Lehmler Hans-Joachim, Fortis-Santiago Azarih, Nauduri Dhananjaya, Bummer Paul M
Department of Occupational and Environmental Health, University of Iowa, Iowa City, IA 52242, USA.
J Lipid Res. 2005 Mar;46(3):535-46. doi: 10.1194/jlr.M400406-JLR200. Epub 2004 Dec 16.
The interaction of four long-chain nicotinates, compounds that are of interest as potential chemopreventive agents, with dipalmitoylphosphatidylcholine (DPPC) was investigated in monolayers at the air-water interface and in fully hydrated bilayers. For the monolayer studies, the compression isotherms of mixtures of the respective nicotinate with DPPC were recorded at various compositions on a hydrochloric acid subphase (pH 1.9-2.1, 37 +/- 2 degrees C). The headgroup of the nicotinates (24-29 A2/molecule) is larger than that of the hydrophobic tail (20 A2/molecule). The pure nicotinates exhibit a temperature- and chain length-dependent transition from an expanded to a condensed phase. Analysis of the concentration dependence of the average molecular area at constant film pressure and the concentration dependence of the breakpoint of the phase transition from the expanded to the condensed state suggests that all four DPPC-nicotinate mixtures are partially miscible at the air-water interface. Although a complex phase behavior with several phase transitions was observed, differential scanning calorimetry studies of the four mixtures are also indicative of the partial miscibility of DPPC and the respective nicotinate. Overall, the complex phase behavior most likely results from the head-tail mismatch of the nicotinates and the geometric packing constraints in the two-component lipid bilayer.
研究了四种长链烟酸酯(作为潜在化学预防剂具有研究价值的化合物)与二棕榈酰磷脂酰胆碱(DPPC)在空气-水界面的单分子层以及完全水合双层中的相互作用。对于单分子层研究,在盐酸亚相(pH 1.9 - 2.1,37 ± 2℃)上,以不同组成记录了各烟酸酯与DPPC混合物的压缩等温线。烟酸酯的头部基团(24 - 29 Ų/分子)大于疏水尾部的头部基团(20 Ų/分子)。纯烟酸酯表现出从膨胀相到凝聚相的温度和链长依赖性转变。在恒定膜压力下对平均分子面积的浓度依赖性以及从膨胀态到凝聚态的相变断点的浓度依赖性分析表明,所有四种DPPC - 烟酸酯混合物在空气-水界面处部分互溶。尽管观察到了具有多个相变的复杂相行为,但对这四种混合物的差示扫描量热法研究也表明DPPC与相应的烟酸酯部分互溶。总体而言,这种复杂的相行为很可能是由于烟酸酯的头尾不匹配以及双组分脂质双层中的几何堆积限制所致。