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| Main Authors: | , , , , , , , , , , |
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| Format: | Preprint |
| Published: |
2024
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2410.00532 |
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Table of Contents:
- Advanced microscopy techniques are essential in biomedical research for visualising and tracking biomolecules within living cells and their compartments. Conventional fluorescence microscopy methods, however, often struggle with accurately measuring the absolute concentrations of fluorescent probes in living cells. To overcome these limitations, we introduce an open-source analysis tool, smICA (Single-Molecule Image to Concentration Analyser). The smICA method offers quantitative mapping of absolute fluorophore concentrations, lifetime-resolved filtering methods of the signal, intensity-based cell segmentation, and requires only a few photons per pixel. Our approach also reduces the time required to determine the mean concentration per cell compared to the standard FCS measurement performed in multiple posts. To highlight the robustness of the method, we validated it against standard fluorescence correlation spectroscopy (FCS) measurements by performing in vitro (polymers in aqueous solution) and in vivo (polymers and EGFP in living cells) experiments. Finally, we present exemplary studies on the time evolution of fluorescently labelled mRNA concentration in living cells. The presented methodology, along with the software, is a promising tool for quantitative single-cell studies, including, but not limited to, protein expression, biomolecule degradation (such as proteins and mRNA), and monitoring enzymatic reactions.