Powell G L, Grothusen J R, Zimmerman J K, Evans C A, Fish W W
J Biol Chem. 1981 Dec 25;256(24):12740-7.
Three separate techniques have been employed to estimate the critical micelle concentration: spin labeling using 6-doxylstearoyl-CoA, gel permeation chromatography, and analytical ultracentrifugation. The first method is a labeling technique. The latter two methods utilize no potentially interfering probe and provide a value for the aggregation number for palmitoyl-CoA. All three methods provide a critical micelle concentration for palmitoyl-CoA no lower than 30 to 60 microM. The latter methods provide an aggregation number near 40 and certainly no larger than 200. These values are inconsistent with the values suggested earlier (Zahler, W. L., Barden, R. E., and Cleland, W. W. (1968) Biochim. Biophys. Acta 164, 1-11). The spin-labeled analogues, 6- and 16-doxylstearoyl-CoA, were shown not to micellize, yet these analogues were good inhibitors for citrate synthase. These observations will require the re-examination of a large body of literature in which inhibition of enzymes by fatty acyl-CoA at concentrations below 30 microM was simply ascribed to the formation of micelles.
使用6-脱氧硬脂酰辅酶A的自旋标记法、凝胶渗透色谱法和分析超速离心法。第一种方法是一种标记技术。后两种方法不使用可能产生干扰的探针,并能提供棕榈酰辅酶A的聚集数。所有这三种方法得出的棕榈酰辅酶A的临界胶束浓度均不低于30至60微摩尔。后两种方法得出的聚集数接近40,肯定不大于200。这些值与早期提出的值不一致(扎勒,W.L.,巴登,R.E.,和克莱兰,W.W.(1968年)《生物化学与生物物理学报》164,1 - 11)。自旋标记类似物6-和16-脱氧硬脂酰辅酶A并未形成胶束,但这些类似物是柠檬酸合酶的良好抑制剂。这些观察结果将需要重新审视大量文献,在这些文献中,脂肪酸辅酶A在浓度低于30微摩尔时对酶的抑制作用被简单地归因于胶束的形成。