Fluorogenic, Two-Photon-Triggered Photoclick Chemistry in Live Mammalian Cells
Citations Over TimeTop 1% of 2013 papers
Abstract
The tetrazole-based photoclick chemistry has provided a powerful tool to image proteins in live cells. To extend photoclick chemistry to living organisms with improved spatiotemporal control, here we report the design of naphthalene-based tetrazoles that can be efficiently activated by two-photon excitation with a 700 nm femtosecond pulsed laser. A water-soluble, cell-permeable naphthalene-based tetrazole was identified that reacts with acrylamide with the effective two-photon cross-section for the cycloaddition reaction determined to be 3.8 GM. Furthermore, the use of this naphthalene-tetrazole for real-time, spatially controlled imaging of microtubules in live mammalian cells via the fluorogenic, two-photon-triggered photoclick chemistry was demonstrated.
Related Papers
- → Recent Progress in Metal-Catalyzed [2+2+2] Cycloaddition Reactions(2021)96 cited
- → Acetylene and Ethylene: Universal C2 Molecular Units in Cycloaddition Reactions(2021)27 cited
- → Detonation properties and sensitivities of a series of -NHNH-/-N = N- bridged tetrazole-based energetic materials(2023)1 cited
- → Investigation of some tetrazole derivatives of 1,8‐naphthyridines(1970)17 cited
- → Addition Reactions: Cycloaddition(2014)