Advanced Medical Bioimaging Core Facility, Charité-Universitätsmedizin, 10117 Berlin, Germany.
Faculty of Physics and Center for Nanoscience, Ludwig Maximilian University, 80799 Munich, Germany.
Nano Lett. 2022 Apr 13;22(7):2682-2690. doi: 10.1021/acs.nanolett.1c04520. Epub 2022 Mar 15.
Several variants of multicolor single-molecule localization microscopy (SMLM) have been developed to resolve the spatial relationship of nanoscale structures in biological samples. The oligonucleotide-based SMLM approach "DNA-PAINT" robustly achieves nanometer localization precision and can be used to count binding sites within nanostructures. However, multicolor DNA-PAINT has primarily been realized by "Exchange-PAINT", which requires sequential exchange of the imaging solution and thus leads to extended acquisition times. To alleviate the need for fluid exchange and to speed up the acquisition of current multichannel DNA-PAINT, we here present a novel approach that combines DNA-PAINT with simultaneous multicolor acquisition using spectral demixing (SD). By using newly designed probes and a novel multichannel registration procedure, we achieve simultaneous multicolor SD-DNA-PAINT with minimal crosstalk. We demonstrate high localization precision (3-6 nm) and multicolor registration of dual- and triple-color SD-DNA-PAINT by resolving patterns on DNA origami nanostructures and cellular structures.
已经开发出了几种多色单分子定位显微镜(SMLM)变体,以解析生物样本中纳米级结构的空间关系。基于寡核苷酸的 SMLM 方法“DNA-PAINT”能够稳健地实现纳米级定位精度,并且可用于计数纳米结构内的结合位点。然而,多色 DNA-PAINT 主要通过“交换 PAINT”来实现,这需要依次交换成像溶液,因此会导致采集时间延长。为了减轻对流体交换的需求并加快当前多通道 DNA-PAINT 的采集速度,我们在这里提出了一种新方法,该方法将 DNA-PAINT 与使用光谱解混(SD)的同时多色采集相结合。通过使用新设计的探针和新颖的多通道注册程序,我们实现了最小串扰的同时多色 SD-DNA-PAINT。我们通过解析 DNA 折纸纳米结构和细胞结构上的图案,证明了双和三色彩色 SD-DNA-PAINT 的高定位精度(3-6nm)和多色注册。