Tran John C, Doucette Alan A
Department of Chemistry, Dalhousie University, 6274 Coburg Road, Halifax, Nova Scotia, Canada B3H 4J3.
Anal Chem. 2008 Mar 1;80(5):1568-73. doi: 10.1021/ac702197w. Epub 2008 Jan 30.
Although well-established as a technique for protein purification, the application of continuous elution tube gel electrophoresis to proteome fractionation remains problematic. Difficulties associated with sample collection, particularly at the high mass range or at low sample loadings, continue to plague the technique. Furthermore, an upper mass limit is imposed as slow-moving higher molecular weight proteins are progressively diluted during the collection phase. In short, with current technology, effective separation over a broad mass range has not been achieved. In this work, we present improved techniques for continuous elution tube gel electrophoresis to accommodate broad mass range separation of proteins. Our device enables rapid partitioning of a proteome into discrete mass range fractions in the solution phase. High recovery is achieved at submicrogram to milligram sample loadings. We demonstrate comprehensive, reproducible separations of protein mixtures, as well as separation of a proteome in as fast as 1 h, over mass ranges from below 10 to 250 kDa. Finally, we identified proteins from a prefractionated standard protein mixture using liquid chromatography tandem mass spectrometric (LC-MS/MS) analysis.
尽管连续洗脱管凝胶电泳作为一种蛋白质纯化技术已得到广泛认可,但将其应用于蛋白质组分级分离仍存在问题。与样品收集相关的困难,尤其是在高质量范围或低样品加载量时,仍然困扰着该技术。此外,由于在收集阶段移动缓慢的高分子量蛋白质会逐渐被稀释,因此存在一个质量上限。简而言之,就目前的技术而言,尚未实现宽质量范围内的有效分离。在这项工作中,我们提出了改进的连续洗脱管凝胶电泳技术,以适应蛋白质的宽质量范围分离。我们的装置能够在溶液相中快速将蛋白质组划分为离散的质量范围级分。在亚微克到毫克的样品加载量下可实现高回收率。我们展示了蛋白质混合物的全面、可重复分离,以及在1小时内对质量范围从低于10 kDa到250 kDa的蛋白质组进行分离。最后,我们使用液相色谱串联质谱(LC-MS/MS)分析从预分级的标准蛋白质混合物中鉴定出蛋白质。