| 研究課題/領域番号 |
23K22483
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| 補助金の研究課題番号 |
22H01212 (2022-2023)
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| 研究種目 |
基盤研究(B)
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| 配分区分 | 基金 (2024)
補助金 (2022-2023) |
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| 応募区分 | 一般 |
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| 審査区分 |
小区分14030:プラズマ応用科学関連
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| 研究機関 | 九州大学 |
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研究代表者 |
Attri Pankaj 九州大学, システム情報科学研究院, 学術研究員 (40868361)
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| 研究分担者 |
田中 宏昌 名古屋大学, 低温プラズマ科学研究センター, 教授 (00508129)
栗田 弘史 豊橋技術科学大学, 工学(系)研究科(研究院), 准教授 (70512177)
竹内 希 東京工業大学, 工学院, 准教授 (80467018)
白谷 正治 九州大学, システム情報科学研究院, 教授 (90206293)
古閑 一憲 九州大学, システム情報科学研究院, 教授 (90315127)
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| 研究期間 (年度) |
2022-04-01 – 2027-03-31
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| 研究課題ステータス |
交付 (2024年度)
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| 配分額 *注記 |
17,290千円 (直接経費: 13,300千円、間接経費: 3,990千円)
2026年度: 2,340千円 (直接経費: 1,800千円、間接経費: 540千円)
2025年度: 2,340千円 (直接経費: 1,800千円、間接経費: 540千円)
2024年度: 2,340千円 (直接経費: 1,800千円、間接経費: 540千円)
2023年度: 2,990千円 (直接経費: 2,300千円、間接経費: 690千円)
2022年度: 6,630千円 (直接経費: 5,100千円、間接経費: 1,530千円)
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| キーワード | Computational study / Protein / Plasma Chemistry / Non-thermal plasma / Nitrogen conversion / Plant protein / COMSOL Multiphysics / CO2 and N2 plasma / Fluorescence / Plasma agriculture / plasma medicine / peptides / proteins / anticancer treatment |
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| 研究開始時の研究の概要 |
Modified the amino acids through plasma and understood the structure changes in proteins and peptides in the absence and presence of co-solvents. Additionally, to understand the effect of plasma-modified protein action on cancer cells, we will bind the protein with drugs and inhibit their action.
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| 研究実績の概要 |
We developed steamer discharge plasma working on N2, CO2, and Air feed gas. We also developed reaction chemistry for CO2, N2, and Air plasma to understand the production of short-lived species. Our 0D and 1D models are ready nowadays; we are focused on developing 2D models. 2D models in two different phases took a very long time to standardize due to complications in fluid flow in two distinct phases. Our 2D model is very close to the experimental conditions of the gas and liquid phase. OD and 1D model COMSOL model were helpful in predicting the very short reactive species those were are not possible to detect through the physical parameters. like We also measured the reactive species in the gas and liquid phase. Further, we measured the changes in the reactive species using a chemical analysis Kit and Fluorescence spectroscopy for the liquid phase analysis, and FT-IR used for the gas phase analysis. We analyzed our plasma system on the radish seeds to find out the change in germination index and growth. Also new analyzed the production of the NO3- species inside the seeds. We also checked the production of reactive production in the gas phase like CO, and O3 using FTIR. And detected the NH4+, NO3-, NO2- and H2O2 concentrations in the water using chemical analysis. Later, we also checked the production of OH radical in the water using the Fluorescence spectroscopy. The detection of OH, N2 second positive system, NO, CO, Alpha-H were detected in the gas phase using Optical emission spectroscopy. Our Simulation results are in the good agreement with the experimental results
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| 現在までの達成度 (区分) |
現在までの達成度 (区分)
2: おおむね順調に進展している
理由
According to the plan, we have developed CO2 and N2 streamer plasma to modify the peptides and proteins. Additionally, we also developed reaction chemistry to understand the production of short-lived species. Our 0D and 1D model is ready nowadays we are focused on developing 2D model. 2D models in two different phases took a very long time to standardize due to complications in fluid flow in two different phases.
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| 今後の研究の推進方策 |
We will use the cyclic dipeptides and treat them with plasma using Air, CO2, and N2 plasma. The modification in the peptides will be analysed by the variety of state-of-the-art analytical methods, such as circular dichroism, fluorescence spectroscopy, and mass spectrometry, again supported by computational methods, such as Molecular dynamics simulations, which will be used to understand the change in peptides. We will also use some synthesized organic drugs to interact with the protein and check the interaction using the MD simulation. We also plan to check the effect of catalase protein effect with and without inhibitors on the cancer cells. Later we evaluate the structural modification in the catalase enzyme using CD, fluorescence, and MS spectroscopy.
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