A molecular probe for detecting cholinesterase activity in MRI

S Sajal Sen (Department of Chemistry, The University of Texas at Austin, 105 East 24th Street Stop A 5300, Austin, Texas 78712-1224, United States) M Miranda Dawson (Department of Biological Engineering, Massachusetts Institute of Technology) G Gregory D. Thiabaud (Department of Biological Engineering, Massachusetts Institute of Technology) K Kyle Backman (Department of Biological Engineering, Massachusetts Institute of Technology) I Itay Fayer (Department of Biological Engineering, Massachusetts Institute of Technology) S Sayani Das (Department of Biological Engineering, Massachusetts Institute of Technology) E Eliza Whitmire (Department of Biological Engineering, Massachusetts Institute of Technology) C Catherine Kung (Department of Biological Engineering, Massachusetts Institute of Technology) A Ali Barandov (Department of Biological Engineering, Massachusetts Institute of Technology) A Alan Jasanoff (Department of Biological Engineering, Massachusetts Institute of Technology)

Abstract

Cholinesterase (ChE) enzymes terminate action of the neurotransmitter acetylcholine at synapses and neuromuscular junctions throughout the body. Noninvasive strategies for monitoring these enzymes could be important for studying basic biology of cholinergic systems and disorders that affect their function. To address this goal, we developed an imaging probe that allows activity of ChE to be detected using MRI. The probe, called ChERT, undergoes enzymatic processing that reduces its solubility, promoting accumulation near sites of cholinesterase activity. Following wide-field brain delivery, ChERT produces MRI contrast changes in brain regions known to be enriched in cholinesterases; these are suppressed in the presence of a selective enzymatic inhibitor, confirming their specificity. After abdominal delivery, ChERT labels regions of the gut where ChE expression is expected. In both the brain and periphery, colocalization of ChERT with ChE could be confirmed and visualized at higher resolution by fluorescence microscopy, owing to optical properties of the probe architecture. The ChERT agent thus provides a potentially versatile basis for assessment of cholinergic phenotypes throughout the body.

Article Details

Volume / Issue Vol. 122, Issue 41
Published October 14, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

S

Sajal Sen

Department of Chemistry, The University of Texas at Austin, 105 East 24th Street Stop A 5300, Austin, Texas 78712-1224, United States

M

Miranda Dawson

Department of Biological Engineering, Massachusetts Institute of Technology

G

Gregory D. Thiabaud

Department of Biological Engineering, Massachusetts Institute of Technology

K

Kyle Backman

Department of Biological Engineering, Massachusetts Institute of Technology

I

Itay Fayer

Department of Biological Engineering, Massachusetts Institute of Technology

S

Sayani Das

Department of Biological Engineering, Massachusetts Institute of Technology

E

Eliza Whitmire

Department of Biological Engineering, Massachusetts Institute of Technology

C

Catherine Kung

Department of Biological Engineering, Massachusetts Institute of Technology

A

Ali Barandov

Department of Biological Engineering, Massachusetts Institute of Technology

A

Alan Jasanoff

Department of Biological Engineering, Massachusetts Institute of Technology