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Determination of the sialylation level and of the ratio alpha-(2 -> 3)/alpha-(2 -> 6) sialyl linkages of N-glycans by methylation and GC/MS analysis

机译:通过甲基化和GC / MS分析确定N-聚糖的唾液酸化水平和比例α-(2-> 3)/α-(2-> 6)唾液酸键

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A methodology for the determination of the sialylation pattern of N-glycans, extent of sialylation and the ratio between alpha-(2-->3) and alpha-(2-->6) sialyl linkages, is presented based on the labelling of the C-3 and C-6 hydroxyl groups of Gal residues obtained after permethylation, saponification, selective desialylation of sialylated oligosaccharides and methanolysis. Deuteromethylation and GC/MS analysis of Gal derivatives allow to determine the sialylation level of glycans. O-Ethyl ether labelling followed by GC analysis of the resulting Gal derivatives allows to obtain the ratio between alpha-(2-->3) and alpha-(2-->6) sialyl linkages. The method was applied to LNT (LcOse(4): beta-D-Galp-(1 -->3)-beta-D-GlcpNAc-(1-->3)-beta-D-Galp-(1-->4)-D-Glcp), LSTa (IV(3)NeuAcLcOse(4): alpha-Neu-p5Ac-(2-->3)-beta-D-Galp-(1--> 3)-beta-D-GlcpNAc-(1-->3)-beta-D-Galp-(1-->4)-D-Glcp), LSTc (IV(6)NeuAcn LcOse(4): alpha-Neup5Ac-(2-->6)-beta-D-Galp-(1-->4)-beta-D-GlcpNAc-(1-->3)-beta-D-Ga lp-(1-->4)-D-Glcp) and a bisialylated biantennary N-glycan in which sialic acid is bound to Gal residues via an alpha-(2-->6) linkage. Using this method, it was found that 92.8% of N-glycans in bovine fetuin is sialylated and that the ratio of alpha-(2-->6) versus alpha-(2-->3) sialyl linkages was 31:19. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 21]
机译:基于N的标记,提出了一种确定N-聚糖唾液酸化模式,唾液酸化程度以及α-(2-> 3)和α-(2-> 6)唾液酸键之间的比率的方法。经过甲基化,皂化,唾液酸化寡糖选择性脱唾液酸化和甲醇分解后获得的Gal残基的C-3和C-6羟基。 Gal衍生物的氘代甲基化和GC / MS分析可以确定聚糖的唾液酸化水平。用O-乙基醚标记,然后对所得的Gal衍生物进行GC分析,可以得到α-(2-> 3)和α-(2-> 6)唾液酸键之间的比率。该方法应用于LNT(LcOse(4):beta-D-Galp-(1-> 3)-beta-D-GlcpNAc-(1-> 3)-beta-D-Galp-(1-- > 4)-D-Glcp),LSTa(IV(3)NeuAcLcOse(4):alpha-Neu-p5Ac-(2-> 3)-beta-D-Galp-(1-> 3)-beta- D-GlcpNAc-(1-> 3)-beta-D-Galp-(1-> 4)-D-Glcp),LSTc(IV(6)NeuAcn LcOse(4):alpha-Neup5Ac-(2- -> 6)-beta-D-Galp-(1-> 4)-beta-D-GlcpNAc-(1-> 3)-beta-D-Ga lp-(1-> 4)-D- (Glcp)和双唾液酸化双触角N-聚糖,其中唾液酸通过alpha-(2-> 6)键与Gal残基结合。使用该方法,发现牛胎球蛋白中的92.8%的N-聚糖被唾液酸化,并且α-(2-→6)与α-(2-→3)唾液酸键的比例为31:19。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:21]

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