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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Micropipet writing technique for production of two-dimensional lipid bilayer nanotube-vesicle networks on functionalized and patterned surfaces
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Micropipet writing technique for production of two-dimensional lipid bilayer nanotube-vesicle networks on functionalized and patterned surfaces

机译:在功能化和图案化表面上生产二维脂质双层纳米管-囊泡网络的微吸管书写技术

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We present a micropipet-assisted writing technique for formation of two-dimensional networks of phospholipid vesicles and nanotubes on functionalized and patterned substrates. The substrates are patterned with vesicle-adhesive circular spots (5-7.5 mum in diameter) consisting of a basal layer of biotin on gold and an apical coating of NeutrAvidin in a sandwich manner. The area surrounding the adhesive spots is coated with a phosphatidylcholine bilayer membrane, preventing protein and liposome adhesion. Networks were formed by aspirating a biotin-functionalized giant unilamellar or multilamellar liposome (5-50 mum in diameter) into a similar to3 mum inner diameter borosilicate glass micropipet. By using a pressurizedair microejection system, a portion of the liposome is then ejected back into the solution while forming a first vesicle similar to3 mum in diameter. This vesicle is placed on an adhesive spot. When the micropipet is moved, a nanotube connection is formed from the first vesicle and is pulled to the next adhesive spot where a second vesicle is ejected. This procedure can then be repeated until the lipid material is consumed in the pipet. The method allows for formation of networks with a large number of nodes and vertexes with well-defined geometry and surface adhesion, and represents a first step toward very large scale integration of nanotube-vesicle networks in, for example, nanofluidic applications. [References: 38]
机译:我们提出了一种在功能化和图案化基质上形成磷脂囊泡和纳米管的二维网络的微吸管辅助书写技术。用金黄色的生物素基底层和中性抗生物素蛋白的顶涂层以三明治的方式组成的囊状粘附性圆形斑点(直径为5-7.5微米)对基材进行构图。粘附点周围的区域涂有磷脂酰胆碱双层膜,可防止蛋白质和脂质体粘附。通过将生物素功能化的巨型单层或多层脂质体(直径5至50微米)吸入内径类似于3微米的硼硅酸盐玻璃微吸管中来形成网络。通过使用加压空气显微喷射系统,然后将一部分脂质体喷射回溶液中,同时形成直径类似于3微米的第一囊泡。将该囊泡放置在粘合点上。当微量移液管移动时,纳米管连接从第一个囊泡形成,并被拉到下一个粘附点,第二个囊泡被排出。然后可以重复此过程,直到吸液管中的脂质物质被消耗掉为止。该方法允许形成具有大量具有明确定义的几何形状和表面粘附力的节点和顶点的网络,并且代表了例如在纳米流体应用中朝着纳米管-囊泡网络的超大规模集成的第一步。 [参考:38]

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