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Séminaire Chimie ED459

Synthesis of modified-tRNA to explore biological targets : application to the study of Fem transferase in Bacteria

Prof. Mélanie Éthève-Quelquejeu (équipe Chimie et Biologie, Nucléos(t)ides et Immunologie pour la Thérapie, LCBPT Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS, Université Paris-Descartes)

publié le , mis à jour le

Le Jeudi 03 décembre 2015 à 13h45
UM FdS, salle de cours SC-16.01

In addition to their role in protein synthesis aminoacyl-tRNAs (aa-tRNA) participate in various metabolic pathways as a source of ester-activated amino acids in bacteria. In order to explore the role of aa-tRNA in the biosynthesis of the peptidoglygan, a major component of the cell wall of bacteria, we develop versatile methods for the synthesis of modified aa-tRNA. We report here the synthesis of stable analogues of aa-tRNA, fluoro-tRNA and peptidyl-RNA. These novel analogues of RNAs have been developed using two strategies. The first strategy involves an enzymatic ligation by T4 RNA ligase and the second strategy is base on the solid phase synthesis and the click chemistry. One peptidyl-RNA conjugates was found to inhibit the non-ribosomal FemXWv aminoacyl-transferase with an IC50 of 90 ±9 pM ; and one was used to successfully obtain the crystallographic structure of FemXWv in Complex with the Peptidyl-RNA.

These modified tRNAs are interesting tools to investigate in the field of RNA biology.

(la conférence sera donnée en français)

Contact local IBMM : Prof. Michaël Smietana (DACAN)

Agenda

séminaire

  • Jeudi 3 décembre 2015 13:45-15:00 -

    Synthesis of modified-tRNA to explore biological targets : application to the study of Fem transferase in Bacteria

    Résumé : Séminaire Chimie ED459 – Mélanie Éthève-Quelquejeu

    Lieu : UM FdS, salle SC-16.01


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