Glatz C E, Vislocky J M
Biochim Biophys Acta. 1979 May 25;573(2):382-93. doi: 10.1016/0005-2760(79)90071-7.
A model arterial system of heparin immobilized on an agarose gel was used to study the amount and kinetics of binding of porcine serum lipoproteins to heparin. Binding occurred to lipoproteins in the density range 1.006 less than d less than 1.062, but there was no binding with high density lipoprotein. A theoretical model of the kinetic experiments was formulated and used to demonstrate that the rate of the binding reaction could be considered instantaneous relative to the rate of transport of lipoproteins. Extrapolation of these results to arterial levels of glycosaminoglycans and lipoprotein indicate that complexes of lipoprotein and the glycosaminoglycans could account for much of the cholesterol entrapment in atherosclerotic lesions.
一个固定在琼脂糖凝胶上的肝素模型动脉系统被用于研究猪血清脂蛋白与肝素结合的量及动力学。结合发生在密度范围为1.006<d<1.062的脂蛋白上,但与高密度脂蛋白没有结合。建立了动力学实验的理论模型,并用于证明相对于脂蛋白的运输速率,结合反应的速率可被视为瞬时的。将这些结果外推至动脉水平的糖胺聚糖和脂蛋白表明,脂蛋白与糖胺聚糖的复合物可能是动脉粥样硬化病变中大部分胆固醇滞留的原因。