Department of Chemistry, Yale University, 225 Prospect Street, New Haven, CT, 06511, USA.
Department of Molecular Biophysics and Biochemistry and Interdepartmental Neuroscience Program, Yale University, 333 Cedar Street, New Haven, CT, 06511, USA.
Angew Chem Int Ed Engl. 2017 Aug 21;56(35):10408-10412. doi: 10.1002/anie.201704783. Epub 2017 Jul 24.
Super-resolution imaging of live cells over extended time periods with high temporal resolution requires high-density labeling and extraordinary fluorophore photostability. Herein, we achieve this goal by combining the attributes of the high-density plasma membrane probe DiI-TCO and the photostable STED dye SiR-Tz. These components undergo rapid tetrazine ligation within the plasma membrane to generate the HIDE probe DiI-SiR. Using DiI-SiR, we visualized filopodia dynamics in HeLa cells over 25 min at 0.5 s temporal resolution, and visualized dynamic contact-mediated repulsion events in primary mouse hippocampal neurons over 9 min at 2 s temporal resolution. HIDE probes such as DiI-SiR are non-toxic and do not require transfection, and their apparent photostability significantly improves the ability to monitor dynamic processes in live cells at super-resolution over biologically relevant timescales.
通过高密度标记和非凡的荧光团光稳定性,实现对活细胞进行长时间、高时间分辨率的超分辨率成像。在此,我们通过结合高密度质膜探针 DiI-TCO 和光稳定 STED 染料 SiR-Tz 的特性来实现这一目标。这些成分在质膜内快速进行四嗪连接,生成 HIDE 探针 DiI-SiR。使用 DiI-SiR,我们以 0.5 秒的时间分辨率在 HeLa 细胞中可视化了 25 分钟的丝状伪足动力学,并且以 2 秒的时间分辨率在原代小鼠海马神经元中可视化了 9 分钟的动态接触介导排斥事件。像 DiI-SiR 这样的 HIDE 探针无毒性,不需要转染,其明显的光稳定性显著提高了在超分辨率下监测活细胞中生物相关时间尺度内动态过程的能力。