Oncode Institute, Hubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Van der Maasweg 9, 2629 HZ, Delft, The Netherlands.
ACS Nano. 2023 Oct 24;17(20):20179-20193. doi: 10.1021/acsnano.3c05959. Epub 2023 Oct 4.
Single-molecule fluorescence imaging experiments generally require sub-nanomolar protein concentrations to isolate single protein molecules, which makes such experiments challenging in live cells due to high intracellular protein concentrations. Here, we show that single-molecule observations can be achieved in live cells through a drastic reduction in the observation volume using overmilled zero-mode waveguides (ZMWs- subwavelength-size holes in a metal film). Overmilling of the ZMW in a palladium film creates a nanowell of tunable size in the glass layer below the aperture, which cells can penetrate. We present a thorough theoretical and experimental characterization of the optical properties of these nanowells over a wide range of ZMW diameters and overmilling depths, showing an excellent signal confinement and a 5-fold fluorescence enhancement of fluorescent molecules inside nanowells. ZMW nanowells facilitate live-cell imaging as cells form stable protrusions into the nanowells. Importantly, the nanowells greatly reduce the cytoplasmic background fluorescence, enabling the detection of individual membrane-bound fluorophores in the presence of high cytoplasmic expression levels, which could not be achieved with TIRF microscopy. Zero-mode waveguide nanowells thus provide great potential to study individual proteins in living cells.
单分子荧光成像实验通常需要亚纳摩尔级的蛋白质浓度来分离单个蛋白质分子,由于细胞内蛋白质浓度较高,因此在活细胞中进行此类实验具有挑战性。在这里,我们通过使用过度研磨的零模波导(ZMW-金属膜中的亚波长尺寸孔)大幅减小观察体积,展示了在活细胞中可以实现单分子观察。在钯膜中对 ZMW 进行过度研磨会在孔径下方的玻璃层中创建一个可调节尺寸的纳米井,细胞可以穿透该纳米井。我们对这些纳米井的光学性质进行了广泛的理论和实验表征,涵盖了广泛的 ZMW 直径和过度研磨深度范围,结果表明纳米井具有出色的信号限制能力和荧光分子的 5 倍荧光增强。ZMW 纳米井可促进活细胞成像,因为细胞会形成稳定的突起进入纳米井。重要的是,纳米井大大降低了细胞质背景荧光,使得即使在细胞质表达水平较高的情况下也能够检测到单个膜结合荧光团,这是 TIRF 显微镜无法实现的。因此,零模波导纳米井为在活细胞中研究单个蛋白质提供了巨大的潜力。