Baykal-Caglar Eda, Hassan-Zadeh Ebrahim, Saremi Bahar, Huang Juyang
Department of Physics, Texas Tech University, Lubbock, TX, USA.
Biochim Biophys Acta. 2012 Nov;1818(11):2598-604. doi: 10.1016/j.bbamem.2012.05.023. Epub 2012 May 28.
Giant unilamellar vesicles (GUVs) containing cholesterol often have a wide distribution in lipid composition. In this study, GUVs of 1,2-dioleoyl-sn-glycero-3-phosphocholine(DOPC)/1,2-distearoyl-sn-glycero-3-phosphocholine(DSPC)/cholesterol and 1,2-diphytanoyl-sn-glycero-3-phosphocholine(diPhyPC)/1,2-dipalmitoyl-sn-glycero-3-phosphocholine(DPPC)/cholesterol were prepared from dry lipid films using the standard electroformation method as well as a modified method from damp lipid films, which are made from compositional uniform liposomes prepared using the Rapid Solvent Exchange (RSE) method. We quantified the lipid compositional distributions of GUV by measuring the miscibility transition temperature of GUVs using fluorescence microscopy, since a narrower distribution in the transition temperature should correspond to a more uniform distribution in GUV lipid composition. Cholesterol molecules can demix from other lipids in dry state and form cholesterol crystals. Using optical microscopy, micron-sized crystals were observed in some dry lipid films. Thus, a major cause of GUV lipid compositional heterogeneity is the demixing of lipids in the dry film state. By avoiding the dry film state, GUVs prepared from damp lipid films have a better uniformity in lipid composition, and the standard deviations of miscibility transition temperature are about 2.5 times smaller than that of GUVs prepared from dry lipid films. Comparing the two ternary systems, diPhyPC/DPPC/cholesterol GUVs has a larger cholesterol compositional heterogeneity, which directly correlates with the low maximum solubility of cholesterol in diPhyPC lipid bilayers (40.2±0.5mol%) measured by light scattering. Our data indicate that cholesterol interacts far less favorably with diPhyPC than it does with other PCs. The damp lipid film method also has a potential of preparing GUVs from cell membranes containing native proteins without going through a dry state.
含有胆固醇的巨型单层囊泡(GUVs)在脂质组成上往往具有广泛的分布。在本研究中,使用标准电形成方法以及一种从潮湿脂质膜改进而来的方法,由干燥脂质膜制备了1,2 - 二油酰基 - sn - 甘油 - 3 - 磷酸胆碱(DOPC)/1,2 - 二硬脂酰基 - sn - 甘油 - 3 - 磷酸胆碱(DSPC)/胆固醇和1,2 - 二植烷酰基 - sn - 甘油 - 3 - 磷酸胆碱(diPhyPC)/1,2 - 二棕榈酰基 - sn - 甘油 - 3 - 磷酸胆碱(DPPC)/胆固醇的GUVs,潮湿脂质膜是由使用快速溶剂交换(RSE)方法制备的组成均匀的脂质体制成的。我们通过使用荧光显微镜测量GUVs的混溶转变温度来量化GUV的脂质组成分布,因为转变温度分布越窄应对应于GUV脂质组成中更均匀的分布。胆固醇分子在干燥状态下会与其他脂质分离并形成胆固醇晶体。使用光学显微镜,在一些干燥脂质膜中观察到微米级晶体。因此,GUV脂质组成异质性的一个主要原因是干燥膜状态下脂质的分离。通过避免干燥膜状态,由潮湿脂质膜制备的GUVs在脂质组成上具有更好的均匀性,混溶转变温度的标准偏差比由干燥脂质膜制备的GUVs小约2.5倍。比较这两个三元体系,diPhyPC/DPPC/胆固醇GUVs具有更大的胆固醇组成异质性,这与通过光散射测量的胆固醇在diPhyPC脂质双层中的低最大溶解度(40.2±0.5mol%)直接相关。我们的数据表明,胆固醇与diPhyPC的相互作用远不如与其他磷脂酰胆碱(PCs)有利。潮湿脂质膜方法还具有在不经过干燥状态的情况下从含有天然蛋白质的细胞膜制备GUVs的潜力。