1987 Fiscal Year Final Research Report Summary
Regulatory Factor of Smooth Muscle Contraction: Relation of Leiotonin with Myosin Light Chain Kinase
Project/Area Number |
61480112
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Research Category |
Grant-in-Aid for General Scientific Research (B)
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Allocation Type | Single-year Grants |
Research Field |
Neurophysiology and muscle physiology
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Research Institution | National Institute for Physiological Sciences |
Principal Investigator |
EBASHI Setsuro Director General of Physiological Sciences, 生理学研究所, 所長 (10009863)
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Co-Investigator(Kenkyū-buntansha) |
ISHIZAKI Yasuki Postdoctral Fellow of JSPS, 生理学研究所, 学術振興会特別研究員 (90183003)
SUZUKI Masashi Research Associate, 生理学研究所, 助手 (70187764)
MIKAWA Takashi Research Associate, 生理学研究所, 助手 (50143417)
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Project Period (FY) |
1986 – 1987
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Keywords | Regulation in smooth muscle / Leiotonin / ミオシン軽鎖キナーゼ |
Research Abstract |
A new method of preparing leiotonin was developed. It was incidentally found that dimethyl sulfoxide (DMSO) is a very useful agent for protein fractionation, not only for the above purpose but also for general ones. Using DMSO, a fraction exhibiting much larger actomyosin-activating activity, or leiotonin activity, than myosin light chain kinase (MLCK) activity (L/K > 100, taking L/K of 0.1 M extract as 1) was obtained both from chicken gizzard and boving stomach without particular treatment. Using special procedures, a preparation void of MLCK avtivity (L/K > 3,000) could be obtained. The component responsibe for the leiotonin activity was a protein of 155 kDa, indistinguishable from MLCK in its molecular weight. A fragment produced by trypsin under specified conditions exhibited also a definite leiotonin activity without MLCK activity. This may correspond to the old preparation of leiotonin. The primary sequence of the 155 kDa component responsible for leiotonin activity (and/or MLCK activity) has been determined up to 120 kDa from the C- terminal. As a whole the idea that smooth muscle regulation is mediated by leiotonin has further been substantiated.
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Research Products
(14 results)
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[Publications] Yanagisawa, M., Hamada, Y., Katsuragawa, Y., Imamura, M., Mikawa, T., Masaki, T.: "Complete primary structure of vertebrate smooth muscle myosin heavy chain deduced from its cDNA sequence, Implications on topography and function of myosin." J. Biol. Chem.198. 143-157 (1987)
Description
「研究成果報告書概要(欧文)」より
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[Publications] Ebashi, S., Mikawa, T., Kuwayama, H., Suzuki, M., Ikemoto, H., Ishizaki, Y., Koga, R.: "Ca^<2+> regulation in smooth muscle; dissociation of myosin light chain kinase activity from activation of actin-myosin interaction." In Regulation and Contraction of Smooth Muscle (eds by N.L. Stephens et al.) Alan R. Liss, Inc.109-117 (1987)
Description
「研究成果報告書概要(欧文)」より
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