Evidence map›Paper›PMID 24328347›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2013

DNA-modified electrodes fabricated using copper-free click chemistry for enhanced protein detection.

Ariel L Furst, Michael G Hill, Jacqueline K Barton

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-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

13 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. On-Surface Azide-Alkyne Cycloaddition Reaction: Does It Click with Ruthenium Catalysts?Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Electrical Probes of DNA-Binding Proteins.Methods in enzymology · 2017
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Label-free electrochemical detection of human methyltransferase from tumors.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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 at 2 institutions in 1 country.

Ariel L FurstDepartment of Chemistry and Chemical Engineering, California Institute of Technology , Pasadena, California 91125, United States.
Michael G Hill
Jacqueline K Barton
California Institute of Technology · USOccidental College · US

Funding

ELECTROCHEMICAL DNA-BASED SENSORSR01GM061077 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BARTON, JACQUELINE K · 2000 to 2017
$5.2M
NIGMS NIH HHS GM61077NIGMS NIH HHS R01 GM061077
6 · The paper itself

Abstract

A method of DNA monolayer formation has been developed using copper-free click chemistry that yields enhanced surface homogeneity and enables variation in the amount of DNA assembled; extremely low-density DNA monolayers, with as little as 5% of the monolayer being DNA, have been formed. These DNA-modified electrodes (DMEs) were characterized visually, with AFM, and electrochemically, and were found to facilitate DNA-mediated reduction of a distally bound redox probe. These low-density monolayers were found to be more homogeneous than traditional thiol-modified DNA monolayers, with greater helix accessibility through an increased surface area-to-volume ratio. Protein binding efficiency of the transcriptional activator TATA-binding protein (TBP) was also investigated on these surfaces and compared to that on DNA monolayers formed with standard thiol-modified DNA. Our low-density monolayers were found to be extremely sensitive to TBP binding, with a signal decrease in excess of 75% for 150 nM protein. This protein was detectable at 4 nM, on the order of its dissociation constant, with our low-density monolayers. The improved DNA helix accessibility and sensitivity of our low-density DNA monolayers to TBP binding reflects the general utility of this method of DNA monolayer formation for DNA-based electrochemical sensor development.

Indexed as

Click ChemistryElectrodesChemistry Techniques, AnalyticalCopperDNAMicroscopy, Atomic ForceModels, MolecularMolecular StructureProteinsTATA-Box Binding ProteinCopperDNAProteinsTATA-Box Binding Protein

Identifiers

PMID24328347
PMCPMC3947573
OpenAlexW2020731023

What OpenQuestion holds

Textmetadata
LicenceTDM
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.