The Trypanosoma brucei sphingolipid synthase, an essential enzyme and drug target

Mina, J.G.; Pan, S.Y.; Wansadhipathi, N.K.; Bruce, C.; Shams-Eldin, H.; Schwarz, R.T.; Steel, P.G.; Denny, P.W.

Abstract

Sphingolipids are important components of eukaryotic membranes, particularly the plasma membrane, and are involved in a diverse array of signal transduction processes. In the Eukaryota the biosynthetic pathway for the formation of these lipid species is largely conserved. However, in contrast to mammals which produce sphingomyelin (SM), several pathogenic fungi and protozoa synthesize inositol phosphorylceramide (IPC) as the primary phosphosphingolipid. This process is catalyzed by the enzyme IPC synthase, a recognized target for anti-fungals encoded by the AUR1 gene in yeast. Recently, functional orthologues of the AUR1p have been identified in a group of insect vector-borne pathogenic protozoa, the Kinetoplastida, which are responsible for a range of so-called neglected diseases. Of these the Trypanosoma brucei species are the causative agents of human African trypanosomiasis in many of the most under-developed regions of Africa. The available treatments for these diseases are limited, of decreasing efficacy, and often demonstrate severe side-effects. Against this background the T. brucei sphingolipid synthase, an orthologue of the yeast AUR1p, may represent a promising target for novel anti-protozoals. Our studies identify an isoform of this protein as a novel bi-functional enzyme capable of catalyzing the synthesis of both IPC and SM, both known to be present in the parasite. Furthermore, the synthase is essential for parasite growth and can be inhibited by a known anti-fungal at low nanomolar levels in vitro. Most notably this drug demonstrates trypanocidal activity against cultured bloodstream form parasites. Thus, the T. brucei sphingolipid synthase represents a valid and promising drug target.

Citation

Mina, J., Pan, S., Wansadhipathi, N., Bruce, C., Shams-Eldin, H., Schwarz, R., …Denny, P. (2009). The Trypanosoma brucei sphingolipid synthase, an essential enzyme and drug target. Molecular and Biochemical Parasitology, 168(1), 16-23. https://doi.org/10.1016/j.molbiopara.2009.06.002

• Journal Article Type: Article
• Acceptance Date: Jun 11, 2009
• Online Publication Date: Jun 21, 2009
• Publication Date: Nov 1, 2009
• Deposit Date: Aug 13, 2009
• Publicly Available Date: Sep 3, 2009
• Journal: Molecular and Biochemical Parasitology
• Print ISSN: 0166-6851
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 168
• Issue: 1
• Pages: 16-23
• DOI: https://doi.org/10.1016/j.molbiopara.2009.06.002
• Keywords: Trypanosoma, Trypanosomiasis, Sphingolipid synthase, Drug target.
• Public URL: https://durham-repository.worktribe.com/output/1558498