Shaikh Saame Raza, Locascio Daniel S, Soni Smita P, Wassall Stephen R, Stillwell William
Department of Biochemistry and Molecular Biology, Brody School of Medicine, East Carolina University, 600 Moye Boulevard, Greenville, NC 27834, USA.
Biochim Biophys Acta. 2009 Nov;1788(11):2421-6. doi: 10.1016/j.bbamem.2009.08.019. Epub 2009 Sep 6.
A central tenet of the lipid raft model is the existence of non-raft domains. In support of this view, we have established in model membranes that a phosphatidylethanolamine (PE)-containing docosahexaenoic acid (DHA) forms organizationally distinct non-raft domains in the presence of sphingomyelin (SM) and cholesterol (Chol). We have shown that formation of DHA-rich domains is driven by unfavorable molecular interactions between the rigid Chol molecule and the highly flexible DHA acyl chain. However, the molecular interactions between SM and the DHA-containing PE, which could also contribute to the formation of DHA-rich non-raft domains, have not been sufficiently investigated. To address this issue, we use differential scanning calorimetry (DSC) to study the phase behavior of mixtures of SM with either 1-palmitoyl-2-docosahexaenoyl-sn-glycero-3-phosphoethanolamine (16:0-22:6PE) or 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (16:0-18:1PE), an oleic acid (OA)-containing control, over a wide range of concentrations. Deconvolution of binary DSC scans shows that both 16:0-22:6PE and 16:0-18:1PE phase separate from SM. Analysis of transition temperatures and partial phase diagrams, constructed from the DSC scans for the first time, shows that 16:0-22:6PE displays greater non-ideal mixing with SM compared to 16:0-18:1PE. Our findings support a model in which DHA- and OA-containing PEs differentially phase separate from SM over a wide range of molar ratios to initiate the formation of non-raft domains, which is greatly enhanced by DHA, but not OA, in the presence of cholesterol.
脂筏模型的一个核心原则是存在非脂筏结构域。为支持这一观点,我们已在模型膜中证实,在鞘磷脂(SM)和胆固醇(Chol)存在的情况下,含二十二碳六烯酸(DHA)的磷脂酰乙醇胺(PE)会形成组织上不同的非脂筏结构域。我们已经表明,富含DHA的结构域的形成是由刚性的Chol分子与高度灵活的DHA酰基链之间不利的分子相互作用驱动的。然而,SM与含DHA的PE之间的分子相互作用,这也可能有助于富含DHA的非脂筏结构域的形成,尚未得到充分研究。为解决这个问题,我们使用差示扫描量热法(DSC)来研究SM与1-棕榈酰-2-二十二碳六烯酰-sn-甘油-3-磷酸乙醇胺(16:0-22:6PE)或1-棕榈酰-2-油酰-sn-甘油-3-磷酸乙醇胺(16:0-18:1PE,一种含油酸(OA)的对照物)在广泛浓度范围内混合物的相行为。二元DSC扫描的去卷积显示,16:0-22:6PE和16:0-18:1PE都与SM发生相分离。首次根据DSC扫描构建的转变温度和部分相图分析表明,与16:0-18:1PE相比,16:0-22:6PE与SM表现出更大的非理想混合。我们的研究结果支持这样一个模型,即含DHA和OA的PE在广泛的摩尔比范围内与SM发生不同的相分离,从而引发非脂筏结构域的形成,在胆固醇存在的情况下,DHA而非OA会极大地增强这种形成。