Oxidation of lipid membrane cholesterol by cholesterol oxidase and its effects on raft model membrane structure

The effects of a peripheral protein - cholesterol oxidase (3β-hydroxysteroid oxidase, ChOx) on the characteristics of model lipid membranes composed of cholesterol, cholesterol:sphingomyelin (1:1), and the raft model composed of DOPC:Chol:SM (1:1:1) were investigated using two membrane model systems: the flat monolayer prepared by the Langmuir technique and the curved model consisting of liposome of the same lipids. The planar monolayers and liposomes were employed to follow membrane cholesterol oxidation to cholestenone catalyzed by ChOx and changes in the lipid membrane structure accompanying this reaction. Changes in the structure of liposomes in the presence of the enzyme were reflected in the changes of hydrodynamic diameter and fluorescence microscopy images, while changes of surface properties of planar membranes were evaluated by grazing incidence X-ray diffraction (GIXD) and Brewster angle microscopy. UV-Vis absorbance measurements confirmed the activity of the enzyme in the tested systems. A better understanding of the interactions between the enzyme and the cell membrane may help in finding alternative ways to decrease excessive cholesterol levels than the common approach of treating hypercholesterolemia with statins, which are not free from undesirable side effects, repeatedly reported in the literature and observed by the patients.

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Publication Details

Journal
Colloids and Surfaces B Biointerfaces
Published
2024-08-30
DOI
https://doi.org/10.1016/j.colsurfb.2024.114191
Citations
8
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
1.87

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article

Oxidation of lipid membrane cholesterol by cholesterol oxidase and its effects on raft model membrane structure

Renata Bilewicz, Dorota Matyszewska, Philippe Fontaine, Michalina Zaborowska et al.
8 citations
Colloids and Surfaces B Biointerfaces
Lipid Membrane Structure and Behavior
1.87
article

Oxidation of lipid membrane cholesterol by cholesterol oxidase and its effects on raft model membrane structure

Renata Bilewicz, Dorota Matyszewska, Philippe Fontaine, Michalina Zaborowska, Teresa Bizoń
article en
8 citations

Abstract

The effects of a peripheral protein - cholesterol oxidase (3β-hydroxysteroid oxidase, ChOx) on the characteristics of model lipid membranes composed of cholesterol, cholesterol:sphingomyelin (1:1), and the raft model composed of DOPC:Chol:SM (1:1:1) were investigated using two membrane model systems: the flat monolayer prepared by the Langmuir technique and the curved model consisting of liposome of the same lipids. The planar monolayers and liposomes were employed to follow membrane cholesterol oxidation to cholestenone catalyzed by ChOx and changes in the lipid membrane structure accompanying this reaction. Changes in the structure of liposomes in the presence of the enzyme were reflected in the changes of hydrodynamic diameter and fluorescence microscopy images, while changes of surface properties of planar membranes were evaluated by grazing incidence X-ray diffraction (GIXD) and Brewster angle microscopy. UV-Vis absorbance measurements confirmed the activity of the enzyme in the tested systems. A better understanding of the interactions between the enzyme and the cell membrane may help in finding alternative ways to decrease excessive cholesterol levels than the common approach of treating hypercholesterolemia with statins, which are not free from undesirable side effects, repeatedly reported in the literature and observed by the patients.

Colloids and Surfaces B BiointerfacesVol. 245
Synchrotron soleil (FR), University of Warsaw (PL)
European Commission, Narodowe Centrum Nauki, European Regional Development Fund
Openalex Percentile: Top 14%
Lipid Membrane Structure and Behavior
1.87
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Oxidation of lipid membrane cholesterol by cholesterol oxidase and its effects on raft model membrane structure — Renata Bilewicz, Dorota Matyszewska, et al. · Colloids and Surfaces B Biointerfaces (2024) | TGRS Research Map | TGRS