Evidence map›Paper›PMID 42465379›Full record

ArticlebioRxiv : the preprint server for biology2026

Graph neural network modeling of receptor interaction kinetics from single-molecule imaging data.

Khai Nguyen, Khuloud Jaqaman

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

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

2 authors.

Khai NguyenDepartment of Biophysics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Khuloud JaqamanDepartment of Biophysics, UT Southwestern Medical Center, Dallas, TX 75390, USA.

Funding

Mechanisms and Functional Consequences of Signaling Protein Organization at MembranesR35GM119619 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI DASGUPTA, APARAJITA KAMALESH · 2016 to 2025
$4.3M
NIGMS NIH HHS R35 GM119619
6 · The paper itself

Abstract

Single-molecule (SM) imaging (SMI)-based approaches have the powerful ability to capture receptor interactions - necessary for cell signaling - in their native live-cell environment. Yet, due to substoichiometric labeling, SMI generally provides only partial information on these interactions. We developed Deep-FISIK, which utilizes graph neural networks and multi-head attention for message-passing, to predict from SMI data the kinetics of homotypic interactions of the full receptor system. The input to Deep-FISIK are the SM detections in SMI experiments, without the need for explicit tracking. Thus, Deep-FISIK is compatible with labeling a higher fraction of receptors in the SMI experiments, increasing the prediction accuracy of the interaction kinetics parameters. Deep-FISIK's performance is robust in the presence of a variety of deviations from the training data, indicating Deep-FISIK's applicability to many receptor systems and SMI experiments.

Identifiers

PMID42465379
PMCPMC13370353

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.