Abstract
BackgroundEffective and economical methods for quantitative analysis of high throughput mass spectrometry data are essential to meet the goals of directly identifying, characterizing, and quantifying proteins from a particular cell state. Multidimensional Protein Identification Technology (MudPIT) is a common approach used in protein identification. Two types of methods are used to detect differential protein expression in MudPIT experiments: those involving stable isotope labelling and the so-called label-free methods. Label-free methods are based on the relationship between protein abundance and sampling statistics such as peptide count, spectral count, probabilistic peptide identification scores, and sum of peptide Sequest XCorr scores (ΣXCorr). Although a number of label-free methods for protein quantification have been described in the literature, there are few publicly available tools that implement these methods. We describe ProtQuant, a Java-based tool for label-free protein quantification that uses the previously published ΣXCorr method for quantification and includes an improved method for handling missing data.ResultsProtQuant was designed for ease of use and portability for the bench scientist. It implements the ΣXCorr method for label free protein quantification from MudPIT datasets. ProtQuant has a graphical user interface, accepts multiple file formats, is not limited by the size of the input files, and can process any number of replicates and any number of treatments. In addition,ProtQuant implements a new method for dealing with missing values for peptide scores used for quantification. The new algorithm, called ΣXCorr*, uses "below threshold" peptide scores to provide meaningful non-zero values for missing data points. We demonstrate that ΣXCorr* produces an average reduction in false positive identifications of differential expression of 25% compared to ΣXCorr.ConclusionProtQuant is a tool for protein quantification built for multi-platform use with an intuitive user interface. ProtQuant efficiently and uniquely performs label-free quantification of protein datasets produced with Sequest and provides the user with facilities for data management and analysis. Importantly, ProtQuant is available as a self-installing executable for the Windows environment used by many bench scientists.
Highlights
Effective and economical methods for quantitative analysis of high throughput mass spectrometry data are essential to meet the goals of directly identifying, characterizing, and quantifying proteins from a particular cell state
ProtQuant is available as a self-installing executable for the Windows environment used by many bench scientists
Multidimensional Protein Identification Technology (MudPIT) coupled with database searching is a common approach in biological studies to identify proteins [2]
Summary
Effective and economical methods for quantitative analysis of high throughput mass spectrometry data are essential to meet the goals of directly identifying, characterizing, and quantifying proteins from a particular cell state. Label-free methods are based on the relationship between protein abundance and sampling statistics such as peptide count, spectral count, probabilistic peptide identification scores, and sum of peptide Sequest XCorr scores (ΣXCorr). Multidimensional Protein Identification Technology (MudPIT) coupled with database searching is a common approach in biological studies to identify proteins [2]. MudPIT involves site-specific proteolytic digestion of proteins to peptides, separation of peptides by two-dimensional liquid chromatography (LC) (strong cation exchange and reverse phase), and analysis of peptides by tandem mass spectrometry (MS/MS), followed by database searching for protein identification. Protein identification using database searching algorithms like Sequest [3], MASCOT [4] and OMSSA [5] are based on thresholds for specific scoring parameters for each algorithm that are used to filter the peptide identifications most likely to be correct. It is important to note that only 10–50% of spectra assignments generated in LC-MS/MS experiments are correct [7] and a majority of peptide assignments to spectra are removed by filtering
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