Catalytic mechanisms and specificities of glutathione peroxidases: Variations of a basic scheme

• Published in: Biochimica et biophysica acta Vol. 1790; no. 11; pp. 1486 - 1500
• Main Authors: Toppo, Stefano, Flohé, Leopold, Ursini, Fulvio, Vanin, Stefano, Maiorino, Matilde
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.11.2009
• Subjects: Animals; Catalysis; Enzyme kinetics; Glutathione Peroxidase - chemistry; Glutathione Peroxidase - genetics; Glutathione Peroxidase - metabolism; Glutathione Peroxidase - physiology; Glutathione peroxidases; Humans; Hydroperoxide; Models, Biological; Models, Chemical; Models, Molecular; Molecular phylogenesis; Oxidation-Reduction; Phylogeny; Redox signaling; Selenium; Substrate Specificity; Hydroperoxide; Selenium; Enzyme kinetics; Glutathione peroxidases; Redox signaling; Molecular phylogenesis
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/j.bbagen.2009.04.007

Kinetics and molecular mechanisms of GPx-type enzymes are reviewed with emphasis on structural features relevant to efficiency and specificity. In Sec-GPxs the reaction takes place at a single redox centre with selenocysteine as redox-active residue (peroxidatic Sec, U P). In contrast, most of the non-vertebrate GPx have the U P replaced by a cysteine (peroxidatic Cys, C P) and work with a second redox centre that contains a resolving cysteine (C R). While the former type of enzymes is more or less specific for GSH, the latter are reduced by “redoxins”. The common denominator of the GPx family is the first redox centre comprising the (seleno)cysteine, tryptophan, asparagine and glutamine. In this architectural context the rate of hydroperoxide reduction by U P or C P, respectively, is enhanced by several orders of magnitude compared to that of free selenolate or thiolate. Mammalian GPx-1 dominates H 2O 2 metabolism, whereas the domain of GPx-4 is the reduction of lipid hydroperoxides with important consequences such as counteracting 12/15-lipoxygenase-induced apoptosis and regulation of inflammatory responses. Beyond, the degenerate GSH specificity of GPx-4 allows selenylation and oxidation to disulfides of protein thiols. Heterodimer formation of yeast GPx with a transcription factor is discussed as paradigm of a redox sensing that might also be valid in vertebrates.