%0 Conference Paper
%F Oral 
%T Physical modeling of active bacterial DNA segregation
%+ Laboratoire Charles Coulomb (L2C)
%A Walter, Jean-Charles
%< sans comité de lecture
%Z L2C:17-237
%B Quantitative Methods in Gene Regulation IV
%C Cambridge, United Kingdom
%8 2017-12-18
%D 2017
%Z Physics [physics]/Physics [physics]/Biological Physics [physics.bio-ph]Conference papers
%X Efficient bacterial chromosome segregation typically requires the coordinated action of a three-component, fueled by adenosine triphosphate machinery called the partition complex. We present a phenomenological model accounting for the dynamic activity of this system that is also relevant for the physics of catalytic particles in active environments. The model is obtained by coupling simplelinear reaction-diffusion equations with a proteophoresis, or “volumetric” chemophoresis, force field that arises from protein-protein interactions and provides a physically viable mechanism for complex translocation. This minimal description captures most known experimental observations: dynamic oscillations of complex components, complex separation and subsequent symmetricalpositioning. The predictions of our model are in phenomenological agreement with and provide substantial insight into recent experiments. From a non-linear physics view point, this system explores the active separation of matter at micrometric scales with a dynamical instability between static positioning and travelling wave regimes triggered by the dynamical spontaneous breaking ofrotational symmetry.
%G English
%L hal-01881265
%U https://hal.science/hal-01881265
%~ CNRS
%~ L2C
%~ MIPS
%~ UNIV-MONTPELLIER
%~ UM-2015-2021