Evidence map›Paper›PMID 39483526›Full record

ArticleBioinformatics advances2024

PatchProt: hydrophobic patch prediction using protein foundation models.

Dea Gogishvili, Emmanuel Minois-Genin, Jan van Eck, Sanne Abeln

Abstract read
In one paragraph

Article in Bioinformatics advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. PLM-eXplain: divide and conquer the protein embedding space.Bioinformatics (Oxford, England) · 2026
    Article
  2. The Human Omnibus of Targetable Pockets.Journal of cheminformatics · 2025
    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.

Dea GogishviliBioinformatics, Computer Science Department, Vrije Universiteit Amsterdam, Amsterdam, 1081 HV, The Netherlands.ORCID https://orcid.org/0000-0001-8809-0861
Emmanuel Minois-GeninBioinformatics, Computer Science Department, Vrije Universiteit Amsterdam, Amsterdam, 1081 HV, The Netherlands.ORCID https://orcid.org/0009-0007-7032-478X
Jan van EckAI Technology for Life, Department of Computing and Information Sciences, Department of Biology, Utrecht University, Utrecht, 3584 CS, The Netherlands.ORCID https://orcid.org/0009-0002-3877-2965
Sanne AbelnBioinformatics, Computer Science Department, Vrije Universiteit Amsterdam, Amsterdam, 1081 HV, The Netherlands.ORCID https://orcid.org/0000-0002-2779-7174

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Hydrophobic patches on protein surfaces play important functional roles in protein-protein and protein-ligand interactions. Large hydrophobic surfaces are also involved in the progression of aggregation diseases. Predicting exposed hydrophobic patches from a protein sequence has shown to be a difficult task. Fine-tuning foundation models allows for adapting a model to the specific nuances of a new task using a much smaller dataset. Additionally, multitask deep learning offers a promising solution for addressing data gaps, simultaneously outperforming single-task methods. Results: In this study, we harnessed a recently released leading large language model Evolutionary Scale Models (ESM-2). Efficient fine-tuning of ESM-2 was achieved by leveraging a recently developed parameter-efficient fine-tuning method. This approach enabled comprehensive training of model layers without excessive parameters and without the need to include a computationally expensive multiple sequence analysis. We explored several related tasks, at local (residue) and global (protein) levels, to improve the representation of the model. As a result, our model, PatchProt, cannot only predict hydrophobic patch areas but also outperforms existing methods at predicting primary tasks, including secondary structure and surface accessibility predictions. Importantly, our analysis shows that including related local tasks can improve predictions on more difficult global tasks. This research sets a new standard for sequence-based protein property prediction and highlights the remarkable potential of fine-tuning foundation models enriching the model representation by training over related tasks. Availability and implementation: https://github.com/Deagogishvili/chapter-multi-task.

Identifiers

PMID39483526
PMCPMC11525051

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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.