Zechner R
Institute of Medical Biochemistry, Karl Franzens University Graz, Austria.
Biochim Biophys Acta. 1990 May 1;1044(1):20-5. doi: 10.1016/0005-2760(90)90213-h.
Lipoprotein lipase (LPL) is an important enzyme in lipid and energy metabolism of all vertebrates. Measurement of its activity in human postheparin plasma has become a standard procedure for diagnosis of Type I hyperlipoproteinemia and other types of hypertriglyceridemias. This paper presents a rapid and simple purification procedure for human lipoprotein lipase and the production of specific polyclonal antibodies. In the isolation procedure, the fat moiety of human milk obtained by centrifugation was delipidated and a buffer-extractable fraction chromatographed sequentially on heparin-Sepharose and phenyl-Sepharose. This three-step procedure provides a high yield of apparently pure LPL with very high specific activity against radiolabeled triacylglycerol substrates. The apparent molecular weight of LPL on SDS-PAGE was 60 kDa. Amino acid analysis and NH2-terminal sequencing proved the identity and the apparent homogeneity of the isolated enzyme. alpha-Lactoferrin and antithrombin III, common contaminants in earlier isolation procedures, were not detectable immunologically. Purified LPL was used to produce in the rabbit a specific polyclonal antiserum that inhibited LPL activity from human postheparin plasma and other tissues. In postheparin plasma from normal individuals, anti-LPL IgG was used in Western blotting to show LPL protein. In preheparin plasma, or in certain patients with Type I hyperlipoproteinemia, no specific signal was detected. The improved purification procedure presented here allows the rapid isolation of human LPL and production of antibodies to the protein, both of which will greatly facilitate future studies of this important enzyme.
脂蛋白脂肪酶(LPL)是所有脊椎动物脂质和能量代谢中的一种重要酶。测定其在人肝素后血浆中的活性已成为诊断I型高脂蛋白血症和其他类型高甘油三酯血症的标准程序。本文介绍了一种快速简便的人脂蛋白脂肪酶纯化方法以及特异性多克隆抗体的制备。在分离过程中,将通过离心获得的人乳脂肪部分脱脂,并将可缓冲提取的部分依次在肝素-琼脂糖和苯基-琼脂糖上进行层析。这个三步程序可获得高产率的明显纯的LPL,其对放射性标记的三酰甘油底物具有非常高的比活性。SDS-PAGE上LPL的表观分子量为60 kDa。氨基酸分析和氨基末端测序证明了分离出的酶的同一性和明显的均一性。早期分离程序中常见的污染物α-乳铁蛋白和抗凝血酶III在免疫学上无法检测到。纯化的LPL用于在兔体内产生特异性多克隆抗血清,该抗血清可抑制人肝素后血浆和其他组织中的LPL活性。在正常个体的肝素后血浆中,抗LPL IgG用于蛋白质印迹以显示LPL蛋白。在肝素前血浆或某些I型高脂蛋白血症患者中,未检测到特异性信号。本文介绍的改进纯化程序可快速分离人LPL并产生针对该蛋白的抗体,这两者将极大地促进对这种重要酶的未来研究。