Evidence map›Paper›PMID 42049499›Full record

ArticleJournal of chemical information and modeling2026

Predicting Peptide Aggregation with Protein Language Model Embeddings.

Ethan Eschbach, Kristine Deibler, Deepa Korani, Sebastian Swanson

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2026. 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

4 authors.

Ethan EschbachMolecular AI, Novo Nordisk, Lexington, Massachusetts 02421, United States.
Kristine DeiblerMolecular AI, Novo Nordisk, Lexington, Massachusetts 02421, United States.
Deepa KoraniMolecular AI, Novo Nordisk, Lexington, Massachusetts 02421, United States.
Sebastian SwansonMolecular AI, Novo Nordisk, Lexington, Massachusetts 02421, United States.ORCID 0000-0002-0114-0051

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyloid fibrils, a form of peptide aggregates, are associated with multiple diseases and hinder the development of therapeutics. The experimental characterization of aggregating peptides is resource-intensive, and data are scarce, limiting the development of accurate models. We present a deep-learning model, PALM (Predicting Aggregation with Language Model embeddings), which uses transfer learning to predict aggregation from embeddings extracted from a pretrained protein language model (pLM). PALM is trained on the WaltzDB-2.0 dataset to classify peptides and identify aggregation-prone regions within a sequence at single-residue resolution. Compared to existing models, it exhibits competitive performance on diverse held-out experimental datasets. We find that PALM fails to identify single mutations that increase the rate of aggregation of the amyloid beta peptide; however, training the PALM architecture on a larger dataset, CANYA NNK1-3, substantially improves performance in this task. These results show that transfer learning with pLM embeddings improves performance when training on small datasets, but highlight that challenging tasks, such as predicting the effect of single mutations, require more experimental data.

Indexed as

Deep LearningPeptidesProtein AggregatesModels, MolecularPrediction AlgorithmsPredictive Learning ModelsPeptidesProtein Aggregates

Identifiers

PMID42049499
PMCPMC13170650

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.