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Journal Article

Long-term single-molecule tracking in living cells using weak-affinity protein labeling

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Kompa,  Julian
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Johnsson,  Kai
Chemical Biology, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Catapano, C., Dietz, M. S., Kompa, J., Jang, S., Freund, P., Johnsson, K., et al. (2025). Long-term single-molecule tracking in living cells using weak-affinity protein labeling. Angewandte Chemie International Edition, 64(1): e202413117, pp. 1-8. doi:10.1002/anie.202413117.


Cite as: https://hdl.handle.net/21.11116/0000-0010-405B-0
Abstract
Single-particle tracking (SPT) has become a powerful tool to monitor the dynamics of membrane proteins in living cells. However, permanent labeling strategies for SPT suffer from photobleaching as a major limitation, restricting observation times, and obstructing the study of long-term cellular processes within single living cells. Here, we use exchangeable HaloTag Ligands (xHTLs) as an easy-to-apply labeling approach for live-cell SPT and demonstrate extended observation times of individual live cells of up to 30 minutes. Using the xHTL/HT7 labeling system, we measure the ligand-induced activation kinetics of the epidermal growth factor receptor (EGFR) in single living cells. Furthermore, we generate spatial maps of receptor diffusion in cells, report non-uniform distributions of receptor activation, and the formation of spatially confined ‘hot spots’ of EGFR activation. This approach represents a general strategy to monitor protein dynamics in a functional context and for extended observation times in single living cells.