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dc.contributor.authorKeya, Jakia Jannaten
dc.contributor.authorInoue, Daisukeen
dc.contributor.authorSuzuki, Yukien
dc.contributor.authorKozai, Toshiyaen
dc.contributor.authorIshikuro, Daikien
dc.contributor.authorKodera, Noriyukien
dc.contributor.authorUchihashi, Takayukien
dc.contributor.authorKabir, Arif Md. Rashedulen
dc.contributor.authorEndo, Masayukien
dc.contributor.authorSada, Kazukien
dc.contributor.authorKakugo, Akiraen
dc.contributor.alternative遠藤, 政幸ja
dc.date.accessioned2017-12-01T05:21:14Z-
dc.date.available2017-12-01T05:21:14Z-
dc.date.issued2017-07-21-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/228139-
dc.description.abstractIn vitro gliding assay of microtubules (MTs) on kinesins has provided us with valuable biophysical and chemo-mechanical insights of this biomolecular motor system. Visualization of MTs in an in vitro gliding assay has been mainly dependent on optical microscopes, limited resolution of which often render them insufficient sources of desired information. In this work, using high speed atomic force microscopy (HS-AFM), which allows imaging with higher resolution, we monitored MTs and protofilaments (PFs) of tubulins while gliding on kinesins. Moreover, under the HS-AFM, we also observed splitting of gliding MTs into single PFs at their leading ends. The split single PFs interacted with kinesins and exhibited translational motion, but with a slower velocity than the MTs. Our investigation at the molecular level, using the HS-AFM, would provide new insights to the mechanics of MTs in dynamic systems and their interaction with motor proteins.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2017.en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.subjectMotor protein functionen
dc.subjectPolymersen
dc.titleHigh-Resolution Imaging of a Single Gliding Protofilament of Tubulins by HS-AFMen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific Reportsen
dc.identifier.volume7-
dc.relation.doi10.1038/s41598-017-06249-1-
dc.textversionpublisher-
dc.identifier.artnum6166-
dc.identifier.pmid28733669-
dcterms.accessRightsopen access-
dc.identifier.eissn2045-2322-
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