Evidence map›Paper›PMID 40520595›Full record

ArticleComputational and structural biotechnology journal2025

Fine-tuning protein language models to understand the functional impact of missense variants.

Ali Saadat, Jacques Fellay

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Which chemical features are captured by ChemBERTa's attention?Journal of computer-aided molecular design · 2026
    Article
  2. Article
  3. INBAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. 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

2 authors.

Ali SaadatSchool of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Jacques FellaySchool of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elucidating the functional effects of missense variants is crucial yet challenging. To investigate their impact, we fine-tuned protein language models, including ESM2 and ProtT5, to classify 20 protein features at amino acid resolution. In addition, we trained a fully connected neural network classifier on frozen embeddings and compared its performance to fine-tuning in order to quantify the added value of task-specific adaptation. We then used the fine-tuned models to: 1) identify protein features enriched in either pathogenic or benign missense variants, and 2) compare the predicted feature profiles of proteins with reference and alternate alleles to understand how missense variants affect protein functionality. We show that our models can be used to reclassify variants of uncertain significance and provide mechanistic insights into the functional consequences of missense mutations.

Indexed as

Fine-tuningMechanistic interpretationMissense variantProtein language modelsToken classification

Identifiers

PMID40520595
PMCPMC12166733

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.