PHYSICOCHEMICAL STUDIES OF 2 MAJOR SUBPOPULATIONS OF LOW-DENSITY LIPOPROTEINS BY DIFFERENTIAL SCANNING CALORIMETRY AND NMR-SPECTROSCOPY

被引:6
作者
BIHARIVARGA, M
TOLGYESI, F
PELCZER, J
MOK, T
LEE, DM
机构
[1] OKLAHOMA MED RES FDN,LIPOPROT & ATHEROSCLEROSIS RES PROGRAM,825 NE 13TH ST,OKLAHOMA CITY,OK 73104
[2] UNIV OKLAHOMA,HLTH SCI CTR,DEPT BIOCHEM & MOLEC BIOL,OKLAHOMA CITY,OK 73190
[3] SEMMELWEIS UNIV MED,H-1085 BUDAPEST 8,HUNGARY
[4] EGIS PHARMACEUT WORKS,BUDAPEST,HUNGARY
关键词
cholesterol ester; d.s.c; heterogeneity; LDL; n.m.r; physicochemical; structural alteration; subfractions; Transition temperature;
D O I
10.1016/0141-8130(90)90034-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two subpopulations, layer 2 (density 1.025-1.029 g/ml) and layer 3 (density 1.032-1.043 g/ml) of low density lipoproteins (LDL) were isolated from fresh human plasma of normal lipidaemic subjects by density gradient ultracentrifugation. Chemical analyses demonstrated the ratios of triglyceride/cholesterol ester decreased with increasing densities of subfractions. These subfractions together with triglyceride-rich lipoproteins (layer 1, density < 1.019 g/ml) were subjected to physicochemical studies by differential scanning calorimetry (d.s.c.) and nuclear magnetic resonance (n.m.r.) spectroscopy. The average transition temperature (Tt) of layer 2 was 34.20±0.83°C and that of layer 3 was 37.25±0.35°C. In addition, many of the layer 3, but not layer 2 and layer 1, samples showed structural alteration and gave rise to an average Tt of 39.18±1.24°C. The structural alteration could be detected with polarizing light microscopy showing birefringent spherulites at body temperature. The peak Tt values obtained by d.s.c. were in good agreement with those by n.m.r. spectroscopy. These results demonstrate the physicochemical heterogeneity within the LDL density region and suggest that layer 3 subpopulation is much more labile than the others. © 1990.
引用
收藏
页码:207 / 212
页数:6
相关论文
共 29 条
  • [1] EQUILIBRIUM BANDING OF LOW-DENSITY LIPOPROTEINS .2. ANALYSIS OF BANDING PATTERNS
    ADAMS, GH
    SCHUMAKER, VN
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1970, 202 (02) : 315 - +
  • [2] HUMAN SERUM-LIPOPROTEINS - EVIDENCE FOR 3 CLASSES OF LIPOPROTEINS IN SF 0-2
    ALBERS, JJ
    ALADJEM, F
    CHEN, CH
    [J]. BIOCHEMISTRY, 1972, 11 (01) : 57 - &
  • [3] STRUCTURE OF LOW-DENSITY LIPOPROTEIN IN COMPLEXES FORMED WITH ARTERIAL MATRIX COMPONENTS
    BIHARIVARGA, M
    CAMEJO, G
    HORN, MC
    SZABO, D
    LOPEZ, F
    GRUBER, E
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1983, 5 (01) : 59 - 62
  • [4] BIHARIVARGA M, 1982, ATHEROSCLEROSIS, V7, P413
  • [5] RADIOIMMUNOASSAY STUDIES OF HUMAN APOLIPOPROTEIN-E
    BLUM, CB
    ARON, L
    SCIACCA, R
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1980, 66 (06) : 1240 - 1250
  • [6] DECKELBAUM RJ, 1977, J BIOL CHEM, V252, P744
  • [7] DECKELBAUM RJ, 1977, J LIPID RES, V18, P164
  • [8] THERMAL TRANSITIONS IN HUMAN PLASMA LOW-DENSITY LIPOPROTEINS
    DECKELBAUM, RJ
    SHIPLEY, GG
    SMALL, DM
    LEES, RS
    GEORGE, PK
    [J]. SCIENCE, 1975, 190 (4212) : 392 - 394
  • [9] LIPOPROTEINS, CORONARY HEART DISEASE, AND ATHEROSCLEROSIS
    GOFMAN, JW
    GLAZIER, F
    TAMPLIN, A
    STRISOWER, B
    DELALLA, O
    [J]. PHYSIOLOGICAL REVIEWS, 1954, 34 (03) : 589 - 607
  • [10] LOW-DENSITY LIPOPROTEIN PATHWAY AND ITS RELATION TO ATHEROSCLEROSIS
    GOLDSTEIN, JL
    BROWN, MS
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1977, 46 : 897 - 930