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  1. 原著論文

Characterization of cells expressing MRI reporters for the analysis of epigenetics.

https://repo.qst.go.jp/records/84776
https://repo.qst.go.jp/records/84776
4b165793-d05a-4c0a-9ed5-490f7bc60223
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-10-12
タイトル
タイトル Characterization of cells expressing MRI reporters for the analysis of epigenetics.
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
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Kimihiko, Sugaya

× Kimihiko, Sugaya

WEKO 1022937

Kimihiko, Sugaya

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Kimihiko, Sugaya

× Kimihiko, Sugaya

WEKO 1022938

en Kimihiko, Sugaya

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抄録
内容記述タイプ Abstract
内容記述 Epigenetics is thought to be involved in highly advanced life phenomena, and its regulation has created new opportunities in regenerative medicine. Mintbody (modification-specific intracellular antibody) can track a posttranslational protein modification in epigenetics using a genetic system encoded within a single chain of variable fragments tagged with a fluorescent protein. Magnetic resonance imaging (MRI) is a technique that allows observation of specific molecules in living organisms. The ferritin heavy chain (FTH1) is one of the MRI reporters used in mammals. The combination of FTH1 with mintbody may show remarkable ability as a reporter for MRI to investigate epigenetics in the deep part of a living organism. This article discusses the suitability and safety of FTH1 for use in the analysis of epigenetics by MRI. Cells expressing the FTH1 hybrid of mintbody showed insufficiently increased sensitivity by MRI even in the presence of excess iron. After incubation with ferric ammonium citrate, DNA damage was found in cells expressing the FTH1 hybrid of mintbody. The use of FTH1 as a genetically encoded reporter for MRI appears to be limited by the requirement of metal and its relatively low sensitivity. These results suggest future directionality and the possibility of studying epigenetics in vivo.
書誌情報 Analytical biochemistry

巻 633, p. 114395, 発行日 2021-09
出版者
出版者 Elsevier
ISSN
収録物識別子タイプ ISSN
収録物識別子 0003-2697
PubMed番号
識別子タイプ PMID
関連識別子 34600867
DOI
識別子タイプ DOI
関連識別子 10.1016/j.ab.2021.114395
関連サイト
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.ab.2021.114395
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