Demonstration of the phosphorylation-dependent interaction of tryptophan hydroxylase with the 14-3-3 protein

Biochem Biophys Res Commun. 1993 Jul 15;194(1):144-9. doi: 10.1006/bbrc.1993.1796.

Abstract

The molecular mechanism of the phosphorylation-dependent activation of tryptophan hydroxylase is studied with respect to the role of the 14-3-3 protein. Reexamination of the system reconstituted with the purified TRH and the 14-3-3 protein showed that the level of the TRH activity correlated with the extent of the Ca2+/calmodulin- or the cAMP-dependent phosphorylation in TRH. The experiment confirmed the requirement of the 14-3-3 protein for the activation, but the 14-3-3 protein added into the assay mixture did not affect either the extent nor the specificity of the phosphorylation. However, the analysis of the assay mixture on a pteridine-based affinity column indicated the formation of a complex between TRH and the 14-3-3 protein, where the complex formation depended on the phosphorylation of TRH. The complex between the phosphorylated TRH and the 14-3-3 protein could also be detected by analysis of crude brainstem extract previously phosphorylated by endogeneous Ca2+/calmodulin-dependent protein kinase. The 14-3-3 protein, therefore, appears to be a phosphorylation-dependent TRH-binding protein whose interaction causes the activation of TRH.

MeSH terms

  • 14-3-3 Proteins
  • Animals
  • Brain Stem / enzymology*
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Kinetics
  • Molecular Weight
  • Nerve Tissue Proteins / isolation & purification
  • Nerve Tissue Proteins / metabolism*
  • Phosphorylation
  • Protein Binding
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinases / metabolism
  • Rats
  • Tyrosine 3-Monooxygenase / isolation & purification
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • 14-3-3 Proteins
  • Nerve Tissue Proteins
  • Tyrosine 3-Monooxygenase
  • Protein Kinases
  • Protein Kinase C
  • Calcium-Calmodulin-Dependent Protein Kinases