Bates Mark, Huang Bo, Dempsey Graham T, Zhuang Xiaowei
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Science. 2007 Sep 21;317(5845):1749-53. doi: 10.1126/science.1146598. Epub 2007 Aug 16.
Recent advances in far-field optical nanoscopy have enabled fluorescence imaging with a spatial resolution of 20 to 50 nanometers. Multicolor super-resolution imaging, however, remains a challenging task. Here, we introduce a family of photo-switchable fluorescent probes and demonstrate multicolor stochastic optical reconstruction microscopy (STORM). Each probe consists of a photo-switchable "reporter" fluorophore that can be cycled between fluorescent and dark states, and an "activator" that facilitates photo-activation of the reporter. Combinatorial pairing of reporters and activators allows the creation of probes with many distinct colors. Iterative, color-specific activation of sparse subsets of these probes allows their localization with nanometer accuracy, enabling the construction of a super-resolution STORM image. Using this approach, we demonstrate multicolor imaging of DNA model samples and mammalian cells with 20- to 30-nanometer resolution. This technique will facilitate direct visualization of molecular interactions at the nanometer scale.
远场光学纳米显微镜的最新进展已实现了空间分辨率为20至50纳米的荧光成像。然而,多色超分辨率成像仍然是一项具有挑战性的任务。在此,我们引入了一族光开关荧光探针,并展示了多色随机光学重建显微镜(STORM)。每个探针由一个可在荧光态和暗态之间循环的光开关“报告”荧光团,以及一个促进报告分子光激活的“激活剂”组成。报告分子和激活剂的组合配对允许创建具有许多不同颜色的探针。对这些探针的稀疏子集进行迭代的、特定颜色的激活,能够以纳米精度对其进行定位,从而构建超分辨率的STORM图像。使用这种方法,我们展示了对DNA模型样品和哺乳动物细胞的20至30纳米分辨率的多色成像。这项技术将有助于在纳米尺度上直接可视化分子相互作用。