| Literature DB >> 23361008 |
Shaileja Chopra1, Andrés Palencia, Cornelia Virus, Ashutosh Tripathy, Brenda R Temple, Adrian Velazquez-Campoy, Stephen Cusack, John S Reader.
Abstract
Leucyl-tRNA synthetases (LeuRSs) have an essential role in translation and are promising targets for antibiotic development. Agrocin 84 is a LeuRS inhibitor produced by the biocontrol agent Agrobacterium radiobacter K84 that targets pathogenic strains of A. tumefaciens, the causative agent of plant tumours. Agrocin 84 acts as a molecular Trojan horse and is processed inside the pathogen into a toxic moiety (TM84). Here we show using crystal structure, thermodynamic and kinetic analyses, that this natural antibiotic employs a unique and previously undescribed mechanism to inhibit LeuRS. TM84 requires tRNA(Leu) for tight binding to the LeuRS synthetic active site, unlike any previously reported inhibitors. TM84 traps the enzyme-tRNA complex in a novel 'aminoacylation-like' conformation, forming novel interactions with the KMSKS loop and the tRNA 3'-end. Our findings reveal an intriguing tRNA-dependent inhibition mechanism that may confer a distinct evolutionary advantage in vivo and inform future rational antibiotic design.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23361008 DOI: 10.1038/ncomms2421
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919