Evaluation of the metal ion requirement of the human deoxyhypusine hydroxylase from HeLa cells using a novel enzyme assay

被引:19
作者
Csonga, R
Ettmayer, P
Auer, M
Eckerskorn, C
Eder, J
Klier, H
机构
[1] SANDOZ GMBH,DEPT IMMUNODERMATOL,A-1235 VIENNA,AUSTRIA
[2] MAX PLANCK INST BIOCHEM,D-82152 MARTINSRIED,GERMANY
关键词
eukaryotic initiation factor 5A; hypusine; posttranslational modification; mimosine; ciclopirox olamine; metal chelation; AMINO-ACID; SACCHAROMYCES-CEREVISIAE; HYPUSINE; INHIBITION; PEPTIDE; GROWTH;
D O I
10.1016/0014-5793(96)00020-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypusine synthesis in the eukaryotic initiation factor 5A is a unique two-step posttranslational modification. After deoxyhypusine is generated by the deoxyhypusine synthase, the deoxyhypusine hydroxylase (EC 1.14.99.29) catalyzes the formation of mature hypusine, A rapid assay for monitoring the deoxyhypusine hydroxylase activity was established, employing the oxidative cleavage of the hypusyl residue and subsequent extraction of the generated aldehydes. As metal ion chelators have been reported to inhibit the deoxyhypusine hydroxylase, the mechanism of this inhibition and the effect of transition metal ions on the enzyme activity were investigated. A ferric ion appears to be essential for enzymatic activity, the inhibition of which is entirely attributed to the metal ion binding capacity of the chelators.
引用
收藏
页码:209 / 214
页数:6
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