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January 28, 2016

  • Date:14MondayMarch 2016

    Hydrodynamics of a small swimming robot

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    Time
    14:15 - 14:15
    Location
    Dannie N. Heineman Laboratory
    LecturerAryesh Mukherjee, WIS
    Organizer
    Department of Physics of Complex Systems
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    AbstractShow full text abstract about Fish and insects live in fluid environments and use numerous...»
    Fish and insects live in fluid environments and use numerous techniques to survive in a hostile environment. Small insects beat their wings many times a second, and can couple fluid vortices to the elasticity of their wings to generate optimal flight modes within short time scales. Motivated by such observations, we borrowed such passive techniques to design a small swimming robot, equipped with a flexible tail. The robot is capable of swimming at high speeds, but more importantly its thrust is maximized at a frequency where the elasticity of the tail couples strongly with the fluid environment, beyond just added mass effects. In this talk we will discuss the physical principles that govern the kinematics of this robotic device.
    Lecture
  • Date:14MondayMarch 2016

    Hydrodynamics of a small swimming robot

    More information
    Time
    14:15 - 14:15
    Location
    Dannie N. Heineman Laboratory
    LecturerAryesh Mukherjee, WIS
    Organizer
    Department of Physics of Complex Systems
    Contact
    AbstractShow full text abstract about Fish and insects live in fluid environments and use numerous...»
    Fish and insects live in fluid environments and use numerous techniques to survive in a hostile environment. Small insects beat their wings many times a second, and can couple fluid vortices to the elasticity of their wings to generate optimal flight modes within short time scales. Motivated by such observations, we borrowed such passive techniques to design a small swimming robot, equipped with a flexible tail. The robot is capable of swimming at high speeds, but more importantly its thrust is maximized at a frequency where the elasticity of the tail couples strongly with the fluid environment, beyond just added mass effects. In this talk we will discuss the physical principles that govern the kinematics of this robotic device.
    Lecture
  • Date:15TuesdayMarch 2016

    Measuring enzymatic activity in vitro and in vivo

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    Time
    10:00 - 10:30
    Location
    Wolfson Building for Biological Research
    LecturerDr. Agnes Zotter
    Dept. of Biomolecular Sciences-WIS
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Live-cell imaging allows the investigation of dynamic proces...»
    Live-cell imaging allows the investigation of dynamic processes inside living cells, where macromolecular crowding is proposed to influence various properties of proteins. We have previously demonstrated how Förster Resonance Energy Transfer (FRET) can be used to determine binding dynamics between proteins in living cells. Here we follow catalysis within HeLa cells in real time, to determine ezymatic reaction parameters (Km, kcat) from single cell measurements and to relate them to their values in vitro under different conditions. Measurement protocols were developed for two enzymes, fluorescently labeled TEM1 β-lactamase and β-galactosidase degrading fluorogenic substrates. The enzymatic reactions were initiated by microinjection of the substrate and monitored by FRET and/or detecting the intensity change of the cleaved molecule. Our experimental setup enables us to determine enzymatic constants inside the cell. This allows determining cell-to-cell variability in catalytic efficiency. Moreover, we used mutations that affect Km and kcat to see how in vitro changes are manifested in live cells. In addition to the in vivo work, we investigate the enzymatic reaction in vitro and in HeLa cell extracts. For data analysis of the single progress curves three models were compared, (i) analytic approximation of the Lambert function, (ii) the Lambert W-function including an exponential fit and (iii) computer simulation. Our results show that there is a big difference in the catalytic efficiency in vitro compared to in vivo data, what explanation needs further studies (cellular crowding, pH, in-cell redox conditions, etc.).
    Lecture
  • Date:15TuesdayMarch 2016

    Designer cellulosomes: Nano-biotechnological building-blocks toward significant economical and environmental goals

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    Time
    10:30 - 11:00
    Location
    Wolfson Building for Biological Research
    LecturerDr. Johanna Stern
    Dept. of Biomolecular Sciences
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Degradation of the plant cell wall is of major interest in a...»
    Degradation of the plant cell wall is of major interest in a wide variety of fields: for ecological concerns, for renewability of energy and advanced biotechnology. However, this process is extremely difficult and only a relatively small number of microorganisms have evolved to utilize it as a carbon source. Some anaerobic bacteria produce an extracellular multi-enzyme complex named the cellulosome, which is considered an exceptionally efficient plant biomass-degrading system. The Lego-like nature of the cellulosomal subunits enables the mixing and matching of different cohesin-dockerin pairs to control the composition and architecture of an artificial cellulosome-like system, referred to as designer cellulosomes. Here, we explored the option of expanding the designer cellulosome concept by two major approaches: by extending the diversity of the enzymatic repertoire and by creating novel types of chimaeric scaffoldins that resulted in more elaborate architectures.

    Lecture
  • Date:15TuesdayMarch 2016

    New molecular defined iron complexes for catalyzed reduction and

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    Time
    11:00 - 12:00
    Location
    Helen and Milton A. Kimmelman Building
    LecturerProf. Christophe Darcel
    University of Rennes
    Organizer
    Department of Molecular Chemistry and Materials Science
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    Lecture
  • Date:15TuesdayMarch 2016

    Stress-Induced Mutation: Evolution, adaptation, and the role of communication

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    Time
    11:15 - 11:15
    Location
    Ullmann Building of Life Sciences
    LecturerProf. Lilach Hadany
    Department of Molecular Biology and Ecology of Plants, Tel Aviv University
    Organizer
    Department of Plant and Environmental Sciences
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    Lecture
  • Date:15TuesdayMarch 2016

    Science Time - Popular Lecture

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    Time
    12:00 - 13:00
    Location
    Dolfi and Lola Ebner Auditorium
    LecturerProf. Nir Davidson
    The butterfly effect chaos and quantum theory meet in the microscopic world
    Organizer
    Communications and Spokesperson Department
    Homepage
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    Lecture
  • Date:15TuesdayMarch 2016

    MCB Student Seminar

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    Time
    12:30 - 13:30
    Title
    Dynamic proteomics of HSV-1 infected cells reveals effects of cellular heterogeneity on viral infection outcome Neuron-glia interactions in Drosophila melanogaster mushroom body development
    Location
    Wolfson Building for Biological Research
    LecturerDr. Nir Drayman & Neta Kollet
    Organizer
    Department of Molecular Cell Biology
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    Lecture
  • Date:15TuesdayMarch 2016

    Dissecting the role of horizontal cells for retinal processing

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    Time
    12:30 - 12:30
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerDr. Karin Dedek
    Neurosensorics University of Oldenburg, Germany
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about In the mammalian retina, visual information is transduced in...»
    In the mammalian retina, visual information is transduced into electrical signals by photoreceptors. These signals are transmitted from photoreceptors to bipolar cells and on to ganglion cells, which inform the brain about contrast, form, color, object motion and other features of the visual world. On its route through the retina, visual information is modulated by inhibitory networks formed by horizontal and amacrine cells. Here, I focus on horizontal cells. At so-called triad synapses, these interneurons receive glutamatergic input from photoreceptors and provide feedback and feedforward signals to photoreceptors and bipolar cells, respectively. In recent years, we used different techniques to analyze the role of horizontal cells: we 1) deleted electrical synapses between horizontal cells, 2) ablated the entire horizontal cell population, and 3) selectively silenced horizontal cells by input deprivation. From these studies we gathered that horizontal cells are important for the spatial and temporal tuning of ganglion cells and are necessary to maintain the integrity of the first synapse in the visual system.
    Lecture
  • Date:15TuesdayMarch 2016

    "Cryo Microscopies: From detailed macromolecular architecture by cryoEM to whole cells by cryo Soft X-rays Tomography"

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    Time
    14:00 - 14:00
    Location
    Helen and Milton A. Kimmelman Building
    LecturerProf. Jose-Maria Carazo
    National Center of Biotechnology Madrid
    Organizer
    Department of Chemical and Structural Biology
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    Lecture
  • Date:16WednesdayMarch 2016

    Magnetic Resonance Seminar

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    Time
    11:00 - 11:00
    Title
    Studies in Breast and Pancreas MRI
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Noam Nissan
    Departments of Chemical Physics and Biological Regulation Weizmann Institute of Science
    Organizer
    Department of Chemical and Biological Physics
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    Lecture
  • Date:16WednesdayMarch 2016

    In-vivo flux through the mammalian TRC40 (GET) pathway

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    Time
    15:00 - 15:00
    LecturerProf. Blanche Schwappach
    Department of Molecular Biology, University Medical Center Göttingen
    Organizer
    Department of Molecular Genetics
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    Lecture
  • Date:17ThursdayMarch 2016

    Magnetic Resonance Seminar

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    Time
    09:30 - 09:30
    Title
    Biomedical applications with a stray-field NMR scanner
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Uri Nevo, Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University
    Organizer
    Department of Chemical and Biological Physics
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  • Date:17ThursdayMarch 2016

    cancelled

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    Time
    11:15 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    Lecturercancelled
    Organizer
    Faculty of Physics
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    AbstractShow full text abstract about TBA ...»
    TBA
    Colloquia
  • Date:17ThursdayMarch 2016

    Single cell resolution of DC- T cell interactome in the antigen-challenged lymph node

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    Time
    14:00 - 14:30
    Title
    THE OFER LIDER RESEARCH-IN-PROGRESS SEMINAR 2016 IMMUNOLOGY DEPARTMENT
    Location
    Wolfson Building for Biological Research
    LecturerDr. Caterina Curato
    Prof. Steffen Jung’s lab
    Organizer
    Department of Systems Immunology
    Contact
    Lecture
  • Date:17ThursdayMarch 2016

    TCR sequencing reveals the architecture of the T cells compartments

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    Time
    14:30 - 15:00
    Title
    THE OFER LIDER RESEARCH-IN-PROGRESS SEMINAR 2016 IMMUNOLOGY DEPARTMENT
    Location
    Wolfson Building for Biological Research
    LecturerDr. Michal Mark
    Organizer
    Department of Systems Immunology
    Contact
    Lecture
  • Date:17ThursdayMarch 2016

    Life Science Lecture

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    Time
    15:00 - 16:30
    Location
    Dolfi and Lola Ebner Auditorium
    LecturerProf. Maya Schuldiner
    Department of Molecular Genetics
    Contact
    Lecture
  • Date:17ThursdayMarch 2016

    "CAMELOT" The legendary musical in English

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    Time
    20:00 - 22:30
    Location
    Michael Sela Auditorium
    Contact
    Cultural Events
  • Date:19SaturdayMarch 2016

    Ben Ben Baruch - Stand Up

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    Time
    21:00 - 21:00
    Location
    Michael Sela Auditorium
    Contact
    Cultural Events
  • Date:20SundayMarch 2016

    The response of peatland microbial communities to climate change

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    Time
    11:00 - 11:00
    Location
    Sussman Family Building for Environmental Sciences
    LecturerMax Kolton
    School of Biology Georgia Institute of Technology
    Organizer
    Department of Earth and Planetary Sciences
    Contact
    AbstractShow full text abstract about Fears of global climate change and its potential outcomes ha...»
    Fears of global climate change and its potential outcomes have stimulated intensive efforts to update current climate models. Nevertheless, most of the existing models lack inputs specific to peatlands and/or to microorganisms. Peatlands store up to 30% of the world’s soil carbon and contribute up to 30% of atmospheric methane, thus their response to climate change is of special interest. Peatlands are mostly found at northern high latitudes where nutrient poor conditions foster Sphagnum as a keystone plant species. My studies focus on understanding the response of peatland ecosystems to climate change at the Marcell Experimental Forest (MEF) in northern Minnesota, USA. At MEF, the U.S. DOE has created a unique multi-faceted large scale climate manipulation experiment known as SPRUCE (Spruce and Peatland Response Under Climatic and Environmental Change), initiated in June 2014. From June 2014 to June 2015, we evaluated the responses of microbial communities, both in structure and metabolic potential, to 5 soil warming treatments (+0°C; +2.25°C; +4.5°C; +6.75°C; +9°C). Methane flux was correlated with temperature in the treatments, suggesting that increases in soil temperature apparently drive the emission response. However, multiple lines of evidence, including laboratory incubations, indicate that CH4 emission increased due to surface processes and not degradation of deep carbon. Characterization of in situ microbial communities indicated no significant effect of temperature or time on community composition or function. Specifically, the potential activity of extracellular lignin oxidative enzymes showed that one year of soil warming had a limited effect on microbial activity. While the physiology and ecology of Sphagnum have been well-studied, the structure, function and response of their microbiome to climate change is less understood. Sphagnum-associated, nitrogen-fixing bacteria are thought to play a major role in plant functioning and the peatland nitrogen cycle. Therefore, we conducted intensive sampling of the S. magellanicum phyllosphere-associated microbial communities. Our results revealed a significant geographical effect on general and nitrogen-fixing microbial communities. Interestingly, the nitrogen-fixing core-microbiome contained only 2 members, taxonomically affiliated with Nostoc azollae (symbiotic Cyanobacteria) and Methyloferula stellate (an obligate methanotroph). Potentially synergistic interactions between these nitrogen-fixing bacteria not only provide the plant with sufficient nitrogen, but may also reduce methane emission from peatlands. Our observations of evolutionary conserved nitrogen-fixing bacteria among representative peatland sites further knowledge of the benefits of the microbiome to Sphagnum host fitness and to ecosystem function.
    Lecture

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