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Evidence for a cyanine link between propargylamine drugs and monoamine oxidase clarifies the inactivation mechanism

Research output: Contribution to journalArticle

Author(s)

Alen Albreht, Irena Vovk, Janez Mavri, Jose Marco-Contelles, Rona R. Ramsay

School/Research organisations

Abstract

Successful propargylamine drugs such as deprenyl inactivate monoamine oxidase (MAO), a target in multi-faceted approaches to prevent neurodegeneration in the aging population, but the chemical structure and mechanism of the irreversible inhibition are still debated. We characterized the covalent cyanine structure linking the multi-target propargylamine inhibitor ASS234 and the flavin adenine dinucleotide in MAO-A using a combination of ultra-high performance liquid chromatography, spectroscopy, mass spectrometry, and computational methods. The partial double bond character of the cyanine chain gives rise to 4 interconverting geometric isomers of the adduct which were chromatographically separated at low temperatures. The configuration of the cyanine linker governs adduct stability with segments of much higher flexibility and rigidity than previously hypothesized. The findings indicate the importance of intramolecular electrostatic interactions in the MAO binding site and provide key information relevant to incorporation of the propargyl moiety into novel multi-target drugs. Based on the structure, we propose a mechanism of MAO inactivation applicable to all propargylamine inhibitors.
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Details

Original languageEnglish
Article number169
Number of pages11
JournalFrontiers in Chemistry
Volume6
DOIs
Publication statusPublished - 28 May 2018

    Research areas

  • Monoamine oxidase, Propargylamine, Inhibition mechanism, Electrostatic interactions, Quantum chemical calculations, Isomers, Interconversion, Structure

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