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巨分子单层囊泡与疏水玻璃表面和硅油-水界面的相互作用机制:吸附、变形、破裂、动态形状变化、内部囊泡形成和脱附。

Interaction Mechanisms of Giant Unilamellar Vesicles with Hydrophobic Glass Surfaces and Silicone Oil-Water Interfaces: Adsorption, Deformation, Rupture, Dynamic Shape Changes, Internal Vesicle Formation, and Desorption.

机构信息

International Center for Materials Nanoarchitectonics (WPI-MANA) , National Institute for Materials Science , 1-1 Namiki , Tsukuba , Ibaraki 305-0044 , Japan.

出版信息

Langmuir. 2019 Dec 10;35(49):16136-16145. doi: 10.1021/acs.langmuir.9b02472. Epub 2019 Nov 20.

DOI:10.1021/acs.langmuir.9b02472
PMID:31697503
Abstract

Phospholipid monolayers at oil-water interfaces are often obtained via vesicle adsorption. However, the interaction mechanisms of vesicles with these oil-water interfaces remain unclear. Herein, we studied the adsorption of giant unilamellar vesicles (GUVs) of approximately 2-5 μm diameter onto silicone oil-water interfaces and glass surfaces modified with hexamethyldisilazane (HMDS) and octadecyltrimethoxysilane (ODTMS) using fluorescence microscopy. The GUVs exhibited various modes of interaction, adsorbing on the silanized glass surfaces without sizable deformation, whereas GUVs bound to the silicone oil-water interface exhibited large deformation. After adsorption, GUV rupture occurred within 350, 110, and 3 ms on HMDS-modified glass, ODTMS-modified glass, and silicone oil-water interface, respectively. On glass surfaces, GUV rupture was often initiated and proceeded with pore formation near the surface. The monolayer patches formed by GUV rupture on HMDS-modified glass remained for at least 1 h over an area approximately twice of that estimated from the original GUV. On the ODTMS-modified glass and silicone oil surfaces, the monolayer patch structures disappeared in milliseconds owing to lipid diffusion across the interface. When adsorbed on the oil-water interface, the GUVs spontaneously underwent dynamic shape changes, internal vesicle formation, and desorption without rupture. Thus, it can be concluded that these different pathways arose from different lipid-surface affinities.

摘要

磷脂单层在油水界面通常通过囊泡吸附获得。然而,囊泡与这些油水界面的相互作用机制仍不清楚。在此,我们使用荧光显微镜研究了大约 2-5 μm 直径的巨大单层囊泡(GUV)在硅油-水界面和经六甲基二硅氮烷(HMDS)和十八烷基三甲氧基硅烷(ODTMS)修饰的玻璃表面上的吸附。GUV 表现出各种相互作用模式,在未经修饰的玻璃表面上吸附时没有明显变形,而在硅油-水界面上结合的 GUV 则发生了较大的变形。吸附后,GUV 在 HMDS 修饰的玻璃、ODTMS 修饰的玻璃和硅油-水界面上分别在 350、110 和 3 ms 内破裂。在玻璃表面上,GUV 破裂通常是在靠近表面的地方形成孔开始并进行的。在 HMDS 修饰的玻璃上,由 GUV 破裂形成的单层补丁至少保持 1 小时,面积大约是原始 GUV 估计面积的两倍。在 ODTMS 修饰的玻璃和硅油表面上,由于脂质在界面上的扩散,单层补丁结构在几毫秒内消失。当吸附在油水界面上时,GUV 会自发地经历动态形状变化、内部囊泡形成和脱附而不会破裂。因此,可以得出结论,这些不同的途径是由不同的脂质-表面亲和力引起的。

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