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November 02, 2015
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Date:10TuesdayNovember 2015Lecture
On the origins of agency
More information Time 10:00 - 11:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Scott Kelso
Florida Atlantic UniversityOrganizer Department of Systems ImmunologyHomepage Contact -
Date:10TuesdayNovember 2015Lecture
A transcriptional program induced by trophic factor withdrawal controls the peripheral nervous system development
More information Time 10:00 - 10:30Location Wolfson Building for Biological ResearchLecturer Dr. Maya Maor Organizer Department of Biomolecular SciencesContact Abstract Show full text abstract about Cell death an axonal elimination govern the peripheral nervo...» Cell death an axonal elimination govern the peripheral nervous system development. These processes have long thought to be controlled by transcriptional programs. However, the nature of these programs remains elusive. Here I performed comprehensive transcriptome analysis of sensory neurons in response to trophic deprivation. Functional analysis of two upregulated transcriptional components, dual phosphatase Dusp16 and the pro-apoptotic protein Puma, revealed unexpectedly opposing roles in axonal elimination both in vitro and in vivo. Additional experiments uncovered both genetic and biochemical interactions between Puma and Dusp16. These results revealed a transcriptional program of regressive and progressive elements, whose balance controls developmental peripheral nervous system wiring through specific subcellular functions. -
Date:10TuesdayNovember 2015Lecture
Trailing membrane protein mRNAs on their way to the membrane in Escherichia coli: the effect of CspE
More information Time 10:30 - 11:00Location Wolfson Building for Biological ResearchLecturer Dr. Daniel Ben-halevy
Dept. of Biological Chemistry-WISOrganizer Department of Biomolecular SciencesContact Abstract Show full text abstract about Previous studies have suggested that mRNAs encoding integral...» Previous studies have suggested that mRNAs encoding integral membrane proteins (MPRs) are delivered to membrane-bound ribosomes, but how they actually target the membrane remains unknown. We have previously proposed that MPRs may be recognized through uracil-rich segments that encode hydrophobic transmembrane helices. Recently we showed that MPRs are specifically recognized by the E. coli protein, CspE, in a translation independent manner. To further investigate the hypothesis of translation-independent targeting of MPRs to membrane-associated ribosomes, we performed a high-throughput analysis of the cellular distribution of mRNAs. The results confirmed that MPRs are overrepresented on the membrane, as expected. Surprisingly, however, the results also showed that MPRs are relatively abundant in the cytosolic, ribosomal-free fraction. We propose that the “free” form of MPRs represents a stage during their targeting to the membrane in a translation-independent manner. Remarkably, we demonstrate that cold shock proteins, which were shown to interact with MPRs, play a role in linking the intriguing subcellular localization of MPRs with their translation into integral membrane proteins. -
Date:10TuesdayNovember 2015Lecture
Stretching boundaries: Rigidity and Flexibility in Microbial Biofilms
More information Time 11:15 - 11:15Location Ullmann Building of Life SciencesLecturer Dr. Ilana Kolodkin-Gal
Department of Molecular Genetics, The Weizmann Institute of ScienceOrganizer Department of Plant and Environmental SciencesContact -
Date:10TuesdayNovember 2015Lecture
Aiming at the sweet spot of disease
More information Time 14:00 - 15:00Location Helen and Milton A. Kimmelman BuildingLecturer Dr. Vered Padler-Karavani
Laboratory of Glycoimmunology Department of Cell Research and Immunology Tel Aviv UniversityOrganizer Department of Chemical and Structural BiologyContact -
Date:10TuesdayNovember 2015Lecture
MCB Student Seminar
More information Time 14:15 - 14:15Title Novel p53 target genes secreted by the liver are involved in non-cell-autonomous regulation Growth dynamics of gut microbiota inferred from single metagenomic samplesLocation Wolfson Building for Biological ResearchLecturer Meital Charni, Tal Korem Organizer Department of Molecular Cell BiologyContact -
Date:10TuesdayNovember 2015Lecture
MCB Student Seminar
More information Time 14:15 - 15:30Title Novel p53 target genes secreted by the liver are involved in non-cell-autonomous regulation Growth dynamics of gut microbiota inferred from single metagenomic samplesLocation Wolfson Building for Biological ResearchLecturer Meital Charni, Tal Korem Organizer Department of Molecular Cell BiologyContact -
Date:12ThursdayNovember 2015Colloquia
Physical computation in animal collectives
More information Time 11:15 - 12:30Location Edna and K.B. Weissman Building of Physical SciencesLecturer Iain D. Couzin
PrincetonOrganizer Faculty of PhysicsContact Abstract Show full text abstract about Understanding how social influence shapes biological process...» Understanding how social influence shapes biological processes is a central challenge in con-temporary science, essential for achieving progress in a variety of fields ranging from the or-ganization and evolution of coordinated collective action among cells, or animals, to the dy-namics of information exchange in human societies. Using an integrated experimental and theoretical approach I will address how, and why, animals exhibit highly-coordinated collective behavior. I will demonstrate new imaging technology that allows us to reconstruct (automatcally) the dynamic, time-varying networks that correspond to the visual cues employed by organisms when making movement decisions [1]. Sensory networks are shown to provide a much more accurate representation of how social influence propagates in groups, and their analysis allows us to identify, for any instant in time, the most socially-influential individuals within groups, and to predict the magnitude of complex behavioral cascades before they actually occur [2]. I will also investigate the coupling between spatial and information dynamics in groups and reveal that emergent problem solving is the predominant mechanism by which mobile groups sense, and respond to complex environmental gradients [3]. Evolutionary modeling demonstrates such ‘physical computation’ readily evolves within populations of selfish organisms, and allowing individuals to compute collectively the spatial distribution of rsources and to allocate themselves effectively among distinct, and distant, resource patches,
Without requiring information about the number, location or size of patches [4].
Finally I will reveal the critical role uninformed, or unbiased, individuals play in effecting fast and democratic consensus decision-making in collectives [5-7], and will test these predictions with experiments involving schooling fish [6] and wild baboons [8].
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Date:12ThursdayNovember 2015Lecture
Life Science Lecture
More information Time 15:00 - 16:30Location Dolfi and Lola Ebner AuditoriumLecturer Prof. Irit Sagi
Dept. of Biological RegulationsOrganizer Department of Biomolecular SciencesContact -
Date:15SundayNovember 2015Lecture
The War on Science: Climate Change in an Era of Doubt
More information Time 11:00 - 11:00Location Sussman Family Building for Environmental SciencesLecturer William Newman
UCLAOrganizer Department of Earth and Planetary SciencesContact -
Date:15SundayNovember 2015Lecture
Innate immune regulation of intestinal mucosal inflammation
More information Time 13:30 - 13:30Location Wolfson Building for Biological ResearchLecturer Dr. Roni Nowarski
Yale UniversityOrganizer Department of Systems ImmunologyContact -
Date:15SundayNovember 2015Lecture
Circadian Clock Control by Polyamine Levels through a Mechanism that Declines with Age
More information Time 15:00 - 16:00Lecturer Prof. Gad Asher
Dept. of Biological Chemistry, Weizmann Institute of ScienceContact -
Date:16MondayNovember 2015Conference
The Helen and Martin Kimmel Stem Cell Institute: Regulation of Normal and Leukemic Hematopoietic Ste
More information Time All dayLocation The David Lopatie Conference CentreChairperson Tsvee LapidotHomepage Contact -
Date:16MondayNovember 2015Lecture
Analyzing genomic circuitry by genetic perturbation analyses
More information Time 09:15 - 11:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Frank Holstege
UMC UtrechtOrganizer Department of Systems ImmunologyContact -
Date:16MondayNovember 2015Lecture
Self-Assembly Control of Chemical Structures on the Nano-Scale: Design, Synthesis, and Function
More information Time 11:00 - 12:00Location Helen and Milton A. Kimmelman BuildingLecturer Prof. Makoto Fujita
Department of Applied Chemistry School of Engineering The University of TokyoOrganizer Department of Molecular Chemistry and Materials ScienceContact -
Date:16MondayNovember 2015Lecture
Probabilistic inference of immune repertoires diversity
More information Time 14:15 - 14:15Location Edna and K.B. Weissman Building of Physical SciencesLecturer Yuval Elhanati
École Normale Supérieure, ParisOrganizer Department of Physics of Complex SystemsContact Abstract Show full text abstract about The adaptive immune system can recognize many different path...» The adaptive immune system can recognize many different pathogens by maintaining a large diversity of cells with different membrane receptors. We study the complex stochastic processes that generate and shape this ensemble of immune receptors developing probabilistic models from statistical inference of high throughput sequencing data. Our technique based on transfer matrices learns the probabilistic properties of the generation process, and finds it to be amazingly universal across individuals. We then model also selection pressures on the generated cells, in terms of the composition of their receptors, again finding universality, and reduction in diversity. In general our methods allows us to characterize and study the diversity distribution of immune repertoires using available sample data. This can be invaluable as a baseline for future study of the system as well as clinical applications, but might also expand our knowledge on statistical properties of interacting ensembles. -
Date:17TuesdayNovember 2015Lecture
Steady-state and dynamic analyses of transcription regulation
More information Time 10:00 - 11:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Frank Holstege
UMC UtrechtOrganizer Department of Systems ImmunologyContact -
Date:17TuesdayNovember 2015Lecture
Dolichol (physiologically important superlipid) - biosynthesis in Arabidopsis
More information Time 11:15 - 11:15Location Ullmann Building of Life SciencesLecturer Dr. Adam Jozwiak
Prof. Asaph Aharoni’s lab. Dept. of Plant and Environmental Sciences The Weizmann Institute of ScienceOrganizer Department of Plant and Environmental SciencesContact -
Date:17TuesdayNovember 2015Lecture
Science Time - Popular Lecture
More information Time 12:00 - 13:00Title Learning from ants how to walk the golden path between conformism and individualityLocation Dolfi and Lola Ebner AuditoriumLecturer Prof. Nir Gov
Learning from ants how to walk the golden path between conformism and individualityOrganizer Communications and Spokesperson DepartmentHomepage Contact -
Date:18WednesdayNovember 2015Lecture
Super resolution Conical Diffraction Microscopy - BioAxial
More information Time 10:00 - 11:00Location Ullmann Building of Life SciencesLecturer Gabriel Y.SIRAT and Louis-P.BRAITBART
Bioaxial,Paris,FranceOrganizer Department of Life Sciences Core FacilitiesContact Abstract Show full text abstract about Super-resolution Conical Diffraction Microscopy (CoDiM) pack...» Super-resolution Conical Diffraction Microscopy (CoDiM) packaged in an easy-to-use add-on accessory to confocal microscopes unveils molecular mechanisms in live samples below 90nm resolution.
Gabriel Y. SIRAT and Louis-P. BRAITBART
Bioaxial, 24 rue du Faubourg Saint-Jacques, 75014 Paris, France
gabriel.sirat@bioaxial.com; philippe.braitbart@bioaxial.com
Recent progress in sub-diffraction light microscopy has allowed researchers to look into cells with an unrivalled level of detail and specificity. Still current advanced imaging techniques too often remain plagued by overwhelming complexity, cost and high photo-toxicity which dramatically restrict their range of application and scientific output. Here we present a super-resolution technique based on cutting-edge conical diffraction optics and advanced emitter localization opening up a range of life science applications yet unexplored by high-performance super-resolution imaging.
BioAxial’s user-friendly super-resolution CODIM100 add-on module has been specifically designed to perform live cell imaging at resolutions exceeding 90 nm. Our system does not require any specific sample preparation, is compatible with all standard immunostaining and fluorescent proteins such as GFP, produces very limited phototoxicity and bleaching and integrates seamlessly in regular confocal microscopy workflows. Minimization of photo damage ensures the biological fidelity of the experimental paradigm and the biological relevance of functional measurements.
In this presentation we will discuss the underlying principle of the BioAxial optical technology, image formation and analysis processes with attendees. We will also show the latest applications that BioAxial has developed together with its different academic partners.
For more information on BioAxial, Conical Diffraction Microscopy and the CODIM100, please visit www.bioaxial.com
