ReviewBiophysical journal2026
Reimagining computational macromolecular modeling: AI-driven approaches.
Review in Biophysical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Simulation of cell-size systems at long timescales with flexible protein structures.bioRxiv : the preprint server for biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Macromolecules, such as proteins, antibodies, nanobodies, and other affinity binders, play essential roles in therapeutic and diagnostic applications due to their high specificity and functionality. Understanding their structure is critical for deciphering their biological activity and drug discovery; however, the inherent complexity of these molecules poses significant challenges. Computational approaches have emerged as powerful tools for modeling macromolecular structures and interactions, offering faster and more cost-effective alternatives to experimental techniques. This review highlights state-of-the-art computational methods used in macromolecule modeling, with a strong focus on artificial intelligence (AI)- and machine learning (ML)-based approaches. Key advanced AI/ML techniques that have revolutionized the field are discussed. We also discuss therapeutic applications of AI/ML approaches and explore how these technologies are transforming drug discovery by accurately predicting macromolecular structures, designing novel therapeutic molecules, modeling protein-protein and protein-drug interactions, estimating binding affinities, and improving cheminformatics analyses. Finally, the review outlines ongoing shortcomings, such as data integration, interpretability, and model validation, and offers perspectives on future directions. We assess the strengths and limitations of each computational approach and present challenges unique to different macromolecule types. By providing a comprehensive overview of current computational strategies, this review serves as a valuable resource for developing innovative approaches in drug development while showcasing the state of the art in computational macromolecular modeling.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.