Iminosugar-based glycopolypeptides: glycosidase inhibition with bioinspired glycoprotein analogue micellar self-assemblies

被引:76
作者
Bonduelle, Colin [1 ,2 ]
Huang, Jin [3 ]
Mena-Barragan, Teresa [4 ]
Ortiz Mellet, Carmen [4 ]
Decroocq, Camille [5 ,6 ]
Etame, Emile [5 ,6 ]
Heise, Andreas [3 ]
Compain, Philippe [5 ,6 ,7 ]
Lecommandoux, Sebastien [1 ,2 ]
机构
[1] Univ Bordeaux, IPB, ENSCBP, F-33607 Pessac, France
[2] CNRS, Lab Chim Polymeres Organ, UMR5629, Pessac, France
[3] Dublin City Univ, Sch Chem Sci, Dublin 9, Ireland
[4] Univ Seville, Fac Chem, Dept Organ Chem, Seville 41012, Spain
[5] Univ Strasbourg, Lab Synth Orgn & Mol Bioact, F-67087 Strasbourg, France
[6] CNRS, UMR 7509, Ecole Europeenne Chim Polymeres & Mat, F-67087 Strasbourg, France
[7] Inst Univ France, F-75005 Paris, France
基金
爱尔兰科学基金会;
关键词
RING-OPENING POLYMERIZATION; CLICK CLUSTERS; MULTIVALENT; FUNCTIONALIZATION; GLYCOPOLYMERS; GLYCOPEPTIDES; GLYCOBIOLOGY; POLYPEPTIDES; LECTINS; BINDING;
D O I
10.1039/c3cc48190e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biomimetic nanoparticles prepared by self-assembly of iminosugar-based glycopolypeptides evidenced remarkablemultivalency properties when inhibiting alpha-mannosidase activity. This approach paves the way to obtain biologically active drug delivery systems having glycosidase inhibition potency.
引用
收藏
页码:3350 / 3352
页数:3
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