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January 01, 2015

  • Date:11MondayMay 202014ThursdayMay 2020

    Conference on Representation Theory and Algebraic Analysis

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    Time
    All day
    Title
    in honor of Joseph Berstein’s 75th birthday.
    Organizer
    Department of Mathematics
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    Lecture
  • Date:11MondayMay 2020

    Chemistry Colloquium

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    Time
    11:00 - 12:15
    Title
    The Macromolecular Structure of Mucus, Our Bodies’ First Line of Defense Against Pathogens
    Location
    https://weizmann.zoom.us/j/92049901272
    LecturerProf. Debbie Fass
    WIS Department of Structural Biology
    Organizer
    Faculty of Chemistry
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    AbstractShow full text abstract about Respiratory viruses such as coronavirus spread from person t...»
    Respiratory viruses such as coronavirus spread from person to person through droplets of saliva or mucus. Face masks decrease the dissemination of such droplets and thereby minimize viral propagation from someone who may be contagious. Mucus did not evolve, though, to help pathogens spread. Quite the opposite.
    Mucus arose early in the evolution of multicellular animals to exclude undesirable bacteria from body tissues, a primitive type of immunity. The cooperation between cilia* and mucus also helped prevent aquatic organisms from being smothered by sediments and enabled them to clean or collect particulate matter from their exteriors. Producing mucus was likely a prerequisite for evolution of the gut and of the types of respiratory organs necessary for terrestrial life. Today, mucus protects the large, exposed interior surfaces of our respiratory and gastrointestinal tracts from bacteria, viruses, parasites, and chemical/physical hazards.
    But what material is mucus? Mucus is a hydrogel made of heavily glycosylated protein molecules called “mucins,” each of which is nearly 3 megadaltons in size. Individual giant mucin molecules are disulfide bonded to one another, generating an extended mesh. Using cryo-electron microscopy and X-ray crystallography, we have discovered the three-dimensional structure of mucins and gained insight into the mechanism by which they assemble step-wise into hydrogels.
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    * cell-surface, rope-like structures that beat in coordinated waves

    Colloquia
  • Date:12TuesdayMay 2020

    Using small molecules to study translational control by eIF1A

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    Time
    10:00 - 10:45
    Location
    Nella and Leon Benoziyo Building for Biological Sciences
    LecturerDaniel Hayat
    Members - Dept. of Biomolecular Sciences-WIS
    Organizer
    Department of Biomolecular Sciences
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    AbstractShow full text abstract about Eukaryotic initiation factor 1A (eIF1A) is a key translation...»
    Eukaryotic initiation factor 1A (eIF1A) is a key translation initiation regulatory factor yet little is known about its exact role in the translation process of mammalian cells. Previous work in our lab have shown that eIF1A interacts with ribosomal proteins RPS3 and RPS10 and these interactions are disrupted by eIF1A cancer-associated mutants. As the activities of eIF1A are critically dependent on its ability to bind the ribosome, we targeted eIF1A-RPS10 complex to identify eIF1A inhibitors, using high throughput drug screen. We found 21 eIF1A inhibitors which affected eIF1A known translational roles and divided them to groups according to the protein they bind. Several inhibitors which can differentiate between eIF1A known functions were identified and inhibitor 1Ai-5662 showed dramatic affect in decreasing uveal melanoma cells viability. Our results show the benefits of using small molecules research approach.
    Lecture
  • Date:12TuesdayMay 2020

    TBA

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    Time
    10:00 - 10:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Allon Klein
    Organizer
    Department of Molecular Cell Biology
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    Lecture
  • Date:12TuesdayMay 2020

    From sensory perception to decision making in bats

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    Time
    12:30 - 12:30
    LecturerProf. Yossi Yovel
    Faculty of Life Sciences Tel Aviv University
    Organizer
    Department of Brain Sciences
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    Lecture
  • Date:12TuesdayMay 2020

    Scientific Council meeting

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    Time
    14:00 - 16:00
    Location
    The David Lopatie Conference Centre
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    Academic Events
  • Date:13WednesdayMay 2020

    Developmental Club Series 2019-20

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    Time
    10:00 - 10:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Efrat Shema
    Organizer
    Department of Molecular Genetics
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    Lecture
  • Date:14ThursdayMay 2020

    TBA

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    Time
    11:15 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerRolf Kuiper
    University of Tubingen, Germnay
    Organizer
    Faculty of Physics
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    AbstractShow full text abstract about TBA ...»
    TBA
    Colloquia
  • Date:17SundayMay 2020

    POSTPONED: Frontiers in Immunology (EFIS onTour)

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    Time
    08:00 - 08:00
    Location
    The David Lopatie Conference Centre
    Chairperson
    Steffen Jung
    Organizer
    Department of Systems Immunology
    Conference
  • Date:17SundayMay 2020

    Zoom Lecture: The fascinating frictional properties of layered materials: Insights from atomistic modeling

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    Time
    11:00 - 12:00
    LecturerProf. Michael Urbakh
    School of Chemistry, Tel Aviv University
    Organizer
    Department of Molecular Chemistry and Materials Science
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    AbstractShow full text abstract about Zoom Lecture: : https://weizmann.zoom.us/j/91487772614 ...»
    Zoom Lecture: : https://weizmann.zoom.us/j/91487772614

    Structural superlubricity may provide a viable route to the reduction of friction and wear. In this talk I will present results of fully atomistic numerical simulations of static and dynamical properties of graphite/hexagonal boron nitride (h-BN) heterojunctions, performed adopting a recently developed inter-layer potential. We found that structural superlubricity at interfaces between graphite and h-BN persists even for the aligned contacts sustaining external loads. A negative friction coefficient, where friction is reduced upon increasing normal load, is predicted. It is demonstrated that further control over the physical properties of 2D layered materials can be gained via tuning the aspect-ratio of nanoribbons. The sliding dynamics of the edge-pulled nanoribbons is found to be determined by the interplay between in-plane ribbon elasticity and interfacial lattice mismatch. Our results are expected to be of general nature and should be applicable to other van der Waals heterostructures.
    Lecture
  • Date:19TuesdayMay 2020

    Resistance Mechanisms of Salmonella Typhimurium to Antimicrobial Peptides

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    Time
    10:00 - 10:45
    Location
    Nella and Leon Benoziyo Building for Biological Sciences
    LecturerGal Kapach
    Members - Dept. of Biomolecular Sciences-WIS
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Bacterial resistance to antibiotics is a major concern world...»
    Bacterial resistance to antibiotics is a major concern worldwide, leading to an extensive search for alternative drugs. Promising candidates are antimicrobial peptides, innate immunity molecules, which were shown to be highly efficient against multidrug resistant bacteria. Therefore, it is essential to study bacterial resistance mechanisms against them. In Salmonella Typhimurium (S.Typhimurium), a pathogenic bacterium that causes inflammation of the gastrointestinal tract, resistance to antimicrobial peptide is mainly mediated by surface modifications. These reduce the molecular interactions between the bacterial surface and the peptides. Searching for new resistance mechanisms to antimicrobial peptides, we revealed two novel strategies that evolved in a S. Typhimurium resistant line. One involves mutations in the AcrAB-TolC efflux pump and the second is acquired by the loss of the periplasmic chaperone Skp. Our data provide a deeper understanding on the role of the AcrAB-TolC system and Skp in S. Typhimurium.

    Lecture
  • Date:19TuesdayMay 2020

    TBA

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    Time
    10:00 - 10:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Itai Yanai
    Organizer
    Department of Molecular Cell Biology
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    Lecture
  • Date:19TuesdayMay 2020

    Prof. Yohai Kaspi - How does the climate system work?

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    Time
    12:00 - 12:00
    Title
    How does the climate system work?
    Location
    Dolfi and Lola Ebner Auditorium
    LecturerProf. Yohai Kaspi
    Organizer
    Communications and Spokesperson Department
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    Lecture
  • Date:19TuesdayMay 2020

    Individual differences in decision-making under uncertainty: a neuroeconomic approach

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    Time
    12:30 - 12:30
    LecturerProf. Ifat Levy
    Decision Neuroscience Lab Yale School of Medicine
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Individuals differ substantially in their attitudes to uncer...»
    Individuals differ substantially in their attitudes to uncertainty: some avoid is at all costs, while others are tolerant of, or even seek, uncertainty. These differences are important, because uncertainty is everywhere – how we cope with uncertainty can have significant implications for our mental health and quality of life. I will describe a series of studies in which we characterize individual differences in decision-making under uncertainty, and use these characterizations to study the neural mechanisms of decision-making under uncertainty and variations in these mechanisms in mental illness.
    Lecture
  • Date:20WednesdayMay 2020

    Developmental Club Series 2019-20

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    Time
    10:00 - 10:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Yonatan Stelzer
    Organizer
    Department of Molecular Genetics
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    Lecture
  • Date:24SundayMay 2020

    Departmental Seminar by Daria Amiad-Pavlov

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    Time
    13:00 - 14:00
    Organizer
    Department of Molecular Genetics
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    Lecture
  • Date:25MondayMay 2020

    Chemistry Colloquium

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    Time
    11:00 - 12:15
    Title
    On the nature of cellular contractility
    Location
    https://weizmann.zoom.us/j/93163029720
    LecturerProf. Eran Bouchbinder
    WIS Department of Chemical and Biological Physics
    Organizer
    Faculty of Chemistry
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    Colloquia
  • Date:25MondayMay 2020

    POSTPONED: Braginsky Center for the interface between the Science and the Humanities

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    Time
    14:00 - 15:00
    Location
    Dolfi and Lola Ebner Auditorium
    LecturerProf. Menachem Fisch
    Organizer
    Braginsky Center for the Interface between Science and the Humanities
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    Lecture
  • Date:26TuesdayMay 2020

    To be announced

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    Time
    09:00 - 10:00
    Title
    Stem Cells, Regeneration and Aging Breakfast Seminar
    Location
    Max and Lillian Candiotty Building
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    Lecture
  • Date:26TuesdayMay 2020

    Computational design of enzyme repertoires

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    Time
    10:00 - 10:45
    Location
    Nella and Leon Benoziyo Building for Biological Sciences
    LecturerRosalie Lipsh-Sokolik
    Members - Dept. of Biomolecular Sciences-WIS
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Antibodies are produced to target any antigen using a fini...»
    Antibodies
    are produced to target any antigen using a finite set of gene fragments generating a huge diversity (>1010)
    distinct structures. In contrast, we are unaware of a system that can produce analogous diversity in enzymes. Inspired by antibody repertoires,
    I have developed the first strategy to design, synthesise, and experimentally
    test repertoires comprising millions of enzymes. Using evolution-guided atomistic design
    simulations, I designed thousands of protein fragments that exhibited
    high structure and sequence diversity, including within the active-site pocket, which can be genetically assembled into full-length enzymes. I also developed an ML-based algorithm to select a subset of the designed fragments that would give rise to stable
    and active proteins. Applied to a family of xylanases (sophisticated enzymes which are
    critical in biomass degradation) I designed a repertoire comprising a million enzymes at a cost of 0.3¢
    per enzyme. Screening with an activity-based probe revealed thousands of functional xylanases based on nearly 1,000 unique backbones. Advanced machine-learning methods uncovered important elements that discriminate active from inactive designs, enabling us
    to design even more effective enzyme repertoires targeting, in principle, any desired substrate. Thus, enzyme repertoire design will enable a new generation of highly efficient and selective enzymes, while teaching us essential rules in biomolecular design.
    Lecture

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