Evidence map›Paper›PMID 41060756›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

A molecular probe for detecting cholinesterase activity in MRI.

Sajal Sen, Miranda Dawson, Gregory D Thiabaud, Kyle Backman, Itay Fayer, Sayani Das, Eliza Whitmire, Catherine Kung, Ali Barandov, Alan Jasanoff

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sajal Sen *Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-1189-4156
Miranda Dawson *Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-3226-9122
Gregory D ThiabaudDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-5189-8445
Kyle BackmanDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0009-0008-4741-5509
Itay FayerDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Sayani DasDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Eliza WhitmireDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0009-0006-1437-5729
Catherine KungDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Ali BarandovDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Alan JasanoffDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-2834-6359

Funding

Hemogenetic imaging technology for circuit-specific analysis of primate brain functionUG3MH126868 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JASANOFF, ALAN · 2021 to 2023
$1.8M
Nanosensors for sensitive brain-wide neurochemical imagingR01NS120592 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JASANOFF, ALAN · 2021 to 2021
$1.4M
Intracellular calcium sensing with molecular fMRIUF1NS107712 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JASANOFF, ALAN · 2018 to 2018
$1.4M
Supplement to Neurobiological Engineering Training ProgramT32EB019940 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JASANOFF, ALAN · 2015 to 2025
$1.4M
Multimodal probes for multiscale calcium imagingR21EY032369 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JASANOFF, ALAN · 2021 to 2022
$464k
G. Harold and Leila Y. Mathers Foundation (Mathers Foundation) n/aHHS | National Institutes of Health (NIH) UF1 NS107712 R21 EY032369 R01 NS120592 UG3 MH126868NEI NIH HHS R21 EY032369NIBIB NIH HHS T32 EB019940NIMH NIH HHS UG3 MH126868NINDS NIH HHS R01 NS120592NINDS NIH HHS UF1 NS107712
6 · The paper itself

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.

Indexed as

CholinesterasesMagnetic Resonance ImagingMolecular ProbesAnimalsBrainMiceCholinesterasesMolecular Probesbraincontrast agentmolecular imagingneurochemistryperipheral nervous system

Identifiers

PMID41060756
PMCPMC12541304

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.