Summary
The aim of this grant is to understand how cellular, tissue-scale and organismal left-right asymmetry arises
from the chirality of molecular constituents. In many instances the actomyosin cortex, a thin and
mechanically active layer of dynamically cross-linked filaments and molecular motors at the surface of cells,
drives the emergence of chiral morphogenetic events. In the nematode Caenorhabditis elegans, mesoscale
chiral active torques generated by this active layer establish the embryo’s left-right body axis. Here we want
to understand how mesoscale actomyosin active torques are generated at the molecular level, and how active
torque generation in the actomyosin surface drives chiral morphogenesis of cells, tissues and organisms.
Cells and tissues represent a new class of active chiral materials where both the force and the torque balance
need to be considered, and we will perform a systematic and cross-scale characterization of active chiral
biological matter. We will pursue an interdisciplinary approach at the interface of physics and biology. At the
molecular-scale, we will use optical tweezers to measure active torques generated by single molecules of the
molecular myosin and the actin polymerizing protein formin. At the cell-scale, we will reconstitute chiral
actomyosin flows in vitro and characterize chiral dynamics of single molecules in vivo. At the tissue-scale,
we will investigate chiral cell movements in a multicellular environment and unravel the physical basis of
chiral tissue flow in vertebrates. Theory is essential at all stages, and we will build a molecular-scale model
of actomyosin torque generation that will be coarse-grained to a generalized hydrodynamic description of
active chiral matter. This interdisciplinary and cross-scale approach will provide fundamentally new insights
into active chiral materials and the mechanisms by which left-right asymmetries arise in development.
from the chirality of molecular constituents. In many instances the actomyosin cortex, a thin and
mechanically active layer of dynamically cross-linked filaments and molecular motors at the surface of cells,
drives the emergence of chiral morphogenetic events. In the nematode Caenorhabditis elegans, mesoscale
chiral active torques generated by this active layer establish the embryo’s left-right body axis. Here we want
to understand how mesoscale actomyosin active torques are generated at the molecular level, and how active
torque generation in the actomyosin surface drives chiral morphogenesis of cells, tissues and organisms.
Cells and tissues represent a new class of active chiral materials where both the force and the torque balance
need to be considered, and we will perform a systematic and cross-scale characterization of active chiral
biological matter. We will pursue an interdisciplinary approach at the interface of physics and biology. At the
molecular-scale, we will use optical tweezers to measure active torques generated by single molecules of the
molecular myosin and the actin polymerizing protein formin. At the cell-scale, we will reconstitute chiral
actomyosin flows in vitro and characterize chiral dynamics of single molecules in vivo. At the tissue-scale,
we will investigate chiral cell movements in a multicellular environment and unravel the physical basis of
chiral tissue flow in vertebrates. Theory is essential at all stages, and we will build a molecular-scale model
of actomyosin torque generation that will be coarse-grained to a generalized hydrodynamic description of
active chiral matter. This interdisciplinary and cross-scale approach will provide fundamentally new insights
into active chiral materials and the mechanisms by which left-right asymmetries arise in development.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/742712 |
| Start date: | 01-01-2018 |
| End date: | 31-03-2024 |
| Total budget - Public funding: | 2 500 000,00 Euro - 2 500 000,00 Euro |
Cordis data
Original description
The aim of this grant is to understand how cellular, tissue-scale and organismal left-right asymmetry arisesfrom the chirality of molecular constituents. In many instances the actomyosin cortex, a thin and
mechanically active layer of dynamically cross-linked filaments and molecular motors at the surface of cells,
drives the emergence of chiral morphogenetic events. In the nematode Caenorhabditis elegans, mesoscale
chiral active torques generated by this active layer establish the embryo’s left-right body axis. Here we want
to understand how mesoscale actomyosin active torques are generated at the molecular level, and how active
torque generation in the actomyosin surface drives chiral morphogenesis of cells, tissues and organisms.
Cells and tissues represent a new class of active chiral materials where both the force and the torque balance
need to be considered, and we will perform a systematic and cross-scale characterization of active chiral
biological matter. We will pursue an interdisciplinary approach at the interface of physics and biology. At the
molecular-scale, we will use optical tweezers to measure active torques generated by single molecules of the
molecular myosin and the actin polymerizing protein formin. At the cell-scale, we will reconstitute chiral
actomyosin flows in vitro and characterize chiral dynamics of single molecules in vivo. At the tissue-scale,
we will investigate chiral cell movements in a multicellular environment and unravel the physical basis of
chiral tissue flow in vertebrates. Theory is essential at all stages, and we will build a molecular-scale model
of actomyosin torque generation that will be coarse-grained to a generalized hydrodynamic description of
active chiral matter. This interdisciplinary and cross-scale approach will provide fundamentally new insights
into active chiral materials and the mechanisms by which left-right asymmetries arise in development.
Status
SIGNEDCall topic
ERC-2016-ADGUpdate Date
27-04-2024
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