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dc.contributor.authorNakamura, Hidekien
dc.contributor.authorRho, Elmeren
dc.contributor.authorLee, Christopher T.en
dc.contributor.authorItoh, Kieen
dc.contributor.authorDeng, Daqien
dc.contributor.authorWatanabe, Satoshien
dc.contributor.authorRazavi, Shivaen
dc.contributor.authorMatsubayashi, Hideaki T.en
dc.contributor.authorZhu, Cunchengen
dc.contributor.authorJung, Eleanoren
dc.contributor.authorRangamani, Padminien
dc.contributor.authorWatanabe, Shigekien
dc.contributor.authorInoue, Takanarien
dc.contributor.alternative中村, 秀樹ja
dc.contributor.alternative伊藤, 喜重ja
dc.contributor.alternative渡邉, 哲史ja
dc.contributor.alternative松林, 英明ja
dc.contributor.alternative渡辺, 重喜ja
dc.contributor.alternative井上, 尊生ja
dc.date.accessioned2023-11-01T01:09:37Z-
dc.date.available2023-11-01T01:09:37Z-
dc.date.issued2023-10-31-
dc.identifier.urihttp://hdl.handle.net/2433/285964-
dc.description細胞の中のものを「押す」方法を開発 --細胞内構造体の“かたち”と機能の関係を明らかに--. 京都大学プレスリリース. 2023-09-25.ja
dc.description.abstractForm and function are often interdependent throughout biology. Inside cells, mitochondria have particularly attracted attention since both their morphology and functionality are altered under pathophysiological conditions. However, directly assessing their causal relationship has been beyond reach due to the limitations of manipulating mitochondrial morphology in a physiologically relevant manner. By engineering a bacterial actin regulator, ActA, we developed tools termed “ActuAtor” that inducibly trigger actin polymerization at arbitrary subcellular locations. The ActuAtor-mediated actin polymerization drives striking deformation and/or movement of target organelles, including mitochondria, Golgi apparatus, and nucleus. Notably, ActuAtor operation also disperses non-membrane-bound entities such as stress granules. We then implemented ActuAtor in functional assays, uncovering the physically fragmented mitochondria being slightly more susceptible to degradation, while none of the organelle functions tested are morphology dependent. The modular and genetically encoded features of ActuAtor should enable its application in studies of the form-function interplay in various intracellular contexts.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2023 The Authors.en
dc.rightsThis is an open access article under the CC BY-NC-ND license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectmolecular actuatorsen
dc.subjectactin polymerizationen
dc.subjectphysical manipulationen
dc.subjectform-function interplayen
dc.subjectstress granulesen
dc.subjectmitochondriaen
dc.titleActuAtor, a Listeria-inspired molecular tool for physical manipulation of intracellular organizations through de novo actin polymerizationen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleCell Reportsen
dc.identifier.volume42-
dc.identifier.issue10-
dc.relation.doi10.1016/j.celrep.2023.113089-
dc.textversionpublisher-
dc.identifier.artnum113089-
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicine; Kyoto University Hakubi Center for Advanced Research; Kyoto University Graduate School of Engineering, Department of Synthetic Chemistry and Biological Chemistry, Katsura Int'tech Center, Graduate School of Engineering, Kyoto Universityen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Mechanical and Aerospace Engineering, University of California San Diegoen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Biomedical Engineering, Johns Hopkins University School of Medicineen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Mechanical and Aerospace Engineering, University of California San Diegoen
dc.addressDepartment of Mechanical and Aerospace Engineering, University of California San Diegoen
dc.addressDepartment of Mechanical and Aerospace Engineering, University of California San Diegoen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicineen
dc.addressDepartment of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicine; Department of Biomedical Engineering, Johns Hopkins University School of Medicineen
dc.identifier.pmid37734382-
dc.relation.urlhttps://www.t.kyoto-u.ac.jp/ja/research/topics/20230921-
dcterms.accessRightsopen access-
datacite.awardNumber21H00397-
datacite.awardNumber22H05087-
datacite.awardNumber22H05091-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-21H00397/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-ORGANIZER-22H05087/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-22H05091/-
dc.identifier.pissn2639-1856-
dc.identifier.eissn2211-1247-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle細胞内タンパク質分子集団の自己組織化による結晶マイクロマシンの発動ja
jpcoar.awardTitle動的溶液科学の推進ja
jpcoar.awardTitle合成生物学技術による生きた細胞内での自己凝縮過程評価系の構築ja
出現コレクション:学術雑誌掲載論文等

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