Authors
Das, R., Dutta, S., Bhattacharjee, S.
Abstract
Emerging Plasmodium falciparum resistance to frontline artemisinin (ART) derivatives threatens global malaria control efforts. Current protocols assigning ART-sensitive (ART-S) or -resistant (ART-R) phenotypes to parasite strains with Kelch13 (K13) mutations remain time-intensive for real-time surveillance. Ring-survival assay (RSA), an ex vivo gold standard mandates laboratory-adaptation under culture conditions and frequently does not replicate clinical ART-responsiveness, thereby limiting its utility for rapidly triaging newly emerging K13 variants. In contrast, advent of artificial intelligence (AI)-derived models hold potential to screen >100 K13 variants within hours, enabling rapid near-real-time prediction of ART-S/R. Here, we engineered a panel of forty representative K13 variants by computing their relative deviations from wild-type K13 across ten physicochemical and structural descriptors, yielding a compact feature set which captures mutation-induced perturbations in folding, stability, and solvent exposure. These can be further utilized to train and validate AI classifier to predict resistance.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 10 Nov 2026.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 1
- Comments 0