Evidence map›Paper›PMID 24683272›Full record

ArticleMacromolecules2013

Presentation of large DNA molecules for analysis as nanoconfined dumbbells.

Kristy L Kounovsky-Shafer, Juan P Hernández-Ortiz, Kyubong Jo, Theo Odijk, Juan J de Pablo, David C Schwartz

Abstract read
In one paragraph

Article in Macromolecules, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Single-molecule DNA-mapping and whole-genome sequencing of individual cells.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Measuring the wall depletion length of nanoconfined DNA.The Journal of chemical physics · 2018
    Article
  9. Article
  10. Electrostatic confinement and manipulation of DNA molecules for genome analysis.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Article
  12. Article
  13. Maligner: a fast ordered restriction map aligner.Bioinformatics (Oxford, England) · 2016
    Article
  14. Identifying DNA methylation in a nanochannel.Science and technology of advanced materials · 2016
    Article
  15. Review
  16. Article
  17. Article
  18. Hydrodynamics of DNA confined in nanoslits and nanochannels.The European physical journal. Special topics · 2014
    Article
  19. 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

6 authors.

Kristy L Kounovsky-ShaferLaboratory for Molecular and Computational Genomics, Department of Chemistry, Laboratory of Genetics, and UW-Biotechnology Center, University of Wisconsin-Madison, Madison, WI 53706-1580.
Juan P Hernández-OrtizDepartamento de Materiales, Universidad Nacional de Colombia, Sede Medellín, Kra 80 # 65-223.
Kyubong JoBloque M3-050, Medellín Colombia, Department of Chemistry, Sogang University, Seoul, Korea.
Theo OdijkLorentz Institute for Theoretical Physics, University of Leiden, The Netherlands.
Juan J de PabloInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637.
David C SchwartzLaboratory for Molecular and Computational Genomics, Department of Chemistry, Laboratory of Genetics, and UW-Biotechnology Center, University of Wisconsin-Madison, Madison, WI 53706-1580.

Funding

NEW PHYSICAL METHODOLOGIES FOR GENOMIC ANALYSISR01HG000225 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI SCHWARTZ, DAVID C. · 1991 to 2014
$5.2M
NHGRI NIH HHS R01 HG000225
6 · The paper itself

Abstract

The analysis of very large DNA molecules intrinsically supports long-range, phased sequence information, but requires new approaches for their effective presentation as part of any genome analysis platform. Using a multi-pronged approach that marshaled molecular confinement, ionic environment, and DNA elastic properties-but tressed by molecular simulations-we have developed an efficient and scalable approach for presentation of large DNA molecules within nanoscale slits. Our approach relies on the formation of DNA dumbbells, where large segments of the molecules remain outside the nanoslits used to confine them. The low ionic environment, synergizing other features of our approach, enables DNA molecules to adopt a fully stretched conformation, comparable to the contour length, thereby facilitating analysis by optical microscopy. Accordingly, a molecular model is proposed to describe the conformation and dynamics of the DNA molecules within the nanoslits; a Langevin description of the polymer dynamics is adopted in which hydrodynamic effects are included through a Green's function formalism. Our simulations reveal that a delicate balance between electrostatic and hydrodynamic interactions is responsible for the observed molecular conformations. We demonstrate and further confirm that the "Odijk regime" does indeed start when the confinement dimensions size are of the same order of magnitude as the persistence length of the molecule. We also summarize current theories concerning dumbbell dynamics.

Identifiers

PMID24683272
PMCPMC3964590

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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.