Kato Masaru, Gyoten Yukari, Sakai-Kato Kumiko, Nakajima Tohru, Toyo'oka Toshimasa
Department of Analytical Chemistry, School of Pharmaceutical Sciences and COE Program in the 21st Century, University of Shizuoka, Shizuoka, Japan.
Electrophoresis. 2005 Oct;26(19):3682-8. doi: 10.1002/elps.200500124.
Plastic microchips are very promising analytical devices for the high-speed analysis of biological compounds. However, due to its hydrophobicity, their surface strongly interacts with nonpolar analytes or species containing hydrophobic domains, resulting in a significant uncontrolled adsorption on the channel walls. This paper describes the migration of fluorescence-labeled amino acids and proteins using the poly(methyl methacrylate) microchip. A cationic starch derivative significantly decreases the adsorption of analytes on the channel walls. The migration time of the analytes was related to their molecular weight and net charge or pI of the analytes. FITC-BSA migrated within 2 min, and the theoretical plate number of the peak reached 480,000 plates/m. Furthermore, proteins with a wide range of pI values and molecular weights migrated within 1 min using the microchip.
塑料微芯片是用于生物化合物高速分析的非常有前景的分析装置。然而,由于其疏水性,其表面与非极性分析物或含有疏水结构域的物质强烈相互作用,导致在通道壁上出现显著的不受控制的吸附。本文描述了使用聚甲基丙烯酸甲酯微芯片对荧光标记的氨基酸和蛋白质的迁移情况。一种阳离子淀粉衍生物显著降低了分析物在通道壁上的吸附。分析物的迁移时间与其分子量以及分析物的净电荷或pI有关。异硫氰酸荧光素标记的牛血清白蛋白(FITC-BSA)在2分钟内迁移,峰的理论塔板数达到480,000块/米。此外,使用该微芯片,具有广泛pI值和分子量的蛋白质在1分钟内迁移。