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胆固醇的溶解性及其在膜之间的交换。

The solubility of cholesterol and its exchange between membranes.

作者信息

Bruckdorfer K R, Sherry M K

出版信息

Biochim Biophys Acta. 1984 Jan 11;769(1):187-96. doi: 10.1016/0005-2736(84)90022-1.

Abstract

It has been proposed that exchange between membrane cholesterol pools occurs by desorption of molecules into the aqueous environment rather than by formation of a transitory collision complex between the membranes. The rate of exchange is likely to be determined by the rate of dissociation of cholesterol from the membrane bilayer and by the concentration of cholesterol monomers or aggregates of cholesterol molecules in solution. The aim of this study was to measure the effects of agents known to increase cholesterol exchange rates on cholesterol solubility, critical micellar concentration and on the activation energy of exchange. A comparison was also made with regard to these parameters, of the exchange of cholesterol to that of 4-cholesten-3-one, another steroid which exchanges more rapidly than cholesterol. Acetone and dimethylsulphoxide increased cholesterol exchange between liposomes and erythrocytes, but only modestly increased the apparent solubility of cholesterol in saline and had no effect on the activation energy of the exchange process. However, acetone and dimethylsulphoxide increased the critical micellar concentration of the cholesterol 3-fold, although tetraethylammonium iodide, which had a smaller effect on exchange, did not. 4-Cholesten-3-one had a lower solubility and critical micellar concentration than that of cholesterol, but had the same activation energy for exchange. It is concluded that the apparent solubility of steroid aggregates are unlikely to determine the rate of exchange, but that agents which substantially increase exchange also increase the critical micellar concentration. The low critical micellar concentration of cholestenone suggests that the actual monomer concentration in an exchange system is low and that the rate of dissociation of the molecules from the liposomes must determine the exchange rate. This is not reflected in the activation energy measurements since these are a composite of all the elements of the exchange process.

摘要

有人提出,膜胆固醇池之间的交换是通过分子解吸到水性环境中发生的,而不是通过膜之间形成瞬时碰撞复合物。交换速率可能由胆固醇从膜双层解离的速率以及溶液中胆固醇单体或胆固醇分子聚集体的浓度决定。本研究的目的是测量已知能提高胆固醇交换速率的试剂对胆固醇溶解度、临界胶束浓度和交换活化能的影响。还对胆固醇与4-胆甾烯-3-酮(另一种比胆固醇交换更快的类固醇)的交换在这些参数方面进行了比较。丙酮和二甲基亚砜增加了脂质体和红细胞之间的胆固醇交换,但仅适度增加了胆固醇在盐水中的表观溶解度,并且对交换过程的活化能没有影响。然而,丙酮和二甲基亚砜使胆固醇的临界胶束浓度增加了3倍,尽管对交换影响较小的碘化四乙铵没有这种作用。4-胆甾烯-3-酮的溶解度和临界胶束浓度低于胆固醇,但具有相同的交换活化能。得出的结论是,类固醇聚集体的表观溶解度不太可能决定交换速率,但大幅增加交换的试剂也会增加临界胶束浓度。胆甾烯酮的低临界胶束浓度表明交换系统中实际的单体浓度较低,并且分子从脂质体解离的速率必须决定交换速率。这在活化能测量中没有体现出来,因为这些是交换过程所有要素的综合结果。

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