The Ivan Huc Group
Our group has developed a unique know-how in the design, synthesis and characterization of artificial folded molecular architectures (foldamers) based on aromatic oligoamides. These objects differ notably from peptides or nucleotides, from which they are inspired, and from their analogues, and give access to structural motifs and thus to functions beyond those of biopolymers.
Our main research lines include the development of synthetic and design methodologies towards molecular objects as large and complex as small proteins ; the investigation of receptors and molecular motors based on these folded architectures ; the study of potential biological applications of aromatic oligoamide foldamers, in particular to recognize protein surfaces ; and exploration of properties such as electron transport which may be of use in new materials. These projects have fostered a very active collaboration with x-ray crystallographers and our involvement in the set-up of an x-ray diffraction facility.
We are affiliated to the CBMN Laboratory, a joint research unit of the CNRS, the University of Bordeaux, and the Bordeaux Polytechnic Institute. Our laboratory space is embedded in the European Institute of Chemistry and Biology, a research team incubator that promotes emergence and interdisciplinary research on the University of Bordeaux campus.
Symposium on Foldamers 2016We are pleased to announce that registration is now open to attend the Bordeaux 2016 Symposium on Foldamers which will take place at the European Institute of Chemistry and Biology, on the campus of the University of Bordeaux, France, on September 26-28 2016. Read more
Cover picture : Angew. Chem. Int. Ed., 2016, May20/05/2016 Read more See all news
Latest publicationsM. Jewginski, L. Fischer, C. Colombo, I. Huc*, C. D. Mackereth*
Solution observation of dimerization and helix handedness induction in a human carbonic anhydrase–helical aromatic amide foldamer complex
See the publication H. Noguchia, M. Takafujia, V. Maurizot, I. Huc*, H. Ihara∗
Chiral separation by a terminal chirality triggered P-helical quinolineoligoamide foldamer
See the publication X. Li, T. Qi, K. Srinivas, S. Massip, V. Maurizot, I. Huc*
Synthesis and multibromination of nanosized helical aromatic amide foldamers via segment-doubling condensation
See the publication