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Studies on the Reaction Mechanism of the Cytochrome oxidase based on the Crystal Structure

Studies on the Reaction Mechanism of the Cytochrome oxidase based on the Crystal Structure
基于晶体结构的细胞色素氧化酶反应机理研究
批准号:
02044126
负责人:
YOSHIKAWA Shinya
金额:
$5.44万
依托单位国家:
日本
项目类别:
Grant-in-Aid for international Scientific Research
财政年份:
1990
资助国家:
日本
项目状态:
已结题
起止时间:
1990 至 1992

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英文摘要
Among many factors affecting crystallization conditions of cytochrome c oxidase, structure of detergent for stabilizing the solubilized enzyme protein has turned out to be the most critical. We have discovered seven species of synthetic non ionic detergents which provide crystallizable enzyme preparations. An alkyloxyethylene, BL8SY(CH_3(CH_2)_<11>O(CH_2CH_2)_<11>OH), most extensively examined so far, gave tetragonal crystals which diffract x-ray with the correlation coefficient larger than 0.5 at 6A resolution and 0.8 at 7A resolution. Occasionally X-ray diffraction was found at higher than 5A. Heavy atom derivatives of the hexagonal crystal were obtained by Hg, W and Au compounds. For molecular replacement analysis, 2D crystals in various space groups were prepared and the electron diffractions obtained indicates a three dimensional structure significantly different from that previously given by Henderson et al. Furthermore, formation of dimer affects clearly the 3D structure of the … More monomer.Preparation methods of yeast and bacterial(Paracoccas)enzymes have improved to establish much better methods than previously published ones in terms of the yeald, purity and reproducibility. The bacterial enzyme gave two dimensional crystals. The yeast preparation we obtained is soluble to any neutral buffer without any detergent. This property is quite promising for 3D crystallization.Method for infrared anisotropy of the single crystal of carbonyl cytochrome c oxidase has been essentially established. The most critical point was how to make small and polished tubes of CaF_2 for both infrared and optical measurements for a single crystal at various direction. During this investigation, crystallization conditions for fully reduced and fully reduced CO forms were examined to obtain X-ray diffraction. The space groups and lattice constants of these derivatives obtained coincide with those of the resting oxidized form within the experimental accuracy, suggesting that the conformational changes during the electron transfer and ligand binding are not so large as affecting quaternary structure of the enzyme molecule. Thus, once a crystal at an oxidation state are obtained at a certain level of resolution, crystals with the same quality may be easily obtained at other oxidation and binding states probably by treatment of the crystal with appropriate oxidant, reductant or ligand. Less
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W.S.Caughey,A.Dong,V.Sampath,S.YOSHIKAWA and X.-J.Zhao: "Probing heartY cytochrome c oxidase structure and function by infrared spectroscpy" J.Bioenergetics.(1993)
W.S.Caughey、A.Dong、V.Sampath、S.YOSHIKAWA 和 X.-J.Zhao:“通过红外光谱探测心脏细胞色素 C 氧化酶的结构和功能”J.Bioenergetics.(1993)
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"Single crystals of bovine heart cytochrome c oxidase at fully oxidized resting,fully reduced and CO bound fully reduced states are isomorphous with each other." J.Mol.Biol.122. 298-302 (1992)
“牛心脏细胞色素 C 氧化酶的单晶在完全氧化静止状态、完全还原状态和 CO 结合完全还原状态下是彼此同晶的。”
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T.OGURA,S.TAKAHASHI,K.Sinzawa-Itoh,S.YOSHIKAWA and T.KITAGAWA: "Observation of the fe^<4+>=O Stretching Raman Band for Cytochrome Oxidase Compound B at Ambient Temperature." J.Biol.Chem.265. 14721-14723 (1990)
T.OGURA、S.TAKAHASHI、K.Sinzawa-Itoh、S.YOSHIKAWA 和 T.KITAGAWA:“在环境温度下观察细胞色素氧化酶化合物 B 的 fe^<4 >=O 拉伸拉曼带。”
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M.Tsubaki, K.Shinzawa-Itoh and S.Yoshikawa: "Effects of crystallization on the heme-carbon monoxide moiety of bovine heart cytochrome c oxidase carbonyl." Biophys. J.(1992)
M.Tsubaki、K.Shinzawa-Itoh 和 S.Yoshikawa:“结晶对牛心细胞色素 C 氧化酶羰基的血红素一氧化碳部分的影响。”
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43
    Elucidation of the mammalian mitochondrial respiration mechanism at the atomic level.
    • 批准号:
      22247012
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $28.29万
    • 财政年份:
      2010
    • 负责人:
      YOSHIKAWA Shinya
    • 依托单位:
    The atomic mechanism of the functions of protein complexes which drive mitochondrial energy transduction.
    • 批准号:
      16087208
    • 项目类别:
      Grant-in-Aid for Scientific Research on Priority Areas
    • 资助金额:
      $54.46万
    • 财政年份:
      2004
    • 负责人:
      YOSHIKAWA Shinya
    • 依托单位:
    Studies on the proton pumping in mitochondrial electrotransfer system.
    • 批准号:
      09308026
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $22.02万
    • 财政年份:
      1997
    • 负责人:
      YOSHIKAWA Shinya
    • 依托单位:
    Preparation of crystals of cytochrome c oxidase and cytochrome bcl complex
    • 批准号:
      06453220
    • 项目类别:
      Grant-in-Aid for General Scientific Research (B)
    • 资助金额:
      $4.54万
    • 财政年份:
      1994
    • 负责人:
      YOSHIKAWA Shinya
    • 依托单位:
    海外基金