Biochemistry, Department of Biosciences, Åbo Akademi University, Turku, Finland.
Langmuir. 2013 Feb 19;29(7):2319-29. doi: 10.1021/la3051324. Epub 2013 Feb 4.
We prepared cholesteryl phosphocholine (CholPC) by chemical synthesis and studied its interactions with small (ceramide and cholesterol) and large headgroup (sphingomyelin (SM) and phosphatidylcholine) colipids in bilayer membranes. We established that CholPC could form bilayers (giant uni- and multilamellar vesicles, as well as extruded large unilamellar vesicles) with both ceramides and cholesterol (initial molar ratio 1:1). The extruded bilayers appeared to be fluid, although highly ordered, even when the ceramide had an N-linked palmitoyl acyl chain. In binary systems containing CholPC and either palmitoyl SM or 1,2-dipalmitoyl-sn-glycero-3-phospholine, CholPC markedly destabilized the gel phase of the respective large headgroup lipid. In 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) bilayers, CholPC was much less efficient than cholesterol in ordering the acyl chains. In complex bilayers containing POPC and cholesterol or palmitoyl ceramide, CholPC appeared to prefer interacting with the small headgroup lipids over POPC. When the degree of order in CholPC/PCer bilayers was compared to Chol/PSM bilayers, CholPC/PCer bilayers were more disordered (based on DPH anisotropy). This finding may result from different headgroup orientation and dynamics in CholPC and PSM. Our results overall can be understood if one takes into account the molecular shape of CholPC (large polar headgroup and modest size hydrophobic part) when interpreting molecular interactions between small and large headgroup colipids. The results are also consistent with the proposed umbrella model" for explaining cholesterol/colipid interactions.
我们通过化学合成制备了胆甾基磷酸胆碱(CholPC),并研究了其在双层膜中与小(神经酰胺和胆固醇)和大头部基团(鞘磷脂(SM)和磷脂酰胆碱)脂质的相互作用。我们确定 CholPC 可以与神经酰胺和胆固醇(初始摩尔比为 1:1)形成双层(巨大的单和多层囊泡,以及挤出的大单层囊泡)。即使神经酰胺具有 N-连接的棕榈酰酰基链,挤出的双层膜似乎仍然是流体,尽管高度有序。在含有 CholPC 和棕榈酰 SM 或 1,2-二棕榈酰基-sn-甘油-3-磷酸胆碱的二元体系中,CholPC 明显破坏了各自的大头部基团脂质的凝胶相。在 1-棕榈酰基-2-油酰基-sn-甘油-3-磷酸胆碱(POPC)双层膜中,CholPC 对酰链有序化的效率远低于胆固醇。在含有 POPC 和胆固醇或棕榈酰神经酰胺的复杂双层膜中,CholPC 似乎更喜欢与小头部基团脂质相互作用,而不是与 POPC 相互作用。当将 CholPC/PCer 双层膜中的有序度与 Chol/PSM 双层膜进行比较时,CholPC/PCer 双层膜更加无序(基于 DPH 各向异性)。这一发现可能是由于 CholPC 和 PSM 的头部基团取向和动力学不同所致。如果在解释小头部基团脂质和大头部基团脂质之间的分子相互作用时考虑到 CholPC 的分子形状(大极性头部基团和适度大小的疏水区),那么我们的结果总体上是可以理解的。这些结果也与解释胆固醇/脂质相互作用的“伞形模型”一致。