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Highly sensitive capillary electrophoresis analysis of N-linked oligosaccharides in glycoproteins following fluorescence derivatization with rhodamine 110 and laser-induced fluorescence detection

机译:罗丹明110荧光衍生化和激光诱导荧光检测后糖蛋白中N-连接寡糖的高灵敏毛细管电泳分析

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摘要

We describe a highly sensitive CE with laser-induced fluorescence (LIF) detection for the analysis of N-linked oligosaccharides in glycoproteins using rhodamine 110 as a fluorescence derivatization reagent. One CE separation is performed using a fused-silica capillary and neutral pH buffer conditions and allows for the separation of sialo-oligosaccharides according to the number of sialic acids. An alternate separation is performed using the same capillary and acidic pH buffer conditions, enabling the separation of asialo-oligosaccharides according to their sizes. The derivatization and separation conditions for the analysis of sialo- and asialo-oligosaccharides were optimized. Furthermore, we applied the proposed method for the analyses of N-linked sialo- and asialo-oligosaccharides in glycoproteins (ribonuclease B, fetuin, and recombinant human erythropoietin).
机译:我们描述了一种高灵敏度的CE与激光诱导荧光(LIF)检测,用于使用罗丹明110作为荧光衍生试剂来分析糖蛋白中的N-连接寡糖。使用熔融硅胶毛细管和中性pH缓冲液条件进行一次CE分离,并根据唾液酸的数量进行唾液寡糖的分离。使用相同的毛细管和酸性pH缓冲液条件进行替代分离,从而能够根据脱唾液酸寡糖的大小进行分离。优化了唾液寡糖和去唾液寡糖分析的衍生化和分离条件。此外,我们将提出的方法用于糖蛋白(核糖核酸酶B,胎球蛋白和重组人促红细胞生成素)中N-连接的唾液寡糖和去唾液酸寡糖的分析。

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