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Gaining Confidence in the Elusive Histidine Phosphoproteome

[Image: see text] 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...

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Detalles Bibliográficos
Autores principales: Potel, Clement M., Lin, Miao-Hsia, Prust, Nadine, van den Toorn, Henk W. P., Heck, Albert J. R., Lemeer, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506798/
https://www.ncbi.nlm.nih.gov/pubmed/30969750
http://dx.doi.org/10.1021/acs.analchem.9b00734
Descripción
Sumario:[Image: see text] 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.