Bayerl T M, Werner G D, Sackmann E
Technische Universität München, Physik Department, Garching bei München, F.R.G.
Biochim Biophys Acta. 1989 Sep 4;984(2):214-24. doi: 10.1016/0005-2736(89)90219-8.
The interaction of sodium deoxycholate, sodium cholate and octyl glucoside with sonicated vesicles of L alpha-dimyristoyl-phosphatidylcholine (DMPC) and L alpha-dipalmitoylphosphatidylcholine (DPPC) at concentrations below the critical micellization concentration (cmc) of the detergents was studied by high-sensitivity DSC (hs-DSC), Fourier transform infrared spectroscopy (FT-IR) and freeze-fracture electron microscopy. The two phospholipids exhibited a striking different thermotropic behaviour in the presence of these detergents. For DPPC vesicles, the detergents were found to interact exclusively in the aqueous interface region of the bilayer below the membrane saturation concentration Rsat while in DMPC vesicles two coexisting interaction sites below this concentration persist. These are detergents which interact at the aqueous interface region (site 1) and in the acyl chain region (site 2) of the DMPC vesicles. The partition coefficients K of the detergents between DPPC vesicles and the water phase were calculated from the hs-DSC results at two detergent/phospholipid molar ratios Rtot less than or equal to Rsat as 0.35, 0.049 and 0.040 mol-1 for sodium deoxycholate, sodium cholate and octyl glucoside, respectively. In contrast, for DMPC the K values for Rtot less than or equal to Rsat were found to be dependent on Rtot due to the occupation of site 2 by the detergents above a certain Rtot. The model is discussed on the basis of the detergents free energies of transfer from the water phase to site 1 and site 2 of the vesicles, respectively. The solubilization behaviour of DPPC vesicles, dependent on whether the total detergent concentration is above or below the cmc at Rsat, differed significantly as revealed by hs-DSC. This suggests that in the latter case an additional hydrophobic effect could facilitate the formation of disc shaped mixed micelles. Moreover, this different behaviour was employed to measure the cmc values of the detergents studied in the presence of the vesicles by hs-DSC.
通过高灵敏度差示扫描量热法(hs-DSC)、傅里叶变换红外光谱法(FT-IR)和冷冻断裂电子显微镜,研究了脱氧胆酸钠、胆酸钠和辛基葡糖苷在低于洗涤剂临界胶束浓度(cmc)的浓度下与L-α-二肉豆蔻酰磷脂酰胆碱(DMPC)和L-α-二棕榈酰磷脂酰胆碱(DPPC)超声处理囊泡的相互作用。在这些洗涤剂存在下,这两种磷脂表现出显著不同的热致行为。对于DPPC囊泡,发现洗涤剂仅在低于膜饱和浓度Rsat时在双层的水界面区域相互作用,而在DMPC囊泡中,在该浓度以下存在两个共存的相互作用位点。这些是在DMPC囊泡的水界面区域(位点1)和酰基链区域(位点2)相互作用的洗涤剂。根据hs-DSC结果,在两个洗涤剂/磷脂摩尔比Rtot小于或等于Rsat为0.35时,计算出脱氧胆酸钠、胆酸钠和辛基葡糖苷在DPPC囊泡和水相之间的分配系数K分别为0.049和0.040 mol-1。相比之下,对于DMPC,由于在一定Rtot以上洗涤剂占据位点2,Rtot小于或等于Rsat时的K值取决于Rtot。基于洗涤剂分别从水相转移到囊泡位点1和位点2的自由能,对该模型进行了讨论。hs-DSC显示,DPPC囊泡的增溶行为取决于总洗涤剂浓度在Rsat时是高于还是低于cmc,差异显著。这表明在后一种情况下,额外的疏水作用可能促进盘状混合胶束的形成。此外,利用这种不同的行为通过hs-DSC测量了在囊泡存在下所研究洗涤剂的cmc值。