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利用表面等离子体共振对糖蛋白寡糖进行表征

Characterization of glycoprotein oligosaccharides using surface plasmon resonance.

作者信息

Hutchinson A M

机构信息

Department of Natural Products Discovery, Glaxo Research and Development Ltd., Greenford, Middlesex, United Kingdom.

出版信息

Anal Biochem. 1994 Aug 1;220(2):303-7. doi: 10.1006/abio.1994.1341.

Abstract

Surface plasmon resonance was used to characterize the carbohydrate moieties of bovine fetuin. This technique, requiring no sample derivatization or labeling, identified the presence and composition of both N- and O-linked oligosaccharides, using a combination of lectin probes and in situ glycosidase digestion. A complete analysis was achieved using 1.4 micrograms of pure bovine fetuin, and was fully automated using Pharmacia's BIA-core. The presence or absence of specific oligosaccharide structures was determined by the binding of a panel of unlabeled lectins. Monosaccharide order and linkages were determined by sequential digestion using a range of specific exoglycosidases. This novel method implementing in situ digestion was achieved using a modification to the BIAcore software, allowing the flow of reagent over the sensor chip to be stopped for variable lengths of time, thereby permitting enzymatic digestion to occur. This technique can be applied to other commercial SPR biosensors currently available. Glycoanalysis by SPR uses approximately 100- to 1000-fold less protein than comparable analyses using alternative techniques such as gel permeation chromatography of released oligosaccharides, labeled lectin binding, or mass spectrometry.

摘要

表面等离子体共振技术被用于表征牛胎球蛋白的碳水化合物部分。该技术无需对样品进行衍生化或标记,通过结合凝集素探针和原位糖苷酶消化来鉴定N-连接和O-连接寡糖的存在及组成。使用1.4微克纯牛胎球蛋白即可完成全面分析,并且使用Pharmacia公司的BIA-core实现了完全自动化。通过一组未标记凝集素的结合来确定特定寡糖结构的存在与否。通过使用一系列特定的外切糖苷酶进行顺序消化来确定单糖顺序和连接方式。这种实施原位消化的新方法是通过对BIAcore软件进行修改实现的,该修改允许试剂在传感器芯片上流动的时间停止可变长度,从而使酶消化得以发生。该技术可应用于目前可用的其他商业SPR生物传感器。与使用诸如释放寡糖的凝胶渗透色谱、标记凝集素结合或质谱等替代技术的可比分析相比,通过SPR进行糖分析使用的蛋白质大约少100至1000倍。

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