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dc.contributor.authorFerguson, Lindsay
dc.contributor.authorWells, Geoff
dc.contributor.authorBhakta, Sanjib
dc.contributor.authorJohnson, James
dc.contributor.authorGuzman, Junitta
dc.contributor.authorParish, Tanya
dc.contributor.authorPrentice, Robin
dc.contributor.authorBrucoli, Federico
dc.date.accessioned2019-09-05T13:10:45Z
dc.date.available2019-09-05T13:10:45Z
dc.date.issued2019-08-27
dc.identifier.citationLindsay Ferguson, Geoff Wells, Sanjib Bhakta, James Johnson, Junitta Guzman, Tanya Parish, Robin Stacy and Federico Brucoli* Integrated target-based and phenotypic screening approaches for the identification of anti-tubercular agents that bind to the mycobacterial adenylating enzyme MbtA. ChemMedChem, 2019 (published ahead of print) DOI: 10.1002/cmdc.201900217.en
dc.identifier.urihttps://www.dora.dmu.ac.uk/handle/2086/18410
dc.descriptionResearch groups / departments involved in this project: [a] School of Science, University of the West of Scotland, Paisley, PA1 2BE, Scotland, UK [b] UCL School of Pharmacy, University College London, 29/39 Brunswick Square, London, WC1N 1AX, UK [c] Department of Biological Sciences, Institute of Structural and Molecular Biology, Birkbeck, University of London, London, WC1E 7HX, UK [d] TB Discovery Research, Infectious Disease Research Institute, 1616 Eastlake Avenue East, Seattle, WA 98102, USA [e] Seattle Structural Genomics Center for Infectious Disease, Seattle WA, USA [f] Center for Global Infectious Disease Research, Seattle Children’s Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, USA g] Leicester School of Pharmacy, De Montfort University, Leicester, LE1 9BH, UK The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link.en
dc.description.abstractIron is essential for the pathogenicity and virulence of Mycobacterium tuberculosis, which synthesises salicyl-capped siderophores (mycobactins) to acquire this element from the host. MbtA is the adenylating enzyme that catalyses the initial reaction of mycobactins’ biosynthesis and is solely expressed by mycobacteria. A 3,200-member library comprised of lead-like, structurally-diverse compounds was screened against M. tuberculosis for whole-cell inhibitory activity. A set of 846 compounds that inhibited the tubercle bacilli growth were then tested for their ability to bind to MbtA using a fluorescence-based thermal shift assay and NMR-based Water-LOGSY and Saturation Transfer Difference (STD) experiments. We identified an attractive hit-molecule, 5-hydroxy-indol-3-ethylamino-(2-nitro-4-trifluoromethyl)benzene (5), that bound with high affinity to MbtA and produced a MIC90 of 13 µM. The ligand was docked into the MbtA crystal structure and displayed an excellent fit within the MbtA active pocket, adopting a different binding mode to the established MbtA inhibitor Sal-AMS.en
dc.language.isoenen
dc.publisherWileyen
dc.subjectTuberculosis drug discoveryen
dc.subjectphenotypic and target-based screeningen
dc.subjectmycobactins / siderophoresen
dc.subjectmycobacterial iron homeostasisen
dc.subjectNMR Water-LOGSYen
dc.subjectSaturation Transfer Differenceen
dc.subjectNMR spectroscopyen
dc.subjectFluorescent-based Thermal Shift Assayen
dc.titleIntegrated target-based and phenotypic screening approaches for the identification of anti-tubercular agents that bind to the mycobacterial adenylating enzyme MbtAen
dc.typeArticleen
dc.identifier.doihttps://dx.doi.org/10.1002/cmdc.201900217
dc.peerreviewedYesen
dc.funderOther external funder (please detail below)en
dc.projectidContract Nos.: HHSN272201200025C and HHSN272201700059Cen
dc.cclicenceCC-BY-NC-NDen
dc.date.acceptance2019-08
dc.researchinstituteLeicester Institute for Pharmaceutical Innovation - From Molecules to Practice (LIPI)en
dc.funder.otherU.S. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services,en


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