Leonenko Z V, Carnini A, Cramb D T
Department of Chemistry, University of Calgary, 2500 University Dr. N.W., T2N 1N4, Calgary, Alta., Canada.
Biochim Biophys Acta. 2000 Dec 20;1509(1-2):131-47. doi: 10.1016/s0005-2736(00)00288-1.
We have used magnetic alternating current mode atomic force microscopy (MAC-AFM) to investigate the formation of supported phospholipid bilayers (SPB) by the method of vesicle fusion. The systems studied were dioleoylphosphatidylcholine (DOPC) on mica and mica modified with 3-aminopropyl-triethoxy-silane (APTES), and DOPC vesicles with gramicidin incorporated on mica and APTES-modified mica. The AFM images reveal three stages of bilayer formation: localized disklike features that are single bilayer footprints of the vesicles, partial continuous coverage, and finally complete bilayer formation. The mechanism of supported phospholipid bilayers formation is the fusion of proximal vesicles, rather than surface disk migration. This mechanism does not appear to be affected by incorporation of gramicidin or by surface modification. Once formed, the bilayer develops circular defects one bilayer deep. These defects grow in size and number until a dynamic equilibrium is reached.
我们已使用磁交流模式原子力显微镜(MAC-AFM),通过囊泡融合法研究支撑磷脂双层(SPB)的形成。所研究的体系包括云母上的二油酰磷脂酰胆碱(DOPC)以及用3-氨丙基三乙氧基硅烷(APTES)修饰的云母,还有掺入短杆菌肽的DOPC囊泡在云母和APTES修饰云母上的情况。原子力显微镜图像揭示了双层形成的三个阶段:局部盘状特征,即囊泡的单双层印记;部分连续覆盖;最终形成完整的双层。支撑磷脂双层形成的机制是近端囊泡的融合,而非表面盘的迁移。该机制似乎不受短杆菌肽掺入或表面修饰的影响。一旦形成,双层会出现单层深度的圆形缺陷。这些缺陷的尺寸和数量不断增加,直至达到动态平衡。