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用化学合成的寡糖研究 R-10G 和 TRA-1-60/81 的结合特异性,以及角质酶 II 的底物特异性。

Binding specificity of R-10G and TRA-1-60/81, and substrate specificity of keratanase II studied with chemically synthesized oligosaccharides.

机构信息

Research Center for Glycobiotechnology, Ritsumeikan University, Noji-Higashi, 1-1-1, Kusatsu, Shiga, 525-8577, Japan.

Research Center for Glycobiotechnology, Ritsumeikan University, Shiga, 525-8577, Japan.

出版信息

Glycoconj J. 2017 Dec;34(6):789-795. doi: 10.1007/s10719-017-9765-8. Epub 2017 Mar 14.

Abstract

Recently, we established a mouse monoclonal antibody specific to hiPS/ hES cells, R-10G, which recognizes a type of keratan sulfate. Keratan sulfates (KS) comprise a family of glycosaminoglycans consisting of the repeating unit of [Gal-GlcNAc(6S)]. However, there is a diversity in the degree of sulfation at Gal and GlcNAc residues, and also in the mode of linkage, Galβ1 - 3GlcNAc (type 1) or Galβ1 - 4GlcNAc (type 2). To gain more insight into the binding specificity of R-10G, we carried out an ELISA test on avidin-coated plates using polyethylene glycol (PEG)-biotinylated derivatives of a series of N-acetyllactosamine tetrasaccharides (keratan sulfates (KSs)). The results suggested that the minimum epitope structure is Galβ1 - 4GlcNAc(6S)β1 - 3Galβ1 - 4GlcNAc(6S)β1 (type 2- type 2 keratan sulfate). Removal of sulfate from GlcNAc(6S) or addition of sulfate to Gal abolished the binding activity almost completely. We also examined the binding specificity of TRA-1-60/81 in the same assay system. The minimum epitope structure was shown to be Galβ1 - 3GlcNAcβ1 - 3Galβ1 - 4GlcNAcβ1 in agreement with the previous study involving glycan arrays (Natunen et al., Glycobiology, 21, 1125-1130 (2011)). Interestingly, however, TRA-1-60/81 was shown to bind to Galβ1 - 3GlcNAc(6S)β1 - 3Galβ1 - 4GlcNAc(6S)β1 (type 1- type 2 keratan sulfate) dose-dependently, being more than one-third the binding activity toward Galβ1 - 3GlcNAcβ1 - 3Galβ1 - 4GlcNAcβ1 than in the case of TRA-1-60. In addition, a substrate specificity study on keratanase II revealed that keratanase II degraded not only "type 2-type 2 keratan sulfate" but also "type 1-type 2 keratan sulfate", significantly.

摘要

最近,我们建立了一种针对 hiPS/hES 细胞的特异性鼠单克隆抗体 R-10G,它识别一种角蛋白硫酸盐。角蛋白硫酸盐(KS)由重复单元[Gal-GlcNAc(6S)]组成的糖胺聚糖家族组成。然而,Gal 和 GlcNAc 残基的硫酸化程度以及连接方式存在多样性,Galβ1-3GlcNAc(类型 1)或 Galβ1-4GlcNAc(类型 2)。为了更深入地了解 R-10G 的结合特异性,我们在亲和素包被的平板上进行了 ELISA 测试,使用聚乙二醇(PEG)-生物素化的一系列 N-乙酰乳糖胺四糖(角蛋白硫酸盐(KSs))衍生物。结果表明,最小表位结构为 Galβ1-4GlcNAc(6S)β1-3Galβ1-4GlcNAc(6S)β1(类型 2-类型 2 角蛋白硫酸盐)。GlcNAc(6S)上的硫酸根的去除或 Gal 上的硫酸根的添加几乎完全消除了结合活性。我们还在相同的测定系统中检查了 TRA-1-60/81 的结合特异性。最小表位结构显示为 Galβ1-3GlcNAcβ1-3Galβ1-4GlcNAcβ1,与涉及聚糖阵列的先前研究一致(Natunen 等人,Glycobiology,21,1125-1130(2011))。然而,有趣的是,TR-1-60/81 被证明以剂量依赖性方式结合 Galβ1-3GlcNAc(6S)β1-3Galβ1-4GlcNAc(6S)β1(类型 1-类型 2 角蛋白硫酸盐),其结合活性比 TRA-1-60 对 Galβ1-3GlcNAcβ1-3Galβ1-4GlcNAcβ1 的结合活性高三分之一以上。此外,对角蛋白酶 II 的底物特异性研究表明,角蛋白酶 II 不仅降解“类型 2-类型 2 角蛋白硫酸盐”,而且显著降解“类型 1-类型 2 角蛋白硫酸盐”。

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