Computational approach for decoding Malaria Drug Targets from Single-Cell Transcriptomics and finding potential drug molecule

choudhuri, s.; Ghosh, B.

doi:10.1101/2024.01.22.576718

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bioRxiv · 10.1101/2024.01.22.576718

Computational approach for decoding Malaria Drug Targets from Single-Cell Transcriptomics and finding potential drug molecule

choudhuri, s.·Ghosh, B.

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Abstract

Malaria is a deadly disease caused by Plasmodium parasites. While potent drugs are available in the market for malaria treatment, over the years, Plasmodium parasites have successfully developed resistance against many, if not all, front-line drugs. This poses a serious threat to global malaria eradication efforts, and the continued discovery of new drugs is necessary to tackle this debilitating disease. With the advent of recent unprecedented progress in machine learning techniques, single-cell transcriptomic in Plasmodium offers a powerful tool for identifying crucial proteins as a drug target and subsequent computational prediction of potential drugs. In this study, We have implemented a mutual-information-based feature reduction algorithm with a classification algorithm to select important proteins from transcriptomic datasets (sexual and asexual stages) for Plasmodium falciparum and then constructed the protein-protein interaction (PPI) networks of the proteins. The analysis of this PPI network revealed key proteins vital for the survival of Plasmodium falciparum. Based on the function and identification of a few strong binding sites on a couple of these key proteins, we computationally predicted a set of potential drug molecules using a deep learning-based technique. Lead drug molecules that satisfy ADMET and drug-likeliness properties are finally reported out of the generated drugs. The study offers a general computational pipeline to identify crucial proteins using scRNA-seq data sets and further development of potential new drugs.

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choudhuri, s., Ghosh, B.. 2024-01-25. Computational approach for decoding Malaria Drug Targets from Single-Cell Transcriptomics and finding potential drug molecule. https://doi.org/10.1101/2024.01.22.576718

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