Long-Term Live-Cell STED Nanoscopy of Primary and Cultured Cells with the Plasma Membrane HIDE Probe DiI-SiR.

Long-Term Live-Cell STED Nanoscopy of Primary and Cultured Cells with the Plasma Membrane HIDE Probe DiI-SiR.
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与质膜隐藏探针DII-SIR的原代和培养细胞的长期活细胞纳米镜检查。

DOI:
10.1002/anie.201704783
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发表时间:
2017-08-21
期刊:
Angewandte Chemie (International ed. in English)
影响因子:
--
通讯作者:
Schepartz A
Schepartz A
中科院分区:
其他
文献类型:
--
作者:
Thompson AD;Omar MH;Rivera-Molina F;Xi Z;Koleske AJ;Toomre DK;Schepartz A

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Super-resolution imaging of live cells over extended time periods with high temporal resolution requires high-density labeling and extraordinary fluorophore photostability. Here 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 sec temporal resolution, and visualized dynamic contact-mediated repulsion events in primary mouse hippocampal neurons over 9 min at 2 sec 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.
树突稳定性的分子机制。
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