Please use this identifier to cite or link to this item:
Title: Identifying purine nucleoside phosphorylase as the target of quinine using cellular thermal shift assay
Authors: Dziekan, Jerzy Michal
Yu, Han
Chen, Dan
Dai, Lingyun
Wirjanata, Grennady
Larsson, Andreas
Prabhu, Nayana
Sobota, Radoslaw Mikolaj
Bozdech, Zbynek
Nordlund, Pär
Keywords: Science::Biological sciences
Issue Date: 2019
Source: Dziekan, J. M., Yu, H., Chen, D., Dai, L., Wirjanata, G., Larsson, A., Prabhu, N., Sobota, R. M., Bozdech, Z. & Nordlund, P. (2019). Identifying purine nucleoside phosphorylase as the target of quinine using cellular thermal shift assay. Science Translational Medicine, 11(473), eaau3174-.
Project: MOH/IAFCAT2/004/2015
Journal: Science Translational Medicine
Abstract: Mechanisms of action (MoAs) have been elusive for most antimalarial drugs in clinical use. Decreasing responsiveness to antimalarial treatments stresses the need for a better resolved understanding of their MoAs and associated resistance mechanisms. In the present work, we implemented the cellular thermal shift assay coupled with mass spectrometry (MS-CETSA) for drug target identification in Plasmodium falciparum, the main causative agent of human malaria. We validated the efficacy of this approach for pyrimethamine, a folic acid antagonist, and E64d, a broad-spectrum cysteine proteinase inhibitor. Subsequently, we applied MS-CETSA to quinine and mefloquine, two important antimalarial drugs with poorly characterized MoAs. Combining studies in the P. falciparum parasite lysate and intact infected red blood cells, we found P. falciparum purine nucleoside phosphorylase (PfPNP) as a common binding target for these two quinoline drugs. Biophysical and structural studies with a recombinant protein further established that both compounds bind within the enzyme's active site. Quinine binds to PfPNP at low nanomolar affinity, suggesting a substantial contribution to its therapeutic effect. Overall, we demonstrated that implementation of MS-CETSA for P. falciparum constitutes a promising strategy to elucidate the MoAs of existing and candidate antimalarial drugs.
ISSN: 1946-6234
DOI: 10.1126/scitranslmed.aau3174
Rights: © 2019 The Authors. Some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

Page view(s)

Updated on Oct 18, 2021

Google ScholarTM




Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.