Biomicrofluidics. 2010 Jan 27;4(1):14103. doi: 10.1063/1.3298608.
A protein separation technology using the microfluidic device was developed for the more rapid and effective analysis of target protein. This microfluidic separation system was carried out using the aqueous two-phase system (ATPS) and the ionic liquid two-phase system (ILTPS) for purification method of the protein sample, and the three-flow desalting system was used for the removal of salts from the sucrose-rich sample. Partitioning of the protein sample was observed in ATPS or ILTPS with the various pHs. The microdialysis system was applied to remove small molecules, such as sucrose and salts in the microfluidic channel with the different flow rates of buffer phase. A complex purification method, which combines microdialysis and ATPS or ILTPS, was carried out for the effective purification of bacteriorhodopsin (BR) from the purple membrane of Halobacterium salinarium, which was then analyzed by sodium dodecyl sulfatepolyacrylamide gel electrophoresis and matrix-assisted laser desorptionionization time-of-flight. Furthermore, we were able to make a stable three-phase flow controlling the flow rate in the microfluidic channel. Our complex purification methods were successful in purifying and recovering the BR to its required value.
开发了一种使用微流控装置的蛋白质分离技术,以更快速、有效地分析目标蛋白质。该微流分离系统采用双水相体系(ATPS)和离子液体双相体系(ILTPS)作为蛋白质样品的纯化方法,三股流脱盐系统用于去除富含蔗糖的样品中的盐。在不同 pH 值下观察到蛋白质样品在 ATPS 或 ILTPS 中的分配。微透析系统用于在微流道中以不同的缓冲相流速去除小分子,如蔗糖和盐。通过微透析和 ATPS 或 ILTPS 的组合,我们进行了复杂的纯化方法,从盐生盐杆菌的紫色膜中有效纯化菌紫质(BR),然后通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和基质辅助激光解吸电离飞行时间进行分析。此外,我们能够通过控制微流道中的流速来稳定三相流。我们的复杂纯化方法成功地将 BR 纯化并回收至所需值。