Evidence map›Paper›PMID 41272972›Full record

ReviewBiophysical journal2026

Reimagining computational macromolecular modeling: AI-driven approaches.

E Sila Ozdemir, Hyunbum Jang, Ruth Nussinov, Ozlem Keskin, Attila Gursoy

Abstract readReview
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

E Sila OzdemirIndependent Researcher, Seattle, WA 98109.
Hyunbum JangComputational Structural Biology Section, Frederick National Laboratory for Cancer Research in the Cancer Innovation Laboratory, National Cancer Institute, Frederick, MD 21702.
Ruth NussinovComputational Structural Biology Section, Frederick National Laboratory for Cancer Research in the Cancer Innovation Laboratory, National Cancer Institute, Frederick, MD 21702; Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel. Electronic address: nussinor@mail.nih.gov.
Ozlem KeskinDepartment of Chemical and Biological Engineering, Koc University, Istanbul 34450, Turkey. Electronic address: okeskin@ku.edu.tr.
Attila GursoyDepartment of Computer Engineering, Koc University, Istanbul 34450, Turkey. Electronic address: agursoy@ku.edu.tr.

Funding

Biomolecular Recognition and Binding MechanismsZIABC010441 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2009 to 2025
$9.4M
Protein Structure, Stability, and Amyloid FormationZ01BC010440 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2002 to 2008
$1.4M
Biomolecular Recognition and Binding MechanismsZ01BC010441 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2002 to 2008
$1.2M
Method Development: Efficient Computer Vision Based AlgorithmsZ01BC010442 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2002 to 2008
$454k
Intramural NIH HHS Z01 BC010440Intramural NIH HHS Z01 BC010441Intramural NIH HHS Z01 BC010442Intramural NIH HHS ZIA BC010441NCI NIH HHS HHSN261201500003CNCI NIH HHS HHSN261201500003I
6 · The paper itself

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

Artificial IntelligenceMacromolecular SubstancesModels, MolecularHumansMachine LearningMacromolecular Substances

Identifiers

PMID41272972
PMCPMC12701635

What OpenQuestion holds

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Registered trials

None linked

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.