Pages
January 01, 2015
-
Date:11MondayMay 202014ThursdayMay 2020Lecture
Conference on Representation Theory and Algebraic Analysis
More information Time All dayTitle in honor of Joseph Berstein’s 75th birthday.Organizer Department of MathematicsHomepage Contact -
Date:11MondayMay 2020Colloquia
Chemistry Colloquium
More information Time 11:00 - 12:15Title The Macromolecular Structure of Mucus, Our Bodies’ First Line of Defense Against PathogensLocation https://weizmann.zoom.us/j/92049901272Lecturer Prof. Debbie Fass
WIS Department of Structural BiologyOrganizer Faculty of ChemistryContact Abstract Show 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.
______________________________________________________
* cell-surface, rope-like structures that beat in coordinated waves
-
Date:12TuesdayMay 2020Lecture
Using small molecules to study translational control by eIF1A
More information Time 10:00 - 10:45Location Nella and Leon Benoziyo Building for Biological SciencesLecturer Daniel Hayat
Members - Dept. of Biomolecular Sciences-WISOrganizer Department of Biomolecular SciencesContact Abstract Show 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. -
Date:12TuesdayMay 2020Lecture
TBA
More information Time 10:00 - 10:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Allon Klein Organizer Department of Molecular Cell BiologyContact -
Date:12TuesdayMay 2020Lecture
From sensory perception to decision making in bats
More information Time 12:30 - 12:30Lecturer Prof. Yossi Yovel
Faculty of Life Sciences Tel Aviv UniversityOrganizer Department of Brain SciencesContact -
Date:12TuesdayMay 2020Academic Events
Scientific Council meeting
More information Time 14:00 - 16:00Location The David Lopatie Conference CentreContact -
Date:13WednesdayMay 2020Lecture
Developmental Club Series 2019-20
More information Time 10:00 - 10:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Efrat Shema Organizer Department of Molecular GeneticsContact -
Date:14ThursdayMay 2020Colloquia
TBA
More information Time 11:15 - 12:30Location Edna and K.B. Weissman Building of Physical SciencesLecturer Rolf Kuiper
University of Tubingen, GermnayOrganizer Faculty of PhysicsContact Abstract Show full text abstract about TBA ...» TBA -
Date:17SundayMay 2020Conference
POSTPONED: Frontiers in Immunology (EFIS onTour)
More information Time 08:00 - 08:00Location The David Lopatie Conference CentreChairperson Steffen JungOrganizer Department of Systems Immunology -
Date:17SundayMay 2020Lecture
Zoom Lecture: The fascinating frictional properties of layered materials: Insights from atomistic modeling
More information Time 11:00 - 12:00Lecturer Prof. Michael Urbakh
School of Chemistry, Tel Aviv UniversityOrganizer Department of Molecular Chemistry and Materials ScienceContact Abstract Show 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. -
Date:19TuesdayMay 2020Lecture
Resistance Mechanisms of Salmonella Typhimurium to Antimicrobial Peptides
More information Time 10:00 - 10:45Location Nella and Leon Benoziyo Building for Biological SciencesLecturer Gal Kapach
Members - Dept. of Biomolecular Sciences-WISOrganizer Department of Biomolecular SciencesContact Abstract Show 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.
-
Date:19TuesdayMay 2020Lecture
TBA
More information Time 10:00 - 10:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Itai Yanai Organizer Department of Molecular Cell BiologyContact -
Date:19TuesdayMay 2020Lecture
Prof. Yohai Kaspi - How does the climate system work?
More information Time 12:00 - 12:00Title How does the climate system work?Location Dolfi and Lola Ebner AuditoriumLecturer Prof. Yohai Kaspi Organizer Communications and Spokesperson DepartmentHomepage Contact -
Date:19TuesdayMay 2020Lecture
Individual differences in decision-making under uncertainty: a neuroeconomic approach
More information Time 12:30 - 12:30Lecturer Prof. Ifat Levy
Decision Neuroscience Lab Yale School of MedicineOrganizer Department of Brain SciencesContact Abstract Show 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. -
Date:20WednesdayMay 2020Lecture
Developmental Club Series 2019-20
More information Time 10:00 - 10:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Yonatan Stelzer Organizer Department of Molecular GeneticsContact -
Date:24SundayMay 2020Lecture
Departmental Seminar by Daria Amiad-Pavlov
More information Time 13:00 - 14:00Organizer Department of Molecular GeneticsContact -
Date:25MondayMay 2020Colloquia
Chemistry Colloquium
More information Time 11:00 - 12:15Title On the nature of cellular contractilityLocation https://weizmann.zoom.us/j/93163029720Lecturer Prof. Eran Bouchbinder
WIS Department of Chemical and Biological PhysicsOrganizer Faculty of ChemistryHomepage Contact -
Date:25MondayMay 2020Lecture
POSTPONED: Braginsky Center for the interface between the Science and the Humanities
More information Time 14:00 - 15:00Location Dolfi and Lola Ebner AuditoriumLecturer Prof. Menachem Fisch Organizer Braginsky Center for the Interface between Science and the HumanitiesContact -
Date:26TuesdayMay 2020Lecture
To be announced
More information Time 09:00 - 10:00Title Stem Cells, Regeneration and Aging Breakfast SeminarLocation Max and Lillian Candiotty BuildingOrganizer Department of Immunology and Regenerative BiologyContact -
Date:26TuesdayMay 2020Lecture
Computational design of enzyme repertoires
More information Time 10:00 - 10:45Location Nella and Leon Benoziyo Building for Biological SciencesLecturer Rosalie Lipsh-Sokolik
Members - Dept. of Biomolecular Sciences-WISOrganizer Department of Biomolecular SciencesContact Abstract Show 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.
