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April 30, 2015
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Date:28SundayMay 2017Lecture
To be announced
More information Time 13:00 - 13:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Dr. Alina Kolpakova
Eli Arama's group, Dept. of Molecular Genetics, WISOrganizer Department of Molecular GeneticsContact -
Date:28SundayMay 2017Cultural Events
Afternoon Music the Moovie - Where is Elle-Kari and what happened to Noriko-San ?
More information Time 16:30 - 17:30Location Michael Sela AuditoriumContact -
Date:29MondayMay 2017Colloquia
"Solving hard computational problems with coupled lasers"
More information Time 11:00 - 12:15Location Gerhard M.J. Schmidt Lecture HallLecturer Prof. Nir Davidson
Department of Physics of Complex Systems WISOrganizer Faculty of ChemistryContact -
Date:29MondayMay 2017Lecture
Combination therapies and drug resistance in Triple Negative Breast Cancer
More information Time 14:00 - 15:00Title Cancer Research ClubLocation Max and Lillian Candiotty BuildingLecturer Prof. Sima Lev
Department of Molecular Cell Biology, Weizmann InstituteOrganizer Department of Immunology and Regenerative BiologyContact Abstract Show full text abstract about Triple negative breast cancer (TNBC) is a highly aggressive,...» Triple negative breast cancer (TNBC) is a highly aggressive, heterogeneous disease with high rates of metastasis and poor prognosis. Currently, there are no targeted therapies for TNBC and adjuvant chemotherapy is the mainstay treatment. Identification of molecular targets and potent combination therapies for TNBC is a major challenge of extensive biomedical research and our own studies. Given that drug resistance is a critical clinical problem, a drug combination that could overcome drug resistance could offer a promising therapeutic opportunity. We have recently identified potent combination therapies for TNBC which are not only potent but could also overcome drug resistance and further defined the molecular mechanisms underlying their therapeutic benefit. -
Date:01ThursdayJune 2017Lecture
Through the looking glass: The red queens race and other tales of immunovirology
More information Time 11:15 - 11:15Title Virology ClubLocation Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Dr. Leslie Lobel Organizer Department of Molecular GeneticsContact -
Date:04SundayJune 201705MondayJune 2017Conference
From Molecular beams to photosynthesis-Conference in honor of Ron Naaman
More information Time 08:00 - 08:00Location The David Lopatie Conference CentreChairperson David CahenHomepage -
Date:04SundayJune 2017Lecture
Metabolome analysis:Finding a Needle in a Haystack
More information Time 09:00 - 10:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Dr. Sergey Malitsky Organizer Department of Life Sciences Core FacilitiesContact -
Date:04SundayJune 2017Lecture
Deciphering the wastewater resistome and its potential impact on downstream environments
More information Time 11:00 - 11:00Location Sussman Family Building for Environmental SciencesLecturer Eddie Cytryn, PhD
Institute of Soil, Water and Environmental Sciences Volcani Center, Agricultural Research OrganizationOrganizer Department of Earth and Planetary SciencesContact Abstract Show full text abstract about Wastewater treatment plants consolidate high loads of fecal ...» Wastewater treatment plants consolidate high loads of fecal and environmental bacteria and residual concentrations of antibiotics and consequentially, effluents released from these facilities may contribute to antibiotic resistance in downstream ecosystems. This is especially relevant in arid and semi-arid environments, where treated wastewater (TWW) is used for irrigation. The goal of this study was to pinpoint key antibiotic resistance genes (ARGs) in wastewater effluents and to determine the impact of TWW irrigation on antibiotic resistance in terrestrial and food-associated microbiomes. The diversity and abundance of ARGs was evaluated in wastewater effluents, in TWW -irrigated soils and in crops irrigated with TWW using state of the art molecular, genomic and bioinformatic analyses. Three specific methods were applied: (A) a novel high-throughput amplicon sequencing methodology that specifically targeted ARGs associated with integron gene cassettes in effluents from 12 wastewater treatment facilities across Europe and in pristine vs. wastewater effluent-saturated soil; (B) quantitative PCR that assessed the abundance of selected ARGs along freshwater- and TWW-irrigated, water-soil-crop continuum; and (C) comparative in-silico-based analyses of human gut, wastewater and soil metagenomes to determine specific associations between wastewater and soil resistomes. Our results reveal that wastewater effluents contain a diverse array of ARGs, and that specific ARGs and class 1 integrons (mobile genetic elements that often harbor ARGs) are profuse and strongly associated with wastewater effluents. In contrast we found that other ARGs that are ubiquitous to soil regardless of TWW irrigation suggesting that these elements are common in environmental microbiomes. Collectively, the study indicates the distribution of ARGs in the environment is highly complex and is impacted by both natural and anthropogenic factors, and that while the impact of wastewater-derived ARGs in TWW-irrigated soils is limited, there is evidence that plasmid- and integron-associated ARGs are disseminated to soil microbiomes.
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Date:04SundayJune 2017Lecture
Aggregation of a bacterial extracellular matrix protein
More information Time 11:00 - 12:00Location Perlman Chemical Sciences BuildingLecturer Dr. Liraz Chai
Institute of Chemistry, HUJIOrganizer Department of Molecular Chemistry and Materials ScienceContact -
Date:04SundayJune 2017Lecture
To be announced
More information Time 13:00 - 13:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Inna Averbukh
Naama Barkai's and Benny Shilo's groups, Dept. of Molecular Genetics, WISOrganizer Department of Molecular GeneticsContact -
Date:04SundayJune 2017Lecture
RECYCLE THE BRAIN: Glutamine repeats (polyQ) shape cell recycling in health and neurodegeneration
More information Time 14:00 - 15:00Location Max and Lillian Candiotty BuildingLecturer Dr. Avraham Ashkenazi
Cambridge Institute for Medical Research, University of CambridgeOrganizer Department of Immunology and Regenerative Biology , Department of Biomolecular SciencesContact -
Date:04SundayJune 2017Lecture
A key role of c-Abl tyrosine kinase in metabolic physiology
More information Time 15:00 - 16:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Yosef Shaul
Department of Molecular GeneticsContact -
Date:04SundayJune 2017Lecture
When Lithium Travels in Solid State Disorder
More information Time 15:00 - 16:00Location Perlman Chemical Sciences BuildingLecturer Prof. Jennifer Rupp
Dept. Materials Science, MITOrganizer Department of Molecular Chemistry and Materials ScienceContact -
Date:05MondayJune 2017Lecture
AMO Special Seminar
More information Time 11:00 - 11:00Title Photon Processing in the Frequency DomainLocation Edna and K.B. Weissman Building of Physical SciencesLecturer Prof. Alexander Gaeta
Columbia UniversityOrganizer Department of Physics of Complex SystemsContact Abstract Show full text abstract about Nonlinear optical processes play a central role in many quan...» Nonlinear optical processes play a central role in many quantum information devices. I will describe our recent work in which we explore the use of quantum frequency conversion based on four-wave mixing to process photons with high quantum efficiency without adding noise. I will describe how we use this conversion process to create a single-photon Ramsey interferometer, temporally magnify photon wavepackets, and perform frequency multiplexing to create a quasi-deterministic photon source. -
Date:06TuesdayJune 2017Lecture
"Mechanisms of bone surface sensing by osteoclasts"
More information Time 09:00 - 09:00Location Helen and Milton A. Kimmelman BuildingLecturer Michal Shemesh
WIS Departments of Structural Biology and Molecular Cell BiologyOrganizer Department of Chemical and Structural BiologyContact -
Date:06TuesdayJune 2017Lecture
Regulating the 20S proteasome degradation pathway
More information Time 10:00 - 10:30Location Wolfson Building for Biological ResearchLecturer Dr. Maya Olshina
Members - Dept. of Biomolecular Sciences-WISOrganizer Department of Biomolecular SciencesContact Abstract Show full text abstract about The protein degradation machinery in cells plays a critical ...» The protein degradation machinery in cells plays a critical role in the maintenance of homeostasis, preventing the accumulation of damaged or misfolded proteins and controlling the levels of regulatory proteins. The predominant degradation pathway involves the ubiquitin-dependent 26S proteasome, however recent evidence has identified an alternate ubiquitin-independent pathway involving only the 20S core particle of the proteasome. The regulatory mechanisms controlling its function are poorly understood, and only a small number of regulators have been identified. Using a combination of bioinformatics, structural and in vivo analyses, as well as native mass spectrometry techniques, new 20S proteasome regulatory proteins were identified, hinting towards an as yet undescribed regulatory network of the 20S proteasome. -
Date:06TuesdayJune 2017Lecture
Computational Design of Novel Enzymes Guided By Evolutionary Data
More information Time 10:30 - 10:00Location Wolfson Building for Biological ResearchLecturer Gideon Lapidoth
Members - Dept. of Biomolecular Sciences-WISOrganizer Department of Biomolecular SciencesContact Abstract Show full text abstract about The ability to computationally design efficient, specific ...» The ability to computationally design efficient,
specific enzymes is a rigorous test of our understanding of the principles of catalysis and molecular recognition.
Successful designs have to date shown several limitations:
they only targeted simple reactions, involving two to three catalytic residues with low efficiencies and selectivities, and impaired stability. We developed a new algorithm using Rosetta to combine compatible backbone fragments from natural enzymes of the
same enzyme superfamily to generate novel conformations. The designs’ sequences are then optimized, guided by sequence conservation data to improve stability and expressibility. We used the algorithm to design novel TIM barrel fold enzymes belonging to the
GH10 family capable of hydrolyzing xylan, an abundant plant polysaccharide, with Kcat/Km values similar to those of natural xylanases. The designed enzyme conformations differ from one another and from any other known natural xylanase conformations and have
different substrate specificities.
The algorithm is completely automated and can be
applied to other enzymes of modular fold to efficiently and broadly explore the potential selectivities of the superfamily. -
Date:06TuesdayJune 2017Lecture
Andor Dragonfly - High speed confocal imaging Platform
More information Time 10:30 - 11:30Location Max and Lillian Candiotty BuildingLecturer Dr. Bruno Combettes
Business Development Manager ANDOR TechnologyOrganizer Department of Life Sciences Core FacilitiesContact -
Date:06TuesdayJune 2017Colloquia
Life Sciences Colloquium
More information Time 11:00 - 12:00Title A chemo-evolutionary basis for polypharmacologyLocation Gerhard M.J. Schmidt Lecture HallLecturer Prof. Brian K. Shoichet
UCSFHomepage Contact -
Date:06TuesdayJune 2017Lecture
Processing of Chemical Signals by Enzymatic and Organic Reactions
More information Time 11:00 - 12:00Location Helen and Milton A. Kimmelman BuildingLecturer Dr. Sergey Semenov
Dept. of Chemistry and Chemical Biology Harvard UniversityOrganizer Department of Molecular Chemistry and Materials ScienceContact
