Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101701
Title: Identification of LasR ligands through a virtual screening approach
Authors: Skovstrup, Søren
Le Quement, Sebastian Thordal
Hansen, Thomas
Jakobsen, Tim Holm
Harmsen, Morten
Tolker-Nielsen, Tim
Nielsen, Thomas E.
Givskov, Michael
Taboureau, Olivier
Keywords: DRNTU::Science::Medicine::Biomedical engineering
Issue Date: 2013
Source: Skovstrup, S., Le Quement, S. T., Hansen, T., Jakobsen, T. H., Harmsen, M., Tolker-Nielsen, T., et al. (2013). Identification of LasR Ligands through a Virtual Screening Approach. ChemMedChem, 8(1), 157-163.
Series/Report no.: ChemMedChem
Abstract: With the widespread occurrence of bacterial resistance to antibiotics, the development of new strategies beyond conventional treatments is a pursuit taken by public health institutions worldwide. LasR, a transcription factor that controls quorum sensing in Pseudomonas aeruginosa, has emerged as an attractive therapeutic target for the next generation of antimicrobial agents. In the present study, a virtual screening workflow combining pharmacophore- and structure-based approaches was used to identify new LasR ligands. Five novel inducers and three inhibitors of LasR activity were validated experimentally by use of a cell-based assay. Interestingly, these compounds are molecularly distinct from the native signal molecule, N-3-oxododecanoyl-L-homoserine lactone (OHN), and may serve as lead structures for the design of new drugs. The binding modes of these compounds to the OHN binding site in LasR were predicted and used to identify the key interactions that contribute to the induction and inhibition of LasR activity.
URI: https://hdl.handle.net/10356/101701
http://hdl.handle.net/10220/19785
ISSN: 1860-7179
DOI: 10.1002/cmdc.201200434
Rights: © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SCELSE Journal Articles

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