Carrier ampholyte‐free solution isoelectric focusing as a prefractionation method for the proteomic analysis of complex protein mixtures
- 16 July 2003
- journal article
- research article
- Published by Wiley in Electrophoresis
- Vol. 24 (14), 2359-2368
- https://doi.org/10.1002/elps.200305502
Abstract
The field of proteomics requires methods that offer high sensitivity and wide dynamic range. One of the strategies used to improve the dynamic range is sample prefractionation, such as microsolution isoelectric focusing (IEF). We have modified a commercial solution IEF instrument, the Rotofor®, to prefractionate protein mixtures by carrier ampholyte-free solution IEF. The focusing chamber of the Rotofor was divided into several compartments by polyacrylamide membranes with imbedded Immobiline mixtures of specific pH values. When an electric field is applied, each protein migrates to the compartment confined by membranes with pH values flanking its isoelectric point. The approach was demonstrated for the focusing of myoglobin into a predicted compartment, as well as the separation of a complex soluble yeast protein mixture into several distinct fractions. The proteins were dissolved in water or 30% isopropanol. The method is applicable to both gel-based and solution-phase protein identification methods, without the need for further sample preparation.Keywords
This publication has 22 references indexed in Scilit:
- Quantitative proteome analysis by solid-phase isotope tagging and mass spectrometryNature Biotechnology, 2002
- Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometryNature, 2002
- Identification of the apolipoprotein E4 isoform in cerebrospinal fluid with preparative two-dimensional electrophoresis and matrix assisted laser desorption/ionization-time of flight-mass spectrometryElectrophoresis, 2001
- Evaluation of two-dimensional gel electrophoresis-based proteome analysis technologyProceedings of the National Academy of Sciences, 2000
- Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two dimensional gelsProceedings of the National Academy of Sciences, 1996
- Improvement of an "In-Gel" Digestion Procedure for the Micropreparation of Internal Protein Fragments for Amino Acid SequencingAnalytical Biochemistry, 1995
- Internal protein sequence analysis: Enzymatic digestion for less than 10 μg of protein bound to polyvinylidene difluoride or nitrocellulose membranesAnalytical Biochemistry, 1992
- Preparative purification of human monoclonal antibody isoforms in a multi-compartment electrolyser with immobiline membranesJournal of Chromatography A, 1990
- Preparative protein purification in a multi-compartment electrolyser with immobiline membranesJournal of Chromatography A, 1989
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970