Intracellular reduction of the cupric ion of bleomycin copper complex and transfer of the cuprous ion to a cellular protein.
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- TAKAHASHI KATSUTOSHI
- Research Laboratories, Pharmaceutical Division, Nippon Kayaku Co.
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- YOSHIOKA OSAMU
- Research Laboratories, Pharmaceutical Division, Nippon Kayaku Co.
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- MATSUDA AKIRA
- Research Laboratories, Pharmaceutical Division, Nippon Kayaku Co.
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- UMEZAWA HAMAO
- Institute of Microbial Chemistry
書誌事項
- タイトル別名
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- Intracellular reduction of the cupric i
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The cupric ion of the bleomycin copper complex has been shown to be reduced and transferred to a cellular protein by the following mechanism: Bleomycin-Cu2+→Bleomycin+Cu+ X Cu++M→M-Cu+ The intracellular reducing agents (X) are suggested to be sulfhydryl compounds, because their action is inhibited by N-ethylmaleimide. The active group of the cellular protein (M) that binds with the cuprous ion is suggested to be a sulfhydryl group. The action of the bleomycin copper complex in causing DNA fragmentation in cells can be explained by the mechanism presented in this paper. This mechanism in cells is also supported by the temperature dependency of the action of the bleomycin copper complex on cells.
収録刊行物
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- The Journal of Antibiotics
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The Journal of Antibiotics 30 (10), 861-869, 1977
公益財団法人 日本感染症医薬品協会
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詳細情報 詳細情報について
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- CRID
- 1390001204155027072
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- NII論文ID
- 130003499280
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- NII書誌ID
- AA0069330X
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- COI
- 1:CAS:528:DyaE1cXhsFE%3D
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- ISSN
- 18811469
- 00218820
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- NDL書誌ID
- 1913645
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- PubMed
- 73538
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可