Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.10.28.684999

Predicting single-stranded DNA oligonucleotides 3D structures: an open issue

Abstract

Single-stranded Nucleic Acids (ssNAs) play major biological functions and represent an interesting biotechnological tool. Their function depends strictly on the specific foldings they can adopt. Therefore, information about ssNAs tridimensional structures is fundamental to investigate their functions. In this context, in silico 3D structure prediction can facilitate ssNAs design. Many algorithms have been developed with this aim, mainly focused on RNA. However, the growing interest in single-stranded DNA (ssDNA), due to their greater stability as compared to RNA, has highlighted the need to adapt these methods for ssDNA. This study assessed three RNA 3D structure prediction methods (RNAComposer, SimRNA, and Vfold3D), based on their performance in the Critical Assessment of protein Structure Prediction 15 and/or 16, to evaluate their applicability to ssDNA. At this scope, a dataset of 93 experimentally determined ssDNA structures, including challenging motifs such as G-quadruplexes, was built. Various metrics, such as RMSD, GDT TS, and INF were employed to benchmark the accuracy of the predictions. The three tools showed similar and moderate performances. In addition, they show strong difficulties in modeling G-quadruplexes, and structures containing motifs strongly increasing the intrinsic flexibility of ssDNA. Despite the recent efforts in the prediction of the 3D folding of ssNAs, it is clear that a significant improvement of the methods is needed. This should involve taking into account the conformational variability of this kind of molecules and paying attention to their specific 3D motifs. Author summarySingle-stranded oligonucleotides (ssNAs) are RNA or single-stranded DNA molecules involved in crucial biological processes, such as gene expression, DNA replication, and transcription. In addition, they represent a powerful biotechnlogical tool exploitable in therapeutics, diagnostics and biosensing. This is due to their capacity of recognizing different kind of molecular targets, thanks to the tridimensional foldings they can adopt. It is therefore clear that the knowledge of the ssNAs structure is fundamental to master these molecules. With this aim, much effort has been paid in developing computational tools for the prediction of ssNAs 3D structures. However, their application is mostly limited to RNA sequences, even if the interest in ssDNAs is rapidly increasing. Moreover, an extensive benchmark on their performances is missing. We focused this work on assessing the performances of three ssNA structure prediction tools, which best performed in the two latest Critical Assessment of protein Structure Prediction contests, on a large dataset of ssDNA, in order to establish the strengths and limits of the available tools. This knowledge will be helpful in finding new solutions for better understanding the ssNAs folding and their structure-function relationship.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bengaouer, S., Binet, T., Octave, S., Padiolleau, S., Avalle, B., MAFFUCCI, I.. 2025-10-28. Predicting single-stranded DNA oligonucleotides 3D structures: an open issue. https://doi.org/10.1101/2025.10.28.684999

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Comparative functional genomics reveals distributed SERPINE1 like characteristics among Drosophila serpins

Serpins (serine protease inhibitors) regulate proteolytic activity through a suicide-substrate inhibitory mechanism, whereby the serpin covalently traps and inactivates their target protease. Serpins are broadly conserved across eukaryotes, but the evolutionary and functional relationships between human SERPINE1, and Drosophila Serpins in incompletely defined. To identify candidate Drosophila functional analogs of SERPINE1/PAI-1, a multi-omics framework was applied to thoroughly compare the serpins across species. The multi-level analysis integrated orthology prediction, protein sequence and structural characterization, phylogenetic reconstruction, bulk tissue transcriptomics, single-cell transcriptomics, and aging-associated expression analysis. Candidate serpins (Spn42Da, Spn42Db, Spn42Dc, Spn42Dd, Spn28B, and Spn28F) were evaluated using DIOPT, AlphaFold/ChimeraX structural comparisons, reactive center loop analyses, phylogenetic distances, GTEx, Human Protein Atlas, FlyAtlas2, Fly Cell Atlas, and Aging Fly Cell Atlas datasets. Comparative analyses demonstrated full-length sequence and reactive center loop (RCL) divergence despite preservation of the canonical serpin fold. Tissue, cell-type, and age-associated expression analysis revealed distinct candidate-specific patterns. Spn42Dd comparisons uncovered similarities to human SERPINE1 in sequence/structural and broad expression but did not represent the strongest overall cross-species expression correlations. Spn42Da and Spn42Db received the highest cross species integrated support. Quality check of the ranking confirmed that Spn42Da and Spn42Db were stable top candidates across orthology, sequence alignment, and expression domains. The multi-domain analysis was unable to identify a single definitive Drosophila serpin as the closest counterpart to human SERPINE1, indicating that cross-species similarity is distributed across multiple candidate serpins. This study therefore provides a quantitative method for prioritizing potential evolutionary and functional analogs across highly divergent species.

bioinformatics↗

CellChat Hotspot: A Targeted Approach to Cell Cell Communication Analysis With Spatial transcriptomics Validation.

Abstract. In recent years, single cell RNA sequencing (scRNA seq) has enabled the investigation of intercellular communication through Cell Cell Communication (CCC) tools such as CellChat. Despite their potential, these approaches remain challenging to interpret, particularly when global analyses generate complex interaction networks that may include biologically irrelevant signals. To address this limitation, we developed a framework termed CellChat Hotspot, designed to improve the biological interpretability of inferred communication networks. This approach integrates gene set enrichment analysis with a context driven filtering strategy, selecting both genes and cells based on their functional relevance prior to communication inference. Applied to stage II colon cancer data, CellChat Hotspot enabled the identification of condition-specific interaction patterns associated with recurrence. Non recurrent patients showed enrichment of immune related processes, whereas recurrent cases were characterized by pathways associated with invasion and metastasis. Notably, a loss of interaction in the HSPG pathway between CALB1+ and stromal cells was observed in recurrent patients, suggesting a potential disruption of cell matrix adhesion mechanisms. To verify the reliability of this finding, we applied the framework to spatial transcriptomics data, which confirmed the presence of the HSPG2 DAG1 interaction in non-recurrent tumors and its near absence in recurrent ones. Overall, this framework provides a biologically guided strategy for studying intercellular communication in complex systems such as the tumor microenvironment.

bioinformatics↗

DiffTernary: a Diffusion Model for Molecular Glue Ternary Complex Docking

Molecular glues (MGs) modulate protein function by inducing or stabilizing protein interactions. However, accurately modeling MG ternary complexes remains challenging. Here, we present DiffTernary, a diffusion-based docking method for the joint prediction of relative protein arrangement and MG binding pose. We introduce Ternary-PDB, a dataset of 76,702 experimentally determined ternary complexes curated from the Protein Data Bank using structural filters and a release cutoff aligned with AlphaFold 3 (AF3). When trained on this dataset, DiffTernary achieved acceptable protein-protein interaction (PPI) predictions (DockQ > 0.23) for 50.0% of MGBench complexes with a single prediction, compared with 51.1% for AF3. In comparisons with AF3, OpenFold3, ESMFold2, Protenix-v1 and Protenix-v2, DiffTernary ranked second with a best-of-25 PPI prediction success rate of 78.4%, behind ESMFold2 (90.9%) and ahead of AF3 (72.7%). A separate DiffTernary model trained on TernaryDB achieved a mean DockQ of 0.306 on the 94 complexes in the TernaryDB MGD test set with a single prediction, compared with 0.228 for DeepTernary. Confidence-based selection among 40 samples yielded acceptable PPI predictions for 41.5% of complexes, compared with 30.9% for DeepTernary. An E2Former variant increased training and sampling throughput 6.90-fold and 4.37-fold, respectively, under the evaluated configurations. Together, DiffTernary and Ternary-PDB provide an efficient docking approach for MG complex prediction and a valuable structural resource for MG discovery and design.

bioinformatics↗