Ebbe Nordlander
Professor
Evaluation of Au(III) complexes as Plasmodium falciparum aquaglyceroporin (PfAQP) inhibitors by in silico and in vitro methods
Author
Summary, in English
The onset of resistance to artemisinin for malaria treatment has stimulated the quest for novel antimalarial drugs. Herein, the gold(III) coordination complexes Aubipy [Au(bipy)Cl]+ (bipy = 2,2'-bipyridine), Auphen [Au(phen)Cl]+ (phen = phenanthroline), Auterpy [Au(terpy)Cl]2+ (terpy = 2,2';6',2″-terpyridine), and corresponding hydrolyzed species, have been investigated as inhibitors of the Plasmodium falciparum aquaglyceroporin (PfAQP) protein by computational methods. Through an in-silico approach using an Umbrella Sampling protocol to sample how Aubipy, Auphen, and Auterpy permeate through the PfAQP, their permeability coefficients were estimated using the Inhomogeneous Solubility Diffusion (ISD) model with promising results. The efficacy of the gold complexes was then probed by an in vitro assay testing the growth inhibition in chloroquine sensitive and resistant P. falciparum strains. In accordance with the computational data, Auterpy achieved the highest efficiency with an IC50 in the nanomolar range (590 nM) on resistant strain cultures, additionally revealing a good selectivity as compared to its activity against the human aquaglyceroporin 3.
Department/s
- Malaria and Babesia
- Division of Clinical Chemistry and Pharmacology
- Centre for Analysis and Synthesis
- LU Profile Area: Light and Materials
- Chemical Physics
Publishing year
2024-11-23
Language
English
Pages
821-836
Publication/Series
Journal of Biological Inorganic Chemistry
Volume
29
Issue
7-8
Document type
Journal article
Publisher
Springer
Topic
- Pharmaceutical Sciences
- Infectious Medicine
Status
Published
Research group
- Malaria and Babesia
ISBN/ISSN/Other
- ISSN: 1432-1327