• Since 2016 Biology engineer, lab manager, quality manager assistant at UMR INSERM CHU-1248 (ex 850), Individual Profiling and Prevention of Risks with Immunosuppressive Therapies and Transplantation, Limoges, France
  • 2013-2015 Research assistant in Sandra Wolin’s lab at Yale University, New Haven, CT, USA
  • 2008-2013 EPHE degree training and then engineer at INSERM U869 (now U1212), RNA: natural and artificial regulations, Bordeaux, France
  • 2007 Research assistant training, at UMR 5247, IBMM, team MFSA, Montpellier, France
  • 2008-2011 M. Sc. in Earth and Life Sciences with honours, Ecole Pratique des Hautes Etudes (EPHE), Paris, France
  • 2007 B. Sc. in Biochemistry, University of La Rochelle, France
  • 2006 « D.U.T » (Technologic and Academic Degree) in bioengineering, specialty: biological and biochemical analysis, with honours, University of La Rochelle, France.
  • 2004 « Baccalauréat » in laboratory science and technology, specialty: Biochemistry Bioengineering, Lycée Jacques Monod, Lescar, France

2016-nowaday:

  • Pharmacoepigenetics : 

DNA sequence variations in metabolic enzymes, membrane transporters or cellular targets have been shown to explain inter-individual variability in immunosuppressive drug response. On the other hand epigenetic changes which dynamically and reversibly alter gene expression might contribute to intra-individual vvariability.  We investigate epigenic changes occurring following immunosuppressive treatments in mice.

  • Pharmacogenetics:
    • We investigate polymorphisms in candidate pharmacogenes which could be associated with graft function and subsequent graft outcomes in transplantation.
    • Thanks to NGS we screen kidney grafted patients’ whole exome in order to identify unknown rare mutation, which could be associated to extreme phenotypes in transplantation. 
  • Transporters:
    • We try to identify substrates and inhibitors of protein of interest in order to document drug-drug interactions in transplantation
    • We investigate in vitro the effect of gene mutations on their structure or function.

2013-2015:

  • We studied noncoding RNA in the human immunodeficiency virus (HIV-1). Retroviruses encapsidate specific ncRNA from the host cell in addition to their own genomes into newly generated virions. We characterized the RNAs within infectious HIV-1 virions produced in human T lymphosarcoma cell line by high-throughput sequencing. We also investigated how the virus selectively incorporates a noncoding host RNA, 7SL, into virions budding.

2008-2013:

  • We studied genes expression regulation by small noncoding RNA in the major human gastric pathogen: Helicobacter pylori. The bacteria transcriptome sequencing gave us a lot of targets and we characterized a new familly of type I Toxin-Antitoxin (TA) system present on the chromosome of the bacteria, named aapA/IsoA 1 to 6. We investigated the interaction mechanism between the two RNA components of the TA system. This work led us to investigate the role of numerous enzymes in the RNA maturation/degradation pathway.

2007:

  • We developed a new and advantageous method of alkanesulphonyl chloride synthesis for the preparation of sulfonamides and sulfonylureas which have pharmaceutical profit.