54 research outputs found
Optical dispersions through intracellular inhomogeneities
Transport of intensity equation (TIE) exhibits a non-interferometric
correlation between intensity and phase variations of intermediate fields
(e.g., light and electron) in biological imaging. Previous TIE formulations
have generally assumed a free space propagation of monochromatic coherent field
functions crossing phase distributions along a longitudinal direction. Here, we
modify the TIE with fractal (or self-similar) organization models based on
intracellular refractive index turbulence. We then implement the TIE simulation
over a broad range of fractal dimensions and wavelengths. Simulation results
show how the intensity propagation through the spatial fluctuation of
intracellular refractive index interconnects fractal-dimensionality with
intensity dispersion (or transmissivity) within the picometer to micrometer
wavelength range. In addition, we provide a spatial-autocorrelation of phase
derivatives which allows the direct measurement and reconstruction of
intracellular fractal profiles from optical and electron microscopy imaging.Comment: 22 pages, 18 figures, 4 table
Mechanical Characterization of One-Headed Myosin-V Using Optical Tweezers
Class V myosin (myosin-V) is a cargo transporter that moves along an actin filament with large (βΌ36-nm) successive steps. It consists of two heads that each includes a motor domain and a long (23 nm) neck domain. One of the more popular models describing these steps, the hand-over-hand model, assumes the two-headed structure is imperative. However, we previously succeeded in observing successive large steps by one-headed myosin-V upon optimizing the angle of the acto-myosin interaction. In addition, it was reported that wild type myosin-VI and myosin-IX, both one-headed myosins, can also generate successive large steps. Here, we describe the mechanical properties (stepsize and stepping kinetics) of successive large steps by one-headed and two-headed myosin-Vs. This study shows that the stepsize and stepping kinetics of one-headed myosin-V are very similar to those of the two-headed one. However, there was a difference with regards to stability against load and the number of multisteps. One-headed myosin-V also showed unidirectional movement that like two-headed myosin-V required 3.5 kBT from ATP hydrolysis. This value is also similar to that of smooth muscle myosin-II, a non-processive motor, suggesting the myosin family uses a common mechanism for stepping regardless of the steps being processive or non-processive. In this present paper, we conclude that one-headed myosin-V can produce successive large steps without following the hand-over-hand mechanism
Three-Dimensional Microstructural Visualization of Mitosis using Focused Ion Beam-Scanning Electron Microscope (FIB-SEM) and 3Mv Ultra-High Voltage Electron Microscope (UHVEM) Tomography with Nanoscale Resolution at Whole Cell Level
Observation of Mechanical Process for Myosin-Ii by a Dark-Field Microscopy Combined with an Optical Trap
Structural Visualization of Mitotic Cycle by Three-Dimensional Focused Ion Beam-Scanning Electron Microscope (FIB-SEM) with Nanoscale Resolution at Whole Cell Level
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