Evidence map›Paper›PMID 29361056›Full record

ArticleNucleic acids research2018

In vitro isolation of small-molecule-binding aptamers with intrinsic dye-displacement functionality.

Haixiang Yu, Weijuan Yang, Obtin Alkhamis, Juan Canoura, Kyung-Ae Yang, Yi Xiao

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Rationally Designed DNA-Based Scaffolds and Switching Probes for Protein Sensing.Advances in biochemical engineering/biotechnology · 2024
    Review
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  18. Updates on Aptamer Research.International journal of molecular sciences · 2019
    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 at 2 institutions in 1 country.

Haixiang YuDepartment of Chemistry and Biochemistry, Florida International University, 11200 SW Eighth Street, Miami, FL 33199, USA.
Weijuan YangDepartment of Chemistry and Biochemistry, Florida International University, 11200 SW Eighth Street, Miami, FL 33199, USA.
Obtin AlkhamisDepartment of Chemistry and Biochemistry, Florida International University, 11200 SW Eighth Street, Miami, FL 33199, USA.
Juan CanouraDepartment of Chemistry and Biochemistry, Florida International University, 11200 SW Eighth Street, Miami, FL 33199, USA.
Kyung-Ae YangDivision of Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA.
Yi XiaoDepartment of Chemistry and Biochemistry, Florida International University, 11200 SW Eighth Street, Miami, FL 33199, USA.
Florida International University · USColumbia University · US

Funding

Aptamer-Based, Exonuclease-Amplified, Colorimetric, Onsite Screening of Methylenedioxypyrovalerone (MDPV) and Mephedrone in Oral FluidR15DA036821 · NIDA · FLORIDA INTERNATIONAL UNIVERSITY · PI XIAO, YI · 2015 to 2015
$337k
NIDA NIH HHS R15 DA036821
6 · The paper itself

Abstract

Aptamer-based sensors offer a powerful tool for molecular detection, but the practical implementation of these biosensors is hindered by costly and laborious sequence engineering and chemical modification procedures. We report a simple strategy for directly isolating signal-reporting aptamers in vitro through systematic evolution of ligands by exponential enrichment (SELEX) that transduce binding events into a detectable change of absorbance via target-induced displacement of a small-molecule dye. We first demonstrate that diethylthiatricarbocyanine (Cy7) can stack into DNA three-way junctions (TWJs) in a sequence-independent fashion, greatly altering the dye's absorbance spectrum. We then design a TWJ-containing structured library and isolate an aptamer against 3,4-methylenedioxypyrovalerone (MDPV), a synthetic cathinone that is an emerging drug of abuse. This aptamer intrinsically binds Cy7 within its TWJ domain, but MDPV efficiently displaces the dye, resulting in a change in absorbance within seconds. This assay is label-free, and detects nanomolar concentrations of MDPV. It also recognizes other synthetic cathinones, offering the potential to detect newly-emerging designer drugs, but does not detect structurally-similar non-cathinone compounds or common cutting agents. Moreover, we demonstrate that the Cy7-displacement colorimetric assay is more sensitive than a conventional strand-displacement fluorescence assay. We believe our strategy offers an effective generalized approach for the development of sensitive dye-displacement colorimetric assays for other small-molecule targets.

Indexed as

Aptamers, NucleotideBase SequenceBenzodioxolesBiosensing TechniquesCarbocyaninesColorimetryColoring AgentsDNAMolecular StructurePyrrolidinesSELEX Aptamer TechniqueSynthetic CathinoneAptamers, NucleotideBenzodioxolesCarbocyaninesColoring AgentsDNAindotricarbocyaninePyrrolidinesSynthetic Cathinone

Identifiers

PMID29361056
PMCPMC5934630
OpenAlexW2791188661

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.