Ellipsometry studies of lipoprotein adsorption

被引:31
作者
Malmsten, M
Siegel, G
Wood, WG
机构
[1] Inst Surface Chem, SE-11486 Stockholm, Sweden
[2] Free Univ Berlin, Inst Physiol, D-14195 Berlin, Germany
[3] Inst Clin Lab Diagnost, Clin Hanse City Stralsund, D-18410 Stralsund, Germany
关键词
adsorption; arteriosclerosis; atherosclerosis; ellipsometry; HDL; LDL; lipoprotein (a); proteoglycans; proteoheparan sulfate;
D O I
10.1006/jcis.1999.6689
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption of a number of lipoproteins, i.e., low-density lipoprotein (LDL), oxidized LDL (oxLDL), high-density lipoprotein (HDL), and lipoprotein (a), at silica and methylated silica as well as at the latter surface modified through adsorption of proteoheparan sulfate, was investigated with in situ ellipsometry at close to physiological conditions. It was found that LDL, oxLDL, HDL, and lipoprotein (a) all adsorbed more extensively at silica than at methylated silica. Upon exposure of the methylated silica surface to proteoheparan sulfate, this proteoglycan adsorbs through its hydrophobic moiety, thereby forming a layer similar to that in the biological system, with the polysaccharide chains forming brushes oriented toward the aqueous solution. Analogous to the biological system, both lipoprotein (a) and LDL were found to deposit at such surfaces, the latter particularly in the simultaneous presence of Ca2+. After HDL pre-exposure, however, no LDL deposition was observed, even at high LDL and Ca2+ concentrations. These findings correlate well with those obtained from clinical investigations on risk factors for atherosclerosis. (C) 2000 Academic Press.
引用
收藏
页码:338 / 346
页数:9
相关论文
共 66 条
[1]   Isolation of low density lipoprotein subfraction containing apolipoprotein B-like protein from Japanese eel Anguilla japonica plasma using dextran sulfate cellulose [J].
Ando, S ;
Matsuzaki, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1997, 116 (02) :191-196
[2]   BLOOD ANTIOXIDANTS (VITAMIN-E AND BETA-CAROTENE) IN LONG-TERM LOW-DENSITY-LIPOPROTEIN APHERESIS [J].
ASSOGBA, U ;
LEPAGE, S ;
BRUCKERT, E ;
BONNEFONTROUSSELOT, D ;
DAIROU, F ;
DEGENNES, JL ;
DELATTRE, J .
CLINICA CHIMICA ACTA, 1995, 235 (02) :147-157
[3]  
Azzam RM, 1989, ELLIPSOMETRY POLARIZ
[4]  
BANTJES A, 1985, MAKROMOL CHEM S, V9, P99
[5]  
BRASH JL, 1984, THROMB HAEMOSTASIS, V51, P326
[6]   PREFERENTIAL ADSORPTION OF HIGH-DENSITY LIPOPROTEIN FROM BLOOD-PLASMA ONTO BIOMATERIAL SURFACES [J].
BREEMHAAR, W ;
BRINKMAN, E ;
ELLENS, DJ ;
BEUGELING, T ;
BANTJES, A .
BIOMATERIALS, 1984, 5 (05) :269-274
[7]   INHIBITION OF BINDING OF LOW-DENSITY LIPOPROTEIN TO ITS CELL-SURFACE RECEPTOR IN HUMAN FIBROBLASTS BY POSITIVELY CHARGED PROTEINS [J].
BROWN, MS ;
DEUEL, TF ;
BASU, SK ;
GOLDSTEIN, JL .
JOURNAL OF SUPRAMOLECULAR STRUCTURE, 1978, 8 (03) :223-234
[8]  
Burstein M, 1973, Adv Lipid Res, V11, P67
[9]  
Cockerill GW, 1999, INT REV CYTOL, V188, P257
[10]   SPECIFIC, SATURABLE, AND HIGH AFFINITY BINDING OF I-125 LOW DENSITY LIPOPROTEIN TO GLASS BEADS [J].
DANA, SE ;
BROWN, MS ;
GOLDSTEIN, JL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 74 (04) :1369-1376