Recent advances in glycosome biogenesis and its implications for drug discovery

The phylum Euglenozoa, within the Eukaryote domain, includes diverse protists such as the medically significant kinetoplastids, characterized by their unique kinetoplast DNA. Both kinetoplastids and their sister class Diplonemea possess glycosomes - specialized microbodies that compartmentalize glycolysis and other metabolic pathways. Glycosomes likely evolved in a common ancestor of kinetoplastid and diplonemids, conferring metabolic flexibility and reducing cellular toxicity. These organelles are essential for parasite survival and thus, represent promising drug targets for treating kinetoplastid diseases. While the basic principles of peroxisome and glycosome biogenesis are conserved, distinct features in glycosome biogenesis machinery and a lower level of sequence conservation enables pathogen specific drug design for developing new therapies. This review summarizes our current knowledge on glycosome biogenesis, recent advances, and therapeutic potential for treating trypanosomatid infections.

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Publication Details

Journal
Biological Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1515/hsz-2025-0183
Primary Topic
Trypanosoma species research and implications
Type
article
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article

Recent advances in glycosome biogenesis and its implications for drug discovery

Vishal C. Kalel, Lary C. Walker, Ralf Erdmann, Chethan K. Krishna et al.
Biological Chemistry
Trypanosoma species research and implications
article

Recent advances in glycosome biogenesis and its implications for drug discovery

Vishal C. Kalel, Lary C. Walker, Ralf Erdmann, Chethan K. Krishna, Lisa Hohnen
article en

Abstract

The phylum Euglenozoa, within the Eukaryote domain, includes diverse protists such as the medically significant kinetoplastids, characterized by their unique kinetoplast DNA. Both kinetoplastids and their sister class Diplonemea possess glycosomes - specialized microbodies that compartmentalize glycolysis and other metabolic pathways. Glycosomes likely evolved in a common ancestor of kinetoplastid and diplonemids, conferring metabolic flexibility and reducing cellular toxicity. These organelles are essential for parasite survival and thus, represent promising drug targets for treating kinetoplastid diseases. While the basic principles of peroxisome and glycosome biogenesis are conserved, distinct features in glycosome biogenesis machinery and a lower level of sequence conservation enables pathogen specific drug design for developing new therapies. This review summarizes our current knowledge on glycosome biogenesis, recent advances, and therapeutic potential for treating trypanosomatid infections.

Biological ChemistryVol. 406(10-12)
Ruhr University Bochum (DE)
Openalex Percentile: Top 51%
Trypanosoma species research and implications
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