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OpenPepXL: An Open-Source Tool for Sensitive Identification of Cross-Linked Peptides in XL-MS.
Netz, Eugen; Dijkstra, Tjeerd M H; Sachsenberg, Timo; Zimmermann, Lukas; Walzer, Mathias; Monecke, Thomas; Ficner, Ralf; Dybkov, Olexandr; Urlaub, Henning; Kohlbacher, Oliver.
Afiliação
  • Netz E; Biomolecular Interactions, Max Planck Institute for Developmental Biology, Tübingen, Germany; Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen, Germany; Applied Bioinformatics, Dept. of Computer Science, University of Tübingen, Tübingen, Germany. Electronic addr
  • Dijkstra TMH; Biomolecular Interactions, Max Planck Institute for Developmental Biology, Tübingen, Germany; Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen, Germany; Applied Bioinformatics, Dept. of Computer Science, University of Tübingen, Tübingen, Germany; Center for Wome
  • Sachsenberg T; Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen, Germany; Applied Bioinformatics, Dept. of Computer Science, University of Tübingen, Tübingen, Germany.
  • Zimmermann L; Biomolecular Interactions, Max Planck Institute for Developmental Biology, Tübingen, Germany; Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen, Germany; Institute for Translational Bioinformatics, University Hospital Tübingen, Tübingen, Germany.
  • Walzer M; Institute for Translational Bioinformatics, University Hospital Tübingen, Tübingen, Germany; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
  • Monecke T; X-Ray Crystallography Facility, Institute of Pharmaceutical Biotechnology, University of Ulm, Ulm, Germany; Department of Molecular Structural BiologyInstitute for Microbiology and GeneticsGZMB, Georg-August-University Göttingen, Göttingen, Germany.
  • Ficner R; Department of Molecular Structural BiologyInstitute for Microbiology and GeneticsGZMB, Georg-August-University Göttingen, Göttingen, Germany.
  • Dybkov O; Department for Cellular BiochemistryMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  • Urlaub H; Bioanalytical Mass SpectrometryMax Planck Institute for Biophysical Chemistry, Göttingen, Germany; BioanalyticsInstitute for Clinical Chemistry, University Medical Center, Göttingen, Germany.
  • Kohlbacher O; Biomolecular Interactions, Max Planck Institute for Developmental Biology, Tübingen, Germany; Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen, Germany; Applied Bioinformatics, Dept. of Computer Science, University of Tübingen, Tübingen, Germany; Institute for T
Mol Cell Proteomics ; 19(12): 2157-2168, 2020 12.
Article em En | MEDLINE | ID: mdl-33067342
Cross-linking MS (XL-MS) has been recognized as an effective source of information about protein structures and interactions. In contrast to regular peptide identification, XL-MS has to deal with a quadratic search space, where peptides from every protein could potentially be cross-linked to any other protein. To cope with this search space, most tools apply different heuristics for search space reduction. We introduce a new open-source XL-MS database search algorithm, OpenPepXL, which offers increased sensitivity compared with other tools. OpenPepXL searches the full search space of an XL-MS experiment without using heuristics to reduce it. Because of efficient data structures and built-in parallelization OpenPepXL achieves excellent runtimes and can also be deployed on large compute clusters and cloud services while maintaining a slim memory footprint. We compared OpenPepXL to several other commonly used tools for identification of noncleavable labeled and label-free cross-linkers on a diverse set of XL-MS experiments. In our first comparison, we used a data set from a fraction of a cell lysate with a protein database of 128 targets and 128 decoys. At 5% FDR, OpenPepXL finds from 7% to over 50% more unique residue pairs (URPs) than other tools. On data sets with available high-resolution structures for cross-link validation OpenPepXL reports from 7% to over 40% more structurally validated URPs than other tools. Additionally, we used a synthetic peptide data set that allows objective validation of cross-links without relying on structural information and found that OpenPepXL reports at least 12% more validated URPs than other tools. It has been built as part of the OpenMS suite of tools and supports Windows, macOS, and Linux operating systems. OpenPepXL also supports the MzIdentML 1.2 format for XL-MS identification results. It is freely available under a three-clause BSD license at https://openms.org/openpepxl.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Software / Reagentes de Ligações Cruzadas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Mol Cell Proteomics Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Software / Reagentes de Ligações Cruzadas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Mol Cell Proteomics Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2020 Tipo de documento: Article