RPIPLM: Prediction of ncRNA-protein interaction by post-training a dual-tower pretrained biological model with supervised contrastive learning

The field of biological research has been profoundly impacted by the emergence of biological pre-trained models, which have resulted in remarkable advancements in life sciences and medicine. However, the current landscape of biological pre-trained language models suffers from a shortcoming, i.e., their inability to grasp the intricacies of molecular interactions, such as ncRNA-protein interactions. It is in this context that our paper introduces a two-tower computational framework, termed RPIPLM, which brings forth a new paradigm for the prediction of ncRNA-protein interactions. The core of RPIPLM lies in its harnessing of the pre-trained RNA language model and protein language model to process ncRNA and protein sequences, thereby enabling the transfer of the general knowledge gained from self-supervised learning of vast data to ncRNA-protein interaction tasks. Additionally, to learn the intricate interaction patterns between RNA and protein embeddings across diverse scales, we employ a fusion of scaled dot-product self-attention mechanism and Multi-scale convolution operations on the output of the dual-tower architecture, effectively capturing both global and local information. Furthermore, we introduce supervised contrastive learning into the training of RPIPLM, enabling the model to effectively capture discriminative information by distinguishing between interacting and non-interacting samples in the learned representations. Through extensive experiments and an interpretability study, we demonstrate the effectiveness of RPIPLM and its superiority over other methods, establishing new state-of-the-art performance. RPIPLM is a powerful and scalable computational framework that holds the potential to unlock enormous insights from vast biological data, thereby accelerating the discovery of molecular interactions.

Authors

Institutions

Publication Details

Journal
PLoS ONE
Published
2025-08-14
DOI
https://doi.org/10.1371/journal.pone.0329174
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.81
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

RPIPLM: Prediction of ncRNA-protein interaction by post-training a dual-tower pretrained biological model with supervised contrastive learning

Yiwei Liu, Y Wang, Ting Bao, Peng Yin et al.
1 citations
PLoS ONE
RNA and protein synthesis mechanisms
0.81
article

RPIPLM: Prediction of ncRNA-protein interaction by post-training a dual-tower pretrained biological model with supervised contrastive learning

Yiwei Liu, Y Wang, Ting Bao, Peng Yin, Shumin Wang
article en
1 citations

Abstract

The field of biological research has been profoundly impacted by the emergence of biological pre-trained models, which have resulted in remarkable advancements in life sciences and medicine. However, the current landscape of biological pre-trained language models suffers from a shortcoming, i.e., their inability to grasp the intricacies of molecular interactions, such as ncRNA-protein interactions. It is in this context that our paper introduces a two-tower computational framework, termed RPIPLM, which brings forth a new paradigm for the prediction of ncRNA-protein interactions. The core of RPIPLM lies in its harnessing of the pre-trained RNA language model and protein language model to process ncRNA and protein sequences, thereby enabling the transfer of the general knowledge gained from self-supervised learning of vast data to ncRNA-protein interaction tasks. Additionally, to learn the intricate interaction patterns between RNA and protein embeddings across diverse scales, we employ a fusion of scaled dot-product self-attention mechanism and Multi-scale convolution operations on the output of the dual-tower architecture, effectively capturing both global and local information. Furthermore, we introduce supervised contrastive learning into the training of RPIPLM, enabling the model to effectively capture discriminative information by distinguishing between interacting and non-interacting samples in the learned representations. Through extensive experiments and an interpretability study, we demonstrate the effectiveness of RPIPLM and its superiority over other methods, establishing new state-of-the-art performance. RPIPLM is a powerful and scalable computational framework that holds the potential to unlock enormous insights from vast biological data, thereby accelerating the discovery of molecular interactions.

PLoS ONEVol. 20(8)
Shenzhen Technology University (CN), University of Chinese Academy of Sciences (CN), Shenzhen MSU-BIT University, Inner Mongolia Medical University (CN)
Reduced inequalities
Openalex Percentile: Top 25%
RNA and protein synthesis mechanisms
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.