Evidence map›Paper›PMID 29569930›Full record

ArticleNano letters2018

Double Barrel Nanopores as a New Tool for Controlling Single-Molecule Transport.

Paolo Cadinu, Giulia Campolo, Sergii Pud, Wayne Yang, Joshua B Edel, Cees Dekker, Aleksandar P Ivanov

Abstract read
In one paragraph

Article in Nano letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. A subcellular cookie cutter for spatial genomics in human tissue.Analytical and bioanalytical chemistry · 2022
    Article
  12. Article
  13. Review
  14. Real-Time and Label-Free Measurement of Deubiquitinase Activity with a MspA Nanopore.Chembiochem : a European journal of chemical biology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors.

Paolo CadinuDepartment of Chemistry , Imperial College London , Exhibition Road , SW7 2AZ London , United Kingdom.
Giulia CampoloDepartment of Chemistry , Imperial College London , Exhibition Road , SW7 2AZ London , United Kingdom.
Sergii PudDepartment of Bionanoscience, Kavli Institute of Nanoscience Delft , Delft University of Technology , Van der Maasweg 9 , 2629 HZ Delft , The Netherlands.ORCID 0000-0002-1393-9135
Wayne YangDepartment of Bionanoscience, Kavli Institute of Nanoscience Delft , Delft University of Technology , Van der Maasweg 9 , 2629 HZ Delft , The Netherlands.
Joshua B EdelDepartment of Chemistry , Imperial College London , Exhibition Road , SW7 2AZ London , United Kingdom.ORCID 0000-0001-5870-8659
Cees DekkerDepartment of Bionanoscience, Kavli Institute of Nanoscience Delft , Delft University of Technology , Van der Maasweg 9 , 2629 HZ Delft , The Netherlands.ORCID 0000-0001-6273-071X
Aleksandar P IvanovDepartment of Chemistry , Imperial College London , Exhibition Road , SW7 2AZ London , United Kingdom.ORCID 0000-0003-1419-1381

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to control the motion of single biomolecules is key to improving a wide range of biophysical and diagnostic applications. Solid-state nanopores are a promising tool capable of solving this task. However, molecular control and the possibility of slow readouts of long polymer molecules are still limited due to fast analyte transport and low signal-to-noise ratios. Here, we report on a novel approach of actively controlling analyte transport by using a double-nanopore architecture where two nanopores are separated by only a ∼ 20 nm gap. The nanopores can be addressed individually, allowing for two unique modes of operation: (i) pore-to-pore transfer, which can be controlled at near 100% efficiency, and (ii) DNA molecules bridging between the two nanopores, which enables detection with an enhanced temporal resolution (e.g., an increase of more than 2 orders of magnitude in the dwell time) without compromising the signal quality. The simplicity of fabrication and operation of the double-barrel architecture opens a wide range of applications for high-resolution readout of biological molecules.

Indexed as

MotionDNAElectrodesNanoporesNanotechnologyDNAbiophysicsdouble nanopore architectureSingle-molecule sensing

Identifiers

PMID29569930
PMCPMC5969804

What OpenQuestion holds

Textmetadata
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.