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Purification and characterisation of the fission yeast Ndc80 complex

https://hiroshima.repo.nii.ac.jp/records/2008706
https://hiroshima.repo.nii.ac.jp/records/2008706
b02495d2-c4f3-4ace-b7aa-b83a8fa2b4d4
名前 / ファイル ライセンス アクション
ProteinExprPurif_135_61.pdf ProteinExprPurif_135_61.pdf (2.3 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Purification and characterisation of the fission yeast Ndc80 complex
言語 en
作成者 Matsuo, Yuzy

× Matsuo, Yuzy

en Matsuo, Yuzy

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Maurer, Sebastian P.

× Maurer, Sebastian P.

en Maurer, Sebastian P.

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Surrey, Thomas

× Surrey, Thomas

en Surrey, Thomas

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Toda, Takashi

× Toda, Takashi

en Toda, Takashi

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 © 2017 The Francis Crick Institute. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
主題
主題Scheme Other
主題 Dis1
主題
主題Scheme Other
主題 Fission yeast
主題
主題Scheme Other
主題 Kinetochore
主題
主題Scheme Other
主題 Ndc80 complex
主題
主題Scheme Other
主題 Microtubule
主題
主題Scheme Other
主題 TIRF microscopy
内容記述
内容記述 The Ndc80 complex is a conserved outer kinetochore protein complex consisting of Ndc80 (Hec1), Nuf2, Spc24 and Spc25. This complex comprises a major, if not the sole, platform with which the plus ends of the spindle microtubules directly interact. In fission yeast, several studies indicate that multiple microtubule-associated proteins including the Dis1/chTOG microtubule polymerase and the Mal3/EB1 microtubule plus-end tracking protein directly or indirectly bind Ndc80, thereby ensuring stable kinetochore-microtubule attachment. However, the purification of the Ndc80 complex from this yeast has not been achieved, which hampers the in-depth investigation as to how the outer kinetochore attaches to the plus end of the spindle microtubule. Here we report the two-step purification of the fission yeast Ndc80 holo complex from bacteria. First, we purified separately two sub-complexes consisting of Ndc80-Nuf2 and Spc24-Spc25. Then, these two sub-complexes were mixed and applied to size-exclusion chromatography. The reconstituted Ndc80 holo complex is composed of four subunits with equal stoichiometry. The complex possesses microtubule-binding activity, and Total Internal Reflection Fluorescence (TIRF)-microscopy assays show that the complex binds the microtubule lattice. Interestingly, unlike the human complex, the fission yeast complex does not track depolymerising microtubule ends. Further analysis shows that under physiological ionic conditions, the Ndc80 holo complex does not detectably bind Dis1, but instead it interacts with Mal3/EB1, by which the Ndc80 complex tracks the growing microtubule plus end. This result substantiates the notion that the Ndc80 complex plays a crucial role in establishment of the dynamic kinetochore-microtubule interface by cooperating with chTOG and EB1.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported by Cancer Research UK and the Francis Crick Institute which receives its core funding from Cancer Research UK (FC001163, FC001184), the UK Medical Research Council (FC001163, FC001184), and the Wellcome Trust (FC001163, FC001184) (T.S., T.T.), the Japan Society for the Promotion of Science KAKENHI Scientific Research (A) (16H02503) (T.T.), Challenging Exploratory Research (16K14672) (T.T.), the Naito Foundation (T.T.), the Uehara Memorial Foundation (T.T) and a Marie Curie fellowship (PIEF-GA-2009-253043) (S.P.M.).
出版者
出版者 Elsevier
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.1016/j.pep.2017.05.002
関連情報
識別子タイプ PMID
関連識別子 28502666
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.pep.2017.05.002
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1046-5928
開始ページ
開始ページ 61
書誌情報 Protein Expression and Purification
Protein Expression and Purification

巻 135, p. 61-69, 発行日 2017-07
旧ID 48782
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