4.6 Article

Corra: Computational framework and tools for LC-MS discovery and targeted mass spectrometry-based proteomics

期刊

BMC BIOINFORMATICS
卷 9, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2105-9-542

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资金

  1. National Heart, Lung, and Blood Institute Seattle Proteome Center [N01-HV-8179]
  2. National Cancer Institute [N01CO-12400]
  3. National Institute of Diabetes & Digestive Kidney Disease [1R21-DK71275]
  4. Swiss National Science Foundation [31000-10767]
  5. Entertainment Industry Foundation (EIF)
  6. EIF Women's Cancer Research Fund
  7. National Institute of Diabetes & Digestive Kidney Disease
  8. R21 [PAR-04076]
  9. Functional Proteomics Center, Zurich, Switzerland

向作者/读者索取更多资源

Background: Quantitative proteomics holds great promise for identifying proteins that are differentially abundant between populations representing different physiological or disease states. A range of computational tools is now available for both isotopically labeled and label-free liquid chromatography mass spectrometry (LC-MS) based quantitative proteomics. However, they are generally not comparable to each other in terms of functionality, user interfaces, information input/output, and do not readily facilitate appropriate statistical data analysis. These limitations, along with the array of choices, present a daunting prospect for biologists, and other researchers not trained in bioinformatics, who wish to use LC-MS-based quantitative proteomics. Results: We have developed Corra, a computational framework and tools for discovery-based LC-MS proteomics. Corra extends and adapts existing algorithms used for LC-MS-based proteomics, and statistical algorithms, originally developed for microarray data analyses, appropriate for LC-MS data analysis. Corra also adapts software engineering technologies (e. g. Google Web Toolkit, distributed processing) so that computationally intense data processing and statistical analyses can run on a remote server, while the user controls and manages the process from their own computer via a simple web interface. Corra also allows the user to output significantly differentially abundant LC-MS-detected peptide features in a form compatible with subsequent sequence identification via tandem mass spectrometry (MS/MS). We present two case studies to illustrate the application of Corra to commonly performed LC-MS-based biological workflows: a pilot biomarker discovery study of glycoproteins isolated from human plasma samples relevant to type 2 diabetes, and a study in yeast to identify in vivo targets of the protein kinase Ark1 via phosphopeptide profiling. Conclusion: The Corra computational framework leverages computational innovation to enable biologists or other researchers to process, analyze and visualize LC-MS data with what would otherwise be a complex and not user-friendly suite of tools. Corra enables appropriate statistical analyses, with controlled false-discovery rates, ultimately to inform subsequent targeted identification of differentially abundant peptides by MS/MS. For the user not trained in bioinformatics, Corra represents a complete, customizable, free and open source computational platform enabling LC-MS-based proteomic workflows, and as such, addresses an unmet need in the LC-MS proteomics field.

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