Winsborrow B G, Smith I C, Jarrell H C
Institute of Biological Sciences, National Research Council of Canada, Ottawa, Ontario.
Biophys J. 1991 Mar;59(3):729-41. doi: 10.1016/S0006-3495(91)82286-X.
It has been shown previously that two types of motion are adequate to describe the partially relaxed 2H NMR line shapes (inversion recovery experiment) for the backbone portion of the glycolipid 1,2-di-O-tetradecyl-3-O-(beta-D-glucopyranosyl)-sn-glycerol (beta-DTGL) in the highly ordered gel phase (Auger, M.A., D. Carrier, I.C.P. Smith, and H. C. Jarrell. 1990. J. Am. Chem. Soc. 112:1373-1381). This study extends the latter investigation to the more fluid liquid-crystalline phase, where more complex motions are anticipated. Analyses of the powder line shapes and oriented sample relaxation data for both the glycerol backbone and head group regions of this lipid have been performed. The dynamics of glycerol at the C3 position in the gel state have been described by large angle jumps about the C2-C3 bond with a correlation time in the fast-limit motional regime (omega o tau c much less than 1) and site populations 0.46, 0.34, and 0.20. The present data show that in the liquid-crystalline phase the internal jump rate is maintained, and two additional motions are necessary to describe the dependence of the relaxation rate on the orientation of the director with respect to the magnetic field direction. These are rotation about the molecular long axis with a correlation time in the slow-limit motional regime very near to the T1 minimum (omega o tau c approximately 0.65), and molecular fluctuations about the order director (modeled by a Maier-Saupe restoration potential). This treatment was also extended to the glucose head group where additional segmental motion about the glycosidic bond has been reported previously. While the two motions dominating relaxation at the glycerol C3 segment reproduce the general relaxation features of the glucose head group, the results suggest that additional motion about the glycosidic linkage must be present. This study is a stringent test of the motional model chosen earlier because relaxation data were obtained at two 2H NMR frequencies using two relaxation experiments (T1Z and T1Q) and two types of sample preparation (oriented and dispersed multibilayers). The results strongly uphold the choice of model and indicate the utility of both oriented samples and the T1Q experiment.
先前的研究表明,两种类型的运动足以描述糖脂1,2 - 二 - O - 十四烷基 - 3 - O -(β - D - 吡喃葡萄糖基) - sn - 甘油(β - DTGL)主链部分在高度有序凝胶相中的部分弛豫2H NMR线形(反转恢复实验)(奥热,M.A.,D. 卡里尔,I.C.P. 史密斯,和H.C. 贾雷尔。1990年。《美国化学会志》112:1373 - 1381)。本研究将后者的调查扩展到更具流动性的液晶相,预计在该相中会有更复杂的运动。已对该脂质的甘油主链和头部基团区域的粉末线形和取向样品弛豫数据进行了分析。凝胶态下C3位置甘油的动力学已通过围绕C2 - C3键的大角度跳跃来描述,相关时间处于快速极限运动状态(ωoτc远小于1),位点占有率分别为0.46、0.34和0.20。目前的数据表明,在液晶相中内部跳跃速率得以维持,并且需要另外两种运动来描述弛豫速率对指向矢相对于磁场方向的取向的依赖性。这两种运动分别是围绕分子长轴的旋转,相关时间处于非常接近T1最小值的慢速极限运动状态(ωoτc约为0.65),以及围绕有序指向矢的分子涨落(由迈尔 - 绍佩恢复势建模)。这种处理方法也扩展到了葡萄糖头部基团,先前已有报道表明围绕糖苷键存在额外的片段运动。虽然在甘油C3片段主导弛豫的两种运动重现了葡萄糖头部基团的一般弛豫特征,但结果表明围绕糖苷键必定存在额外的运动。本研究是对先前选择的运动模型的严格检验,因为弛豫数据是在两个2H NMR频率下使用两个弛豫实验(T1Z和T1Q)以及两种类型的样品制备(取向和分散的多层膜)获得的。结果有力地支持了模型的选择,并表明了取向样品和T1Q实验的实用性。