Exploring the mode of action of ebselen in Trypanosoma brucei hexokinase inhibition

• Published in: International journal for parasitology -- drugs and drug resistance 2013-12, Vol.3, p.154-160
• Main Authors: Joice, April C., Harris, Michael T., Kahney, Elizabeth W., Dodson, Heidi C., Maselli, Andrew G., Whitehead, Daniel C., Morris, James C.
• Format: Article
• Language: English
• Subjects: Ebselen; Hexokinase; Inhibitors; Trypanosoma brucei
• ISSN: 2211-3207; 2211-3207
• DOI: 10.1016/j.ijpddr.2013.08.002

[Display omitted] •Trypanosoma brucei hexokinase 1 is irreversibly inhibited by ebselen.•Mutation of Cys residues did not change hexamer abundance.•Active variants bearing Cys mutations were inhibited by ebselen.•ESI–MS/MS indicated that the essential Cys327 was oxidized by ebselen. Glycolysis is essential to Trypanosoma brucei, the causative agent of African sleeping sickness, suggesting enzymes in the pathway could be targets for drug development. Ebselen (2-phenyl-1,2-benzisoselenazol-3(2H)-one, EbSe) was identified in a screen as a potent inhibitor of T. brucei hexokinase 1 (TbHK1), the first enzyme in the pathway. EbSe has a history of promiscuity as an enzyme inhibitor, inactivating proteins through seleno-sulfide conjugation with Cys residues. Indeed, dilution of TbHK1 and inhibitor following incubation did not temper inhibition suggesting conjugate formation. Using mass spectrometry to analyze EbSe-based modifications revealed that two Cys residues (C327 and C369) were oxidized after treatment. Site-directed mutagenesis of C327 led to enzyme inactivation indicating that C327 was essential for catalysis. C369 was not essential, suggesting that EbSe inhibition of TbHK1 was the consequence of modification of C327 via thiol oxidation. Additionally, neither EbSe treatment nor mutation of the nine TbHK1 Cys residues appreciably altered enzyme quaternary structure.