Evidence map›Paper›PMID 27256891›Full record

ArticleIET nanobiotechnology2016

Characterisation of optically driven microstructures for manipulating single DNA molecules under a fluorescence microscope.

Kyohei Terao, Chihiro Masuda, Ryo Inukai, Murat Gel, Hidehiro Oana, Masao Washizu, Takaaki Suzuki, Hidekuni Takao, Fusao Shimokawa, Fumikazu Oohira

Abstract read
In one paragraph

Article in IET nanobiotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Driving Forces for Single DNA Stretching Assessed byChemical & biomedical imaging · 2023
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. 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

10 authors.

Kyohei TeraoJST-PREST, Saitama 332-0012, Japan. terao@eng.kagawa-u.ac.jp.
Chihiro MasudaDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.
Ryo InukaiDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.
Murat GelCSIRO, Material Science and Engineering, Clayton, VIC 3030, Australia.
Hidehiro OanaDepartment of Mechanical Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
Masao WashizuDepartment of Mechanical Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
Takaaki SuzukiDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.
Hidekuni TakaoDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.
Fusao ShimokawaDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.
Fumikazu OohiraDepartment of Intelligent Mechanical Systems Engineering, Kagawa University, Takamatsu 761-0396, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optical tweezers are powerful tools for manipulating single DNA molecules using fluorescence microscopy, particularly in nanotechnology-based DNA analysis. We previously proposed a manipulation technique using microstructures driven by optical tweezers that allows the handling of single giant DNA molecules of millimetre length that cannot be manipulated by conventional techniques. To further develop this technique, the authors characterised the microstructures quantitatively from the view point of fabrication and efficiency of DNA manipulation under a fluorescence microscope. The success rate and precision of the fabrications were evaluated. The results indicate that the microstructures are obtained in an aqueous solution with a precision ∼50 nm at concentrations in the order of 10(6) particles/ml. The visibility of these microstructures under a fluorescence microscope was also characterised, along with the elucidation of the fabrication parameters needed to fine tune visibility. Manipulating yeast chromosomal DNA molecules with the microstructures illustrated the relationship between the efficiency of manipulation and the geometrical shape of the microstructure. This report provides the guidelines for designing microstructures used in single DNA molecule analysis based on on-site DNA manipulation, and is expected to broaden the applications of this technique in the future.

Indexed as

Optical TweezersDNAEquipment DesignMicroscopy, FluorescenceMicrotechnologyDNA

Identifiers

PMID27256891
PMCPMC8676171

What OpenQuestion holds

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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.