Alkylation of rabbit muscle creatine kinase surface methionine residues inhibits enzyme activity in vitro

Steinritz, Dirk; Lüling, Robin; Siegert, Markus; Mückter, Harald; Popp, Tanja; Reinemer, Peter; Gudermann, Thomas; Thiermann, Horst und John, Harald (2021): Alkylation of rabbit muscle creatine kinase surface methionine residues inhibits enzyme activity in vitro. In: Archives of toxicology, Bd. 95, Nr. 10: S. 3253-3261

Abstract

Creatine kinase (CK) catalyzes the formation of phosphocreatine from adenosine triphosphate (ATP) and creatine. The highly reactive free cysteine residue in the active site of the enzyme (Cys283) is considered essential for the enzymatic activity. In previous studies we demonstrated that Cys283 is targeted by the alkylating chemical warfare agent sulfur mustard (SM) yielding a thioether with a hydroxyethylthioethyl (HETE)-moiety. In the present study, the effect of SM on rabbit muscle CK (rmCK) activity was investigated with special focus on the alkylation of Cys283 and of reactive methionine (Met) residues. For investigation of SM-alkylated amino acids in rmCK, micro liquid chromatography-electrospray ionization high-resolution tandem-mass spectrometry measurements were performed using the Orbitrap technology. The treatment of rmCK with SM resulted in a decrease of enzyme activity. However, this decrease did only weakly correlate to the modification of Cys283 but was conclusive for the formation of Met70-HETE and Met179-HETE. In contrast, the activity of mutants of rmCK produced by side-directed mutagenesis that contained substitutions of the respective Met residues (Met70Ala, Met179Leu, and Met70Ala/Met179Leu) was highly resistant against SM. Our results point to a critical role of the surface exposed Met70 and Met179 residues for CK activity.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin ; Medizin > Walther-Straub-Institut für Pharmakologie und Toxikologie
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• Sprache: Englisch