4.6 Article

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

Journal

JOURNAL OF LIPID RESEARCH
Volume 64, Issue 10, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jlr.2023.100430

Keywords

Supplementary key words antioxidant; dicarboxylic acid; flavone; flavonol; lipid/peroxidation; oxidized lipid; phospholipid/phosphatidylcholine; physical biochemistry

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Products of lipid peroxidation can cause detrimental structural changes in cell membranes, including the formation of water pores. However, the influence of dicarboxylic acids on cell membranes is still not well understood. This study focused on dodecanedioic acid (DDA) as a model product and investigated the impact of different flavonoids on DDA aggregation. The results showed that the addition of flavonoids disrupted the formation of DDA aggregates, leading to a decrease in DDA concentration in cell membranes.
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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