Evaluation of Parameters for Confident Phosphorylation Site Localization Using an Orbitrap Fusion Tribrid Mass Spectrometer

J Proteome Res. 2017 Sep 1;16(9):3448-3459. doi: 10.1021/acs.jproteome.7b00337. Epub 2017 Aug 11.

Abstract

Confident identification of sites of protein phosphorylation by mass spectrometry (MS) is essential to advance understanding of phosphorylation-mediated signaling events. However, the development of novel instrumentation requires that methods for MS data acquisition and its interrogation be evaluated and optimized for high-throughput phosphoproteomics. Here we compare and contrast eight MS acquisition methods on the novel tribrid Orbitrap Fusion MS platform using both a synthetic phosphopeptide library and a complex phosphopeptide-enriched cell lysate. In addition to evaluating multiple fragmentation regimes (HCD, EThcD, and neutral-loss-triggered ET(ca/hc)D) and analyzers for MS/MS (orbitrap (OT) versus ion trap (IT)), we also compare two commonly used bioinformatics platforms, Andromeda with PTM-score, and MASCOT with ptmRS for confident phosphopeptide identification and, crucially, phosphosite localization. Our findings demonstrate that optimal phosphosite identification is achieved using HCD fragmentation and high-resolution orbitrap-based MS/MS analysis, employing MASCOT/ptmRS for data interrogation. Although EThcD is optimal for confident site localization for a given PSM, the increased duty cycle compared with HCD compromises the numbers of phosphosites identified. Finally, our data highlight that a charge-state-dependent fragmentation regime and a multiple algorithm search strategy are likely to be of benefit for confident large-scale phosphosite localization.

Keywords: Andromeda; EThcD; MASCOT; Orbitrap Fusion; PTM-score; mass spectrometry; phosphoproteomics; phosphorylation site; phosphosite localization; ptmRS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Benchmarking
  • Cell Line, Tumor
  • Humans
  • Mass Spectrometry / instrumentation
  • Mass Spectrometry / methods*
  • Osteoblasts / cytology
  • Osteoblasts / metabolism*
  • Peptide Fragments / analysis*
  • Phosphoproteins / chemistry
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Protein Processing, Post-Translational*
  • Proteomics / methods*
  • Software

Substances

  • Peptide Fragments
  • Phosphoproteins