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脱水过程中麦芽糊精从磷脂酰胆碱多层膜中的排除:对膜相行为的影响

Exclusion of maltodextrins from phosphatidylcholine multilayers during dehydration: effects on membrane phase behaviour.

作者信息

Koster Karen L, Maddocks Kami J, Bryant Gary

机构信息

Department of Biology, The University of South Dakota, Vermillion, SD 57069, USA.

出版信息

Eur Biophys J. 2003 May;32(2):96-105. doi: 10.1007/s00249-003-0277-z. Epub 2003 Feb 13.

DOI:10.1007/s00249-003-0277-z
PMID:12734697
Abstract

The effect of increasing solute size on phosphatidylcholine phase behaviour at a range of hydrations was investigated using differential scanning calorimetry. Dehydration of phospholipid membranes gives rise to a compressive stress within the bilayers that promotes fluid-to-gel phase transitions. According to the Hydration Forces Explanation, sugars in the intermembrane space minimize the compressive stress and limit increases in the fluid-gel transition temperature, T(m), by acting as osmotic and volumetric spacers that hinder the close approach of membranes. However, the sugars must remain between the bilayers in order to limit the rise in T(m). Large polymers are excluded from the interlamellar space during dehydration and do not limit the dehydration-induced rise in T(m). In this study, we used maltodextrins with a range of molecular weights to investigate the size-exclusion limit for polymers between phosphatidylcholine bilayers. Solutes with sizes ranging from glucose to dextran 1000 limited the rise in lipid T(m) during dehydration, suggesting that they remain between dehydrated bilayers. At the lowest hydrations the solutions vitrified, and T(m) was further depressed to about 20 degrees C below the transition temperature for the lipid in excess water, T(o). The depression of T(m) below T(o) occurs when the interlamellar solution vitrifies between fluid phase bilayers. The larger maltodextrins, dextran 5000 and 12,000, had little effect on the T(m) of the PCs at any hydration, nor did vitrification of these larger polymers affect the lipid phase behaviour. This suggests that the larger maltodextrins are excluded from the interlamellar region during dehydration.

摘要

利用差示扫描量热法研究了在一系列水合作用下溶质尺寸增加对磷脂酰胆碱相行为的影响。磷脂膜脱水会在双层膜内产生压缩应力,从而促进流体相到凝胶相的转变。根据水合力解释,膜间空间中的糖通过充当阻碍膜紧密靠近的渗透和体积间隔物,使压缩应力最小化,并限制流体 - 凝胶转变温度T(m)的升高。然而,糖必须保留在双层膜之间才能限制T(m)的升高。在脱水过程中,大聚合物被排除在层间空间之外,不会限制脱水诱导的T(m)升高。在本研究中,我们使用了一系列分子量的麦芽糊精来研究磷脂酰胆碱双层膜之间聚合物的尺寸排阻极限。从葡萄糖到葡聚糖1000的溶质限制了脱水过程中脂质T(m)的升高,表明它们保留在脱水双层膜之间。在最低水合作用下,溶液玻璃化,T(m)进一步降低至比过量水中脂质的转变温度T(o)低约20℃。当层间溶液在流体相双层膜之间玻璃化时,T(m)会低于T(o)。较大的麦芽糊精,葡聚糖5000和12000,在任何水合作用下对磷脂酰胆碱的T(m)几乎没有影响,这些较大聚合物的玻璃化也不影响脂质相行为。这表明在脱水过程中较大的麦芽糊精被排除在层间区域之外。

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