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Rotating-frame relaxation studies of slow motions in fluorinated phospholipid model membranes.

机译:氟化磷脂模型膜中慢动作的旋转框架松弛研究。

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摘要

Rotating-frame relaxation experiments have been carried out on 19F-labeled dimyristoylphosphatidylcholine model membranes. The lipids are labeled with a single CF2 group in the 4-, 8-, or 12-position of the 2-acyl chain. Both oriented lipid bilayers and multilamellar liposomes have been investigated. The relaxation rate has been measured as a function of the locking-field strength, the sample orientation, the label position, and the temperature. Our results have confirmed that extensive slow motions exist in the bilayer and dominate the low-frequency relaxation. The relaxation rate is quite sensitive to the label position. However, many other features of the relaxation are very similar for all three lipid isomers. The temperature dependence of the relaxation rate for the multilamellar liposomes differs from the oriented bilayers, which may imply that the motions are also different. To fit our data, a working model consisting of a superposition of an anisotropic reorientation term and a director fluctuation term has been proposed. We have also verified that almost all of the relaxation process is caused by modulations of the intramolecular interactions. Based on this, a view of the slow motions at a molecular level is discussed in this paper.
机译:已经在19 F标记的二肉豆蔻酰基磷脂酰胆碱模型膜上进行了旋转框架松弛实验。脂质在2-酰基链的4、8或12位标记有单个CF2基团。定向脂质双层和多层脂质体均已被研究。测量了松弛率,它是锁定场强度,样品方向,标签位置和温度的函数。我们的结果证实双层中存在广泛的慢动作,并且主导了低频弛豫。松弛率对标签位置非常敏感。然而,对于所有三种脂质异构体,弛豫的许多其他特征非常相似。多层脂质体松弛速率的温度依赖性与取向的双层不同,这可能意味着运动也不同。为了拟合我们的数据,提出了一个由各向异性重取向项和指向矢波动项的叠加组成的工作模型。我们还证实,几乎所有的弛豫过程都是由分子内相互作用的调节引起的。基于此,本文讨论了分子水平上的慢动作。

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