| Project/Area Number |
13557004
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
General physiology
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| Research Institution | Jikei University School of Medicine |
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Principal Investigator |
KURIHARA Satoshi Jikei University, School of Medicine, Professor, 医学部, 教授 (90057026)
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| Co-Investigator(Kenkyū-buntansha) |
KUSAKARI Yoichiro Jikei University, School of Medicine, Research Assistant, 医学部, 助手 (80338889)
WATANABE Michiko Jikei University, School of Medicine, Research Assistant, 医学部, 助手 (10158660)
SUDA Norio Jikei University, School of Medicine, Lecturer, 医学部, 講師 (80201581)
INOUYE Satoshi Chisso Corporation, Chief Research Chemist, 横浜研究所, 次席研究員
田中 悦子 東京慈恵会医科大学, 医学部, 講師 (70256410)
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| Project Period (FY) |
2001 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥6,300,000 (Direct Cost: ¥6,300,000)
Fiscal Year 2003: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2002: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2001: ¥3,500,000 (Direct Cost: ¥3,500,000)
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| Keywords | native aepuorin / Ca^<2+> / recombinant aequorin / apoaequorin / light / Mg^<2+> / pH / mouse / 変異型組み換えイクオリン / Caイオン / Mgイオン / 変異型組換えイクオリン / イクオリン / 遺伝子組換え / 変異イクオリン / Ca応答性 |
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| Research Abstract |
Native aequorin has been used for measurement of intracellular Ca^<2+> transients. However, it is difficult to get a large number of jellyfish that is used for extraction of aequorin. We intended to produce apoasquorin using E.coli and then recombinant aequoin began being produced by mixing the apoaequorin and celenterazine. We recorded a relation between pCa and the light signal normalized by the peak light at pCa 2, which was performed by instantaneously mixing the recombinant aequorin and solutions with various concentrations of Ca^<2+>. The recombinant aequorin was slightly sensitive to Ca^<2+> in a range between pCa5 and pCa6. The level of Ca^<2+>-independent light in recombinant aequorin was lower than that of native aequorin. Mg^<2+> inhibited the light signal of the recombinant aequorin. We altered pH in the solution and confirmed that the light of aequorin was not significantly sensitive to pH change. Then, we injected the recombinant aequorin into superficial cells of the left ventricular papillary muscles of mouse to confirm whether the recombinant aequorin can be used for the measurement of the intracellular Ca^<2+> transients (CaT) in cardiac muscles. The peak of CaT measured with the recombinant aequorin was larger than that with native aequorin. The tail of CaT in the recombinant aequorin was slightly faster than that in the native aequorin. Thus, the recombinant aequorin can be used for the measurement of intracellular Ca^<2+> concentration. We established the method to produce a large amount of the recombinant aequorin. We can expect various recombinant aequorin with different characteristics, which is useful for cellular physiology.
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