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使用凝集素分析IgG中的糖基化变化。

Analysis of glycosylation changes in IgG using lectins.

作者信息

Sumar N, Bodman K B, Rademacher T W, Dwek R A, Williams P, Parekh R B, Edge J, Rook G A, Isenberg D A, Hay F C

机构信息

Department of Immunology, University College and Middlesex School of Medicine, London, U.K.

出版信息

J Immunol Methods. 1990 Jul 20;131(1):127-36. doi: 10.1016/0022-1759(90)90242-n.

Abstract

A simple rapid assay based on the ability of lectins to bind carbohydrates has been developed to analyse changes in the oligosaccharide chains of IgG. Bandeiraea simplicifolia lectin and Ricinus communis agglutinin have been used to detect terminal N-acetylglucosamine and galactose moieties respectively in IgG using immunodot-blotting. IgG samples (approximately 1 micrograms) were dot-blotted onto nitrocellulose followed by boiling of the blots to expose the carbohydrate moieties. The blots were then treated with biotinylated lectins followed by either streptavidin-biotin-hydrogen peroxidase conjugate or 125I-labelled streptavidin. The colour was developed using chloronaphthol and the blots read on a densitometer. The labelled blots were cut and read on a gamma counter. The use of a monoclonal antibody to N-acetylglucosamine is also discussed. The results obtained using this method are comparable to those obtained by structural analysis.

摘要

基于凝集素与碳水化合物结合能力开发了一种简单快速的检测方法,用于分析IgG寡糖链的变化。已使用单叶豆凝集素和蓖麻凝集素,通过免疫斑点印迹法分别检测IgG中的末端N-乙酰葡糖胺和半乳糖部分。将IgG样品(约1微克)点印迹到硝酸纤维素膜上,然后将印迹膜煮沸以暴露碳水化合物部分。然后用生物素化的凝集素处理印迹膜,接着用链霉亲和素-生物素-过氧化氢酶缀合物或125I标记的链霉亲和素处理。使用氯萘酚显色,并在密度计上读取印迹膜。将标记的印迹膜切割下来并在γ计数器上读取。还讨论了使用抗N-乙酰葡糖胺单克隆抗体的情况。用该方法获得的结果与通过结构分析获得的结果相当。

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