Westcott J Y, Sloan S, Wenzel S E
National Jewish Medical and Research Center, Denver, Colorado 80206, USA.
Anal Biochem. 1997 Jun 1;248(2):202-10. doi: 10.1006/abio.1997.2132.
Leukotriene E4 (LTE4) is a major leukotriene metabolite in urine. Urinary LTE4 concentration is often utilized as an index of total leukotriene synthesis. A novel method employing immunofiltration for the purification of urinary LTE4 was developed. This immunofiltration method is based upon the addition of excess anti-LTE4 antibody to urine which binds LTE4. Separation of bound LTE4 (high M(r)) from high levels of unbound contaminants (low M(r)) is then accomplished by filtration through a 10,000 M(r) cut-off filter. The LTE4-antibody complex is separated by precipitation of the antibody with methanol which is subsequently removed by centrifugation. Following evaporation of the methanol, enzyme immunoassay is utilized for quantitation. This methodology was validated by determining the recovery of tritiated and unlabeled LTE4 added to urine and buffer and by comparison of results obtained with urine samples measured after HPLC purification (correlation r2 = 0.72). Reproducibility of the assay was assessed by analyzing the same sample on two different days (standard deviation of 18%). The mean urinary LTE4 levels in healthy subjects and asthmatics measured utilizing this method were found to be identical to levels determined by HPLC/immunoassay. The ease and accuracy of this assay make it amenable for the analysis of large numbers of samples.
白三烯E4(LTE4)是尿液中的一种主要白三烯代谢产物。尿LTE4浓度常被用作总白三烯合成的指标。开发了一种采用免疫过滤法纯化尿LTE4的新方法。这种免疫过滤方法基于向尿液中添加过量的抗LTE4抗体,该抗体可结合LTE4。然后通过10,000 M(r)截留过滤器过滤,将结合的LTE4(高分子量)与高水平的未结合污染物(低分子量)分离。通过用甲醇沉淀抗体来分离LTE4-抗体复合物,随后通过离心去除甲醇。甲醇蒸发后,采用酶免疫测定法定量。通过测定添加到尿液和缓冲液中的氚标记和未标记LTE4的回收率,并比较经高效液相色谱(HPLC)纯化后测量的尿液样本所得结果(相关系数r2 = 0.72),验证了该方法。通过在两天内分析同一样本来评估该测定法的重现性(标准差为18%)。发现使用该方法测量的健康受试者和哮喘患者的尿LTE4平均水平与通过HPLC/免疫测定法测定的水平相同。该测定法的简便性和准确性使其适用于大量样本的分析。