Lo Stanley F, Young Velta, Rhead William J
Department of Pathology, Medical College of Wisconsin, Milwaukee, WI, USA.
Methods Mol Biol. 2010;603:433-43. doi: 10.1007/978-1-60761-459-3_42.
A patient suspected of an inborn error of metabolism will commonly have urine organic acid analysis performed as part of their workup. The traditional urine organic acid method involves extraction of the acidic fraction from urine samples using an organic solvent, derivatization of extracted compounds, and identification using gas chromatography-mass spectrometry (GC-MS). Unfortunately, the extraction step results in the loss of many neutral and positively charged compounds, which may be of interest to metabolic physicians and biochemical geneticists. By replacing the traditional extraction step with an enzymatic treatment of the sample with urease, an abundance of organic molecules are available for separation and quantitation by GC-MS. The urease method is a useful adjunct to newborn screening follow-up and it has the additional benefit of being able to identify many classes of biochemical compounds, such as amino acids, acylglycines, neurotransmitters, and carbohydrates. The method below describes the urease treatment, derivatization, and the organic acids, and other biochemical metabolites that can be identified.
疑似患有先天性代谢缺陷的患者通常会进行尿有机酸分析,作为其检查的一部分。传统的尿有机酸检测方法包括:使用有机溶剂从尿液样本中提取酸性成分,对提取的化合物进行衍生化处理,然后使用气相色谱 - 质谱联用仪(GC - MS)进行鉴定。不幸的是,提取步骤会导致许多中性和带正电荷的化合物丢失,而这些化合物可能是代谢内科医生和生化遗传学家感兴趣的。通过用脲酶对样品进行酶处理来取代传统的提取步骤,大量有机分子可用于通过GC - MS进行分离和定量。脲酶法是新生儿筛查后续检查的有用辅助方法,它还有一个额外的好处,即能够鉴定许多类别的生化化合物,如氨基酸、酰基甘氨酸、神经递质和碳水化合物。以下方法描述了脲酶处理、衍生化以及可鉴定的有机酸和其他生化代谢物。