Affiliation:
1. Department of Chemical Science and Engineering Tokyo Institute of Technology Tokyo 152‐8552 Japan
2. Department of Biology Faculty of Sciences Kyushu University Fukuoka 819‐0395 Japan
3. Laboratoire de Bioimagerie et Pathologies UMR 7021 CNRS Université de Strasbourg 74 route du Rhin Illkirch 67401 France
4. Department of Chemistry Tokyo Institute of Technology Tokyo 152‐8552 Japan
Abstract
AbstractHigh‐resolution spatio‐temporal monitoring of the cell membrane lipid order provides visual insights into the complex and sophisticated systems that control cellular physiological functions. Solvatochromic fluorescent probes are highly promising noninvasive visualization tools for identifying the ordering of the microenvironment of plasma membrane microdomains. However, conventional probes, although capable of structural analysis, lack the necessary long‐term photostability required for live imaging at the cellular level. Here, an ultra‐high‐light‐resistant solvatochromic fluorescence probe, 2‐N,N‐diethylamino‐7‐(4‐methoxycarbonylphenyl)‐9,9‐dimethylfluorene (FπCM) is reported, which enables live lipid order imaging of cell division. This probe and its derivatives exhibit sufficient fluorescence wavelengths, brightness, polarity responsiveness, low phototoxicity, and remarkable photostability under physiological conditions compared to conventional solvatochromic probes. Therefore, these probes have the potential to overcome the limitations of fluorescence microscopy, particularly those associated with photobleaching. FπCM probes can serve as valuable tools for elucidating mechanisms of cellular processes at the bio‐membrane level.
Funder
Nagase Science Technology Foundation
Japan Science and Technology Agency
Agence Nationale de la Recherche
Japan Society for the Promotion of Science
Kyushu University
Cited by
3 articles.
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