Hayakawa C, Aono S, Keino H, Mizutani N, Watanabe K, Ikemoto M, Totani M, Murachi T, Kashiwamata S
Department of Pediatrics, Nagoya University School of Medicine, Japan.
Eur J Pediatr. 1991 Sep;150(11):800-3. doi: 10.1007/BF02026716.
In Japan, hyperargininemia has been reported in only 5 unrelated families and four patients are alive at present. In this study we examined arginase protein in erythrocytes of these Japanese patients using two analytical methods of immunoblotting and two-dimensional gel electrophoresis. Immunoblotting study with anti-E. coli-expressed human liver arginase rabbit IgG revealed lack of cross-reacting materials in the erythrocyte lysates from these patients. On two-dimensional gels, arginase protein was detected in any control subject, but it was completely absent in all the patients studied. These results suggest that either arginase protein in erythrocytes is not produced or it is structurally labile in these patients.
在日本,仅在5个无亲缘关系的家族中报告过高精氨酸血症,目前有4名患者存活。在本研究中,我们使用免疫印迹和二维凝胶电泳这两种分析方法,检测了这些日本患者红细胞中的精氨酸酶蛋白。用抗大肠杆菌表达的人肝脏精氨酸酶兔IgG进行的免疫印迹研究表明,这些患者的红细胞裂解物中缺乏交叉反应物质。在二维凝胶上,在任何对照受试者中都检测到了精氨酸酶蛋白,但在所有研究的患者中该蛋白完全缺失。这些结果表明,在这些患者中,红细胞中的精氨酸酶蛋白要么未产生,要么在结构上不稳定。