Boroske E, Trahms L
Biophys J. 1983 Jun;42(3):275-83. doi: 10.1016/S0006-3495(83)84395-1.
Motional changes of the dipalmitoyl lecithin molecule associated with the pretransition in multibilayers are investigated by proton-enhanced 13C-NMR and proton spin-locking experiments. The nitrogen-bound methyl groups of the polar head exhibit faster motion and more disorder in the intermediate phase compared with the gel phase. Although little or no change occurs in the hydrocarbon chain order at the pretransition, the corresponding motional correlation time changes by one order of magnitude. This is consistent with a model involving rotational motion of the hydrocarbon chains about their long axes: in the gel phase the motion is such that neighboring chains make an oscillating disrotatory motion, while in contrast, in the intermediate phase a quasi-free chain rotation takes place. Earlier contradicting results of Davies, J., 1979, Biophys. J., 27:339-358, and ourselves, Trahms, L., and E. Boroske, 1979, Biochim, Biophys. Acta. 552:189-193, are explained by this model.
通过质子增强的13C-NMR和质子自旋锁定实验,研究了多层膜中与预转变相关的二棕榈酰卵磷脂分子的运动变化。与凝胶相相比,极性头部的氮结合甲基在中间相表现出更快的运动和更高的无序度。尽管在预转变时烃链顺序几乎没有变化,但相应的运动相关时间变化了一个数量级。这与一个涉及烃链绕其长轴旋转运动的模型一致:在凝胶相中,运动使得相邻链进行振荡反向旋转运动,而相比之下,在中间相中发生准自由链旋转。戴维斯(1979年,《生物物理杂志》,第27卷:339 - 358页)以及我们自己(特拉姆斯和E. 博罗斯克,1979年,《生物化学与生物物理学报》,第552卷:189 - 193页)早期相互矛盾的结果,都由该模型得到了解释。