High-resolution SEM in cell biology

1993 ◽  
Vol 3 (6) ◽  
pp. 205-208 ◽  
Author(s):  
T ALLEN ◽  
M GOLDBERG
Keyword(s):  
2000 ◽  
Vol 6 (S2) ◽  
pp. 1148-1149
Author(s):  
U. Ziese ◽  
A.H. Janssen ◽  
T.P. van der Krift ◽  
A.G. van Balen ◽  
W.J. de Ruijter ◽  
...  

Electron tomography is a three-dimensional (3D) imaging method with transmission electron microscopy (TEM) that provides high-resolution 3D images of structural arrangements. Conventional TEM images are in first approximation mere 2D-projections of a 3D sample under investigation. With electron tomographya series of images is acquired of a sample that is tilted over a large angular range (±70°) with small angular tilt increments (so called tilt-series). For the subsequent 3D-reconstruction, the images of the tilt series are aligned relative to each other and the 3D-reconstruction is computed. Electron tomography is the only technique that can provide true 3D information with nm-scale resolution of individual and unique samples. For (cell) biology and material science applications the availability of high-resolution 3D images of structural arrangements within individual samples provides unique architectural information that cannot be obtained otherwise. Routine application of electron tomography will comprise a major revolutionary step forward in the characterization of complex materials and cellular arrangements.


2015 ◽  
Vol 337 (2) ◽  
pp. v
Author(s):  
Urban Lendahl
Keyword(s):  

2010 ◽  
Vol 190 (4) ◽  
pp. 491-500 ◽  
Author(s):  
Tobias C. Walther ◽  
Matthias Mann

The global analysis of protein composition, modifications, and dynamics are important goals in cell biology. Mass spectrometry (MS)–based proteomics has matured into an attractive technology for this purpose. Particularly, high resolution MS methods have been extremely successful for quantitative analysis of cellular and organellar proteomes. Rapid advances in all areas of the proteomic workflow, including sample preparation, MS, and computational analysis, should make the technology more easily available to a broad community and turn it into a staple methodology for cell biologists.


2008 ◽  
Vol 3 (8) ◽  
pp. 1278-1286 ◽  
Author(s):  
Stephan Speier ◽  
Daniel Nyqvist ◽  
Martin Köhler ◽  
Alejandro Caicedo ◽  
Ingo B Leibiger ◽  
...  

2010 ◽  
Author(s):  
Gerhard Krampert ◽  
Ingo Kleppe ◽  
Thomas Kalkbrenner ◽  
Klaus Weisshart ◽  
Ralf Wolleschensky ◽  
...  

2019 ◽  
Vol 30 ◽  
pp. 16-29 ◽  
Author(s):  
Mostafa Bakhti ◽  
Katharina Scheibner ◽  
Sophie Tritschler ◽  
Aimée Bastidas-Ponce ◽  
Marta Tarquis-Medina ◽  
...  

Cells ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 35
Author(s):  
Shane M. Hickey ◽  
Ben Ung ◽  
Christie Bader ◽  
Robert Brooks ◽  
Joanna Lazniewska ◽  
...  

Fluorescence microscopy has become a critical tool for researchers to understand biological processes at the cellular level. Micrographs from fixed and live-cell imaging procedures feature in a plethora of scientific articles for the field of cell biology, but the complexities of fluorescence microscopy as an imaging tool can sometimes be overlooked or misunderstood. This review seeks to cover the three fundamental considerations when designing fluorescence microscopy experiments: (1) hardware availability; (2) amenability of biological models to fluorescence microscopy; and (3) suitability of imaging agents for intended applications. This review will help equip the reader to make judicious decisions when designing fluorescence microscopy experiments that deliver high-resolution and informative images for cell biology.


2019 ◽  
Author(s):  
C. Shan Xu ◽  
Song Pang ◽  
Kenneth J. Hayworth ◽  
Harald F. Hess

AbstractIsotropic high-resolution imaging of large volumes provides unprecedented opportunities to advance connectomics and cell biology research. Conventional Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) offers unique benefits such as high resolution (< 10 nm in x, y, and z), robust image alignment, and minimal artifacts for superior tracing of neurites. However, its prevailing deficiencies in imaging speed and duration cap the maximum possible image volume. We have developed technologies to overcome these limitations, thereby expanding the image volume of FIB-SEM by more than four orders of magnitude from 103µm3to 3 x 107µm3while maintaining an isotropic resolution of 8 x 8 x 8 nm3voxels. These expanded volumes are now large enough to support connectomic studies, in which the superior z resolution enables automated tracing of fine neurites and reduces the time-consuming human proofreading effort. Moreover, by trading off imaging speed, the system can readily be operated at even higher resolutions achieving voxel sizes of 4 x 4 x 4 nm3, thereby generating ground truth of the smallest organelles for machine learning in connectomics and providing important insights into cell biology. Primarily limited by time, the maximum volume can be greatly extended.Here we provide a detailed description of the enhanced FIB-SEM technology, which has transformed the conventional FIB-SEM from a laboratory tool that is unreliable for more than a few days to a robust imaging platform with long term reliability: capable of years of continuous imaging without defects in the final image stack. An in-depth description of the systematic approach to optimize operating parameters based on resolution requirements and electron dose boundary conditions is also explicitly disclosed. We further explore how this technology unleashes the full potential of FIB-SEM systems, revolutionizing volume electron microscopy (EM) imaging for biology by gaining access to large sample volumes with single-digit nanoscale isotropic resolution.


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