J
Junichiro Yajima
Researcher at University of Tokyo
Publications - 30
Citations - 814
Junichiro Yajima is an academic researcher from University of Tokyo. The author has contributed to research in topics: Kinesin & Microtubule. The author has an hindex of 12, co-authored 26 publications receiving 724 citations. Previous affiliations of Junichiro Yajima include Florida State University College of Arts and Sciences & Gakushuin University.
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Journal ArticleDOI
Kinesin–microtubule binding depends on both nucleotide state and loading direction
Sotaro Uemura,Kenji Kawaguchi,Junichiro Yajima,Masaki Edamatsu,Yoko Y. Toyoshima,Shin'ichi Ishiwata +5 more
TL;DR: It is found that both a weak and a strong binding state exist in each head of kinesin corresponding to a small and a large unbinding force, respectively; that is, weak for the ADP state and strong for the nucleotide-free and adenosine 5′-[β,γ-imido]triphosphate states.
Journal ArticleDOI
A torque component present in mitotic kinesin Eg5 revealed by three-dimensional tracking.
TL;DR: Three-dimensional tracking of a quantum dot attached to the microtubule in a motility assay is used to directly visualize the corkscrew motion of a sliding microtubules, confirming that two-headed Eg5 is much less processive than two- headed kinesin-1.
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A Novel Action of Terpendole E on the Motor Activity of Mitotic Kinesin Eg5
Junko Nakazawa,Junichiro Yajima,Takeo Usui,Masashi Ueki,Akira Takatsuki,Masaya Imoto,Yoko Y. Toyoshima,Hiroyuki Osada +7 more
TL;DR: It is demonstrated that terpendole E (TerE) is a novel Eg5 inhibitor isolated from a fungal strain that inhibited both motor and microtubule-stimulated ATPase activities of human Eg5, but did not affect conventional kinesin from either Drosophila or bovine brain.
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Direct Long-Term Observation of Kinesin Processivity at Low Load
TL;DR: This work fused kinesin to gelsolin, creating a construct that severs and caps rhodamine-phalloidin actin filaments, setting exactly one kinesIn molecule on one end of each fluorescent actin filament, and uses the new system to show that, contrary to a recent report, kines in run length at low load is independent of ATP concentration in the muM to mM range of ATP concentrations.
Journal ArticleDOI
The human chromokinesin Kid is a plus end-directed microtubule-based motor.
Junichiro Yajima,Masaki Edamatsu,Junko Watai-Nishii,Noriko Tokai-Nishizumi,Tadashi Yamamoto,Yoko Y. Toyoshima +5 more
TL;DR: The initial characterization of Kid as a microtubule‐based motor using optical trapping microscopy shows results consistent with Kid having a role in chromosome congression in vivo, where it would be responsible for the polar ejection forces acting on the chromosome arms.