Creation of protein-base nanocarrier with a protease dependent molecule release mechanism
| Project/Area Number |
26620132
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Bio-related chemistry
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| Research Institution | Nagoya University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
NAKAJIMA Hiroshi 大阪市立大学, 大学院理学研究科, 教授 (00283151)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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| Keywords | フェリチン / 一酸化炭素 / 鉄チオラト錯体 / 一酸化炭素放出分子 / ドラッグデリバリー / エンテロバクチン |
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| Outline of Final Research Achievements |
A ferric iron-tris catechol complex, which is a mimicry of enterobactin, a strong chelator for iron(III) ion found in nature was successfully prepared on the entrance of the 3-fold axis channel of ferritin. The X-ray crystal structure of the complex appeared to plug the ferritin channel and confine penetrated molecules into the ferritin cavity, while experimental data revealed that our original target molecules, antithrombotics passed through the channel, irrespective of formation or deformation of the iron catechol complex.
By contrast, the ferritin with the iron catechol complex was competent to capture an iron carbonyl complex, which we recently developed as a photo-dependent CO release molecule ([Fe-CO]). Bio-compatible CO releasers adaptable to organisms have been focused as an important tool to study signal transduction mechanism in the cells. We will develop a novel bio-compatible CO releaser based on the newly obtained composite, ferritin-[Fe-CO].
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Report
(3 results)
Research Products
(18 results)
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[Presentation] フェリチンへの分子取り込みの制御2014
Author(s)
近藤美緒・中島洋・中尾貴大・渡辺芳人
Organizer
第45回 中部化学関係学協会支部連合秋季大会
Place of Presentation
春日井、愛知
Year and Date
2014-11-29 – 2014-11-30
Related Report
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