Jiang Yanfei, Pryse Kenneth M, Melnykov Artem, Genin Guy M, Elson Elliot L
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri.
Department of Mechanical Engineering and Materials Science, Washington University, St. Louis, Missouri.
Biophys J. 2017 Jun 6;112(11):2367-2376. doi: 10.1016/j.bpj.2017.04.013.
Measurement of the sizes of nanoscopic particles is a difficult challenge, especially in two-dimensional systems such as cell membranes. We have extended inverse fluorescence correlation spectroscopy (iFCS) to endow it with unique advantages for measuring particle size from the nano- to the microscale. We have augmented iFCS with an analysis of moments of fluorescence fluctuations and used it to measure stages of phase separation in model lipid bilayer membranes. We observed two different pathways for the growth of phase domains. In one, nanoscopic gel domains appeared first and then gradually grew to micrometer size. In the other, the domains reached micrometer size quickly, and their number gradually increased. These measurements demonstrate the value of iFCS measurements through their ability, to our knowledge, to provide new information about the mechanism of lipid phase separation and potentially about the physical basis of naturally occurring nanodomains such as lipid rafts.
测量纳米级粒子的大小是一项艰巨的挑战,尤其是在二维系统中,如细胞膜。我们扩展了反向荧光相关光谱技术(iFCS),使其在测量从纳米到微米尺度的粒子大小时具有独特优势。我们通过对荧光涨落矩的分析增强了iFCS,并将其用于测量模型脂质双层膜中的相分离阶段。我们观察到相域生长的两种不同途径。一种途径是,纳米级凝胶域首先出现,然后逐渐生长到微米大小。另一种途径是,这些域迅速达到微米大小,并且其数量逐渐增加。据我们所知,这些测量通过iFCS测量的能力证明了其价值,即能够提供有关脂质相分离机制以及潜在地有关诸如脂筏等天然存在的纳米域的物理基础的新信息。