Automated Assignment of MS/MS Cleavable Cross-Links in Protein 3D-Structure Analysis

CID-MS/MS cleavable cross-linkers hold an enormous potential for an automated analysis of cross-linked products, which is essential for conducting structural proteomics studies. The created characteristic fragment ion patterns can easily be used for an automated assignment and discrimination of cros...

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Veröffentlicht in:Journal of the American Society for Mass Spectrometry 2015-01, Vol.26 (1), p.83-97
Hauptverfasser: Götze, Michael, Pettelkau, Jens, Fritzsche, Romy, Ihling, Christian H., Schäfer, Mathias, Sinz, Andrea
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Sprache:eng
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Zusammenfassung:CID-MS/MS cleavable cross-linkers hold an enormous potential for an automated analysis of cross-linked products, which is essential for conducting structural proteomics studies. The created characteristic fragment ion patterns can easily be used for an automated assignment and discrimination of cross-linked products. To date, there are only a few software solutions available that make use of these properties, but none allows for an automated analysis of cleavable cross-linked products. The MeroX software fills this gap and presents a powerful tool for protein 3D-structure analysis in combination with MS/MS cleavable cross-linkers. We show that MeroX allows an automatic screening of characteristic fragment ions, considering static and variable peptide modifications, and effectively scores different types of cross-links. No manual input is required for a correct assignment of cross-links and false discovery rates are calculated. The self-explanatory graphical user interface of MeroX provides easy access for an automated cross-link search platform that is compatible with commonly used data file formats, enabling analysis of data originating from different instruments. The combination of an MS/MS cleavable cross-linker with a dedicated software tool for data analysis provides an automated workflow for 3D-structure analysis of proteins. MeroX is available at www.StavroX.com . Graphical Abstract ᅟ
ISSN:1044-0305
1879-1123
DOI:10.1007/s13361-014-1001-1