Abstract

BackgroundMass spectrometry (MS) based label-free protein quantitation has mainly focused on analysis of ion peak heights and peptide spectral counts. Most analyses of tandem mass spectrometry (MS/MS) data begin with an enzymatic digestion of a complex protein mixture to generate smaller peptides that can be separated and identified by an MS/MS instrument. Peptide spectral counting techniques attempt to quantify protein abundance by counting the number of detected tryptic peptides and their corresponding MS spectra. However, spectral counting is confounded by the fact that peptide physicochemical properties severely affect MS detection resulting in each peptide having a different detection probability. Lu et al. (2007) described a modified spectral counting technique, Absolute Protein Expression (APEX), which improves on basic spectral counting methods by including a correction factor for each protein (called Oi value) that accounts for variable peptide detection by MS techniques. The technique uses machine learning classification to derive peptide detection probabilities that are used to predict the number of tryptic peptides expected to be detected for one molecule of a particular protein (Oi). This predicted spectral count is compared to the protein's observed MS total spectral count during APEX computation of protein abundances.ResultsThe APEX Quantitative Proteomics Tool, introduced here, is a free open source Java application that supports the APEX protein quantitation technique. The APEX tool uses data from standard tandem mass spectrometry proteomics experiments and provides computational support for APEX protein abundance quantitation through a set of graphical user interfaces that partition thparameter controls for the various processing tasks. The tool also provides a Z-score analysis for identification of significant differential protein expression, a utility to assess APEX classifier performance via cross validation, and a utility to merge multiple APEX results into a standardized format in preparation for further statistical analysis.ConclusionThe APEX Quantitative Proteomics Tool provides a simple means to quickly derive hundreds to thousands of protein abundance values from standard liquid chromatography-tandem mass spectrometry proteomics datasets. The APEX tool provides a straightforward intuitive interface design overlaying a highly customizable computational workflow to produce protein abundance values from LC-MS/MS datasets.

Highlights

  • Mass spectrometry (MS) based label-free protein quantitation has mainly focused on analysis of ion peak heights and peptide spectral counts

  • This paper describes a new software tool, the Absolute Protein Expression (APEX) Quantitative Proteomics Tool, an implementation of the APEX technique for the quantitation of proteins based on LCMS/MS proteomics results

  • The APEX tool has a graphical user interface (Figure 5) where the parameter controls for each processing task are encapsulated in a different tabbed panel in the interface

Read more

Summary

Results

Http://www.biomedcentral.com/1471-2105/9/529 ties that vary and result in a mix of observed and nonobserved peptides These input proteins are specified by a protein accession list and the corresponding protein sequences are supplied in a standard FASTA format file. The protein sequences are input in a FASTA format file They undergo an in silico trypsin digestion and peptide properties are computed for each peptide. Computing APEX Quantitation Values The third and primary processing task of the APEX tool uses the Oi values and an MS data file in protXML format as input to generate abundance values for each protein according to equation 1. Protein and peptide objects serve as container objects for sequence, annotation, and numerical data fields required for APEX computation Data loaders populate these structures from FASTA or protXML files. Developers can add new processing tasks by extending an abstract process panel class that presents parameter controls and by add-

Conclusion
Background
Results and discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call