Evidence map›Paper›PMID 40847907›Full record

ArticleAnalytical chemistry2025

Multiplexed Single-Molecule Detection of Nucleic Acid Biomarkers with a Distance-Tuned Single FRET Pair.

Srishty Sethi, Kalani M Wijesinghe, Md Monirul Islam, J Chuck Harrell, Soma Dhakal

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Article in Analytical chemistry, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Srishty SethiDepartment of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
Kalani M WijesingheDepartment of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
Md Monirul IslamDepartment of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
J Chuck HarrellDepartment of Pathology, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298, United States.
Soma DhakalDepartment of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284, United States.ORCID 0000-0002-3734-139X

Funding

Single-Molecule High-Confidence Detection of miRNA Cancer BiomarkersR61CA278445 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DHAKAL, SOMA · 2023 to 2025
$616k
NCI NIH HHS R61 CA278445
6 · The paper itself

Abstract

Biomarkers have gained tremendous attention in recent years, as they offer reliable detection of diseases such as cancers and other health conditions. However, with the recent realization that one biomarker can be associated with more than one disease (cross-talk), there is a significant shift toward simultaneous monitoring of more than one biomarker to increase the accuracy of diagnosis. Despite a sizable effort made over the last several years, multiplexing using the common techniques including surface-enhanced Raman spectroscopy (SERS), microarrays, RT-qPCR, nanostring, fluorescence, and others requires target amplification, target labeling, or the use of additional probes/actuators, and hence, these requirements complicate the experiments and data analyses. Using single-molecule fluorescence resonance energy transfer (smFRET) and 4-way DNA junction strategy, we introduced a relatively simple platform for simultaneous detection of multiple nucleic acid biomarkers. While the traditional way of smFRET-multiplexing requires multiple excitation sources and multiple FRET pairs (donor-acceptor dyes), our approach requires only one set of excitation sources and one FRET pair. Specifically, we presented four sensors that provide nonoverlapping FRET traces upon target binding, thus offering a clear multiplexed detection. Further, the 4-way DNA strategy enables detection down to low femtomolar (×10

Indexed as

DNAFluorescence Resonance Energy TransferSingle Molecule ImagingBiomarkersFluorescent DyesHumansBiomarkersDNAFluorescent Dyes

Identifiers

PMID40847907
PMCPMC12403156

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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.