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

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/.

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Publication Details

Journal
Advanced Science
Published
2024-12-12
DOI
https://doi.org/10.1002/advs.202404212
Citations
23
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
5.38

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article

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

Duolin Wang, Mahdi Pourmirzaei, Usman L. Abbas, Negin Manshour et al.
23 citations
Advanced Science
Protein Structure and Dynamics
5.38
article

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

Duolin Wang, Mahdi Pourmirzaei, Usman L. Abbas, Negin Manshour, Qing Shao, Farzaneh Esmaili, Dong Xu, Biplab Poudel, Jin Chen, Shuai Zeng, Yuexu Jiang
article en
23 citations

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/.

Advanced ScienceVol. 12(5)
University of Kentucky (US), University of Alabama at Birmingham (US), University of Missouri (US)
National Science Foundation, Foundation for the National Institutes of Health, Alzheimer's Association, University of Missouri, University of Kentucky, National Centre for Supercomputing Applications, National Institutes of Health, National Cancer Institute, Office of Advanced Cyberinfrastructure, National Center for Advancing Translational Sciences
Openalex Percentile: Top 3%
Protein Structure and Dynamics
5.38
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