Semmler K, Meyer H W, Quinn P J
King's College London, Division of Life Sciences, UK.
Biochim Biophys Acta. 2000 Dec 20;1509(1-2):385-96. doi: 10.1016/s0005-2736(00)00321-7.
The structure and thermotropic phase behaviour of a fully hydrated binary mixture of dipalmitoylphosphatidylcholine and a branched-chain phosphatidylcholine, 1, 2-di(4-dodecyl-palmitoyl)-sn-glycero-3-phosphocholine, were examined using differential scanning calorimetry, synchrotron X-ray diffraction and freeze-fracture electron microscopy. The branched-chain lipid forms a nonlamellar phase when dispersed alone in aqueous medium. Mixed aqueous dispersions of the two phospholipids containing less than 33 mol% of the branched-chain lipid form lamellar phases over the whole temperature range were studied (4 degrees C to 60 degrees C). When present in proportions greater than 33 mol% it induces a hexagonal phase in mixed aqueous dispersions with dipalmitoylphosphatidylcholine at temperatures above the fluid phase transition. At temperatures below 35 degrees C a hexagonal phase coexists with a gel bilayer phase. The lamellar<-->nonlamellar transition can be explained satisfactorily on the basis of the shape of the molecule expressed in terms of headgroup and chain cross-sectional areas. At temperatures below 35 degrees C macroscopic phase separation of two gel phases takes place. Freeze-fracture electron microscopy revealed that one gel phase consists of bilayers with a highly regular, periodic superstructure (macro-ripples) whereas the other phase forms flat, planar bilayers. The macro-ripple phase appears to represent a relaxation structure required to adapt to the packing constraints imposed by the incorporation of the branched-chain lipid into the dipalmitoylphosphatidylcholine host bilayer. The data suggest that structural changes that take place on cooling the mixed dispersion below the lamellar<-->nonlamellar phase transition temperature cannot be adequately described using the molecular form concept. Instead it is necessary to take into account the detailed molecular form of the guest lipid as well as its physical properties.
利用差示扫描量热法、同步加速器X射线衍射和冷冻断裂电子显微镜,研究了二棕榈酰磷脂酰胆碱与一种支链磷脂酰胆碱(1,2-二(4-十二烷基-棕榈酰)-sn-甘油-3-磷酸胆碱)的完全水合二元混合物的结构和热致相行为。当支链脂质单独分散在水性介质中时会形成非层状相。研究了两种磷脂的混合水分散体,其中支链脂质含量低于33摩尔%,在整个温度范围(4℃至60℃)内形成层状相。当比例大于33摩尔%时,它会在高于流体相转变温度时,在与二棕榈酰磷脂酰胆碱的混合水分散体中诱导形成六方相。在低于35℃的温度下,六方相与凝胶双层相共存。基于以头基和链横截面积表示的分子形状,可以令人满意地解释层状<-->非层状转变。在低于35℃的温度下,会发生两种凝胶相的宏观相分离。冷冻断裂电子显微镜显示,一种凝胶相由具有高度规则、周期性超结构(大波纹)的双层组成,而另一种相形成扁平的平面双层。大波纹相似乎代表了一种松弛结构,以适应将支链脂质掺入二棕榈酰磷脂酰胆碱主体双层所带来的堆积限制。数据表明,将混合分散体冷却至层状<-->非层状相转变温度以下时发生的结构变化,无法用分子形式概念充分描述。相反,有必要考虑客体脂质的详细分子形式及其物理性质。