| Project/Area Number |
02044080
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| Research Category |
Grant-in-Aid for international Scientific Research
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| Allocation Type | Single-year Grants |
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| Section | Joint Research |
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| Research Institution | Kyoto University |
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Principal Investigator |
IMOTO Keiji (1991) Kyoto University Faculty of Medicine, Associate professor, 医学部, 助教授 (00176512)
沼 正作 (1990) 京都大学, 医学部, 教授 (50025516)
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| Co-Investigator(Kenkyū-buntansha) |
TSIEN Richard W. Stanford University, Department of Molecular and Cellular Physiology, Professor, 分子細胞生理学教室, 教授
BEAM Kurt G. Colorado State University Department of Physiology, Professor, 獣医学部生理学教室, 教授
STUHMER Walter Max-Planck-Institut fur Biophysikalische Chemie, Abteilung Membranbiophysik, Res, プランク生物物理化学研究所・膜生物物理部門, 研究員
MICHEL Hartmut Max-Planck-Institut fur Biophysik, Abteilung Membranbiochemie, Direcotr, プランク生物物理研究所・膜生化学部門, 部長
NAKAI Junichi Kyoto University Faculty of Medicine, Instructor, 医学部, 助手 (80237198)
FUKUDA Kazuhiko Kyoto University Faculty of Medicine, Instructor, 医学部, 助手 (90199224)
TANABE Tsutomu Kyoto University Faculty of Medicine, Instructor, 医学部, 助手 (70183069)
WALTER Stuhm マックス, プランク生物物理化学研究所・膜生物物理部門, 研究員
HARTMUT Mich マックス, プランク生物物理研究所・膜生化学部門, 部長
SAKMANN Bert マックス, プランク医学研究所・細胞生理学部門, 部長
井本 敬二 京都大学, 医学部, 助教授 (00176512)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥14,300,000 (Direct Cost: ¥14,300,000)
Fiscal Year 1991: ¥7,500,000 (Direct Cost: ¥7,500,000)
Fiscal Year 1990: ¥6,800,000 (Direct Cost: ¥6,800,000)
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| Keywords | Nicotinic acetylcholine receptor / Na^+ channel / Ca^<2+> channel / cDNA expression / Site-directed mutagenesis / Ion selectivity / Excitation-contraction coupling / Voltage sensing mechanism |
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| Research Abstract |
We expressed muscarinic acetylcholine receptor (mAChR I) and nicotinic acetylcholine receptor subunits in CHO cells, and purified and characterized the products. We also tried the baculo virus system, which turned out to be more efficient. Using purified samples, we investigated conditions for crystallisations of the proteins.
By analysing site-specifically mutated nicotine acetylcholine receptor, we showed that the residues in the intermediate ring is a determinant of ion selectivity, and that a ring-like structure of uncharged polar residues, together with the neighbouring intermediate ring, forms a short channel constriction close to the cytoplasmic side of the membrane. We analysed spontaneous openings of an acetylcholine receptor channel composed of bovine muscle alpha-, beta- and delta-subunits.
We extended our previous work on tetrodotoxin sensitivity and found that tetrodotoxin sensitivity and single-channel conductance are affected by mutations in two clusters of amino acid resi
… More
dues locating in the SS2 region of repeats I-IV. This strongly supports that the SS2 region of each repeat forms the eternal mouth and/or the pore wall of the channel.
From analysis of a series of chimeric constructs made of skeletal and cardiac dihydropyridine (DHP) receptors, we demonstrated that the region between repeats II and III is critical for skeletal-type excitation-contraction coupling, and that repeat I determines kinetics of activation of the chimeric receptors. We showed that intramembranous charge movement is restored by expressing DHP receptor in myotubes of dysgenic mice, indicating that the DHP receptor is closely related to the voltage-sensing mechanism. We cloned a brain calcium channel and determined its primary structure. Functional expression of this channel in Xenopus oocytes is enormously enhanced by coexpression of skeletal muscle alpha_2- and beta-subunits. This channel is a high-threshold calcium channel, insensitive to nifedipine and omega-conotoxin. Blot analysis suggests it is predominantly expressed in cerebellar purkinje and granular cells. Less
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