School of Physics and Astronomy, University of Leeds , Leeds LS2 9JT, United Kingdom.
Nano Lett. 2014 Oct 8;14(10):5984-8. doi: 10.1021/nl503024v. Epub 2014 Sep 3.
The diffusion behavior of biological components in cellular membranes is vital to the function of cells. By collapsing the complexity of planar 2D membranes down to one dimension, fundamental investigations of bimolecular behavior become possible in one dimension. Here we develop lipid nanolithography methods to produce membranes, under fluid, with widths as low as 6 nm but extending to microns in length. We find reduced lipid mobility, as the width is reduced below 50 nm, suggesting different lipid packing in the vicinity of boundaries. The insertion of a membrane protein, M2, into these systems, allowed characterization of protein diffusion using high-speed AFM to demonstrate the first membrane protein 1D random walk. These quasi-1D lipid bilayers are ideal for testing and understanding fundamental concepts about the roles of dimensionality and size on physical properties of membranes from energy transfer to lipid packing.
生物分子在细胞膜中的扩散行为对细胞的功能至关重要。通过将平面 2D 细胞膜的复杂性折叠到一维,在一维中可以对双分子行为进行基础研究。在这里,我们开发了脂质纳米光刻方法来制造在流体下的膜,其宽度低至 6nm,但长度可达数微米。我们发现,当宽度低于 50nm 时,脂质的流动性降低,这表明在边界附近存在不同的脂质堆积。将膜蛋白 M2 插入这些系统中,允许使用高速 AFM 对蛋白质扩散进行表征,从而证明了第一个膜蛋白 1D 随机行走。这些准 1D 脂质双层非常适合测试和理解关于维度和尺寸对膜的物理性质(从能量转移到脂质堆积)的基本概念,例如能量转移和脂质堆积。