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タイトル: Live-cell imaging of endogenous mRNAs with a small molecule.
著者: Sato, Shin-ichi
Watanabe, Mizuki
Katsuda, Yousuke
Murata, Asako
Wang, Dan Ohtan
Uesugi, Motonari  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-8515-445X (unconfirmed)
著者名の別形: 佐藤, 慎一
キーワード: fluorescence
live-cell imaging
RNA
RNA dynamics
small molecules
発行日: 23-Dec-2014
出版者: wiley
誌名: Angewandte Chemie
巻: 54
号: 6
開始ページ: 1855
終了ページ: 1858
抄録: Determination of subcellular localization and dynamics of mRNA is increasingly important to understanding gene expression. A new convenient and versatile method is reported that permits spatiotemporal imaging of specific non-engineered RNAs in living cells. The method uses transfection of a plasmid encoding a gene-specific RNA aptamer, combined with a cell-permeable synthetic small molecule, the fluorescence of which is restored only when the RNA aptamer hybridizes with its cognitive mRNA. The method was validated by live-cell imaging of the endogenous mRNA of β-actin. Application of the technology to mRNAs of a total of 84 human cytoskeletal genes allowed us to observe cellular dynamics of several endogenous mRNAs including arfaptin-2, cortactin, and cytoplasmic FMR1-interacting protein 2. The RNA-imaging technology and its further optimization might permit live-cell imaging of any RNA molecules.
著作権等: This is the peer reviewed version of the following article: Sato, S.-i., Watanabe, M., Katsuda, Y., Murata, A., Wang, D. O. and Uesugi, M. (2015), Live-Cell Imaging of Endogenous mRNAs with a Small Molecule. Angew. Chem. Int. Ed., 54: 1855–1858, which has been published in final form at http://dx.doi.org/10.1002/anie.201410339.
許諾条件により本文ファイルは2015-12-23に公開.
この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
This is not the published version. Please cite only the published version.
URI: http://hdl.handle.net/2433/198615
DOI(出版社版): 10.1002/anie.201410339
PubMed ID: 25537455
出現コレクション:学術雑誌掲載論文等

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