Abstract
Visualizing signaling systems in the brain with high spatial resolution is critical to understanding brain function and to develop therapeutics. Especially, enzymes are often regulated on the post-translational level, resulting in a disconnect between protein levels and activity. Conventional antibody-based methods have limitations, including potential cross-reactivity and the inability of antibodies to discriminate between active and inactive enzyme states. Monoacylglycerol lipase (MAGL), an enzyme degrading the neuroprotective endocannabinoid 2-arachidonoylglycerol, is the target of inhibitors currently in clinical trials for the treatment of several neurological disorders. To support translational and (pre)clinical studies and fully realize the therapeutic opportunities of MAGL inhibitors, it is essential to map the spatial distribution of MAGL activity throughout the brain in both health and disease. Here, we introduce selective fluorescent activity-based probes for MAGL enabling direct visualization of its enzymatic activity in lysates, cultured cells, and tissue sections. We show that oxidative stress, which inactivates MAGL through the oxidation of regulatory cysteines, reduces probe labeling, thereby validating the probes activity-dependence. Extending this approach, we developed an activity-based histology protocol to visualize MAGL activity in fresh-frozen mouse and human brain tissues. This approach revealed robust MAGL activity in astrocytes and presynaptic terminals within the mouse hippocampus and further allows detection of MAGL activity in the human cerebral cortex. Collectively, these findings establish selective activity-based probes as powerful tools mapping MAGL activity with high spatial resolution across mammalian brain tissue.
| Original language | English |
|---|---|
| Pages (from-to) | 4622-4635 |
| Number of pages | 14 |
| Journal | ACS Chemical Neuroscience |
| Volume | 16 |
| Issue number | 24 |
| Early online date | 28 Nov 2025 |
| DOIs | |
| Publication status | Published - 17 Dec 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Authors. Published by American Chemical Society
Funding
We are grateful to the brain donors and their families for their commitment to The Netherlands Brain Bank donor program. We thank Prof. dr. Sakimura (Niigata University) for providing the MAGL KO animals and E. Tischler, B. Pinter for their technical support. Research reported in the publication was supported by Oncode Accelerator, a Dutch National Growth Fund project under grant number NGFPO2201. D.v.d.V. and M.v.d.S. acknowledge funding from the Institute of Chemical Immunology (project ICI0000030). D.v.d.V., I.H., and M.v.d.S. acknowledge funding from the Institute of Chemical Neuroscience (iCNS). I.K. holds the Naus Family Chair in Addiction Sciences in the Department of Psychological and Brain Sciences at Indiana University Bloomington. This work was funded by the NKFIH EXCELLENCE program 151377 (I.K.) and the National Institutes of Health grant P30DA056410 (I.K.) and the Intramural Program of the NIH/NIAAA to P.P., and it has been approved by OGC and the NIH Ethics Office.
| Funders | Funder number |
|---|---|
| Institute of Chemical Immunology | ICI0000030 |
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | NGFPO2201 |
| Nemzeti Kutat?si Fejleszt?si ?s Innov?ci?s Hivatal | NA |
| National Institutes of Health | P30DA056410 |
| Indiana University Bloomington | NA |
| Institute of Chemical Neuroscience | NA |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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