Imaging, Tracking and Computational Analyses of Virus Entry and Egress with the Cytoskeleton

Viruses have a dual nature: particles are “passive substances” lacking chemical energy transformation, whereas infected cells are “active substances” turning-over energy. How passive viral substances convert to active substances, comprising viral replication and assembly compartments has been of intense interest to virologists, cell and molecular biologists and immunologists. Infection starts with virus entry into a susceptible cell and delivers the viral genome to the replication site. This is a multi-step process, and involves the cytoskeleton and associated motor proteins. Likewise, the egress of progeny virus particles from the replication site to the extracellular space is enhanced by the cytoskeleton and associated motor proteins. This overcomes the limitation of thermal diffusion, and transports virions and virion components, often in association with cellular organelles. This review explores how the analysis of viral trajectories informs about mechanisms of infection. We discuss the methodology enabling researchers to visualize single virions in cells by fluorescence imaging and tracking. Virus visualization and tracking are increasingly enhanced by computational analyses of virus trajectories as well as in silico modeling. Combined approaches reveal previously unrecognized features of virus-infected cells. Using select examples of complementary methodology, we highlight the role of actin filaments and microtubules, and their associated motors in virus infections. In-depth studies of single virion dynamics at high temporal and spatial resolutions thereby provide deep insight into virus infection processes, and are a basis for uncovering underlying mechanisms of how cells function

Connecting mitochondrial dynamics and life-or-death events via Bcl-2 family proteins

International audienceThe morphology of a population of mitochondria is the result of several interacting dynamical phenomena, including fission, fusion, movement, elimination and biogenesis. Each of these phenomena is controlled by underlying molecular machinery, and when defective can cause disease. New understanding of the relationships between form and function of mitochondria in health and disease is beginning to be unraveled on several fronts. Studies in mammals and model organisms have revealed that mitochondrial morphology, dynamics and function appear to be subject to regulation by the same proteins that regulate apoptotic cell death. One protein family that influences mitochondrial dynamics in both healthy and dying cells is the Bcl-2 protein family. Connecting mitochondrial dynamics with life-death pathway forks may arise from the intersection of Bcl-2 family proteins with the proteins and lipids that determine mitochondrial shape and function. Bcl-2 family proteins also have multifaceted influences on cells and mitochondria, including calcium handling, autophagy and energetics, as well as the subcellular localization of mitochondrial organelles to neuronal synapses. The remarkable range of physical or functional interactions by Bcl-2 family proteins is challenging to assimilate into a cohesive understanding. Most of their effects may be distinct from their direct roles in apoptotic cell death and are particularly apparent in the nervous system. Dual roles in mitochondrial dynamics and cell death extend beyond BCL-2 family proteins. In this review, we discuss many processes that govern mitochondrial structure and function in health and disease, and how Bcl-2 family proteins integrate into some of these processes

Strategies to optimize cationic polymers for gene delivery via endosomal escape

Cationic polymers with different backbones were characterized regarding their performance at different steps of the gene delivery process. The interaction with plasmid DNA (pDNA), cytotoxicity, uptake of pDNA, endosomal escape and protein expression in different cell lines were investigated using methods like fluorometric assays, dynamic light scattering, flow cytometry and confocal laser scanning microscopy. Starting with homopolymers of different degrees of polymerization and different cationic moieties, a positive correlation between toxicity and endosomal escape was demonstrated. By combination with hydrophobic functionalities either within block copolymers resulting in cationic micelles or within statistic copolymers, the transfection efficiency was increased even in hard-to-transfect leukemia cells. To reduce the accompanying toxicity, further hydrophilic neutral and/or anionic functionalities were introduced either within block copolymers or as an additional layer outside the preformed cationic micelles. Different factors influenced the efficiency-toxicity ratio of the polymers, such as the ratio, type and combination method of cationic and anionic/hydrophilic moieties. The introduction of only anionic moieties was most promising and led to an increase in viability while maintaining high transfection efficiencies comparable to the cationic micelle. The combination of cationic micelle and anionic-hydrophilic block copolymer exhibited the highest shielding efficiency with decreased but still moderate transfection efficiency, rendering it suitable for long circulation times and targeted delivery. This thesis illustrates the high suitability of cationic polymers for gene delivery and their optimization in different parameters towards high cell viability while maintaining superior gene delivery efficiency. Hence, polymers represent promising tools for future gene therapy and further (in vivo) studies are required to transfer these results to humans

Probes, hardware and software for next-generation super-resolution microscopy

Super-resolution microscopy enables optical imaging using fluorescence probes below the diffraction limit. In stochastic super-resolution microscopy, molecules are „switched“ between non-fluorescent dark-state (OFF-state) and fluorescent bright-state (ON-state) in order to pinpoint their position with sub-diffraction precision. The most prominent techniques of localization-based super-resolution microscopy are photo-activated localization microscopy (PALM) and stochastic optical reconstruction microscopy (STORM). Here, the switching between dark- and bright-state is accomplished using photophysical or photochemical processes. A recently introduced super-resolution microscopy method called DNA-PAINT (deoxyribonucleic acid - point accumulation for imaging in nanoscale topography) is based on DNA-DNA interaction. In contrast to STORM or PALM, the fluorescence molecules do not switch between dark and bright states. The so-called „blinking“ in DNA-PAINT is created by transient hybridization of short fluorescent DNA strands (imagers) to their targets. The work in this dissertation focuses on three different advancements in the technological aspect of super-resolution microscopy. Probes In the first project of this thesis, I demonstrate the combination of single-molecule Förster resonance energy transfer (FRET) with DNA-PAINT imaging to overcome some current limitations of the DNA-based super-resolution microscopy. I evaluate the novel probe design with in vitro experiments using DNA nanostructures and prove the performance of the FRET-based probes in a cellular context. Hardware In the second project, I describe a cost-efficient single-molecule microscope platform, which is an order of magnitude more affordable, while still yielding high-performance imaging capacity. Using two-dimensional (2D) and three-dimensional (3D) super-resolution in vitro experiments using DNA nanostructures, I asses the performance of the microscopy platform. Finally, I present exemplary experiments for multiplexed cellular imaging. Software In the last project, I present a software package that is developed to assist during super-resolution data analysis. It is based on the deep learning concept of the artificial neural network (ANN) and designed to automate the classification of nano-scaled patterns found in super-resolution images. I evaluate the performance of the software package using super-resolution in vitro experiments of DNA nanostructures as well as targets in cellular samples.Die superauflösende Mikroskopie ermöglicht die optische Abbildung mittels Fluoreszenzsonden unterhalb der Beugungsgrenze. In stochastischen Superauflösungsmikroskopie werden Moleküle zwischen dem nicht-fluoreszierenden Zustand (OFF-Zustand) und dem fluoreszierenden Zustand (ON-Zusstand) “geschaltet“, um ihre Position präziser als die Beugungsgrenze zu bestimmen. Die bekanntesten Mikroskopietechniken der lokalisationsbasierten Superauflösungsmikroskopie sind photo-activated localization microscopy (PALM) und stochastic optical reconstruction microscopy (STORM). Hier wird die Umschaltung zwischen Dunkel- und Hellzustand mithilfe photophysikalischer oder photochemischer Prozesse durchgeführt. Eine kürzlich eingeführte Methode der Superauflösungsmikroskopie namens DNA-PAINT (deoxyribonucleic acid - point accumulation for imaging in nanoscale topography) basiert auf der DNA-DNA Wechselwirkung. Im Vergleich zu STORM oder PALM wechseln die Fluoreszenzmoleküle nicht zwischen dem dunklen und dem hellen Zustand. Das sogenannte “Blinken“ in DNA-PAINT wird durch transiente Hybridisierung kurzer fluoreszierender DNA Stränge (Imager) an ihre Ziele erzeugt. Die Arbeiten in dieser Dissertation konzentriert sich auf drei unterschiedliche Fortschritte im technologischen Aspekt der Superauflösungsmikroskopie. Sonden Im ersten Projekt dieser Arbeit zeige ich die Kombination von Einzelmolekül-Förster-Resonanzenergietransfer (englisch Förster resonance energy transfer (FRET)) mit DNA-PAINT Mikroskopie, um einige aktuelle Einschränkungen der DNA basierten Superauflösungsmikroskopie zu überwinden. Ich evaluiere das neuartige Sondendesign mithilfe von in vitro Experimenten mit DNA nanostructure und zeige die Leistungsfähigkeit der FRET-basierten Sonden im zellulären Kontext. Hardware Im zweiten Projekt beschreibe ich eine kosteneffiziente Mikroskop-Plattform für Einzelmolekülstudien, die um eine Größenordnung erschwinglicher ist und dennoch eine leistungsstarke Abbildungsfähigkeit bietet. Unter Verwendung von zweidimensionalen (2D) und dreidimensionalen (3D) in vitro Superauflösungsexperimenten von DNA Nanostrukturen bewerte ich die Leistung der Mikroskopie-Plattform. Schließlich zeige ich exemplarische Experimente für die zelluläre Bildgebung in mehreren Farben. Software Im letzten Projekt stelle ich ein Softwarepaket vor, das zur Unterstützung der Analyse von Daten in Superauflösungsmikroskopie entwickelt wurde. Es basiert auf dem Konzept des tiefen Lernens (englisch deep learning) mithilfe von künstlichen neuronalen Netzen und wurde entwickelt, um die Klassifikation von nanoskaligen Mustern zu automatisieren, die in superaufgelösten Bildern zu finden sind. Ich evaluiere die Leistung des Softwarepakets anhand von in vitro Superauflösungsexperimenten von DNA Nanostrukturen sowie von in Zellproben

Optimierung der kardialen Programmierung von Stammzellen und der Reifung in vitro generierter Kardiomyozyten

Herz-Kreislauf-Erkrankungen sind mit 17,9 Mio. Sterbefällen pro Jahr die Haupttodesursache in der westlichen Welt. Stammzellderivierte Kardiomyozyten bieten hier neue Möglichkeiten zur Verbesserung der kardialen Regeneration. Die vorliegende Habilitationsschrift beschäftigt sich mit der Optimierung der kardialen Stammzellprogrammierung mit dem Ziel der Herstellung reifer kardialer Zelltypen für Zellersatztherapie und in vitro Anwendungen

Special oils for halal and safe cosmetics

Three types of non conventional oils were extracted, analyzed and tested for toxicity. Date palm kernel oil (DPKO), mango kernel oil (MKO) and Ramputan seed oil (RSO). Oil content for tow cultivars of dates Deglect Noor and Moshkan was 9.67% and 7.30%, respectively. The three varieties of mango were found to contain about 10% oil in average. The red yellow types of Ramputan were found to have 11 and 14% oil, respectively. The phenolic compounds in DPKO, MKO and RSO were 0.98, 0.88 and 0.78 mg/ml Gallic acid equivalent, respectively. Oils were analyzed for their fatty acid composition and they are rich in oleic acid C18:1 and showed the presence of (dodecanoic acid) lauric acid C12:0, which reported to appear some antimicrobial activities. All extracted oils, DPKO, MKO and RSO showed no toxic effect using prime shrimp bioassay. Since these oils are stable, melt at skin temperature, have good lubricity and are great source of essential fatty acids; they could be used as highly moisturizing, cleansing and nourishing oils because of high oleic acid content. They are ideal for use in such halal cosmetics such as Science, Engineering and Technology 75 skin care and massage, hair-care, soap and shampoo products