Evidence map›Paper›PMID 42324907›Full record

ArticleSmall methods2026

Dual Quantum Dot Molecular FRET Probes for Picomolar DNA Hexaplexing.

Ruifang Su, Federico Pini, Nour Fayad, Kimihiro Susumu, Marta M Natile, Igor L Medintz, Thibault Gallavardin, Thomas J Sørensen, Niko Hildebrandt

Abstract read
In one paragraph

Article in Small methods, 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

9 authors.

Ruifang SuInstitut CARMeN, UMR 6064, CNRS, Université de Rouen Normandie, INSA Rouen Normandie, ENSICAEN, Université de Caen Normandie, Rouen, France.
Federico PiniInstitut CARMeN, UMR 6064, CNRS, Université de Rouen Normandie, INSA Rouen Normandie, ENSICAEN, Université de Caen Normandie, Rouen, France.ORCID https://orcid.org/0000-0002-6963-7742
Nour FayadInstitut CARMeN, UMR 6064, CNRS, Université de Rouen Normandie, INSA Rouen Normandie, ENSICAEN, Université de Caen Normandie, Rouen, France.
Kimihiro SusumuOptical Sciences Division, Code 5600, U.S. Naval Research Laboratory, Washington, D.C., USA.
Marta M NatileConsiglio Nazionale delle Ricerche (CNR), Istituto di Chimica della Materia Condensata e Tecnologie per l'Energia (ICMATE), Padova, Italy.ORCID https://orcid.org/0000-0001-5591-2670
Igor L MedintzCenter for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C., USA.
Thibault GallavardinInstitut CARMeN, UMR 6064, CNRS, Université de Rouen Normandie, INSA Rouen Normandie, ENSICAEN, Université de Caen Normandie, Rouen, France.ORCID https://orcid.org/0000-0002-3339-2288
Thomas J SørensenNano-Science Center & Department of Chemistry, University of Copenhagen, Copenhagen, Denmark.
Niko HildebrandtDepartment of Engineering Physics, McMaster University, Hamilton, Ontario, Canada.ORCID https://orcid.org/0000-0001-8767-9623

Funding

Agence Nationale de la Recherche ANR-11-LABX-0029;ANR-18-EURE-0020XLCHEMNatural Sciences and Engineering Research Council of Canada CERC-2022-00072Université Franco-Italienne ScholarshipF.P.Villum Fonden Grant14922
6 · The paper itself

Abstract

Semiconductor quantum dots (QD) combine bright and color-tunable photoluminescence (PL) with large surfaces. Thus, merging multiplexed PL detection and specific biorecognition on a single QD is in principle possible. By attaching multiple DNAs per QD and adjusting terbium (Tb) to QD Förster resonance energy transfer (FRET) with sub-nanometer resolution, we designed dual-color FRET-nanoprobes with six distinguishable signals. The hexaplexing molecular probes combined two PL colors with three PL decays while requiring only a single excitation wavelength for rapid and simple biosensing. Implementation into a sensitive diagnostic assay was demonstrated via the specific quantification of six different DNA targets at picomolar concentrations (2 to 40 femtomole) from a single 200 µL sample. The orthogonality of specific biorecognition and FRET multiplexing on the nanosurface makes the QD-based FRET probes extendable to the sensitive quantification of potentially any biomarker or biological interaction at even higher multiplexing capability. Our results demonstrate that luminescent nanoprobes are capable of translating sophisticated multiplexing approaches into relatively simple biosensing methods.

Indexed as

DNAFluorescence Resonance Energy TransferMolecular ProbesQuantum DotsBiosensing TechniquesTerbiumDNAMolecular ProbesTerbiumbiomarkersbiosensingenergy transfermultiplexingnanoparticles

Identifiers

PMID42324907
PMCPMC13505750

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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.