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


ABSTRACT: 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.

SUBMITTER: Thompson AD 

PROVIDER: S-EPMC5576494 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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

Thompson Alexander D AD   Omar Mitchell H MH   Rivera-Molina Felix F   Xi Zhiqun Z   Koleske Anthony J AJ   Toomre Derek K DK   Schepartz Alanna A  

Angewandte Chemie (International ed. in English) 20170724 35


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   ...[more]

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