Weyant R S, Chan W C, Austin G E
Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia 30322.
Am J Clin Pathol. 1988 Mar;89(3):384-9. doi: 10.1093/ajcp/89.3.384.
An automated method for analytical subcellular fractionation which utilizes routinely available reagents and equipment is described. Tissues are fractionated in Percoll density gradients and marker enzyme analysis of gradient fractions is performed with the Cobas-Bio centrifugal analyzer. Manual assays for cytochrome oxidase and protein were adapted for use with the instrument along with commercially available 5'-nucleotidase, lactate dehydrogenase, and acid phosphatase assay kits. Crude liver homogenate fractions containing different levels of enzyme activity were used to examine the linearity of the enzyme assays. The assays were shown to be linear at high and low levels of activity. Within-run precision studies using high and low activity liver homogenate pools were also performed, and a coefficient of variation of less than or equal to 5.5% was obtained for all assays. This method was used to analyze subcellular fractions from a Percoll density gradient separation of mouse liver homogenate material. The method allowed for a complete marker analysis, consisting of 96 separate kinetic assays, within 2 hours. The versatility of this method and the ease with which it can be performed should expand the use of analytical subcellular fractionation in the diagnostic laboratory.
本文描述了一种利用常规可得试剂和设备的自动化亚细胞分级分离分析方法。组织在Percoll密度梯度中进行分级分离,并用Cobas-Bio离心分析仪对梯度级分进行标记酶分析。针对该仪器对细胞色素氧化酶和蛋白质的手动测定方法进行了调整,同时使用了市售的5'-核苷酸酶、乳酸脱氢酶和酸性磷酸酶检测试剂盒。使用含有不同酶活性水平的粗肝匀浆级分来检测酶测定的线性。结果表明,这些测定在高活性和低活性水平下均呈线性。还使用高活性和低活性肝匀浆池进行了批内精密度研究,所有测定的变异系数均小于或等于5.5%。该方法用于分析从小鼠肝匀浆材料的Percoll密度梯度分离中得到的亚细胞级分。该方法能够在2小时内完成包括96个独立动力学测定的完整标记分析。这种方法的多功能性及其易于操作的特点应会扩大诊断实验室中亚细胞分级分离分析的应用。