Hauer C R, Leimbacher W, Hunziker P, Neuheiser F, Blau N, Heizmann C W
Department of Pediatrics, University of Zurich, Switzerland.
Biochem Biophys Res Commun. 1992 Jan 31;182(2):953-9. doi: 10.1016/0006-291x(92)91824-a.
The most frequent variant of atypical phenylketonuria, an inborn error of metabolism, is characterized by a low activity of the 6-pyruvoyl tetrahydropterin synthase. We purified and characterized this enzyme from salmon liver known to contain high levels. After digestion, peptides were sequenced by tandem mass spectrometry and/or automated Edman microsequence analysis. Both a free amine terminus and an N-acetylated amine terminus were found, indicating the presence of two isoforms. The peptide sequences determined here have a high degree of homology with the protein sequence deduced from cDNA for rat 6-pyruvoyl tetrahydropterin synthase (1), however, the amine termini of these proteins differ significantly.
非典型苯丙酮尿症是一种先天性代谢缺陷疾病,其最常见的变异形式表现为6-丙酮酰四氢蝶呤合酶活性低下。我们从已知该酶含量高的鲑鱼肝中纯化并鉴定了这种酶。酶解后,通过串联质谱和/或自动埃德曼微量序列分析对肽段进行测序。发现了一个游离胺末端和一个N-乙酰化胺末端,表明存在两种同工型。这里确定的肽序列与从大鼠6-丙酮酰四氢蝶呤合酶的cDNA推导的蛋白质序列具有高度同源性(1),然而,这些蛋白质的胺末端存在显著差异。