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dc.contributor.authorPey, A.L.*
dc.contributor.authorMartinez, A.*
dc.contributor.authorCharubala, R.*
dc.contributor.authorMaitland, Derek J.*
dc.contributor.authorTeigen, K.*
dc.contributor.authorCalvo, A.*
dc.contributor.authorPfleiderer, W.*
dc.contributor.authorWood, John M.*
dc.contributor.authorSchallreuter, Karin U.*
dc.date.accessioned2017-11-07T11:46:23Z
dc.date.available2017-11-07T11:46:23Z
dc.date.issued2006
dc.identifier.citationPey AL, Martinez A, Charubala R, Maitland DJ, Teigen K, Calvo A, Pfleiderer W, Wood JM and Schallreuter KU (2006) Specific interaction of the diastereomers 7(R)- and 7(S)-tetrahydrobiopterin with phenylalanine hydroxylase: implications for understanding primapterinuria and vitiligo. The Faseb Journal. 20(12): 2130-2132.en_US
dc.identifier.urihttp://hdl.handle.net/10454/13682
dc.descriptionnoen_US
dc.description.abstractPterin-4a-carbinolamine dehydratase (PCD) is an essential component of the phenylalanine hydroxylase (PAH) system, catalyzing the regeneration of the essential cofactor 6(R)-L-erythro-5,6,7,8-tetrahydrobiopterin [6(R)BH4]. Mutations in PCD or its deactivation by hydrogen peroxide result in the generation of 7(R,S)BH4, which is a potent inhibitor of PAH that has been implicated in primapterinuria, a variant form of phenylketonuria, and in the skin depigmentation disorder vitiligo. We have synthesized and separated the 7(R) and 7(S) diastereomers confirming their structure by NMR. Both 7(R)- and 7(S)BH4 function as poor cofactors for PAH, whereas only 7(S)BH4 acts as a potent competitive inhibitor vs. 6(R)BH4 (Ki=2.3–4.9 μM). Kinetic and binding studies, as well as characterization of the pterin-enzyme complexes by fluorescence spectroscopy, revealed that the inhibitory effects of 7(R,S)BH4 on PAH are in fact specifically based on 7(S)BH4 binding. The molecular dynamics simulated structures of the pterin-PAH complexes indicate that 7(S)BH4 inhibition is due to its interaction with the polar region at the pterin binding site close to Ser-251, whereas its low efficiency as cofactor is related to a suboptimal positioning toward the catalytic iron. 7(S)BH4 is not an inhibitor for tyrosine hydroxylase (TH) in the physiological range, presumably due to the replacement of Ser-251 by the corresponding Ala297. Taken together, our results identified structural determinants for the specific regulation of PAH and TH by 7(S)BH4, which in turn aid in the understanding of primapterinuria and acute vitiligo. —Pey, A. L., Martinez, A., Charubala, R., Maitland, D. J., Teigen, K., Calvo, A., Pfleiderer, W., Wood, J. M., Schallreuter, K. U. Specific interaction of the diastereomers 7(R)- and 7(S)-tetrahydrobiopterin with phenylalanine hydroxylase: implications for understanding primapterinuria and vitiligoen_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttps://doi.org/10.1096/fj.06-5835fjeen_US
dc.subjectPterin 4a-carbinolamine dehydratase; NMR; Isothermal titration calorimetry; Primapterinuria; Vitiligoen_US
dc.titleSpecific interaction of the diastereomers 7(R)- and 7(S)-tetrahydrobiopterin with phenylalanine hydroxylase: implications for understanding primapterinuria and vitiligoen_US
dc.status.refereedyesen_US
dc.typeArticleen_US
dc.type.versionNo full-text in the repositoryen_US


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