Two-Dimensional Microcolumn Separation Platform for Proteomics Consisting of On-Line Coupled Capillary Isoelectric Focusing and Capillary Electrochromatography. 1. Evaluation of the Capillary-Based Two-Dimensional Platform with Proteins, Peptides, and Human Serum
- 4 July 2006
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Proteome Research
- Vol. 5 (8) , 2001-2008
- https://doi.org/10.1021/pr060185u
Abstract
In this report, an on-line coupling of capillary isoelectric focusing (CIEF) to capillary electrochromatography (CEC) is developed via a nanoinjector valve for performing two-dimensional (2D) proteomics separation. CIEF constitutes the first separation dimension, while CEC operates as the second separation dimension. Besides the orthogonal migration mechanisms of the two capillary-based separation modes, which lead to a 2D system whose overall peak capacity is the product of the peak capacity of the individual modes, the solvent of the CIEF mode is a weak eluent for the reversed-phase CEC (RP-CEC) mode, thus, allowing the transferring of focused fractions from CIEF to CEC without inducing band broadening, and instead zone sharpening would result. In fact, the transferred focused protein fraction from the CIEF column to the CEC column will stay tightly adsorbed to the inlet top of the CEC column until it will be eluted and separated into its protein components with a hydro-organic mobile phase. The theoretical peak capacity of the CIEF−CEC 2D platform is estimated at nCIEF (= 560) × nCEC (= 97) = 54 320. This peak capacity is more than needed for proteomics profiling. Also, only a fraction of this peak capacity is needed when looking at heart cuts for performing subproteomics. The 2D platform described here offers the convenience to generate the needed peak capacity to solve a given proteomic separation problem. This is facilitated by the RP-CEC dimension, which ensures rapid isocratic separation of proteins and peptides and rapid solvent change and column equilibration and avoids lengthy gradient elution. The RP-CEC column is based on neutral C17 monolith, which offers high separation efficiency and relatively high column permeability. To the best of our knowledge, the proposed 2D platform combining CIEF and CEC is reported for the first time for proteins and proteomics. Keywords: Capillary Isoelectric Focusing • Capillary Electrochromatography • Capillary-Based Two-Dimensional Separations • ProteomicsKeywords
This publication has 22 references indexed in Scilit:
- Capillary electrochromatography with monolithic stationary phases. 4. Preparation of neutral stearyl - acrylate monoliths and their evaluation in capillary electrochromatography of neutral and charged small species as well as peptides and proteinsElectrophoresis, 2005
- Capillary electrochromatography with monolithic stationary phases: II. Preparation of cationic stearyl-acrylate monoliths and their electrochromatographic characterizationJournal of Chromatography A, 2003
- Comprehensive two dimensional separation based on coupling micellar electrokinetic chromatography with capillary isoelectric focusingPresented at Pittcon 2002.The Analyst, 2002
- Comprehensive Two-Dimensional High-Performance Liquid Chromatography for the Isolation of Overexpressed Proteins and Proteome MappingAnalytical Biochemistry, 1998
- Macroporous Polyacrylamide/Poly(ethylene glycol) Matrixes as Stationary Phases in Capillary ElectrochromatographyAnalytical Chemistry, 1997
- A Transparent Flow Gating Interface for the Coupling of Microcolumn LC with CZE in a Comprehensive Two-Dimensional SystemAnalytical Chemistry, 1997
- Comprehensive on-line RPLC-CZE-MS of peptidesJournal of the American Society for Mass Spectrometry, 1997
- Concepts and comparisons in multidimensional separationJournal of High Resolution Chromatography, 1987
- High-performance electrophoresisJournal of Chromatography A, 1985
- Two-dimensional electrophoresis and ionophoresisJournal of Colloid Science, 1951