Lange A, Marsh D, Wassmer K H, Meier P, Kothe G
Biochemistry. 1985 Jul 30;24(16):4383-92. doi: 10.1021/bi00337a020.
The electron spin resonance spectra of the 1-myristoyl-2-[6-(4,4-dimethyloxazolidine-N-oxyl)myristoyl]-sn-glycero- 3-phosphocholine spin-label in highly oriented, fully hydrated bilayers of 1,2-dimyristoyl-sn-glycero-3-phosphocholine have been studied as a function of temperature and magnetic field orientation. The oriented spectra show clear indications of slow motional components (rotational correlation times greater than 3 ns) even in the fluid phase (T greater than 23 degrees C), indicating that motional narrowing theory is not applicable to the spectral analysis. The spectra have been simulated by a comprehensive line-shape model that incorporates trans-gauche isomerization in addition to restricted anisotropic motion of the lipid long molecular axis and that is valid in all motional regimes. In the gel (L beta') phase the spin-label chains are found to be tilted at 28 degrees with respect to the normal of the orienting plane. In the intermediate (P beta') phase there is a continuous distribution of tilt angles between 0 degrees and 25 degrees. In fluid (L alpha) phase there is no net tilt of the lipid chains. The chains rotate at an intermediate rate about their long axis in the fluid phase (tau R,parallel = 1.4-6.6 ns for T = 50-25 degrees C), but the reorientation of the chain axis is much slower (tau R, perpendicular= 13-61 ns for T = 50-25 degrees C), whereas trans-gauche isomerization (at the C-6 position) is rapid (tau J less than or equal to 0.2 ns). Below the chain melting transition both chain reorientation and chain rotation are at the ESR rigid limit (tau R greater than or equal to 100 ns), and trans-gauche isomerization is in the slow-motion regime (tau J = 3.7-9.5 ns for T = 22-2 degrees C). The chain order parameter increases continuously with decreasing temperature in the fluid phase (SZZ = 0.47-0.61 for T = 50-25 degrees C), increases abruptly on going below the chain melting transition, and then increases continuously in the intermediate phase (SZZ = 0.79-0.85 for T = 22-14 degrees C) to an approximately constant value in the gel phase (SZZ congruent to 0.86 for T = 10-2 degrees C).(ABSTRACT TRUNCATED AT 400 WORDS)
研究了1-肉豆蔻酰基-2-[6-(4,4-二甲基恶唑烷-N-氧基)肉豆蔻酰基]-sn-甘油-3-磷酸胆碱自旋标记物在高度取向、完全水合的1,2-二肉豆蔻酰基-sn-甘油-3-磷酸胆碱双层膜中的电子自旋共振光谱,该光谱是温度和磁场取向的函数。即使在流体相(T大于23℃)中,取向光谱也清晰显示出慢速运动成分(旋转相关时间大于3纳秒)的迹象,这表明运动窄化理论不适用于光谱分析。通过一个综合线形模型对光谱进行了模拟,该模型除了考虑脂质长分子轴的受限各向异性运动外,还纳入了反式-顺式异构化,并且在所有运动状态下均有效。在凝胶(Lβ')相中,发现自旋标记链相对于取向平面的法线倾斜28°。在中间(Pβ')相中,倾斜角在0°至25°之间连续分布。在流体(Lα)相中,脂质链没有净倾斜。在流体相中,链围绕其长轴以中等速率旋转(对于T = 50 - 25℃,τR,平行 = 1.4 - 6.6纳秒),但链轴的重新取向要慢得多(对于T = 50 - 25℃,τR,垂直 = 13 - sixty-one纳秒),而反式-顺式异构化(在C-6位置)很快(τJ小于或等于0.2纳秒)。在链熔化转变温度以下,链的重新取向和链的旋转都处于电子自旋共振刚性极限(τR大于或等于100纳秒),并且反式-顺式异构化处于慢运动状态(对于T = 22 - 2℃,τJ = 3.7 - 9.5纳秒)。在流体相中,链序参数随着温度降低而连续增加(对于T = 五十 - 25℃,SZZ = 0.47 - 0.61),在低于链熔化转变温度时突然增加,然后在中间相中连续增加(对于T = 22 - 14℃,SZZ = 0.79 - 0.85),在凝胶相中达到近似恒定值(对于T = 10 - 2℃,SZZ约等于0.86)。(摘要截短于400字)