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Abundance-based classifier for the prediction of mass spectrometric peptide detectability upon enrichment (PPA).
Muntel, Jan; Boswell, Sarah A; Tang, Shaojun; Ahmed, Saima; Wapinski, Ilan; Foley, Greg; Steen, Hanno; Springer, Michael.
Afiliação
  • Muntel J; From the ‡Departments of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA;
  • Boswell SA; §Department of Systems Biology, Harvard Medical School, Boston, MA.
  • Tang S; From the ‡Departments of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA;
  • Ahmed S; From the ‡Departments of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA;
  • Wapinski I; §Department of Systems Biology, Harvard Medical School, Boston, MA.
  • Foley G; §Department of Systems Biology, Harvard Medical School, Boston, MA.
  • Steen H; From the ‡Departments of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA; Michael_springer@hms.harvard.edu hanno.steen@childrens.harvard.edu.
  • Springer M; §Department of Systems Biology, Harvard Medical School, Boston, MA Michael_springer@hms.harvard.edu hanno.steen@childrens.harvard.edu.
Mol Cell Proteomics ; 14(2): 430-40, 2015 Feb.
Article em En | MEDLINE | ID: mdl-25473088
ABSTRACT
The function of a large percentage of proteins is modulated by post-translational modifications (PTMs). Currently, mass spectrometry (MS) is the only proteome-wide technology that can identify PTMs. Unfortunately, the inability to detect a PTM by MS is not proof that the modification is not present. The detectability of peptides varies significantly making MS potentially blind to a large fraction of peptides. Learning from published algorithms that generally focus on predicting the most detectable peptides we developed a tool that incorporates protein abundance into the peptide prediction algorithm with the aim to determine the detectability of every peptide within a protein. We tested our tool, "Peptide Prediction with Abundance" (PPA), on in-house acquired as well as published data sets from other groups acquired on different instrument platforms. Incorporation of protein abundance into the prediction allows us to assess not only the detectability of all peptides but also whether a peptide of interest is likely to become detectable upon enrichment. We validated the ability of our tool to predict changes in protein detectability with a dilution series of 31 purified proteins at several different concentrations. PPA predicted the concentration dependent peptide detectability in 78% of the cases correctly, demonstrating its utility for predicting the protein enrichment needed to observe a peptide of interest in targeted experiments. This is especially important in the analysis of PTMs. PPA is available as a web-based or executable package that can work with generally applicable defaults or retrained from a pilot MS data set.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Espectrometria de Massas / Algoritmos Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Espectrometria de Massas / Algoritmos Idioma: En Ano de publicação: 2015 Tipo de documento: Article