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タイトル: Live-cell Imaging with Genetically Encoded Protein Kinase Activity Reporters
著者: Maryu, Gembu
Miura, Haruko
Uda, Youichi
Komatsubara, Akira T.
Matsuda, Michiyuki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-5876-9969 (unconfirmed)
Aoki, Kazuhiro  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-7263-1555 (unconfirmed)
著者名の別形: 真流, 玄武
三浦, 晴子
松田, 道行
青木, 一洋
キーワード: kinase
FRET
phosphorylation
KTR
発行日: 2018
出版者: Japan Society for Cell Biology
誌名: Cell structure and function
巻: 43
号: 1
開始ページ: 61
終了ページ: 74
抄録: Protein kinases play pivotal roles in intracellular signal transduction, and dysregulation of kinases leads to pathological results such as malignant tumors. Kinase activity has hitherto been measured by biochemical methods such as in vitro phosphorylation assay and western blotting. However, these methods are less useful to explore spatial and temporal changes in kinase activity and its cell-to-cell variation. Recent advances in fluorescent proteins and live-cell imaging techniques enable us to visualize kinase activity in living cells with high spatial and temporal resolutions. Several genetically encoded kinase activity reporters, which are based on the modes of action of kinase activation and phosphorylation, are currently available. These reporters are classified into single-fluorophore kinase activity reporters and Förster (or fluorescence) resonance energy transfer (FRET)-based kinase activity reporters. Here, we introduce the principles of genetically encoded kinase activity reporters, and discuss the advantages and disadvantages of these reporters.
著作権等: ©2018 The Author(s). This is an open access article distributed under the terms of the Creative Commons BY (Attribution) License (https://creativecommons.org/licenses/by/4.0/legalcode), which permits the unrestricted distribution, reproduction and use of the article provided the original source and authors are credited.
URI: http://hdl.handle.net/2433/232993
DOI(出版社版): 10.1247/csf.18003
PubMed ID: 29553079
出現コレクション:学術雑誌掲載論文等

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