Automated LC-LC-MS-MS platform using binary ion-exchange and gradient reversed-phase chromatography for improved proteomic analyses

被引:140
作者
Davis, MT [1 ]
Beierle, J
Bures, ET
McGinley, MD
Mort, J
Robinson, JH
Spahr, CS
Yu, W
Luethy, R
Patterson, SD
机构
[1] Amgen Inc, Dept Biochem, Thousand Oaks, CA 91320 USA
[2] Amgen Inc, Dept Computat Biol, Thousand Oaks, CA 91320 USA
[3] Celeva Genom, Rockville, MD 20850 USA
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 752卷 / 02期
关键词
proteomics;
D O I
10.1016/S0378-4347(00)00547-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:281 / 291
页数:11
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