Yang E, Huestis W H
Department of Chemistry, Stanford University, California 94305.
Biochemistry. 1993 Nov 16;32(45):12218-28. doi: 10.1021/bi00096a035.
The mechanism of phospholipid transfer between membranes has been studied as a function of the configuration and concentration of donor and recipient membranes. The study was motivated by the observation that dimyristoylphosphatidylcholine transfers from sonicated vesicles to erythrocytes at a 4-fold faster rate at pH 5.5 than at pH 7.4. It is unexpected that the solubility of phosphatidylcholine should be affected by pH changes in this range; indeed, the more hydrophilic homolog dilauroylphosphatidylcholine transfers at closely similar rates at pH 5.5 and 7.4. The behavior of the more hydrophobic lipid is not consistent with transfer solely as a monomer passing through the aqueous phase. The effects of membrane proximity on phospholipid transfer were examined in dilution experiments employing intact erythrocytes, resealed ghosts, erythrocyte membrane buds, and sonicated vesicles as both donor and recipient membranes. For both hydrophobic and less hydrophobic lipids, the kinetics of intermembrane transfer were affected significantly by dilution at constant donor:recipient ratios. The results were fit to a kinetic model containing contributions from both through-solution monomer transfer and transient collisional transfer. The model predicts that the mechanism of intermembrane transfer varies with experimental conditions such as membrane concentration, donor and acceptor membrane area, and surface curvature. Through-solution monomer transfer predominates for less hydrophobic lipids at all values of pH and membrane concentration, and for more hydrophobic lipids at very high membrane dilutions. Transient collisional transfer contributes significantly to the rate for relatively hydrophobic lipids in concentrated donor-acceptor systems, an effect that is particularly evident at pH values below 6. The size and surface configuration of donor and recipient membranes also alter the relative contributions of through-solution and collisional transfer.
膜之间磷脂转移的机制已作为供体膜和受体膜的构型及浓度的函数进行了研究。该研究的动机是观察到二肉豆蔻酰磷脂酰胆碱从超声处理的囊泡转移到红细胞的速率在pH 5.5时比在pH 7.4时快4倍。出乎意料的是,磷脂酰胆碱的溶解度竟然会受此pH范围内变化的影响;实际上,亲水性更强的同系物二月桂酰磷脂酰胆碱在pH 5.5和7.4时的转移速率非常相似。这种疏水性更强的脂质的行为并不符合仅作为单体穿过水相进行转移的情况。在稀释实验中,使用完整红细胞、重封的血影、红细胞膜芽以及超声处理的囊泡作为供体膜和受体膜,研究了膜接近度对磷脂转移的影响。对于疏水性和疏水性较弱的脂质,在供体与受体比例恒定的情况下,膜间转移动力学均受到稀释的显著影响。结果符合一个动力学模型,该模型包含通过溶液的单体转移和瞬时碰撞转移的贡献。该模型预测,膜间转移机制会随实验条件而变化,如膜浓度、供体和受体膜面积以及表面曲率。对于疏水性较弱的脂质,在所有pH值和膜浓度下,通过溶液的单体转移占主导;对于疏水性更强的脂质,在膜高度稀释时也是如此。在浓的供体 - 受体体系中,瞬时碰撞转移对相对疏水性脂质的转移速率有显著贡献,这种效应在pH值低于6时尤为明显。供体膜和受体膜的大小及表面构型也会改变通过溶液转移和碰撞转移的相对贡献。