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1. Accurate prediction of nucleic acid binding proteins using protein language model

   https://doi.org/10.1093/bioadv/vbaf008  

   Wu, Siwen; Xu, Jinbo; Guo, Jun-tao (December 2024, Bioinformatics Advances)

   Bateman, Alex (Ed.)

   Abstract MotivationNucleic acid binding proteins (NABPs) play critical roles in various and essential biological processes. Many machine learning-based methods have been developed to predict different types of NABPs. However, most of these studies have limited applications in predicting the types of NABPs for any given protein with unknown functions, due to several factors such as dataset construction, prediction scope and features used for training and testing. In addition, single-stranded DNA binding proteins (DBP) (SSBs) have not been extensively investigated for identifying novel SSBs from proteins with unknown functions. ResultsTo improve prediction accuracy of different types of NABPs for any given protein, we developed hierarchical and multi-class models with machine learning-based methods and a feature extracted from protein language model ESM2. Our results show that by combining the feature from ESM2 and machine learning methods, we can achieve high prediction accuracy up to 95% for each stage in the hierarchical approach, and 85% for overall prediction accuracy from the multi-class approach. More importantly, besides the much improved prediction of other types of NABPs, the models can be used to accurately predict single-stranded DBPs, which is underexplored. Availability and implementationThe datasets and code can be found at https://figshare.com/projects/Prediction_of_nucleic_acid_binding_proteins_using_protein_language_model/211555. 

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2. EquiPNAS: improved protein–nucleic acid binding site prediction using protein-language-model-informed equivariant deep graph neural networks

   https://doi.org/10.1093/nar/gkae039  

   Roche, Rahmatullah; Moussad, Bernard; Shuvo, Md Hossain; Tarafder, Sumit; Bhattacharya, Debswapna (January 2024, Nucleic Acids Research)

   Abstract Protein language models (pLMs) trained on a large corpus of protein sequences have shown unprecedented scalability and broad generalizability in a wide range of predictive modeling tasks, but their power has not yet been harnessed for predicting protein–nucleic acid binding sites, critical for characterizing the interactions between proteins and nucleic acids. Here, we present EquiPNAS, a new pLM-informed E(3) equivariant deep graph neural network framework for improved protein–nucleic acid binding site prediction. By combining the strengths of pLM and symmetry-aware deep graph learning, EquiPNAS consistently outperforms the state-of-the-art methods for both protein–DNA and protein–RNA binding site prediction on multiple datasets across a diverse set of predictive modeling scenarios ranging from using experimental input to AlphaFold2 predictions. Our ablation study reveals that the pLM embeddings used in EquiPNAS are sufficiently powerful to dramatically reduce the dependence on the availability of evolutionary information without compromising on accuracy, and that the symmetry-aware nature of the E(3) equivariant graph-based neural architecture offers remarkable robustness and performance resilience. EquiPNAS is freely available at https://github.com/Bhattacharya-Lab/EquiPNAS. 

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3. The Landscape of RNA-Protein Interactions in Plants: Approaches and Current Status

   https://doi.org/10.3390/ijms22062845  

   Burjoski, Vesper; Reddy, Anireddy S. (March 2021, International Journal of Molecular Sciences)

   null (Ed.)

   RNAs transmit information from DNA to encode proteins that perform all cellular processes and regulate gene expression in multiple ways. From the time of synthesis to degradation, RNA molecules are associated with proteins called RNA-binding proteins (RBPs). The RBPs play diverse roles in many aspects of gene expression including pre-mRNA processing and post-transcriptional and translational regulation. In the last decade, the application of modern techniques to identify RNA–protein interactions with individual proteins, RNAs, and the whole transcriptome has led to the discovery of a hidden landscape of these interactions in plants. Global approaches such as RNA interactome capture (RIC) to identify proteins that bind protein-coding transcripts have led to the identification of close to 2000 putative RBPs in plants. Interestingly, many of these were found to be metabolic enzymes with no known canonical RNA-binding domains. Here, we review the methods used to analyze RNA–protein interactions in plants thus far and highlight the understanding of plant RNA–protein interactions these techniques have provided us. We also review some recent protein-centric, RNA-centric, and global approaches developed with non-plant systems and discuss their potential application to plants. We also provide an overview of results from classical studies of RNA–protein interaction in plants and discuss the significance of the increasingly evident ubiquity of RNA–protein interactions for the study of gene regulation and RNA biology in plants. 

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4. mebipred : identifying metal-binding potential in protein sequence

   https://doi.org/10.1093/bioinformatics/btac358  

   Aptekmann, A A; Buongiorno, J; Giovannelli, D; Glamoclija, M; Ferreiro, D U; Bromberg, Y (July 2022, Bioinformatics)

   Cowen, Lenore (Ed.)

   Abstract Motivationmetal-binding proteins have a central role in maintaining life processes. Nearly one-third of known protein structures contain metal ions that are used for a variety of needs, such as catalysis, DNA/RNA binding, protein structure stability, etc. Identifying metal-binding proteins is thus crucial for understanding the mechanisms of cellular activity. However, experimental annotation of protein metal-binding potential is severely lacking, while computational techniques are often imprecise and of limited applicability. Resultswe developed a novel machine learning-based method, mebipred, for identifying metal-binding proteins from sequence-derived features. This method is over 80% accurate in recognizing proteins that bind metal ion-containing ligands; the specific identity of 11 ubiquitously present metal ions can also be annotated. mebipred is reference-free, i.e. no sequence alignments are involved, and is thus faster than alignment-based methods; it is also more accurate than other sequence-based prediction methods. Additionally, mebipred can identify protein metal-binding capabilities from short sequence stretches, e.g. translated sequencing reads, and, thus, may be useful for the annotation of metal requirements of metagenomic samples. We performed an analysis of available microbiome data and found that ocean, hot spring sediments and soil microbiomes use a more diverse set of metals than human host-related ones. For human microbiomes, physiological conditions explain the observed metal preferences. Similarly, subtle changes in ocean sample ion concentration affect the abundance of relevant metal-binding proteins. These results highlight mebipred’s utility in analyzing microbiome metal requirements. Availability and implementationmebipred is available as a web server at services.bromberglab.org/mebipred and as a standalone package at https://pypi.org/project/mymetal/. Supplementary informationSupplementary data are available at Bioinformatics online. 

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5. HybridDBRpred: improved sequence-based prediction of DNA-binding amino acids using annotations from structured complexes and disordered proteins

   https://doi.org/10.1093/nar/gkad1131  

   Zhang, Jian; Basu, Sushmita; Kurgan, Lukasz (December 2023, Nucleic Acids Research)

   Abstract Current predictors of DNA-binding residues (DBRs) from protein sequences belong to two distinct groups, those trained on binding annotations extracted from structured protein-DNA complexes (structure-trained) vs. intrinsically disordered proteins (disorder-trained). We complete the first empirical analysis of predictive performance across the structure- and disorder-annotated proteins for a representative collection of ten predictors. Majority of the structure-trained tools perform well on the structure-annotated proteins while doing relatively poorly on the disorder-annotated proteins, and vice versa. Several methods make accurate predictions for the structure-annotated proteins or the disorder-annotated proteins, but none performs highly accurately for both annotation types. Moreover, most predictors make excessive cross-predictions for the disorder-annotated proteins, where residues that interact with non-DNA ligand types are predicted as DBRs. Motivated by these results, we design, validate and deploy an innovative meta-model, hybridDBRpred, that uses deep transformer network to combine predictions generated by three best current predictors. HybridDBRpred provides accurate predictions and low levels of cross-predictions across the two annotation types, and is statistically more accurate than each of the ten tools and baseline meta-predictors that rely on averaging and logistic regression. We deploy hybridDBRpred as a convenient web server at http://biomine.cs.vcu.edu/servers/hybridDBRpred/ and provide the corresponding source code at https://github.com/jianzhang-xynu/hybridDBRpred. 

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