LPTMS Internship proposal: Critical behaviour in the creep dynamics

We focus on the creep dynamics of a magnetic domain wall. Indeed, at tiny magnetic fields, the wall creeps only via thermal activation over pinning centers. A localized instability triggers a cascade, akin to aftershocks following a large earthquake in a compact active region. How large are these reorganisations? The goal of this project is to show that their size diverges, decreasing the temperature revealing the existence of a disordered, out-of-equilibrium critical point. In this internship we introduce a model for the domain wall and adapt the Dijkstra algorithm to study the creep dynamics.

The internship can then lead to a PhD project in collaboration with D. Vandembroucq (PMMH, ESPCI)

Contact:
alberto.rosso[a]cnrs.fr or alberto.rosso[a]universite-paris-saclay.fr


LPTMS Internship proposal: Using statistical physics to unravel how gene selection leads to robust developmental traits

Internship_Gene_Reg.pdf

Contact : Antoine Fruleux (antoine.fruleux@universite-paris-saclay.fr)


LPTMS Internship and PhD Proposal: Frustrated self-assembly with multiple particle types

Self-organization is key to the function of living cells – but sometimes goes wrong! In Alzheimer’s and many other diseases, normally soluble proteins thus clump up into pathological fiber-like aggregates. While biologists typically explain this on the grounds of detailed molecular interactions, we have started proving that such fibers are actually expected from very general physical principles. We thus show that geometrical frustration builds up when mismatched objects self-assemble, and leads to non-trivial aggregate morphologies, including fibers.
While we have shown that collections of identical particles form aggregates of various dimensionalities, realistic biological examples often involve multiple proteins. We will thus investigate how collections of several types of different particles typically interact and interfere. Our study will first consist in developing multi-geometries variants of the lattice-based numerical model presented in the illustration. We will then ask whether species with different geometries tend to phase separate, or conversely whether the mutiplicity of interactions they offer eases geometrical frustration and favors co-assembly. We will also wonder how this combinatorics affects the dimensionality of the aggregates, and whether we can identify generic features of the particles that distinguish between the two scenarios. We will then conduct off-lattice simulations to assess the robustness of these scenarios. Finally, we will attempt to construct a mean-field theory describing the co-assembly of a large variety of particles (> 10 or so) thus revealing the interplay between frustration and combinatorial freedom in self-assembly.
Beyond protein aggregation, this project opens investigations into a new class of “disordered” systems where the disorder is carried by each identical particle, as opposed to sprinkled throughout the system. This will help define the much-debated notion of frustration in dilute systems. This project will be conducted in collaboration with Pierre Ronceray (Turing Center for Living Systems, Marseille), who will co-direct a possible PhD project.

Expected skills:
A taste for statistical mechanics and numerical simulations connected to analytical aspects.
Location:
PMMH at ESPCI & Sorbonne U. and/or LPTMS at U. Paris-Saclay (Orsay)
Contact:
martin.lenz@espci.fr or martin.lenz@u-psud.fr
http://lptms.u-psud.fr/membres/mlenz/

pdf



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