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首页> 外文期刊>Chemistry and Physics of Lipids >Structural role of mismatched C-C bonds in a series of d-erythro- sphingomyelins as studied by DSC and electron microscopy
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Structural role of mismatched C-C bonds in a series of d-erythro- sphingomyelins as studied by DSC and electron microscopy

机译:DSC和电子显微镜研究了一系列d-赤型-鞘磷脂中错配的C-C键的结构作用

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摘要

A series of d-erythro (2S, 3R) sphingomyelins (SMs) whose acyl chain was 16, 18, 20, 22, and 24 carbons long, respectively, was synthesized by the acylation of d-erythro-sphingosylphosphorylcholine. For all the SM dispersions, reversible and reproducible thermal behavior was observed to show the gel-to-gel and the main gel-to-liquid crystal phase transition in heating scan. The main transition enthalpy (ΔHM) decreased linearly with increasing acyl chain length. The vesicular structures were observed for all the gel phases at temperatures just below the main transition, but the mean diameter of these vesicles changed markedly from ~1.5 to 100nm with increasing acyl chain length. On this basis, the decrease in ΔHM with increasing acyl chain length was discussed from the viewpoint of the effect of the mismatched C-C bonds in the acyl chain on the van der Waals attractive force between the matched acyl chain segment and the sphingoshine chain of the gel phase at temperatures just below the main transition.
机译:通过d-赤型-鞘氨醇磷酸化胆碱的酰化反应,合成了一系列酰基链长度分别为16、18、20、22和24个碳的d-赤型(2S,3R)鞘磷脂(SMs)。对于所有的SM分散体,观察到可逆和可再现的热行为,在加热扫描中显示出凝胶到凝胶和主要的凝胶到液晶的相变。主过渡焓(ΔHM)随着酰基链长度的增加而线性降低。在刚好低于主转变温度的温度下,所有凝胶相都观察到了囊泡结构,但是随着酰基链长度的增加,这些囊泡的平均直径从约1.5nm到100nm发生了显着变化。在此基础上,从酰基链中CC键错配对凝胶中匹配的酰基链段与鞘氨醇之间的范德华吸引力的影响出发,讨论了随着酰基链长度的增加ΔHM的降低。相温度低于主要转变温度。

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