| Project/Area Number |
02304062
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| Research Category |
Grant-in-Aid for Co-operative Research (A)
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| Allocation Type | Single-year Grants |
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| Research Field |
物質生物化学
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| Research Institution | Kyushu University |
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Principal Investigator |
IMOTO Taiji Kyushu Univ., Faculty of Pharmaceutical Sciences Professor., 薬学部, 教授 (90038282)
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| Co-Investigator(Kenkyū-buntansha) |
SAKIYAMA Fumio Osaka Univ. Division of Protein Chemistry Professor., 蛋白質研究所, 教授 (40029947)
OHTSUKA Eiko Hokkaido Univ., Faculty of Pharmaceutical Sciences Professor., 薬学部, 教授 (80028836)
OHTA Takahisa Tokyo Univ., Faculty of Agricultural chemistry Professor., 農学部, 教授 (30011844)
IWANAGA Sadaaki Kyushu Univ., Faculty of Sciences, Professor., 理学部, 教授 (90029942)
ASHIDA Tamaichi Nagoya Univ., Faculty of Engineerings, Professor., 工学部, 教授 (10029936)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥31,500,000 (Direct Cost: ¥31,500,000)
Fiscal Year 1991: ¥16,500,000 (Direct Cost: ¥16,500,000)
Fiscal Year 1990: ¥15,000,000 (Direct Cost: ¥15,000,000)
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| Keywords | Protein Engineering / NMR / X-ray crystallography / Replacement of amino acid / Chemical modification / Comparative biochemistry / cDNA / Protein expression system / アルドラ-ゼ / NADHーシトクロムb5 / 血液凝固因子 / アロステリック現象 / T4エンドヌクレア-ゼ / ATPase. / 核酸修復酵素 / Lー乳酸脱水素酵素 / ATPase / キメラタンパク質 / モジュ-ル / Znープロテア-ゼ / ボ-マン・バ-ク型インヒビタ- |
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| Research Abstract |
We have accomplished various Investigations described below for the establishment of the basis of 'Protein Engineering'.
1, The approach by replacing amino acid : (1) Glu23 residue of T4 endonuclease was proved to be Important in glycosylase activity. (2) Thrl56 residue of H^+ ATPase was found to be important to evoke activity. (3) The structure-function relationship of NADHcytochrome b_5 was examined to understand the cause of hereditary methemoglobinemia. (4) The role of Trp108 in lysozyme on evoking activity became apparent.
2, The approach by constructing expression system of aimed protein : (1) The binding site of bovine tissue factor was present in the region between Gal and EGF domain in blood coagulation factor VII. (2) The active sites and the catalytic mechanism of neutral protease from Bacillus subtilis var. amylosacchariticus were elucidated. (3) The binding mode of L-lysine and ATP with lysyl tRNA synthase from Bacillus stearothermophilus were analyzed.
3, The approach by com
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paring primarx and tertiary structure of proteins : (1) HIs210 residue of lysylendopeptidase was proved to be important in high-selectivity on evoking activity. (2) The relationship between structure and function in phospholipase A_2 from Habu snake was analyzed. (3) The catalytic mechanism of human aldolase was analyzed by preparing its various chimeric proteins. (4) The structure, function and heredity of both triosephosphate isomerase and ribonuclease were examined discussed by the analysis of their module structures.
4, The approach by means of chemical modification : (1) RNase T1 and trypsin became stable by introducing novel polyethyleneglycol and amylose derivative.
5, The approach by use of NMR and X-ray crystallography : (1) The allosteric phenomena of L-lactic acid dehydrogenase from Bifidobacterium longum was analyzed. (2) The tertiary structure of neocarzinostatin was determined by use of NMR and distance geometry algorism. (3) The function of Bowman-Birk protease inhibitor was examined from the X-ray crystallographic analysis of its complex with trypsin. Less
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