Jonas A, Bottum K, Kézdy K E
Department of Biochemistry, College of Medicine at Urbana-Champaign, University of Illinois 61801.
Biochim Biophys Acta. 1991 Aug 20;1085(1):71-6. doi: 10.1016/0005-2760(91)90233-8.
The objectives of this study were to determine the structural changes in defined, reconstituted high density lipoproteins (rHDL) resulting from spontaneous phospholipid depletion in the presence or absence of low-density lipoproteins (LDL), to establish the precursor-product relationships among the rHDL particles and to assess the differences in behavior of rHDL particles containing apo A-I or apo A-II. The rHDL particles were prepared by the sodium cholate dialysis method, and were incubated in buffer at 50 degrees C, or in buffer containing different concentrations of LDL at 37 degrees C, for up to 24 h. The changes in the rHDL particle distributions with time were followed by non-denaturing gradient gel electrophoresis, and the rHDL were isolated at various time points for chemical analysis. We found that rHDL particles containing apo A-I or apo A-II lose phospholipid and gain cholesterol when incubated with LDL. Increasing LDL concentrations remove increasingly larger amounts of phospholipid. With phospholipid loss the apo A-I containing particles undergo major structural rearrangements that give rise to 78 A and 106 A particles from 86 A and 94 A precursors. The 78 A products appear to be the most stable, lipid-poor species. Reconstituted HDL particles prepared with apo A-II (94 and 101 A in diameter) are more resistant to structural rearrangements than the apo A-I counterparts under similar reaction conditions.
本研究的目的是确定在存在或不存在低密度脂蛋白(LDL)的情况下,因自发磷脂耗竭而导致的特定重组高密度脂蛋白(rHDL)的结构变化,建立rHDL颗粒之间的前体-产物关系,并评估含有载脂蛋白A-I或载脂蛋白A-II的rHDL颗粒行为的差异。rHDL颗粒通过胆酸钠透析法制备,并在50℃的缓冲液中,或在含有不同浓度LDL的缓冲液中于37℃孵育长达24小时。通过非变性梯度凝胶电泳跟踪rHDL颗粒分布随时间的变化,并在不同时间点分离rHDL进行化学分析。我们发现,含有载脂蛋白A-I或载脂蛋白A-II的rHDL颗粒与LDL孵育时会失去磷脂并获得胆固醇。LDL浓度增加会去除越来越多的磷脂。随着磷脂的流失,含有载脂蛋白A-I的颗粒会发生重大结构重排,从86 Å和94 Å的前体产生78 Å和106 Å的颗粒。78 Å的产物似乎是最稳定、脂质含量低的物种。在类似反应条件下,用载脂蛋白A-II制备的重组HDL颗粒(直径94和101 Å)比载脂蛋白A-I对应的颗粒更能抵抗结构重排。