Evidence map›Paper›PMID 40610378›Full record

ArticleACS synthetic biology2025

Direct Modeling of DNA and RNA Aptamers with AlphaFold 3: A Promising Tool for Predicting Aptamer Structures and Aptamer-Target Interactions.

Steven Ochoa, Valeria Tohver Milam

Abstract read
In one paragraph

Article in ACS synthetic biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Predicting Single-Stranded DNA Oligonucleotides 3D Structures: An Open Issue.Computational and structural biotechnology journal · 2026
    Article
  11. Review
  12. 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

2 authors.

Steven OchoaSchool of Materials Science and Engineering, Georgia Institute of Technology, 771 Ferst Dr. NW, Atlanta, Georgia 30332-0245, United States.ORCID 0009-0003-7509-7425
Valeria Tohver MilamSchool of Materials Science and Engineering, Georgia Institute of Technology, 771 Ferst Dr. NW, Atlanta, Georgia 30332-0245, United States.ORCID 0000-0002-5303-7777

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aptamers, single-stranded nucleic acids that fold into unique three-dimensional shapes, bind selectively to non-nucleotide target molecules, making them promising ligands for diagnostic and therapeutic applications. The ability to accurately predict folded aptamer structures and their molecular interactions would significantly enhance the rational design of nucleic acid-based affinity reagents. However, predicting the 3D structures of aptamers remains challenging due to their complex folding patterns and limited experimental structure data compared to proteins. AlphaFold 3 is the latest structure prediction tool by Google DeepMind that has recently expanded to include nucleic acids and small molecule targets, offering new possibilities for the direct 3D modeling of aptamer sequences. This study evaluates the accuracy of AlphaFold 3 by comparing its predictions to experimentally resolved aptamer structures in the Protein Data Bank (PDB) and to well-characterized aptamers not included in the PDB. AlphaFold 3 effectively modeled a range of PDB-resolved aptamer structures, including those with noncanonical secondary structure elements such as G-quadruplexes and pseudoknots. For non-PDB aptamers, AlphaFold predictions were considerably less confident yet showed reasonable overlap with experimental data, accurately predicting G-quadruplex conformations and, in some cases, correctly localizing known binding interfaces in aptamer-protein complexes. Despite these attributes, AlphaFold 3 predictions appear limited by biases in its training data, reflecting the relative scarcity and redundancy of nongenomic nucleic acid structures in the PDB. These findings highlight the potential of AlphaFold 3 for aptamer modeling but underscore the need for further refinement to reliably predict complex, underrepresented structures. AlphaFold 3 represents a powerful step toward in silico aptamer design and offers a promising glimpse into a future where artificial intelligence accelerates discoveries and advancements in aptamers as effective affinity reagents.

Indexed as

Aptamers, NucleotideDNAG-QuadruplexesLigandsModels, MolecularNucleic Acid ConformationSoftwareAptamers, NucleotideDNALigandscanonicalligandnoncanonicaloligonucleotideProtein Data Banksecondary structure predictionstructure-binding

Identifiers

PMID40610378
PMCPMC12362623

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Registered trials

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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.