Artigo Acesso aberto Revisado por pares

DIA-Umpire: comprehensive computational framework for data-independent acquisition proteomics

2015; Nature Portfolio; Volume: 12; Issue: 3 Linguagem: Inglês

10.1038/nmeth.3255

ISSN

1548-7105

Autores

Chih‐Chiang Tsou, Dmitry M. Avtonomov, Brett Larsen, Monika Tucholska, Hyungwon Choi, Anne‐Claude Gingras, Alexey I. Nesvizhskii,

Tópico(s)

Metabolomics and Mass Spectrometry Studies

Resumo

The computational workflow of DIA-Umpire allows untargeted peptide identificationdirectly from DIA (data-independent acquisition) proteomics data without dependence on a spectral library for data extraction As a result of recent improvements in mass spectrometry (MS), there is increased interest in data-independent acquisition (DIA) strategies in which all peptides are systematically fragmented using wide mass-isolation windows ('multiplex fragmentation'). DIA-Umpire ( http://diaumpire.sourceforge.net/ ), a comprehensive computational workflow and open-source software for DIA data, detects precursor and fragment chromatographic features and assembles them into pseudo–tandem MS spectra. These spectra can be identified with conventional database-searching and protein-inference tools, allowing sensitive, untargeted analysis of DIA data without the need for a spectral library. Quantification is done with both precursor- and fragment-ion intensities. Furthermore, DIA-Umpire enables targeted extraction of quantitative information based on peptides initially identified in only a subset of the samples, resulting in more consistent quantification across multiple samples. We demonstrated the performance of the method with control samples of varying complexity and publicly available glycoproteomics and affinity purification–MS data.

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