Interaction between lectins and neoglycoproteins containing new sialylated glycosynthons

被引:6
作者
Duverger, E
Coppin, A
Strecker, G
Monsigny, M [1 ]
机构
[1] Univ Orleans, F-45071 Orleans 2, France
[2] CNRS, Ctr Biophys Mol, F-45071 Orleans, France
[3] Univ Sci & Tech Lille Flandres Artois, Chim Biol Lab, UMR 8756, F-59655 Villeneuve Dascq, France
关键词
N-acetyl neuraminic acid; lectin; glycosynthon; oligosaccharide; sialic acid;
D O I
10.1023/A:1007131931851
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
Neoglycoconjugates are useful tools to study carbohydrate/protein interactions. In order to discover new lectins, to define their fine specificity or to study their intracellular trafficking, there is a need for neoglycoconjugates containing complex oligosaccharides. We recently set up a simple way to transform native oligosaccharides into glycosynthons. The present paper describes i) the synthesis of such glycosynthons starting with sialylated oligosides, ii) the preparation of sialylated neoglycoproteins and iii) their binding to sialic acid-specific lectins assessed by surface plasmon resonance experiments.
引用
收藏
页码:793 / 800
页数:8
相关论文
共 14 条
  • [1] Carbohydrate recognition systems: Functional triads in cell-cell interactions
    Crocker, PR
    Feizi, T
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1996, 6 (05) : 679 - 691
  • [2] DRICKAMER K, 1993, ANNU REV CELL BIOL, V9, P237, DOI 10.1146/annurev.cb.09.110193.001321
  • [3] COLORIMETRIC DETERMINATION OF NEUTRAL SUGARS BY A RESORCINOL SULFURIC-ACID MICROMETHOD
    MONSIGNY, M
    PETIT, C
    ROCHE, AC
    [J]. ANALYTICAL BIOCHEMISTRY, 1988, 175 (02) : 525 - 530
  • [4] Glycotargeting:: The preparation of glyco-amino acids and derivatives from unprotected reducing sugars
    Monsigny, M
    Quétard, C
    Bourgerie, S
    Delay, D
    Pichon, C
    Midoux, P
    Mayer, R
    Roche, AC
    [J]. BIOCHIMIE, 1998, 80 (02) : 99 - 108
  • [5] OKAZAKI I, 1995, J MOL RECOGNIT, V8, P95, DOI 10.1002/jmr.300080117
  • [6] Novel glycosynthons for glycoconjugate preparation:: Oligosaccharylpyroglutamylanilide derivatives
    Quétard, C
    Bourgerie, S
    Normand-Sdiqui, N
    Mayer, R
    Strecker, G
    Midoux, P
    Roche, AC
    Monsigny, M
    [J]. BIOCONJUGATE CHEMISTRY, 1998, 9 (02) : 268 - 276
  • [7] Quetard C., 1997, CARBOHYDR LETT, V2, P415
  • [8] SUGAR-SPECIFIC ENDOCYTOSIS OF GLYCOPROTEINS BY LEWIS LUNG-CARCINOMA CELLS
    ROCHE, AC
    BARZILAY, M
    MIDOUX, P
    JUNQUA, S
    SHARON, N
    MONSIGNY, M
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1983, 22 (03) : 131 - 140
  • [9] SDIQUI N, 1995, CARBOHYDR LETT, V1, P269
  • [10] Elucidation of the mechanism enhancing the avidity of lectin with oligosaccharides on the solid phase surface
    Shinohara, Y
    Hasegawa, Y
    Kaku, H
    Shibuya, N
    [J]. GLYCOBIOLOGY, 1997, 7 (08) : 1201 - 1208