Current Selection : 24 Research Groups
Research in Marine Biology, Cell Biology and Molecular Biology
Analytical Chemistry, Electrochemistry, Electrochemical Sensors, Optical Detection Principles, Ion Optodes, Exhaustive Sensors, Photoelectric Conversion, Light Activated Extraction, Nanosphere Reagents, Materials Characterization, Polymers and Polymer Modifications, Environmental Analysis, Biomedical Analysis.
The research of the group focuses on fundamental physical and analytical chemistry of colloids, surfaces, and polymers. Applications of these concepts are pursued in industrial process control and environmental chemistry.
Chemistry, spectroscopy and applications of surfaces, interfaces and chiral nanomaterials: Development and application of spectroscopic techniques to probe solid-liquid interfaces, preparation and applications of chiral nanomaterials, enantiodifferentiation, vibrational optical activity, self-assembly of plasmonic nanomaterials.
We are mainly interested in synthesizing topologically complex molecules, using the hydrophobic effect as a driving force. Molecules with complex topologies are entangled macrocycles composed of one or many components, named knots and links, respectively. The formation of knots and links represent an original, but efficient, way to control the three–dimensional shape of molecules, making these structures ideal candidates for a variety of biological applications, such as sequence- and structure-specific binding to proteins and DNA. However, they remain extremely difficult to produce using the current methods of chemistry, and their potential applications constitute an entirely unexplored field.
We want to understand in physical and molecular terms how cells talk to each other during development. This means our research is highly interdisciplinary: physics, cell biology, molecular biology, biochemistry, genetics... Indeed some of us in the lab are biologists, other physicists, chemists, engineers.
We are interested in the signaling events that control tissue growth: how is the shape and final size of a tissue achieved during embryogenesis?
We focus on two types of proliferation modes: growth control by morphogen gradients and asymmetric cell division in stem cells. We do this using two model systems: Drosophila and Zebrafish.
Spectroscopie laser cw, spectroscopie Raman et luminescence, et chimie du solide dans les fluorures (matériaux optiques potentiels) et hydrures (stockage d’hydrogène); caractérisation des propriétés structurales et dynamiques des échantillons par combinaison des techniques structurales et spectroscopiques, et optimisation des stratégies de synthèse en vue d’échantillons avec des propriétés améliorées; applications de la spectroscopie Raman : échantillons biochimiques, équilibres conformationnels.
Analytical chemistry and mass spectrometry of low molecular weight compounds (pharmaceuticals) and macromolcules (peptides, proteins). Mass spectrometry imaging, Ionization, High resolution MS and data independent acquisition, ion mobility mass spectrometry, coupling MS with separation sciences, data analysis, MS libraries, bioanalysis, metabolism, metabolomics, lipidomics, proteomics, ultra-fast quantitative analysis.
Methodology and signal processing in Nuclear Magnetic Resonance; elucidation of structures of natural products
We study the molecular mechanisms of membrane traffic, especially clathrin-mediated endocytosis. We aim to understand the assembly, function and regulation of the complex molecular machineries that drive the formation of endocytic vesicles. Our main experimental organism is budding yeast. We use a combination of quantitative live-cell imaging, electron microscopy, genetics, biochemistry and structural biology.
We study the formation of spatial and temporal structures in individual biological cells and cells assemblies. The focus of our work is on theoretical descriptions of cytoskeletal dynamics. The cytoskeleton is a network of filamentous proteins, which is kept permanently out of thermodynamic equilibrium. It enables cells to divide, determines their shape and plays an important role in cell locomotion. In our descriptions, we rely heavily on concepts from non-linear dynamics and from non-equilibrium statistical mechanics.
We study excited-state proton transfer from photoacids to proton acceptors in solutions and at biologically relevant interfaces. In particular, we investigate the influence of the environment (polarity, viscosity, pH etc.) on the mechanism and dynamics of the proton transfer reaction. A thorough understanding of the influence of the environmental parameters can yield valuable information about the complex local environment in biological systems. The main experimental approaches are based on time-resolved optical spectroscopic techniques such as optically gated fluorescence and surface second harmonic generation.
Synthetic organic chemistry, chirality and molecular recognition: Organometallic reactivity and asymmetric transformations; Synthetic, physical and biological applications of highly stable (chiral) carbenium ions; NMR enantiodifferentiation of chiral substances; Hexacoordinated phosphorus chemistry
Organic Synthesis, Supramolecular Chemistry, Bioorganic Chemistry, Functional Systems, Unorthodox Interactions
Synthetic chemistry, asymmetric catalysis, reaction mechanism, characterization of reactive intermediates
Supramolecular chemistry of f-elements.
Synthesis of luminescent and magnetically active polymetallic materials. Thermodynamics of self-assembly. Molecular near-infrared to visible upconversion using linear optics. Thermotropic luminescent liquid crystals.
The focus of our group is to reach an in-depth theoretical understanding of regio- and enantion-selective processes.
Biologie cellulaire et moléculaire; mécanismes de biogenèse des membranes et du trafic membranaire; biochimie et génétique des membranes et du trafic membranaire; triage des protéines via la route de sécrétion; fonctions intracellulaires des sphingolipides et stérols.
My research group focuses on understanding how mechanics of lipid membranes can influence the life of cells. The enveloppe of living cells is made of lipid bilayers which impermeability and deformability ensure changes in cell shape while keeping its specific content. We are interested in understanding how membrane mechanical properties can constraint several cell processes at the molecular, cellular and multi-cellular scales. In particular, we focused on how membrane tension and rigidity influence intracellular membrane traffic (in particular endocytosis and Golgi trafficking) and cell division (in particular cytokinesis). We recently started to be interested in multi-cellular systems, in particular epithelia, where membrane tension is proposed to play a role in cell reorganization during organ morphogenesis.
The major aim of my group is to understand the integration of signalling, cytoskeleton and membrane trafficking in phagocytosis and its relevance to host-pathogen interactions. To this end, we use the social amoeba Dictyostelium as a model organism as it is a is genetically and biochemically tractable professional phagocyte very similar to phagocytes of the innate immune system in morphology and behaviour.
We study the fundamental mechanism of lipid self-assembly. The assembled lipid nanostructures are tested for use in applications in the field of biophysics, electrochemistry, materials science and biomedical engineering.
Ultrafast photochemistry: development and applications of optical spectroscopic methods, investigations of ultrafast photoinduced molecular processes in condensed phase and at liquid interfaces.
Quantum embedding theory for multi-level simulations, density functional theory, computational spectroscopy, and computational chemistry.