Analysis Tool for Proteomics Research (ATP) is our next generation approach for processing, storing and analyzing mass spectrometry-based proteomics data base on our previously developed bioinformatics graphical comparative analysis tools (BIGCAT) software . This software is being developed for the efficient management, visualization, identification, characterization and comparison of peptides and proteins from tandem mass spectrometry experiments. The basic framework of the software suite consists of a back-end relational database to store primary LC-MS/MS data and the peptide/protein identification data from various database search algorithms. The interactive front-end software applications are interfaced to the relational database for managing, visual interpreting, and analyzing the LC-MS/MS results (Figure 1). As an open source and multi-functional analysis software suite, it enables users to 1) customize source code scheme to facilitate specialized experiment aims, 2) manage and load LC-MS/MS data and protein identification, 3) graphically display and evaluate protein identifications using various views and threshold modifications, 4) compare, merge, and run cluster results from multiple LC-MS/MS experiments, 5) search for neutral losses that are indications of modified peptides, and 6) search immunological peptide motifs. The overall goal is to increase the efficiency and simplicity of managing proteomics data while providing means of publishing and analyzing data on the web in a biologically intuitive and robust way.
We thank Vanderbilt University's Advanced Computing Center for Research and Education (ACCRE), which provides technique support for parallel computing service. Also, thank to Jennifer Jennings for providing proteomics data, data loading, testing, and suggestions on further developing this package. We thank Sumei Chang for providing Oracle Database Administration. This work is supported by NIH Grants GM064779, AR055231, and AI40079.
McAfee KJ, Duncan DT, Assink M, Link AJ: Analyzing proteomes and protein function using graphical comparative analysis of tandem mass spectrometry results.Molecular & Cellular Proteomics 2006, 5: 1497–1513. 10.1074/mcp.T500027-MCP200View ArticleGoogle Scholar