TY  - JOUR
ID  - open3331
UR  - http://crdd.osdd.net/open/3331/
IS  - 1
A1  - Rahman, Abdur
A1  - Tamseel, Sabahat
A1  - Dutta, Smritikana
A1  - Khan, Nawaal
A1  - Faaiz, Mohammad
A1  - Rastogi, Harshita
A1  - Nath, Jyoti Rani
A1  - Haldar, Kasturi
A1  - Chowdhury, Pramit
A1  - Ashish, 
A1  - Bhattacharjee, Souvik
Y1  - 2024/11//
N2  - The potency of frontline antimalarial drug artemisinin (ART) derivatives is triggered by heme-induced cleavage of the endoperoxide bond to form reactive heme-ART alkoxy radicals and covalent heme-ART adducts, which are highly toxic to the parasite. ART-resistant (ART-R) parasites with mutations in the Plasmodium falciparum Kelch-containing protein Kelch13 (PfKekch13) exhibit impaired hemoglobin uptake, reduced yield of hemoglobin-derived heme, and thus decreased ART activation. However, any direct involvement of PfKelch13 in heme-mediated ART activation has not been reported. Here, we show that the purified recombinant PfKelch13 wild-type (WT) protein displays measurable binding affinity for iron and heme, the main effectors for ART activation. The heme-binding property is also exhibited by the native PfKelch13 protein from parasite culture. The two ART-R recombinant PfKelch13 mutants (C580Y and R539T) display weaker heme binding affinities compared to the ART-sensitive WT and A578S mutant proteins, which further translates into reduced yield of heme-ART derivatives when ART is incubated with the heme molecules bound to the mutant PfKelch13 proteins. In conclusion, this study provides the first evidence for ART activation via the heme-binding propensity of PfKelch13. This mechanism may contribute to the modulation of ART-R levels in malaria parasites through a novel function of PfKelch13.
PB  - Springer Science and Business Media LLC
JF  - Commun. Biol.
VL  - 7
TI  - Artemisinin-resistant Plasmodium falciparum Kelch13 mutant proteins display reduced heme-binding affinity and decreased artemisinin activation
ER  -