| First Author | Vowinckel J | Year | 2012 |
| Journal | FEBS Lett | Volume | 586 |
| Issue | 21 | Pages | 3819-24 |
| PubMed ID | 23022564 | Mgi Jnum | J:201289 |
| Mgi Id | MGI:5512934 | Doi | 10.1016/j.febslet.2012.09.027 |
| Citation | Vowinckel J, et al. (2012) Histaminylation of glutamine residues is a novel posttranslational modification implicated in G-protein signaling. FEBS Lett 586(21):3819-24 |
| abstractText | Posttranslational modifications (PTM) have been shown to be essential for protein function and signaling. Here we report the identification of a novel modification, protein transfer of histamine, and provide evidence for its function in G protein signaling. Histamine, known as neurotransmitter and mediator of the inflammatory response, was found incorporated into mastocytoma proteins. Histaminylation was dependent on transglutaminase II. Mass spectrometry confirmed histamine modification of the small and heterotrimeric G proteins Cdc42, Galphao1 and Galphaq. The modification was specific for glutamine residues in the catalytic core, and triggered their constitutive activation. TGM2-mediated histaminylation is thus a novel PTM that functions in G protein signaling. Protein alphamonoaminylations, thus including histaminylation, serotonylation, dopaminylation and norepinephrinylation, hence emerge as a novel class of regulatory PTMs. |
