Literature DB >> 15307793

A proteome strategy for fractionating proteins and peptides using continuous free-flow electrophoresis coupled off-line to reversed-phase high-performance liquid chromatography.

Robert L Moritz1, Hong Ji, Frédéric Schütz, Lisa M Connolly, Eugene A Kapp, Terence P Speed, Richard J Simpson.   

Abstract

Extensive prefractionation is now considered to be a necessary prerequisite for the comprehensive analysis of complex proteomes where the dynamic range of protein abundances can vary from approximately 10(6) for cells to approximately 10(10) for tissues such as blood. Here, we describe a high-resolution 2D protein separation system that uses a continuous free-flow electrophoresis (FFE) device to fractionate complex protein mixtures by solution-phase isoelectric focusing (IEF) into 96 well-defined pools, each separated by approximately 0.02-0.10 pH unit depending on the gradient created, followed by rapid (approximately 6 min per analysis) reversed-phase high-performance liquid chromatography (RP-HPLC) of each FFE pool. Fractionated proteins are readily visualized in a virtual 2D format using software that plots protein loci, pI in the first dimension and relative hydrophobicity (i.e., RP-HPLC retention time) in the second dimension. By coupling a diode-array detector in line with a multiwavelength fluorescence detector, separated proteins can be monitored in the RP-HPLC eluent by both UV absorbance and intrinsic fluorescence simultaneously from a single experiment. Triplicate analyses of standard proteins using a pH 3-10 gradient conducted over a 3-day period revealed a high system reproducibility with a SD of 0.57 (0.05 pH unit) within the FFE pools and 0.003 (0.18 s) for protein retention times in the second-dimension RP-HPLC step. In addition, we demonstrate that the FFE-IEF/RP-HPLC separation strategy can also be applied to complex mixtures of low molecular weight compounds such as peptides. With the facile ability to measure the pH of the isoelectric focused pools, peptide pI values can be estimated and used to qualify peptide identifications made using either MS/MS sequencing approaches or pI discriminated peptide mass fingerprinting. The calculated peak capacity of this 2D liquid-based FFE-IEF/RP-HPLC system is 6720.

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Year:  2004        PMID: 15307793     DOI: 10.1021/ac049717l

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  12 in total

1.  Quantitative phosphoproteomic analysis of the tumor necrosis factor pathway.

Authors:  Greg T Cantin; John D Venable; Daniel Cociorva; John R Yates
Journal:  J Proteome Res       Date:  2006-01       Impact factor: 4.466

2.  Integration of 18O labeling and solution isoelectric focusing in a shotgun analysis of mitochondrial proteins.

Authors:  Jinshan Wang; Peter Gutierrez; Nathan Edwards; Catherine Fenselau
Journal:  J Proteome Res       Date:  2007-11-10       Impact factor: 4.466

Review 3.  Immobilized pH gradient isoelectric focusing as a first-dimension separation in shotgun proteomics.

Authors:  Benjamin J Cargile; Joel R Sevinsky; Amal S Essader; James L Stephenson; Jonathan L Bundy
Journal:  J Biomol Tech       Date:  2005-09

Review 4.  Proteomics and the analysis of proteomic data: an overview of current protein-profiling technologies.

Authors:  Erol E Gulcicek; Christopher M Colangelo; Walter McMurray; Kathryn Stone; Kenneth Williams; Terence Wu; Hongyu Zhao; Heidi Spratt; Alexander Kurosky; Baolin Wu
Journal:  Curr Protoc Bioinformatics       Date:  2005-07

Review 5.  Protein analysis by shotgun/bottom-up proteomics.

Authors:  Yaoyang Zhang; Bryan R Fonslow; Bing Shan; Moon-Chang Baek; John R Yates
Journal:  Chem Rev       Date:  2013-02-26       Impact factor: 60.622

6.  Development of a Chip/Chip/SRM platform using digital chip isoelectric focusing and LC-Chip mass spectrometry for enrichment and quantitation of low abundance protein biomarkers in human plasma.

Authors:  Agnes Rafalko; Shujia Dai; William S Hancock; Barry L Karger; Marina Hincapie
Journal:  J Proteome Res       Date:  2011-12-27       Impact factor: 4.466

7.  Analysis of phosphorylation sites on proteins from Saccharomyces cerevisiae by electron transfer dissociation (ETD) mass spectrometry.

Authors:  An Chi; Curtis Huttenhower; Lewis Y Geer; Joshua J Coon; John E P Syka; Dina L Bai; Jeffrey Shabanowitz; Daniel J Burke; Olga G Troyanskaya; Donald F Hunt
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-07       Impact factor: 11.205

8.  Investigating the secretome: lessons about the cells that comprise the heart.

Authors:  Miroslava Stastna; Jennifer E Van Eyk
Journal:  Circ Cardiovasc Genet       Date:  2012-02-01

9.  Application of free-flow electrophoresis/2-dimentional gel electrophoresis for fractionation and characterization of native proteome of Pseudomonas putida KT2440.

Authors:  Chi-Won Choi; Young S Hong; Seung Il Kim
Journal:  J Microbiol       Date:  2008-08-31       Impact factor: 3.422

Review 10.  High-field asymmetric waveform ion mobility spectrometry for mass spectrometry-based proteomics.

Authors:  Kristian E Swearingen; Robert L Moritz
Journal:  Expert Rev Proteomics       Date:  2012-10       Impact factor: 3.940

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