Evidence map›Paper›PMID 42358792›Full record

ArticleChemical & biomedical imaging2026

Multiplexed Detection of Reactive Biomolecules via Chemoresponsive DNA Accumulation on Fluorescence-Encoded Beads.

Tatsuya Nishihara, Masato Sugawara, Reoto Mio, Yuto Motohashi, Kazuhito Tanabe

Abstract read
In one paragraph

Article in Chemical & biomedical imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

5 authors.

Tatsuya NishiharaDepartment of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.ORCID https://orcid.org/0000-0002-6020-8757
Masato SugawaraDepartment of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.
Reoto MioDepartment of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.
Yuto MotohashiDepartment of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.
Kazuhito TanabeDepartment of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.ORCID https://orcid.org/0000-0003-2440-2293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multiplex analysis of reactive biomolecules is crucial in diagnostics and life science research. However, conventional methods using small-molecule-based fluorescent probes are limited in the number of simultaneously detectable targets because of the spectral overlap of their fluorescence wavelengths. Herein we present a sequencing-free multiplexed analysis platform using chemoresponsive DNA-based fluorescent probes. A target-responsive moiety was installed in the phosphate backbone of the probe to strategically destabilize the DNA duplex. Reaction with a target molecule such as hydrogen peroxide or nitroreductase cleaved this moiety, restoring duplex stability and thereby triggering the accumulation of fluorescent product DNAs on beads functionalized with a complementary sequence. By encoding beads with distinct fluorescence intensity ratios and sizes, we achieved the simultaneous and specific detection of multiple targets in a single sample. The system performed well even with complex biological samples. This modular "reaction-to-accumulation" strategy offers a generalizable approach for developing DNA-based multiplex detection systems tailored to different target molecules.

Indexed as

Beads accumulationFluorescent sensorH2O2Multiplex analysisNitroreductaseProbe DNA

Identifiers

PMID42358792
PMCPMC13291999

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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.