Related Experiment Video
Updated: Jun 27, 2026

Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds
Published on: October 15, 2019
Caged Monomethyl Auristatin F (MMAF) for Cell-Specific Activation Using a 488-nm-Optimized Photolabile Group
Yuhang Lai1, Francesco Russo1, Alexandre Fürstenberg1
1School of Chemistry and Biochemistry, University of Geneva, CH-1211 Geneva, Switzerland.
Abstract:
Photolabile protecting groups (PPGs) are central tools for achieving precise spatial and temporal control of bioactive molecules in living systems. Their practical utility is critically dependent on efficient uncaging under biologically compatible conditions. Here, we report a coumarin-based PPG specifically optimized for 488 nm excitation, a ubiquitous laser line in fluorescence microscopy, enabling uncaging under irradiation conditions comparable to those used for GFP imaging. We applied the optimized PPG to cage the C-terminal carboxylate of monomethyl auristatin F (cMMAF), converting a membrane-impermeant antimitotic agent into a cell-permeant prodrug that regenerates an impermeant MMAF upon photoactivation. We showcase its utility through the light-triggered release of MMAF using irradiance typically used for imaging. We demonstrate the ability to confine the pharmacological activity of MMAF to a single cell, sparing adjacent cells (neighboring effect).
More Related Videos
10:10Spatiotemporally Controlled Nuclear Translocation of Guests in Living Cells Using Caged Molecular Glues as Photoactivatable Tags
Published on: January 17, 2019
11:20An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation
Published on: August 30, 2017