Gruner S M, Tate M W, Kirk G L, So P T, Turner D C, Keane D T, Tilcock C P, Cullis P R
Department of Physics, Princeton University, New Jersey 08544.
Biochemistry. 1988 Apr 19;27(8):2853-66. doi: 10.1021/bi00408a029.
The polymorphic phase behavior of aqueous dispersions of dioleoylphosphatidylethanolamine (DOPE) and its N-methylated analogues, DOPE-Me, DOPE-Me2, and DOPC, has been investigated by X-ray diffraction. In the fully hydrated lamellar (L alpha) phase at 2 degrees C, the major structural difference is a large increase in the interlamellar water width from DOPE to DOPE-Me, with minor increases with successive methylation. Consistent with earlier reports, inverted hexagonal (HII) phases are observed upon heating at 5-10 degrees C in DOPE and at 65-75 degrees C in DOPE-Me and are not observed to at least 85 degrees C in DOPE-Me2 or DOPC. In DOPE, the L alpha-HII transition is facile and is characterized by a relatively narrow temperature range of coexistence of L alpha and HII domains, each with long-range order. DOPE-Me exhibits complex nonequilibrium behavior below the occurrence of the HII phase: Upon heating, the L alpha lattice spontaneously disorders on a time scale of days; on cooling from the HII phase, the disorder rises on a time scale of minutes. It is shown that, in copious water, the disordered state transforms very slowly into phases with cubic symmetry. This process is assisted by the generation of small amounts of lipid degradation products. The relative magnitudes of the monolayer spontaneous radius of curvature, R0 [Kirk, G. L., Gruner, S. M., & Stein, D. L. (1984) Biochemistry 23, 1093; Gruner, S. M. (1985) Proc. Natl. Acad. Sci. U.S.A. 82, 3665], are inferred from the HII lattice spacings vs temperature and are shown to increase with increasing methylation. The relative magnitudes of R0 are categorized as small for DOPE, intermediate for DOPE-Me, and large for DOPC. It is suggested, and examples are used to illustrate, that small R0 lipid systems exhibit facile, low-temperature L alpha-HII transitions, intermediate R0 systems exhibit complex nonequilibrium transition behavior and are likely to form cubic phases, and large R0 systems are stable as L alpha phases. The relationship between the cubic phases and minimal periodic surfaces is discussed. It is suggested that minimal periodic surfaces represent geometries in which near constant, intermediate R0 values can be obtained concomitantly with monolayers of near constant thickness, thereby leading to equilibrium cubic phases. Thus, the relative magnitude of the spontaneous radius of curvature may be used to predict mesomorphic behavior.(ABSTRACT TRUNCATED AT 400 WORDS)
通过X射线衍射研究了二油酰磷脂酰乙醇胺(DOPE)及其N-甲基化类似物DOPE-Me、DOPE-Me2和二油酰磷脂酰胆碱(DOPC)的水分散体的多晶型相行为。在2℃完全水合的层状(Lα)相中,主要结构差异是从DOPE到DOPE-Me层间水宽度大幅增加,随着连续甲基化增加幅度较小。与早期报道一致,在5-10℃加热DOPE时以及在65-75℃加热DOPE-Me时观察到反相六角(HII)相,而在DOPE-Me2或DOPC中至少到85℃都未观察到。在DOPE中,Lα-HII转变很容易发生,其特征是Lα和HII域共存的温度范围相对较窄,且每个域都具有长程有序。DOPE-Me在HII相出现之前表现出复杂的非平衡行为:加热时,Lα晶格在数天时间尺度上自发无序;从HII相冷却时,无序在数分钟时间尺度上增加。结果表明,在大量水中,无序状态非常缓慢地转变为具有立方对称性的相。这个过程由少量脂质降解产物的产生所促进。从HII晶格间距与温度的关系推断出单层自发曲率半径R0的相对大小[柯克,G.L.,格鲁纳,S.M.,&斯坦,D.L.(1984)《生物化学》23,1093;格鲁纳,S.M.(1985)《美国国家科学院院刊》82,3665],并表明其随着甲基化程度的增加而增加。R0的相对大小分类为DOPE小、DOPE-Me中等、DOPC大。有人提出并用实例说明,R0小的脂质系统表现出容易的低温Lα-HII转变,R0中等的系统表现出复杂的非平衡转变行为且可能形成立方相,R0大的系统作为Lα相是稳定的。讨论了立方相与最小周期表面之间的关系。有人提出,最小周期表面代表这样的几何形状,在其中可以同时获得接近恒定的中间R0值以及接近恒定厚度的单层,从而导致平衡立方相。因此,自发曲率半径的相对大小可用于预测介晶行为。(摘要截断于400字)