Mechanisms of Neurotransmitter Biosynthesis

描述（由申请人提供）：苯丙氨酸羟化酶、酪氨酸羟化酶和色氨酸羟化酶组成非血红素铁蝶呤依赖性芳香族氨基酸羟化酶家族。每种酶都催化其底物的芳族侧链在中枢神经系统正常功能的关键反应中的羟基化：苯丙氨酸代谢、儿茶酚胺生物合成和5-羟色胺生物合成。除了它们的生理重要性之外，这些酶的独特之处在于它们是唯一的非血红素铁酶，其生理反应是未活化的芳香族系统的羟基化。本提案解决了几个悬而未决的问题，这些酶的催化和调节机制。共同的催化机制将使用快速反应方法和光谱学的组合进行研究，目的是表征催化中的单个铁物种。蛋白质动力学在酪氨酸和苯丙氨酸羟化酶催化中的作用将通过确定底物对与溶剂的肽键交换动力学的影响来研究。苯丙氨酸和酪氨酸羟化酶的调节对它们的正常功能至关重要。肽键交换的动力学将用于评估苯丙氨酸羟化酶变构调节的文献模型，而荧光方法将用于评估酪氨酸羟化酶通过磷酸化调节的结构模型。这些酶中的活性位点铁原子由2-组氨酸-1-羧酸酯面三联体结合。苯丙氨酸羟化酶中的这两个组氨酸将被类似物取代，并使用稳态动力学、产物分配和动力学同位素效应的组合来确定对单个动力学步骤的影响。芳香族氨基酸羟化酶在中枢神经系统的正常功能中起着关键作用。苯丙氨酸羟化酶的丧失会导致苯丙酮尿症;需要酪氨酸羟化酶来产生神经递质多巴胺、去甲肾上腺素和肾上腺素;需要色氨酸羟化酶来合成神经递质血清素。

DESCRIPTION (provided by applicant): Phenylalanine hydroxylase, tyrosine hydroxylase, and tryptophan hydroxylase make up the family of non-heme iron pterin-dependent aromatic amino acid hydroxylases. Each enzyme catalyzes the hydroxylation of the aromatic side chain of its substrate in a reaction critical for proper functioning of the central nervous system: phenylalanine metabolism, catecholamine biosynthesis, and serotonin biosynthesis. In addition to their physiological importance, these enzymes are unique in that they are the only nonheme iron enzymes whose physiological reaction is the hydroxylation of unactivated aromatic systems. The present proposal addresses several outstanding questions regarding the catalytic and regulatory mechanisms of these enzymes. The common catalytic mechanism will be studied using a combination of rapid reaction methods and spectroscopy, with the goal of characterizing individual iron species in catalysis. The role of protein dynamics in catalysis by tyrosine and phenylalanine hydroxylase will be studied by determining the effects of substrates on the kinetics of peptide bond exchange with solvent. The regulation of phenylalanine and tyrosine hydroxylase is critical to their proper function. The kinetics of peptide bond exchange will be used to evaluate a literature model for allosteric regulation of phenylalanine hydroxylase, while fluorescence methods will be used to evaluate a structural model for the regulation of tyrosine hydroxylase by phosphorylation. The active site iron atom in these enzymes is bound by a 2-Histidine-1-carboxylate facial triad. These two histidines in phenylalanine hydroxylase will be replaced with analogs and the effects on individual kinetic steps determined, using a combination of steady state kinetics, product partitioning, and kinetic isotope effects. The aromatic amino acid hydroxylases play critical roles in the proper functioning of the central nervous system. Loss of phenylalanine hydroxylase results in phenylketonuria; tyrosine hydroxylase is required to make the neurotransmitters dopamine, norepinephrine, and epinephrine; and tryptophan hydroxylase is required to synthesize the neurotransmitter serotonin.