METACyt Biochemical Analysis Center, Department of Chemistry, Indiana University, Bloomington, IN 47405, USA.
Rapid Commun Mass Spectrom. 2010 Jun 15;24(11):1565-74. doi: 10.1002/rcm.4536.
A simple, sensitive, and reproducible quantitative liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was designed for the simultaneous quantification of monosaccharides derived from glycoprotein and blood serum using a multiple-reaction monitoring (MRM) approach. Sialic acids and neutral monosaccharides were efficiently separated using an amino-bonded silica phase column. Neutral monosaccharide molecules were detected as their aldol acetate anion adducts M + CH(3)CO(2) using electrospray ionization in negative ion MRM mode, while sialic acids were detected as deprotonated ions M-H. The new method did not require a reduction step, and exhibited very high sensitivity to carbohydrates with limits of detection of 1 pg for the sugars studied. The linearity of the described approach spanned over three orders of magnitude (pg to ng). The method was validated for monosaccharides originating from N-linked glycans attached to glycoproteins and glycoproteins found in human blood serum. The method effectively quantified monosaccharides originating from as little as 1 microg of glycoprotein and 5 microL of blood serum. The method was robust, reproducible, and highly sensitive. It did not require reduction, derivatization or postcolumn addition of reagents.
建立了一种简单、灵敏、重现性好的定量液相色谱/串联质谱(LC/MS/MS)方法,采用多反应监测(MRM)模式,可同时定量分析糖蛋白和血清中衍生的单糖。采用氨基键合硅胶柱可有效分离唾液酸和中性单糖。中性单糖分子采用电喷雾电离负离子 MRM 模式,检测到其醛醇乙酸盐阴离子加合物 M+CH(3)CO(2),而唾液酸则检测到去质子化离子 M-H。该方法不需要还原步骤,对碳水化合物具有很高的灵敏度,检测限为研究糖的 1 pg。所描述的方法线性范围跨越三个数量级(pg 至 ng)。该方法对来源于糖蛋白上 N 连接聚糖的单糖和人血清中的糖蛋白进行了验证。该方法可有效定量来源于 1 μg 糖蛋白和 5 μL 血清的单糖。该方法稳定、重现性好且灵敏度高。它不需要还原、衍生化或柱后添加试剂。