Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Anal Chem. 2010 Dec 15;82(24):9967-76. doi: 10.1021/ac1019039. Epub 2010 Nov 16.
A simple, low-cost capillary electrophoresis-mass spectrometry (CE-MS) method is demonstrated for the simultaneous analysis of amino acids and small carboxylic acids (glycerate, lactate, fumarate, succinate, malate, tartrate, citrate, iso-citrate, cis-aconitate, and shikimate). All CE-MS experiments were performed using a single uncoated fused-silica capillary and with a single separation electrolyte, formic acid. For CE polarity, the CE inlet was set as the anode, and the MS side was set as the cathode. By using high-speed sheath gas flow, the apparent mobilities of all compounds were sped up; thus, the migration times of the carboxylic acids were reduced. In positive ion mode ESI-MS detection, small carboxylic acids were detected faintly as m/z = M + 18 or M + 23, after protonated molecule detection (m/z = M + 1) of the amino acids. In negative ion mode, all of these small carboxylic acids were detected clearly as deprotonated molecules (m/z = M - 1), after detection of the amino acids. By changing the polarity of the MS during CE separation, both amino acids and small carboxylic acids were detectable in a single electrophoresis analysis run. With this method, the diurnal metabolic changes of pineapple leaves were observed as reflecting Crassulacean acid metabolism.
一种简单、低成本的毛细管电泳-质谱(CE-MS)方法被证明可用于同时分析氨基酸和小羧酸(甘油酸、乳酸、富马酸、琥珀酸、苹果酸、酒石酸、柠檬酸、异柠檬酸、顺乌头酸和莽草酸)。所有的 CE-MS 实验都使用单根未涂层的熔融石英毛细管和单一分离电解质(甲酸)进行。对于 CE 极性,将 CE 入口设置为阳极,MS 侧设置为阴极。通过使用高速鞘气流量,所有化合物的表观迁移率都得到了提高,从而缩短了羧酸的迁移时间。在正离子模式 ESI-MS 检测中,在检测到氨基酸的质子化分子(m/z = [M + 1](+)后,小羧酸作为 m/z = M + 18 或 M + 23 微弱地被检测到。在负离子模式下,在检测到氨基酸后,所有这些小羧酸都作为去质子化分子(m/z = [M - 1](-))被清晰地检测到。通过在 CE 分离过程中改变 MS 的极性,可以在单次电泳分析运行中同时检测氨基酸和小羧酸。使用这种方法,可以观察菠萝叶的昼夜代谢变化,以反映景天酸代谢。