Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, Oxford, United Kingdom.
MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Biophys J. 2018 Jun 19;114(12):2945-2950. doi: 10.1016/j.bpj.2018.05.007.
The spatiotemporal organization and dynamics of the plasma membrane and its constituents are central to cellular function. Fluorescence-based single-particle tracking has emerged as a powerful approach for studying the single molecule behavior of plasma-membrane-associated events because of its excellent background suppression, at the expense of imaging speed and observation time. Here, we show that interferometric scattering microscopy combined with 40 nm gold nanoparticle labeling can be used to follow the motion of membrane proteins in the plasma membrane of live cultured mammalian cell lines and hippocampal neurons with up to 3 nm precision and 25 μs temporal resolution. The achievable spatiotemporal precision enabled us to reveal signatures of compartmentalization in neurons likely caused by the actin cytoskeleton.
质膜及其成分的时空组织和动态是细胞功能的核心。基于荧光的单粒子跟踪已成为研究质膜相关事件中单分子行为的有力方法,因为它具有出色的背景抑制能力,但牺牲了成像速度和观察时间。在这里,我们表明,干涉散射显微镜结合 40nm 金纳米粒子标记可用于以高达 3nm 的精度和 25μs 的时间分辨率跟踪活培养的哺乳动物细胞系和海马神经元的质膜中膜蛋白的运动。可实现的时空精度使我们能够揭示神经元中可能由肌动蛋白细胞骨架引起的隔室化特征。