Rhode H, Elei E, Taube I, Podskarbi T, Horn A
Institute of Biochemistry, Medical Faculty, Friedrich Schiller University, Jena, Germany.
Clin Chim Acta. 1998 Jun 8;274(1):71-87. doi: 10.1016/s0009-8981(98)00052-7.
An enzymatically optimized, miniaturized (20 microl) fluorimetric assay of galactose-1-phosphate-uridyltransferase using dried blood spots for newborn screening is presented. The Beutler reaction principle has been adapted to the microtiter plate technology and acetone/methanol was used for complete deproteinization. A special ultramicro multiwell screening plate resistant to organic solvents has been developed and employed. The assay is simple, sensitive and inexpensive, due to small reagent volumes and the low prices of ultramicro screening plates. The reaction is linear with galactose-1-phosphate-uridyltransferase activity up to 120 min of incubation time. It shows low imprecision and good correlation to a quantitative validation test. For standardization the use of plate means or medians of activity or fluorescence values is proposed. Individual blank measurement prevents false negative assessments.
本文介绍了一种酶法优化的、小型化(20微升)的荧光测定法,用于利用干血斑进行新生儿半乳糖-1-磷酸尿苷转移酶筛查。Beutler反应原理已应用于微量滴定板技术,并使用丙酮/甲醇进行完全脱蛋白。已开发并采用了一种特殊的耐有机溶剂超微量多孔筛查板。由于试剂用量少且超微量筛查板价格低廉,该测定法简单、灵敏且成本低。在长达120分钟的孵育时间内,反应与半乳糖-1-磷酸尿苷转移酶活性呈线性关系。它显示出低不精密度,并且与定量验证试验具有良好的相关性。为实现标准化,建议使用板均值或活性或荧光值的中位数。单独的空白测量可防止假阴性评估。