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. 1995 Apr;68(4 Suppl):286S–290S.

Mechanical measurements of single actomyosin motor force.

H Miyata 1, H Yoshikawa 1, H Hakozaki 1, N Suzuki 1, T Furuno 1, A Ikegami 1, K Kinosita Jr 1, T Nishizaka 1, S Ishiwata 1
PMCID: PMC1281950  PMID: 7787092

Abstract

To elucidate the mechanism of force generation by actomyosin motor, a measuring system was constructed, in which an in vitro motility assay was combined with an optical trapping technique. An actin filament of several micron long was attached to a gelsolin-coated polystyrene bead, and was allowed to interact with a small number (approximately 1/1 micron actin filament) of rabbit skeletal heavy meromyosin (an active subfragment of myosin) molecules bound to a nitrocellulose-coated coverglass. The bead position was determined at 33-ms intervals. We measured the force generation event at relatively low (100-400 nM) ATP concentration so that the occurrence of individual force generation events could be detected with our time resolution. The actin-bound bead held in the optical trap moved in a stepwise manner in the direction of the actin filament only in the presence of ATP. At the trap strength of 0.3 pN/nm, the maximum size of the step was 11 nm, and the maximum force associated with the movement was 3.3 pN.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Finer J. T., Simmons R. M., Spudich J. A. Single myosin molecule mechanics: piconewton forces and nanometre steps. Nature. 1994 Mar 10;368(6467):113–119. doi: 10.1038/368113a0. [DOI] [PubMed] [Google Scholar]
  2. Furuno T., Ulmer K. M., Sasabe H. Scanning electron microscopy of negatively stained catalase on a silicon wafer. Microsc Res Tech. 1992 Mar 1;21(1):32–38. doi: 10.1002/jemt.1070210105. [DOI] [PubMed] [Google Scholar]
  3. Goldman Y. E. Kinetics of the actomyosin ATPase in muscle fibers. Annu Rev Physiol. 1987;49:637–654. doi: 10.1146/annurev.ph.49.030187.003225. [DOI] [PubMed] [Google Scholar]
  4. Hackney D. D. Evidence for alternating head catalysis by kinesin during microtubule-stimulated ATP hydrolysis. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6865–6869. doi: 10.1073/pnas.91.15.6865. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ishijima A., Harada Y., Kojima H., Funatsu T., Higuchi H., Yanagida T. Single-molecule analysis of the actomyosin motor using nano-manipulation. Biochem Biophys Res Commun. 1994 Mar 15;199(2):1057–1063. doi: 10.1006/bbrc.1994.1336. [DOI] [PubMed] [Google Scholar]
  6. Kron S. J., Toyoshima Y. Y., Uyeda T. Q., Spudich J. A. Assays for actin sliding movement over myosin-coated surfaces. Methods Enzymol. 1991;196:399–416. doi: 10.1016/0076-6879(91)96035-p. [DOI] [PubMed] [Google Scholar]
  7. Miyata H., Hakozaki H., Yoshikawa H., Suzuki N., Kinosita K., Jr, Nishizaka T., Ishiwata S. Stepwise motion of an actin filament over a small number of heavy meromyosin molecules is revealed in an in vitro motility assay. J Biochem. 1994 Apr;115(4):644–647. doi: 10.1093/oxfordjournals.jbchem.a124389. [DOI] [PubMed] [Google Scholar]
  8. Rayment I., Holden H. M., Whittaker M., Yohn C. B., Lorenz M., Holmes K. C., Milligan R. A. Structure of the actin-myosin complex and its implications for muscle contraction. Science. 1993 Jul 2;261(5117):58–65. doi: 10.1126/science.8316858. [DOI] [PubMed] [Google Scholar]
  9. Svoboda K., Block S. M. Force and velocity measured for single kinesin molecules. Cell. 1994 Jun 3;77(5):773–784. doi: 10.1016/0092-8674(94)90060-4. [DOI] [PubMed] [Google Scholar]
  10. Uyeda T. Q., Warrick H. M., Kron S. J., Spudich J. A. Quantized velocities at low myosin densities in an in vitro motility assay. Nature. 1991 Jul 25;352(6333):307–311. doi: 10.1038/352307a0. [DOI] [PubMed] [Google Scholar]
  11. Wakabayashi K., Tokunaga M., Kohno I., Sugimoto Y., Hamanaka T., Takezawa Y., Wakabayashi T., Amemiya Y. Small-angle synchrotron x-ray scattering reveals distinct shape changes of the myosin head during hydrolysis of ATP. Science. 1992 Oct 16;258(5081):443–447. doi: 10.1126/science.1411537. [DOI] [PubMed] [Google Scholar]

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