Mechanistic studies on the enzymatic processing of fluorinated methionine analogs by Trichomonas vaginalis methionine γ-lyase
Moya, Ignace A and Westrop, Gareth D and Coombs, Graham H and Honek, John F (2011) Mechanistic studies on the enzymatic processing of fluorinated methionine analogs by Trichomonas vaginalis methionine γ-lyase. Biochemical Journal. (https://doi.org/10.1042/BJ20101986)
Full text not available in this repository.Request a copyAbstract
L-Trifluoromethionine (TFM), a potential prodrug, was reported to be toxic toward human pathogens that express L-methionine γ-lyase (MGL; EC: 4.4.1.11), a pyridoxal phosphate-containing enzyme that converts L-methionine to α-ketobutyrate, ammonia and methyl mercaptan. It has been hypothesized that the extremely reactive thiocarbonyl difluoride is produced when the enzyme acts upon TFM, resulting in cellular toxicity. The potential application of the fluorinated thiomethyl group in other areas of biochemistry and medicinal chemistry requires additional studies. Therefore a detailed investigation of the theoretical and experimental chemistry and biochemistry of these fluorinated groups (CF3S- and CF2HS-) has been undertaken to trap and identify chemical intermediates produced by enzyme processing of molecules containing these fluorinated moieties. MGL from Trichomonas vaginalis (TvMGL) and a chemical model system of the reaction were utilized in order to investigate the cofactor-dependent activation of TFM and previously uninvestigated L-difluoromethionine (DFM). The differences in toxicity between TFM and DFM were evaluated against Escherichia coli expressing TvMGL1, as well as the intact human pathogen, T. vaginalis. The relationship between the chemical structure of the reactive intermediates produced from the enzymatic processing of these analogs and their cellular toxicity are discussed.
-
-
Item type: Article ID code: 32496 Dates: DateEvent10 June 2011PublishedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 10 Aug 2011 12:59 Last modified: 08 Apr 2024 19:19 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/32496