Ohki S, Marcus E, Sukumaran D K, Arnold K
Department of Biophysical Sciences, State University of New York at Buffalo 142149.
Biochim Biophys Acta. 1994 Sep 14;1194(2):223-32. doi: 10.1016/0005-2736(94)90303-4.
Interaction of melittin with lipid membranes was studied systematically with respect to its adsorption onto membranes, its effect on membrane leakage and fusion, and micellization at various melittin/lipid ratios. It was found that melittin has a strong affinity for adsorption onto lipid membranes. The analysis of the measured electrophoretic mobilities by use of a Gouy-Chapman double layer theory, shows that melittin is adsorbed onto the phosphatidylserine membrane several times more than the phosphatidylcholine membrane. However, it was observed that the phosphatidylcholine membrane is more susceptible to membrane leakage, vesicle fusion and micellization at a lower level of melittin adsorbed than the phosphatidylserine membrane. For small unilamellar phosphatidylcholine vesicles in 0.1 M NaCl, membrane leakage started at melittin to lipid ratio of 1:2000, a large increase in the rate of membrane leakage occurred at a ratio of about 1:500 or higher, membrane fusion occurred at a ratio of 1:200, and membrane micellization at a ratio of 1:10. On the other hand, for small unilamellar phosphatidylserine vesicles, the respective concentrations of melittin to result in membrane leakage, vesicle fusion, and membrane micellization were several times higher. Surface pressure measurements of lipid monolayers showed that the increase in surface pressure of the phosphatidylcholine monolayer due to the presence of melittin in the subphase solution was greater than that for the phosphatidylserine monolayer at any melittin concentration in the subphase solution. These experimental results indicate that melittin tends to be adsorbed on the surface of the negatively charged phosphatidylserine membrane due to the electrostatic binding so that the melittin molecule can stay out more on the surface of the membrane, while melittin appears to be adsorbed more into the hydrophobic membrane core for the electrically neutral phosphatidylcholine membrane.
系统研究了蜂毒肽与脂质膜的相互作用,涉及它在膜上的吸附、对膜泄漏和融合的影响以及在不同蜂毒肽/脂质比例下的胶束化作用。发现蜂毒肽对脂质膜具有很强的吸附亲和力。利用古依 - 查普曼双层理论对测量的电泳迁移率进行分析表明,蜂毒肽在磷脂酰丝氨酸膜上的吸附量是磷脂酰胆碱膜的几倍。然而,观察到在较低的蜂毒肽吸附水平下,磷脂酰胆碱膜比磷脂酰丝氨酸膜更容易发生膜泄漏、囊泡融合和胶束化。对于在0.1 M NaCl中的小单层磷脂酰胆碱囊泡,膜泄漏在蜂毒肽与脂质比例为1:2000时开始,在比例约为1:500或更高时膜泄漏速率大幅增加,膜融合在比例为1:200时发生,膜胶束化在比例为1:10时发生。另一方面,对于小单层磷脂酰丝氨酸囊泡,导致膜泄漏、囊泡融合和膜胶束化的蜂毒肽相应浓度要高几倍。脂质单分子层的表面压力测量表明,在亚相溶液中任何蜂毒肽浓度下,由于亚相溶液中存在蜂毒肽导致的磷脂酰胆碱单分子层表面压力增加都大于磷脂酰丝氨酸单分子层。这些实验结果表明,由于静电结合,蜂毒肽倾向于吸附在带负电荷的磷脂酰丝氨酸膜表面,使得蜂毒肽分子能更多地留在膜表面,而对于电中性的磷脂酰胆碱膜,蜂毒肽似乎更多地吸附到疏水的膜核心中。