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Gaining Confidence in the Elusive Histidine Phosphoproteome.

Clement M PotelMiao-Hsia LinNadine PrustHenk W P van den ToornAlbert J R HeckSimone Lemeer
Published in: Analytical chemistry (2019)
Recent technological advances have made it possible to investigate the hitherto rather elusive protein histidine phosphorylation. However, confident site-specific localization of protein histidine phosphorylation remains challenging. Here, we address this problem, presenting a mass-spectrometry-based approach that outperforms classical HCD fragmentation without compromising sensitivity. We use the phosphohistidine immonium ion as a diagnostic tool as well as ETD-based fragmentation techniques to achieve unambiguous identification and localization of histidine-phosphorylation sites. The work presented here will allow more confident investigation of the phosphohistidine proteome to reveal the roles of histidine phosphorylation in cellular signaling events.
Keyphrases
  • protein kinase
  • mass spectrometry
  • liquid chromatography
  • genome wide
  • binding protein
  • high resolution
  • single cell