Evidence map›Paper›PMID 39988825›Full record

ArticleJournal of chemical information and modeling2025

ProCeSa: Contrast-Enhanced Structure-Aware Network for Thermostability Prediction with Protein Language Models.

Feixiang Zhou, Shuo Zhang, Huifeng Zhang, Jian K Liu

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2025. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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.

Feixiang ZhouReadline Intelligence, Birmingham B29 6SQ, U.K.
Shuo ZhangSchool of Computer Science, University of Birmingham, Birmingham B15 2TT, U.K.
Huifeng ZhangReadline Intelligence, Birmingham B29 6SQ, U.K.
Jian K LiuSchool of Computer Science, University of Birmingham, Birmingham B15 2TT, U.K.ORCID 0000-0002-5391-7213

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins play a fundamental role in biology, and their thermostability is essential for their proper functionality. The precise measurement of thermostability is crucial, traditionally relying on resource-intensive experiments. Recent advances in deep learning, particularly in protein language models (PLMs), have significantly accelerated the progress in protein thermostability prediction. These models utilize various biological characteristics or deep representations generated by PLMs to represent the protein sequences. However, effectively incorporating structural information, based on the PLM embeddings, while not considering atomic protein structures, remains an open and formidable challenge. Here, we propose a novel Protein Contrast-enhanced Structure-Aware (ProCeSa) model that seamlessly integrates both sequence and structural information extracted from PLMs to enhance thermostability prediction. Our model employs a contrastive learning scheme guided by the categories of amino acid residues, allowing it to discern intricate patterns within protein sequences. Rigorous experiments conducted on publicly available data sets establish the superiority of our method over state-of-the-art approaches, excelling in both classification and regression tasks. Our results demonstrate that ProCeSa addresses the complex challenge of predicting protein thermostability by utilizing PLM-derived sequence embeddings, without requiring access to atomic structural data.

Indexed as

ProteinsTemperatureDeep LearningModels, MolecularProtein ConformationProtein StabilityProteins

Identifiers

PMID39988825
PMCPMC11898056

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LicenceCC BY
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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.