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缓冲液组成对8-氨基萘-1,3,6-三磺酸标记的单糖和复合碳水化合物毛细管电泳中分离效率和分辨率的影响。

The influence of buffer composition on separation efficiency and resolution in capillary electrophoresis of 8-aminonaphthalene-1,3,6-trisulfonic acid labeled monosaccharides and complex carbohydrates.

作者信息

Klockow A, Amado R, Widmer H M, Paulus A

机构信息

Ciba, Corporate Analytical Research, Zurich, Switzerland.

出版信息

Electrophoresis. 1996 Jan;17(1):110-9. doi: 10.1002/elps.1150170119.

Abstract

The effect of buffer conditions -- varying in salt type, pH, and concentration -- on the separation of 8-aminonaphthalene-1,3,6-trisulfonic acid (ANTS)-labeled monosaccharides and complex-type carbohydrates was investigated. Different buffer systems for high and low electroosmotic flow conditions were chosen: a phosphate and a citrate background electrolyte, each at pH 2.5, a phosphate buffer, pH 9.0, and a borate buffer at pH 9.5. All buffer systems displayed differences in resolution and selectivity. Phosphate and borate buffer demonstrated the greatest selectivity changes for ANTS-labeled carbohydrates. While separation in the phosphate system relies mainly on differences in the charge-to-mass-ratio, additional selectivity can be achieved with borate complexation of glycoconjugates. The use of borate buffers improved monosaccharide separations whereas complex carbohydrates showed a loss in resolution. The citrate background electrolyte at low pH caused no significant changes in the separation performance. The pH 9.0 phosphate buffer showed a reversed migration order of the ANTS conjugates with a decreased resolution, compared to the pH 2.5 phosphate buffer, due to the strong electroosmotic flow generated under high pH conditions. An ovalbumin-derived oligosaccharide library demonstrates the significance of buffer selectivity for complex carbohydrate separations. The separation in the acidic phosphate and the alkaline borate buffer generates a different pattern and only the combination of both buffer systems allows an appropriate assessment of sample complexity.

摘要

研究了缓冲条件(盐类型、pH值和浓度各不相同)对8-氨基萘-1,3,6-三磺酸(ANTS)标记的单糖和复合碳水化合物分离的影响。针对高和低电渗流条件选择了不同的缓冲系统:pH值为2.5的磷酸盐和柠檬酸盐背景电解质、pH值为9.0的磷酸盐缓冲液以及pH值为9.5的硼酸盐缓冲液。所有缓冲系统在分辨率和选择性方面均表现出差异。磷酸盐和硼酸盐缓冲液对ANTS标记的碳水化合物表现出最大的选择性变化。在磷酸盐系统中,分离主要依赖于质荷比的差异,而通过糖缀合物与硼酸盐的络合可以实现额外的选择性。使用硼酸盐缓冲液可改善单糖的分离,而复合碳水化合物的分辨率则有所下降。低pH值的柠檬酸盐背景电解质在分离性能方面未引起显著变化。与pH值为2.5的磷酸盐缓冲液相比,pH值为9.0的磷酸盐缓冲液由于在高pH条件下产生强烈的电渗流,导致ANTS缀合物的迁移顺序颠倒且分辨率降低。一个源自卵清蛋白的寡糖文库证明了缓冲液选择性对复合碳水化合物分离的重要性。在酸性磷酸盐和碱性硼酸盐缓冲液中的分离产生了不同的模式,只有两种缓冲系统的组合才能对样品复杂性进行适当评估。

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