Design and synthesize antiviral molecules targetting human pathogenic viruses (HIV, HCV, SRAS, LCMV, Dengue...) for which there is no treatment and to design more potent antiviral molecules than those currently used in therapy.
Establish the relationships between the aminoacid sequence of CAZymes and their specificity. We work in various areas from the exploration of the gut microbiota to the search of novel enzymes for biofuel production or blood group conversion.
Characterize at the biochemical level the molecules involved in these processes, define the way they interact and study their tridimensional structure by X-ray crystallography.
Characterize and describe the molecular architectures and functional mechanisms of carbohydrate-active enzymes, sensor domains and lectins, and of enzymes, receptors and cell adhesion molecules with a neurobiological interest.
Identify, isolate and characterize the structure and function of multifunctional macromolecular complexes that rule essential processes of viral infection involving viral replication, transcription and host interactions.
Unravel the molecular mechanisms of emerging viruses by characterizing the structures and the enzymatic activities of proteins forming the viral replication and transcription complex. Develop new antiviral strategies.