Gross M, Gathof B S, Kölle P, Gresser U
Purinlabor, Medizinischen Poliklinik, Klinikum Innenstadt, Ludwig-Maximilians-Universität München, Germany.
Electrophoresis. 1995 Oct;16(10):1927-9. doi: 10.1002/elps.11501601318.
We report a new screening method for adenylosuccinate lyase (ASase) deficiency using capillary electrophoresis (CE). This enzyme defect causes secondary autism and psychomotor retardation in early childhood. In all body fluids of these patients, two succinylpurine metabolites can be found that are normally not detectable: succinyladenosine and succinylaminoimidazole carboxamide (SAICA) riboside. A Beckman P/ACE 2050 capillary electrophoresis system was used with a 47.1 cm capillary, 75 microns ID, and the P/ACE Beckman UV absorbance detector. Untreated urine, injected for 1 s, was separated in a pH 8.63 borate buffer at 20 kV. The two succinylpurines (migration times 13.36 and 13.60 min) were detected at 254 nm only in urine of patients with ASase deficiency but not in control samples.
我们报告了一种使用毛细管电泳(CE)筛查腺苷酸琥珀酸裂解酶(ASase)缺乏症的新方法。这种酶缺陷会在幼儿期导致继发性自闭症和精神运动发育迟缓。在这些患者的所有体液中,可以发现两种正常情况下无法检测到的琥珀酰嘌呤代谢物:琥珀酰腺苷和琥珀酰氨基咪唑甲酰胺(SAICA)核苷。使用了贝克曼P/ACE 2050毛细管电泳系统,配备一根47.1厘米长、内径75微米的毛细管以及P/ACE贝克曼紫外吸收检测器。未经处理的尿液进样1秒,在pH 8.63的硼酸盐缓冲液中于20 kV电压下进行分离。仅在ASase缺乏症患者的尿液中,于254纳米处检测到了两种琥珀酰嘌呤(迁移时间分别为13.36分钟和13.60分钟),而在对照样本中未检测到。