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METHOD:PUBLISH
X-WR-CALNAME:Institute for Bioengineering of Catalonia
X-ORIGINAL-URL:https://ibecbarcelona.eu/ca/
X-WR-CALDESC:Esdeveniments per Institute for Bioengineering of Catalonia
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X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Europe/Madrid
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20160327T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20161030T010000
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TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20170326T010000
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TZOFFSETTO:+0100
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DTSTART:20171029T010000
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TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20180325T010000
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BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170707T110000
DTEND;TZID=Europe/Madrid:20170707T130000
DTSTAMP:20260506T001044
CREATED:20170703T113940Z
LAST-MODIFIED:20170703T113940Z
UID:96076-1499425200-1499432400@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Maria Valls
DESCRIPTION:“Development of an advanced 3D culture system for human cardiac tissue engineering”\nMaria Valls\, Biomimetic systems for cell engineering group\nMaria will be defending her PhD thesis on Friday 7th June at 11:00 in the Aula Magna of the UB’s Faculty of Biology. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-maria-valls-2/
LOCATION:Aula Magna\, Facultad de Biología\, UB
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170707T110000
DTEND;TZID=Europe/Madrid:20170707T130000
DTSTAMP:20260506T001044
CREATED:20170703T113940Z
LAST-MODIFIED:20170703T113940Z
UID:30229-1499425200-1499432400@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Maria Valls
DESCRIPTION:“Development of an advanced 3D culture system for human cardiac tissue engineering”\nMaria Valls\, Biomimetic systems for cell engineering group\nMaria will be defending her PhD thesis on Friday 7th June at 11:00 in the Aula Magna of the UB’s Faculty of Biology. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-maria-valls/
LOCATION:Aula Magna\, Facultad de Biología\, UB
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170711T100000
DTEND;TZID=Europe/Madrid:20170711T180000
DTSTAMP:20260506T001044
CREATED:20170324T092603Z
LAST-MODIFIED:20170324T102221Z
UID:28653-1499767200-1499796000@ibecbarcelona.eu
SUMMARY:Career Development for Scientists
DESCRIPTION:Training activity in Leadership&management skills. \nThe goal of this workshop on career development for scientists is to give participants a competitive edge on the job market by developing both the intellectual framework to make informed career choices as well as by providing practical help for the actual application and selection process\, be it within or outside the academic environment. \nDates: \n11th and 12th July 2017 \nIn person class sessions: 14 hours\, from 10:00 to 18:00 \nTarget Group: \nPhDs and Postdoctoral researchers. \nProvider: Tobias Maier.
URL:https://ibecbarcelona.eu/ca/event/career-development-for-scientists/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170711T100000
DTEND;TZID=Europe/Madrid:20170711T180000
DTSTAMP:20260506T001044
CREATED:20170324T092603Z
LAST-MODIFIED:20170324T092603Z
UID:96021-1499767200-1499796000@ibecbarcelona.eu
SUMMARY:Career Development for Scientists
DESCRIPTION:Training activity in Leadership&management skills. \nThe goal of this workshop on career development for scientists is to give participants a competitive edge on the job market by developing both the intellectual framework to make informed career choices as well as by providing practical help for the actual application and selection process\, be it within or outside the academic environment. \nDates: \n11th and 12th July 2017 \nIn person class sessions: 14 hours\, from 10:00 to 18:00 \nTarget Group: \nPhDs and Postdoctoral researchers. \nProvider: Tobias Maier.
URL:https://ibecbarcelona.eu/ca/event/career-development-for-scientists-2/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170713
DTEND;VALUE=DATE:20170714
DTSTAMP:20260506T001044
CREATED:20170324T080526Z
LAST-MODIFIED:20170324T102200Z
UID:28629-1499904000-1499990399@ibecbarcelona.eu
SUMMARY:Science Communication to a non-scientific audience
DESCRIPTION:Training activity in Transferable skills. \nThe aim of the course is to prepare participants to communicate their research better to a non- scientific audience\, be it online or offline. \nDates: \n13th July 2017 from 9 to 6pm. \nIn person class sessions = 8 hours. One whole day. \nTarget group: \nAll IBEC members. Preference will be given to PhDs and postdocs. \nProvider: Tobias Maier.
URL:https://ibecbarcelona.eu/ca/event/science-communication-to-a-non-scientific-audience/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170713
DTEND;VALUE=DATE:20170714
DTSTAMP:20260506T001044
CREATED:20170324T080526Z
LAST-MODIFIED:20170324T080526Z
UID:96014-1499904000-1499990399@ibecbarcelona.eu
SUMMARY:Science Communication to a non-scientific audience
DESCRIPTION:Training activity in Transferable skills. \nThe aim of the course is to prepare participants to communicate their research better to a non- scientific audience\, be it online or offline. \nDates: \n13th July 2017 from 9 to 6pm. \nIn person class sessions = 8 hours. One whole day. \nTarget group: \nAll IBEC members. Preference will be given to PhDs and postdocs. \nProvider: Tobias Maier.
URL:https://ibecbarcelona.eu/ca/event/science-communication-to-a-non-scientific-audience-2/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170714T100000
DTEND;TZID=Europe/Madrid:20170714T110000
DTSTAMP:20260506T001044
CREATED:20170630T073735Z
LAST-MODIFIED:20170630T073735Z
UID:30516-1500026400-1500030000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Maria Vinaixa
DESCRIPTION:Mass spectrometry and metabolomics data analysis for synthetic biology\n Maria Vinaixa\, Synthetic Biology for Fine and Speciality Chemicals (SYNBIOCHEM)\, Manchester Institute of Biotechnology\nSynthetic biology builds upon the creation of new biologically inspired standardized parts that can be put together using design or simulations tools to build circuits that will create de-novo biological functions or modify existing ones. Using synthetic biology\, microbial cell factories can be engineered to provide new sustainable bio-routes for the production of fuels\, biopharmaceuticals\, fragrances\, and food flavors among others. In this regard\, the SYNBIOCHEM Centre (www.synbiochem.co.uk) has set-up an automated Design/Build/Test/Learn pipeline designed to provide access to target fine chemicals through iterative\, rapid and predictable engineering of production pathways and microbial strains. This pipeline moves from Design of new parts (e.g. enzymes\, regulatory circuits\, metabolic pathways)\, through to combinatorial high-throughput Build approaches (directed evolution\, components\, pathways and strain assembly) and high-throughput analytics in Test (product extraction\, instrumental analysis\, data analysis and sharing) feeding back to improved designs via an active Learning stage at each cycle iteration. This pipeline allows unprecedented possibilities for retro biosynthesis of non-natural products and for the expansion of natural products chemical diversity. Screening for the small-molecule structure diversity emanating from such pipeline is an analytically daunting challenge. In this regard\, mass spectrometry (MS) is a key analytical technology offering the high throughput screening capabilities as well as the versatility needed to cope with such chemical diversity. However\, curating MS data and merging it with all other types of data generated through iterative D/B/T/L cycle so that it can be used to learn and redesign remains a challenge. Despite Metabolomics has powered computational solutions for MS data analysis; such solutions do only partially cover the needs within a synthetic biology context. Thus\, we are building the next generation computational toolbox for MS data analysis and storage so it can be harvested across the entire pipeline. In this seminar\, main capabilities and functionalities on such toolbox are going to be discussed.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-maria-vinaixa/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170714T100000
DTEND;TZID=Europe/Madrid:20170714T110000
DTSTAMP:20260506T001044
CREATED:20170630T073735Z
LAST-MODIFIED:20170630T073735Z
UID:96075-1500026400-1500030000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Maria Vinaixa
DESCRIPTION:Mass spectrometry and metabolomics data analysis for synthetic biology\n Maria Vinaixa\, Synthetic Biology for Fine and Speciality Chemicals (SYNBIOCHEM)\, Manchester Institute of Biotechnology\nSynthetic biology builds upon the creation of new biologically inspired standardized parts that can be put together using design or simulations tools to build circuits that will create de-novo biological functions or modify existing ones. Using synthetic biology\, microbial cell factories can be engineered to provide new sustainable bio-routes for the production of fuels\, biopharmaceuticals\, fragrances\, and food flavors among others. In this regard\, the SYNBIOCHEM Centre (www.synbiochem.co.uk) has set-up an automated Design/Build/Test/Learn pipeline designed to provide access to target fine chemicals through iterative\, rapid and predictable engineering of production pathways and microbial strains. This pipeline moves from Design of new parts (e.g. enzymes\, regulatory circuits\, metabolic pathways)\, through to combinatorial high-throughput Build approaches (directed evolution\, components\, pathways and strain assembly) and high-throughput analytics in Test (product extraction\, instrumental analysis\, data analysis and sharing) feeding back to improved designs via an active Learning stage at each cycle iteration. This pipeline allows unprecedented possibilities for retro biosynthesis of non-natural products and for the expansion of natural products chemical diversity. Screening for the small-molecule structure diversity emanating from such pipeline is an analytically daunting challenge. In this regard\, mass spectrometry (MS) is a key analytical technology offering the high throughput screening capabilities as well as the versatility needed to cope with such chemical diversity. However\, curating MS data and merging it with all other types of data generated through iterative D/B/T/L cycle so that it can be used to learn and redesign remains a challenge. Despite Metabolomics has powered computational solutions for MS data analysis; such solutions do only partially cover the needs within a synthetic biology context. Thus\, we are building the next generation computational toolbox for MS data analysis and storage so it can be harvested across the entire pipeline. In this seminar\, main capabilities and functionalities on such toolbox are going to be discussed.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-maria-vinaixa-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170714T100000
DTEND;TZID=Europe/Madrid:20170714T110000
DTSTAMP:20260506T001044
CREATED:20170630T073735Z
LAST-MODIFIED:20170630T073735Z
UID:96077-1500026400-1500030000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Maria Vinaixa
DESCRIPTION:Mass spectrometry and metabolomics data analysis for synthetic biology\n Maria Vinaixa\, Synthetic Biology for Fine and Speciality Chemicals (SYNBIOCHEM)\, Manchester Institute of Biotechnology\nSynthetic biology builds upon the creation of new biologically inspired standardized parts that can be put together using design or simulations tools to build circuits that will create de-novo biological functions or modify existing ones. Using synthetic biology\, microbial cell factories can be engineered to provide new sustainable bio-routes for the production of fuels\, biopharmaceuticals\, fragrances\, and food flavors among others. In this regard\, the SYNBIOCHEM Centre (www.synbiochem.co.uk) has set-up an automated Design/Build/Test/Learn pipeline designed to provide access to target fine chemicals through iterative\, rapid and predictable engineering of production pathways and microbial strains. This pipeline moves from Design of new parts (e.g. enzymes\, regulatory circuits\, metabolic pathways)\, through to combinatorial high-throughput Build approaches (directed evolution\, components\, pathways and strain assembly) and high-throughput analytics in Test (product extraction\, instrumental analysis\, data analysis and sharing) feeding back to improved designs via an active Learning stage at each cycle iteration. This pipeline allows unprecedented possibilities for retro biosynthesis of non-natural products and for the expansion of natural products chemical diversity. Screening for the small-molecule structure diversity emanating from such pipeline is an analytically daunting challenge. In this regard\, mass spectrometry (MS) is a key analytical technology offering the high throughput screening capabilities as well as the versatility needed to cope with such chemical diversity. However\, curating MS data and merging it with all other types of data generated through iterative D/B/T/L cycle so that it can be used to learn and redesign remains a challenge. Despite Metabolomics has powered computational solutions for MS data analysis; such solutions do only partially cover the needs within a synthetic biology context. Thus\, we are building the next generation computational toolbox for MS data analysis and storage so it can be harvested across the entire pipeline. In this seminar\, main capabilities and functionalities on such toolbox are going to be discussed.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-maria-vinaixa-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170714T100000
DTEND;TZID=Europe/Madrid:20170714T110000
DTSTAMP:20260506T001044
CREATED:20170630T073735Z
LAST-MODIFIED:20170630T073735Z
UID:96078-1500026400-1500030000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Maria Vinaixa
DESCRIPTION:Mass spectrometry and metabolomics data analysis for synthetic biology\n Maria Vinaixa\, Synthetic Biology for Fine and Speciality Chemicals (SYNBIOCHEM)\, Manchester Institute of Biotechnology\nSynthetic biology builds upon the creation of new biologically inspired standardized parts that can be put together using design or simulations tools to build circuits that will create de-novo biological functions or modify existing ones. Using synthetic biology\, microbial cell factories can be engineered to provide new sustainable bio-routes for the production of fuels\, biopharmaceuticals\, fragrances\, and food flavors among others. In this regard\, the SYNBIOCHEM Centre (www.synbiochem.co.uk) has set-up an automated Design/Build/Test/Learn pipeline designed to provide access to target fine chemicals through iterative\, rapid and predictable engineering of production pathways and microbial strains. This pipeline moves from Design of new parts (e.g. enzymes\, regulatory circuits\, metabolic pathways)\, through to combinatorial high-throughput Build approaches (directed evolution\, components\, pathways and strain assembly) and high-throughput analytics in Test (product extraction\, instrumental analysis\, data analysis and sharing) feeding back to improved designs via an active Learning stage at each cycle iteration. This pipeline allows unprecedented possibilities for retro biosynthesis of non-natural products and for the expansion of natural products chemical diversity. Screening for the small-molecule structure diversity emanating from such pipeline is an analytically daunting challenge. In this regard\, mass spectrometry (MS) is a key analytical technology offering the high throughput screening capabilities as well as the versatility needed to cope with such chemical diversity. However\, curating MS data and merging it with all other types of data generated through iterative D/B/T/L cycle so that it can be used to learn and redesign remains a challenge. Despite Metabolomics has powered computational solutions for MS data analysis; such solutions do only partially cover the needs within a synthetic biology context. Thus\, we are building the next generation computational toolbox for MS data analysis and storage so it can be harvested across the entire pipeline. In this seminar\, main capabilities and functionalities on such toolbox are going to be discussed.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-maria-vinaixa-4/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170718T110000
DTEND;TZID=Europe/Madrid:20170718T130000
DTSTAMP:20260506T001044
CREATED:20170713T140323Z
LAST-MODIFIED:20170713T140323Z
UID:30519-1500375600-1500382800@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Marta Pozuelo
DESCRIPTION:“Bioengineering single-protein wires”\nMarta Pozuelo\, Nanoprobes and Nanoswitches Group\nMaria will be defending her PhD thesis on Tuesday 18th July at 11:00 in the sala de graus Eduard Fontserè\, Facultad de Física (UB). \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-marta-pozuelo/
LOCATION:Sala de Graus Eduard Fontseré\, Martí i Franquès\, 1-11\, Barcelona\, 08028
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170718T110000
DTEND;TZID=Europe/Madrid:20170718T130000
DTSTAMP:20260506T001044
CREATED:20170713T140323Z
LAST-MODIFIED:20170713T140323Z
UID:96079-1500375600-1500382800@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Marta Pozuelo
DESCRIPTION:“Bioengineering single-protein wires”\nMarta Pozuelo\, Nanoprobes and Nanoswitches Group\nMarta will be defending her PhD thesis on Tuesday 18th July at 11:00 in the sala de graus Eduard Fontserè\, Facultad de Física (UB). \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-marta-pozuelo-2/
LOCATION:Sala de Graus Eduard Fontseré\, Martí i Franquès\, 1-11\, Barcelona\, 08028
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170718T110000
DTEND;TZID=Europe/Madrid:20170718T130000
DTSTAMP:20260506T001044
CREATED:20170713T140323Z
LAST-MODIFIED:20170713T140323Z
UID:96080-1500375600-1500382800@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Marta Pozuelo
DESCRIPTION:“Bioengineering single-protein wires”\nMarta Pozuelo\, Nanoprobes and Nanoswitches Group\nMaria will be defending her PhD thesis on Tuesday 18th July at 11:00 in the sala de graus Eduard Fontserè\, Facultad de Física (UB). \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-marta-pozuelo-3/
LOCATION:Sala de Graus Eduard Fontseré\, Martí i Franquès\, 1-11\, Barcelona\, 08028
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170718T110000
DTEND;TZID=Europe/Madrid:20170718T130000
DTSTAMP:20260506T001044
CREATED:20170713T140323Z
LAST-MODIFIED:20170713T140323Z
UID:96081-1500375600-1500382800@ibecbarcelona.eu
SUMMARY:IBEC PhD Defence: Marta Pozuelo
DESCRIPTION:“Bioengineering single-protein wires”\nMarta Pozuelo\, Nanoprobes and Nanoswitches Group\nMaria will be defending her PhD thesis on Tuesday 18th July at 11:00 in the sala de graus Eduard Fontserè\, Facultad de Física (UB). \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/ca/event/ibec-phd-defence-marta-pozuelo-4/
LOCATION:Sala de Graus Eduard Fontseré\, Martí i Franquès\, 1-11\, Barcelona\, 08028
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170725T100000
DTEND;TZID=Europe/Madrid:20170725T110000
DTSTAMP:20260506T001044
CREATED:20170717T120502Z
LAST-MODIFIED:20170717T120502Z
UID:30584-1500976800-1500980400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Ronen Zaidel-Bar
DESCRIPTION:Regulation of actomyosin contractility in C. elegans\nRonen Zaidel-Bar\, Mechanobiology Institute Singapore and Tel-Aviv University Medical School\nThe actomyosin cortex is responsible for cell shape and for dynamic processes such as cell polarization and cytokinesis. We are studying the regulation of cortical contractility in the C. elegans zygote\, using genetic loss of function and live-imaging. In my talk\, I will discuss recent findings regarding two proteins: the actin cross-linking protein plastin (PLST-1) and the transmembrane receptor E-cadherin (HMR-1). Consistent with previous in-vitro reconstitution studies\, we show that an optimal level of cross-linking by plastin is required for the generation of coordinated long-range contractions in the cortex; without the connectivity afforded by plastin\, zygote polarization and cytokinesis are severely perturbed. E-cadherin is well known for its role as a cell-cell adhesion receptor. \nSurprisingly\, we discovered a role for non-junctional E-cadherin clusters in regulating cortical contractility. E-cadherin clusters inhibit RhoA and non-muscle myosin II activity at the cortex and form a physical barrier that slows actin flows. In the absence of non-junctional E-cadherin cytokinesis proceeds faster\, but the cortex is also at a risk of detaching from the plasma membrane. Thus\, our studies in the C. elegans zygote are shedding light on structural and regulatory mechanisms underlying cortex function.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-ronen-zaidel-bar/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170725T100000
DTEND;TZID=Europe/Madrid:20170725T110000
DTSTAMP:20260506T001044
CREATED:20170717T120502Z
LAST-MODIFIED:20170717T120502Z
UID:96085-1500976800-1500980400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Ronen Zaidel-Bar
DESCRIPTION:Regulation of actomyosin contractility in C. elegans\nRonen Zaidel-Bar\, Mechanobiology Institute Singapore and Tel-Aviv University Medical School\nThe actomyosin cortex is responsible for cell shape and for dynamic processes such as cell polarization and cytokinesis. We are studying the regulation of cortical contractility in the C. elegans zygote\, using genetic loss of function and live-imaging. In my talk\, I will discuss recent findings regarding two proteins: the actin cross-linking protein plastin (PLST-1) and the transmembrane receptor E-cadherin (HMR-1). Consistent with previous in-vitro reconstitution studies\, we show that an optimal level of cross-linking by plastin is required for the generation of coordinated long-range contractions in the cortex; without the connectivity afforded by plastin\, zygote polarization and cytokinesis are severely perturbed. E-cadherin is well known for its role as a cell-cell adhesion receptor. \nSurprisingly\, we discovered a role for non-junctional E-cadherin clusters in regulating cortical contractility. E-cadherin clusters inhibit RhoA and non-muscle myosin II activity at the cortex and form a physical barrier that slows actin flows. In the absence of non-junctional E-cadherin cytokinesis proceeds faster\, but the cortex is also at a risk of detaching from the plasma membrane. Thus\, our studies in the C. elegans zygote are shedding light on structural and regulatory mechanisms underlying cortex function.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-ronen-zaidel-bar-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170725T100000
DTEND;TZID=Europe/Madrid:20170725T110000
DTSTAMP:20260506T001044
CREATED:20170717T120502Z
LAST-MODIFIED:20170717T120502Z
UID:96086-1500976800-1500980400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Ronen Zaidel-Bar
DESCRIPTION:Regulation of actomyosin contractility in C. elegans\nRonen Zaidel-Bar\, Mechanobiology Institute Singapore and Tel-Aviv University Medical School\nThe actomyosin cortex is responsible for cell shape and for dynamic processes such as cell polarization and cytokinesis. We are studying the regulation of cortical contractility in the C. elegans zygote\, using genetic loss of function and live-imaging. In my talk\, I will discuss recent findings regarding two proteins: the actin cross-linking protein plastin (PLST-1) and the transmembrane receptor E-cadherin (HMR-1). Consistent with previous in-vitro reconstitution studies\, we show that an optimal level of cross-linking by plastin is required for the generation of coordinated long-range contractions in the cortex; without the connectivity afforded by plastin\, zygote polarization and cytokinesis are severely perturbed. E-cadherin is well known for its role as a cell-cell adhesion receptor. \nSurprisingly\, we discovered a role for non-junctional E-cadherin clusters in regulating cortical contractility. E-cadherin clusters inhibit RhoA and non-muscle myosin II activity at the cortex and form a physical barrier that slows actin flows. In the absence of non-junctional E-cadherin cytokinesis proceeds faster\, but the cortex is also at a risk of detaching from the plasma membrane. Thus\, our studies in the C. elegans zygote are shedding light on structural and regulatory mechanisms underlying cortex function.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-ronen-zaidel-bar-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170725T100000
DTEND;TZID=Europe/Madrid:20170725T110000
DTSTAMP:20260506T001044
CREATED:20170717T120502Z
LAST-MODIFIED:20170717T120502Z
UID:96087-1500976800-1500980400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Ronen Zaidel-Bar
DESCRIPTION:Regulation of actomyosin contractility in C. elegans\nRonen Zaidel-Bar\, Mechanobiology Institute Singapore and Tel-Aviv University Medical School\nThe actomyosin cortex is responsible for cell shape and for dynamic processes such as cell polarization and cytokinesis. We are studying the regulation of cortical contractility in the C. elegans zygote\, using genetic loss of function and live-imaging. In my talk\, I will discuss recent findings regarding two proteins: the actin cross-linking protein plastin (PLST-1) and the transmembrane receptor E-cadherin (HMR-1). Consistent with previous in-vitro reconstitution studies\, we show that an optimal level of cross-linking by plastin is required for the generation of coordinated long-range contractions in the cortex; without the connectivity afforded by plastin\, zygote polarization and cytokinesis are severely perturbed. E-cadherin is well known for its role as a cell-cell adhesion receptor. \nSurprisingly\, we discovered a role for non-junctional E-cadherin clusters in regulating cortical contractility. E-cadherin clusters inhibit RhoA and non-muscle myosin II activity at the cortex and form a physical barrier that slows actin flows. In the absence of non-junctional E-cadherin cytokinesis proceeds faster\, but the cortex is also at a risk of detaching from the plasma membrane. Thus\, our studies in the C. elegans zygote are shedding light on structural and regulatory mechanisms underlying cortex function.
URL:https://ibecbarcelona.eu/ca/event/ibec-seminar-ronen-zaidel-bar-4/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
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