Department of Physics and Center for Nanoscience , Ludwig Maximilian University , 80539 Munich , Germany.
Max Planck Institute of Biochemistry , 82152 Martinsried , Germany.
Nano Lett. 2019 Apr 10;19(4):2641-2646. doi: 10.1021/acs.nanolett.9b00508. Epub 2019 Mar 13.
Optical super-resolution techniques reach unprecedented spatial resolution down to a few nanometers. However, efficient multiplexing strategies for the simultaneous detection of hundreds of molecular species are still elusive. Here, we introduce an entirely new approach to multiplexed super-resolution microscopy by designing the blinking behavior of targets with engineered binding frequency and duration in DNA-PAINT. We assay this kinetic barcoding approach in silico and in vitro using DNA origami structures, show the applicability for multiplexed RNA and protein detection in cells, and finally experimentally demonstrate 124-plex super-resolution imaging within minutes.
光学超分辨率技术的空间分辨率达到空前的水平,可达到几纳米。然而,高效的多路复用策略仍然难以实现对数百种分子物种的同时检测。在这里,我们通过在 DNA-PAINT 中设计具有工程化结合频率和持续时间的靶标闪烁行为,引入了一种全新的多路超分辨率显微镜方法。我们在计算机和体外使用 DNA 折纸结构对这种动力学条形码方法进行了评估,展示了在细胞中进行多路 RNA 和蛋白质检测的适用性,最后在几分钟内实现了 124 路超分辨率成像的实验验证。