Ohura T, Kominami E, Tada K, Katunuma N
Clin Chim Acta. 1984 Jan 16;136(1):29-37. doi: 10.1016/0009-8981(84)90244-4.
A sensitive and convenient radioisotopic assay for ornithine aminotransferase (OAT) and an enzyme immunoassay for human ornithine aminotransferase were developed for studying decrease in activity of this enzyme in gyrate atrophy of the choroid and retina with hyperornithinemia. Picogram amounts of human OAT could be detected by the enzyme immunoassay. The OAT activity in cultured fibroblasts from two patients was 6% and 2% of that in control fibroblasts, and did not increase on addition of a high concentration of vitamin B6. The decreased activity, assayed by enzyme immunoassay, was associated with decreased enzyme concentration, suggesting that deficiency of OAT in these patients is not due to production of a structurally altered enzyme lacking catalytic activity, but to decreased production of enzyme protein. When cells from patients were repeatedly subcultured, selective loss of both the activity and concentration of OAT was observed, without changes in activities of several other enzymes tested.
为研究脉络膜和视网膜回旋性萎缩伴高鸟氨酸血症时鸟氨酸转氨酶(OAT)活性降低的情况,开发了一种灵敏且便捷的放射性同位素法检测鸟氨酸转氨酶以及一种人鸟氨酸转氨酶的酶免疫分析法。通过酶免疫分析法可检测到皮克量的人OAT。两名患者培养的成纤维细胞中的OAT活性分别为对照成纤维细胞的6%和2%,添加高浓度维生素B6后活性并未增加。通过酶免疫分析法测定,活性降低与酶浓度降低相关,这表明这些患者中OAT的缺乏并非由于产生了缺乏催化活性的结构改变的酶,而是由于酶蛋白产生减少。当对患者的细胞进行反复传代培养时,观察到OAT的活性和浓度均选择性丧失,而所检测的其他几种酶的活性未发生变化。