Alivisatos S G, Deliconstantinos G, Papaphilis A, Theodosiadis G P
Biochim Biophys Acta. 1981 May 20;643(3):642-9. doi: 10.1016/0005-2736(81)90360-6.
The 'binding' of cholesterol on to dog brain synaptosomal plasma membranes from aqueous cholesterol 'solutions' was studied. 'Binding' of exogenous cholesterol is a slow process, strictly depending on the concentration of cholesterol and the quantity of the membranes present. It appears that binding probably occurs in three distinct successive stages. The first stage occurs very rapidly, and consists of a large deposition-like accumulation of cholesterol onto the membranes. This stage is characterized by the lack of functional changes of integral proteins. It is followed or accompanied by a slower type of binding, probably at 'specific binding sites', the nature of which is, in all probability, cooperative. Thus, when the glucoside of cholesterol is used at lower concentrations as compared to cholesterol it increases the binding of cholesterol, while at higher concentrations relative to cholesterol, it antagonizes its binding. This stage, which evokes strong functional changes of integral proteins, merges without interruption into an incorporation of cholesterol as a structural element into the membranous framework (nonspecific binding).
研究了胆固醇从水性胆固醇“溶液”与犬脑突触体细胞膜的“结合”。外源性胆固醇的“结合”是一个缓慢的过程,严格取决于胆固醇的浓度和膜的数量。结合似乎可能发生在三个不同的连续阶段。第一阶段非常迅速地发生,包括胆固醇大量沉积样地积聚在膜上。该阶段的特征是整合蛋白缺乏功能变化。随后是或伴随着一种较慢类型的结合,可能发生在“特异性结合位点”,其性质很可能是协同性的。因此,当胆固醇糖苷与胆固醇相比以较低浓度使用时,它会增加胆固醇的结合,而当相对于胆固醇以较高浓度使用时,它会拮抗其结合。这个引起整合蛋白强烈功能变化的阶段不间断地融入到胆固醇作为结构元件并入膜框架的过程中(非特异性结合)。