Function of the photo-induced triplet radical pair in the photo-sensor BLUF protein
Function of the photo-induced triplet radical pair in the photo-sensor BLUF protein
批准号:
21370069
负责人:
MINO Hiroyuki
金额:
$12.31万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2009
资助国家:
日本
项目状态:
已结题
起止时间:
2009 至 2011
中文摘要
A photo-induced radical pair of FADH·and Y8·in BLUF protein SyPixD was studied by electron paramagnetic resonance(EPR)spectroscopy.The EPR signal has been characterized by a Pake doublet signal with complete S=1 spin state。The temperature dependence of the spin-lattice relaxation of the radical pair of flavin and tyrosine in SyPixD was investigated by pulsed electron paramagnetic resonance(EPR)spectroscopy.Based on the temperature dependence of spin.Lattice relaxation time T-1,the exchange coupling of the radical pair was estimated as2J=6to8厘米^<;-1>;,defined as-2JS-1*S-2.The radical pair was utilized as a probe to analyze the oligomer of SyPixD.The relative arrangement of PixD proteins in the complex was investigated by pulsed electron-electron double resonance(PELDOR)with the orientation selection。Based on the decameric structure in the crystal,the possible structure for the PELDOR results was evaluated.The transient EPR measurements have been performed to investigate the reaction pathway to produce radical-pair.The results show that the radical-pair was produced in the range of 200-263K.The possible reaction mechanism was proposed.
英文摘要
A photo-induced radical pair of FADH・and Y8・in BLUF protein SyPixD was studied by electron paramagnetic resonance(EPR) spectroscopy. The EPR signal has been characterized by a Pake doublet signal with complete S=1 spin state. The temperature dependence of the spin-lattice relaxation of the radical pair of flavin and tyrosine in SyPixD was investigated by pulsed electron paramagnetic resonance(EPR) spectroscopy. Based on the temperature dependence of spin. lattice relaxation time T-1, the exchange coupling of the radical pair was estimated as 2J=6 to 8 cm^<-1>, defined as-2JS-1* S-2.The radical pair was utilized as a probe to analyze the oligomer of SyPixD. The relative arrangement of PixD proteins in the complex was investigated by pulsed electron-electron double resonance(PELDOR) with the orientation selection. Based on the decameric structure in the crystal, the possible structure for the PELDOR results was evaluated.The transient EPR measurements have been performed to investigate the reaction pathway to produce radical-pair. The results show that the radical-pair was produced in the range of 200-263 K. The possible reaction mechanism was proposed.
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ESEEM studies of the doublet signal with spin S = 1 in the blue light sensor BLUF protein SyPixD
蓝光传感器 BLUF 蛋白 SyPixD 中自旋 S = 1 的双峰信号的 ESEEM 研究
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[Kondo, T., Masuda, S., Mino, H.]
通讯作者:
H.
The position of the Mn^2+binding site at the first dark state for photoactivation in Photosystem II manganese cluster
Photosystem II 锰簇中用于光活化的第一暗状态下 Mn^2 结合位点的位置
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Mizue Asada, Hiroyuki Mino]
通讯作者:
Hiroyuki Mino
Pulsed EPR analysis of the photo-induced triplet radical pair in the BLUF protein SyPixD : Determination of the protein-protein distance and orientation in the oligomeric protein
BLUF 蛋白 SyPixD 中光诱导三重态自由基对的脉冲 EPR 分析:测定寡聚蛋白中的蛋白-蛋白距离和方向
DOI:
10.1007/s00723-011-0237-1
发表时间:
2011
期刊:
Applied Magnetic Resonance
影响因子:
1
作者:
[Toru Kondo, Shinji Masuda and Hiroyuki Mino]
通讯作者:
Shinji Masuda and Hiroyuki Mino
The formation of an radical pair FADH.-Y8. in SyPixD investigated by pulsed and transient EPR
形成自由基对FADH.-Y8。
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[三野広幸, 近藤徹, 筒井和彦, 増田真二]
通讯作者:
増田真二
法による青色光センサータンパク質SyPixD重合体のタンパク間相互作用の解析
蓝光传感器蛋白SyPixD聚合物的蛋白质-蛋白质相互作用分析方法
DOI:
--
发表时间:
2009
期刊:
影响因子:
--
作者:
[近藤徹, 筒井和彦, 増田真二, 三野広幸]
通讯作者:
三野広幸
共 11 条
Quantum teleportation of radical pair in photosynthetic biomembrane
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批准号:22654051
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.05万
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财政年份:2010
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负责人:MINO Hiroyuki
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依托单位:
国内基金
海外基金
光受体蛋白AppA的BLUF域超快动力学机理研究
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批准号:31971233
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项目类别:面上项目
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资助金额:58.0万元
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批准年份:2019
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负责人:丁蓓
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依托单位: