Paddy M R, Dahlquist F W, Dratz E A, Deese A J
Biochemistry. 1985 Oct 8;24(21):5988-95. doi: 10.1021/bi00342a045.
Deuterium nuclear magnetic resonance (2H NMR) spectra from aqueous dispersions of phosphatidylcholines in which perdeuterated palmitic acid is esterified at the sn-1 position have several very useful features. The powder spectra show six well-resolved 90 degree edges which correspond to the six positions closest to the methyl end of the acyl chain. The spectral overlap inherent in the multiple powder pattern line shape of these dispersions can be removed by using a "dePaking" procedure [Bloom, M., Davis, J.H., & Mackay, A. (1981) Chem. Phys. Lett. 80, 198-202] which calculates the spectra that would result if the lipid bilayers were oriented in the magnetic field. This procedure produces six well-resolved doublets whose NMR properties can be observed without interference from the resonances of other labeled positions. The presence of a single double bond in the sn-2 chain increases the order of the saturated 16:0 sn-1 chain at every position in the bilayer compared with a saturated sn-2 chain at the same reduced temperature. Surprisingly, addition of five more double bonds to the sn-2 chain only slightly reduces the order of the 16:0 sn-1 chain at many positions in the bilayer compared with the single double bond. Calculating oriented spectra from a spin-lattice (T1) relaxation series of powder spectra allows one to obtain the T1 relaxation times of six positions on the acyl chain simultaneously. As an example of the utility of these molecules, we demonstrate that the dependence of the spin-lattice (T1) relaxation rate as a function of orientational order for two unsaturated phospholipids differs significantly from the corresponding fully saturated analogue. Interpreting this difference using current models of acyl chain dynamics suggests that the bilayers containing either of the two unsaturated phospholipids are significantly more deformable than bilayers made from the fully saturated phospholipid.
来自磷脂酰胆碱水分散体的氘核磁共振(2H NMR)光谱具有几个非常有用的特征,其中在sn-1位被全氘代棕榈酸酯化。粉末光谱显示出六个分辨率良好的90度边缘,它们对应于酰基链甲基末端最近的六个位置。通过使用“去包络”程序[Bloom, M., Davis, J.H., & Mackay, A. (1981) Chem. Phys. Lett. 80, 198 - 202]可以消除这些分散体多重粉末图案线形中固有的光谱重叠,该程序计算如果脂质双层在磁场中取向时将产生的光谱。此程序产生六个分辨率良好的双峰,其NMR特性可以在不受其他标记位置共振干扰的情况下观察到。与在相同降低温度下具有饱和sn-2链相比,sn-2链中存在单个双键会增加双层中每个位置饱和16:0 sn-1链的有序度。令人惊讶的是,与单个双键相比,在sn-2链中再添加五个双键只会略微降低双层中许多位置16:0 sn-1链的有序度。从粉末光谱的自旋晶格(T1)弛豫系列计算取向光谱可以同时获得酰基链上六个位置的T1弛豫时间。作为这些分子实用性的一个例子,我们证明了两种不饱和磷脂的自旋晶格(T)弛豫速率对取向有序度的依赖性与相应的完全饱和类似物有显著差异。使用当前的酰基链动力学模型解释这种差异表明,含有两种不饱和磷脂中任何一种的双层比由完全饱和磷脂制成的双层更具可变形性。