Viera L I, Alonso-Romanowski S, Borovyagin V, Feliz M R, Disalvo E A
Area de Biomembranas, Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas, INIFTA, Facultad de Ciencias Exactas, UNLP, La Plata, Argentina.
Biochim Biophys Acta. 1993 Jan 18;1145(1):157-67. doi: 10.1016/0005-2736(93)90393-e.
When dipalmitoylphosphatidylcholine bilayers dried under vacuum in different concentrations of trehalose are rehydrated in buffer without the sugar they show different physicochemical properties in the gel state in comparison to the normal gel state. Dry DPPC/trehalose mixtures are readily dispersed in buffer below the phase transition showing by electron microscopy a morphology similar to liposomes prepared by dispersing the lipids in buffer above the phase transition temperature. In these conditions, an increase in the peak at 570 nm of merocyanine after the dehydration-rehydration process in the presence of the sugar is observed and the water permeation increases to values comparable to those found in the fluid state as indicated by the activation energy values and the osmotic volume. The trehalose-dried liposomes rehydrated in buffer show a similar osmotic response to hypertonic gradient as DPPC liposomes without sugar near the phase transition temperature. In accordance with this behavior the trehalose-dried liposomes are lysed below the phase transition temperature by lysoderivatives. These modifications of the gel state of hydrated phospholipids by trehalose can only be achieved if a drastic dehydration is performed in the presence of the sugar. After rehydration the changes in the gel state can be detected after dyalizing the rehydrated membranes in media without trehalose during at least 24 h. These results suggest that trehalose is still intercalated between the phospholipids after restoring water to the dried liposomes either at temperatures below or above the phase transition.
当在不同浓度海藻糖存在下真空干燥的二棕榈酰磷脂酰胆碱双层在无糖缓冲液中复水时,与正常凝胶态相比,它们在凝胶态下呈现出不同的物理化学性质。干燥的DPPC/海藻糖混合物在低于相变温度时很容易分散在缓冲液中,电子显微镜显示其形态类似于在高于相变温度的缓冲液中分散脂质制备的脂质体。在这些条件下,观察到在糖存在下脱水 - 复水过程后,部花青在570 nm处的峰增加,并且水渗透增加到与流体态相当的值,这由活化能值和渗透体积表明。在相变温度附近,在缓冲液中复水的海藻糖干燥脂质体对高渗梯度显示出与无糖DPPC脂质体相似的渗透反应。根据这种行为,海藻糖干燥的脂质体在相变温度以下被溶菌衍生物裂解。只有在糖存在下进行剧烈脱水,海藻糖才能对水合磷脂的凝胶态进行这些修饰。复水后,在至少24小时内在无海藻糖的介质中透析复水的膜后,可以检测到凝胶态的变化。这些结果表明,在低于或高于相变温度的温度下,向干燥脂质体恢复水分后,海藻糖仍插层在磷脂之间。