Evidence map›Paper›PMID 23550815›Full record

ArticleACS nano2013

Designing a polycationic probe for simultaneous enrichment and detection of microRNAs in a nanopore.

Kai Tian, Zhaojian He, Yong Wang, Shi-Jie Chen, Li-Qun Gu

Abstract read
In one paragraph

Article in ACS nano, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Biological Nanopores: Engineering on Demand.Life (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. PNA-Based MicroRNA Detection Methodologies.Molecules (Basel, Switzerland) · 2020
    Review
  13. Article
  14. Review
  15. Review
  16. Label-Free Detection of DNA Mutations by Nanopore Analysis.ACS applied materials & interfaces · 2018
    Article
  17. Membrane protein-based biosensors.Journal of the Royal Society, Interface · 2018
    Review
  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.

Kai TianDepartment of Biological Engineering and Dalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri 65211, United States.
Zhaojian He
Yong Wang
Shi-Jie Chen
Li-Qun Gu

Funding

Programmable Multi-Target Detection Using an Aptamer-Integrated NanoporeR01GM079613 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI GU, LI-QUN (ANDREW) · 2007 to 2011
$1.3M
Nanopore single-molecule dielectrophoresis and biomedical detectionR01GM114204 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI GU, LI-QUN (ANDREW) · 2015 to 2017
$887k
A Phase 1 Study/DNA-Based Vaccine vs Prostatic Acid PaseK23RR016489 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI MCNEEL, DOUGLAS G · 2002 to 2006
$709k
NCRR NIH HHS C06-RR-016489-01NCRR NIH HHS K23 RR016489NIGMS NIH HHS GM079613NIGMS NIH HHS R01 GM079613NIGMS NIH HHS R01 GM114204
6 · The paper itself

Abstract

The nanopore sensor can detect cancer-derived nucleic acid biomarkers such as microRNAs (miRNAs), providing a noninvasive tool potentially useful in medical diagnostics. However, the nanopore-based detection of these biomarkers remains confounded by the presence of numerous other nucleic acid species found in biofluid extracts. Their nonspecific interactions with the nanopore inevitably contaminate the target signals, reducing the detection accuracy. Here we report a novel method that utilizes a polycationic peptide-PNA probe as the carrier for selective miRNA detection in the nucleic acid mixture. The cationic probe hybridized with microRNA forms a dipole complex, which can be captured by the pore using a voltage polarity that is opposite the polarity used to capture negatively charged nucleic acids. As a result, nontarget species are driven away from the pore opening, and the target miRNA can be detected accurately without interference. In addition, we demonstrate that the PNA probe enables accurate discrimination of miRNAs with single-nucleotide difference. This highly sensitive and selective nanodielectrophoresis approach can be applied to the detection of clinically relevant nucleic acid fragments in complex samples.

Indexed as

Drug DesignNanoporesBase SequenceElectricityMicroRNAsModels, MolecularMolecular ProbesNucleic Acid ConformationPeptide Nucleic AcidsPeptidesTime FactorsMicroRNAsMolecular ProbesPeptide Nucleic AcidsPeptides

Identifiers

PMID23550815
PMCPMC3675772

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.