Evidence map›Paper›PMID 39665266›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

S-PLM: Structure-Aware Protein Language Model via Contrastive Learning Between Sequence and Structure.

Duolin Wang, Mahdi Pourmirzaei, Usman L Abbas, Shuai Zeng, Negin Manshour, Farzaneh Esmaili, Biplab Poudel, Yuexu Jiang, Qing Shao, Jin Chen and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Contrastive learning unites sequence and structure in a global representation of protein space.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. CLASPP: A unified model for predicting post-translational modifications.bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. CACLENS: A Multitask Deep Learning System for Enzyme Discovery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Duolin WangDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Mahdi PourmirzaeiDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Usman L AbbasChemical & Materials Engineering, University of Kentucky, Lexington, KY, 40506, USA.
Shuai ZengDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Negin ManshourDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Farzaneh EsmailiDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Biplab PoudelDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Yuexu JiangDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Qing ShaoChemical & Materials Engineering, University of Kentucky, Lexington, KY, 40506, USA.
Jin ChenDepartment of Medicine and Department of Biomedical Informatics and Data Science, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Dong XuDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.ORCID https://orcid.org/0000-0002-4809-0514

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Multi-view self-supervised deep learning for biological sequences and beyondR35GM126985 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI DONG XU · 2018 to 2026
$3.8M
Structure-Function-Aware Large Protein Language Models for Enhanced Biomedical ApplicationsR01LM014510 · NLM · UNIVERSITY OF KENTUCKY · PI Qing Shao · 2024 to 2026
$994k
Foundation for the National Institutes of Health R35GM126985Medicine (AIM) at the University of Kentucky NCI P30 CA177558Medicine (AIM) at the University of Kentucky UL1TR001998National Science Foundation #2138259NCATS NIH HHS UL1 TR001998NCI NIH HHS P30 CA177558NCSA CIS230053NIGMS NIH HHS R35 GM126985NIH HHS R01LM014510NLM NIH HHS R01 LM014510University of Kentucky and Alzheimer's Association AARG-23-1144638University of Kentucky Center for Computational Sciences and Information Technology Services Research Computing
6 · The paper itself

Abstract

Proteins play an essential role in various biological and engineering processes. Large protein language models (PLMs) present excellent potential to reshape protein research by accelerating the determination of protein functions and the design of proteins with the desired functions. The prediction and design capacity of PLMs relies on the representation gained from the protein sequences. However, the lack of crucial 3D structure information in most PLMs restricts the prediction capacity of PLMs in various applications, especially those heavily dependent on 3D structures. To address this issue, S-PLM is introduced as a 3D structure-aware PLM that utilizes multi-view contrastive learning to align the sequence and 3D structure of a protein in a coordinated latent space. S-PLM applies Swin-Transformer on AlphaFold-predicted protein structures to embed the structural information and fuses it into sequence-based embedding from ESM2. Additionally, a library of lightweight tuning tools is provided to adapt S-PLM for diverse downstream protein prediction tasks. The results demonstrate S-PLM's superior performance over sequence-only PLMs on all protein clustering and classification tasks, achieving competitiveness comparable to state-of-the-art methods requiring both sequence and structure inputs. S-PLM and its lightweight tuning tools are available at https://github.com/duolinwang/S-PLM/.

Indexed as

Computational BiologyMachine LearningProteinsProtein ConformationProteinscontrastive learningdeep learningprotein function predictionprotein language modelprotein structure

Identifiers

PMID39665266
PMCPMC11791933

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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.