Kang Dukjin, Moon Myeong Hee
Department of Chemistry, Yonsei University, Seoul 120-749, Korea.
Anal Chem. 2004 Jul 1;76(13):3851-5. doi: 10.1021/ac0496704.
A miniaturized frit inlet asymmetrical flow field-flow fractionation (mFI-AFlFFF) channel has been constructed and tested for the separation of proteins. By scaling down the geometrical channel dimension of a conventional FI-AFlFFF system, flow rate ranges that can be manipulated were decreased to 20-30 microL/min, which reduces the injection amount of sample materials. The end effect contribution to plate height was evaluated by varying the inner diameter of the connection tubing between the injector and the channel inlet at various injection flow rates, and the results showed that the use of silica capillary tubing of the shortest possible distance is essential in reducing the initial band broadening prior to the sample injection to the microscale channel. The capability of the microFI-AFlFFF system was demonstrated with the separation of protein standards, polystyrenesulfonates, and ssDNA strains and for the characterization of replication protein A-ssDNA binding complex regulated by redox status.
已构建并测试了一种用于蛋白质分离的小型化 frit 入口不对称流场-流分级分离(mFI-AFlFFF)通道。通过缩小传统 FI-AFlFFF 系统的几何通道尺寸,可操控的流速范围降至 20 - 30 微升/分钟,这减少了样品材料的进样量。在不同进样流速下,通过改变进样器与通道入口之间连接管的内径来评估端效应对方板高度的贡献,结果表明,使用尽可能短距离的硅胶毛细管对于减少样品注入微尺度通道之前的初始谱带展宽至关重要。通过对蛋白质标准品、聚苯乙烯磺酸盐和单链 DNA 菌株的分离以及对受氧化还原状态调节的复制蛋白 A - 单链 DNA 结合复合物的表征,证明了 microFI-AFlFFF 系统的能力。