DNA conformational behavior and functions in microcapsules
| Project/Area Number |
17K05611
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Biological physics/Chemical physics/Soft matter physics
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| Research Institution | Nagoya University |
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Principal Investigator |
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| Project Period (FY) |
2017-04-01 – 2020-03-31
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| Project Status |
Completed (Fiscal Year 2019)
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| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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| Keywords | DNA / カプセル / DNA折り畳み / 人工細胞モデル / DNA凝縮 / 高分子カプセル / マイクロカプセル / DNA高次構造変化 |
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| Outline of Final Research Achievements |
In eukaryotic cells, DNA macromolecules with a length exceeding 1 meter are densely folded and exist in cells with a size of several μm. Artificial experimental models are needed to explain the higher order structure and behavior of DNA in cellular-like environment. In this study, we constructed an "artificial cell model" method for encapsulating very ling genomic DNA in polymer capsules of several μm size. Using this experimental model, we made clear the behavior of DNA confined in the cell-sized space. The experimental methodology proposed in this study is promising for gene delivery and related biomedical applications.
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| Academic Significance and Societal Importance of the Research Achievements |
核酸のカプセル化は、遺伝子送達、ゲノム保護などの応用を対象とする重要な技術である。これまでのカプセル化の技術により短いDNAまたはオリゴマーDNAのカプセル化が示されたが、カプセルの大きさより数倍～数十倍ほど長いゲノムDNAのカプセル化が困難であった。本研究で開発した人工細胞モデルの構築方法を用いて、長鎖DNAのカプセル化はほぼ100%効率で成功した。この技術、細胞内での長鎖DNAの状態を明らかにするための使用に加えて、バイオ・医療分野においても応用できると期待される。
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Report
(4 results)
Research Products
(14 results)
