scholarly journals Coupled Broad Ion Beam–Scanning Electron Microscopy (BIB–SEM) for polishing and three dimensional (3D) serial section tomography (SST)

2020 ◽  
Vol 214 ◽  
pp. 112989
Author(s):  
Ali Gholinia ◽  
Matthew E. Curd ◽  
Etienne Bousser ◽  
Kevin Taylor ◽  
Thijs Hosman ◽  
...  
2011 ◽  
Vol 6 (6) ◽  
pp. 845-858 ◽  
Author(s):  
Andrew J Bushby ◽  
Kenneth M Y P'ng ◽  
Robert D Young ◽  
Christian Pinali ◽  
Carlo Knupp ◽  
...  

2012 ◽  
Vol 18 (1) ◽  
pp. 171-178 ◽  
Author(s):  
Bijoyendra Bera ◽  
Naga Siva Kumar Gunda ◽  
Sushanta K. Mitra ◽  
Douglas Vick

AbstractSedimentary carbonate rocks are one of the principal porous structures in natural reservoirs of hydrocarbons such as crude oil and natural gas. Efficient hydrocarbon recovery requires an understanding of the carbonate pore structure, but the nature of sedimentary carbonate rock formation and the toughness of the material make proper analysis difficult. In this study, a novel preparation method was used on a dolomitic carbonate sample, and selected regions were then serially sectioned and imaged by focused ion beam–scanning electron microscopy. The resulting series of images were used to construct detailed three-dimensional representations of the microscopic pore spaces and analyze them quantitatively. We show for the first time the presence of nanometer-scale pores (50–300 nm) inside the solid dolomite matrix. We also show the degree of connectivity of these pores with micron-scale pores (2–5 μm) that were observed to further link with bulk pores outside the matrix.


mSphere ◽  
2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Winnie Kerstens ◽  
Anneke Kremer ◽  
Michelle Holtappels ◽  
Peter Borghgraef ◽  
Saskia Lippens ◽  
...  

ABSTRACT The determination of the exact location of a protein in the cell is essential to the understanding of biological processes. Here, we report for the first time the visualization of a protein of interest in Saccharomyces cerevisiae using focused ion beam scanning electron microscopy (FIB-SEM). As a proof of concept, the integral endoplasmic reticulum (ER) membrane protein Erg11 has been C-terminally tagged with APEX2, which is an engineered peroxidase that catalyzes an electron-dense deposition of 3,3′-diaminobenzidine (DAB), as such marking the location of the fused protein of interest in electron microscopic images. As DAB is unable to cross the yeast cell wall to react with APEX2, cell walls have been partly removed by the formation of spheroplasts. This has resulted in a clear electron-dense ER signal for the Erg11 protein using FIB-SEM. With this study, we have validated the use of the APEX2 tag for visualization of yeast proteins in electron microscopy. Furthermore, we have introduced a methodology that enables precise and three-dimensional (3D) localization studies in yeast, with nanometer resolution and without the need for antibody staining. Because of these properties, the described technique can offer valuable information on the molecular functions of studied proteins. IMPORTANCE With this study, we have validated the use of the APEX2 tag to define the localization of proteins in the model yeast S. cerevisiae. As such, FIB-SEM can identify the exact 3D location of a protein of interest in the cell with nanometer-scale resolution. Such detailed imaging could provide essential information on the elucidation of various biological processes. APEX2, which adds electron density to a fused protein of interest upon addition of the substrate DAB, originally was used in mammalian studies. With this study, we expand its use to protein localization studies in one of the most important models in molecular biology.


2013 ◽  
Vol 19 (S2) ◽  
pp. 1868-1869 ◽  
Author(s):  
M. De Winter ◽  
G.M. Pennock ◽  
J.A. Post ◽  
M.R. Drury

Extended abstract of a paper presented at Microscopy and Microanalysis 2013 in Indianapolis, Indiana, USA, August 4 – August 8, 2013.


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