Synthesis of sphere-type monodispersed oligosaccharide-polypeptide dendrimers

被引:32
作者
Baigude, H
Katsuraya, K
Okuyama, K
Tokunaga, S
Uryu, T
机构
[1] Teikyo Univ Sci & Technol, Dept Environm & Mat Engn, Yamanashi 4090193, Japan
[2] Wayo Womens Univ, Chiba 2728533, Japan
[3] Univ Tokyo, Inst Ind Sci, Meguro Ku, Tokyo 1538505, Japan
关键词
D O I
10.1021/ma030021o
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A sphere-type fully substituted oligosaccharide-beta-alanine-poly(lysine) dendrimer having a sharp molecular weight distribution was synthesized. Sphere-type poly(lysine) dendrimers were prepared using 1,4-diaminobutane as an initiator core and N,N'-bis(tert-butyloxycarbonyl)-L-lysine as a branching unit. beta-Alanine was bound to the poly(lysine) dendrimer generation 3 to form beta-alanine-poly(lysine) dendrimer generation 3, which has 16 terminal amino groups on its surface. A series of sphere-type oligosaccharide-beta-alanine-poly(lysine) dendrimers were obtained by binding such an oligosaccharide as maltose, lactose, cellobiose, maltotriose, or a mixture of lactose and maltose to the surface of the beta-alanine-poly(lysine) dendrimer scaffolding by reductive amination using the borane-pyridine complex. Oligosaccharide-beta-alanine-poly(lysine) dendrimers having 32 oligosaccharide residues were obtained in high yields. NMR and MALDI-TOF mass measurements revealed that the oligosaccharide-polypeptide dendrimers have a monodispersed molecular weight distribution, the molecular weight of which was 13 418.36, 13 472.50, and 13 507.28 g/mol for cellobiose, maltose, and lactose, respectively, indicating that a complete substitution of the amino group by the oligosaccharide occurred.
引用
收藏
页码:7100 / 7106
页数:7
相关论文
共 36 条
  • [1] André S, 2001, CHEMBIOCHEM, V2, P822, DOI 10.1002/1439-7633(20011105)2:11<822::AID-CBIC822>3.0.CO
  • [2] 2-W
  • [3] GLOBULAR CARBOHYDRATE MACROMOLECULE SUGAR BALLS .1. SYNTHESIS OF NOVEL SUGAR-PERSUBSTITUTED POLY(AMIDO AMINE) DENDRIMERS
    AOI, K
    ITOH, K
    OKADA, M
    [J]. MACROMOLECULES, 1995, 28 (15) : 5391 - 5393
  • [4] Synthesis of glycodendrimers by modification of poly(propylene imine) dendrimers
    Ashton, PR
    Boyd, SE
    Brown, CL
    Nepogodiev, SA
    Meijer, EW
    Peerlings, HWI
    Stoddart, JF
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 1997, 3 (06) : 974 - 984
  • [5] Synthesis of dicarboxylate oligosaccharide multilayer terminal functionality upon poly(lysine) dendrimer scaffolding
    Baigude, H
    Katsuraya, K
    Okuyama, K
    Yachi, Y
    Sato, S
    Uryu, T
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (21) : 3622 - 3633
  • [6] About dendrimers: Structure, physical properties, and applications
    Bosman, AW
    Janssen, HM
    Meijer, EW
    [J]. CHEMICAL REVIEWS, 1999, 99 (07) : 1665 - 1688
  • [7] MACROMOLECULAR ASSEMBLAGE IN THE DESIGN OF A SYNTHETIC AIDS VACCINE
    DEFOORT, JP
    NARDELLI, B
    HUANG, WL
    HO, DD
    TAM, JP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 3879 - 3883
  • [8] Gordon M, 1997, J MED, V28, P108
  • [9] GORDON M, 1994, J MED, V25, P163
  • [10] Guittard J, 1996, J MASS SPECTROM, V31, P1409, DOI 10.1002/(SICI)1096-9888(199612)31:12<1409::AID-JMS440>3.3.CO