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

被引:1
作者
Zaborowska-Mazurkiewicz, Michalina [1 ]
Bizon, Teresa [2 ]
Matyszewska, Dorota [3 ]
Fontaine, Philippe [4 ]
Bilewicz, Renata [1 ]
机构
[1] Univ Warsaw, Fac Chem, Pasteura 1, PL-02093 Warsaw, Poland
[2] Univ Warsaw, Fac Phys, Pasteura 5, PL-02093 Warsaw, Poland
[3] Univ Warsaw, Fac Chem, Biol & Chem Res Ctr, Zwirki & Wigury 101, PL-02089 Warsaw, Poland
[4] Synchrotron Soleil, Dept 128, F-91190 Saint Aubin, France
关键词
Cholesterol; Langmuir monolayer; Cholesterol oxidase; Cholesterol oxidation; Lipid raft; Liposomes; INCIDENCE X-RAY; ENZYME-CATALYZED OXIDATION; BREWSTER-ANGLE MICROSCOPY; LIPOSOME SIZE; MONOLAYERS; SPHINGOMYELIN; DIFFRACTION; IMMOBILIZATION; SCATTERING; BIOSENSOR;
D O I
10.1016/j.colsurfb.2024.114191
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The effects of a peripheral protein - cholesterol oxidase (3(3-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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页数:12
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共 63 条
[1]  
ALSNIELSEN J, 1994, PHYS REP, V246, P252
[2]   ROLE OF ENDOGENOUS AND EXOGENOUS CHOLESTEROL IN LIVER AS THE PRECURSOR FOR BILE-ACIDS IN RATS [J].
AYAKI, Y ;
TSUMADATE, T ;
ENDO, S ;
OGURA, M .
STEROIDS, 1981, 38 (05) :495-509
[3]   Steady-state oxidation of cholesterol catalyzed by cholesterol oxidase in lipid bilayer membranes on platinum electrodes [J].
Bokoch, MP ;
Devadoss, A ;
Palencsár, MS ;
Burgess, JD .
ANALYTICA CHIMICA ACTA, 2004, 519 (01) :47-55
[4]   Cross-Talk between Lipoproteins and Inflammation: The Role of Microvesicles [J].
Chiva-Blanch, Gemma ;
Badimon, Lina .
JOURNAL OF CLINICAL MEDICINE, 2019, 8 (12)
[5]   Oxygen access to the active site of cholesterol oxidase through a narrow channel is gated by an Arg-Glu pair [J].
Coulombe, R ;
Yue, KQ ;
Ghisla, S ;
Vrielink, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (32) :30435-30441
[7]  
Eeman M, 2010, BIOTECHNOL AGRON SOC, V14, P719
[8]   Evidence for lipid/cholesterol ordering in model lipid membranes [J].
Ege, Canay ;
Ratajczak, Maria K. ;
Majewski, Jaroslaw ;
Kjaer, Kristian ;
Lee, Ka Yee C. .
BIOPHYSICAL JOURNAL, 2006, 91 (01) :L1-L3
[9]   Current and future treatment of hyperlipidemia: The role of statins [J].
Farnier, M ;
Davignon, J .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 82 (4B) :3J-10J
[10]   Monomolecular films of cholesterol oxidase and S-Layer proteins [J].
Ferraz, Helen Conceicao ;
Guimaraes, Juliana Aguilar ;
Moitinho Alves, Tito Livio ;
Leopoldo Constantino, Carlos Jose .
APPLIED SURFACE SCIENCE, 2011, 257 (15) :6535-6539