Evidence map›Paper›PMID 41018615›Full record

ArticleACS omega2025

DNA Origami-Based Luminescent Biosensors Enabling Smartphone Detection of Nucleic Acid Sequences.

Shuhei Kido, Nozomu Takahashi, Hiroshi Miyazaki, Sachiko Kono, Keita Saito, Akinori Kuzuya

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
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  5. 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

6 authors.

Shuhei KidoCranebio Co., Ltd., 2-13-4 Sotokanda, Chiyoda-Ku, Tokyo 101-0021, Japan.ORCID https://orcid.org/0009-0000-5803-1350
Nozomu TakahashiCranebio Co., Ltd., 2-13-4 Sotokanda, Chiyoda-Ku, Tokyo 101-0021, Japan.
Hiroshi MiyazakiCranebio Co., Ltd., 2-13-4 Sotokanda, Chiyoda-Ku, Tokyo 101-0021, Japan.
Sachiko KonoCranebio Co., Ltd., 2-13-4 Sotokanda, Chiyoda-Ku, Tokyo 101-0021, Japan.
Keita SaitoCranebio Co., Ltd., 2-13-4 Sotokanda, Chiyoda-Ku, Tokyo 101-0021, Japan.
Akinori KuzuyaDepartment of Chemistry and Materials Engineering, Kansai University, 3-3-35 Yamate, Suita, Osaka 564-8680, Japan.ORCID https://orcid.org/0000-0003-0003-2996

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA origami enables the precise assembly of complex nanostructures, facilitating the visual detection of various molecular targets. Previously, we developed DNA origami-based nanosensors, termed "pliers", which allowed the detection of inorganic and organic single-molecule targets through shape transitions. However, these methods require costly analytical instruments, such as atomic force microscopy and fluorescence detection. To establish a more accessible and quantitative detection approach, we developed a luminescence-based DNA origami biosensor for nucleic acid detection. By redesigning the sensor module, we improved the structural stability and sensitivity. The integration of split luciferase enabled signal amplification proportional to the target RNA concentration, allowing for precise detection using a smartphone. Additionally, combining this method with PCR successfully detected as few as 100 copies of

Identifiers

PMID41018615
PMCPMC12461322

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.