Evidence map›Paper›PMID 22452720›Full record

ArticleJournal of the American Chemical Society2012

Quantitation of femtomolar protein levels via direct readout with the electrochemical proximity assay.

Jiaming Hu, Tanyu Wang, Joonyul Kim, Curtis Shannon, Christopher J Easley

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 172 citations in OpenAlex.

  1. Review
  2. Modular DNA origami-based electrochemical detection of DNA and proteins.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Review
  5. Rationally Designed DNA-Based Scaffolds and Switching Probes for Protein Sensing.Advances in biochemical engineering/biotechnology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Device integration of electrochemical biosensors.Nature reviews bioengineering · 2023
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Electrospun Nanofibers for Cancer Therapy.Advances in experimental medicine and biology · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Jiaming HuDepartment of Chemistry and Biochemistry, Auburn University, Auburn, Alabama 36849, USA.
Tanyu Wang
Joonyul Kim
Curtis Shannon
Christopher J Easley
Auburn University · US

Funding

Unmasking mechanisms of lipolytic dynamics in adipose tissue using high-resolution microfluidic samplingR01DK093810 · NIDDK · AUBURN UNIVERSITY AT AUBURN · PI EASLEY, CHRISTOPHER J · 2012 to 2023
$3.8M
NIDDK NIH HHS R01 DK093810
6 · The paper itself

Abstract

We have developed a separation-free, electrochemical assay format with direct readout that is amenable to highly sensitive and selective quantitation of a wide variety of target proteins. Our first generation of the electrochemical proximity assay (ECPA) is composed of two thrombin aptamers which form a cooperative complex only in the presence of target molecules, moving a methylene blue (MB)-conjugated oligonucleotide close to a gold electrode. Without washing steps, electrical current is increased in proportion to the concentration of a specific target protein. By employing a DNA-based experimental model with the aptamer system, we show that addition of a short DNA competitor can reduce background current of the MB peak to baseline levels. As such, the detection limit of aptamer-based ECPA for human thrombin was 50 pM via direct readout. The dual-probe nature of ECPA gave high selectivity and 93% recovery of signal from 2.5 nM thrombin in 2% bovine serum albumin (BSA). To greatly improve the flexibility of ECPA, we then proved the system functional with antibody-oligonucleotide conjugates as probes; the insulin detection limit was 128 fM with a dynamic range of over 4 orders of magnitude in concentration, again with high assay selectivity. ECPA thus allows separation-free, highly sensitive, and highly selective protein detection with a direct electrochemical readout. This method is extremely flexible, capable of detecting a wide variety of protein targets, and is amenable to point-of-care protein measurement, since any target with two aptamers or antibodies could be assayed via direct electrochemical readout.

Indexed as

Electrochemical TechniquesAnimalsAptamers, NucleotideCattleDNAElectrodesGoldHumansSerum Albumin, BovineThrombinAptamers, NucleotideDNAGoldSerum Albumin, BovineThrombin

Identifiers

PMID22452720
PMCPMC4992576
OpenAlexW2328559027

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.