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Fluorescent Membrane Tension Probes for Super-Resolution Microscopy: Combining Mechanosensitive Cascade Switching with Dynamic-Covalent Ketone Chemistry

José García‐Calvo, Jimmy Maillard, Ina Fureraj, Karolína Straková, Adai Colom, Vincent Mercier, Aurélien Roux, Eric Vauthey, Naomi Sakai, Alexandre Fürstenberg, Stefan Matile

2020Journal of the American Chemical Society70 citationsDOIOpen Access PDF

Abstract

We report the design, synthesis, and evaluation of fluorescent flipper probes for single-molecule super-resolution imaging of membrane tension in living cells. Reversible switching from bright-state ketones to dark-state hydrates, hemiacetals, and hemithioacetals is demonstrated for twisted and planarized mechanophores in solution and membranes. Broadband femtosecond fluorescence up-conversion spectroscopy evinces ultrafast chalcogen-bonding cascade switching in the excited state in solution. According to fluorescence lifetime imaging microscopy, the new flippers image membrane tension in live cells with record red shifts and photostability. Single-molecule localization microscopy with the new tension probes resolves membranes well below the diffraction limit.

Topics & Concepts

ChemistryMembraneFluorescenceMicroscopyFluorescence microscopeOpticsBiochemistryPhysicsAdvanced Fluorescence Microscopy TechniquesForce Microscopy Techniques and ApplicationsLipid Membrane Structure and Behavior
Fluorescent Membrane Tension Probes for Super-Resolution Microscopy: Combining Mechanosensitive Cascade Switching with Dynamic-Covalent Ketone Chemistry | Litcius