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PMID: 8502995 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Feedback regulation mechanisms for the control of GTP cyclohydrolase I activity.

Science (New York, N.Y.) ·Vol. 260 ·No. 5113 ·1993-06-04 ·Pages 1507-10

Harada T, Kagamiyama H, Hatakeyama K

Abstract

Guanosine triphosphate (GTP) cyclohydrolase I, the rate-limiting enzyme in the biosynthesis of tetrahydrobiopterin (BH4), is subject to feedback inhibition by BH4, a cofactor for phenylalanine hydroxylase. Inhibition was found to depend specifically on BH4 and the presence of another protein (p35). The inhibition occurred through BH4-dependent complex formation between p35 protein and GTP cyclohydrolase I. Furthermore, the inhibition was specifically reversed by phenylalanine, and, in conjunction with p35, phenylalanine reduced the cooperativity of GTP cyclohydrolase I. These findings also provide a molecular basis for high plasma BH4 concentrations observed in patients with hyperphenylalaninemia caused by phenylalanine hydroxylase deficiency.

MeSH Terms
Animals Biological Factors/physiology Biopterin/analogs & derivatives,physiology Chromatography, Gel Feedback GTP Cyclohydrolase/antagonists & inhibitors,metabolism Humans In Vitro Techniques Liver/metabolism Phenylalanine/physiology Phenylalanine Hydroxylase/metabolism Protein Binding Rats Recombinant Proteins/metabolism Tissue Extracts
Chemicals
Biological Factors Recombinant Proteins Tissue Extracts Biopterin Phenylalanine Phenylalanine Hydroxylase GTP Cyclohydrolase sapropterin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Harada T
Department of Biochemistry, Osaka Medical College, Japan.
Kagamiyama H
Hatakeyama K
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1993-06-04
Pages
1507-10
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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