Hoogenraad N, Luisa de Martinis M, Danks D M
J Inherit Metab Dis. 1983;6(4):149-52. doi: 10.1007/BF02310869.
An unusual form of ornithine transcarbamylase deficiency was found in a male child who became unconscious at 8 months. Two maternal uncles had died during similar illnesses at 6 years and 11 years, respectively. Detailed studies of the enzyme showed 10% residual activity, a very low Km for carbamyl phosphate (0.015 mmol/l) and near normal amounts of immunoreactive protein with a smaller than normal subunit (molecular weight 37 800 instead of 39 700). This information was obtained from a 10 mg liver biopsy core using protein separation on SDS-polyacrylamide gel, electrophoretic transfer to nitrocellulose filters and probing with antibody to the enzyme. Resolution of the exact mutation causing this change will be of interest to those who are studying the processing of mitochondrial enzymes during transport from the cytoplasm.
在一名8个月时失去意识的男童身上发现了一种罕见形式的鸟氨酸转氨甲酰酶缺乏症。该男童的两位舅舅分别在6岁和11岁时因类似疾病去世。对该酶的详细研究表明,其残余活性为10%,氨基甲酰磷酸的米氏常数(Km)极低(0.015 mmol/l),免疫反应性蛋白含量接近正常,但亚基比正常的小(分子量为37 800,而非39 700)。这些信息是通过对10 mg肝活检组织进行以下操作获得的:在SDS-聚丙烯酰胺凝胶上进行蛋白质分离,电泳转移至硝酸纤维素滤膜,并用该酶的抗体进行检测。确定导致这种变化的确切突变,将引起那些研究线粒体酶从细胞质转运过程的人员的兴趣。