Nagata Hideya, Tabuchi Mari, Hirano Ken, Baba Yoshinobu
Department of Molecular and Pharmaceutical Biotechnology, Graduate School of Pharmaceutical Sciences, The University of Tokushima, The 21ST Century COE Program, CREST(JST), Tokushima, Japan.
Electrophoresis. 2005 Jun;26(11):2247-53. doi: 10.1002/elps.200410395.
Separation of sodium dodecyl sulfate (SDS)-protein complexes is difficult on plastic microchips due to protein adsorption onto the wall. In this paper, we elucidated the reasons for the difficulties in separating SDS-protein complexes on plastic microchips, and we then demonstrated an effective method for separating proteins using polymethyl methacrylate (PMMA) microchips. Separation difficulties were found to be dependent on adsorption of SDS onto the hydrophobic surface of the channel, by which cathodic electroosmotic flow (EOF; reversed flow) was generated. Our developed method effectively utilized the reversed flow from this cathodic EOF as a driving force for sample proteins using permanently uncoated but dynamic SDS-coated PMMA microchips. High-speed (6 s) separation of proteins and peptides up to 116 kDa was successfully achieved using this system.
由于蛋白质会吸附在塑料微芯片壁上,因此在塑料微芯片上分离十二烷基硫酸钠(SDS)-蛋白质复合物很困难。在本文中,我们阐明了在塑料微芯片上分离SDS-蛋白质复合物存在困难的原因,然后展示了一种使用聚甲基丙烯酸甲酯(PMMA)微芯片分离蛋白质的有效方法。研究发现,分离困难取决于SDS在通道疏水表面的吸附,由此产生了阴极电渗流(EOF;逆流)。我们开发的方法使用永久未涂层但动态涂有SDS的PMMA微芯片,有效地将这种阴极EOF产生的逆流用作样品蛋白质的驱动力。使用该系统成功实现了高达116 kDa的蛋白质和肽的高速(6秒)分离。