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Targeting Mycobacterium tuberculosis Biotin Protein Ligase (MtBPL) with Nucleoside-Based Bisubstrate Adenylation Inhibitors.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2015 Sep 24; Vol. 58 (18), pp. 7349-7369. Date of Electronic Publication: 2015 Sep 03. - Publication Year :
- 2015
-
Abstract
- Mycobacterium tuberculosis (Mtb), responsible for both latent and symptomatic tuberculosis (TB), remains the second leading cause of mortality among infectious diseases worldwide. Mycobacterial biotin protein ligase (MtBPL) is an essential enzyme in Mtb and regulates lipid metabolism through the post-translational biotinylation of acyl coenzyme A carboxylases. We report the synthesis and evaluation of a systematic series of potent nucleoside-based inhibitors of MtBPL that contain modifications to the ribofuranosyl ring of the nucleoside. All compounds were characterized by isothermal titration calorimetry (ITC) and shown to bind potently with K(D)s ≤ 2 nM. Additionally, we obtained high-resolution cocrystal structures for a majority of the compounds. Despite fairly uniform biochemical potency, the whole-cell Mtb activity varied greatly with minimum inhibitory concentrations (MIC) ranging from 0.78 to >100 μM. Cellular accumulation studies showed a nearly 10-fold enhancement in accumulation of a C-2'-α analogue over the corresponding C-2'-β analogue, consistent with their differential whole-cell activity.
- Subjects :
- Antitubercular Agents chemical synthesis
Antitubercular Agents pharmacology
Bacterial Proteins metabolism
Biotinylation
Carbon-Nitrogen Ligases metabolism
Crystallography, X-Ray
Microbial Sensitivity Tests
Models, Molecular
Mycobacterium tuberculosis drug effects
Nucleosides chemical synthesis
Nucleosides pharmacology
Protein Conformation
Stereoisomerism
Structure-Activity Relationship
Thermodynamics
Antitubercular Agents chemistry
Bacterial Proteins antagonists & inhibitors
Carbon-Nitrogen Ligases antagonists & inhibitors
Mycobacterium tuberculosis enzymology
Nucleosides chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 58
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 26299766
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.5b00719