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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Long N-acyl fatty acids on sphingolipids are responsible for miscibility with phospholipids to form liquid-ordered phase.
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Long N-acyl fatty acids on sphingolipids are responsible for miscibility with phospholipids to form liquid-ordered phase.

机译:鞘脂上的长N酰基脂肪酸负责与磷脂混溶以形成液相。

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摘要

The structure and thermotropic phase behaviour of aqueous dispersions of dipalmitoylphosphatidylcholine and glucosylceramide rich in C-24 fatty acyl residues was investigated by synchrotron X-ray diffraction methods. Binary mixtures comprised of molar ratios 2.5:100, 6.5:100, 12.6:100, 25:100, 40:100 and 50:100, glucolipid:phospholipid were examined in heating and cooling scans of 2 degrees /min between 25 and 85 degrees C. Small-angle reflections indicated coexisting lamellar structures over the entire temperature range investigated. Reversible thermotropic changes were observed in one lamellar structure that is consistent with transitions between gel, ripple and fluid lamellar phases of pure phospholipid. The temperature of these transitions, however, were progressively shifted up by about 5 degrees C in the mixture containing the highest proportion of glucolipid and coincided with a published endothermic peak observed in this mixture. A higher-temperature endotherm was associated with molecular rearrangements on transition of the gel phase phospholipid to the fluid phase. This rearrangement was associated with the appearance of identifiable transient intermediate structures in the small-angle scattering region. The glucolipid formed stoichiometric mixtures with the phospholipid at all temperatures investigated and there was no evidence of phase separation of pure glucolipid. Analysis of the wide-angle scattering profiles during an initial heating scan of a binary mixture comprised of 40:60 glucolipid:phospholipid was consistent with a phase transition of pure phospholipid at about 43 degrees C coexisting with a liquid-ordered phase formed from the two lipids. This was confirmed by analysis of the small-angle scattering peaks of this mixture recorded at 25 and 65 degrees C which showed that a glucolipid-rich phase coexisted with almost pure bilayers of phospholipid at both temperatures. The glucolipid-rich phase consisted of 45:55 mole ratio glucolipid:phospholipid at 25 degrees C with pure phospholipid in gel phase and 42:58 mole ratio at 65 degrees C when the phospholipid was in the fluid phase. The results are discussed with reference to the role of the length of the N-acyl substituent of the sphingolipids in formation of complexes with phospholipids.
机译:用同步加速器X射线衍射方法研究了富含C-24脂肪酰基残基的二棕榈酰磷脂酰胆碱和葡萄糖基神经酰胺水分散液的结构和热致相行为。在25和85度之间以2度/ min的加热和冷却扫描检查了摩尔比为2.5:100、6.5:100、12.6:100、25:100、40:100和50:100的二元混合物,糖脂:磷脂C.小角度反射表明在研究的整个温度范围内共存的层状结构。在一种层状结构中观察到可逆的热致变化,与纯磷脂的凝胶,波纹和流体层状相之间的转变一致。然而,在包含最高比例的糖脂的混合物中,这些转变的温度逐渐升高了约5摄氏度,并且与在该混合物中观察到的已公布的吸热峰一致。高温吸热与凝胶相磷脂向液相过渡的分子重排有关。这种重排与小角度散射区域中可识别的瞬态中间结构的出现有关。在所有研究的温度下,糖脂与磷脂形成化学计量的混合物,没有证据表明纯糖脂会发生相分离。在初始加热扫描过程中,对由40:60的糖脂:磷脂组成的二元混合物进行的广角散射曲线分析与纯磷脂在约43摄氏度下与由两者形成的液相有序相共存的相变相一致脂质。这通过分析在25和65℃下记录的该混合物的小角散射峰来证实,该峰显示出在两个温度下富含葡萄糖的相与几乎纯净的双层双层共存。富含糖脂的相由摩尔比为25:45的45:55的糖脂:磷脂和凝胶相中的纯磷脂组成,以及当磷脂为液相时在65°C的摩尔比为42:58。参考鞘脂的N-酰基取代基的长度在与磷脂形成复合物中的作用来讨论结果。

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