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Crystal-C: A Computational Tool for Refinement of Open Search Results.
Chang, Hui-Yin; Kong, Andy T; da Veiga Leprevost, Felipe; Avtonomov, Dmitry M; Haynes, Sarah E; Nesvizhskii, Alexey I.
Affiliation
  • Chang HY; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Kong AT; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • da Veiga Leprevost F; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Avtonomov DM; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Haynes SE; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Nesvizhskii AI; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
J Proteome Res ; 19(6): 2511-2515, 2020 06 05.
Article in En | MEDLINE | ID: mdl-32338005
ABSTRACT
Shotgun proteomics using liquid chromatography coupled to mass spectrometry (LC-MS) is commonly used to identify peptides containing post-translational modifications. With the emergence of fast database search tools such as MSFragger, the approach of enlarging precursor mass tolerances during the search (termed "open search") has been increasingly used for comprehensive characterization of post-translational and chemical modifications of protein samples. However, not all mass shifts detected using the open search strategy represent true modifications, as artifacts exist from sources such as unaccounted missed cleavages or peptide co-fragmentation (chimeric MS/MS spectra). Here, we present Crystal-C, a computational tool that detects and removes such artifacts from open search results. Our analysis using Crystal-C shows that, in a typical shotgun proteomics data set, the number of such observations is relatively small. Nevertheless, removing these artifacts helps to simplify the interpretation of the mass shift histograms, which in turn should improve the ability of open search-based tools to detect potentially interesting mass shifts for follow-up investigation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteomics / Tandem Mass Spectrometry Language: En Journal: J Proteome Res Journal subject: BIOQUIMICA Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteomics / Tandem Mass Spectrometry Language: En Journal: J Proteome Res Journal subject: BIOQUIMICA Year: 2020 Type: Article Affiliation country: United States