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Protein-nucleic acid interactions (PNI) play crucial roles in various life processes, including gene expression regulation, DNA replication, repair, recombination, and RNA processing and translation. However, accurately predicting these interactions remains challenging due to their complexity. This paper proposes a deep learning-based multi-task learning framework for predicting protein-nucleic acid interactions. The integrated framework comprises four independent deep learning models: PNI-FCN, PNI-Transformer, PNI-MAMBA, and PNI-MAMBA2. PNI-FCN leverages fully connected neural networks, PNI-Transformer utilizes Transformer networks, and both PNI-MAMBA and PNI-MAMBA2 are built upon Mamba network architectures. A novel binding site attention mechanism is introduced to capture key binding site information. The multi-task learning objective function combines the binary classification cross-entropy loss with a binding site loss to guide the model's focus on critical regions. Experiments on merged DNA and RNA datasets demonstrate the effectiveness of the proposed framework in accurately predicting protein-nucleic acid interactions and identifying binding PNI sites. Notably, the architectural framework leveraging PNI-MAMBA (s)-encompassing both PNI-MAMBA and PNI-MAMBA2-demonstrates superior overall performance, thereby enhancing both the accuracy and robustness of predictions. This work offers significant insights into the underlying molecular mechanisms and lays a strong foundation for the development of targeted therapeutic interventions.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.147419 | DOI Listing |
Brief Bioinform
August 2025
School of Information and Artificial Intelligence, Anhui Agricultural University, 130 Changjiang Road, Shushan District, Hefei, Anhui 230036, China.
Protein-nucleic acid binding sites play a crucial role in biological processes such as gene expression, signal transduction, replication, and transcription. In recent years, with the development of artificial intelligence, protein language models, graph neural networks, and transformer architectures have been adopted to develop both structure-based and sequence-based predictive models. Structure-based methods benefit from the spatial relationship between residues and have shown promising performance.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Center for Artificial Intelligence Driven Drug Discovery, Faculty of Applied Sciences, Macao Polytechnic University, Macau. Electronic address:
Protein-nucleic acid interactions (PNI) play crucial roles in various life processes, including gene expression regulation, DNA replication, repair, recombination, and RNA processing and translation. However, accurately predicting these interactions remains challenging due to their complexity. This paper proposes a deep learning-based multi-task learning framework for predicting protein-nucleic acid interactions.
View Article and Find Full Text PDFElife
September 2025
Department of Biochemistry & Biophysics and Bioengineering, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States.
Cryptic pockets are of growing interest as potential drug targets, particularly to control protein-nucleic acid interactions that often occur via flat surfaces. However, it remains unclear whether cryptic pockets contribute to protein function or if they are merely happenstantial features that can easily be evolved away to achieve drug resistance. Here, we explore whether a cryptic pocket in the Interferon Inhibitory Domain (IID) of viral protein 35 (VP35) of Zaire ebolavirus aids its ability to bind double-stranded RNA (dsRNA).
View Article and Find Full Text PDFPrep Biochem Biotechnol
September 2025
Department of Biotechnology, Vignan's Foundation for Science, Technology and Research, Vadlamudi, Andhra Pradesh, India.
Enteric fever caused by remains a critical public health challenge due to rising incidence and increasing antimicrobial resistance. The development of effective polysaccharide conjugate vaccines targeting Salmonella Paratyphi requires high-purity O-antigen polysaccharide (PS) conjugated to immunogenic carrier proteins. This study optimized a robust and scalable purification-conjugation methodology, specifically tailored for O-antigen from Initial purification utilized ultrafiltration via tangential flow filtration (TFF), followed by sequential cation- and anion-exchange chromatography steps, significantly reducing protein, nucleic acid, and endotoxin contaminants.
View Article and Find Full Text PDFJACS Au
August 2025
Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, U.K.
Rapid, accurate, and accessible diagnostics for pathogenic infections are of vital importance for the prevention of disease transmission and mitigation of future pandemics. Biosensors employing the CRISPR nuclease Cas13 have enabled robust detection of viral RNA. However, existing Cas13-based diagnostics primarily utilize fluorescent or lateral flow assay (LFA) readouts, impeding detection in complex sample media.
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