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In vitro partial relipidation of apolipoproteins in plasma.

机译:脂质蛋白在血浆中的体外偏复体。

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摘要

In vitro recombination of lipids with apolipoproteins is achieved when a concentrated solution of plasma lipids in petroleum ether is mixed with delipidated plasma. Combination of phospholipids and unesterified fatty acids are observed in amounts comparable with those originally present in the native unextracted plasma; triglycerides combine partially and cholesterol only slightly. On agarose gel immunoelectrophoresis, a component in the delipidated plasma which is reactive with high density lipoprotein antibodies migrates more slowly than high density lipoprotein in the undelipidated control plasma. However, the component reacting with low density lipoprotein antibodies in the delipidated plasma moves more rapidly than low density lipoprotein in the native plasma. These changes are reversed by recombination of lipid with delipidated plasma. All lipids present in the plasma phase after relipidation travel with the lipoproteins during zonal electrophoresis. The apparent concentrations of proteins reacting with high density and low density lipoprotein antibodies decrease when no lipid is present in plasma on assay by single radial immunodiffusion and immunoelectrophoresis, using commercially available lipoprotein antibodies. On relipidation, full immunochemical properties of high density lipoprotein are restored, but relipidated low density lipoprotein exhibits only partial immunochemical restoration.
机译:当通过玻璃醚中的血浆脂质的浓缩溶液与倒样的等离子体混合时,实现了用脂蛋白的脂质的体外重组。磷脂和未缔酸化脂肪酸的组合以与最初存在于原生未提示的血浆中的相当的量相当;甘油三酯仅略微结合部分和胆固醇。在琼脂糖凝胶免疫电泳中,具有高密度脂蛋白抗体反应性的德普化血浆中的组分在未填充的对照等离子体中比高密度脂蛋白迁移得更缓慢。然而,在天然血浆中与低密度脂蛋白抗体与低密度脂蛋白抗体反应的组分比天然血浆中的低密度脂蛋白更快地移动。这些变化通过通过玻璃化血浆重组而逆转。在分层电泳期间,在重新筛选后,血浆相的所有脂质存在于脂蛋白的血浆相。当通过单径径向免疫反转和免疫电泳的等离子体中没有脂质在等离子体中存在血浆时,使用市售的脂蛋白抗体在等离子体上存在血浆时,蛋白质的表观浓度降低。在再湿化上,恢复高密度脂蛋白的全免疫化学性质,但重新化的低密度脂蛋白表现出仅部分免疫化学修复。

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  • 作者

    B E Cham; B R Knowles;

  • 作者单位
  • 年度 1976
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  • 原文格式 PDF
  • 正文语种 eng
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