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一种无需除去过量试剂即可用于还原胺化糖的毛细管电泳分析的新条件。

A novel condition for capillary electrophoretic analysis of reductively aminated saccharides without removal of excess reagents.

机构信息

Faculty of Pharmaceutical Sciences, Kinki University, Kowakae, Higashi-Osaka, Osaka, Japan.

出版信息

Electrophoresis. 2013 Dec;34(22-23):3198-205. doi: 10.1002/elps.201200612. Epub 2013 Oct 23.

Abstract

We have identified novel CE conditions for the separation of 7-amino-4-methylcoumarin-labeled monosaccharides and oligosaccharides from glycoproteins. Using a neutrally coated capillary and alkaline borate buffer containing hydroxypropylcellulose and ACN, saccharide derivatives form anionic borate complexes, which move from the cathode to the anode in an electric field and are detected near the anodic end. Excess labeling reagents and other fluorescent products remain at the cathodic end. Fluorimetric detection using an LED as a light source enables determination of monosaccharide derivatives with good linearity between at least 0.4 and 400 μM, may correspond to 140 amol to 140 fmol. The lower LOD (S/N = 5) is only 80 nM in the sample solution (ca. 28 amol). The results were comparable to reported values using fluorometric detection LC. The method was also applied to the analysis of oligosaccharides that were enzymatically released from glycoproteins. Fine resolution enables profiling of glycans in glycoproteins. The applicability of the method was examined by applying it to other derivatives labeled with nonacidic tags such as ethyl p-aminobenzoate- and 2-aminoacridone-labeled saccharides.

摘要

我们已经确定了用于从糖蛋白中分离 7-氨基-4-甲基香豆素标记的单糖和寡糖的新型 CE 条件。使用中性涂层毛细管和含有羟丙基纤维素和 ACN 的碱性硼酸盐缓冲液,糖衍生物形成阴离子硼酸盐配合物,在电场中从阴极向阳极移动,并在阳极末端附近检测到。过量的标记试剂和其他荧光产物仍留在阴极末端。使用 LED 作为光源进行荧光检测可实现单糖衍生物的良好线性度,至少在 0.4 和 400 μM 之间,可能对应于 140 amol 至 140 fmol。在样品溶液中的较低 LOD(S/N = 5)仅为 80 nM(约 28 amol)。结果与使用荧光检测 LC 报告的值相当。该方法还应用于从糖蛋白中酶解释放的寡糖的分析。精细分辨率可实现糖蛋白中聚糖的分析。该方法的适用性通过将其应用于用非酸性标签(如乙基对氨基苯甲酸酯和 2-氨基吖啶酮标记的糖)标记的其他衍生物进行了检验。

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