Evidence map›Paper›PMID 26325477›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2015

High-Throughput Universal DNA Curtain Arrays for Single-Molecule Fluorescence Imaging.

Ignacio F Gallardo, Praveenkumar Pasupathy, Maxwell Brown, Carol M Manhart, Dean P Neikirk, Eric Alani, Ilya J Finkelstein

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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
  2. Mechanism of Cas9 inhibition by AcrIIA11.Nucleic acids research · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Single Molecule Imaging of DNA-Protein Interactions Using DNA Curtains.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  11. Article
  12. Article
  13. Molecular basis of the dual role of the Mlh1-Mlh3 endonuclease in MMR and in meiotic crossover formation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Patterns (New York, N.Y.) · 2021
    Article
  15. Article
  16. Oriented Soft DNA Curtains for Single-Molecule Imaging.Langmuir : the ACS journal of surfaces and colloids · 2021
    Article
  17. Article
  18. DNA Manipulation and Single-Molecule Imaging.Molecules (Basel, Switzerland) · 2021
    Review
  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

7 authors.

Ignacio F Gallardo
Praveenkumar Pasupathy
Maxwell Brown
Carol M ManhartDepartment of Molecular Biology and Genetics, Cornell University , Ithaca, New York 14853, United States.
Dean P Neikirk
Eric AlaniDepartment of Molecular Biology and Genetics, Cornell University , Ithaca, New York 14853, United States.
Ilya J Finkelstein

Funding

Roles for Mismatch Repair Proteins in Maintaining Genome StabilityR01GM053085 · NIGMS · CORNELL UNIVERSITY ITHACA · PI ALANI, ERIC E. · 1995 to 2019
$7.3M
Mechanisms of chromatin remodeling and roadblock clearance by DNA motor proteinsR00GM097177 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI FINKELSTEIN, ILYA J · 2013 to 2015
$747k
Characterizing an Endonuclease Ensemble in Meiotic Crossing OverF32GM112435 · NIGMS · CORNELL UNIVERSITY · PI MANHART, CAROL M · 2014 to 2016
$164k
NIGMS NIH HHS F32 GM112435NIGMS NIH HHS GM53085NIGMS NIH HHS R00 GM097177NIGMS NIH HHS R01 GM053085
6 · The paper itself

Abstract

Single-molecule studies of protein-DNA interactions have shed critical insights into the molecular mechanisms of nearly every aspect of DNA metabolism. The development of DNA curtains-a method for organizing arrays of DNA molecules on a fluid lipid bilayer-has greatly facilitated these studies by increasing the number of reactions that can be observed in a single experiment. However, the utility of DNA curtains is limited by the challenges associated with depositing nanometer-scale lipid diffusion barriers onto quartz microscope slides. Here, we describe a UV lithography-based method for large-scale fabrication of chromium (Cr) features and organization of DNA molecules at these features for high-throughput single-molecule studies. We demonstrate this approach by assembling 792 independent DNA arrays (containing >900,000 DNA molecules) within a single microfluidic flowcell. As a first proof of principle, we track the diffusion of Mlh1-Mlh3-a heterodimeric complex that participates in DNA mismatch repair and meiotic recombination. To further highlight the utility of this approach, we demonstrate a two-lane flowcell that facilitates concurrent experiments on different DNA substrates. Our technique greatly reduces the challenges associated with assembling DNA curtains and paves the way for the rapid acquisition of large statistical data sets from individual single-molecule experiments.

Indexed as

Oligonucleotide Array Sequence AnalysisDNAMicroscopy, FluorescenceNanotechnologyDNA

Identifiers

PMID26325477
PMCPMC4624423

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Registered trials

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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.