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High-Resolution Imaging of Myosin Motor in Action by a High-Speed Atomic Force Microscope

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 538))

Abstract

The atomic force microscope (AFM) is a powerful tool for imaging biological molecules on a substrate, in solution. However, there is no effective time axis with AFM; commercially available AFMs require minutes to capture an image, but many interesting biological processes occur at much higher rate. Hence, what we can observe using the AFM is limited to stationary molecules, or those moving very slowly. We sought to increase markedly the scan speed of the AFM, so that in the future it can be used to study the dynamic behaviour of biomolecules. For this purpose, we have developed various devices optimised for high-speed scanning. Combining these devices has produced an AFM that can capture a 100 × 100 pixel image within 80 ms, thus generating a movie consisting of many successive images of a sample in aqueous solution. This is demonstrated by imaging myosin V molecules moving on mica, in solution.

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References

  • Ando, T., Kodera, N., Takai, E., Maruyama, D., Saito, K. & Toda, A. (2001) A high-speed atomic force microscope for studying biological macromolecules. Porc. Natl Acad. Sci. USA, 98, 12468–12472.

    Article  CAS  Google Scholar 

  • Ando, T., Kodera, N., Takai, E., Maruyama, D., Saito K. & Toda, A. A high-speed atomic force microscope for studying biological macromolecules in action. Jpn. J. Appl. Phys. 41, 4851–4856.

    Google Scholar 

  • Binnig, G., Quate, CF. & Gerber, C. (1986) Atomic force microscope. Phys. Rev. Lett., 56, 930–933.

    Article  PubMed  Google Scholar 

  • Sakamoto, T., Amitani, I., Yokota, E. & Ando, T. (2000) Direct observation of processive movement by individual myosin V molecules. Biochem. Biophys. Res. Commun. 272, 586–590.

    Article  PubMed  CAS  Google Scholar 

  • Sulcheck, T., Hsieh, R., Adams, J.D., Minne, S.C., Quate, CF. & Adderton, D.M. (2000) Highspeed atomic force microscopy in liquid. Rev. Sci. Instrum., 71, 2097–2099.

    Article  Google Scholar 

  • Viani, M.V., Schaffer, T.E., Paloczi, G.T., Pietrasanta, L.L., Smith, B.L. et. al. (1999) Fast imaging and fast force spectroscopy of single biopolymers with a new atomic force microscope designed for small cantilevers. Rev. Sci. Instrum., 70, 4300–4303

    Article  CAS  Google Scholar 

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© 2003 Springer Science+Business Media New York

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Kodera, N., Kinoshita, T., Ito, T., Ando, T. (2003). High-Resolution Imaging of Myosin Motor in Action by a High-Speed Atomic Force Microscope. In: Sugi, H. (eds) Molecular and Cellular Aspects of Muscle Contraction. Advances in Experimental Medicine and Biology, vol 538. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9029-7_11

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  • DOI: https://doi.org/10.1007/978-1-4419-9029-7_11

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-4764-4

  • Online ISBN: 978-1-4419-9029-7

  • eBook Packages: Springer Book Archive

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