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全合成C16:0-乳糖基神经酰胺的双层性质

Bilayer properties of totally synthetic C16:0-lactosyl-ceramide.

作者信息

Saxena K, Zimmermann P, Schmidt R R, Shipley G G

机构信息

Department of Biophysics, Center for Advanced Biomedical Research, Boston University School of Medicine, Boston, Massachusetts 02118 USA.

出版信息

Biophys J. 2000 Jan;78(1):306-12. doi: 10.1016/S0006-3495(00)76593-3.

Abstract

Differential scanning calorimetry (DSC) and x-ray diffraction have been used to study the structural and thermal properties of totally synthetic D-erythro-N-palmitoyl-lactosyl-C(18)-sphingosine (C16:0-LacCer). Over the temperature range 0-90 degrees C, fully hydrated C16:0-LacCer shows complex thermal transitions characteristic of polymorphic behavior of exclusively bilayer phases. On heating at 5 degrees C/min, hydrated C16:0-LacCer undergoes a complex two-peak endothermic transition with maxima at 69 degrees C and 74 degrees C and a total enthalpy of 14.6 kcal/mol C16:0-LacCer. At a slower heating rate (1.5 degrees C/min), two endothermic transitions are observed at 66 degrees C and 78 degrees C. After cooling to 0 degrees C, the subsequent heating run shows three overlapping endothermic transitions at 66 degrees C, 69 degrees C, and 71.5 degrees C, followed by a chain-melting endothermic transition at 78 degrees C. Two thermal protocols were used to completely convert C16:0-LacCer to its stable, high melting temperature (78 degrees C) form. As revealed by x-ray diffraction, over the temperature range 20-78 degrees C this stable phase exhibits a bilayer structure, periodicity d approximately 65 A with an ordered chain packing mode. At the phase transition (78 degrees C) chain melting occurs, and C16:0-LacCer converts to a liquid crystalline bilayer (L(alpha)) phase of reduced periodicity d approximately 59 A. On cooling from the L(alpha) phase, C16:0-LacCer converts to metastable bilayer phases undergoing transitions at 66-72 degrees C. These studies allow comparisons to be made with the behavior of the corresponding C16:0-Cer (. J. Lipid Res. 36:1936-1944) and C16:0-GluCer and C16:0-GalCer (. J. Lipid Res. 40:839-849). Our systematic studies are aimed at understanding the role of oligosaccharide complexity in regulating glycosphingolipid structure and properties.

摘要

差示扫描量热法(DSC)和X射线衍射已被用于研究全合成的D-赤藓糖型-N-棕榈酰乳糖基-C(18)-鞘氨醇(C16:0-LacCer)的结构和热性质。在0至90摄氏度的温度范围内,完全水合的C16:0-LacCer呈现出复杂的热转变,这是仅双层相多晶型行为的特征。以5摄氏度/分钟的速率加热时,水合的C16:0-LacCer经历复杂的双峰吸热转变,最大值分别在69摄氏度和74摄氏度,总焓为14.6千卡/摩尔C16:0-LacCer。在较慢的加热速率(1.5摄氏度/分钟)下,在66摄氏度和78摄氏度观察到两个吸热转变。冷却至0摄氏度后,随后的加热过程显示在66摄氏度、69摄氏度和71.5摄氏度有三个重叠的吸热转变,随后在78摄氏度有链熔化吸热转变。使用两种热方案将C16:0-LacCer完全转化为其稳定的高熔点(78摄氏度)形式。如X射线衍射所示,在20至78摄氏度的温度范围内,这种稳定相呈现双层结构,周期d约为65埃,具有有序的链堆积模式。在相变(78摄氏度)时发生链熔化,C16:0-LacCer转化为周期约为59埃的液晶双层(L(α))相。从L(α)相冷却时,C16:0-LacCer转化为在66至72摄氏度发生转变的亚稳双层相。这些研究使得能够与相应的C16:0-Cer(《脂质研究杂志》36:1936 - 1944)以及C16:0-GluCer和C16:0-GalCer(《脂质研究杂志》4:839 - 849)的行为进行比较。我们的系统研究旨在了解寡糖复杂性在调节糖鞘脂结构和性质中的作用。

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