The analysis of heparin-protein interactions using evanescent wave biosensor with regioselectively desulfated heparins as the ligands

被引:21
作者
Kamei, K
Wu, XF
Xu, XY
Minami, K
Huy, NT
Takano, R
Kato, H
Hara, S
机构
[1] Kyoto Inst Technol, Dept Appl Biol, Sakyo Ku, Kyoto 6068585, Japan
[2] Natl Cardiovasc Ctr, Inst Res, Osaka 5658565, Japan
关键词
D O I
10.1006/abio.2001.5193
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Evanescent wave biosensor has been recently employed as a powerful tool for analyses of macromolecular interactions. In the present study, evanescent wave biosensor analysis was developed to analyze the heparin-protein interaction using as ligands a series of heparin derivatives regioselectively desulfated by chemical methods, particularly to evaluate the effect of each sulfate group of heparin. The method for immobilizing heparin on the cuvette of the evanescent wave biosensor equipment was optimized to obtain the high response required for accurate measurement. The best result was achieved when the amino group introduced at the reducing end of heparin was coupled with carboxymethyl dextran on the surface of the cuvette using glycolchitosan as a multivalent linker. The established system appeared to describe well the interactions of heparin with such proteins as acidic and basic fibroblast growth factors and tissue factor pathway inhibitor. (C) 2001 Academic Press.
引用
收藏
页码:203 / 213
页数:11
相关论文
共 34 条
  • [1] A MODIFIED URONIC ACID CARBAZOLE REACTION
    BITTER, T
    MUIR, HM
    [J]. ANALYTICAL BIOCHEMISTRY, 1962, 4 (04) : 330 - &
  • [2] MECHANISM OF THE ANTICOAGULANT ACTION OF HEPARIN
    BJORK, I
    LINDAHL, U
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1982, 48 (03) : 161 - 182
  • [3] TISSUE FACTOR PATHWAY INHIBITOR AND THE REVISED THEORY OF COAGULATION
    BROZE, GJ
    [J]. ANNUAL REVIEW OF MEDICINE, 1995, 46 : 103 - 112
  • [4] DANISHEFSKY I., 1965, METHOD CARBOHYD CHEM, V5, P407
  • [5] Edward Conrad H, 1998, HEPARIN BINDING PROT, P7, DOI [DOI 10.1016/B978-012186060-8/50003-6, 10.1016/B978-012186060-8/50003-6]
  • [6] EFFECT OF HEPARIN ON THE INHIBITION OF FACTOR-XA BY TISSUE FACTOR PATHWAY INHIBITOR - A SEGMENT, GLY(212)-PHE(243), OF THE 3RD KUNITZ DOMAIN IS A HEPARIN-BINDING SITE
    ENJYOJI, K
    MIYATA, T
    KAMIKUBO, Y
    KATO, H
    [J]. BIOCHEMISTRY, 1995, 34 (17) : 5725 - 5735
  • [7] BIOSPECIFIC INTERACTION ANALYSIS USING SURFACE-PLASMON RESONANCE DETECTION APPLIED TO KINETIC, BINDING-SITE AND CONCENTRATION ANALYSIS
    FAGERSTAM, LG
    FROSTELLKARLSSON, A
    KARLSSON, R
    PERSSON, B
    RONNBERG, I
    [J]. JOURNAL OF CHROMATOGRAPHY, 1992, 597 (1-2): : 397 - 410
  • [8] Heparin structure and interactions with basic fibroblast growth factor
    Faham, S
    Hileman, RE
    Fromm, JR
    Linhardt, RJ
    Rees, DC
    [J]. SCIENCE, 1996, 271 (5252) : 1116 - 1120
  • [9] GALLAGHER JT, 1992, ADV EXP MED BIOL, V313, P49
  • [10] Histidine-rich glycoprotein binds to human IgG and C1q and inhibits the formation of insoluble immune complexes
    Gorgani, NN
    Parish, CR
    Smith, SBE
    Altin, JG
    [J]. BIOCHEMISTRY, 1997, 36 (22) : 6653 - 6662