Screening-based discovery and structural dissection of a novel family 18 chitinase inhibitor

Alexander W. Schüttelkopf, Ole A. Andersen, Francesco V. Rao, Matthew Allwood, Clare Lloyd, Ian M. Eggleston, Daan M. F. van Aalten

    Research output: Contribution to journalArticlepeer-review

    44 Citations (Scopus)

    Abstract

    Family 18 chitinases play key roles in the life cycles of a variety of organisms ranging from bacteria to man. Very recently it has been shown that one of the mammalian chitinases is highly overexpressed in the asthmatic lung and contributes to the pathogenic process through recruitment of inflammatory cells. Although several potent natural product chitinase inhibitors have been identified, their chemotherapeutic potential or their use as cell biological tools is limited due to their size, complex chemistry, and limited availability. We describe a virtual screening-based approach to identification of a novel, purine-based, chitinase inhibitor. This inhibitor acts in the low micromolar (Ki = 2.8 ± 0.2 µm) range in a competitive mode. Dissection of the binding mode by x-ray crystallography reveals that the compound, which consistsof two linked caffeine moieties, binds in the active site through extensive and not previously observed stacking interactions with conserved solvent exposetryptophans. Such exposed aromatics are also present in the structures of many other carbohydrate processing enzymes. The compound exhibits favorable chemical properties and is likely to be useful as a general scaffold for development of pan-family 18 chitinase inhibitors.

    Original languageEnglish
    Pages (from-to)27278-27285
    Number of pages8
    JournalJournal of Biological Chemistry
    Volume281
    Issue number37
    DOIs
    Publication statusPublished - 15 Sep 2006

    Fingerprint

    Dive into the research topics of 'Screening-based discovery and structural dissection of a novel family 18 chitinase inhibitor'. Together they form a unique fingerprint.

    Cite this