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吡啶基化 N-连接中性和唾液酸化寡糖的三维洗脱图谱

Three-dimensional elution mapping of pyridylaminated N-linked neutral and sialyl oligosaccharides.

作者信息

Takahashi N, Nakagawa H, Fujikawa K, Kawamura Y, Tomiya N

机构信息

GlycoLab, Nakano Vinegar Company Ltd., Handa-City, Japan.

出版信息

Anal Biochem. 1995 Mar 20;226(1):139-46. doi: 10.1006/abio.1995.1201.

DOI:10.1006/abio.1995.1201
PMID:7540366
Abstract

We propose a three-dimensional (3-D) sugar-mapping technique for pyridylaminated (PA) neutral and sialyl oligosaccharides as a powerful structural characterization of N-linked oligosaccharides using only picomoles of samples. The new map consists of the elution data from 42 different sialyl oligosaccharides, 26 of which are mono-, 7 of which are di-, 7 of which are tri-, and 2 of which are tetra-sialylated oligosaccharides. The 20 standard sialyl oligosaccharides were released from human serum and calf fetuin by digestion with glycoamidase A. The other 22 standard sialyl oligosaccharides were obtained by subsequent digestion of the above 20 sialyl oligosaccharides with beta-galactosidase, beta-N-acetylhexosaminidase, alpha-fucosidase, and alpha 2-->3 specific sialidase. The present 3-D mapping method involves the following four steps: First, a neutral and sialyl PA-oligosaccharide mixture is separated by HPLC on the diethylaminoethyl (DEAE) column according to the sialic acid content, and the elution data are considered as one of the three dimensions (Z-axis). Then, neutral, mono-, di-, tri-, and tetra-sialyl oligosaccharides are individually separated on the octadecylsilyl (ODS)-silica (X-axis) and amide-silica (Y-axis) columns. The fourth step is to plot the coordinates on a two-dimensional (2-D) map. Thus, for each of the groups separated on the DEAE column, a 2-D map can be achieved. By repeating the whole process for each group of different sialylation, the layers of the 2-D map lined up on the Z-axis form a 3-D map.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们提出了一种用于吡啶基胺化(PA)中性和唾液酸化寡糖的三维(3-D)糖图谱技术,该技术仅使用皮摩尔级别的样品就能对N-连接寡糖进行强大的结构表征。新图谱包含42种不同唾液酸化寡糖的洗脱数据,其中26种为单唾液酸化、7种为二唾液酸化、7种为三唾液酸化、2种为四唾液酸化寡糖。20种标准唾液酸化寡糖通过用糖酰胺酶A消化从人血清和小牛胎球蛋白中释放出来。另外22种标准唾液酸化寡糖是通过用β-半乳糖苷酶、β-N-乙酰己糖胺酶、α-岩藻糖苷酶和α2→3特异性唾液酸酶对上述20种唾液酸化寡糖进行后续消化获得的。目前的三维图谱方法包括以下四个步骤:首先,中性和唾液酸化PA-寡糖混合物在二乙氨基乙基(DEAE)柱上通过高效液相色谱(HPLC)根据唾液酸含量进行分离,洗脱数据被视为三维之一(Z轴)。然后,中性、单、二、三、四唾液酸化寡糖分别在十八烷基硅烷(ODS)-硅胶(X轴)和酰胺-硅胶(Y轴)柱上分离。第四步是在二维(2-D)图谱上绘制坐标。因此,对于在DEAE柱上分离的每组,都可以获得一个二维图谱。通过对每组不同唾液酸化重复整个过程,在Z轴上排列的二维图谱层形成一个三维图谱。(摘要截断于250字)

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