2001 Fiscal Year Final Research Report Summary
Analysis of structure-function relationships on smooth muscle myosin using NMR and X-ray crystallography.
| Project/Area Number |
09480172
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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 | 一般 |
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| Research Field |
Biophysics
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| Research Institution | University of Tokyo |
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Principal Investigator |
TANOKURA Masaru University of Tokyo, Graduate School of Agricultural and Life Sciences, Professor, 大学院・農学生命科学研究科, 教授 (60136786)
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| Co-Investigator(Kenkyū-buntansha) |
SASAKI Hiroshi Oita Medical University, Faculty of Medicine, Research associate, 医学部, 助手 (80272467)
NISHIYAMA Makoto University of Tokyo, Biotechnology Research Center, Associate Professor, 生物生産工学研究センター, 助教授 (00208240)
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| Project Period (FY) |
1997 – 1999
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| Keywords | myosin / smooth muscle / motor protein / NMR / nuclear magnetic resonance |
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| Research Abstract |
Myosin is an enzyme transducing the chemical energy from the hydrolysis of ATP into directed mechanical movement, in conjunction with actin. In this research, we use the NMR, which is a good probe to observe the microenvironments, and X-ray crystallography, which allows us a precise three-dimensional structure determination, to investigate the mechanism of energy conversion by myosin with atomic level.
From the pH- and temperature-dependent changes of the signals in the ^<31>P-NMR spectra of smooth muscle sub fragment 1-ADP complex, it is appeared that the interaction between the smooth muscle myosin subfragment 1 and ADP is stronger than that of skeletal muscle myosin subfragment 1 and ADP. In the case of kinesin and ncd motor domains, it was found to exist two different forms of motor domain-ADP complex. In addition, we found a difference between kinesin and ncd motor domains in the chemical shift of the a-phosphate of bound ADP, indicating that the electrostatic or magnetic microenvironments of this site of these motor domains differed from each other.
We established the baculovirus expression system to obtain the recombinant chicken gizzard smooth muscle myosin motor domain as well as mutants for crystallization. We also found that the role of the neck region on the ATPase activity of kinesin.
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Research Products
(10 results)
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[Publications] Suzuki, Y., Ohkura, R., Sugiura, S., Yasuda, R., Kinoshita, K, Tanokura, M., Sutoh, K: "Modulation of actin filament sliding by mutations of the SH2 cysteine in Dictyostelium myosin II"Biochem. Biophys. Res. Commun.. 234・3. 701-706 (1997)
Description
「研究成果報告書概要(和文)」より
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[Publications] Suzuki, Y., Ohkura, R., Sugiura, S., Yasuda, R., Kinoshita, K., Tanokura, M. and Sutoh, K.: "Modulation of actin filament sliding by mutations of the SH2 cysteine in Dictyostelium myosin II"Biochem. Biophys. Res. Commun.. Vol. 234, No. 3. 701-706 (1997)
Description
「研究成果報告書概要(欧文)」より
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