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Toshio Ando

Researcher at Kanazawa University

Publications -  262
Citations -  13063

Toshio Ando is an academic researcher from Kanazawa University. The author has contributed to research in topics: Chemistry & Heavy meromyosin. The author has an hindex of 52, co-authored 247 publications receiving 11015 citations. Previous affiliations of Toshio Ando include Japan Advanced Institute of Science and Technology & University of California, San Francisco.

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A high-speed atomic force microscope for studying biological macromolecules.

TL;DR: In this paper, a high-speed scanner, free of resonant vibrations up to 60 kHz, small cantilevers with high resonance frequencies (450-650 kHz) and small spring constants (150-280 pN/nm), and several electronic devices of wide bandwidth are presented.
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Video imaging of walking myosin V by high-speed atomic force microscopy

TL;DR: This work directly visualize myosin V molecules walking along actin tracks, using high-speed atomic force microscopy, providing corroborative ‘visual evidence’ for previously speculated or demonstrated molecular behaviours, and reveals more detailed behaviours of the molecules, leading to a comprehensive understanding of the motor mechanism.
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Imaging modes of atomic force microscopy for application in molecular and cell biology

TL;DR: The basic principles, advantages and limitations of the most common AFM bioimaging modes are reviewed, including the popular contact and dynamic modes, as well as recently developed modes such as multiparametric, molecular recognition, multifrequency and high-speed imaging.
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Traffic Jams Reduce Hydrolytic Efficiency of Cellulase on Cellulose Surface

TL;DR: The real-time visualization of crystalline cellulose degradation by individual cellulase enzymes through use of an advanced version of high-speed atomic force microscopy is reported here.
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High-speed atomic force microscopy for nano-visualization of dynamic biomolecular processes

TL;DR: The atomic force microscope (AFM) has a unique capability of allowing the high-resolution imaging of biological samples on substratum surfaces in physiological solutions, which has enabled the direct visualization of dynamic structural changes and dynamic interactions occurring in individual biological macromolecules, which is not possible with other techniques as discussed by the authors.