Chiesa C, O'Neill R A
Perkin-Elmer Corporation, Applied Biosystems Division, Foster City, CA 94404.
Electrophoresis. 1994 Aug-Sep;15(8-9):1132-40. doi: 10.1002/elps.11501501171.
Malto-oligosaccharides were derivatized via their reducing ends with different aminoaphthalene mono-, di- and trisulfonic acids by reductive amination. The derivatives were then separated by capillary zone electrophoresis in uncoated fused silica capillaries, using 50 mM triethylammonium phosphate buffer, pH 2.5, as running electrolyte. The effect of degree of charge on speed of analysis and resolution was studied for different aminonaphthalene mono-, di- and trisulfonic acids. Under the conditions used, a higher degree of charge on the derivatives provided both faster analyses and higher resolution. Investigation of the electrophoretic behavior of derivatized oligosaccharides obtained from bovine pancreatic ribonuclease B gave insight into the possibility of applying such electrophoretic systems to the analysis of more complex carbohydrates. The resolution of positional isomers under the conditions described indicated that the high resolving power of this technique allows separations not strictly based on the effects of charge and mass of the analytes, but on structural characteristics as well. The relationship between electrophoretic mobility and molecular structure was investigated for the different derivatives.
通过还原胺化反应,麦芽寡糖在其还原端与不同的氨基萘单磺酸、二磺酸和三磺酸进行衍生化。然后,使用50 mM磷酸三乙铵缓冲液(pH 2.5)作为运行电解质,在未涂层熔融石英毛细管中通过毛细管区带电泳对衍生物进行分离。研究了不同氨基萘单磺酸、二磺酸和三磺酸的电荷程度对分析速度和分辨率的影响。在所使用的条件下,衍生物上更高的电荷程度能实现更快的分析速度和更高的分辨率。对从牛胰核糖核酸酶B获得的衍生化寡糖的电泳行为进行研究,有助于深入了解将这种电泳系统应用于更复杂碳水化合物分析的可能性。在所描述的条件下,位置异构体的分离表明,该技术的高分辨率不仅允许基于分析物的电荷和质量效应进行分离,还能基于结构特征进行分离。研究了不同衍生物的电泳迁移率与分子结构之间的关系。