Clarke James A, Heron Andrew J, Seddon John M, Law Robert V
Department of Chemistry, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom.
Biophys J. 2006 Apr 1;90(7):2383-93. doi: 10.1529/biophysj.104.056499.
To investigate the properties of a pure liquid ordered (Lo) phase in a model membrane system, a series of saturated phosphatidylcholines combined with cholesterol were examined by variable temperature multinuclear (1H, 2H, 13C, 31P) solid-state NMR spectroscopy and x-ray scattering. Compositions with cholesterol concentrations>or=40 mol %, well within the Lo phase region, are shown to exhibit changes in properties as a function of temperature and cholesterol content. The 2H-NMR data of both cholesterol and phospholipids were used to more accurately map the Lo phase boundary. It has been established that the gel-Lo phase coexistence extends to 60 mol % cholesterol and a modified phase diagram is presented. Combined 1H-, 2H-, 13C-NMR, and x-ray scattering data indicate that there are large changes within the Lo phase region, in particular, 1H-magic angle spinning NMR and wide-angle x-ray scattering were used to examine the in-plane intermolecular spacing, which approaches that of a fluid Lalpha phase at high temperature and high cholesterol concentrations. Although it is well known for cholesterol to broaden the gel-to-fluid transition temperature, we have observed, from the 13C magic angle spinning NMR data, that the glycerol region can still undergo a "melting", though this is broadened with increasing cholesterol content and changes with phospholipid chain length. Also from 2H-NMR order parameter data it was observed that the effect of temperature on chain length became smaller with increasing cholesterol content. Finally, from the cholesterol order parameter, it has been previously suggested that it is possible to determine the degree to which cholesterol associates with different phospholipids. However, we have found that by taking into account the relative temperature above the phase boundary this relationship may not be correct.
为了研究模型膜系统中纯液体有序(Lo)相的性质,通过变温多核(1H、2H、13C、31P)固态核磁共振光谱和X射线散射对一系列与胆固醇结合的饱和磷脂酰胆碱进行了研究。胆固醇浓度≥40摩尔%的组合物,完全处于Lo相区域内,结果表明其性质随温度和胆固醇含量而变化。胆固醇和磷脂的2H核磁共振数据被用于更精确地绘制Lo相边界。现已确定凝胶-Lo相共存延伸至60摩尔%的胆固醇,并给出了修正后的相图。1H、2H、13C核磁共振和X射线散射数据相结合表明,在Lo相区域内存在很大变化,特别是,1H魔角旋转核磁共振和广角X射线散射被用于研究面内分子间间距,在高温和高胆固醇浓度下,该间距接近流体Lα相的间距。尽管众所周知胆固醇会拓宽凝胶-流体转变温度,但我们从13C魔角旋转核磁共振数据中观察到,甘油区域仍会发生“熔化”,不过随着胆固醇含量的增加这种熔化会变宽,并且会随磷脂链长度而变化。同样从2H核磁共振序参数据中观察到,随着胆固醇含量的增加,温度对链长度的影响变小。最后,根据胆固醇序参,此前有人提出有可能确定胆固醇与不同磷脂结合的程度。然而,我们发现,考虑到相边界以上的相对温度,这种关系可能并不正确。