Effects of mutations in tyrosine hydroxylase associated with progressive dystonia on the activity and stability of the protein

Montserrat Royo, S. Colette Daubner, Paul F. Fitzpatrick

Research output: Contribution to journalArticlepeer-review

22 Scopus citations


Tyrosine hydroxylase (TyrH) catalyzes the conversion of tyrosine to dihydroxyphenylalanine (DOPA), the rate-limiting step in the biosynthesis of dopamine. Four mutations in the TyrH gene have recently been described in cases of autosomal recessive DOPA-responsive dystonia (Swaans et al., Ann Hum Genet 2000;64:25-31). All four are predicted to result in changes in single amino acid residues in the catalytic domain of the protein: T245P, T283M, R306H, and T463M. To determine the effects of these mutations on the molecular properties of the enzyme, mutant proteins containing the individual single amino acid changes have been expressed in bacteria and purified. Only the T283M mutation results in a decrease in the enzyme kcat value, while the T245P enzyme has a slightly higher value than the wild-type enzyme. The only case in which a Km value for either tyrosine or tetrahydrobiopterin is perturbed is the T245P enzyme, for which the Km value for tyrosine has increased about 50%. In contrast to the minor effects of the mutations on enzyme activity, the stability is decreased significantly by the mutations. The R306H and T283M enzymes are the least stable, losing activity 30- and 50-fold more rapidly than the wild-type enzyme. The apparent Tm value for unfolding was decreased by 3.9, 8.2, and 7.2° for the T245P, R306H, and T463M enzymes, while the T283M enzyme was too unstable for measurement of a Tm value. The results establish that the physiological effects of the mutations are primarily due to the decreased stability of the mutant proteins rather than decreases in their intrinsic activities.

Original languageEnglish (US)
Pages (from-to)14-21
Number of pages8
JournalProteins: Structure, Function and Genetics
Issue number1
StatePublished - Jan 1 2005


  • Human
  • Kinetics
  • Parkinsonism
  • Protein stability
  • Tetrahydrobiopterin

ASJC Scopus subject areas

  • Structural Biology
  • Biochemistry
  • Molecular Biology


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