41 results on '"Iino, Ryota"'
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2. Domain architecture divergence leads to functional divergence in binding and catalytic domains of bacterial and fungal cellobiohydrolases
3. Single-molecule imaging analysis reveals the mechanism of a high-catalytic-activity mutant of chitinase A from Serratia marcescens
4. High-speed near-field fluorescence microscopy combined with high-speed atomic force microscopy for biological studies
5. Processive Chitinase, a Burnt-bridge Brownian Motor Hydrolyzing Crystalline Polysaccharide
6. Single-molecule analysis reveals rotational substeps and chemo-mechanical coupling scheme of Enterococcus hirae V1-ATPase
7. Processive Chitinase is Burnt-Bridge Brownian Motor Operated by Fast Catalysis after Peeling Rail from Crystalline Chitin
8. Single-Nanoparticle Tracking with Angstrom Localization Precision and Microsecond Time Resolution
9. Chemo-Mechanical Coupling of Rotary Molecular Motor Enterococcus Hirae V1-ATPase as Revealed by Single-Molecule Analysis
10. Single-molecule imaging and manipulation of biomolecular machines and systems
11. One-Nanometer Steps in the Motion of a Linear Molecular Motor Serratia marcescens Chitinase A Resolved by Gold Nanoprobe
12. Single-molecule Imaging Analysis of Binding, Processive Movement, and Dissociation of Cellobiohydrolase Trichoderma reesei Cel6A and Its Domains on Crystalline Cellulose
13. Direct Observation of the Allosteric Conformational Change of Kinesin-1 using Gold Nanorod and its Implication for Head-Head Coordination
14. Rotational mechanism of Enterococcus hirae V1-ATPase by crystal-structure and single-molecule analyses
15. The Role of Amino Acid Residues Located at the Catalytic Site in the Rotation of Enterococcus Hirae V1-ATPase
16. Torque Generation of Enterococcus hirae V-ATPase
17. Single-molecule Imaging Analysis of Elementary Reaction Steps of Trichoderma reesei Cellobiohydrolase I (Cel7A) Hydrolyzing Crystalline Cellulose Iα and IIII
18. Single Molecule Observation of F1-ATPase using Artificial Substrate and Amino Acid
19. Basic Properties of Rotary Dynamics of the Molecular Motor Enterococcus hirae V1-ATPase
20. Intersubunit coordination and cooperativity in ring-shaped NTPases
21. Direct Observation of the Forward Stepping Motion of Kinesin-1 using Dark-Field Microscopy with 50-Micro Second Temporal Resolution
22. Direct Observation of the Rotary Motion of FOF1-ATP Synthase Driven by Proton Motive Force
23. Rotary catalysis of the stator ring of F1-ATPase
24. Principal Role of the Arginine Finger in Rotary Catalysis of F1-ATPase
25. Rotary Motion of FOF1-ATP Synthase in the Presence of pmf
26. Direct Observation of Rotary Catalysis of Rotorless F1-ATPase by High-Speed Atomic Force Microscopy
27. Chemomechanical coupling of Pi release on F1-ATPase
28. Direct observation of steps in c-ring rotation of Escherichia coli FOF1-ATP synthase
29. Simple Dark-Field Microscopy with Nanometer Spatial Precision and Microsecond Temporal Resolution
30. Activation and Stiffness of the Inhibited States of F1-ATPase Probed by Single-molecule Manipulation
31. Fluctuation Theorem Applied to F1-ATPase
32. The Role of Pi-Release as the Main Torque Generating Step of F1-Atpase
33. Single-molecule Study on the Temperature-sensitive Reaction of F1-ATPase with a Hybrid F1 Carrying a Single β(E190D)
34. Mechanism of Inhibition by C-terminal α-Helices of the ϵ Subunit of Escherichia coli FoF1-ATP Synthase
35. How is the Temperature Sensitive (TS) Reaction of F1-ATPase Coupled with its Rotation?
36. Single-molecule Imaging of ATP-driven Stepping Rotation of FoF1-ATP Synthase Reconstituted into Supported Membrane
37. Real-time Monitoring of Conformational Dynamics of the ϵ Subunit in F1-ATPase
38. Fluorescence Imaging for Monitoring the Colocalization of Two Single Molecules in Living Cells
39. Ultrafine Membrane Compartments for Molecular Diffusion as Revealed by Single Molecule Techniques
40. F0F1-ATPase/Synthase Is Geared to the Synthesis Mode by Conformational Rearrangement of ϵ Subunit in Response to Proton Motive Force and ADP/ATP Balance
41. Single Molecule Imaging of Green Fluorescent Proteins in Living Cells: E-Cadherin Forms Oligomers on the Free Cell Surface
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