Evidence map›Paper›PMID 26005758›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2015

Heterogeneous Electrochemical Aptamer-Based Sensor Surfaces for Controlled Sensor Response.

Lauren R Schoukroun-Barnes, Ethan P Glaser, Ryan J White

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Accelerating Post-SELEX Aptamer Engineering Using Exonuclease Digestion.Journal of the American Chemical Society · 2021
    Article
  6. Article
  7. Electrochemical Studies of Cation Condensation-Induced Collapse of Surface-Bound DNA.Langmuir : the ACS journal of surfaces and colloids · 2019
    Article
  8. Article
  9. Aptamers for DNA Damage and Repair.International journal of molecular sciences · 2017
    Review
  10. Article
  11. Real-time measurement of small molecules directly in awake, ambulatory animals.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  12. Reagentless, Structure-Switching, Electrochemical Aptamer-Based Sensors.Annual review of analytical chemistry (Palo Alto, Calif.) · 2016
    Article
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

3 authors.

Lauren R Schoukroun-BarnesDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County (UMBC), 1000 Hilltop Circle, Baltimore, Maryland 21250, United States.
Ethan P GlaserDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County (UMBC), 1000 Hilltop Circle, Baltimore, Maryland 21250, United States.
Ryan J WhiteDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County (UMBC), 1000 Hilltop Circle, Baltimore, Maryland 21250, United States.

Funding

Direct, Real-Time Monitoring of Gliotransmitter ReleaseR21MH101692 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI WHITE, RYAN J. · 2014 to 2015
$407k
NIMH NIH HHS R21 MH101692NIMH NIH HHS R21MH101692
6 · The paper itself

Abstract

Structure-switching sensors utilize recognition elements that undergo a conformation change upon target binding that is converted into a quantitative signal. Electrochemical, aptamer-based sensors achieve detection of analytes through a conformation change in an electrode-bound, oligonucleotide aptamer by measuring changes in electron transfer efficiencies. The analytical performance of these sensors is related to the magnitude of the conformation change of the aptamer. The goal of the present work is to develop a general method to predictably tune the analytical performance (sensitivity and linear range) of electrochemical, aptamer-based sensors by utilizing a mixture of rationally designed aptamer sequences that are specific for the same target but with different affinities on the same electrode surface. To demonstrate control over sensor performance, we developed heterogeneous sensors for two representative small molecule targets (adenosine triphosphate and tobramycin). We demonstrate that mixtures of modified sequences can be used to tune the affinity, dynamic range, and sensitivity of the resulting sensors predicted by a bi-Langmuir-type isotherm.

Indexed as

Adenosine TriphosphateAptamers, NucleotideBiosensing TechniquesElectrochemical TechniquesElectrodesElectron TransportNucleic Acid ConformationSensitivity and SpecificityTobramycinAdenosine TriphosphateAptamers, NucleotideTobramycin

Identifiers

PMID26005758
PMCPMC5627764

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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.