scholarly journals Developing and Applying a Correlative Light and Electron Microscopy Technique to Overcome Inherent Transmission Electron Microscopy Shortcomings.

2021 ◽  
Vol 27 (S1) ◽  
pp. 1398-1400
Author(s):  
Jonathan Franks ◽  
Mike Calderone ◽  
Natasha Erdman ◽  
Alan Watson ◽  
Simon Watkins
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Microscopy Technique ◽  
Transmission Electron

Scale structure and taxonomy of some species of Raphidocystis, Raphidiophrys, and Pompholyxophrys (Heliozoea) including descriptions of six new taxa

1985 ◽  
Vol 63 (8) ◽  
pp. 1944-1961 ◽  
Author(s):  
K. H. Nicholls ◽  
M. Dürrschmidt
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
New Zealand ◽  
Light Microscopy ◽  
Light And Electron Microscopy ◽  
Scale Structure ◽  
Taxonomic Descriptions ◽  
Transmission Electron ◽  
New Information ◽  
Freshwater Habitats

Sixteen taxa of the genera Raphidocystis, Raphidiophrys, and Pompholyxophrys from freshwater habitats in Canada, Chile, and New Zealand were studied by light and electron microscopy. Six taxa are described as new: Raphidocystis glabra, Raphidiophrys minuta, Raphidiophrys orbicularis ssp. orbicularis, R. orbicularis ssp. ovalis, Pompholyxophrys stellata, and P. ossea. New information on scale structure and arrangement based on scanning and transmission electron microscopy amplifies the taxonomic descriptions of Raphidiophrys ambigua, R. pallida, R. elegans, R. intermedia, R. marginata, R. symmetrica, Pompholyxophrys punicea, P. exigua, and P. ovuligera, which were previously imperfectly known by light microscopy only.

The proboscis ciliation of the echiuran Bonellia viridis

1979 ◽  
Vol 59 (2) ◽  
pp. 377-384 ◽  
Author(s):  
V. Jaccarini ◽  
P. J. Schembri
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Quantitative Analysis ◽  
Light And Electron Microscopy ◽  
Neck Region ◽  
Dorsal Surface ◽  
Food Particle ◽  
Particle Uptake ◽  
Transmission Electron ◽  
Definite Pattern

Special club-shaped cilia with an expanded tip are seen by both light and electron microscopy on the proboscis of Bonellia viridis in addition to the usual filamentous cilia. Using transmission electron microscopy the club tip is seen to consist of a distally curled axoneme enclosed within a sac-like expansion of the ciliary membrane. The axoneme may describe up to two complete loops inside the membrane sac or may occasionally follow an S-shaped course.A quantitative analysis of the distribution on the proboscis of both filamentous and club cilia is made. No discrete ciliary tracts are present. However, there is a definite pattern of ciliary density distribution. The cilia are densest on both the dorsal and ventral surfaces of the distal fringe of the proboscis. The dorsal fringe cilia are concerned with locomotion and the ventral cilia with food particle uptake. The club cilia are confined to the terminal lobes and neck region of the proboscis. The dorsal surface of the proboscis posterior to the fringe is virtually non-ciliated. The functional significance of the club cilia is discussed.

Visualization of film-forming polymer particles with a liquid cell technique in a transmission electron microscope

The Analyst ◽  
2015 ◽  
Vol 140 (18) ◽  
pp. 6330-6334 ◽  
Author(s):  
Lili Liu ◽  
Yi Liu ◽  
Wenjun Wu ◽  
Christopher. M. Miller ◽  
Elizabeth C. Dickey
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Room Temperature ◽  
Staining Technique ◽  
Polymer Particles ◽  
Microscopy Technique ◽  
Transmission Electron ◽  
Film Forming ◽  
Liquid Cell

Liquid cell transmission electron microscopy technique provides the opportunity to image room-temperature film-forming polymer particles in solution. Together with staining technique, it can also be used as a tool to characterize the internal structure of polymer particles in situ.

scholarly journals Correlative Light and Transmission Electron Microscopy Showed Details of Mitophagy by Mitochondria Quality Control in Propionic Acid Treated SH-SY5Y Cell

Materials ◽  
2020 ◽  
Vol 13 (19) ◽  
pp. 4336
Author(s):  
Minkyo Jung ◽  
Hyosun Choi ◽  
Jaekwang Kim ◽  
Ji Young Mun
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Propionic Acid ◽  
Hippocampal Neurons ◽  
Acid Treatment ◽  
Light And Electron Microscopy ◽  
Quality Monitoring ◽  
Selective Autophagy ◽  
Transmission Electron ◽  
The Brain

Propionic acid is a metabolite of the microbiome and can be transported to the brain. Previous data show that propionic acid changes mitochondrial biogenesis in SH-SY5Y cells and induces abnormal autophagy in primary hippocampal neurons. Maintaining mitochondrial function is key to homeostasis in neuronal cells, and mitophagy is the selective autophagy involved in regulating mitochondrial quality. Monitoring mitophagy though light microscopy or conventional transmission electron microscopy separately is insufficient because phases of mitophagy, including autophagosome and autolysosome in nano-resolution, are critical for studies of function. Therefore, we used correlative light and electron microscopy to investigate mitochondrial quality in SH-SY5Y cells after propionic acid treatment to use the advantages of both techniques. We showed, with this approach, that propionic acid induces mitophagy associated with mitochondrial quality.

scholarly journals Precision of fiducial marker alignment for correlative super‐resolution fluorescence and transmission electron microscopy

2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Adeeba Fathima ◽  
César Augusto Quintana-Cataño ◽  
Christoph Heintze ◽  
Michael Schlierf
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Molecule ◽  
Fluorescent Proteins ◽  
Light And Electron Microscopy ◽  
Super Resolution ◽  
Specific Protein ◽  
Fiducial Markers ◽  
Transmission Electron ◽  
Microscopy Techniques

AbstractRecent advances in microscopy techniques enabled nanoscale discoveries in biology. In particular, electron microscopy reveals important cellular structures with nanometer resolution, yet it is hard, and sometimes impossible to resolve specific protein localizations. Super-resolution fluorescence microscopy techniques developed over the recent years allow for protein-specific localization with ~ 20 nm precision are overcoming this limitation, yet it remains challenging to place those in cells without a reference frame. Correlative light and electron microscopy (CLEM) approaches have been developed to place the fluorescence image in the context of a cellular structure. However, combining imaging methods such as super resolution microscopy and transmission electron microscopy necessitates a correlation using fiducial markers to locate the fluorescence on the structures visible in electron microscopy, with a measurable precision. Here, we investigated different fiducial markers for super-resolution CLEM (sCLEM) by evaluating their shape, intensity, stability and compatibility with photoactivatable fluorescent proteins as well as the electron density. We further carefully determined limitations of correlation accuracy. We found that spectrally-shifted FluoSpheres are well suited as fiducial markers for correlating single-molecule localization microscopy with transmission electron microscopy.

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