Evidence map›Paper›PMID 30680988›Full record

ArticleAnalytical chemistry2019

Split Dapoxyl Aptamer for Sequence-Selective Analysis of Nucleic Acid Sequence Based Amplification Amplicons.

Nanami Kikuchi, Adam Reed, Yulia V Gerasimova, Dmitry M Kolpashchikov

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In one paragraph

Article in Analytical chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

15 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Aptamers isolated against mosquito-borne pathogens.World journal of microbiology & biotechnology · 2021
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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

4 authors at 1 institution in 1 country.

Nanami KikuchiChemistry Department , University of Central Florida , 4111 Libra Drive , Orlando , 32816 , Florida United States.
Adam ReedChemistry Department , University of Central Florida , 4111 Libra Drive , Orlando , 32816 , Florida United States.
Yulia V GerasimovaChemistry Department , University of Central Florida , 4111 Libra Drive , Orlando , 32816 , Florida United States.ORCID 0000-0001-8804-9770
Dmitry M KolpashchikovChemistry Department , University of Central Florida , 4111 Libra Drive , Orlando , 32816 , Florida United States.ORCID 0000-0002-8682-6553
University of Central Florida · US

Funding

Development of a method for visual detection of Mycobacterium tuberculosis complexR21AI123876 · NIAID · UNIVERSITY OF CENTRAL FLORIDA · PI GERASIMOVA, YULIA, ROHDE, KYLE H · 2017 to 2018
$383k
NIAID NIH HHS R21 AI123876
6 · The paper itself

Abstract

Hybridization probes have been used for the detection of single nucleotide variations (SNV) in DNA and RNA sequences in the mix-and-read formats. Among the most conventional are Taqman probes, which require expensive quantitative polymerase chain reaction (qPCR) instruments with melting capabilities. More affordable isothermal amplification format requires hybridization probes that can selectively detect SNVs isothermally. Here we designed a split DNA aptamer (SDA) hybridization probe based on a recently reported DNA sequence that binds a dapoxyl dye and increases its fluorescence ( Kato, T.; Shimada, I.; Kimura, R.; Hyuga, M., Light-up fluorophore-DNA aptamer pair for label-free turn-on aptamer sensors. Chem. Commun. 2016 , 52 , 4041 - 4044 ). SDA uses two DNA strands that have low affinity to the dapoxyl dye unless hybridized to abutting positions at a specific analyte and form a dye-binding site, which is accompanied by up to a 120-fold increase in fluorescence. SDA differentiates SNV in the  inhA gene of Mycobacterium tuberculosis at ambient temperatures and detects a conserved region of the Zika virus after isothermal nucleic acid sequence based amplification (NASBA) reaction. The approach reported here can be used for detection of isothermal amplification products in the mix-and-read format as an alternative to qPCR.

Indexed as

Aptamers, NucleotideBacterial ProteinsDNA, BacterialDNA ProbesDNA, ViralFluorescent DyesLimit of DetectionMycobacterium tuberculosisNucleic Acid Amplification TechniquesNucleic Acid HybridizationOxidoreductasesPoint MutationSpectrometry, FluorescenceSulfonesZika VirusAptamers, NucleotideBacterial ProteinsDNA, BacterialDNA ProbesDNA, ViralFluorescent DyesInhA protein, MycobacteriumOxidoreductasesSulfones

Identifiers

PMID30680988
PMCPMC7720896
OpenAlexW2911393380

What OpenQuestion holds

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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 OpenQuestion graph.