McConathy W J, Koren E, Wieland H, Campos E M, Lee D M, Kloer H U, Alaupovic P
J Chromatogr. 1985 Jul 12;342(1):46-66.
Because of high specificity, immunoaffinity chromatography is the most suitable procedure for the isolation of lipoprotein (LP) particles defined by their apolipoprotein (Apo) composition. The purpose of the present study was to describe immunosorber methodology and its application to the isolation of ApoB-containing lipoproteins from either plasma or isolated lipoprotein density classes. The exploration of various coupling procedures demonstrated that immunosorbers of highest capacity were obtained by cyanogen bromide activation of Sepharose. Among various dissociating agents tested, 3 M sodium thiocyanate was found to be the most effective desorbent for bound lipoproteins. Studies on the non-specific binding of serum albumin to several different immunosorbers showed a negligible retention (1.9%) of albumin. Good recoveries (80-98%) were obtained with all apolipoproteins tested with both anti-ApoA-I and anti-LP-B immunosorbers. By using the optimal experimental conditions, it was shown that the ApoB-containing lipoproteins retained by immunosorbers with antibodies to LP-B had chemical, physical and immunological properties similar, if not identical, to those of their corresponding parent density classes. The application of an alternative immunoaffinity chromatography procedure with serially connected immunosorbers with antibodies to apolipoproteins other than ApoB resulted in the isolation of LP-B, a lipoprotein containing ApoB as its sole protein constitutent. LP-B had chemical and physical properties very similar to those of subclass 2 of low-density lipoproteins (density 1.019-1.063 g/ml, flotation coefficient 0-12). Based on these studies, we suggest that immunoaffinity chromatography in combination with microanalytical procedures for quantification of lipids and apolipoproteins offers a powerful tool for the isolation and functional characterization of lipoprotein particles defined by their apolipoprotein composition.
由于具有高特异性,免疫亲和色谱法是分离由其载脂蛋白(Apo)组成定义的脂蛋白(LP)颗粒的最合适方法。本研究的目的是描述免疫吸附剂方法及其在从血浆或分离的脂蛋白密度类别中分离含ApoB脂蛋白方面的应用。对各种偶联程序的探索表明,通过溴化氰活化琼脂糖可获得容量最高的免疫吸附剂。在测试的各种解离剂中,发现3M硫氰酸钠是结合脂蛋白最有效的解吸剂。对血清白蛋白与几种不同免疫吸附剂的非特异性结合研究表明,白蛋白的保留率可忽略不计(1.9%)。使用抗ApoA-I和抗LP-B免疫吸附剂对所有测试的载脂蛋白都获得了良好的回收率(80-98%)。通过使用最佳实验条件,结果表明,用抗LP-B抗体的免疫吸附剂保留的含ApoB脂蛋白具有与其相应母体密度类别的化学、物理和免疫学性质相似(即使不完全相同)的性质。应用一种替代的免疫亲和色谱程序,使用与ApoB以外的载脂蛋白抗体串联连接的免疫吸附剂,可分离出LP-B,一种以ApoB为唯一蛋白质成分的脂蛋白。LP-B的化学和物理性质与低密度脂蛋白亚类2(密度1.019-1.063 g/ml,漂浮系数0-12)非常相似。基于这些研究,我们认为免疫亲和色谱法与用于脂质和载脂蛋白定量的微量分析程序相结合,为分离和功能表征由其载脂蛋白组成定义的脂蛋白颗粒提供了一个强大的工具。