Impact of chlorogenic acid on surface and phase properties of cholesterol-enriched phosphatidylcholine membranes

This study analyses the insertion of Chlorogenic acid (CGA) in phosphatidylcholine (PC) membranes enriched with cholesterol (Chol). While cholesterol decreases the area per lipid and increases the dipole potential, CGA increases and decreases these values, respectively. When CGA is inserted into cho...

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Veröffentlicht in:Archives of biochemistry and biophysics 2024-03, Vol.753, p.109913, Article 109913
Hauptverfasser: Cejas, Jimena del P., Rosa, Antonio S., González Paz, Agustín N., Disalvo, Edgardo A., Frías, María de los A.
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Sprache:eng
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Zusammenfassung:This study analyses the insertion of Chlorogenic acid (CGA) in phosphatidylcholine (PC) membranes enriched with cholesterol (Chol). While cholesterol decreases the area per lipid and increases the dipole potential, CGA increases and decreases these values, respectively. When CGA is inserted into cholesterol-containing DMPC membranes, these effects cancel out, resulting in values that overlap with those of DMPC monolayers without Chol and CGA. The presence of CGA also compensates the increase of dipole potential produced by Chol which can be explain as a consequence of the orientation of CGA molecule at the interphase opposing the cholesterol dipole moieties and water dipoles. This compensatory effect is less effective when lipids lack carbonyl groups (CO). When monolayers are composed by unsaturated PCs the Chol compensation is found at higher concentrations of CGA due to the direct interaction between CGA and Chol. These results suggest that cholesterol modulates the interaction and distribution of CGA in the lipid membrane, which may have implications for its biological activity. [Display omitted] •CGA compensates cholesterol effect on the lipid membranes compression pattern.•Concentration for compensation depends on Carbonyl Groups and double bonds.•A direct cholesterol-CGA interaction affects the stability of lipid membranes.
ISSN:0003-9861
1096-0384
1096-0384
DOI:10.1016/j.abb.2024.109913