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磷脂囊泡-纳米管网络的生成及其内部分子的传输。

Generation of phospholipid vesicle-nanotube networks and transport of molecules therein.

机构信息

Department of Chemical and Biological Engineering, Chalmers University of Technology, Göteborg, Sweden.

出版信息

Nat Protoc. 2011 Jun;6(6):791-805. doi: 10.1038/nprot.2011.321. Epub 2011 May 19.

DOI:10.1038/nprot.2011.321
PMID:21637199
Abstract

We describe micromanipulation and microinjection procedures for the fabrication of soft-matter networks consisting of lipid bilayer nanotubes and surface-immobilized vesicles. These biomimetic membrane systems feature unique structural flexibility and expandability and, unlike solid-state microfluidic and nanofluidic devices prepared by top-down fabrication, they allow network designs with dynamic control over individual containers and interconnecting conduits. The fabrication is founded on self-assembly of phospholipid molecules, followed by micromanipulation operations, such as membrane electroporation and microinjection, to effect shape transformations of the membrane and create a series of interconnected compartments. Size and geometry of the network can be chosen according to its desired function. Membrane composition is controlled mainly during the self-assembly step, whereas the interior contents of individual containers is defined through a sequence of microneedle injections. Networks cannot be fabricated with other currently available methods of giant unilamellar vesicle preparation (large unilamellar vesicle fusion or electroformation). Described in detail are also three transport modes, which are suitable for moving water-soluble or membrane-bound small molecules, polymers, DNA, proteins and nanoparticles within the networks. The fabrication protocol requires ∼90 min, provided all necessary preparations are made in advance. The transport studies require an additional 60-120 min, depending on the transport regime.

摘要

我们描述了用于制造由双层脂膜纳米管和表面固定囊泡组成的软物质网络的微操作和微注射程序。这些仿生膜系统具有独特的结构灵活性和可扩展性,与通过自上而下的制造方法制备的固态微流控和纳流控装置不同,它们允许对单个容器和互连管道进行动态控制的网络设计。该制造基于磷脂分子的自组装,然后进行微操作,如膜电穿孔和微注射,以实现膜的形状变换并创建一系列互连的隔室。根据其预期功能,可以选择网络的大小和几何形状。膜的组成主要在自组装步骤中控制,而单个容器的内部内容物则通过一系列微针注射来定义。用其他目前可用的巨单层囊泡制备方法(大单层囊泡融合或电成型)无法制备网络。还详细描述了三种适合在网络内移动水溶性或膜结合的小分子、聚合物、DNA、蛋白质和纳米颗粒的运输模式。如果提前做好所有必要的准备,该制造方案大约需要 90 分钟。根据运输模式的不同,运输研究还需要额外的 60-120 分钟。

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