Design and Synthesis of Conformationally Constrained Cyclophilin Inhibitors Showing a Cyclosporin-A Phenotype in C. elegans

Colin J. Dunsmore, Kirk J. Malone, Kevin R. Bailey, Martin A. Wear, Hannah Florance, Sally Shirran, Perdita E. Barran, Antony P. Page, Malcolm D. Walkinshaw, Nicholas J. Turner

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Cyclophilin A (CypA) is a member of the immunophilin family of proteins and receptor for the immunosuppressant drug cyclosporin A (CsA). Here we describe the design and synthesis of a new class of small-molecule inhibitors for CypA that are based upon a dimedone template. Electrospray mass spectrometry is utilised as an initial screen to quantify the protein affinity of the ligands. Active inhibitors and fluorescently labelled derivatives are then used as chemical probes for investigating the biological role of cyclophilins in the nematode Caenorhabditis elegans. Small but effective: We describe the design and synthesis of small-molecule inhibitors for cyclophilin A, based upon a dimedone template. Mass spectrometry was used as an initial screen to quantify the affinity of the ligands for the protein. The biological role of cyclophilins in the nematode Caenorhabditis elegans was investigated with active inhibitors and fluorescent derivatives as chemical probes. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
    Original languageEnglish
    Pages (from-to)802-810
    Number of pages8
    JournalChemBioChem: a European journal of chemical biology
    Volume12
    Issue number5
    DOIs
    Publication statusPublished - 21 Mar 2011

    Keywords

    • drug design
    • enzyme inhibitors
    • fluorescent probes
    • mass spectrometry
    • medicinal chemistry
    • ionization mass-spectrometry
    • quantitative-determination
    • caenorhabditis-elegans
    • dissociation-constants
    • ligand complexes
    • cis/trans isomerases
    • binding
    • discovery
    • protein
    • mechanism

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