Ojima N, Shingaki T, Yamamoto T, Masujima T
Department of Analytical Life Science, Institute of Pharmaceutical Sciences, Hiroshima University, Japan.
Electrophoresis. 2001 Oct;22(16):3478-82. doi: 10.1002/1522-2683(200109)22:16<3478::AID-ELPS3478>3.0.CO;2-X.
A droplet of an electroconductive solution was put on the sample plate of a matrix-assisted laser desorption/ionization-time of flight-mass spectroscope (MALDI-TOF-MS) and the outlet terminal of a capillary Electrophoresis (CE) capillary was put into this droplet in order to make an electro-connection and to apply high voltage between the metallic sample plate and the counter pole of the CE. This procedure was simple and gave much more stable interfacing than that of the electrospray method. Furthermore, the separated component was collected and concentrated in a droplet. By mixing each separated sample spot with the MALDI matrix on the sample plate, the spots were analyzed in separated sequences to make three-dimensional mass chromatograms, or applied to the enzyme digestion analysis for peptide sequencing.
将一滴导电溶液滴在基质辅助激光解吸/电离飞行时间质谱仪(MALDI-TOF-MS)的样品板上,并将毛细管电泳(CE)毛细管的出口端放入该液滴中,以实现电连接并在金属样品板和CE的反电极之间施加高压。该过程简单,并且比电喷雾方法提供更稳定的接口。此外,分离出的成分被收集并浓缩在一个液滴中。通过将每个分离的样品点与样品板上的MALDI基质混合,对这些点进行单独的序列分析以制作三维质量色谱图,或应用于酶消化分析以进行肽测序。