pHisphorylation: the emergence of histidine phosphorylation as a reversible regulatory modification - PubMed (original) (raw)

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pHisphorylation: the emergence of histidine phosphorylation as a reversible regulatory modification

Stephen Rush Fuhs et al. Curr Opin Cell Biol. 2017 Apr.

Abstract

Histidine phosphorylation is crucial for prokaryotic signal transduction and as an intermediate for several metabolic enzymes, yet its role in mammalian cells remains largely uncharted. This is primarily caused by difficulties in studying histidine phosphorylation because of the relative instability of phosphohistidine (pHis) and lack of specific antibodies and methods to preserve and detect it. The recent synthesis of stable pHis analogs has enabled development of pHis-specific antibodies and their use has started to shed light onto this important, yet enigmatic posttranslational modification. We are beginning to understand that pHis has broader roles in protein and cellular function including; cell cycle regulation, phagocytosis, regulation of ion channel activity and metal ion coordination. Two mammalian histidine kinases (NME1 and NME2), two pHis phosphatases (PHPT1 and LHPP), and a handful of substrates were previously identified. These new tools have already led to the discovery of an additional phosphatase (PGAM5) and hundreds of putative substrates. New methodologies are also being developed to probe the pHis phosphoproteome and determine functional consequences, including negative ion mode mass spectroscopy and unnatural amino acid incorporation. These new tools and strategies have the potential to overcome the unique challenges that have been holding back our understanding of pHis in cell biology.

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Figures

Figure 1

Figure 1. pHis Isomers and Structural Analogs

Structural drawings of (A) the phosphoester amino acids; pSer, pThr and pTyr are contrasted with (B) histidine, 3-phosphohistidine (3-pHis) and 1-phosphohistidine (1-pHis). Examples of phosphohistidine structural analogs designed for antibody generation include; (C) phosphofurylalanine and the two phosphoryltriazolylalanine analogs (3-pTza) and (1-pTza). (D) Second-generation, pyrazole-based pHis analogs; 4-Phosphopyrazol-2-yl alanine (pPza) and phosphono-pyrazolyl ethylamine (pPye).

Figure 2

Figure 2. Summary of pHis Cellular Functions

An illustration of the pHis related proteins discussed in this review and their various functions, enzymatic reactions and subcellular localizations. NME1/2 protein histidine kinase functions are in yellow, pHis enzyme intermediates are in green, phosphohistidine phosphatases are in white and pHis substrates are in bold. Beneath each protein’s gene name is the specific amino acid position number of the pHis residue in red. Cellular functions of specific pHis proteins are in blue. The subcellular localization of pHis related proteins and functions are in grey. Curved arrows represent reactions catalyzed by enzymes that utilize pHis intermediates. For LHPP, phospholysine and 3-phsphohistidine are substrates in vitro, however no known substrates have yet been identified in vivo.

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