Evidence map›Paper›PMID 42080436›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Sequence-Encoded Frustration Directs the Formation of Abridged G-Quadruplex Architectures.

Yuncheng Qian, Mohamed Y Ali, Andreas I Karsisiotis, Paul Dillon, Scarlett A Dvorkin, Peter A C McPherson, Mateus Webba da Silva

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Yuncheng QianBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.
Mohamed Y AliBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.
Andreas I KarsisiotisBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.
Paul DillonBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.
Scarlett A DvorkinBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.
Peter A C McPhersonBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.ORCID 0000-0001-6961-1158
Mateus Webba da SilvaBiomedical Sciences Research Institute, Ulster University, Coleraine, UK.

Funding

BBSRC
6 · The paper itself

Abstract

Frustration-competing interactions that cannot be simultaneously optimized-shapes energy landscapes in proteins and soft matter, but has rarely been exploited as a programmable design principle in nucleic acids. Here we demonstrate that sequence-encoded frustration programmes DNA G-quadruplex folding, yielding stable "abridged" architectures with fewer guanine tetrads than the sequence would nominally permit. Using an integrated structural, spectroscopic, thermodynamic, and computational approach, we map a frustration-biased folding landscape featuring a thermodynamically stabilized G-triplex intermediate, whose identity we assign via TD-DFT computed electronic circular dichroism spectra, and resolve the dominant unfolding pathway at atomic resolution. These results demonstrate programmable frustration as a predictive design principle for controlling nucleic acid topology and dynamics, offering new strategies for engineering functional DNA-based systems and for interpreting genomic G-quadruplex plasticity.

Indexed as

DNAG-QuadruplexesBase SequenceCircular DichroismNucleic Acid ConformationThermodynamicsDNAabridged G‐quadruplexcompetitive cappingdensity functional theoryfolding frustrationG‐triplexmetadynamicsSRCD

Identifiers

PMID42080436
PMCPMC13266908

What OpenQuestion holds

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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.