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Accelerated formation of cubic phases in phosphatidylethanolamine dispersions.

机译:磷脂酰乙醇胺分散体中立方相的加速形成。

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摘要

By means of x-ray diffraction we show that several sodium salts and the disaccharides sucrose and trehalose strongly accelerate the formation of cubic phases in phosphatidylethanolamine (PE) dispersions upon temperature cycling through the lamellar liquid crystalline-inverted hexagonal (Lalpha-HII) phase transition. Ethylene glycol does not have such an effect. The degree of acceleration increases with the solute concentration. Such an acceleration has been observed for dielaidoyl PE (DEPE), dihexadecyl PE, and dipalmitoyl PE. It was investigated in detail for DEPE dispersions. For DEPE (10 wt% of lipid) aqueous dispersions at 1 M solute concentration, 10-50 temperature cycles typically result in complete conversion of the Lalpha phase into cubic phase. Most efficient is temperature cycling executed by laser flash T-jumps. In that case the conversion completes within 10-15 cycles. However, the cubic phases produced by laser T-jumps are less ordered in comparison to the rather regular cubic structures produced by linear, uniform temperature cycling at 10 degrees C/min. Temperature cycles at scan rates of 1-3 degrees C/min also induce the rapid formation of cubic phases. All solutes used induce the formation of Im3m (Q229) cubic phase in 10 wt% DEPE dispersions. The initial Im3m phases appearing during the first temperature cycles have larger lattice parameters that relax to smaller values with continuation of the cycling after the disappearance of the Lalpha phase. A cooperative Im3m --> Pn3m transition takes place at approximately 85 degrees C and transforms the Im3m phase into a mixture of coexisting Pn3m (Q224) and Im3m phases. The Im3m/Pn3m lattice parameter ratio is 1. 28, as could be expected from a representation of the Im3m and Pn3m phases with the primitive and diamond infinite periodic minimal surfaces, respectively. At higher DEPE contents ( approximately 30 wt%), cubic phase formation is hindered after 20-30 temperature cycles. The conversion does not go through, but reaches a stage with coexisting Ia3d (Q230) and Lalpha phases. Upon heating, the Ia3d phase cooperatively transforms into a mixture of, presumably, Im3m and Pn3m phases at about the temperature of the Lalpha-HII transition. This transformation is readily reversible with the temperature. The lattice parameters of the DEPE cubic phases are temperature-insensitive in the Lalpha temperature range and decrease with the temperature in the range of the HII phase.
机译:通过X射线衍射,我们显示了几种钠盐以及二糖蔗糖和海藻糖在通过层状液晶转化的六角形(Lalpha-HII)相转变的温度循环后,强烈加速了磷脂酰乙醇胺(PE)分散体中立方相的形成。 。乙二醇没有这种作用。加速程度随溶质浓度的增加而增加。对于二烯丙基PE(DEPE),二十六烷基PE和二棕榈酰PE已经观察到这种加速。已对DEPE分散液进行了详细研究。对于浓度为1 M的DEPE(脂质的10 wt%)水分散体,10-50个温度循环通常会导致Lalpha相完全转化为立方相。最有效的是通过激光闪光T跳执行温度循环。在这种情况下,转换将在10-15个周期内完成。然而,与通过线性,均匀的温度循环(以10摄氏度/分钟的速度)产生的相当规则的立方结构相比,由激光T型跃迁产生的立方相的排列较不规则。扫描速度为1-3摄氏度/分钟的温度循环也会引起立方相的快速形成。使用的所有溶质均会在10 wt%的DEPE分散液中诱导形成Im3m(Q229)立方相。在第一个温度循环中出现的初始Im3m相具有较大的晶格参数,随着Lalpha相消失后循环的继续,该参数会松弛为较小的值。 Im3m-> Pn3m的协同转变发生在大约85摄氏度,并将Im3m相转变为共存的Pn3m(Q224)和Im3m相的混合物。 Im3m / Pn3m晶格参数比为1. 28,这可以从分别具有基本面和菱形无限周期性最小曲面的Im3m和Pn3m相的表示中预期到。在较高的DEPE含量(约30 wt%)下,在20-30个温度循环后,立方相的形成受到阻碍。转换不会进行,但会达到与Ia3d(Q230)和Lalpha相共存的阶段。加热后,Ia3d相在大约Lalpha-HII转变温度下协同转变为Im3m和Pn3m相的混合物。该转变易于随温度逆转。 DEPE立方相的晶格参数在Lalpha温度范围内对温度不敏感,并随HII相范围内的温度而降低。

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