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Non-Vesicular Lipid Transport Machinery in : Functional Implications in Host-Parasite Interaction

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Jul 14
PMID 37445815
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Abstract

Eukaryotic cells have distinct membrane-enclosed organelles, each with a unique biochemical signature and specialized function. The unique identity of each organelle is greatly governed by the asymmetric distribution and regulated intracellular movement of two important biomolecules, lipids, and proteins. Non-vesicular lipid transport mediated by lipid-transfer proteins (LTPs) plays essential roles in intra-cellular lipid trafficking and cellular lipid homeostasis, while vesicular transport regulates protein trafficking. A comparative analysis of non-vesicular lipid transport machinery in protists could enhance our understanding of parasitism and basis of eukaryotic evolution. , the trypanosomatid parasite, greatly depends on receptor-ligand mediated signalling pathways for cellular differentiation, nutrient uptake, secretion of virulence factors, and pathogenesis. Lipids, despite being important signalling molecules, have intracellular transport mechanisms that are largely unexplored in . We have identified a repertoire of sixteen (16) potential lipid transfer protein (LTP) homologs based on a domain-based search on TriTrypDB coupled with bioinformatics analyses, which signifies the presence of well-organized lipid transport machinery in this parasite. We emphasized here their evolutionary uniqueness and conservation and discussed their potential implications for parasite biology with regards to future therapeutic targets against visceral leishmaniasis.

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References
1.
Mishkind M, Vermeer J, Darwish E, Munnik T . Heat stress activates phospholipase D and triggers PIP accumulation at the plasma membrane and nucleus. Plant J. 2009; 60(1):10-21. DOI: 10.1111/j.1365-313X.2009.03933.x. View

2.
Chiapparino A, Maeda K, Turei D, Saez-Rodriguez J, Gavin A . The orchestra of lipid-transfer proteins at the crossroads between metabolism and signaling. Prog Lipid Res. 2015; 61:30-9. DOI: 10.1016/j.plipres.2015.10.004. View

3.
Sunter J, Gull K . Shape, form, function and pathogenicity: from textbook descriptions to biological understanding. Open Biol. 2017; 7(9). PMC: 5627057. DOI: 10.1098/rsob.170165. View

4.
Blom T, Somerharju P, Ikonen E . Synthesis and biosynthetic trafficking of membrane lipids. Cold Spring Harb Perspect Biol. 2011; 3(8):a004713. PMC: 3140686. DOI: 10.1101/cshperspect.a004713. View

5.
Thakur L, Singh K, Shanker V, Negi A, Jain A, Matlashewski G . Atypical leishmaniasis: A global perspective with emphasis on the Indian subcontinent. PLoS Negl Trop Dis. 2018; 12(9):e0006659. PMC: 6159859. DOI: 10.1371/journal.pntd.0006659. View