Methylxanthine drugs are chitinase inhibitors: investigation of inhibition and binding modes

Francesco V. Rao, Ole A. Andersen, Kalpit A. Vora, Julie A. DeMartino, Daan M. F. van Aalten

    Research output: Contribution to journalArticlepeer-review

    85 Citations (Scopus)

    Abstract

    Family 18 chitinases play key roles in a range of pathogenic organisms and are overexpressed in the asthmatic lung. By screening a library of marketed drug molecules, we have identified methylxanthine derivatives as possible inhibitor leads. These derivatives, theophylline, caffeine, and pentoxifylline, are used therapeutically as antiinflammatory agents, with pleiotropic mechanisms of action. Here it is shown that they are also competitive inhibitors against a fungal family 18 chitinase, with pentoxifylline being the most potent (Ki of 37 µM). Crystallographic analysis of chitinase-inhibitor complexes revealed specific interactions with the active site, mimicking the reaction intermediate analog, allosamidin. Mutagenesis identified the key active site residues, conserved in mammalian chitinases, which contribute to inhibitor affinity. Enzyme assays also revealed that these methylxanthines are active against human chitinases.

    Original languageEnglish
    Pages (from-to)973-980
    Number of pages8
    JournalChemistry & Biology
    Volume12
    Issue number9
    DOIs
    Publication statusPublished - 1 Sep 2005

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