Evidence map›Paper›PMID 41993498›Full record

ArticlebioRxiv : the preprint server for biology2026

Phenotypic screening for small molecules that lower PrP in cultured cells.

Jeannine A Frei, Andrew G Reidenbach, Leo Mh Xu, Raja Mohan Gopalakrishnan, Dominick Casalana, Daniel A Sprague, Mark-Anthony Bray, Amy Q Wang, Vanessa Laversenne, Brian Erickson and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jeannine A FreiProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID 0000-0003-0004-4022
Andrew G ReidenbachProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.
Leo Mh XuProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.
Raja Mohan GopalakrishnanProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.
Dominick CasalanaFacilitated Access to Screening Technologies (FAST) Lab, Novartis Institutes for Biomedical Research, Cambridge, MA, 02139, USA.
Daniel A SpragueProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.
Mark-Anthony BrayFacilitated Access to Screening Technologies (FAST) Lab, Novartis Institutes for Biomedical Research, Cambridge, MA, 02139, USA.ORCID 0000-0002-9748-3592
Amy Q WangEarly Translation Branch, Division of Preclinical Innovation, National Center for Advancing Translational Sciences, Rockville, MD, 20850, USA.
Vanessa LaversenneProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID 0000-0002-1929-477X
Brian EricksonIQ Proteomics, Framingham, MA, 01702, USA.
Craig BraunIQ Proteomics, Framingham, MA, 01702, USA.
Samarjit PatnaikEarly Translation Branch, Division of Preclinical Innovation, National Center for Advancing Translational Sciences, Rockville, MD, 20850, USA.
Mckenzie HallEarly Translation Branch, Division of Preclinical Innovation, National Center for Advancing Translational Sciences, Rockville, MD, 20850, USA.
Douglas AuldFacilitated Access to Screening Technologies (FAST) Lab, Novartis Institutes for Biomedical Research, Cambridge, MA, 02139, USA.
Eric Vallabh MinikelProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID 0000-0003-2206-1608
Sonia M VallabhProgram in Brain Health, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID 0000-0003-3824-2702

Funding

Mechanism of Action of Prion Protein-Lowering Small MoleculesR01NS131663 · NINDS · BROAD INSTITUTE, INC. · PI Sonia Minikel Vallabh · 2023 to 2026
$1.6M
NINDS NIH HHS R01 NS131663
6 · The paper itself

Abstract

PrP lowering is a validated therapeutic hypothesis in prion disease. To identify small molecules that reduce PrP levels, we performed phenotypic screening in cultured cells. To prioritize PrP specificity in our primary screen, we generated mouse N2a cells stably expressing GFP and used high content imaging analysis to select compounds that lowered PrP without affecting GFP signal or cell viability. Screening a curated library of 3,492 compounds with annotated mechanisms of action identified two small molecules, EYH (PubChem CID: 71678945) and LCZ (PubChem CID: 24970350), that selectively and dose-dependently lowered PrP. Proteomics on whole cell lysates identified PrP as the #1 or #2 most potently downregulated out of 8,722 proteins detected. Both compounds minimally affected

Identifiers

PMID41993498
PMCPMC13081808

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.