Due to the rapid globalization there is an increasing danger for pandemic outbreaks. The high death toll of fast spreading diseases like the Ebola infection demand the fast development of new medicines. Thus, the automation of pharmaceutical processes is an indispensable but challenging task. In cooperation with the Institute for Virology, Philipps-University, Marburg, Germany, recently, algorithms to detect and evaluate subviral particle tracks in live-cell fluorescence image sequences were developed. In steady interdisciplinary exchange between pharmacists and engineers it turned out that new measures to identify and classify subviral particle motion are required. This article focuses on the evaluation and optimization of a new method to classify subviral particle motion using fractal dimension estimation. The influence of global and local interpolation methods on fractal dimension estimation is investigated. The methods are tested on simulated data and applied to real image sequences. The results prospect a high benefit of using the presented methods for an effective classification of subviral particle behavior.
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http://dx.doi.org/10.1109/EMBC.2019.8857721 | DOI Listing |
Subcell Biochem
December 2024
Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Madrid, Spain.
Virus-like particles (VLPs) are formed by viral proteins that, when overexpressed, spontaneously self-assemble into particles that structurally are similar to infectious virus or subviral particles (e.g. the viral capsid).
View Article and Find Full Text PDFVaccines (Basel)
September 2024
Institute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, 1090 Vienna, Austria.
Approximately 10-20% of subjects vaccinated with HBsAg-based hepatitis B virus (HBV) vaccines are non-responders. BM32 is a recombinant grass pollen allergy vaccine containing the HBV-derived preS surface antigen as an immunological carrier protein. PreS includes the binding site of HBV to its receptor on hepatocytes.
View Article and Find Full Text PDFbioRxiv
September 2024
Arbovirus Immunity Section, Vaccine Research Center, NIAID, NIH; Bethesda, 20892, USA.
Flavivirus assembly at the endoplasmic reticulum is driven by the structural proteins envelope (E) and premembrane (prM). Here, contrary to the established paradigm for flavivirus assembly, we demonstrate that the biogenesis of flavivirus particles does not require an intact prM nor proteolytic activation. The expression of E preceded by a truncated version of prM (M-E) was sufficient for the formation of non-infectious Zika virus subviral particles and pseudo-infectious reporter virions.
View Article and Find Full Text PDFFront Immunol
September 2024
Botany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, Egypt.
Background: The relationship between chronic hepatitis B (CHB) infection and natural killer (NK) cell dysfunction is well-established, but the specific role of HBV viral antigens in driving NK cell impairment in patients with CHB remains unclear. This study investigates the modulatory effects of hepatitis B virus subviral particles (HBVsvp, a representative model for HBsAg) on the phenotypic regulation (activating and inhibitory receptors), cytokine production and cytotoxic potential of peripheral blood mononuclear cell-derived natural killer cells (PBMCs-derived NK cell), which contributes to NK cell dysfunction in CHB infection, potentially serving as an effective HBV immune evasion strategy by the virus.
Methods: NK cells were isolated from peripheral blood of patients with CHB (n=5) and healthy individuals (n=5), stimulated with HBVsvp.
J Virol
October 2024
Science Department, Autonomous University of San Luis Potosi, San Luis Potosí, Mexico.
Cryo-electron microscopy and tomography have allowed us to unveil the remarkable structure of icosahedral viruses. However, in the past few years, the idea that these viruses must have perfectly symmetric virions, but in some cases, it might not be true. This has opened the door to challenging paradigms in structural virology and raised new questions about the biological implications of "unusual" or "defective" symmetries and structures.
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