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通过糖肽酶、外切糖苷酶和高效液相色谱联用对N-连接寡糖进行结构分析。

Structural analysis of N-linked oligosaccharides by a combination of glycopeptidase, exoglycosidases, and high-performance liquid chromatography.

作者信息

Tomiya N, Kurono M, Ishihara H, Tejima S, Endo S, Arata Y, Takahashi N

机构信息

Mie Research Laboratory, Sanwa Kagaku Kenkyusho Co. Ltd., Japan.

出版信息

Anal Biochem. 1987 Jun;163(2):489-99. doi: 10.1016/0003-2697(87)90253-3.

Abstract

A simple, sensitive, and rapid method for the analysis of structures of N-linked carbohydrates is reported. The method involves four steps: preparation of carbohydrate chains from glycopeptides by N-oligosaccharide glycopeptidase digestion; derivatization of the reducing ends of carbohydrate chains with a fluorescent reagent, 2-aminopyridine, by using sodium cyanoborohydride; separation of oligosaccharide derivatives by reverse-phase high-performance liquid chromatography; and structural analysis of oligosaccharides by sequential exoglycosidase digestion. The elution positions of 50 standard oligosaccharide derivatives were determined by HPLC. The structure of an unknown oligosaccharide can be characterized by comparison of its elution position with those of the standard compounds. The method was applied to elucidate the structures of oligosaccharides in the myeloma IgG protein, Yot.

摘要

报道了一种用于分析N-连接碳水化合物结构的简单、灵敏且快速的方法。该方法包括四个步骤:通过N-寡糖糖肽酶消化从糖肽制备碳水化合物链;使用氰基硼氢化钠,用荧光试剂2-氨基吡啶对碳水化合物链的还原端进行衍生化;通过反相高效液相色谱分离寡糖衍生物;以及通过顺序外切糖苷酶消化对寡糖进行结构分析。通过高效液相色谱法测定了50种标准寡糖衍生物的洗脱位置。未知寡糖的结构可通过将其洗脱位置与标准化合物的洗脱位置进行比较来表征。该方法被用于阐明骨髓瘤IgG蛋白Yot中寡糖的结构。

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