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Histone H2AX Y142 phosphorylation is a low abundance modification

  • Abubakar A. Hatimy
  • , Martin J.G. Browne
  • , Andrew Flaus
  • , Steve M.M. Sweet
  • Genome Damage and Stability Centre
  • University of Galway

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

9 Citations (Scopus)

Abstract

We employ targeted mass spectrometry to compare the levels of H2AX S139 phosphorylation (γH2AX) and Y142 phosphorylation. We use synthetic peptides to facilitate MS optimisation and estimate relative detection efficiencies for the different modifications. Despite phosphopeptide enrichment from large amounts of starting material, we are unable to detect endogenous H2AX Y142 phosphorylation, indicating that it is present in low abundance (<1%). We also calculate the relative levels of H2AX compared to other H2A isoforms and quantify the proportion of H2AX that is phosphorylated on S139 (γH2AX) after ionising radiation.

Original languageEnglish
Pages (from-to)139-145
Number of pages7
JournalInternational Journal of Mass Spectrometry
Volume391
DOIs
Publication statusPublished - 30 Nov 2015

Keywords

  • Chromatin
  • DNA damage
  • Histone
  • Phosphorylation
  • Selected reaction monitoring

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