scholarly journals A comparative study of high resolution microscopy imaging modalities using a three-dimensional resolution measure

2009 ◽  
Vol 17 (26) ◽  
pp. 24377 ◽  
Author(s):  
Jerry Chao ◽  
Sripad Ram ◽  
E. Sally Ward ◽  
Raimund J. Ober
Author(s):  
H.A. Cohen ◽  
T.W. Jeng ◽  
W. Chiu

This tutorial will discuss the methodology of low dose electron diffraction and imaging of crystalline biological objects, the problems of data interpretation for two-dimensional projected density maps of glucose embedded protein crystals, the factors to be considered in combining tilt data from three-dimensional crystals, and finally, the prospects of achieving a high resolution three-dimensional density map of a biological crystal. This methodology will be illustrated using two proteins under investigation in our laboratory, the T4 DNA helix destabilizing protein gp32*I and the crotoxin complex crystal.


2019 ◽  
Author(s):  
Kozgunova Elena ◽  
Gohta Goshima

AbstractHigh-resolution microscopy is a valuable tool to study cellular processes, such as signalling, membrane trafficking, or cytoskeleton remodelling. Several techniques of inclined illumination microscopy allow imaging at near single molecular level; however, the application of these methods to plant cells is limited, due to thick cell walls and necessity to excise a part of the tissue for sample preparation. In this study, we developed simple, easy-to-use microfluidic device for highly inclined and laminated optical sheet (HILO) microscopy using a model plant Physcomitrella patens. We demonstrated that microfluidic device can be used to culture living cells and enables high-resolution HILO imaging of microtubules without perturbing their dynamics. In addition, our microdevice enables the supply and robust washout of compounds during HILO microscopy imaging, for example to perform microtubule regrowth assay. Furthermore, we tested long-term (48 h) HILO imaging using a microdevice and visualised the developmental changes in the microtubule dynamics during tissue regeneration. The microfluidic device designed in this study provides a novel tool to conduct long-term HILO microscopy and washout assays using plant cells.


1990 ◽  
Vol 217 ◽  
Author(s):  
H. W. Deckman ◽  
J. H. Dunsmuir ◽  
K. L. D'Amico ◽  
S. R. Ferguson ◽  
B. P. Flannery

ABSTRACTWe have developed several x-ray microtomography systems which function as quantitative three dimensional x-ray microscopes. In this paper we describe the evolutionary path followed from making the first high resolution experimental microscopes to later generations which can be routinely used for investigating materials. Developing the instrumentation for reliable quantitative x-ray microscopy using synchrotron and laboratory based x-ray sources has led to other imaging modalities for obtaining temporal and spatial two dimensional information.


Author(s):  
T. J. Headley

Oxide phases having the hollandite structure have been identified in multiphase ceramic waste forms being developed for radioactive waste disposal. High resolution studies of phases in the waste forms described in Ref. [2] were initiated to examine them for fine scale structural differences compared to natural mineral analogs. Two hollandites were studied: a (Ba,Cs,K)-titan-ate with minor elements in solution that is produced in the waste forms, and a synthesized BaAl2Ti6O16 phase containing ∼ 4.7 wt% Cs2O. Both materials were consolidated by hot pressing at temperatures above 1100°C. Samples for high resolution microscopy were prepared both by ion-milling (7kV argon ions) and by crushing and dispersing the fragments on holey carbon substrates. The high resolution studies were performed in a JEM 200CX/SEG operating at 200kV.


Author(s):  
Kenneth H. Downing ◽  
Hu Meisheng ◽  
Hans-Rudolf Went ◽  
Michael A. O'Keefe

With current advances in electron microscope design, high resolution electron microscopy has become routine, and point resolutions of better than 2Å have been obtained in images of many inorganic crystals. Although this resolution is sufficient to resolve interatomic spacings, interpretation generally requires comparison of experimental images with calculations. Since the images are two-dimensional representations of projections of the full three-dimensional structure, information is invariably lost in the overlapping images of atoms at various heights. The technique of electron crystallography, in which information from several views of a crystal is combined, has been developed to obtain three-dimensional information on proteins. The resolution in images of proteins is severely limited by effects of radiation damage. In principle, atomic-resolution, 3D reconstructions should be obtainable from specimens that are resistant to damage. The most serious problem would appear to be in obtaining high-resolution images from areas that are thin enough that dynamical scattering effects can be ignored.


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