Evidence map›Paper›PMID 41834072›Full record

ArticleChemPlusChem2026

Nanopipette-DNA-Nanopore Hybrid System for Small Molecule Detection.

Hiromu Akai, Kan Shoji

Abstract read
In one paragraph

Article in ChemPlusChem, 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. Review
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.

Hiromu AkaiDepartment of Mechanical Engineering, Nagaoka University of Technology, Nagaoka, Niigata, Japan.
Kan ShojiDepartment of Mechanical Engineering, Nagaoka University of Technology, Nagaoka, Niigata, Japan.ORCID 0000-0002-7198-9683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hybrid nanopores composed of a solid-state nanopore and a DNA origami nanopore are excellent candidates for highly molecular-selective nanopore sensors owing to the high designability and functionalization potential of DNA origami structures. Although the detection of macromolecules, including ssDNAs and proteins, has been demonstrated using hybrid nanopores, their applicability for small-molecule detection has not yet been revealed. The critical issue hindering the application of the hybrid nanopore is the limited understanding of the behavior of DNA origami nanoplates trapped on a solid-state nanopore under high applied potentials. Here, we developed a hybrid nanopore constructed by electrophoretically trapping an adenosine triphosphate (ATP) aptamer-modified DNA origami nanopore onto a nanopipette. This hybrid nanopore generates open/close signals through the binding and dissociation of ATP to the aptamer modified on the central aperture of the DNA origami nanopore. Ion current measurements revealed four distinct kinds of ion current signals in the presence and absence of ATP. Moreover, the ratio of open/close signals in the presence of ATP increased threefold compared with the ATP-free condition or ATP analogs, including cytidine triphosphate, demonstrating specific ATP detection using the hybrid nanopore. We believe that these results provide fundamental insight into the development of versatile hybrid nanopore sensors.

Indexed as

Adenosine TriphosphateDNANanoporesAptamers, NucleotideBiosensing TechniquesDNA NanostructuresAdenosine TriphosphateAptamers, NucleotideDNAaptamersDNA structuresnanopipettesnanoporessmall molecules

Identifiers

PMID41834072
PMCPMC12989472

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.