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基于1型和2型主链序列的发育调控抗原的负离子电喷雾串联质谱分析和微阵列分析

Negative-Ion Electrospray Tandem Mass Spectrometry and Microarray Analyses of Developmentally Regulated Antigens Based on Type 1 and Type 2 Backbone Sequences.

作者信息

Gao Chao, Zhang Yibing, Liu Yan, Feizi Ten, Chai Wengang

机构信息

Glycosciences Laboratory, Department of Medicine, Imperial College London , Hammersmith Campus, London W12 0NN, U.K.

出版信息

Anal Chem. 2015 Dec 1;87(23):11871-8. doi: 10.1021/acs.analchem.5b03471. Epub 2015 Nov 10.

Abstract

Type 1 (Galβ1-3GlcNAc) and type 2 (Galβ1-4GlcNAc) sequences are constituents of the backbones of a large family of glycans of glycoproteins and glycolipids whose branching and peripheral substitutions are developmentally regulated. It is highly desirable to have microsequencing methods that can be used to precisely identify and monitor these oligosaccharide sequences with high sensitivity. Negative-ion electrospray tandem mass spectrometry with collision-induced dissociation has been used for characterization of branching points, peripheral substitutions, and partial assignment of linkages in reducing oligosaccharides. We now extend this method to characterizing entire sequences of linear type 1 and type 2 chain-based glycans, focusing on the type 1 and type 2 units in the internal regions including the linkages connecting type 1 and type 2 disaccharide units. We apply the principles to sequence analysis of closely related isomeric oligosaccharides and demonstrate by microarray analyses distinct binding activities of antibodies and a lectin toward various combinations of type 1 and 2 units joined by 1,3- and 1,6-linkages. These sequence-specific carbohydrate-binding proteins are in turn valuable tools for detecting and distinguishing the type 1 and type 2-based developmentally regulated glycan sequences.

摘要

1型(Galβ1-3GlcNAc)和2型(Galβ1-4GlcNAc)序列是一大类糖蛋白和糖脂聚糖主链的组成部分,其分支和外周取代受发育调控。非常需要有可用于以高灵敏度精确鉴定和监测这些寡糖序列的微测序方法。具有碰撞诱导解离的负离子电喷雾串联质谱已用于表征还原性寡糖中的分支点、外周取代和部分连接归属。我们现在将此方法扩展到表征基于1型和2型链的线性聚糖的完整序列,重点关注内部区域中的1型和2型单元,包括连接1型和2型二糖单元的连接。我们将这些原理应用于密切相关的异构寡糖的序列分析,并通过微阵列分析证明抗体和凝集素对通过1,3-和1,6-连接连接的1型和2型单元的各种组合具有不同的结合活性。这些序列特异性碳水化合物结合蛋白反过来又是检测和区分基于1型和2型发育调控聚糖序列的有价值工具。

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