Bouchez-Mahiout I, Doyen C, Laurière M
Laboratoire de Chimie Biologique, Centre INRA de Versailles-Grignon, Thiverval-Grignon, France.
Electrophoresis. 1999 Jun;20(7):1412-7. doi: 10.1002/(SICI)1522-2683(19990601)20:7<1412::AID-ELPS1412>3.0.CO;2-A.
The detection of glycoproteins based on the periodate oxidation of their carbohydrate moiety, and their conjugation to digoxigenin hydrazide directly on blots, leads to high background staining, especially with polyvinylidene difluoride (PVDF) membranes. The addition of Tween-20 to all incubation solutions, except at the oxidation step, strongly reduced the background staining and allowed us to detect lower amounts of glycans fixed on the blots through the protein moiety. The presence of polysaccharides during the oxidation step was shown to produce side reactions that led to the staining of nonglycosylated proteins; it demonstrated risks that may occur with crude extracts when periodate oxidation is performed in solution. The phenomenon was used to design a total protein-staining assay that can be included along with positive and negative controls in a general strategy based on blotting, which was delineated for the identification of glycoproteins in complex tissue extracts.
基于糖蛋白碳水化合物部分的高碘酸盐氧化以及它们直接在印迹上与地高辛酰肼偶联来检测糖蛋白,会导致高背景染色,尤其是使用聚偏二氟乙烯(PVDF)膜时。除氧化步骤外,在所有孵育溶液中添加吐温-20可显著降低背景染色,并使我们能够通过蛋白质部分检测到印迹上固定的较低量聚糖。结果表明,氧化步骤中多糖的存在会产生副反应,导致非糖基化蛋白质染色;这表明在溶液中进行高碘酸盐氧化时,粗提物可能会出现风险。该现象被用于设计一种总蛋白染色测定法,该方法可与阳性和阴性对照一起纳入基于印迹的通用策略中,该策略已被描述用于鉴定复杂组织提取物中的糖蛋白。