The structure of Mycobacteria 2C-methyl-D-erythritol-2,4-cyclodiphosphatesynthase, an essential enzyme, provides a platform for drug discovery

Lori Buetow, Amanda C. Brown, Tanya Parish, William N. Hunter

    Research output: Contribution to journalArticle

    36 Citations (Scopus)

    Abstract

    Background: The prevalence of tuberculosis, the prolonged and expensive treatment that this disease requires and an increase in drug resistance indicate an urgent need for new treatments. The 1-deoxy-D-xylulose5-phosphate pathway of isoprenoid precursor biosynthesis is an attractive chemotherapeutic target because it occurs in many pathogens, including Mycobacterium tuberculosis, and is absent from humans. To underpin future drug development it is important to assess which enzymes in this biosynthetic pathway are essential in the actual pathogens and to characterize them.

    Results: The fifth enzyme of this pathway, encoded by ispF, is 2C-methyl-D-erythritol-2,4-cyclodiphosphate synthase (IspF). A two-step recombination strategy was used to construct ispF deletion mutants in M. tuberculosis but only wild-type double crossover strains were isolated. The chromosomal copy could be deleted when a second functional copy was provided on an integrating plasmid, demonstrating that ispF is an essential gene under the conditions tested thereby confirming its potential as a drug target. We attempted structure determination of the M. tuberculosis enzyme (MtlspF), but failed to obtain crystals. We instead analyzed the orthologue M. smegmatis IspF (MslspF), sharing 73% amino acid sequence identity, at 2.2 angstrom resolution. The high level of sequence conservation is particularly pronounced in and around the active site. MslspF is a trimer with a hydrophobic cavity at its center that contains density consistent with diphosphate-containing isoprenoids. The active site, created by two subunits, comprises a rigid CDP-Zn2+ binding pocket with a flexible loop to position the 2C-methyl-D-erythritol moiety of substrate. Sequence-structure comparisons indicate that the active site and interactions with ligands are highly conserved.

    Conclusion: Our study genetically validates MtlspF as a therapeutic target and provides a model system for structure-based ligand design.

    Original languageEnglish
    Article number68
    Pages (from-to)-
    Number of pages11
    JournalBMC Structural Biology
    Volume7
    DOIs
    Publication statusPublished - 23 Oct 2007

    Keywords

    • NON-MEVALONATE PATHWAY
    • ISOPRENOID PRECURSOR BIOSYNTHESIS
    • ESCHERICHIA-COLI
    • 2,4-CYCLODIPHOSPHATE SYNTHASE
    • MACROMOLECULAR STRUCTURES
    • HAEMOPHILUS-INFLUENZAE
    • ESSENTIAL GENE
    • TUBERCULOSIS
    • PROTEIN
    • IDENTIFICATION

    Cite this