Tetrahydrobiopterin depletion and ubiquitylation of neuronal nitric oxide synthase

Yasuhiko Kamada, Gary J. Jenkins, Miranda Lau, Anwar Y. Dunbar, Ezra R. Lowe, Yoichi Osawa

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Tetrahydrobiopterin is a necessary cofactor for the synthesis of nitric oxide by the hemeprotein enzyme, NO-synthase (NOS). It is widely thought that inadequate levels of tetrahydrobiopterin lead to tissue injury and organ dysfunction due, in part, to formation of superoxide from pterin-deficient NOS. In the course of studies on the ubiquitylation of neuronal NOS (nNOS), we have found that certain substrate analogs, such as N G-nitro-l-arginine, stabilize the dimeric form of nNOS and protect the enzyme from ubiquitylation. Since tetrahydrobiopterin is known to bind near heme and confers stability to the active dimeric structure of nNOS, we wondered if the loss of tetrahydrobiopterin could be an endogenous signal for nNOS ubiquitylation and degradation. We show here in HEK293 cells stably transfected with nNOS that depletion of tetrahydrobiopterin by treatment with 2,4-diamino-6- hydroxypyrimidine leads to destabilization of the dimeric form and enhances ubiquitylation of nNOS. Sepiapterin, a precursor to tetrahydrobiopterin in the salvage pathway, completely reverses the effect of 2,4-diamino-6- hydroxypyrimidine on nNOS ubiquitylation. Consistent with that found in cells, the in vitro ubiquitylation of nNOS by reticulocyte proteins decreases when tetrahydrobiopterin is present. Thus, inadequate amounts of tetrahydrobiopterin may lead to a sustained decrease in the steady state level of nNOS that is not readily reversed.

Original languageEnglish
Pages (from-to)19-27
Number of pages9
JournalMolecular Brain Research
Volume142
Issue number1
DOIs
Publication statusPublished - Dec 7 2005
Externally publishedYes

Keywords

  • NO synthase
  • Pterin
  • Ubiquitin

ASJC Scopus subject areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience

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