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细胞表面结合蛋白质的碳水化合物作为识别靶点:对其理解的探索历程

Protein-bound carbohydrates on cell-surface as targets of recognition: an odyssey in understanding them.

作者信息

Muramatsu T

机构信息

Department of Biochemistry, Nagoya University School of Medicine, Japan.

出版信息

Glycoconj J. 2000 Jul-Sep;17(7-9):577-95. doi: 10.1023/a:1011078627247.

Abstract

Multidisciplinary approaches by a number of investigators have established that cell-surface carbohydrates are integral components of recognition systems regulating survival, migration, adhesion, growth and differentiation of various cells. Our own experience and contributions to this exciting field are described. We discovered Endo D as the first endoglycosidase acting on glycoproteins, found complementary specificity of two endoglycosidases (Endo D and Endo H), and applied these enzymes for glycoprotein research. Endo-beta-galactosidase C, which hydrolyzes Galalpha1-3Galbeta1-4GlcNAc xenoantigenic determinant, was later found and molecularly cloned. We also found highly branched poly-N-acetyllactosamines in early embryonic cells, and demonstrated developmentally regulated carbohydrate changes during early mammalian development. The binding site for Dolichos biflorus agglutinin was introduced as a new differentiation marker. Basigin and embigin, two related members of the immunoglobulin superfamily, a sialomucin MGC-24 and other glycoproteins were discovered as carriers of developmentally regulated carbohydrate markers. We proposed enhancement of integrin action as a function of sugar chains with Lewis X epitope, and observed a relationship between the expression of carbohydrate markers and invasive properties of human carcinoma. Midkine, a heparin-binding growth factor, was discovered more recently and its interaction with heparin and oversulfated chondroitin sulfate was elucidated. N-Acetylglucosamine-6-sulfotransferase was cloned and used to reconstitute L-selectin ligands. Gene knockout was applied to reveal in vivo function of basigin, syndecan-4 and chondroitin 6-sulfate. Throughout my research on all these subjects, I have been fortunate in obtaining unexpected observations and enjoying fruitful collaborations.

摘要

许多研究人员采用多学科方法证实,细胞表面碳水化合物是调节各种细胞存活、迁移、黏附、生长和分化的识别系统的重要组成部分。本文描述了我们自身在这一令人兴奋的领域中的经验和贡献。我们发现了Endo D,这是首个作用于糖蛋白的内切糖苷酶,发现了两种内切糖苷酶(Endo D和Endo H)的互补特异性,并将这些酶应用于糖蛋白研究。后来发现并分子克隆了水解Galα1-3Galβ1-4GlcNAc异种抗原决定簇的β-半乳糖苷内切酶C。我们还在早期胚胎细胞中发现了高度分支的多聚N-乙酰乳糖胺,并证明了哺乳动物早期发育过程中碳水化合物的发育调控变化。引入了双花扁豆凝集素的结合位点作为一种新的分化标志物。发现免疫球蛋白超家族的两个相关成员基底膜蛋白和胚泡膜蛋白、一种唾液黏蛋白MGC-24以及其他糖蛋白是发育调控碳水化合物标志物的载体。我们提出,具有Lewis X表位的糖链可增强整合素的作用,并观察到碳水化合物标志物的表达与人类癌侵袭特性之间的关系。最近发现了一种肝素结合生长因子中期因子,并阐明了其与肝素和过度硫酸化硫酸软骨素的相互作用。克隆了N-乙酰葡糖胺-6-硫酸转移酶,并用于重构L-选择素配体。应用基因敲除技术揭示基底膜蛋白、多配体蛋白聚糖-4和硫酸软骨素6-硫酸酯在体内的功能。在我对所有这些主题的研究过程中,我有幸获得了意外的发现,并享受了富有成果的合作。

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