Identification of the Binding Site of Apical Membrane Antigen 1 (AMA1) Inhibitors Using a Paramagnetic Probe. (13th February 2019)

• Record Type: Journal Article
• Authors: Akter, Mansura; Drinkwater, Nyssa; Devine, Shane M.; Drew, Simon C.; Krishnarjuna, Bankala; Debono, Cael O.; Wang, Geqing; Scanlon, Martin J.; Scammells, Peter J.; McGowan, Sheena; MacRaild, Christopher A.; Norton, Raymond S.
• Is Part Of: ChemMedChem. Volume 14:Number 5(2019)
• Page Start: 603
• Page End: 612
• Publication Date: 2019-02-13
• Subjects: AMA1 -- drug discovery -- malaria -- NMR spectroscopy -- spin label; Pharmaceutical chemistry -- Periodicals; 615.19005
• DOI: 10.1002/cmdc.201800802
• Languages: English
• ISSNs: 1860-7179

Abstract

Abstract: Apical membrane antigen 1 (AMA1) is essential for the invasion of host cells by malaria parasites. Several small‐molecule ligands have been shown to bind to a conserved hydrophobic cleft in Plasmodium falciparum AMA1. However, a lack of detailed structural information on the binding pose of these molecules has hindered their further optimisation as inhibitors. We have developed a spin‐labelled peptide based on RON2, the native binding partner of AMA1, to probe the binding sites of compounds on Pf AMA1. The crystal structure of this peptide bound to Pf AMA1 shows that it binds at one end of the hydrophobic groove, leaving much of the binding site unoccupied and allowing fragment hits to bind without interference. In paramagnetic relaxation enhancement (PRE)‐based NMR screening, the 1 H relaxation rates of compounds binding close to the probe were enhanced. Compounds experienced different degrees of PRE as a result of their different orientations relative to the spin label while bound to AMA1. Thus, PRE‐derived distance constraints can be used to identify binding sites and guide further hit optimisation. Abstract : Probing binding sites : We designed and developed a spin‐labelled peptide probe that binds to one end of the hydrophobic cleft (green surface) of P. falciparum apical membrane antigen 1 (AMA1) and exerts a paramagnetic relaxation enhancement effect on molecules bound nearby (≈15–20 Å). Thus, the probe better defines the binding site of the molecule in the cleft. This structural information will help guide future hit optimisation efforts in antimalarial drug discovery.