Liu Jing, Kang Mingchao, Liu Zhen
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Se Pu. 2011 Sep;29(9):862-8.
An electrokinetic supercharging (EKS) method with a prefilled water plug at the head column of capillary was developed for on-line preconcentration of sodium dodecyl sulfate (SDS)-protein complexes in capillary sieving electrophoresis (CSE). Conventional EKS is a combination of electrokinetic injection with transient isotachophoresis (tr-ITP). The capillary is first filled with background electrolyte, then an appropriate amount of a leading electrolyte is filled and electro-injection is carried out for certain duration. After that, terminating electrolyte is filled, and tr-ITP is subsequently initiated, followed by capillary electrophoresis (CE) separation. In this work, the performance of EKS was evaluated by integrating multiple sub-methods step by step, and a water plug containing polymer was introduced before electrokinetic injection in order to further improve the concentration effect. The positive effects of the sub-methods were verified, including molecular sieving effect of polymer, field enhanced sample injection (FESI) with and without a water plug, and transient isotachophoretic electrophoresis-based FESI. It was observed that analyte discrimination usually encountered in conventional electrokinetic injection was eliminated due to the similar charge to mass ratios of SDS-protein complexes. Based on these results, a hybrid on-line preconcentration method, EKS with injecting a water plug containing polymer before sample electrokinetic injection, was proposed and used to indiscriminately preconcentrate SDS-protein complexes, which provided a sensitivity enhancement factor of more than 1000. It was very suitable for the analysis of low-abundance proteins, providing the information of their molecular mass.
一种在毛细管柱头部预填充水塞的电动增压(EKS)方法被开发用于毛细管筛分电泳(CSE)中十二烷基硫酸钠(SDS)-蛋白质复合物的在线预浓缩。传统的EKS是电动进样与瞬态等速电泳(tr-ITP)的结合。首先用背景电解质填充毛细管,然后填充适量的前导电解质并进行一定时间的电动进样。之后,填充终止电解质,随后启动tr-ITP,接着进行毛细管电泳(CE)分离。在这项工作中,通过逐步整合多种子方法来评估EKS的性能,并在电动进样前引入含聚合物的水塞以进一步提高浓缩效果。验证了这些子方法的积极作用,包括聚合物的分子筛效应、有无水塞的场增强进样(FESI)以及基于瞬态等速电泳的FESI。观察到由于SDS-蛋白质复合物的电荷质量比相似,消除了传统电动进样中通常遇到的分析物歧视。基于这些结果,提出了一种混合在线预浓缩方法,即在样品电动进样前注入含聚合物水塞的EKS,并用于无差别地预浓缩SDS-蛋白质复合物,其灵敏度增强因子超过1000。它非常适合分析低丰度蛋白质,可提供其分子量信息。