Shah J, Atienza J M, Rawlings A V, Shipley G G
Department of Biophysics, Boston University School of Medicine, MA 02118, USA.
J Lipid Res. 1995 Sep;36(9):1945-55.
The structural and thermotropic properties of alpha-hydroxy fatty acid (HFA) and non-hydroxy fatty acid (NFA) ceramides (CER) have been studied using differential scanning calorimetry (DSC) and X-ray diffraction techniques. The DSC of anhydrous HFA-CER shows a single, sharp reversible transition at 95.6 degrees C (delta H = 15.3 kcal/mol). At intermediate hydrations HFA-CER exhibited more complex behavior but at maximum hydration only a single reversible transition is observed at 80.0 degrees C (delta H = 8.5 kcal/mol). X-ray diffraction of hydrated (74% water) HFA-CER at 20 degrees C shows a lamellar structure with a bilayer periodicity d = 60.7 Angstrum; a single wide angle reflection at 4.2 Angstrum is characteristic of hexagonal chain packing. Above the main transition temperature at 91 degrees C, a hexagonal (HII) phase is observed. In contrast, DSC of anhydrous NFA-CER demonstrates two thermal transitions at 81.3 degrees C (delta H = 6.8 kcal/mol) and 85.9 degrees C (delta H = 3.5 kcal/mol). With increasing hydration, both transitions shift towards lower temperatures; at maximum hydration, on heating, the endothermic transitions occur at 72.7 degrees C (delta H = 9.8 kcal/mol) and 81.1 degrees C (delta H = 4.0 kcal/mol). On cooling, there is hysteresis of both transitions. X-ray diffraction of NFA-CER (80% water) at 20 degrees C shows a well-ordered lamellar structure with a bilayer periodicity d = 58.6 Angstrum and three wide-angle reflections at 4.6 Angstrum, 4.2 Angstrum, and 3.8 Angstrum. At 77 degrees C (between the two transitions), again a lamellar structure exists with reduced bilayer periodicity d = 53.1 Angstrum and four wide-angle reflections at 4.6 Angstrum, 4.2 Angstrum, and 3.8 Angstrum are observed. Above the second transition, only a single low angle reflection at 30.0 Angstrum is observed; a diffuse reflection at 4.6 Angstrum is indicative of a melted chain phase. Thus, HFA-CER exhibits a simple phase behavior involving the reversible conversion of a gel phase to a hexagonal phase (L beta-->HII). However, NFA-CER shows a more complex polymorphic phase behavior involving two gel phases.
利用差示扫描量热法(DSC)和X射线衍射技术研究了α-羟基脂肪酸(HFA)和非羟基脂肪酸(NFA)神经酰胺(CER)的结构和热致性质。无水HFA-CER的DSC显示在95.6℃有一个单一、尖锐的可逆转变(ΔH = 15.3千卡/摩尔)。在中等水合度时,HFA-CER表现出更复杂的行为,但在最大水合度时,仅在80.0℃观察到一个单一的可逆转变(ΔH = 8.5千卡/摩尔)。水合(74%水)HFA-CER在20℃的X射线衍射显示出层状结构,双层周期d = 60.7埃;在4.2埃处的一个单一广角反射是六方链堆积的特征。在91℃的主要转变温度以上,观察到六方(HII)相。相比之下,无水NFA-CER的DSC显示在81.3℃(ΔH = 6.8千卡/摩尔)和85.9℃(ΔH = 3.5千卡/摩尔)有两个热转变。随着水合度增加,两个转变都向较低温度移动;在最大水合度时,加热时吸热转变发生在72.7℃(ΔH = 9.8千卡/摩尔)和81.1℃(ΔH = 4.0千卡/摩尔)。冷却时,两个转变都有滞后现象。NFA-CER(80%水)在20℃的X射线衍射显示出有序的层状结构,双层周期d = 58.6埃,在4.6埃、4.2埃和3.8埃处有三个广角反射。在77℃(两个转变之间),再次存在层状结构,双层周期减小,d = 53.1埃,在4.6埃、4.2埃和3.8埃处观察到四个广角反射。在第二个转变以上,仅在30.0埃处观察到一个单一的低角反射;在4.6埃处的漫反射表明是熔化的链相。因此,HFA-CER表现出简单的相行为,涉及凝胶相到六方相的可逆转变(Lβ→HII)。然而,NFA-CER显示出更复杂的多晶型相行为,涉及两个凝胶相。