Zhang Yang, Zheng Yeting, Tomassini Andrea, Singh Ambarish Kumar, Raymo Françisco M
Program of Polymer and Color Chemistry, Department of Textile Engineering, Chemistry and Science, North Carolina State University, Raleigh, North Carolina 27606, United States.
Laboratory for Molecular Photonics, Department of Chemistry, University of Miami, Coral Gables, Florida 33146-0431, United States.
ACS Appl Opt Mater. 2023 Mar 24;1(3):640-651. doi: 10.1021/acsaom.3c00025. Epub 2023 Feb 27.
Photoactivatable fluorophores provide the opportunity to switch fluorescence on exclusively in a selected area within a sample of interest at a precise interval of time. Such a level of spatiotemporal fluorescence control enables the implementation of imaging schemes to monitor dynamic events in real time and visualize structural features with nanometer resolution. These transformative imaging methods are contributing fundamental insights on diverse cellular processes with profound implications in biology and medicine. Current photoactivatable fluorophores, however, become emissive only after the activation event, preventing the acquisition of fluorescence images and, hence, the visualization of the sample prior to activation. We developed a family of photoactivatable fluorophores capable of interconverting between emissive states with spectrally resolved fluorescence, instead of switching from a nonemissive state to an emissive one. We demonstrated that our compounds allow the real-time monitoring of molecules diffusing across the cellular blastoderm of developing embryos as well as of polymer beads translocating along the intestinal tract of live nematodes. Additionally, they also permit the tracking of single molecules in the lysosomal compartments of live cells and the visualization of these organelles with nanometer resolution. Indeed, our photoactivatable fluorophores may evolve into invaluable analytical tools for the investigation of the fundamental factors regulating the functions and structures of cells at the molecular level.
光可激活荧光团提供了在精确的时间间隔内仅在感兴趣样本的选定区域开启荧光的机会。这种时空荧光控制水平能够实施成像方案,以实时监测动态事件并以纳米分辨率可视化结构特征。这些变革性的成像方法为各种细胞过程提供了重要的见解,对生物学和医学具有深远的影响。然而,目前的光可激活荧光团仅在激活事件后才会发射荧光,这使得在激活之前无法获取荧光图像,从而无法对样本进行可视化。我们开发了一类光可激活荧光团,它们能够在具有光谱分辨荧光的发射状态之间相互转换,而不是从非发射状态切换到发射状态。我们证明,我们的化合物能够实时监测分子在发育中胚胎的细胞胚盘上扩散,以及聚合物珠沿着活线虫肠道的转运。此外,它们还允许在活细胞的溶酶体区室中追踪单个分子,并以纳米分辨率可视化这些细胞器。事实上,我们的光可激活荧光团可能会发展成为用于在分子水平上研究调节细胞功能和结构的基本因素的宝贵分析工具。