PRISM programme - PhD student in Soft Matter for Project PlasticPhase (MSCA COFUND)

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Testo originale dell'annuncio (in inglese)

*PRISM programme* The PRISM (PhD Research Programme for International Training in Sustainable Soft Matter) programme has launched its first call for applications, offering up to 14 fully funded PhD fellowships starting from 1 March 2027 at Paris Sciences & Lettres (PSL) University. The programme trains researchers to address ecological transition challenges through sustainable soft matter science, with projects focused on eco-friendly chemical processes, circular economy, renewable energies, and carbon capture, storage, and valorisation. Co-funded by the European Union under Horizon Europe MSCA COFUND (Grant Agreement 101261637) and partner institutions, PRISM provides interdisciplinary, international, and intersectoral training, including mobility opportunities, secondments, and courses in sustainability, innovation, entrepreneurship, career development, and transferable skills. Applications must be submitted via the PRISM website by 31 October 2026 (23:59 Paris time). *The PhD project* PlasticPhase: Micro- and Nanoplastics as Modulators of Phase Separation and Protein Aggregation Micro- and nanoplastics (MNPs) are tiny plastic particles originating from the breakdown of larger plastic waste. Due to increasing water and soil pollution, they are ubiquitous in the environment, raising concerns about their impact on human health. They can interact with biomolecular condensates which are subcellular compartments confining proteins and nucleic acids organizing cellular biochemistry in space and time. Condensate formation is often mediated through multivalent interactions between biomolecules leading to liquid-liquid phase separation (LLPS). Recent studies hypothesized that LLPS-derived condensates might represent intermediates in the path yielding toxic protein aggregates present in neurodegenerative diseases. This project aims at investigating how MNPs interacts with biocondensates. The central hypothesis is that MNPs affect intracellular phase behavior via two interconnected mechanisms: (i) direct physicochemical interactions, where particles serve as heterogeneous nucleation sites or modify intermolecular interactions, and (ii) indirect effects mediated by stress-response pathways and proteostasis imbalance. These perturbations may drive biomolecular condensates from dynamic, reversible liquid states toward persistent, solid-like assemblies associated with pathological aggregation. Capitalizing AIV team’sexpertise, we will construct model condensates that assemble through LLPS using engineered protein scaffolds, such as multivalent protein domain prone to homodimerize. These synthetic systems mimic the properties of natural condensates, including nucleation, growth, and fusion, allowing for controlled observation in both test tubes and living cells. Additionally, the project will examine UBQLN2, a disease-relevant protein that forms condensates transitioning into stress granules under oxidative or proteotoxic stress, serving as a model for pathological aggregation. In parallel, we will generate a tunable library of MNPs with controlled size, charge, and surface chemistry to systematically investigate their effects on phase separation. Polystyrene nanoparticles of different sizes will serve as model MNPs. These particles can be modified by PEGylation, enabling control over surface interactions and colloidal stability. In addition, particles based on other polymers (e.g., PMMA, PE, PLA,…) will be prepared using nanoprecipitation, a technique mastered at AIV, to represent the diversity of MNPs in the environment. This library will be tested against the synthetic condensates to quantify how specific MNP characteristics influence nucleation rates, growth dynamics, and condensate properties using advanced biophysical techniques. In vitro, researchers will monitor real-time nucleation and coarsening to determine if MNPs lower energy barriers for phase separation. In cellulo, live-cell imaging and Fluorescence Recovery After Photobleac