Evidence map›Paper›PMID 25567007›Full record

ArticleScientific reports2015

Control of microtubule trajectory within an electric field by altering surface charge density.

Naoto Isozaki, Suguru Ando, Tasuku Nakahara, Hirofumi Shintaku, Hidetoshi Kotera, Edgar Meyhöfer, Ryuji Yokokawa

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  8. Review
  9. An Overview of Sub-Cellular Mechanisms Involved in the Action of TTFields.International journal of environmental research and public health · 2016
    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.

Naoto IsozakiDepartment of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Suguru AndoDepartment of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Tasuku NakaharaDepartment of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Hirofumi ShintakuDepartment of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Hidetoshi KoteraDepartment of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Edgar MeyhöferDepartment of Mechanical and Biomedical Engineering, University of Michigan, Ann Arbor 48109, Michigan, USA.
Ryuji Yokokawa1] Department of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan [2] Precursory Research for Embryonic Science and Technology from the Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of challenges for using microtubules (MTs) driven by kinesin motors in microfluidic environments is to control their direction of movement. Although applying physical biases to rectify MTs is prevalent, it has not been established as a design methodology in conjunction with microfluidic devices. In the future, the methodology is expected to achieve functional motor-driven nanosystems. Here, we propose a method to guide kinesin-propelled MTs in multiple directions under an electric field by designing a charged surface of MT minus ends labeled with dsDNA via a streptavidin-biotin interaction. MTs labeled with 20-bp or 50-bp dsDNA molecules showed significantly different trajectories according to the DNA length, which were in good agreement with values predicted from electrophoretic mobilities measured for their minus ends. Since the effective charge of labeled DNA molecules was equal to that of freely dispersed DNA molecules in a buffer solution, MT trajectory could be estimated by selecting labeling molecules with known charges. Moreover, the estimated trajectory enables to define geometrical sizes of a microfluidic device. This rational molecular design and prediction methodology allows MTs to be guided in multiple directions, demonstrating the feasibility of using molecular sorters driven by motor proteins.

Indexed as

ElectricityBiotinDNAFluorobenzenesKinesinsMicrofluidic Analytical TechniquesMicroscopy, FluorescenceMicrotubulesStreptavidinAlexaFluor 488 carboxylic acid tetrafluorophenyl esterBiotinDNAFluorobenzenesKinesinsStreptavidin

Identifiers

PMID25567007
PMCPMC4286733

What OpenQuestion holds

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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.