Schneider W, Marcovitz S, Al-Shammari S, Yago S, Chevalier S
Division of Medical Biochemistry, McGill University Health Centre, Montreal General Hospital, Montreal, Quebec, Canada.
Clin Biochem. 2001 Sep;34(6):469-73. doi: 10.1016/s0009-9120(01)00256-9.
To evaluate a simple assay for macroprolactin for use with the Bayer Immuno 1 analyzer, and to compare the reactivity of macroprolactin in commonly used automated prolactin assays.
Macroprolactin in serum was precipitated in a buffer containing 13.3% polyethylene glycol (PEG) 8000, redissolved, and assayed on the Bayer Immuno 1 for PRL. Presence of macroprolactin was confirmed in some sera by FPLC using a Pharmacia Superose 12 column, followed by prolactin assay of the fractions on the Immuno 1. Sera with and without macroprolactin were then also assayed on the Abbott AxSYM, Bayer Centaur, Beckman Access, and Roche Elecsys.
The PEG precipitation assay is simple and reproducible (CVs < 15%), and we established a normal range of < 20% precipitation of total PRL by PEG. The assay correlates well with the amount of macroprolactin separated by FPLC as a peak with a MW of approximately 180 kDa. Macroprolactin showed the following cross-reactivities in commonly used PRL assays: Roche Elecsys > Bayer Immuno 1 > Abbott AxSYM > Bayer Centaur > Beckman Access, with the Centaur showing more variability than other assays.
Macroprolactin can be easily quantitated using the Immuno 1 PRL assay after PEG precipitation. It cross-reacts to different degrees with common prolactin assays, and is a major source of variability between them.
评估一种适用于拜耳免疫1分析仪的简单的大分子催乳素检测方法,并比较大分子催乳素在常用的自动催乳素检测中的反应性。
血清中的大分子催乳素在含有13.3%聚乙二醇(PEG)8000的缓冲液中沉淀,重新溶解后,在拜耳免疫1分析仪上检测催乳素。通过使用Pharmacia Superose 12柱的快速蛋白质液相色谱法(FPLC)在一些血清中确认大分子催乳素的存在,随后在免疫1分析仪上对各组分进行催乳素检测。然后,对含有和不含有大分子催乳素的血清也在雅培AxSYM、拜耳Centaur、贝克曼Access和罗氏Elecsys上进行检测。
PEG沉淀法简单且可重复(变异系数<15%),我们确定PEG沉淀总催乳素的正常范围<20%。该检测方法与通过FPLC分离出的分子量约为180 kDa的大分子催乳素峰的量相关性良好。大分子催乳素在常用的催乳素检测中表现出以下交叉反应性:罗氏Elecsys>拜耳免疫1>雅培AxSYM>拜耳Centaur>贝克曼Access,其中Centaur的变异性比其他检测方法更大。
PEG沉淀后,使用免疫1催乳素检测方法可轻松定量大分子催乳素。它与常见的催乳素检测方法有不同程度的交叉反应,是它们之间变异性的主要来源。