Oefner P J, Chiesa C
Department of Genetics, Stanford University, CA 94305-5120.
Glycobiology. 1994 Aug;4(4):397-412. doi: 10.1093/glycob/4.4.397.
Capillary electrophoresis has emerged as a highly promising technique for the analysis of mono- and oligosaccharides. The approaches developed for overcoming the lack of chromophoric and fluorophoric functions in most carbohydrates involve the use of indirect photometric detection, amperometry, mass spectrometry, and precolumn derivatization with various tags. The merits and drawbacks of the derivatizing agents, including 2-aminopyridine, 4-amino-benzoic acid and its analogues, which for the first time permitted the reproducible determination of aldoses, uronic acids and even ketoses in the low femtomole range by means of readily available UV detection, and other agents such as 8-aminonaphthalene-1,3,6-trisulphonic acid, 1-phenyl-3-methyl-5-pyrazolone and 3-(4-carboxybenzoyl)-2-quinoline-carboxaldehyde, are discussed in detail. Means to secure electromigration of the usually neutral carbohydrates are: (i) ionization of hydroxyl groups at high pH; (ii) complexation of vicinal or alternate hydroxyl groups with borate or other charged compounds such as alkaline earth metal ions; (iii) derivatization with a reagent possessing ionizable functions; and (iv) partitioning into a pseudostationary phase such as sodium dodecyl sulphate micelles. Each alternative has its own analytical rewards, and combinations of the above mechanisms allow the two-dimensional and perhaps even three-dimensional mapping of oligosaccharides. Pyridylaminated oligosaccharides, for instance, have been separated both according to size by exploiting differences in the charge-to-mass ratio, with the charge being identical for each oligomer under acidic conditions due to protonation of the imino group incorporated by precolumn derivatization, as well as on the basis of structural differences, as a consequence of differences in the ease of borate complexation of the peripheral monosaccharide residues. It is also shown that the 4-aminobenzonitrile derivatives of mono- and disaccharides can be separated by micellar electrokinetic chromatography with a resolving power superior to that achieved by capillary zone electrophoresis of sugar-borate complexes. Based on the progress made, it can be concluded that capillary electrophoresis represents a powerful alternative and complement to existing methodology in the area of carbohydrate analysis.
毛细管电泳已成为一种极具前景的单糖和寡糖分析技术。为克服大多数碳水化合物缺乏发色和荧光功能的问题而开发的方法包括使用间接光度检测、安培法、质谱法以及用各种标签进行柱前衍生化。详细讨论了衍生剂的优缺点,包括2-氨基吡啶、4-氨基苯甲酸及其类似物,它们首次通过易于获得的紫外检测实现了低飞摩尔范围内醛糖、糖醛酸甚至酮糖的可重现测定,以及其他试剂,如8-氨基萘-1,3,6-三磺酸、1-苯基-3-甲基-5-吡唑酮和3-(4-羧基苯甲酰基)-2-喹啉甲醛。确保通常呈中性的碳水化合物发生电迁移的方法有:(i) 在高pH下使羟基离子化;(ii) 使邻位或相间羟基与硼酸盐或其他带电化合物(如碱土金属离子)络合;(iii) 用具有可离子化功能的试剂进行衍生化;(iv) 分配到假固定相(如十二烷基硫酸钠胶束)中。每种方法都有其自身的分析优势,上述机制的组合可实现寡糖的二维甚至三维图谱分析。例如,吡啶基化寡糖已根据电荷与质量比的差异按大小进行分离,由于柱前衍生化引入的亚氨基在酸性条件下质子化,每种寡聚物的电荷相同,同时也基于结构差异进行分离,这是由于外围单糖残基与硼酸盐络合的难易程度不同所致。还表明,单糖和二糖的4-氨基苯腈衍生物可通过胶束电动色谱法分离,其分离能力优于糖-硼酸盐络合物的毛细管区带电泳法。基于所取得的进展,可以得出结论,毛细管电泳是碳水化合物分析领域现有方法的有力替代方法和补充。