Phenylalanine hydroxylase (PheH), tyrosine hydroxylase (TyrH) and tryptophan hydroxylase (TrpH) make upthe family of tetrahydropterin dependent hydroxylases. These enzymes catalyze the iron-dependent aromatichydroxylation of their respective substrates. PheH in the liver catalyzes the hydroxylation of phenylalanine totyrosine. Mutations in PheH result in the inherited disease phenylketonuria. TyrH in the brain and adrenalgland catalyzes the hydroxylation of tyrosine to DOPA, the first step in the biosynthesis of the catecholamineneurotransmitters. Mutations in TyrH have been associated with Parkinson's disease. TrpH in the braincatalyzes the hydroxylation of tryptophan to 5-hydroxytryptophan,the first step in the biosynthesis of theneurotransmitter serotonin. Low levels of serotonin have been associated with depression, violence, andalcoholism. The chemical mechanism of TyrH has been studied extensively, and this proposal will expandonthe previous work. The mechanism of oxygen activation by PheH and TrpH will be studied using 18O kineticisotope effects.The reactivity of the hydroxylating intermediate in all three enzymes will be studied bymeasuring deuterium isotope effects on benzylic and aromatic hydroxylation. Rapid quench EPR andMossbauer spectroscopy will be used for spectroscopic characterization of the proposed hydroxylating intermediate.
| Roberts, Kenneth M; Pavon, Jorge Alex; Fitzpatrick, Paul F (2013) Kinetic mechanism of phenylalanine hydroxylase: intrinsic binding and rate constants from single-turnover experiments. Biochemistry 52:1062-73 |
| Pavon, Jorge Alex; Eser, Bekir; Huynh, Michaela T et al. (2010) Single turnover kinetics of tryptophan hydroxylase: evidence for a new intermediate in the reaction of the aromatic amino acid hydroxylases. Biochemistry 49:7563-71 |
| Pavon, Jorge Alex; Fitzpatrick, Paul F (2009) Demonstration of a peroxide shunt in the tetrahydropterin-dependent aromatic amino acid monooxygenases. J Am Chem Soc 131:4582-3 |
| Pavon, Jorge Alex; Fitzpatrick, Paul F (2006) Insights into the catalytic mechanisms of phenylalanine and tryptophan hydroxylase from kinetic isotope effects on aromatic hydroxylation. Biochemistry 45:11030-7 |
