Titlebook: Information and Operational Technology Security Systems; First International Apostolos P. Fournaris,Konstantinos Lampropoulos,E Conference

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solution where both protein structure and membrane morphology can be revealed. Compared to conventional electron microscopy methods for biology, cryo-ET does not include the use of potentially artifact generating agents for sample fixation or visualization. Despite its obvious advantages, cryo-ET ha

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Konstantinos Solomos,Panagiotis Ilia,Sotiris Ioannidis,Nicolas Kourtelliscule, crystalline sample. While some of the electrons used to probe the crystal interact without altering the crystal, others deposit energy which changes the sample through a series of damage events. It follows that the sample cannot be observed without damaging it, and the frames obtained at the b

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was believed to be maintained with the exception of the presence of .-amino acids in the cell wall of microorganisms. However, .-amino acids were recently found in various higher organisms in proteins and peptides and as free amino acids. In proteins, .-aspartate (Asp) residues have been detected in

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Fady Copty,Andre Kassis,Sharon Keidar-Barner,Dov Murikntral nervous system (CNS). Despite diversity in their subunit composition, their subcellular localization, and their biophysical and pharmacological properties, activation of NMDARs always requires in addition to glutamate the binding of a co-agonist that has long been thought to be glycine. Howeve

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