECHBAUM Manfred MALTAR-STRMECKI Nadica PŘIBYL Jan SEGOTA Suzana

Rok publikování 2023
Druh Článek v odborném periodiku
Časopis / Zdroj JOURNAL OF LIPID RESEARCH
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://www.sciencedirect.com/science/article/pii/S0022227523001037?via%3Dihub
Doi http://dx.doi.org/10.1016/j.jlr.2023.100430
Klíčová slova Supplementary key words antioxidant; dicarboxylic acid; flavone; flavonol; lipid/peroxidation; oxidized lipid; phospholipid/phosphatidylcholine; physical biochemistry
Popis Products of lipid peroxidation induce detrimental structural changes in cell membranes, such as the formation of water pores, which occur in the presence of lipids with partially oxidized chains. However, the influence of another class of products, dicarboxylic acids, is still unclear. These products have greater mobility in the lipid bilayer, which enables their aggregation and the formation of favorable sites for the appearance of pores. Therefore, dodecanedioic acid (DDA) was selected as a model product. Additionally, the influence of several structurally different flavonoids on DDA aggregation via formation of hydrogen bonds with carboxyl groups was investigated. The molecular dynamics of DDA in DOPC lipid bilayer revealed the formation of aggregates extending over the hydrophobic region of the bilayer and increasing its polarity. Consequently, water penetration and the appearance of water wires was observed, representing a new step in the mechanism of pore formation. Furthermore, DDA molecules were found to interact with lipid polar groups, causing them to be buried in the bilayer. The addition of flavonoids to the system disrupted aggregate formation, resulting in the displacement of DDA molecules from the center of the bilayer. The placement of DDA and flavonoids in the lipid bilayer was confirmed by small-angle X-ray scattering. Atomic force microscopy and electron paramagnetic resonance were used to characterize the structural properties. The presence of DDA increased bilayer roughness and decreased the ordering of lipid chains, surface, while flavonoids were found to reduce or reverse these changes.
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