Davis M T, Beierle J, Bures E T, McGinley M D, Mort J, Robinson J H, Spahr C S, Yu W, Luethy R, Patterson S D
Department of Biochemistry, Amgen, Inc., Thousand Oaks, CA 91320, USA.
J Chromatogr B Biomed Sci Appl. 2001 Mar 10;752(2):281-91. doi: 10.1016/s0378-4347(00)00547-8.
A simple multidimensional liquid chromatography system utilizing an isocratic pump and a HPLC system is described for the comprehensive proteomic analysis of complex peptide digest mixtures by coupled LC-LC-MS-MS techniques. A binary ion-exchange separation was achieved through the use of a strong cation-exchange column followed by a reversed-phase column for data-dependent LC-MS-MS analysis of the unbound analytes, and following salt elution (and concomitant column reequilibration), the bound analytes. Off-line validation of the platform showed near quantitative recovery of fractionated peptides and essentially complete ion-exchange partitioning. In comparative analyses of a highly complex peptide digest mixture a >40% increase in the number of peptide and protein identifications was achieved using this multidimensional platform compared to an unfractionated control.
描述了一种利用等度泵和高效液相色谱(HPLC)系统的简单多维液相色谱系统,用于通过联用液相色谱-液相色谱-质谱-质谱(LC-LC-MS-MS)技术对复杂肽消化混合物进行全面的蛋白质组学分析。通过使用强阳离子交换柱,随后是反相柱,实现了二元离子交换分离,用于对未结合分析物进行数据依赖型LC-MS-MS分析,以及在盐洗脱(和伴随的柱再平衡)后对结合分析物进行分析。该平台的离线验证显示,分级肽的回收率接近定量,离子交换分配基本完全。在对高度复杂的肽消化混合物的比较分析中,与未分级对照相比,使用该多维平台可使肽和蛋白质鉴定数量增加>40%。