Sion J P, Laureys M, Gerlo E, Gorus F
Department of Clinical Chemistry, Academic Hospital of the Vrije Universiteit Brussel, Belgium.
J Chromatogr. 1989 Nov 10;496(1):91-100. doi: 10.1016/s0378-4347(00)82555-4.
A rapid high-performance gel permeation chromatographic method to confirm the presence of enzymes with abnormally high relative molecular masses (macroenzymes) in serum is described. The technique requires 200 microliters of serum, can be automated and has been implemented for the analysis of creatine kinase (CK), lactate dehydrogenase, amylase, and alkaline phosphatase (ALP) activities. Serum fractionation according to relative molecular mass is completed within 21 min, and 84-106% of enzyme activities are recovered in the eluted fractions. The elution patterns obtained make possible the differentiation of 40 samples containing at least 10 U/l immunoglobulin-enzyme complexes, aggregated mitochondrial CK or membrane fragments carrying ALP activity from 40 control samples without these high-mass enzyme forms.
描述了一种快速高效的凝胶渗透色谱法,用于确认血清中存在相对分子质量异常高的酶(巨酶)。该技术只需200微升血清,可实现自动化,已用于分析肌酸激酶(CK)、乳酸脱氢酶、淀粉酶和碱性磷酸酶(ALP)的活性。根据相对分子质量进行的血清分级分离在21分钟内完成,洗脱级分中酶活性的回收率为84-106%。所获得的洗脱模式能够将40个含有至少10 U/l免疫球蛋白-酶复合物、聚集的线粒体CK或携带ALP活性的膜片段的样品与40个没有这些高质量酶形式的对照样品区分开来。