Kang Pilsoo, Mechref Yehia, Novotny Milos V
Department of Chemistry, Indiana University, Bloomington, IN 47405, USA.
Rapid Commun Mass Spectrom. 2008;22(5):721-34. doi: 10.1002/rcm.3395.
Permethylation of glycans prior to their mass spectrometric determination has now become a time-honored methodology in glycoconjugate analysis due to the advantage of a simultaneous analysis of neutral and acidic glycans as well as enhanced sensitivity and easier tandem mass spectrometry interpretation. While the different solvent extraction-based versions of this method often suffice in different structural studies, they are generally less satisfactory in the quantitative determinations aiming at minor quantities of the analyzed materials. To overcome these difficulties, we recently introduced a solid-phase capillary permethylation technique (Kang et al., Rapid Commun. Mass Spectrom. 2005; 19: 3421) for microscale determination. Here, we describe a very useful high-throughput extension of the solid-phase methodology utilizing spin columns packed with sodium hydroxide beads. This procedure has been thoroughly optimized to match the analytical performance parameters of the previously used capillary technique. As demonstrated with a high-precision glycomic profiling analysis of human blood serum, this methodological improvement offers simplicity and reproducibility, allowing the complete permethylation of 12-18 samples in less than 20 min.
在进行质谱测定之前对聚糖进行全甲基化,由于其能够同时分析中性和酸性聚糖,以及具有更高的灵敏度和更易于进行串联质谱解释的优点,现已成为糖缀合物分析中一种历史悠久的方法。虽然该方法基于不同溶剂萃取的版本在不同的结构研究中通常足够,但在针对少量分析材料的定量测定中,它们通常不太令人满意。为了克服这些困难,我们最近引入了一种用于微量测定的固相毛细管全甲基化技术(Kang等人,《快速质谱通讯》,2005年;19:3421)。在此,我们描述了一种利用填充有氢氧化钠珠的旋转柱对固相方法进行的非常有用的高通量扩展。该程序已进行了全面优化,以匹配先前使用的毛细管技术的分析性能参数。正如通过对人血清进行的高精度糖组分析所证明的那样,这种方法改进提供了简单性和可重复性,能够在不到20分钟的时间内对12 - 18个样品进行完全全甲基化。